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2025Activity report​​Project-TeamCOMMEDIA

RNSR: 201923240H​​​‌

Creation of the Project-Team:​​​‌ 2019 June 01

Each‌ year, Inria research teams‌​‌ publish an Activity Report​​ presenting their work and​​​‌ results over the reporting‌ period. These reports follow‌​‌ a common structure, with​​ some optional sections depending​​​‌ on the specific team.‌ They typically begin by‌​‌ outlining the overall objectives​​ and research programme, including​​​‌ the main research themes,‌ goals, and methodological approaches.‌​‌ They also describe the​​ application domains targeted by​​​‌ the team, highlighting the‌ scientific or societal contexts‌​‌ in which their work​​ is situated.

The reports​​​‌ then present the highlights‌ of the year, covering‌​‌ major scientific achievements, software​​ developments, or teaching contributions.​​​‌ When relevant, they include‌ sections on software, platforms,‌​‌ and open data, detailing​​ the tools developed and​​​‌ how they are shared.‌ A substantial part is‌​‌ dedicated to new results,​​ where scientific contributions are​​​‌ described in detail, often‌ with subsections specifying participants‌​‌ and associated keywords.

Finally,​​ the Activity Report addresses​​​‌ funding, contracts, partnerships, and‌ collaborations at various levels,‌​‌ from industrial agreements to​​ international cooperations. It also​​​‌ covers dissemination and teaching‌ activities, such as participation‌​‌ in scientific events, outreach,​​​‌ and supervision. The document​ concludes with a presentation​‌ of scientific production, including​​ major publications and those​​​‌ produced during the year.​

Keywords

Computer Science and​‌ Digital Science

  • A6.1.1. Continuous​​ Modeling (PDE, ODE)
  • A6.1.4.​​​‌ Multiscale modeling
  • A6.1.5. Multiphysics​ modeling
  • A6.2.1. Numerical analysis​‌ of PDE and ODE​​
  • A6.3.1. Inverse problems
  • A6.3.2.​​​‌ Data assimilation
  • A6.3.4. Model​ reduction

Other Research Topics​‌ and Application Domains

  • B2.2.1.​​ Cardiovascular and respiratory diseases​​​‌
  • B2.4.1. Pharmaco kinetics and​ dynamics

1 Team members,​‌ visitors, external collaborators

Research​​ Scientists

  • Miguel Angel Fernández​​​‌ Varela [Team leader​, INRIA, Senior​‌ Researcher, HDR]​​
  • Céline Grandmont [INRIA​​​‌, Senior Researcher,​ HDR]
  • Damiano Lombardi​‌ [INRIA, Senior​​ Researcher, from Oct​​​‌ 2025, HDR]​
  • Damiano Lombardi [INRIA​‌, Researcher, until​​ Sep 2025, HDR​​​‌]
  • Frédérique Noël [​CNRS, Researcher]​‌
  • Marina Vidrascu [INRIA​​, Emeritus]

Faculty​​​‌ Members

  • Guillaume Delay [​SORBONNE UNIVERSITE, Associate​‌ Professor Delegation, from​​ Sep 2025]
  • Guillaume​​​‌ Delay [SORBONNE UNIVERSITE​, Associate Professor,​‌ until Aug 2025]​​
  • Fabien Vergnet [SORBONNE​​​‌ UNIVERSITE, Associate Professor​, from Sep 2025​‌]
  • Fabien Vergnet [​​SORBONNE UNIVERSITE, Associate​​​‌ Professor Delegation, until​ Aug 2025]

PhD​‌ Students

  • Marguerite Champion [​​CNRS, until Sep​​​‌ 2025]
  • Abdelkhalak Chetoui​ [DASSAULT SYSTEMES,​‌ CIFRE, from Apr​​ 2025]
  • Davide Pietro​​​‌ Duva [SORBONNE UNIVERSITE​]
  • Corrie James [​‌UVSQ]
  • Gaël Le​​ Ruz [INRIA,​​​‌ from Oct 2025 until​ Nov 2025]
  • Gaël​‌ Le Ruz [SORBONNE​​ UNIVERSITE, until Sep​​​‌ 2025]
  • Romain Lemore​ [SAS CASIS,​‌ CIFRE]
  • Romain Lopez-Surjus​​ [INRIA]
  • Oscar​​​‌ Ruz [ANID Chile​, until Jan 2025​‌]

Technical Staff

  • Carlos​​ Brito Pacheco [INRIA​​​‌, Engineer]
  • Daniele​ Carlo Corti [INRIA​‌, Engineer]

Interns​​ and Apprentices

  • Renee Crispo​​​‌ [INRIA, Intern​, from Apr 2025​‌ until Jul 2025]​​
  • Dongjiao Hong [INRIA​​​‌, Intern, from​ Jun 2025 until Sep​‌ 2025]

Administrative Assistant​​

  • Eugenie-Marie Montagne [INRIA​​​‌]

Visiting Scientists

  • Erik​ Burman [University College​‌ London, from Oct​​ 2025 until Oct 2025​​​‌]
  • Erik Burman [​University College London,​‌ from Apr 2025 until​​ Apr 2025]
  • Buyang​​​‌ Li [The Hong​ Kong Polytechnic University,​‌ from Jun 2025 until​​ Jul 2025]
  • Maxim​​​‌ Olshanskii [University of​ Houston, from Jun​‌ 2025 until Jul 2025​​]

2 Overall objectives​​​‌

COMMEDIA is a joint​ project-team of the Inria​‌ Research Center of Paris​​ and the Jacques-Louis Lions​​​‌ Laboratory (LJLL) of Sorbonne​ Université and CNRS (UMR7598).​‌ The research activity of​​ COMMEDIA focuses on the​​​‌ numerical simulation of bio-fluid​ flows in the human​‌ body, more specifically, blood​​ flows in the cardiovascular​​​‌ system and air flows​ in the respiratory system.​‌ These simulations are intended​​ to complement available clinical​​​‌ data with the following​ purpose: help clinicians or​‌ bio-engineers to enhance the​​ understanding of physiological phenomena,​​ to improve diagnosis and​​​‌ therapy planning or to‌ optimize medical devices. The‌​‌ main objectives of COMMEDIA​​ are:

  • the development of​​​‌ appropriate mathematical models and‌ efficient numerical methods for‌​‌ the simulations and for​​ the interaction of simulations​​​‌ with measured data;
  • the‌ mathematical analysis of these‌​‌ models and numerical techniques;​​
  • the development and validation​​​‌ of scientific computing software‌ which implements these numerical‌​‌ techniques.

A distinctive feature​​ of the mathematical models​​​‌ considered in COMMEDIA is‌ that they often couple‌​‌ different types of partial​​ differential equations (PDEs). This​​​‌ heterogeneous character in the‌ models is a mathematical‌​‌ manifestation of the multi-physics​​ nature of the considered​​​‌ problems.

3 Research program‌

3.1 Multi-physics modeling and‌​‌ simulation

The research activity​​ in terms of modeling​​​‌ and simulation (i.e., the‌ so-called forward problem) is‌​‌ driven by two application​​ domains related to the​​​‌ cardiovascular and the respiratory‌ systems.

3.1.1 Cardiovascular hemodynamics‌​‌

We distinguish between cardiac​​ hemodynamics (blood flow inside​​​‌ the four chambers of‌ the heart) and vascular‌​‌ hemodynamics (blood flow in​​ the vessels of the​​​‌ body).

Cardiac hemodynamics. The‌ numerical simulation of cardiac‌​‌ hemodynamics presents many difficulties.​​ We can mention, for​​​‌ instance, the large deformation‌ of the cardiac chambers‌​‌ and the complex fluid-structure​​ interaction (FSI) phenomena between​​​‌ blood, the valves and‌ the myocardium. Blood flow‌​‌ can be described by​​ the incompressible Navier-Stokes equations​​​‌ which have to be‌ coupled with a bio-physical‌​‌ model of the myocardium​​ electro-mechanics and a mechanical​​​‌ model of the valves.‌ The coupling between the‌​‌ fluid and the solid​​ media is enforced by​​​‌ kinematic and dynamic coupling‌ conditions, which guarantee the‌​‌ continuity of velocity and​​ stresses across the interface.​​​‌ In spite of the‌ significant advances achieved since‌​‌ the beginning of this​​ century (see, e.g., 62​​​‌, 63, 60‌, 65, 53‌​‌), the simulation of​​ all the fluid-structure interaction​​​‌ phenomena involved in the‌ heart hemodynamics remains a‌​‌ complex and challenging problem.​​

Heart valves are definitely​​​‌ a bottleneck of the‌ problem, particularly due to‌​‌ their fast dynamics and​​ the contact phenomena with​​​‌ high pressure-drops. Computational cost‌ is recognized as one‌​‌ of the key difficulties,​​ related to the efficiency​​​‌ of the FSI coupling‌ method and the robustness‌​‌ of the contact algorithm.​​ Furthermore, the numerical discretization​​​‌ of these coupled systems‌ requires to deal with‌​‌ unfitted fluid and solid​​ meshes, which are known​​​‌ to complicate the accuracy‌ and/or the robustness of‌​‌ the numerical approximations (see​​ Section 3.3.2 below).

The​​​‌ ultimate goal of the‌ proposed research activity is‌​‌ the simulation of the​​ complete fluid-structure-contact interaction phenomena​​​‌ involved within the heart.‌ Most of this work‌​‌ will be carried out​​ in close collaboration with​​​‌ the M3DISIM project-team, which‌ has a wide expertise‌​‌ on the modeling, simulation​​ and estimation of myocardium​​​‌ electro-mechanics. We will also‌ consider simplified approaches for‌​‌ cardiac hemodynamics (see, e.g.,​​ 35, 48,​​​‌ 51). The objective‌ is to develop mathematically‌​‌ sound models of reduced​​ valve dynamics with the​​​‌ purpose of enhancing the‌ description of the pressure‌​‌ dynamics right after the​​​‌ opening/closing of the valve​ (traditional models yield spurious​‌ pressure oscillations).

Vascular hemodynamics.​​ The modeling and simulation​​​‌ of vascular hemodynamics in​ large vessels has been​‌ one of the core​​ research topics of some​​​‌ members of COMMEDIA, notably​ as regards the fluid-structure​‌ interaction phenomena. Here we​​ propose to investigate the​​​‌ modeling of pathological scenarios,​ such as the hemorrhage​‌ phenomena in smaller vessels.​​ Modeling of hemorrhage is​​​‌ motivated by the medical​ constatation that, after a​‌ primary vessel wall rupture,​​ secondary vessel wall ruptures​​​‌ are observed. Biologists postulate​ that the mechanical explanation​‌ of this phenomenon might​​ be in the change​​​‌ of applied stress due​ to blood bleeding. We​‌ propose to model and​​ simulate the underlying coupled​​​‌ system, blood vessel flow​ through the external tissue,​‌ to estimate the effect​​ of the subsequent stress​​​‌ variation.

3.1.2 Respiratory flows​

The motivation of the​‌ proposed research activities is​​ to develop a hierarchy​​​‌ of easily parametrizable models​ allowing to describe and​‌ efficiently simulate the physical,​​ mechanical and biological phenomena​​​‌ related to human respiration,​ namely, ventilation, particle deposition,​‌ gas diffusion and coupling​​ with the circulatory system.​​​‌

Ventilation. The current modeling​ approaches (either 3D–0D coupled​‌ models where the 3D​​ Navier-Stokes equations are solved​​​‌ in truncated geometries of​ the bronchial tree with​‌ appropriate lumped boundary conditions,​​ or 0D–3D coupled models​​​‌ where the lung parenchyma​ is described by a​‌ 3D elastic media irrigated​​ by a simplified bronchial​​​‌ tree) provide satisfactory results​ in the case of​‌ mechanical ventilation or normal​​ breathing. Realistic volume-flow phase​​​‌ portraits can also be​ simulated in the case​‌ of forced expiration (see​​ 37, 45,​​​‌ 68), but the​ magnitude of the corresponding​‌ pressure is not physiological.​​ The current models must​​​‌ be enriched since they​ do not yet correctly​‌ describe all the physiological​​ phenomena at play. We​​​‌ hence propose to extend​ the 0D–3D (bronchial tree–parenchyma)​‌ model developed in the​​ team, by considering a​​​‌ non-linear, viscoelastic and possibly​ poro-elastic description of the​‌ parenchyma with appropriate boundary​​ conditions that describe ribs​​​‌ and adjacent organs and​ taking into account an​‌ appropriate resistive model.

So​​ far, the motion of​​​‌ the trachea and proximal​ bronchi has been neglected​‌ in the ventilation models​​ (see, e.g., 70).​​​‌ These features can be​ critical for the modeling​‌ of pathologic phenomena such​​ as sleep apnea and​​​‌ occlusion of the airways.​ This would be a​‌ long-term goal where fluid-structure​​ interaction and the possible​​​‌ contact phenomena will be​ taken into account, as​‌ in the simulation of​​ cardiac hemodynamics (see Section​​​‌ 3.1.1).

Aerosol and​ gas diffusion. The dynamics​‌ of aerosols in the​​ lung have been widely​​​‌ studied from the mathematical​ modeling standpoint. They can​‌ be described by models​​ at different scales: the​​​‌ microscopic one for which​ each particle is described​‌ individually, the mesoscopic (or​​ kinetic) one for which​​​‌ a density of probability​ is considered, or the​‌ macroscopic one where reaction-diffusion​​ equations describing the behavior​​​‌ of the constituant concentration​ are considered. The objective​‌ of COMMEDIA will mainly​​ be to develop the​​ kinetic approach that allows​​​‌ a precise description of‌ the deposition area at‌​‌ controlled computational costs. Part​​ of this study could​​​‌ be done in collaboration‌ with colleagues from the‌​‌ Research Center for Respiratory​​ Diseases at Inserm Tours​​​‌ (UMR1100).

The macroscopic description‌ is also appropriate for‌​‌ the diffusion of gases​​ (oxygen and carbon dioxide)​​​‌ in the bronchial tree‌ (see 64). Regarding‌​‌ the influence of the​​ carrier gas, if the​​​‌ patient inhales a different‌ mixture of air such‌​‌ as a Helium-Oxygen mixture,​​ the diffusion mechanisms could​​​‌ be modified. In this‌ context, the goal is‌​‌ to evaluate if the​​ cross-diffusion (and thus the​​​‌ carrier gas) modifies the‌ quantities of oxygen diffused.‌​‌ Part of this work​​ will be carried out​​​‌ in collaboration with members‌ of the LJLL and‌​‌ of the MAP5.

As​​ a long term goal,​​​‌ we propose to investigate‌ the coupling of these‌​‌ models to models of​​ diffusion in the blood​​​‌ or to perfusion models‌ of the parenchyma, and‌​‌ thus, have access thanks​​ to numerical simulations to​​​‌ new indices of ventilation‌ efficiency (such as dissolved‌​‌ oxygen levels), depending on​​ the pathology considered or​​​‌ the resting or exercise‌ condition of the patient.‌​‌

3.2 Simulation with data​​ interaction

The second research​​​‌ axis of COMMEDIA is‌ devoted to the interaction‌​‌ of numerical simulations with​​ measured data. Several research​​​‌ directions related to two‌ specific applications are described‌​‌ below: blood flows and​​ cardiac electrophysiology, for which​​​‌ the mathematical models have‌ been validated against experimental‌​‌ data. This list is​​ not exhaustive and additional​​​‌ problems (related to cardiac‌ and respiratory flows) shall‌​‌ be considered depending on​​ the degree of maturity​​​‌ of the developed models.‌

3.2.1 Fluid flow reconstruction‌​‌ from medical imaging

A​​ first problem which is​​​‌ currently under study at‌ COMMEDIA is the reconstruction‌​‌ of the flow state​​ from Doppler ultrasound measurements.​​​‌ This is a cheap‌ and largely available imaging‌​‌ modality where the measure​​ can be interpreted as​​​‌ the average on a‌ voxel of the velocity‌​‌ along the direction of​​ the ultrasound beam. The​​​‌ goal is to perform‌ a full-state estimation in‌​‌ a time compatible with​​ a realistic application.

A​​​‌ second problem which is‌ relevant is the flow‌​‌ and wall dynamics reconstruction​​ using 4D-flow MRI. This​​​‌ imaging modality is richer‌ than Doppler ultrasound and‌​‌ provides directly a measure​​ of the 3D velocity​​​‌ field in the voxels.‌ This enables the use‌​‌ of direct estimation methods​​ at a reduced computational​​​‌ cost with respect to‌ the traditional variational data‌​‌ assimilation approaches. Yet, the​​ sensitivity of the results​​​‌ to subsampling and noise‌ is still not well‌​‌ understood.

We also propose​​ to address the issues​​​‌ related to uncertainty quantification.‌ Indeed, measurements are corrupted‌​‌ by noise and the​​ parameters as well as​​​‌ the available data of‌ the system are either‌​‌ hidden or not known​​ exactly (see 59).​​​‌ This uncertainty makes the‌ estimation difficult and has‌​‌ a large impact on​​ the precision of the​​​‌ reconstruction, to be quantified‌ in order to provide‌​‌ a reliable tool.

3.2.2​​​‌ Safety pharmacology

One of​ the the most important​‌ problems in pharmacology is​​ cardio-toxicity (see 58).​​​‌ The objective is to​ predict whether or not​‌ a molecule alters in​​ a significant way the​​​‌ normal functioning of the​ cardiac cells. This problem​‌ can be formulated as​​ inferring the impact of​​​‌ a drug on the​ ionic currents of each​‌ cell based on the​​ measured electrical signal (e.g.,​​​‌ electrograms from Micro-Electrodes Arrays).​ The proposed approach in​‌ collaboration with two industrial​​ partners (NOTOCORD and Ncardia)​​​‌ consists in combining available​ realistic data with virtual​‌ ones obtained by numerical​​ simulations. These two datasets​​​‌ can be used to​ construct efficient classifiers and​‌ regressors using machine learning​​ tools (see 42)​​​‌ and hence providing a​ rapid way to estimate​‌ the impact of a​​ molecule on the electrical​​​‌ activity. The methodological aspects​ of this work are​‌ addressed in Section 3.3.3​​.

3.3 Methodological core​​​‌

The work described in​ this section is aimed​‌ at investigating fundamental mathematical​​ and numerical problems which​​​‌ arise in the first​ two research axes.

3.3.1​‌ Mathematical analysis of PDEs​​

The mathematical analysis of​​​‌ the multi-scale and multi-physics​ models are a fundamental​‌ tool of the simulation​​ chain. Indeed, well-posedness results​​​‌ provide precious insights on​ the properties of solutions​‌ of the systems which​​ can, for instance, guide​​​‌ the design of the​ numerical methods or help​‌ to discriminate between different​​ modeling options.

Fluid-structure interaction.​​​‌ Most of the existing​ results concern the existence​‌ of solutions locally in​​ time or away from​​​‌ contacts. One fundamental problem,​ related to the modeling​‌ and simulation of valve​​ dynamics (see Sections 3.1.1​​​‌ and 3.3.2), is​ the question of whether​‌ or not the model​​ allows for contact (see​​​‌ 57, 55).​ The proposed research activity​‌ is aimed at investigating​​ the case of both​​​‌ immersed rigid or elastic​ structures and explore if​‌ the considered model allows​​ for contact and if​​​‌ existence can be proved​ beyond contact. The question​‌ of the choice of​​ the model is crucial​​​‌ and considering different types​ of fluid (Newtonian or​‌ non-Newtonian), structure (smooth or​​ rough, elastic, viscoelastic, poro-elastic),​​​‌ or various interface conditions​ has an influence on​‌ whether the model allows​​ contact or not.

Fluid–structure​​​‌ mixture. The main motivation​ to study fluid-solid mixtures​‌ (i.e., porous media consisting​​ of a skeleton and​​​‌ connecting pores filled with​ fluid) comes from the​‌ modeling of the lung​​ parenchyma and cerebral hemorrhages​​​‌ (see Sections 3.1.1–​3.1.2). The Biot​‌ model is the most​​ widely used in the​​​‌ literature for the modeling​ of poro-elastic effects in​‌ the arterial wall. Here,​​ we propose to investigate​​​‌ the recent model proposed​ by the M3DISIM project-team​‌ in 47, which​​ allows for nonlinear constitutive​​​‌ behaviors and viscous effects,​ both in the fluid​‌ and the solid. Among​​ the questions which will​​​‌ be addressed, some of​ them in collaboration with​‌ M3DISIM, we mention the​​ justification of the model​​​‌ (or its linearized version)​ by means of homogenization​‌ techniques and its well-posedness.​​

Fluid–particle interaction. Mathematical analysis​​ studies on the Navier-Stokes-Vlasov​​​‌ system for fluid-particle interaction‌ in aerosols can be‌​‌ found in 39,​​ 41. We propose​​​‌ to extend these studies‌ to more realistic models‌​‌ which take into account,​​ for instance, changes in​​​‌ the volume of the‌ particles due to humidity.‌​‌

3.3.2 Numerical methods for​​ multi-physics problems

In this​​​‌ section we describe the‌ main research directions that‌​‌ we propose to explore​​ as regards the numerical​​​‌ approximation of multi-physics problems.‌

Fluid-structure interaction. The spatial‌​‌ discretization of fluid-structure interaction​​ (FSI) problems generally depends​​​‌ on the amount of‌ solid displacement within the‌​‌ fluid. Problems featuring moderate​​ interface displacements can be​​​‌ successfully simulated using (moving)‌ fitted meshes with an‌​‌ arbitrary Lagrangian-Eulerian (ALE) description​​ of the fluid. This​​​‌ facilitates, in particular, the‌ accurate discretization of the‌​‌ interface conditions. Nevertheless, for​​ problems involving large structural​​​‌ deflections, with solids that‌ might come into contact‌​‌ or that might break​​ up, the ALE formalism​​​‌ becomes cumbersome. A preferred‌ approach in this case‌​‌ is to combine a​​ Eulerian formalism in the​​​‌ fluid with an unfitted‌ mesh discretization, in which‌​‌ the fluid-structure interface deforms​​ independently of a background​​​‌ fluid mesh. In general,‌ traditional unfitted mesh approaches‌​‌ (such as the immersed​​ boundary and the fictitious​​​‌ domain methods 67,‌ 38, 54,‌​‌ 36) are known​​ to be inaccurate in​​​‌ space. These difficulties have‌ been recently circumvented by‌​‌ a Nitsche-based cut-FEM methodology​​ (see 33, 43​​​‌). The superior accuracy‌ properties of cut-FEM approaches‌​‌ comes at a price:​​ these methods demand a​​​‌ much more involved computer‌ implementation and require a‌​‌ specific evaluation of the​​ interface intersections.

As regards​​​‌ the time discretization, significant‌ advances have been achieved‌​‌ over the last decade​​ in the development and​​​‌ the analysis of time-splitting‌ schemes that avoid strong‌​‌ coupling (fully implicit treatment​​ of the interface coupling),​​​‌ without compromising stability and‌ accuracy. In the vast‌​‌ majority of these studies,​​ the spatial discretization is​​​‌ based on body fitted‌ fluid meshes and the‌​‌ problem of accuracy remains​​ practically open for the​​​‌ coupling with thick-walled structures‌ (see, e.g., 52).‌​‌ Within the unfitted mesh​​ framework, splitting schemes which​​​‌ avoid strong coupling are‌ much more rare in‌​‌ the literature.

Computational efficiency​​ is a major bottleneck​​​‌ in the numerical simulation‌ of fluid-structure interaction problems‌​‌ with unfitted meshes. The​​ proposed research activity is​​​‌ aimed at addressing these‌ issues. Another fundamental problem‌​‌ that we propose to​​ face is the case​​​‌ of topology changes in‌ the fluid, due to‌​‌ contact or fracture of​​ immersed solids. This challenging​​​‌ problem (fluid-structure-contact-fracture interaction) has‌ major role in many‌​‌ applications (e.g., heart valves​​ repair or replacement, break-up​​​‌ of drug-loaded micro-capsules) but‌ most of the available‌​‌ studies are still merely​​ illustrative. Indeed, besides the​​​‌ numerical issues discussed above,‌ the stability and the‌​‌ accuracy properties of the​​ numerical approximations in such​​​‌ a singular setting are‌ not known.

Fluid–particle interaction‌​‌ and gas diffusion. Aerosols​​ can be described through​​​‌ mesoscopic equations of kinetic‌ type, which provide a‌​‌ trade-off between model complexity​​​‌ and accuracy. The strongly​ coupled fluid-particle system involves​‌ the incompressible Navier-Stokes equations​​ and the Vlasov equation.​​​‌ The proposed research activity​ is aimed at investigating​‌ the theoretical stability of​​ time-splitting schemes for this​​​‌ system. We also propose​ to extend these studies​‌ to more complex models​​ that take into account​​​‌ the radius growth of​ the particles due to​‌ humidity, and for which​​ stable, accurate and mass​​​‌ conservative schemes have to​ be developed.

As regards​‌ gas diffusion, the mathematical​​ models are generally highly​​​‌ non-linear (see, e.g., 64​, 66, 40​‌). Numerical difficulties arise​​ from these strong non​​​‌ linearities and we propose​ to develop numerical schemes​‌ able to deal with​​ the stiff geometrical terms​​​‌ and that guarantee mass​ conservation. Moreover, numerical diffusion​‌ must be limited in​​ order to correctly capture​​​‌ the time scales and​ the cross-diffusion effects.

3.3.3​‌ Statistical learning and mathematical​​ modeling interactions

Machine learning​​​‌ and in general statistical​ learning methods (currently intensively​‌ developed and used, see​​ 34) build a​​​‌ relationship between the system​ observations and the predictions​‌ of the QoI (quantities​​ of interest) based on​​​‌ the a posteriori knowledge​ of a large amount​‌ of data. When dealing​​ with biomedical applications, the​​​‌ available observations are signals​ (think for instance to​‌ images or electro-cardiograms, pressure​​ and Doppler measurements). These​​​‌ data are high dimensional​ and the number of​‌ available individuals to set​​ up precise classification/regression tools​​​‌ could be prohibitively large.​ To overcome this major​‌ problem and still try​​ to exploit the advantages​​​‌ of statistical learning approaches,​ we try to add,​‌ to the a posteriori​​ knowledge of the available​​​‌ data an a priori​ knowledge, based on the​‌ mathematical modeling of the​​ system. A large number​​​‌ of numerical simulations is​ performed in order to​‌ explore a set of​​ meaningful scenarios, potentially missing​​​‌ in the dataset. This​ in silico database of​‌ virtual experiments is added​​ to the real dataset:​​​‌ the number of individuals​ is increased and, moreover,​‌ this larger dataset can​​ be used to compute​​​‌ semi-empirical functions to reduce​ the dimension of the​‌ observed signals.

Several investigations​​ have to be carried​​​‌ out to systematically set​ up this framework. First,​‌ often there is not​​ a single mathematical model​​​‌ describing a physiological phenomenon,​ but hierarchies of models​‌ of different complexity. Every​​ model is characterized by​​​‌ a model error. How​ can this be accounted​‌ for? Moreover, several statistical​​ estimators can be set​​​‌ up and eventually combined​ together in order to​‌ improve the estimations (see​​ 61). Other issues​​​‌ have an actual impact​ and has to be​‌ investigated: what is the​​ optimal number of in​​​‌ silico experiments to be​ added? What are the​‌ most relevant scenarios to​​ be simulated in relation​​​‌ to the statistical learning​ approach considered in order​‌ to obtain reliable results?​​ In order to answer​​​‌ to these questions, discussions​ and collaborations with statistics​‌ and machine learning groups​​ have to be developed.​​​‌

3.3.4 Tensor approximation and​ HPC

Tensor methods have​‌ a recent significant development​​ because of their pertinence​​ in providing a compact​​​‌ representation of large, high-dimensional‌ data. Their applications range‌​‌ from applied mathematics and​​ numerical analysis to machine​​​‌ learning and computational physics.‌ Several tensor decompositions and‌​‌ methods are currently available​​ (see 56). Contrary​​​‌ to matrices, for tensors‌ of order higher or‌​‌ equal to three, there​​ does not exist, in​​​‌ general, a best low‌ rank approximation, the problem‌​‌ being ill posed (see​​ 69). Two main​​​‌ points will be addressed:‌ (i) The tensor construction‌​‌ and the multi-linear algebra​​ operations involved when solving​​​‌ high-dimensional problems are still‌ sequential in most of‌​‌ the cases. The objective​​ is to design efficient​​​‌ parallel methods for tensor‌ construction and computations; (ii)‌​‌ When solving high-dimensional problems,​​ the tensor is not​​​‌ assigned; instead, it is‌ specified through a set‌​‌ of equations and tensor​​ data. Our goal is​​​‌ to devise numerical methods‌ able to (dynamically) adapt‌​‌ the rank and the​​ discretization (possibly even the​​​‌ tensor format) to respect‌ the chosen error criterion.‌​‌ This could, in turn,​​ improve the efficiency and​​​‌ reduce the computational burden.‌

These sought improvements could‌​‌ make the definition of​​ parsimonious discretizations for kinetic​​​‌ theory and uncertainty quantification‌ problems (see Section 3.2.1‌​‌) more efficient and​​ suitable for a HPC​​​‌ paradigm. This work will‌ be carried out in‌​‌ collaboration with Olga Mula​​ (TU Eindhoven) and MATHERIALS​​​‌ project-teams.

4 Application domains‌

4.1 Cardiovascular hemodynamics

The‌​‌ heart is a double​​ pump whose purpose is​​​‌ to deliver blood to‌ the tissue and organs‌​‌ of the body. This​​ function is made possible​​​‌ through the opening and‌ closing of the heart‌​‌ valves. Cardiac diseases generally​​ manifest by affecting the​​​‌ pumping function of the‌ heart. Numerical simulations of‌​‌ cardiac hemodynamics, in normal​​ and pathological conditions, are​​​‌ recognized as a tool‌ of paramount importance for‌​‌ improving the understanding, diagnosis​​ and treatment of cardiac​​​‌ pathologies, and also for‌ the development of implantable‌​‌ devices (see, e.g., 65​​, 46). As​​​‌ an example, we can‌ mention the case of‌​‌ cardiac mitral valve regurgitation,​​ one of the most​​​‌ common heart valve diseases.‌ For this pathology, clinical‌​‌ data are known to​​ be insufficient for determining​​​‌ the optimal timing for‌ surgery, the best surgical‌​‌ strategy and the long-term​​ outcome of a surgical​​​‌ repair. Contrary to imaging‌ techniques, numerical simulations provide‌​‌ local information, such as​​ pressure and stresses, which​​​‌ are of fundamental importance‌ for the prediction of‌​‌ the mechanical behavior of​​ native valves and of​​​‌ implantable devices.

4.2 Respiratory‌ flows

Respiration involves the‌​‌ transport of air through​​ the airways from the​​​‌ mouth to the alveoli‌ of the lungs. These‌​‌ units where diffusion of​​ oxygen and carbon dioxide​​​‌ takes place, are surrounded‌ by a viscoelastic medium‌​‌ (the parenchyma) consisting of​​ blood vessels and collagen​​​‌ fibers. Air flows due‌ to the displacement of‌​‌ the diaphragm, which drives​​ the pulmonary parenchyma. Accidental​​​‌ inhalations of foreign bodies‌ or pathologies such as‌​‌ asthma, emphysema and fibrosis​​ might prevent the lung​​​‌ of fulfilling its function.‌ Therapies mostly use aerosols‌​‌ (set of small particles,​​​‌ solid or liquid), which​ must reach the specific​‌ areas of the lung​​ targeted for treatment. Understanding​​​‌ the airflow mechanisms within​ the respiratory network is​‌ a fundamental ingredient for​​ predicting the particles motion​​​‌ and their deposition (see,​ e.g., 44). Moreover,​‌ understanding of the gas​​ diffusion in the lung​​​‌ is also of major​ importance since the main​‌ function of this organ​​ is to deliver oxygen​​​‌ to the blood.

4.3​ Safety pharmacology

The problem​‌ of safety pharmacology can​​ be summarized as follows:​​​‌ given a molecule which​ is a candidate to​‌ become a drug, is​​ its use dangerous due​​​‌ to side effects? Among​ all the different problems​‌ to be addressed, one​​ of the most relevant​​​‌ questions in pharmacology is​ cardio-toxicity (see 58).​‌ More precisely, the objective​​ is to determine whether​​​‌ or not a molecule​ alters in a significant​‌ way the normal functioning​​ of the cardiac cells.​​​‌ To answer these questions,​ the CiPA initiative promotes​‌ the introduction of novel​​ techniques and their standardisation​​​‌ (see 50). One​ of the proposed tests​‌ of the CiPA panel​​ is to measure the​​​‌ electrical activity using Micro-Electrodes​ Array: these are microchips​‌ that record the electrical​​ activity of an ensemble​​​‌ of cells. The task​ is to infer the​‌ impact of a drug​​ on the ionic currents​​​‌ of each cell based​ on the electrical signal​‌ measured (electrograms) and, in​​ perspective, to be able​​​‌ to assess whether a​ molecule can induce arrhythmia​‌ (see 49).

5​​ Latest software developments, platforms,​​​‌ open data

5.1 Latest​ software developments

5.1.1 FELiScE​‌

  • Name:
    Finite Elements for​​ Life SCiences and Engineering​​​‌ problems
  • Keywords:
    Finite element​ modelling, Cardiac Electrophysiology, Cardiovascular​‌ and respiratory systems
  • Functional​​ Description:
    FELiScE is a​​​‌ finite element developed by​ COMMEDIA project-team. One specific​‌ objective of this code​​ is to provide in​​​‌ a unified software environment​ all the state-of-the-art tools​‌ needed to perform simulations​​ of the complex respiratory​​​‌ and cardiovascular models considered​ in the two teams​‌ – namely involving fluid​​ and solid mechanics, electrophysiology,​​​‌ and the various associated​ coupling phenomena. FELISCE is​‌ written in C++ and​​ open source, and may​​​‌ be later released as​ an opensource library. FELiScE​‌ was registered in July​​ 2014 at the Agence​​​‌ pour la Protection des​ Programmes under the Inter​‌ Deposit Digital Number IDDN.FR.001.350015.000.S.P.2014.000.10000.​​
  • URL:
  • Contact:
    Miguel​​​‌ Angel Fernandez Varela
  • Participants:​
    Romain Lemore, Marguerite Champion,​‌ Daniele Carlo Corti, Miguel​​ Angel Fernandez Varela, Marina​​​‌ Vidrascu, Oscar Ruz, Carlos​ Brito Pacheco

5.1.2 FELiScE-NS​‌

  • Keywords:
    Thin-walled solids, Incompressible​​ flows
  • Functional Description:
    FELiScE-NS​​​‌ is a set of​ finite elements solvers for​‌ incompressible fluids (fractional-step schemes)​​ and non-linear thin-walled structures​​​‌ (3D shells, and 2D​ curved beams) developed in​‌ the framework of the​​ FELiScE library. FELiSCe-NS was​​​‌ registered in 2018 at​ the Agence pour la​‌ Protection des Programmes Inter​​ Deposit Digital Number IDDN.FR.001.270015.000.S.A.2018.000.31200.​​​‌
  • Contact:
    Miguel Angel Fernandez​ Varela
  • Participants:
    Oscar Ruz,​‌ Miguel Angel Fernandez Varela,​​ Marina Vidrascu, Daniele Carlo​​​‌ Corti

5.1.3 ADAPT

  • Name:​
    Adaptive Dynamical Approximation via​‌ Parallel Tensor methods
  • Keywords:​​
    Scientific computing, Tensor decomposition,​​ Partial differential equation
  • Functional​​​‌ Description:
    ADAPT is a‌ library containing methods for‌​‌ scientific computing based on​​ tensors. In many fields​​​‌ of science and engineering‌ we need to approximate‌​‌ the solution of high-dimensional​​ problems. In this library​​​‌ we propose a collection‌ of methods to parsimoniously‌​‌ discretise high-dimensional problems. These​​ methods are mainly based​​​‌ on tensors.
  • Contact:
    Damiano‌ Lombardi
  • Participants:
    Virginie Galland,‌​‌ Damiano Lombardi, Sebastien Riffaud​​

6 New results

6.1​​​‌ Cardiovascular hemodynamics

Participants: Miguel‌ Angel Fernández Varela,‌​‌ Oscar Ruz, Marina​​ Vidrascu.

The thin-walled​​​‌ nature of the atrial‌ wall can lead to‌​‌ numerical locking issues when​​ using 3D models discretized​​​‌ with standard finite elements.‌ In order to circumvent‌​‌ these issues, in 23​​ we introduce a comprehensive​​​‌ electromechanical model of the‌ left atrium based on‌​‌ a 3D-shell formulation. The​​ model integrates both the​​​‌ passive and active components‌ of the atrial tissue,‌​‌ while blood flow and​​ the mitral valve dynamics​​​‌ are described in a‌ lumped parameter fashion. The‌​‌ resulting model is discretized​​ with a finite element​​​‌ approach specifically designed to‌ mitigate numerical locking. The‌​‌ effectiveness of the proposed​​ approach is evaluated by​​​‌ comparing the numerical results‌ with biomarkers reported in‌​‌ the literature, in the​​ case of both healthy​​​‌ and pathological conditions.

6.2‌ Respiratory flows

Participants: Céline‌​‌ Grandmont, Frédèrique Noël​​.

In 21 we​​​‌ propose a new nonlinear‌ coupled 1D model to‌​‌ describe lung ventilation and​​ the transport and diffusion​​​‌ of both oxygen and‌ carbon dioxide in the‌​‌ bronchial tree through the​​ blood. It takes into​​​‌ account the so called‌ Bohr-Haldane effect and is‌​‌ driven by the applied​​ pleural pressure. The ability​​​‌ of this model to‌ recover standard acknowledged values‌​‌ in healthy situations is​​ provided. One key aspect​​​‌ is that, contrary to‌ its 0D counterpart, it‌​‌ naturally takes into account​​ mixing of gases along​​​‌ the tree and a‌ time delay as the‌​‌ gases have to be​​ transported before reaching the​​​‌ alveoli. We further investigate‌ the sensitivity of both‌​‌ the 1D model and​​ its 0D counterpart with​​​‌ respect to the breathing‌ pattern by considering two‌​‌ types of pleural applied​​ pressure: a piecewise constant​​​‌ one and a piecewise‌ exponential one for various‌​‌ values of the breathing​​ period, inspiratory ratio and​​​‌ pressure amplitude. We finally‌ explore which cost functions‌​‌ the observed stereotypical breathing​​ scenario may optimize, underlying​​​‌ the fact that it‌ should be a combination‌​‌ of several criteria: low​​ effort and small lung​​​‌ distension while maintaining carbon‌ dioxide arterial partial pressure‌​‌ at a given level.​​

6.3 Simulation with data​​​‌ interaction

Participants: Miguel Angel‌ Fernández Varela, Gaël‌​‌ Le Ruz, Damiano​​ Lombardi, Fabien Vergnet​​​‌, Marina Vidrascu.‌

In 32 we propose‌​‌ a mathematical model of​​ the photoplethysmography (PPG) measurements.​​​‌ This consists in flashing‌ light on a tissue‌​‌ and measuring the amount​​ of light which comes​​​‌ back. As the tissue‌ evolves, the signal changes‌​‌ in time. The goal​​ of the work consists​​​‌ in going beyond this‌ rough intuitive explanation and‌​‌ providing a more quantitative​​​‌ understanding of this measurement​ process. We propose a​‌ poro-elastic model for the​​ biological tissue coupled with​​​‌ a diffusion approximation of​ the radiative transport equation​‌ in order to describe​​ the light. The model​​​‌ is discretised by means​ of low-order finite elements.​‌ A first validation against​​ real data showed that​​​‌ the model is able​ to provide an interpretation​‌ of the measurement process​​ and that it is​​​‌ possible to estimate haemodynamics​ quantities (such as flow​‌ or relative pressure) based​​ on the PPG signal.​​​‌

In 28 we revisit​ the direct method for​‌ the reconstruction of coefficients​​ in second order elliptic​​​‌ partial differential equations. Two​ model problems are considered:​‌ first the reconstruction of​​ the diffusion coefficient in​​​‌ a scalar elliptic problem​ and second the reconstruction​‌ of the shear modulus​​ in the elastography problem.​​​‌ To highlight the versatility​ of the framework, different​‌ notions of stability are​​ exploited in the two​​​‌ situations. In the scalar​ case, the system is​‌ interpreted as a hyperbolic​​ transport equation and an​​​‌ inf-sup condition on the​ discrete level is leveraged​‌ for the analysis of​​ the numerical method. We​​​‌ obtain error estimates on​ the reconstruction coefficient that​‌ are suboptimal by half​​ an order, which is​​​‌ known to be sharp​ on general meshes. In​‌ the vector case, the​​ minimization of the residual​​​‌ in dual norm and​ a stability result on​‌ the continuous problem lead​​ to error estimates that​​​‌ are optimal compared to​ the approximation. For both​‌ problems, the theoretical results​​ are illustrated by some​​​‌ numerical examples.

In 31​, we adopt an​‌ optimal control viewpoint to​​ formulate a rigorous deterministic​​​‌ filtering theory when the​ dynamics and the observations​‌ are defined on manifolds.​​ Therefore, our result extends​​​‌ the Mortensen observer to​ closed manifolds, namely a​‌ compact manifold without boundary,​​ in both continuous and​​​‌ discrete time, where the​ second ultimately yields a​‌ convergent time discretization of​​ the first. The resulting​​​‌ observer requires the computation​ of the viscosity solution​‌ of a Hamilton-Jacobi-Bellman equation​​ on the state manifold,​​​‌ which we illustrate on​ the sphere.

In 30​‌ we propose a numerical​​ method to approximate the​​​‌ log operation on a​ Riemannian manifold as well​‌ as the Hessian of​​ the squared distance. First,​​​‌ we write the boundary​ value problem of the​‌ geodesics as the minimisation​​ of the geodesic energy​​​‌ with fixed endpoints, and​ write the weak formulation​‌ of the Euler-Lagrange equations.​​ We introduce a fixed-point​​​‌ at continuous level, for​ which, under certain geometrical​‌ assumptions, we can prove​​ that the iterations are​​​‌ well posed and convergent.​ When the fixed-point iterations​‌ are discretised by means​​ of the finite element​​​‌ methods, the discrete iterations​ inherits the properties of​‌ the continuous ones. Moreover,​​ by considering the sensitivity​​​‌ equations of the Euler-Lagrange​ equations we can write​‌ a system of d​​+1 equations (where​​​‌ d is the manifold​ dimension) making it possible​‌ to estimate the Hessian​​ of the squared distance.​​​‌ Some numerical tests on​ the sphere show that​‌ the proposed numerical method​​ converges at the expected​​ order.

6.4 Numerical methods​​​‌ for multi-physics problems

Participants:‌ Miguel Angel Fernández Varela‌​‌.

In 29 we​​ consider a loosely coupled,​​​‌ non-iterative Robin-Robin coupling method‌ proposed and analyzed in‌​‌ [Numer. Algorithms, 99:921-948, 2025]​​ for a parabolic-parabolic interface​​​‌ problem. We modify the‌ first step of the‌​‌ scheme so that several​​ error difference quantities remain​​​‌ higher order convergence without‌ requiring additional assumptions. Numerical‌​‌ results are presented to​​ support our findings.

6.5​​​‌ Tensor approximation and HPC‌

Participants: Damiano Lombardi.‌​‌

In 27 we propose​​ a numerical method to​​​‌ solve large scale matrix‌ equations. In particular, we‌​‌ focus on the matrix​​ equations which arise after​​​‌ space semi-discretisation of non-linear‌ problems (going beyond the‌​‌ case of parametric PDEs).​​ The method leverages the​​​‌ CUR matrix decomposition and‌ Krylov iteration in order‌​‌ to estimate a low-rank​​ decomposition of the solution​​​‌ of the matrix equation.‌ The problem being highly‌​‌ non-linear, we introduce a​​ fixed point. Given the​​​‌ current solution, by exploiting‌ an empirical interpolation method,‌​‌ we are able to​​ select sets of rows​​​‌ and columns. Following the‌ principle of cross approximation‌​‌ we make the residual​​ vanish on the selected​​​‌ rows and columns: the‌ resulting two sets of‌​‌ equations are solved by​​ using a Krylov method,​​​‌ providing an updated solution.‌ Several numerical test-cases make‌​‌ it possible to assess​​ the behavious of the​​​‌ method and its performances.‌

7 Bilateral contracts and‌​‌ grants with industry

7.1​​ Bilateral contracts with industry​​​‌

CASIS

Participants: Miguel Ángel‌ Fernández Varela [coordinator],‌​‌ Damiano Lombardi, Romain​​ Lemore.

Calibration of​​​‌ vascular fluid-structure interaction simulations‌ from 4D-flow MRI data.‌​‌

Dassault Systèmes

Participants: Abdelkhalak​​ Chetoui, Miguel Ángel​​​‌ Fernández Varela, Damiano‌ Lombardi [coordinator].

Reduced‌​‌ order modelling and data​​ assimilation for the haemodynamics​​​‌ of congenital heart diseases.‌

8 Partnerships and cooperations‌​‌

8.1 International initiatives

8.1.1​​ Inria associate team not​​​‌ involved in an IIL‌ or an international program‌​‌

DIAFLOP

Participants: Guillaume Delay​​, Davide Pietro Duva​​​‌, Miguel Angel Fernández‌ Varela, Corrie James‌​‌, Romain Lemore.​​

  • Title:
    Data Integration and​​​‌ Assimilation for FLOw Problems‌
  • Duration:
    2025-207
  • Coordinator:
    Miguel‌​‌ Angel Fernández Varela
  • Partners:​​
    • University College London London,​​​‌ UK
  • Inria contact:
    Miguel‌ Angel Fernández Varela
  • UCL‌​‌ contact:
    Erik Burman
  • Summary:​​
    The purpose of the​​​‌ DIAFLOP Associate Team is‌ to exploit the complementary‌​‌ expertise of both research​​ groups in mathematical analysis,​​​‌ numerical analysis, scientific computing‌ and data assimilation in‌​‌ order to develop innovative​​ forward and inverse techniques​​​‌ in the context of‌ cardiovascular applications. The main‌​‌ scientific goal is to​​ develop new efficient and​​​‌ accurate methods for the‌ integration and assimilation of‌​‌ data in the numerical​​ approximation of solutions to​​​‌ partial differential equations modeling‌ blood flows. This includes‌​‌ both geometrical and kinematical​​ data. A key aspect​​​‌ is the use of‌ both individual and collective‌​‌ data.

8.2 International research​​ visitors

8.2.1 Visits of​​​‌ international scientists

Other international‌ visits to the team‌​‌
Erik Burman
  • Status
    Professor​​
  • Institution of origin:
    UCL​​​‌
  • Country:
    UK
  • Dates:
    March,‌ October 2025 (2 weeks)‌​‌
  • Context of the visit:​​​‌
    Inria-UCL DIAFLOP Associate Team​
  • Mobility program/type of mobility:​‌
    research stay
Buyang Li​​
  • Status
    Professor
  • Institution of​​​‌ origin:
    The Hong Kong​ Polytechnic University
  • Country:
    Hong​‌ Kong
  • Dates:
    June-July 2025​​ (4 weeks)
  • Context of​​​‌ the visit:
    Inria Paris​ Invited Professors Program
  • Mobility​‌ program/type of mobility:
    research​​ stay & lecture
Maxim​​​‌ Olshanskii
  • Status
    Professor
  • Institution​ of origin:
    Uniersity of​‌ Houston
  • Country:
    USA
  • Context​​ of the visit:
    Research​​​‌ collaboration
  • Dates:
    June, July​ 2025 (1 week)
  • Mobility​‌ program/type of mobility:
    research​​ stay & lecture

8.3​​​‌ National initiatives

CoCop: Heart-Lung​ Coupling: aid to monitor​‌ cardio-respiratory functions in intensive​​ care

Participants: Céline Grandmont​​​‌, Frédérique Noël,​ Fabien Vergnet, Romain​‌ Lopez-Surjus.

  • Funding:
    Inria​​ Exploratory Actions
  • Duration:
    2024–2027​​​‌
  • Coordinator:
    Céline Grandmont
  • Partners:​
    ANANKE project-team (Dominique Chapelle,​‌ Philippe Moireau), APHP Lariboisière​​ Hospital (Fabrice Vallée)
  • Summary:​​​‌
    The project seeks to​ respond to the clinical​‌ need for a better​​ understanding of cardio-respiratory functions​​​‌ for patients placed under​ mechanical ventilation. It aims​‌ in particular to propose​​ ventilatory maneuvers or minimally​​​‌ invasive measurements that can​ be carried out at​‌ the bedside of patients,​​ making it possible to​​​‌ estimate the condition of​ the lung, the level​‌ of blood perfusion and​​ help optimize ventilator settings​​​‌ in order to minimize​ damage to the lungs.​‌
MediTwin

Participants: Carlos Brito​​ Pacheco, Abdelkhalak Chetoui​​​‌, Miguel Angel Fernández​ Varela, Damiano Lombardi​‌, Marina Vidrascu.​​

  • Funding:
    Bpifrance
  • Duration:
    2024-2029​​​‌
  • Local coordinator:
    Miguel Angel​ Fernández Varela
  • Partners:
    Dassault​‌ Systèmes
  • Summary:
    Reduced and​​ 3D modeling and simulation​​​‌ of cardiac hemodynamics, notably​ of patohological scenarios such​‌ as the Hypoplastic Left​​ Heart Syndrome (HLHS), whith​​​‌ the purpose of assesing​ different surgicals options.

9​‌ Dissemination

9.1 Promoting scientific​​ activities

9.1.1 Scientific events:​​​‌ organisation

  • Guillaume Delay
    • Co-organizer​ of the Scientific Computing​‌ Seminar, joint event between​​ Inria Paris and Laboratoire​​​‌ Jacques-Louis Lions
    • Co-organizer of​ the Cemracs Summer School​‌ (July-August 2025): web page​​
  • Miguel Angel Fernández Varela​​​‌
    • Co-organiser of the Joint​ Brazil-Chile-Inria MS on Innovative​‌ Numerical Methods for Fluids,​​ 23rd IACM Computational Fluids​​​‌ Conference, Santiago de Chile,​ Chile, March 2025
    • Co-organiser​‌ of the DIAFLOP Inria-UCL​​ Asociated Team Kick-off meeting,​​​‌ London, UK, December 2025​
  • Damiano Lombardi
    • Co-organizer of​‌ the Scientific Computing Seminar,​​ joint event between Inria​​​‌ Paris and Laboratoire Jacques-Louis​ Lions
Member of the​‌ conference program committees
  • Migue​​ Angel Fernández Varela
    • Member​​​‌ of the FIMH 2025​ Program Committee

9.1.2 Journal​‌

Member of the editorial​​ boards
  • Céline Grandmont
    • Mathematical​​​‌ Modelling of Natural Phenomena​
    • Journal of Mathematical Fluid​‌ Mechanics
    • ESAIM: Mathematical Modelling​​ and Numerical Analysis

9.1.3​​​‌ Invited talks

  • Marguerite Champion​
    • Invited speaker, Modeling, Analysis​‌ and Simulation Working Group​​ of MAP5 (Université Paris​​​‌ Cité), November 2025
  • Guillaume​ Delay
    • Invited talk in​‌ mini-symposium ENUMATH 2025, Heidelberg,​​ Germany, September 2025
  • Miguel​​​‌ Angel Fernández Varela
    • Invited​ talk, Inria-LNCC-UDEC Workshop on​‌ Computational Fluids: Challenges and​​ New Trends, Petrópolis, Brazil,​​​‌ March 2025
    • Invited talk,​ 23rd IACM Computational Fluids​‌ Conference, Santiago de Chile,​​ Chile, March 2025
    • Invited​​​‌ talk at Inria-Brasil hybrid​ workshop on Digital Health,​‌ April 2025 (online)
    • Invited​​ speaker, Numerical Analysis of​​ Interface and Multiphysics Problems​​​‌ MATRIX research program, Creswick‌ Campus of The University‌​‌ of Melbourne, Australia, May​​ 2025
    • Invited talk, 20th​​​‌ International Symposium on Computer‌ Methods in Biomechanics and‌​‌ Biomedical Engineering (CMBBE 2025),​​ Barcelona, Spain, September 2025​​​‌
    • Seminar, CHRU of Tours,‌ Tours, France, November 2025‌​‌ (online)
    • Invited talk, Symposium​​ on Stabilized and Cut​​​‌ Finite Element Methods –‌ Celebrating Peter Hansbo, Institut‌​‌ Mittag-Leffler, Stockholm, Sweden, December​​ 2025 (online)
  • Céline Grandmont​​​‌
    • Invited talk, Modeling in‌ Applied Mechanics : A‌​‌ symposium to honour Patrick​​ Le Tallec, Ecole Polytechnique,​​​‌ NovembeDecember 2025
    • Plenary conference,‌ Forum des jeunes Mathématiciennes‌​‌ et Mathématiciens, Bordeaux, November​​ 2025
    • Invited talk, Closure​​​‌ conference of the ARC-ULB‌ projet, Spa, Belgium, December‌​‌ 2025
    • Invited talk, Lung​​ Modelling workshop, October 2025​​​‌
    • Invited talk, ENUMATH 2025,‌ Heidelberg, September 2025
    • Invited‌​‌ talk, Workshop "Mathematical modeling​​ in biology and medicine",​​​‌ Vienna, Jul. 2025
    • Seminar‌ MMCS, Institut Camille Jordan,‌​‌ May 2025
    • Seminar LJLL,​​ Sorbonne Université, May 2025​​​‌
    • Seminar, ULB, Bruxelles, Belgium,‌ April 2025
    • Invited talk,‌​‌ PDEs journey of Université​​ de Lorraine, April 2025​​​‌
  • Corrie James
    • Talk in‌ MS, Math 2 Product,‌​‌ Valencia, Spain, June 2025​​
    • Talk at the Journées​​​‌ Maths Bio Santé, Montpellier,‌ France, November 2025
  • Damiano‌​‌ Lombardi
    • Seminar, LISN (Université​​ Paris Sud, CNRS), October​​​‌ 2025
    • Keynote talk, Joint‌ meeting of Austrian and‌​‌ German mathematical societies, symposium​​ on scientific computing, Linz,​​​‌ September 2025
    • Invited talk,‌ Workshop on Accurate Reduced‌​‌ Order Models for Industrial​​ Applications, Bidart, September 2025​​​‌
  • Frédérique Noël
    • Invited talk,‌ Economic principles in Cell‌​‌ Biology Summer School, Vienna,​​ Austria, July 2025 (online)​​​‌
    • MS talk, International Conference‌ on Computational Bioengineering (ICCB),‌​‌ Rome, Italy, September 2025​​
  • Oscar Ruz
    • Talk at​​​‌ FIMH 2025 Conference, Dallas,‌ USA, June 2025
  • Fabien‌​‌ Vergnet
    • PDE Seminar Laboratoire​​ de Mathématiques de Versailles,​​​‌ Versailles, France, March 2025‌
    • Rencontres Inria-LJLL in Scientific‌​‌ Computing, Inria Paris, Paris,​​ France, March 2025

9.1.4​​​‌ Research administration

  • Céline Grandmont‌
    • Member of the Inria‌​‌ parity and equal opportunities​​ committee (Coordinator of the​​​‌ working group on gender-based‌ and sexual violence, presentations‌​‌ at the Inria project-team​​ comittees of Inria Grenoble​​​‌ and Inria Lille)
    • Member‌ of the LJLL and‌​‌ Inria parity and equal​​ opportunities committees

9.2 Teaching​​​‌ - Supervision - Juries‌ - Educational and pedagogical‌​‌ outreach

  • Licence:
    • Marguerite Champion​​
      • Numerical analysis, 48h, L3,​​​‌ Sorbonne Université
    • Davide Pietro‌ Duva
      • Fourier analysis: L3,‌​‌ 12 hours, Polytech Sorbonne,​​ Sorbonne Université
      • Mathematics for​​​‌ engineering: L3, 30 hours,‌ Polytech Sorbonne, Sorbonne Université‌​‌
    • Marguerite Champion
      • Numerical analysis,​​ 24h, L3, Sorbonne Université​​​‌
      • Python, 32h, L2, Sorbonne‌ Université
    • Corrie James
      • Optimization,‌​‌ 45h, L3, Université de​​ Versailles Saint-Quentin-en-Yvelines
    • Gaël Le​​​‌ Ruz
      • Linear algebra and‌ ODE, 30h, L3, Polytech‌​‌ Sorbonne
      • Numerical Analysis for​​ PDE, 12h, L3, Polytech​​​‌ Sorbonne
    • Fabien Vergnet
      • Numerical‌ analysis and ODE, 66h,‌​‌ L3, Polytech Sorbonne
      • Fourier​​ Analysis 23h, L3, Polytech​​​‌ Sorbonne
      • Mathematical tools for‌ ingeneers, 18h, L3, Polytech‌​‌ Sorbonne
  • Master:
    • Guillaume Delay​​
      • Preparation to Agrégation, 34h,​​​‌ M2, Sorbonne Université
      • Numerical‌ analysis for PDE, 18h,‌​‌ M1, PolyTech Sorbonne
    • Miguel​​ Angel Fernández Varela
      • Mathematical​​​‌ models and numerical methods‌ for hemodynamics simulations, 20h,‌​‌ M2, Sorbonne Université
    • Céline​​​‌ Grandmont
      • Hands-on sessions, PDEs​ Approximation, 46 h, M1,​‌ Sorbonne Université
    • Damiano Lombardi​​
      • Lecture, 1.5h, Modeling the​​​‌ electro-physiology of heart, NovembeDecember​ 2023, Ecole des Mines​‌ Paristech.
    • Frédérique Noël
      • Programming​​ in C++, 36h, M1,​​​‌ Sorbonne Université
      • Numerical linear​ algebra, 18h, M1, Sorbonne​‌ Université

9.2.1 Supervision

  • PhD​​ defended on January 31,​​​‌ 2025: Oscar Ruz ,​ Mathematical modeling and numerical​‌ simulation of left heart​​ hemodynamics with fluid–structure interactions,​​​‌ 26. Supervisors: Dominique​ Chapelle, Miguel Angel Fernández​‌ Varela & Marina Vidrascu​​
  • PhD defended on September​​​‌ 25, 2025: Marguerite Champion​ , Modeling, analysis and​‌ simulation of fluid-structure-interaction with​​ contact, 24. Supervisors:​​​‌ Miguel Angel Fernández Varela​ , Céline Grandmont ,​‌ Fabien Vergnet & Marina​​ Vidrascu
  • PhD defended on​​​‌ December 1, 2025: Gaël​ Le Ruz , Observer​‌ theory in general constrained​​ spaces – from formulations​​​‌ to applications, 25.​ Since October 2022. Supervisors:​‌ Damiano Lombardi & Philippe​​ Moireau
  • PhD in progress:​​​‌ Corrie James , Data-Modeling​ interaction for biomedical applications.​‌ Since October 2023. Supervisors:​​ Muriel Boulakia & Damiano​​​‌ Lombardi
  • PhD in progress:​ Romain Lemore , Modeling​‌ and patient specific fluid-structure​​ interaction simulations of aortic​​​‌ pathological configurations. Since July​ 2024. Supervisors: Miguel Angel​‌ Fernández Varela & Damiano​​ Lombardi
  • PhD in progress:​​​‌ Romain Lopez-Surjus , Mathematical​ and numerical modelling of​‌ the cardio respiratory system.​​ Since October 2024. Supervisors:​​​‌ Céline Grandmont , Frédérique​ Noël & Fabien Vergnet​‌
  • PhD in progress: Davide​​ Pietro Duva , Divergence-free​​​‌ finite elements for direct​ and inverse problems. Since​‌ December 2024. Supervisors: Guillaume​​ Delay & Miguel Angel​​​‌ Fernández Varela
  • PhD in​ progress: Abdelkhalak Chetoui ,​‌ Reduced order modelling and​​ data assimilation for the​​​‌ haemodynamics of congenital heart​ diseases. Since April 2025.​‌ Damiano Lombardi , Miguel​​ Angel Fernández Varela &​​​‌ Hernán Morales
  • Internship: Dongjiao​ Hong . Supervisors: Damiano​‌ Lombardi & Marina Vidrascu​​
  • Internship: Renee Crispo .​​​‌ Supervisor: Miguel Angel Fernández​ Varela

9.2.2 Juries

  • Damiano​‌ Lombardi
    • Co-president of CES​​ (Commission Emploi Scientifique), Inria​​​‌ Paris
    • Participation to the​ SMAI-GAMNI prize selection committee​‌

9.3 Popularization

9.3.1 Productions​​ (articles, videos, podcasts, serious​​​‌ games, ...)

  • Daniele Carlo​ Corti , Miguel Angel​‌ Fernández Varela

9.3.2 Participation in​‌ Live events

  • Marguerite Champion​​
    • Participation in a FIRST​​​‌ event aimed at encouraging​ female high-school students to​‌ pursue scientific studies, Lycée​​ Pierre-Gilles de Gennes (Paris​​​‌ 13), February 2025
  • Céline​ Grandmont
    • Two Interventions at​‌ the SMAI & Musée​​ des arts et métiers​​​‌ Cycle: youtube link
    • Chiche​ intervention, Emilie du Chatelet​‌ Highschool, spring 2025
    • Participation​​ to "Maths C pour​​​‌ Elle week", June 2025​

10 Scientific production

10.1​‌ Major publications

10.2 Publications of the​​ year

International journals

  • 17​​​‌ articleM.Muriel Boulakia​, C.Corrie James​‌ and D.Damiano Lombardi​​. Numerical approximation of​​​‌ the unique continuation problem​ enriched by a database​‌ for the Stokes equations​​.ESAIM: Mathematical Modelling​​​‌ and Numerical Analysis59​3May 2025,​‌ 1399-1435HALDOI
  • 18​​ articleE.Erik Burman​​​‌, G.Guillaume Delay​ and A.Alexandre Ern​‌. The unique continuation​​ problem for the wave​​​‌ equation discretized with a​ high-order space-time nonconforming method​‌.Numerische Mathematik157​​42025, 1259-1284​​​‌HALDOI
  • 19 article​E.Erik Burman,​‌ R.Rebecca Durst,​​ M. A.Miguel Angel​​​‌ Fernández, J.Johnny​ Guzmán and O.Oscar​‌ Ruz. Robin-Robin loose​​ coupling for incompressible fluid-structure​​​‌ interaction: non-linear setting and​ nearly-optimal error analysis.​‌Journal of Scientific Computing​​10434May 2025​​​‌HALDOI
  • 20 article​S. C.Sara Costa​‌ Faya, C.Callan​​ Wesley, M.Marina​​​‌ Vidrascu, M. A.​Miguel Angel Fernández,​‌ P.-J.Pieter-Jan Guns and​​ D.Damiano Lombardi.​​​‌ Validation of a mathematical​ model of arterial wall​‌ mechanics with drug induced​​ vasoconstriction against ex vivo​​​‌ measurements.Cardiovascular Engineering​ and TechnologyJuly 2025​‌HALDOI
  • 21 article​​C.Céline Grandmont,​​​‌ C.Cyril Karamaoun,​ S.Sébastien Martin and​‌ F.Frédérique Noël.​​ Sensitivity and optimality analysis​​​‌ of breathing scenarios for​ 1D or 0D models​‌ of gas diffusion in​​ the lung.Journal​​​‌ of Theoretical Biology615​December 2025HALback​‌ to text
  • 22 article​​O.Oscar Ruz,​​​‌ J.Jérôme Diaz,​ M.Marina Vidrascu,​‌ P.Philippe Moireau,​​ D.Dominique Chapelle and​​​‌ M. A.Miguel Angel​ Fernández. Left heart​‌ hemodynamics simulations with fluid-structure​​ interaction and reduced valve​​​‌ modeling.International Journal​ for Numerical Methods in​‌ Biomedical Engineering419​​August 2025, e70088​​​‌HALDOI

Edition (books,​ proceedings, special issue of​‌ a journal)

  • 23 proceedings​​3D-Shell Electromechanical Modeling of​​​‌ the Left Atrium.​Functional Imaging and Modeling​‌ of the Heart15672​​Dallas (TX), United States​​SpringerJune 2025HAL​​​‌DOIback to text‌

Doctoral dissertations and habilitation‌​‌ theses

Reports‌​‌ & preprints

10.3​​ Cited publications

  • 33 article​​​‌F.F. Alauzet,‌ B.B. Fabrèges,‌​‌ M. A.M. A.​​ Fernández and M.M.​​​‌ Landajuela. Nitsche-XFEM for‌ the coupling of an‌​‌ incompressible fluid with immersed​​ thin-walled structures.Comput.​​​‌ Methods Appl. Mech. Engrg.‌3012016, 300--335‌​‌back to text
  • 34​​ bookE.E. Alpaydin​​​‌. Introduction to machine‌ learning.MIT press‌​‌2009back to text​​
  • 35 articleM.M.​​​‌ Astorino, J.J.‌ Hamers, S. C.‌​‌S. C. Shadden and​​ J.-F.J.-F. Gerbeau.​​​‌ A robust and efficient‌ valve model based on‌​‌ resistive immersed surfaces.​​Int. J. Numer. Meth.​​​‌ Biomed. Engng.289‌2012, 937--959back‌​‌ to text
  • 36 article​​F.F. Baaijens.​​​‌ A fictitious domain/mortar element‌ method for fluid-structure interaction‌​‌.Int. Jour. Num.​​ Meth. Fluids352001​​​‌, 743-761back to‌ text
  • 37 articleL.‌​‌L. Baffico, C.​​C. Grandmont and B.​​​‌B. Maury. Multiscale‌ modeling of the respiratory‌​‌ tract.Math. Models​​ Methods Appl. Sci.20​​​‌12010, 59--93‌back to text
  • 38‌​‌ articleD.D. Boffi​​​‌, N.N. Cavallini​ and L.L. Gastaldi​‌. Finite element approach​​ to immersed boundary method​​​‌ with different fluid and​ solid densities.Math.​‌ Models Methods Appl. Sci.​​21122011,​​​‌ 2523--2550back to text​
  • 39 articleL.L.​‌ Boudin, L.L.​​ Desvillettes, C.C.​​​‌ Grandmont and A.A.​ Moussa. Global existence​‌ of solutions for the​​ coupled Vlasov and Navier-Stokes​​​‌ equations.Differential Integral​ Equations2211-122009​‌, 1247--1271back to​​ text
  • 40 incollectionL.​​​‌L. Boudin, D.​D. Götz and B.​‌B. Grec. Diffusion​​ models of multicomponent mixtures​​​‌ in the lung.​CEMRACS 2009: Mathematical modelling​‌ in medicine30ESAIM​​ Proc.EDP Sci., Les​​​‌ Ulis2010, 90--103​back to text
  • 41​‌ articleL.L. Boudin​​, C.C. Grandmont​​​‌ and A.A. Moussa​. Global existence of​‌ solutions to the incompressible​​ Navier-Stokes-Vlasov equations in a​​​‌ time-dependent domain.J.​ Differential Equations2623​‌2017, 1317--1340back​​ to text
  • 42 book​​​‌L.L. Breiman.​ Classification and regression trees​‌.Routledge2017back​​ to text
  • 43 article​​​‌E.E. Burman and​ M. A.M. A.​‌ Fernández. An unfitted​​ Nitsche method for incompressible​​​‌ fluid-structure interaction using overlapping​ meshes.Comput. Methods​‌ Appl. Mech. Engrg.279​​2014, 497--514back​​​‌ to text
  • 44 article​R. K.R. K.​‌ Calay, J.J.​​ Kurujareon and A. E.​​​‌A. E. Holdo.​ Numerical simulation of respiratory​‌ flow patterns within human​​ lung.Respir. Physiol.​​​‌ Neurobiol.13022002​, 201--221back to​‌ text
  • 45 articleP.​​P. Cazeaux and C.​​​‌C. Grandmont. Homogenization​ of a multiscale viscoelastic​‌ model with nonlocal damping,​​ application to the human​​​‌ lungs.Math. Models​ Methods Appl. Sci.25​‌62015, 1125--1177​​back to text
  • 46​​​‌ articleK. B.K.​ B. Chandran. Role​‌ of Computational Simulations in​​ Heart Valve Dynamics and​​​‌ Design of Valvular Prostheses​.Cardiovasc. Eng. Technol.​‌112010,​​ 18--38back to text​​​‌
  • 47 articleD.D.​ Chapelle and P.P.​‌ Moireau. General coupling​​ of porous flows and​​​‌ hyperelastic formulations—From thermodynamics principles​ to energy balance and​‌ compatible time schemes.​​Eur. J. Mech. B​​​‌ Fluids.462014,​ 82--96back to text​‌
  • 48 articleC.C.​​ Chnafa, S.S.​​​‌ Mendez and F.F.​ Nicoud. Image-Based Simulations​‌ Show Important Flow Fluctuations​​ in a Normal Left​​​‌ Ventricle: What Could be​ the Implications?Ann. Biomed.​‌ Eng.44112016​​, 3346--3358back to​​​‌ text
  • 49 articleT.​T. Colatsky, B.​‌B. Fermini, G.​​G. Gintant, J.​​​‌ B.J. B. Pierson​, P.P. Sager​‌, Y.Y. Sekino​​, D. G.D.​​​‌ G. Strauss and N.​N. Stockbridge. The​‌ comprehensive in vitro proarrhythmia​​ assay (CiPA) initiative—update on​​​‌ progress.J. Pharmacol.​ Toxicol. Methods812016​‌, 15--20back to​​ text
  • 50 articleW.​​​‌ J.W. J. Crumb​, J.J. Vicente​‌, L.L. Johannesen​​ and D. G.D.​​ G. Strauss. An​​​‌ evaluation of 30 clinical‌ drugs against the comprehensive‌​‌ in vitro proarrhythmia assay​​ (CiPA) proposed ion channel​​​‌ panel.J. Pharmacol.‌ Toxicol. Methods812016‌​‌, 251--262back to​​ text
  • 51 articleM.​​​‌M. Fedele, E.‌E. Faggiano, L.‌​‌L. Dedè and A.​​A. Quarteroni. A​​​‌ patient-specific aortic valve model‌ based on moving resistive‌​‌ immersed implicit surfaces.​​Biomech. Model. Mechanobiol.16​​​‌52017, 1779--1803‌back to text
  • 52‌​‌ articleM. A.M.​​ A. Fernández and J.​​​‌J. Mullaert. Convergence‌ and error analysis for‌​‌ a class of splitting​​ schemes in incompressible fluid-structure​​​‌ interaction.IMA J.‌ Numer. Anal.364‌​‌2016, 1748--1782back​​ to text
  • 53 article​​​‌H.H. Gao,‌ L.L. Feng,‌​‌ N.N. Qi,​​ C.C. Berry,​​​‌ B.B.E. Griffith and‌ X.X. Luo.‌​‌ A coupled mitral valve-left​​ ventricle model with fluid-structure​​​‌ interaction.Med. Eng.‌ Phys.4709 2017‌​‌, 128--136back to​​ text
  • 54 articleR.​​​‌R. Glowinski, T.‌T.W. Pan, T.‌​‌T.I. Hesla and D.​​D.D. Joseph. A​​​‌ distributed Lagrange mutiplier/fictitious domain‌ method for particulate flows‌​‌.Int. J. of​​ Multiphase Flow251999​​​‌, 755-794back to‌ text
  • 55 articleC.‌​‌C. Grandmont and M.​​M. Hillairet. Existence​​​‌ of global strong solutions‌ to a beam-fluid interaction‌​‌ system.Arch. Ration.​​ Mech. Anal.2203​​​‌2016, 1283--1333back‌ to text
  • 56 article‌​‌L.L. Grasedyck,​​ D.D. Kressner and​​​‌ C.C. Tobler.‌ A literature survey of‌​‌ low-rank tensor approximation techniques​​.GAMM-Mitt.361​​​‌2013, 53--78back‌ to text
  • 57 article‌​‌M.M. Hillairet.​​ Lack of collision between​​​‌ solid bodies in a‌ 2D incompressible viscous flow‌​‌.Comm. Partial Differential​​ Equations327-92007​​​‌, 1345--1371back to‌ text
  • 58 articleH.‌​‌ M.H. M. Himmel​​. Drug-induced functional cardiotoxicity​​​‌ screening in stem cell-derived‌ human and mouse cardiomyocytes:‌​‌ effects of reference compounds​​.J. Pharmacol. Toxicol.​​​‌ Methods6812013‌, 97--111back to‌​‌ textback to text​​
  • 59 bookJ.J.​​​‌ Kaipio and E.E.‌ Somersalo. Statistical and‌​‌ computational inverse problems.​​160Applied Mathematical Sciences​​​‌Springer-Verlag, New York2005‌back to text
  • 60‌​‌ articleD.D. Kamensky​​, M.-C.M.-C. Hsu​​​‌, Y.Y. Yu‌, J. A.J.‌​‌ A. Evans, M.​​ S.M. S. Sacks​​​‌ and T. J.T.‌ J. R. Hughes.‌​‌ Immersogeometric cardiovascular fluid-structure interaction​​ analysis with divergence-conforming B-splines​​​‌.Comput. Methods Appl.‌ Mech. Engrg.3142017‌​‌, 408--472back to​​ text
  • 61 bookM.​​​‌ J.M. J. van‌ der Laan and S.‌​‌S. Rose. Targeted​​ learning.Springer Series​​​‌ in StatisticsSpringer, New‌ York2011back to‌​‌ text
  • 62 articleM.​​ C.M. C. Lai​​​‌ and C. S.C.‌ S. Peskin. An‌​‌ immersed boundary method with​​ formal second-order accuracy and​​​‌ reduced numerical viscosity.‌J. Comp. Phys.160‌​‌22000, 705--719​​​‌back to text
  • 63​ articleR.R. van​‌ Loon, P. D.​​P. D. Anderson,​​​‌ J.J. de Hart​ and F. P.F.​‌ P. T. Baaijens.​​ A combined fictitious domain/adaptive​​​‌ meshing method for fluid–structure​ interaction in heart valves​‌.International Journal for​​ Numerical Methods in Fluids​​​‌4652004,​ 533-544back to text​‌
  • 64 articleS.S.​​ Martin and B.B.​​​‌ Maury. Modeling of​ the oxygen transfer in​‌ the respiratory process.​​ESAIM Math. Model. Numer.​​​‌ Anal.4742013​, 935--960back to​‌ textback to text​​
  • 65 articleR.R.​​​‌ Mittal, J. H.​J. H. Seo,​‌ V.V. Vedula,​​ Y. J.Y. J.​​​‌ Choi, H.H.​ Liu, H. H.​‌H. H. Huang,​​ S.S. Jain,​​​‌ L.L. Younes,​ T.T. Abraham and​‌ R. T.R. T.​​ George. Computational modeling​​​‌ of cardiac hemodynamics: current​ status and future outlook​‌.J. Comput. Phys.​​3052016, 1065--1082​​​‌back to textback​ to text
  • 66 article​‌J. M.J. M.​​ Oakes, S. C.​​​‌S. C. Shadden,​ C.C. Grandmont and​‌ I. E.I. E.​​ Vignon-Clementel. Aerosol transport​​​‌ throughout inspiration and expiration​ in the pulmonary airways​‌.Int. J. Numer.​​ Methods Biomed. Eng.33​​​‌92017back to​ text
  • 67 articleC.​‌ S.C. S. Peskin​​. The immersed boundary​​​‌ method.Acta Numer.​112002, 479--517​‌back to text
  • 68​​ articleC. J.C.​​​‌ J. Roth, M.​M. Ismail, L.​‌L. Yoshihara and W.​​ A.W. A. Wall​​​‌. A comprehensive computational​ human lung model incorporating​‌ inter-acinar dependencies: Application to​​ spontaneous breathing and mechanical​​​‌ ventilation.Int. J.​ Numer. Method. Biomed. Eng.​‌331e027872016​​back to text
  • 69​​​‌ articleV.V. de​ Silva and L.-H.L.-H.​‌ Lim. Tensor rank​​ and the ill-posedness of​​​‌ the best low-rank approximation​ problem.SIAM J.​‌ Matrix Anal. Appl.30​​32008, 1084--1127​​​‌back to text
  • 70​ articleL.L. Yoshihara​‌, C. J.C.​​ J. Roth and W.​​​‌ A.W. A. Wall​. Fluid-structure interaction including​‌ volumetric coupling with homogenised​​ subdomains for modeling respiratory​​​‌ mechanics.Int. J.​ Numer. Method. Biomed. Eng.​‌334e28122016​​back to text