| Genetic investigation of fibromuscular dysplasia identifies risk loci and shared genetics with common cardiovascular diseases A Georges, ML Yang, TE Berrandou, MK Bakker, O Dikilitas, SR Kiando, ... Nature communications 12 (1), 6031, 2021 | 55 | 2021 |
| National French registry of spontaneous coronary artery dissections: prevalence of fibromuscular dysplasia and genetic analyses: National French SCAD registry: DISCO N Combaret, E Gerbaud, F Dérimay, G Souteyrand, L Cassagnes, ... EuroIntervention 17 (6), 508, 2021 | 45 | 2021 |
| Genome-wide association meta-analysis of spontaneous coronary artery dissection identifies risk variants and genes related to artery integrity and tissue-mediated coagulation D Adlam, TE Berrandou, A Georges, CP Nelson, E Giannoulatou, J Henry, ... Nature Genetics 55 (6), 964-972, 2023 | 39 | 2023 |
| Rare loss-of-function mutations of PTGIR are enriched in fibromuscular dysplasia A Georges, J Albuisson, T Berrandou, D Dupré, A Lorthioir, V D’escamard, ... Cardiovascular Research 117 (4), 1154-1165, 2021 | 29 | 2021 |
| Association of breast cancer risk with polymorphisms in genes involved in the metabolism of xenobiotics and interaction with tobacco smoking: A gene‐set analysis T Berrandou, C Mulot, E Cordina‐Duverger, P Arveux, P Laurent‐Puig, ... International journal of cancer 144 (8), 1896-1908, 2019 | 20 | 2019 |
| Genetic risk score for intracranial aneurysms: prediction of subarachnoid hemorrhage and role in clinical heterogeneity MK Bakker, JP Kanning, G Abraham, AE Martinsen, BS Winsvold, ... Stroke 54 (3), 810-818, 2023 | 18 | 2023 |
| Profiles of polyphenol intake and type 2 diabetes risk in 60,586 women followed for 20 years: Results from the E3N cohort study N Laouali, T Berrandou, J A. Rothwell, S Shah, D El Fatouhi, ... Nutrients 12 (7), 1934, 2020 | 16 | 2020 |
| LDAK-GBAT: Fast and powerful gene-based association testing using summary statistics TE Berrandou, D Balding, D Speed The American Journal of Human Genetics 110 (1), 23-29, 2023 | 15 | 2023 |
| Chromatin accessibility of human mitral valves and functional assessment of MVP risk loci S Kyryachenko, A Georges, M Yu, T Barrandou, L Guo, P Bruneval, ... Circulation research 128 (5), e84-e101, 2021 | 14 | 2021 |
| Genetic Study of PHACTR1 and Fibromuscular Dysplasia, Meta-Analysis and Effects on Clinical Features of Patients: The ARCADIA-POL Study E Warchol-Celinska, T Berrandou, A Prejbisz, A Georges, D Dupré, ... Hypertension 76 (1), e4-e7, 2020 | 12 | 2020 |
| Genomic, Transcriptomic, and Proteomic Depiction of Induced Pluripotent Stem Cells–Derived Smooth Muscle Cells As Emerging Cellular Models for Arterial Diseases L Liu, C Jouve, J Henry, TE Berrandou, JS Hulot, A Georges, ... Hypertension 80 (4), 740-753, 2023 | 7 | 2023 |
| National French registry of spontaneous coronary artery dissections: prevalence of fibromuscular dysplasia and genetic analyses. EuroIntervention.(2021) 17 (6): 508–15. doi: 10 … N Combaret, E Gerbaud, F Dérimay, G Souteyrand, L Cassagnes, ... EIJ-D-20-01046, 0 | 7 | |
| Collaborators. National French registry of spontaneous coronary artery dissections: prevalence of fibromuscular dysplasia and genetic analyses N Combaret, E Gerbaud, F Dérimay, G Souteyrand, L Cassagnes, ... EuroIntervention 17, 508-15, 2021 | 5 | 2021 |
| Genome-wide association meta-analysis of spontaneous coronary artery dissection reveals common variants and genes related to artery integrity and tissue-mediated coagulation D Adlam, TE Berrandou, A Georges, CP Nelson, E Giannoulatou, J Henry, ... medRxiv, 2022.07. 05.22277238, 2022 | 4 | 2022 |
| Genetic association studies of fibromuscular dysplasia identify new risk loci and shared genetic basis with more common vascular diseases A Georges, ML Yang, TE Berrandou, M Bakker, O Dikilitas, L Ma, ... Journal of Hypertension 39, e267, 2021 | 3 | 2021 |
| Variants in the Kallikrein Gene Family and Hypermobile Ehlers-Danlos Syndrome C Gensemer, T Beck, L Guo, T Petrucci, J Morningstar, I Kornblau, ... | 2 | 2024 |
| Characterization of genomic regulation profiles in human mitral valve whole tissue to annotate genetic risk loci for mitral valve prolapse S Kyryachenko, A Georges, M Yu, T Barrandou, P Bruneval, T Rubio, ... medRxiv, 2020.06. 04.20122010, 2020 | 2 | 2020 |
| Rare Loss-of-function Mutations of PTGIR Identified in Fibromuscular Dysplasia and Spontaneous Coronary Artery Dissection A Georges, J Albuisson, T Berrandou, D Dupré, A Lorthioir, V D’Escamard, ... medRxiv, 19012484, 2019 | 1 | 2019 |
| LDAK-PBAT: A Pathway-Based Analysis Tool for Decoding the Genetics of Complex Diseases. TE Berrandou, D Speed medRxiv, 2025.01. 15.25320628, 2025 | | 2025 |
| Genome wide association study meta-analysis of 19,487 individuals with mitral valve prolapse identifies 52 novel genomic regions and highlights pro-fibrosis genes A Small, TE Berrandou, A Georges, J Morningstar, M Huff, TY Yang, J Lee, ... Circulation 150 (Suppl_1), A4143772-A4143772, 2024 | | 2024 |
Nabila Bouatia-NajiINSERM在 inserm.fr 的电子邮件经过验证
