| Mutations of the TGF‐β type II receptor BMPR2 in pulmonary arterial hypertension RD Machado, MA Aldred, V James, RE Harrison, B Patel, EC Schwalbe, ... Human mutation 27 (2), 121-132, 2006 | 525 | 2006 |
| EIF2AK4 mutations cause pulmonary veno-occlusive disease, a recessive form of pulmonary hypertension M Eyries, D Montani, B Girerd, C Perret, A Leroy, C Lonjou, N Chelghoum, ... Nature genetics 46 (1), 65-69, 2014 | 470 | 2014 |
| Mechanisms and therapeutic implications of hypermutation in gliomas M Touat, YY Li, AN Boynton, LF Spurr, JB Iorgulescu, CL Bohrson, ... Nature 580 (7804), 517-523, 2020 | 450 | 2020 |
| Clinical Outcomes of Pulmonary Arterial Hypertension in Carriers of BMPR2 Mutation B Sztrymf, F Coulet, B Girerd, A Yaici, X Jais, O Sitbon, D Montani, ... American journal of respiratory and critical care medicine 177 (12), 1377-1383, 2008 | 383 | 2008 |
| Genome-Wide Association Study in BRCA1 Mutation Carriers Identifies Novel Loci Associated with Breast and Ovarian Cancer Risk FJ Couch, X Wang, L McGuffog, A Lee, C Olswold, KB Kuchenbaecker, ... PLoS genetics 9 (3), e1003212, 2013 | 328 | 2013 |
| Clinical Outcomes of Pulmonary Arterial Hypertension in Patients Carrying an ACVRL1 (ALK1) Mutation B Girerd, D Montani, F Coulet, B Sztrymf, A Yaici, X Jaïs, D Tregouet, ... American journal of respiratory and critical care medicine 181 (8), 851-861, 2010 | 324 | 2010 |
| Identification of six new susceptibility loci for invasive epithelial ovarian cancer KB Kuchenbaecker, SJ Ramus, J Tyrer, A Lee, HC Shen, J Beesley, ... Nature genetics 47 (2), 164-171, 2015 | 307 | 2015 |
| Endoglin germline mutation in a patient with hereditary haemorrhagic telangiectasia and dexfenfluramine associated pulmonary arterial hypertension A Chaouat, F Coulet, C Favre, G Simonneau, E Weitzenblum, F Soubrier, ... Thorax 59 (5), 446-448, 2004 | 294 | 2004 |
| Guidelines for splicing analysis in molecular diagnosis derived from a set of 327 combined in silico/in vitro studies on BRCA1 and BRCA2 variants C Houdayer, V Caux‐Moncoutier, S Krieger, M Barrois, F Bonnet, ... Human mutation 33 (8), 1228-1238, 2012 | 283 | 2012 |
| Identification of hypoxia-response element in the human endothelial nitric-oxide synthase gene promoter F Coulet, S Nadaud, M Agrapart, F Soubrier Journal of Biological Chemistry 278 (47), 46230-46240, 2003 | 269 | 2003 |
| Role of truncating mutations in MME gene in fetomaternal alloimmunisation and antenatal glomerulopathies H Debiec, J Nauta, F Coulet, M van der Burg, V Guigonisy, T Schurmans, ... The Lancet 364 (9441), 1252-1259, 2004 | 260 | 2004 |
| Genotype-phenotype correlations in hereditary hemorrhagic telangiectasia: data from the French-Italian HHT network G Lesca, C Olivieri, N Burnichon, F Pagella, MF Carette, ... Genetics in Medicine 9 (1), 14-22, 2007 | 237 | 2007 |
| Molecular genetic characterization of SMAD signaling molecules in pulmonary arterial hypertension MT Nasim, T Ogo, M Ahmed, R Randall, HM Chowdhury, KM Snape, ... Human mutation 32 (12), 1385-1389, 2011 | 222 | 2011 |
| p53 gene status as a predictor of tumor response to induction chemotherapy of patients with locoregionally advanced squamous cell carcinomas of the head and neck S Temam, A Flahault, S Périé, G Monceaux, F Coulet, P Callard, ... Journal of clinical oncology 18 (2), 385-385, 2000 | 199 | 2000 |
| CDH1 germline mutations and the hereditary diffuse gastric and lobular breast cancer syndrome: a multicentre study PR Benusiglio, D Malka, E Rouleau, A De Pauw, B Buecher, C Noguès, ... Journal of medical genetics 50 (7), 486-489, 2013 | 165 | 2013 |
| Molecular screening of ALK1/ACVRL1 and ENG genes in hereditary hemorrhagic telangiectasia in France G Lesca, H Plauchu, F Coulet, S Lefebvre, G Plessis, S Odent, S Rivière, ... Human mutation 23 (4), 289-299, 2004 | 154 | 2004 |
| Identification in Daily Practice of Patients With Lynch Syndrome (Hereditary Nonpolyposis Colorectal Cancer): Revised Bethesda Guidelines-Based Approach: Versus: Molecular … C Julié, C Trésallet, A Brouquet, C Vallot, U Zimmermann, E Mitry, ... Official journal of the American College of Gastroenterology| ACG 103 (11 …, 2008 | 150 | 2008 |
| Somatic mosaicism and double somatic hits can lead to MSI colorectal tumors I Sourrouille, F Coulet, JH Lefevre, C Colas, M Eyries, M Svrcek, ... Familial cancer 12 (1), 27-33, 2013 | 139 | 2013 |
| Factor V Leiden and G20210A prothrombin mutations are risk factors for very early recurrent miscarriage MF Reznikoff-Etiévant, V Cayol, B Carbonne, A Robert, F Coulet, J Milliez British Journal of Obstetrics and Gynaecology 108 (12), 1251-1254, 2001 | 138 | 2001 |
| Constitutional mismatch repair deficiency syndrome: clinical description in a French cohort N Lavoine, C Colas, M Muleris, S Bodo, A Duval, N Entz-Werle, F Coulet, ... Journal of medical genetics 52 (11), 770-778, 2015 | 133 | 2015 |
