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Florence Coulet
Florence Coulet
Genetics Department, Pitié-Salpêtrière Hospital, Sorbonne University, Paris
Adresse e-mail validée de aphp.fr
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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
5262006
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
4722014
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
4522020
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
3832008
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
3302013
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
3262010
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
3092015
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
2942004
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
2832012
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
2692003
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
2612004
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
2372007
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
2232011
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
1992000
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
1652013
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
1542004
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
1512008
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
1392013
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
1382001
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
1342015
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