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I. Coupier · SciRah

Researcher profile · Semantic Scholar

I. Coupier

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I. Coupier — researcher profile on SciRah

h-index: 35
Works: 94
Citations: 4,606

Most-cited papers

A SUMOylation-defective MITF germline mutation predisposes to melanoma and renal carcinoma
C. Bertolotto, F. Lesueur, Sandy Giuliano, T. Strub +95 more
2011Nature524 citations
Semantic Scholar
Genome-Wide Association Study in BRCA1 Mutation Carriers Identifies Novel Loci Associated with Breast and Ovarian Cancer Risk
F. Couch, Xian-Shu Wang, L. McGuffog, Andrew Lee +259 more
2013PLoS Genetics411 citations Open access
Semantic Scholar
Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer
R. Milne, Karoline B. Kuchenbaecker, K. Michailidou, J. Beesley +466 more
2017Nature Genetics379 citations Open access
Semantic Scholar
The succinate dehydrogenase genetic testing in a large prospective series of patients with paragangliomas.
N. Burnichon, V. Rohmer, L. Amar, P. Herman +16 more
2009Journal of Clinical Endocrinology and Metabolism370 citations
Semantic Scholar
RAD51 135G-->C modifies breast cancer risk among BRCA2 mutation carriers: results from a combined analysis of 19 studies.
A. Antoniou, O. Sinilnikova, J. Simard, M. Léoné +75 more
2007American Journal of Human Genetics265 citations Open access
Semantic Scholar
Frequent hSNF5/INI1 Germline Mutations in Patients with Rhabdoid Tumor
F. Bourdeaut, D. Lequin, L. Brugières, S. Reynaud +22 more
2011Clinical Cancer Research198 citations Open access
Semantic Scholar
Imaging work-up for screening of paraganglioma and pheochromocytoma in SDHx mutation carriers: a multicenter prospective study from the PGL.EVA Investigators.
A. Gimenez-Roqueplo, A. Caumont-Prim, C. Houzard, C. Hignette +17 more
2013Journal of Clinical Endocrinology and Metabolism146 citations
Semantic Scholar
Novel FH mutations in families with hereditary leiomyomatosis and renal cell cancer (HLRCC) and patients with isolated type 2 papillary renal cell carcinoma
B. Gardie, Audrey Remenieras, D. Kattygnarath, J. Bombled +49 more
2011Journal of Medical Genetics132 citations Open access
Semantic Scholar
Birt–Hogg–Dubé syndrome: clinical and genetic studies of 10 French families
Nicolas Kluger, S. Giraud, I. Coupier, M.-F. Avril +4 more
2010British Journal of Dermatology121 citations
Semantic Scholar
Significant contribution of large BRCA1 gene rearrangements in 120 French breast and ovarian cancer families
S. Gad, V. Caux-Moncoutier, S. Pagès‐Berhouet, M. Gauthier-Villars +14 more
2002Oncogene119 citations Open access
Semantic Scholar
Common breast cancer susceptibility alleles are associated with tumour subtypes in BRCA1 and BRCA2 mutation carriers: results from the Consortium of Investigators of Modifiers of BRCA1/2
A. Mulligan, F. Couch, D. Barrowdale, S. Domchek +186 more
2011Breast Cancer Research102 citations Open access
Semantic Scholar
Common alleles at 6q25.1 and 1p11.2 are associated with breast cancer risk for BRCA1 and BRCA2 mutation carriers.
A. Antoniou, Christiana Kartsonaki, O. Sinilnikova, P. Soucy +175 more
2011Human Molecular Genetics84 citations Open access
Semantic Scholar
Familial breast cancer and DNA repair genes: Insights into known and novel susceptibility genes from the GENESIS study, and implications for multigene panel testing
E. Girard, Séverine Eon-Marchais, R. Olaso, A. Renault +60 more
2018International Journal of Cancer71 citations Open access
Semantic Scholar
Mutations of the Imprinted CDKN1C Gene as a Cause of the Overgrowth Beckwith–Wiedemann Syndrome: Clinical Spectrum and Functional Characterization
F. Brioude, I. Netchine, F. Praz, Marilyne Le Jule +27 more
2015Human Mutation71 citations Open access
Semantic Scholar
Variation in the Risk of Colorectal Cancer for Lynch Syndrome: A retrospective family cohort study
Aung Ko Win, J. Dowty, J. Reece, Grant Lee +208 more
2021The Lancet Oncology64 citations Open access
Semantic Scholar
Common variants at the 19p13.1 and ZNF365 loci are associated with ER subtypes of breast cancer and ovarian cancer risk in BRCA1 and BRCA2 mutation carriers
F. Couch, M. Gaudet, A. Antoniou, S. Ramus +186 more
2012Cancer Epidemiology, Biomarkers and Prevention63 citations Open access
Semantic Scholar
Guidelines for reporting secondary findings of genome sequencing in cancer genes: the SFMPP recommendations
P. Pujol, Pierre Vande-Perre, L. Faivre, D. Sanlaville +42 more
2018European Journal of Human Genetics60 citations Open access
Semantic Scholar
ETMR-like infantile cerebellar embryonal tumors in the extended morphologic spectrum of DICER1-related tumors
E. Uro-Coste, J. Masliah-Planchon, A. Siegfried, Maud Blanluet +18 more
2018Acta Neuropathologica53 citations Open access
Semantic Scholar
Variation in breast cancer risk with mutation position, smoking, alcohol, and chest X-ray history, in the French National BRCA1/2 carrier cohort (GENEPSO)
Julie Lecarpentier, C. Noguès, E. Mouret-Fourme, D. Stoppa-Lyonnet +13 more
2011Breast Cancer Research and Treatment53 citations Open access
Semantic Scholar
Impact of an information booklet on satisfaction and decision-making about BRCA genetic testing.
J. Mancini, C. Noguès, C. Adenis, P. Berthet +13 more
2006European Journal of Cancer53 citations
Semantic Scholar
Oral contraceptive use and ovarian cancer risk for BRCA1/2 mutation carriers: an international cohort study
Lieske H. Schrijver, A. Antoniou, Hampus Olsson, T. Mooij +133 more
2021American Journal of Obstetrics and Gynecology52 citations Open access
Semantic Scholar
Patients' characteristics and rate of Internet use to obtain cancer information.
J. Mancini, C. Noguès, C. Adenis, P. Berthet +13 more
2006Journal of public health49 citations Open access
Semantic Scholar
Bar code screening on combed DNA for large rearrangements of the BRCA1 and BRCA2 genes in French breast cancer families
S. Gad, M. Klinger, V. Caux-Moncoutier, Sabine Pages-Berhouet +5 more
2002Journal of Medical Genetics48 citations Open access
Semantic Scholar
Risk assessment of maternally inherited SDHD paraganglioma and phaeochromocytoma
N. Burnichon, J. Mazzella, D. Drui, L. Amar +11 more
2016Journal of Medical Genetics47 citations
Semantic Scholar
A germline mutation in PBRM1 predisposes to renal cell carcinoma
P. Benusiglio, S. Couvé, B. Gilbert-Dussardier, S. Deveaux +18 more
2015Journal of Medical Genetics47 citations
Semantic Scholar
Morphology and genomic hallmarks of breast tumours developed by ATM deleterious variant carriers
A. Renault, N. Mebirouk, L. Fuhrmann, G. Bataillon +38 more
2018Breast Cancer Research43 citations Open access
Semantic Scholar
Brief report: High prevalence of somatic oncogenic driver alterations in non-small cell lung cancer patients with Li-Fraumeni Syndrome.
L. Mezquita, M. Jové, E. Nadal, M. Kfoury +27 more
2020Journal of Thoracic Oncology41 citations Open access
Semantic Scholar
The FANCM:p.Arg658* truncating variant is associated with risk of triple-negative breast cancer
G. Figlioli, M. Bogliolo, Irene Catucci, Laura Caleca +473 more
2019npj Breast Cancer41 citations Open access
Semantic Scholar
Is BRCA1/BRCA2‐related breast carcinogenesis estrogen dependent?
Mehadad Noruzinia, I. Coupier, P. Pujol
2005Cancer41 citations
Semantic Scholar
AURKA F31I Polymorphism and Breast Cancer Risk in BRCA1 and BRCA2 Mutation Carriers: A Consortium of Investigators of Modifiers of BRCA1/2 Study
F. Couch, O. Sinilnikova, R. Vierkant, V. Pankratz +67 more
2007Cancer Epidemiology, Biomarkers and Prevention39 citations Open access
Semantic Scholar
Height and Body Mass Index as Modifiers of Breast Cancer Risk in BRCA1/2 Mutation Carriers: A Mendelian Randomization Study.
F. Qian, Sheng-Feng Wang, Jonathan A. Mitchell, L. McGuffog +143 more
2018Journal of the National Cancer Institute38 citations Open access
Semantic Scholar
BRCA1/2 carriers: their childbearing plans and theoretical intentions about having preimplantation genetic diagnosis and prenatal diagnosis
C. Julian-reynier, R. Fabre, I. Coupier, D. Stoppa-Lyonnet +11 more
2012Genetics in Medicine38 citations Open access
Semantic Scholar
Fidelity of DNA double-strand break repair in heterozygous cell lines harbouring BRCA1 missense mutations
I. Coupier, Céline Baldeyron, Alexandra Rousseau, V. Mosseri +4 more
2004Oncogene38 citations
Semantic Scholar
The predictive ability of the 313 variant–based polygenic risk score for contralateral breast cancer risk prediction in women of European ancestry with a heterozygous BRCA1 or BRCA2 pathogenic variant
Inge M. M. Lakeman, A. J. van den Broek, J. A. Vos, D. Barnes +210 more
2021Genetics in Medicine37 citations Open access
Semantic Scholar
A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers
Juliette Coignard, M. Lush, J. Beesley, T. O'Mara +388 more
2021Nature Communications37 citations Open access
Semantic Scholar
Variation in breast cancer risk associated with factors related to pregnancies according to truncating mutation location, in the French National BRCA1 and BRCA2 mutations carrier cohort (GENEPSO)
J. Lecarpentier, C. Noguès, E. Mouret-Fourme, M. Gauthier-Villars +22 more
2012Breast Cancer Research35 citations Open access
Semantic Scholar
Germline copy number variation of genes involved in chromatin remodelling in families suggestive of Li-Fraumeni syndrome with brain tumours
J. Aury-Landas, G. Bougeard, H. Castel, H. Hernández-Vargas +11 more
2013European Journal of Human Genetics34 citations Open access
Semantic Scholar
Association of PHB 1630 C>T and MTHFR 677 C>T polymorphisms with breast and ovarian cancer risk in BRCA1/2 mutation carriers: results from a multicenter study
A. Jakubowska, D. Rozkrut, A. Antoniou, U. Hamann +112 more
2012British Journal of Cancer33 citations Open access
Semantic Scholar
Classification of 101 BRCA1 and BRCA2 variants of uncertain significance by cosegregation study: A powerful approach.
S. Caputo, L. Golmard, M. Léoné, F. Damiola +156 more
2021American Journal of Human Genetics30 citations Open access
Semantic Scholar
Clinical implications of CTNNA1 germline mutations in asymptomatic carriers
P. Benusiglio, C. Colas, E. Guillerm, Axelle Canard +15 more
2018Gastric Cancer30 citations Open access
Semantic Scholar
Conditional Probability of Survival and Prognostic Factors in Long-Term Survivors of High-Grade Serous Ovarian Cancer
M. Fabbro, P. Colombo, C. Leaha, P. Rouanet +11 more
2020Cancers29 citations Open access
Semantic Scholar
Candidate genetic modifiers for breast and ovarian cancer risk in BRCA1 and BRCA2 mutation carriers
P. Peterlongo, J. Chang-Claude, K. Moysich, A. Rudolph +197 more
2014Cancer Epidemiology, Biomarkers and Prevention29 citations Open access
Semantic Scholar
Breast cancer risk in BRCA1 and BRCA2 mutation carriers and polyglutamine repeat length in the AIB1 gene
D. Hughes, Sophie M. Ginolhac, I. Coupier, L. Barjhoux +26 more
2005International Journal of Cancer29 citations Open access
Semantic Scholar
The TP53 Arg72Pro and MDM2 309G>T polymorphisms are not associated with breast cancer risk in BRCA1 and BRCA2 mutation carriers
O. Sinilnikova, A. Antoniou, J. Simard, S. Healey +64 more
2009British Journal of Cancer27 citations Open access
Semantic Scholar
BAP1 and Breast Cancer Risk
I. Coupier, Pierre-Yves Cousin, D. Hughes, Patricia Legoix-né +3 more
2005Familial Cancer25 citations
Semantic Scholar
Germline CDKN2A/P16INK4A mutations contribute to genetic determinism of sarcoma
F. Jouenne, Isaure Chauvot de Beauchêne, Emeline Bollaert, M. Avril +32 more
2017Journal of Medical Genetics22 citations Open access
Semantic Scholar
GENESIS: a French national resource to study the missing heritability of breast cancer
O. Sinilnikova, Marie-Gabrielle Dondon, Séverine Eon-Marchais, F. Damiola +66 more
2016BMC Cancer21 citations Open access
Semantic Scholar
Clinical relevance of 8q23, 15q13 and 18q21 SNP genotyping to evaluate colorectal cancer risk
S. Baert-Desurmont, F. Charbonnier, E. Houivet, L. Ippolito +52 more
2015European Journal of Human Genetics21 citations Open access
Semantic Scholar
Common BRCA2 variants and modification of breast and ovarian cancer risk in BRCA1 mutation carriers.
D. Hughes, Sophie M. Ginolhac, I. Coupier, M. Corbex +30 more
2005Cancer Epidemiology, Biomarkers and Prevention20 citations
Semantic Scholar
Deletion of Chromosomes 13q and 14q Is a Common Feature of Tumors with BRCA2 Mutations
A. Rouault, G. Banneau, G. MacGrogan, N. Jones +10 more
2012PLoS ONE19 citations Open access
Semantic Scholar

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