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B. Peissel · SciRah

Researcher profile · Semantic Scholar

B. Peissel

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B. Peissel — researcher profile on SciRah

h-index: 46
Works: 155
Citations: 9,547

Most-cited papers

Pathology of breast and ovarian cancers among BRCA1 and BRCA2 mutation carriers: results from the Consortium of Investigators of Modifiers of BRCA1/2 (CIMBA)
N. Mavaddat, D. Barrowdale, I. Andrulis, S. Domchek +129 more
2011Cancer Epidemiology, Biomarkers and Prevention599 citations Open access
Semantic Scholar
Multiple independent variants at the TERT locus are associated with telomere length and risks of breast and ovarian cancer
S. Bojesen, K. Pooley, S. Johnatty, J. Beesley +433 more
2013Nature Genetics560 citations Open access
Semantic Scholar
Genome-wide association studies identify four ER negative–specific breast cancer risk loci
M. García-Closas, F. Couch, S. Lindstrom, K. Michailidou +266 more
2013Nature Genetics442 citations Open access
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 twelve new susceptibility loci for different histotypes of epithelial ovarian cancer
C. Phelan, Karoline B. Kuchenbaecker, J. Tyrer, S. Kar +410 more
2017Nature Genetics399 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
Genome-wide association study identifies 32 novel breast cancer susceptibility loci from overall and subtype-specific analyses
Hao-Yu Zhang, T. Ahearn, J. Lecarpentier, D. Barnes +269 more
2019bioRxiv353 citations Open access
Semantic Scholar
Evaluation of Polygenic Risk Scores for Breast and Ovarian Cancer Risk Prediction in BRCA1 and BRCA2 Mutation Carriers
Karoline B. Kuchenbaecker, L. McGuffog, D. Barrowdale, Andrew Lee +167 more
2017Journal of the National Cancer Institute293 citations Open access
Semantic Scholar
Identification of six new susceptibility loci for invasive epithelial ovarian cancer
Karoline B. Kuchenbaecker, S. Ramus, J. Tyrer, Andrew Lee +285 more
2015Nature Genetics249 citations Open access
Semantic Scholar
PALB2,CHEK2 and ATM rare variants and cancer risk: Data from COGS
M. Southey, D. Goldgar, R. Winqvist, K. Pylkäs +294 more
2016177 citations
Semantic Scholar
Prediction of Breast and Prostate Cancer Risks in Male BRCA1 and BRCA2 Mutation Carriers Using Polygenic Risk Scores
J. Lecarpentier, Valentina Silvestri, Karoline B. Kuchenbaecker, D. Barrowdale +173 more
2017Journal of Clinical Oncology168 citations Open access
Semantic Scholar
Breast cancer risk variants at 6q25 display different phenotype associations and regulate ESR1, RMND1 and CCDC170
A. Dunning, K. Michailidou, Karoline B. Kuchenbaecker, D. Thompson +244 more
2016Nature Genetics157 citations Open access
Semantic Scholar
Association of Type and Location of BRCA1 and BRCA2 Mutations With Risk of Breast and Ovarian Cancer
T. Rebbeck, N. Mitra, F. Wan, O. Sinilnikova +252 more
2015Journal of the American Medical Association (JAMA)147 citations Open access
Semantic Scholar
DNA Glycosylases Involved in Base Excision Repair May Be Associated with Cancer Risk in BRCA1 and BRCA2 Mutation Carriers
A. Osorio, R. Milne, Karoline B. Kuchenbaecker, Tereza Vaclová +193 more
2014PLoS Genetics123 citations Open access
Semantic Scholar
Polygenic risk scores and breast and epithelial ovarian cancer risks for carriers of BRCA1 and BRCA2 pathogenic variants
D. Barnes, M. Rookus, L. McGuffog, Goska Leslie +190 more
2020Genetics in Medicine116 citations Open access
Semantic Scholar
Identification of four novel susceptibility loci for oestrogen receptor negative breast cancer
F. Couch, Karoline B. Kuchenbaecker, K. Michailidou, Gustavo A. Mendoza-Fandino +245 more
2016Nature Communications112 citations Open access
Semantic Scholar
Male breast cancer in BRCA1 and BRCA2 mutation carriers: pathology data from the Consortium of Investigators of Modifiers of BRCA1/2
Valentina Silvestri, D. Barrowdale, A. Mulligan, S. Neuhausen +142 more
2016Breast Cancer Research111 citations Open access
Semantic Scholar
PALB2, CHEK2 and ATM rare variants and cancer risk: data from COGS
M. Southey, D. Goldgar, R. Winqvist, K. Pylkäs +323 more
2016Journal of Medical Genetics102 citations Open access
Semantic Scholar
Common variants at 12p11, 12q24, 9p21, 9q31.2 and in ZNF365 are associated with breast cancer risk for BRCA1 and/or BRCA2 mutation carriers
A. Antoniou, Karoline B. Kuchenbaecker, P. Soucy, J. Beesley +177 more
2012Breast Cancer Research99 citations Open access
Semantic Scholar
The role of genetic breast cancer susceptibility variants as prognostic factors.
P. Fasching, P. Pharoah, A. Cox, H. Nevanlinna +94 more
2012Human Molecular Genetics93 citations Open access
Semantic Scholar
FANCM c.5791C>T nonsense mutation (rs144567652) induces exon skipping, affects DNA repair activity and is a familial breast cancer risk factor.
P. Peterlongo, Irene Catucci, M. Colombo, Laura Caleca +92 more
2015Human Molecular Genetics92 citations Open access
Semantic Scholar
Individuals with FANCM biallelic mutations do not develop Fanconi anemia, but show risk for breast cancer, chemotherapy toxicity and may display chromosome fragility
Irene Catucci, A. Osorio, B. Arver, Guido Neidhardt +24 more
2017Genetics in Medicine89 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
BRCA2 Polymorphic Stop Codon K3326X and the Risk of Breast, Prostate, and Ovarian Cancers.
Huong D. Meeks, Hong-Lin Song, K. Michailidou, M. Bolla +249 more
2016Journal of the National Cancer Institute82 citations Open access
Semantic Scholar
miR-342 Regulates BRCA1 Expression through Modulation of ID4 in Breast Cancer
Elisabetta Crippa, L. Lusa, L. De Cecco, Edoardo Marchesi +7 more
2014PLoS ONE69 citations Open access
Semantic Scholar
Associations of common breast cancer susceptibility alleles with risk of breast cancer subtypes in BRCA1 and BRCA2 mutation carriers
Karoline B. Kuchenbaecker, S. Neuhausen, M. Robson, D. Barrowdale +206 more
2014Breast Cancer Research63 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
Identification of 12 new susceptibility loci for different histotypes of epithelial ovarian cancer
C. Phelan, K. Kuchenbaecker, J. Tyrer, S. Kar +410 more
2017Nature Genetics62 citations Open access
Semantic Scholar
Comparative In Vitro and In Silico Analyses of Variants in Splicing Regions of BRCA1 and BRCA2 Genes and Characterization of Novel Pathogenic Mutations
M. Colombo, G. De Vecchi, Laura Caleca, Claudia Foglia +7 more
2013PLoS ONE59 citations Open access
Semantic Scholar
Identification of fifteen novel germline variants in the BRCA1 3′UTR reveals a variant in a breast cancer case that introduces a functional miR‐103 target site
Brooke L. Brewster, F. Rossiello, J. French, S. Edwards +24 more
2012Human Mutation55 citations
Semantic Scholar
Fine-mapping identifies two additional breast cancer susceptibility loci at 9q31.2
N. Orr, F. Dudbridge, N. Dryden, S. Maguire +209 more
201551 citations Open access
Semantic Scholar
PALB2 germline mutations in familial breast cancer cases with personal and family history of pancreatic cancer
P. Peterlongo, Irene Catucci, G. Pasquini, P. Verderio +7 more
2011Breast Cancer Research and Treatment46 citations
Semantic Scholar
A large-scale assessment of two-way SNP interactions in breast cancer susceptibility using 46,450 cases and 42,461 controls from the breast cancer association consortium.
R. Milne, J. Herranz, K. Michailidou, J. Dennis +139 more
2014Human Molecular Genetics45 citations Open access
Semantic Scholar
Ovarian Cancer Susceptibility Alleles and Risk of Ovarian Cancer in BRCA1 and BRCA2 Mutation Carriers
S. Ramus, A. Antoniou, Karoline B. Kuchenbaecker, P. Soucy +182 more
2012Human Mutation44 citations Open access
Semantic Scholar
Assessing Associations between the AURKA-HMMR-TPX2-TUBG1 Functional Module and Breast Cancer Risk in BRCA1/2 Mutation Carriers
I. Blanco, Karoline B. Kuchenbaecker, D. Cuadras, Xian-Shu Wang +190 more
2015PLoS ONE42 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
Identification of independent association signals and putative functional variants for breast cancer risk through fine-scale mapping of the 12p11 locus
Chen-Jie Zeng, Xing-Yi Guo, J. Long, Karoline B. Kuchenbaecker +233 more
2016Breast Cancer Research41 citations Open access
Semantic Scholar
First description of an acinic cell carcinoma of the breast in a BRCA1 mutation carrier: a case report
C. Ripamonti, M. Colombo, P. Mondini, Manoukian Siranoush +4 more
2013BMC Cancer41 citations Open access
Semantic Scholar
The psychological impact of breast and ovarian cancer preventive options in BRCA1 and BRCA2 mutation carriers
C. Borreani, S. Manoukian, E. Bianchi, C. Brunelli +4 more
2014Clinical Genetics38 citations
Semantic Scholar
Breast and Prostate Cancer Risks for Male BRCA1 and BRCA2 Pathogenic Variant Carriers Using Polygenic Risk Scores
D. Barnes, Valentina Silvestri, Goska Leslie, L. McGuffog +160 more
2021Journal of the National Cancer Institute36 citations Open access
Semantic Scholar
The SNP rs895819 in miR-27a is not associated with familial breast cancer risk in Italians
Irene Catucci, P. Verderio, S. Pizzamiglio, L. Bernard +10 more
2012Breast Cancer Research and Treatment36 citations
Semantic Scholar
Whole‐exome sequencing and targeted gene sequencing provide insights into the role of PALB2 as a male breast cancer susceptibility gene
Valentina Silvestri, Veronica Zelli, V. Valentini, Piera Rizzolo +23 more
2017Cancer34 citations Open access
Semantic Scholar
PALB2 sequencing in Italian familial breast cancer cases reveals a high-risk mutation recurrent in the province of Bergamo
Irene Catucci, P. Peterlongo, S. Ciceri, M. Colombo +20 more
2014Genetics in Medicine34 citations
Semantic Scholar
An original phylogenetic approach identified mitochondrial haplogroup T1a1 as inversely associated with breast cancer risk in BRCA2 mutation carriers
S. Blein, C. Bardel, Vincent Danjean, L. McGuffog +202 more
2015Breast Cancer Research33 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
Adherence to Mediterranean Diet and Metabolic Syndrome in BRCA Mutation Carriers
E. Bruno, S. Manoukian, E. Venturelli, Andreina Oliverio +7 more
2017Integrative Cancer Therapies31 citations Open access
Semantic Scholar
Constitutive BRCA1 Promoter Hypermethylation Can Be a Predisposing Event in Isolated Early-Onset Breast Cancer
J. Azzollini, Chiara Pesenti, S. Pizzamiglio, L. Fontana +11 more
2019Cancers29 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
Functional characterization of the MTC-associated germline RET-K666E mutation: evidence of oncogenic potential enhanced by the G691S polymorphism.
M. G. Borrello, A. Aiello, B. Peissel, M. G. Rizzetti +9 more
2011Endocrine-Related Cancer27 citations Open access
Semantic Scholar
A large de novo 9p21.3 deletion in a girl affected by astrocytoma and multiple melanoma
S. Frigerio, Vittoria Disciglio, S. Manoukian, B. Peissel +9 more
2014BMC Medical Genetics24 citations Open access
Semantic Scholar

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