Frequencies of mutations detected with the screening test targeting founder and recurrent loci in BRCA1 per year and total.

Frequency of BRCA1 dysfunction in ovarian cancer

John P. Geisler
Melanie A. Hatterman-zogg
Jennifer A. Rathe
Richard E. Buller

January 2002

Background: Ovarian cancer is one of the most common hereditary cancers in women. Mutations in the B...

BRCA1 and BRCA2 mutational profile and prevalence in hereditary breast and ovarian cancer (HBOC) probands from Southern Brazil: Are international testing criteria appropriate for this specific population?

Bárbara Alemar (4607857)
Cleandra Gregório (4607863)
Josef Herzog (395277)
Camila Matzenbacher Bittar (4607851)
Cristina Brinckmann Oliveira Netto (4484374)
Osvaldo Artigalas (4607854)
Ida Vanessa D. Schwartz (4607860)
Jordy Coffa (4607866)
Suzi Alves Camey (4607848)
Jeffrey Weitzel (269835)
Patricia Ashton-Prolla (128262)

November 2017

<div>BackgroundGermline pathogenic variants in BRCA1 and BRCA2 (BRCA)...

Cancer Incidence in BRCA1 Mutation Carriers

Thompson, D.
Easton, D. F.
Breast Cancer Linkage Consortium, .

January 2002

Background: Germline BRCA1 mutations confer a substantial lifetime risk of breast and ovarian cancer...

The frequency of mutations detected in BRCA1/2 with NGS among 454 individuals, per year and total (2014–2016).

Artur Kowalik (4164751)
Monika Siołek (5549693)
Janusz Kopczyński (4164760)
Kamila Krawiec (5549687)
Joanna Kalisz (5549690)
Sebastian Zięba (5549699)
Beata Kozak-Klonowska (5549678)
Elżbieta Wypiórkiewicz (4164754)
Jowita Furmańczyk (5549681)
Ewelina Nowak-Ozimek (5549696)
Małgorzata Chłopek (4164769)
Paweł Macek (5549684)
Jolanta Smok-Kalwat (5549702)
Stanisław Góźdź (778173)

July 2018

The frequency of mutations detected in BRCA1/2 with NGS among 454 individuals, per year an...

A BRCA1 founder mutation, identified with haplotype analysis, allowing genotype/phenotype determination and predictive testing

Dorum, A
Moller, P
Kamsteeg, E J
Scheffer, Harmannus
Heimdal, KR
Maehle, LO
Hovig, E
Trope, CG
van der Hout, AH
Buys, CHCM
Meerman, GJT
Burton, M.

December 1997

We searched for a founder mutation in a population from one geographic region of Norway with prevale...

Proportion of pathogenic mutations detected in BRCA1/2 and non-BRCA1/2 genes.

Samuel Guan Wei Ow (3204204)
Pei Yi Ong (6470513)
Soo-Chin Lee (132913)

March 2019

Proportion of pathogenic mutations detected in BRCA1/2 and non-BRCA1/2 genes.</p

A Collaborative Survey of 80 Mutations in the BRCA1 Breast and Ovarian Cancer Susceptibility Gene : Implications for Presymptomatic Testing and Screening

Shattuck Eidens, Donna
Mcclure, Melody
Simard, Jacques
Labrie, Fernand
Narod, Steve
Couch, Fergus
Hoskins, Kent
Weber, Barbara
Castilla, Lucio
Erdos, Mike
Brody, Lawrence
Friedman, Lori
Ostermeyer, Elizabeth
Szabo, Csilla
King, Mary Claire
Jhanwar, Suresh
Offit, Kenneth
Norton, Larry
Gilewski, Teresa
Lubin, Mathew
Osborne, Michael
Black, Donald
Boyd, Marie
Steel, Michael
Ingles, Sue
Haile, Robert
Lindblom, Annika
Olsson, Hakan
Borg, Ake
Bishop, D. Timothy
Solomon, Ellen
Radice, Paolo
Spatti, Giovanbattista
Gayther, Simon
Ponder, Bruce
Warren, William
Stratton, Mike
Liu, Qingyun
Fujimura, Frank
Lewis, Cathryn
Skolnick, Mark H.
Goldgar, David E.

January 1995

OBJECTIVES:To report the initial experience of an international group of investigators in identifyin...

Frequency of gene mutations and germline FLT1 allelic variants in all patients and IMDC intermediate risk patients.

David D. Stenehjem (6263936)
Andrew W. Hahn (6263939)
David M. Gill (6263942)
Daniel Albertson (6263945)
Banumathy Gowrishankar (6263948)
Joseph Merriman (6263951)
Archana M. Agarwal (6263954)
Venkata Thodima (6263957)
Erik B. Harrington (6263960)
Trang H. Au (6263963)
Benjamin L. Maughan (6263966)
Jane Houldsworth (111575)
Sumanta K. Pal (163800)
Neeraj Agarwal (53040)

January 2019

Frequency of gene mutations and germline FLT1 allelic variants in all patients and IMDC intermediate...

BRCA1 and BRCA2 Germline Mutations in Asian and European Populations

Ute Hamann

February 2017

Women who carry a pathogenic mutation in the breast cancer susceptibility genes BRCA1 or BRCA2 (BRCA...

Mutational spectrum in a worldwide study of 29,700 families with BRCA1 or BRCA2 mutations

Rebbeck, T.R.
Friebel, T.M.
Friedman, E.
Hamann, U.
Huo, D.
Kwong, A.
Olah, E.
Olopade, O.I.
Solano, A.R.
Teo, S.H.
Thomassen, M.
Weitzel, J.N.
Chan, T.L.
Couch, F.J.
Goldgar, D.E.
Kruse, T.A.
Palmero, E.I.
Park, S.K.
Torres, D.
Rensburg, E.J. van
McGuffog, L.
Parsons, M.T.
Leslie, G.
Aalfs, C.M.
Abugattas, J.
Adlard, J.
Agata, S.
Aittomaki, K.
Andrews, L.
Andrulis, I.L.
Arason, A.
Arnold, N.
Arun, B.K.
Asseryanis, E.
Auerbach, L.
Azzollini, J.
Balmana, J.
Barile, M.
Barkardottir, R.B.
Barrowdale, D.
Benitez, J.
Berger, A.
Berger, R.
Blanco, A.M.
Blazer, K.R.
Blok, M.J.
Bonadona, V.
Bonanni, B.
Bradbury, A.R.
Brewer, C.
Buecher, B.
Buys, S.S.
Caldes, T.
Caliebe, A.
Caligo, M.A.
Campbell, I.
Caputo, S.M.
Chiquette, J.
Chung, W.K.
Claes, K.B.M.
Collee, J.M.
Cook, J.
Davidson, R.
Hoya, M. de la
Leeneer, K. De
Pauw, A. de
Delnatte, C.
Diez, O.
Ding, Y.C.
Ditsch, N.
Domchek, S.M.
Dorfling, C.M.
Velazquez, C.
Dworniczak, B.
Eason, J.
Easton, D.F.
Eeles, R.
Ehrencrona, H.
Ejlertsen, B.
Engel, C.
Engert, S.
Evans, D.G.
Faivre, L.
Feliubadalo, L.
Ferrer, S.F.
Foretova, L.
Fowler, J.
Frost, D.
Galvao, H.C.R.
Ganz, P.A.
Garber, J.
Gauthier-Villars, M.
Gehrig, A.
Gerdes, A.M.
Gesta, P.
Giannini, G.
Giraud, S.
Glendon, G.
Godwin, A.K.
Greene, M.H.
Mensenkamp, A.R.
Antoniou, A.C.
Nathanson, K.L.

January 2018

Item does not contain fulltextThe prevalence and spectrum of germline mutations in BRCA1 and BRCA2 h...

Tracking of the origin of recurrent mutations of the BRCA1 and BRCA2 genes in the North-East of Italy and improved mutation analysis strategy

Cini, G
Mezzavilla, M
Della Puppa, L
Cupelli, E
Fornasin, A
D'Elia, AV
Dolcetti, R
Damante, G
Bertok, S
Miolo, G
Maestro, R
de Paoli, P
Amoroso, A
Viel, A

February 2016

BACKGROUND: About 20 % of hereditary breast cancers are caused by mutations in BRCA1 and BRCA2 genes...

Mutational spectrum in a worldwide study of 29,700 families with BRCA1 or BRCA2 mutations

Rebbeck, Timothy R.
Friebel, Tara M.
Friedman, Eitan
Hamann, Ute
Huo, Dezheng
Kwong, Ava
Olah, Edith
Olopade, Olufunmilayo I.
Solano, Angela R.
Teo, Soo-Hwang
Thomassen, Mads
Rashid, Muhammad Usman
Rhiem, Kerstin
Robson, Mark
Rodriguez, Gustavo C.
Rogers, Mark T.
Rudaitis, Vilius
Schmidt, Ane Y.
Schmutzler, Rita Katharina
Senter, Leigha
van Rensburg, Elizabeth J.
Gronwald, Jacek
Shah, Payal D.
Sharma, Priyanka
Side, Lucy E.
Simard, Jacques
Singer, Christian F.
Skytte, Anne-Bine
Slavin, Thomas P.
Snape, Katie
Sobol, Hagay
Southey, Melissa
Gutierrez-Barrera, Angelica
McGuffog, Lesley
Steele, Linda
Steinemann, Doris
Sukiennicki, Grzegorz
Sutter, Christian
Szabo, Csilla I.
Tan, Yen Y.
Teixeira, Manuel R.
Terry, Mary Beth
Teulé, Alex
Hahnen, Eric
Thomas, Abigail
Parsons, Michael T.
Thull, Darcy L.
Tischkowitz, Marc
Tognazzo, Silvia
Toland, Amanda Ewart
Topka, Sabine
Trainer, Alison H
Tung, Nadine
van Asperen, Christi J.
Hauke, Jan
van der Hout, Annemieke H.
van der Kolk, Lizet E.
Leslie, Goska
van der Luijt, Rob B.
Van Heetvelde, Mattias
Varesco, Liliana
Varon-Mateeva, Raymonda
Vega, Ana
Villarreal-Garza, Cynthia
von Wachenfeldt, Anna
Henderson, Alex
Walker, Lisa
Wang-Gohrke, Shan
Wappenschmidt, Barbara
Aalfs, Cora M.
Weber, Bernhard H. F.
Yannoukakos, Drakoulis
Yoon, Sook-Yee
Zanzottera, Cristina
Zidan, Jamal
Zorn, Kristin K.
Hentschel, Julia
Hutten Selkirk, Christina G.
Hulick, Peter J.
Chenevix-Trench, Georgia
Spurdle, Amanda B.
Abugattas, Julio
Antoniou, Antonis C.
Nathanson, Katherine L.
Adlard, Julian
Agata, Simona
Aittomäki, Kristiina
Hogervorst, Frans B.L.
Andrews, Lesley
Andrulis, Irene L.
Arason, Adalgeir
Arnold, Norbert
Arun, Banu K.
Asseryanis, Ella
Auerbach, Leo
Azzollini, Jacopo
Balmaña, Judith
Barile, Monica
Honisch, Ellen
Barkardottir, Rosa B.
Barrowdale, Daniel
Benitez, Javier
Berger, Andreas
Berger, Raanan
Blanco, Amie M.
Blazer, Kathleen R.
Blok, Marinus J.
Bonadona, Valérie
Bonanni, Bernardo
Imyanitov, Evgeny N.
Bradbury, Angela R.
Brewer, Carole
Buecher, Bruno
Buys, Saundra S.
Caldes, Trinidad
Caliebe, Almuth
Caligo, Maria A.
Campbell, Ian
Caputo, Sandrine M.
Chiquette, Jocelyne
Isaacs, Claudine
Chung, Wendy K.
Claes, Kathleen B.M.
Collée, J. Margriet
Cook, Jackie
Davidson, Rosemarie
de la Hoya, Miguel
De Leeneer, Kim
de Pauw, Antoine
Delnatte, Capucine
Diez, Orland
Weitzel, Jeffrey N.
Ding, Yuan Chun
Ditsch, Nina
Domchek, Susan M.
Dorfling, Cecilia M.
Velazquez, Carolina
Dworniczak, Bernd
Eason, Jacqueline
Easton, Douglas F.
Eeles, Ros
Ehrencrona, Hans
Izatt, Louise
Ejlertsen, Bent
Engel, Christoph
Engert, Stefanie
Evans, D. Gareth
Faivre, Laurence
Feliubadaló, Lidia
Ferrer, Sandra Fert
Foretova, Lenka
Fowler, Jeffrey
Frost, Debra
Izquierdo, Angel
Galvão, Henrique C. R.
Ganz, Patricia A.
Garber, Judy
Gauthier-Villars, Marion
Gehrig, Andrea
Gerdes, Anne-Marie
Gesta, Paul
Giannini, Giuseppe
Giraud, Sophie
Glendon, Gord
Jakubowska, Anna
Godwin, Andrew K.
Greene, Mark H.
James, Paul
Janavicius, Ramunas
Jensen, Uffe Birk
John, Esther M.
Vijai, Joseph
Kaczmarek, Katarzyna
Karlan, Beth Y.
Chan, TL
Kast, Karin
Investigators, KConFab
Kim, Sung-Won
Konstantopoulou, Irene
Korach, Jacob
Laitman, Yael
Lasa, Adriana
Lasset, Christine
Lázaro, Conxi
Lee, Annette
Couch, Fergus J.
Lee, Min Hyuk
Lester, Jenny
Lesueur, Fabienne
Liljegren, Annelie
Lindor, Noralane M.
Longy, Michel
Loud, Jennifer T.
Lu, Karen H.
Lubinski, Jan
Machackova, Eva
Goldgar, David E.
Manoukian, Siranoush
Mari, Véronique
Martínez-Bouzas, Cristina
Matrai, Zoltan
Mebirouk, Noura
Meijers-Heijboer, Hanne E.J.
Meindl, Alfons
Mensenkamp, Arjen R.
Mickys, Ugnius
Miller, Austin
Kruse, Torben A.
Montagna, Marco
Moysich, Kirsten B.
Mulligan, Anna Marie
Musinsky, Jacob
Neuhausen, Susan L.
Nevanlinna, Heli
Ngeow, Joanne
Nguyen, Huu Phuc
Niederacher, Dieter
Nielsen, Henriette Roed
Palmero, Edenir Inêz
Nielsen, Finn Cilius
Nussbaum, Robert L.
Offit, Kenneth
Öfverholm, Anna
Ong, Kai-ren
Osorio, Ana
Papi, Laura
Papp, Janos
Pasini, Barbara
Pedersen, Inge Sokilde
Park, Sue Kyung
Peixoto, Ana
Peruga, Nina
Peterlongo, Paolo
Pohl, Esther
Pradhan, Nisha
Prajzendanc, Karolina
Prieur, Fabienne
Pujol, Pascal
Radice, Paolo
Ramus, Susan J.
Torres, Diana
Rantala, Johanna

May 2018

To access publisher's full text version of this article click on the hyperlink belowThe prevalence a...

Proportion of pathogenic mutations detected in BRCA1/2 and non-BRCA1/2 genes by Ethnicity (N = 419).

Samuel Guan Wei Ow (3204204)
Pei Yi Ong (6470513)
Soo-Chin Lee (132913)

March 2019

(Excluding n = 41 probands who underwent predictive testing) Proportion of Pathogenic Mutations by E...

Frequency of typical mutations observed among the 2,610 M2 individuals screened.

Liang Chen (73736)
Linzhou Huang (314974)
Donghong Min (138113)
Andy Phillips (11704)
Shiqiang Wang (314975)
Pippa J. Madgwick (314976)
Martin A. J. Parry (95209)
Yin-Gang Hu (138123)

February 2013

Frequency of typical mutations observed among the 2,610 M2 individuals screened.</p

BRCA1 founder mutations and beyond in the Polish population: A single-institution BRCA1/2 next-generation sequencing study

Artur Kowalik (4164751)
Monika Siołek (5549693)
Janusz Kopczyński (4164760)
Kamila Krawiec (5549687)
Joanna Kalisz (5549690)
Sebastian Zięba (5549699)
Beata Kozak-Klonowska (5549678)
Elżbieta Wypiórkiewicz (4164754)
Jowita Furmańczyk (5549681)
Ewelina Nowak-Ozimek (5549696)
Małgorzata Chłopek (4164769)
Paweł Macek (5549684)
Jolanta Smok-Kalwat (5549702)
Stanisław Góźdź (778173)

July 2018

<div>Hereditary mutations in BRCA1/2 genes increase the risk of breast cancer by 60–80% an...

Frequency of BRCA1 dysfunction in ovarian cancer

John P. Geisler
Melanie A. Hatterman-zogg
Jennifer A. Rathe
Richard E. Buller

January 2002

Background: Ovarian cancer is one of the most common hereditary cancers in women. Mutations in the B...

BRCA1 and BRCA2 mutational profile and prevalence in hereditary breast and ovarian cancer (HBOC) probands from Southern Brazil: Are international testing criteria appropriate for this specific population?

Bárbara Alemar (4607857)
Cleandra Gregório (4607863)
Josef Herzog (395277)
Camila Matzenbacher Bittar (4607851)
Cristina Brinckmann Oliveira Netto (4484374)
Osvaldo Artigalas (4607854)
Ida Vanessa D. Schwartz (4607860)
Jordy Coffa (4607866)
Suzi Alves Camey (4607848)
Jeffrey Weitzel (269835)
Patricia Ashton-Prolla (128262)

November 2017

<div>BackgroundGermline pathogenic variants in BRCA1 and BRCA2 (BRCA)...

Cancer Incidence in BRCA1 Mutation Carriers

Thompson, D.
Easton, D. F.
Breast Cancer Linkage Consortium, .

January 2002

Background: Germline BRCA1 mutations confer a substantial lifetime risk of breast and ovarian cancer...

The frequency of mutations detected in BRCA1/2 with NGS among 454 individuals, per year and total (2014–2016).

Artur Kowalik (4164751)
Monika Siołek (5549693)
Janusz Kopczyński (4164760)
Kamila Krawiec (5549687)
Joanna Kalisz (5549690)
Sebastian Zięba (5549699)
Beata Kozak-Klonowska (5549678)
Elżbieta Wypiórkiewicz (4164754)
Jowita Furmańczyk (5549681)
Ewelina Nowak-Ozimek (5549696)
Małgorzata Chłopek (4164769)
Paweł Macek (5549684)
Jolanta Smok-Kalwat (5549702)
Stanisław Góźdź (778173)

July 2018

The frequency of mutations detected in BRCA1/2 with NGS among 454 individuals, per year an...

A BRCA1 founder mutation, identified with haplotype analysis, allowing genotype/phenotype determination and predictive testing

Dorum, A
Moller, P
Kamsteeg, E J
Scheffer, Harmannus
Heimdal, KR
Maehle, LO
Hovig, E
Trope, CG
van der Hout, AH
Buys, CHCM
Meerman, GJT
Burton, M.

December 1997

We searched for a founder mutation in a population from one geographic region of Norway with prevale...

Proportion of pathogenic mutations detected in BRCA1/2 and non-BRCA1/2 genes.

Samuel Guan Wei Ow (3204204)
Pei Yi Ong (6470513)
Soo-Chin Lee (132913)

March 2019

Proportion of pathogenic mutations detected in BRCA1/2 and non-BRCA1/2 genes.</p

A Collaborative Survey of 80 Mutations in the BRCA1 Breast and Ovarian Cancer Susceptibility Gene : Implications for Presymptomatic Testing and Screening

Shattuck Eidens, Donna
Mcclure, Melody
Simard, Jacques
Labrie, Fernand
Narod, Steve
Couch, Fergus
Hoskins, Kent
Weber, Barbara
Castilla, Lucio
Erdos, Mike
Brody, Lawrence
Friedman, Lori
Ostermeyer, Elizabeth
Szabo, Csilla
King, Mary Claire
Jhanwar, Suresh
Offit, Kenneth
Norton, Larry
Gilewski, Teresa
Lubin, Mathew
Osborne, Michael
Black, Donald
Boyd, Marie
Steel, Michael
Ingles, Sue
Haile, Robert
Lindblom, Annika
Olsson, Hakan
Borg, Ake
Bishop, D. Timothy
Solomon, Ellen
Radice, Paolo
Spatti, Giovanbattista
Gayther, Simon
Ponder, Bruce
Warren, William
Stratton, Mike
Liu, Qingyun
Fujimura, Frank
Lewis, Cathryn
Skolnick, Mark H.
Goldgar, David E.

January 1995

OBJECTIVES:To report the initial experience of an international group of investigators in identifyin...

Frequency of gene mutations and germline FLT1 allelic variants in all patients and IMDC intermediate risk patients.

David D. Stenehjem (6263936)
Andrew W. Hahn (6263939)
David M. Gill (6263942)
Daniel Albertson (6263945)
Banumathy Gowrishankar (6263948)
Joseph Merriman (6263951)
Archana M. Agarwal (6263954)
Venkata Thodima (6263957)
Erik B. Harrington (6263960)
Trang H. Au (6263963)
Benjamin L. Maughan (6263966)
Jane Houldsworth (111575)
Sumanta K. Pal (163800)
Neeraj Agarwal (53040)

January 2019

Frequency of gene mutations and germline FLT1 allelic variants in all patients and IMDC intermediate...

BRCA1 and BRCA2 Germline Mutations in Asian and European Populations

Ute Hamann

February 2017

Women who carry a pathogenic mutation in the breast cancer susceptibility genes BRCA1 or BRCA2 (BRCA...

Mutational spectrum in a worldwide study of 29,700 families with BRCA1 or BRCA2 mutations

Rebbeck, T.R.
Friebel, T.M.
Friedman, E.
Hamann, U.
Huo, D.
Kwong, A.
Olah, E.
Olopade, O.I.
Solano, A.R.
Teo, S.H.
Thomassen, M.
Weitzel, J.N.
Chan, T.L.
Couch, F.J.
Goldgar, D.E.
Kruse, T.A.
Palmero, E.I.
Park, S.K.
Torres, D.
Rensburg, E.J. van
McGuffog, L.
Parsons, M.T.
Leslie, G.
Aalfs, C.M.
Abugattas, J.
Adlard, J.
Agata, S.
Aittomaki, K.
Andrews, L.
Andrulis, I.L.
Arason, A.
Arnold, N.
Arun, B.K.
Asseryanis, E.
Auerbach, L.
Azzollini, J.
Balmana, J.
Barile, M.
Barkardottir, R.B.
Barrowdale, D.
Benitez, J.
Berger, A.
Berger, R.
Blanco, A.M.
Blazer, K.R.
Blok, M.J.
Bonadona, V.
Bonanni, B.
Bradbury, A.R.
Brewer, C.
Buecher, B.
Buys, S.S.
Caldes, T.
Caliebe, A.
Caligo, M.A.
Campbell, I.
Caputo, S.M.
Chiquette, J.
Chung, W.K.
Claes, K.B.M.
Collee, J.M.
Cook, J.
Davidson, R.
Hoya, M. de la
Leeneer, K. De
Pauw, A. de
Delnatte, C.
Diez, O.
Ding, Y.C.
Ditsch, N.
Domchek, S.M.
Dorfling, C.M.
Velazquez, C.
Dworniczak, B.
Eason, J.
Easton, D.F.
Eeles, R.
Ehrencrona, H.
Ejlertsen, B.
Engel, C.
Engert, S.
Evans, D.G.
Faivre, L.
Feliubadalo, L.
Ferrer, S.F.
Foretova, L.
Fowler, J.
Frost, D.
Galvao, H.C.R.
Ganz, P.A.
Garber, J.
Gauthier-Villars, M.
Gehrig, A.
Gerdes, A.M.
Gesta, P.
Giannini, G.
Giraud, S.
Glendon, G.
Godwin, A.K.
Greene, M.H.
Mensenkamp, A.R.
Antoniou, A.C.
Nathanson, K.L.

January 2018

Item does not contain fulltextThe prevalence and spectrum of germline mutations in BRCA1 and BRCA2 h...

Tracking of the origin of recurrent mutations of the BRCA1 and BRCA2 genes in the North-East of Italy and improved mutation analysis strategy

Cini, G
Mezzavilla, M
Della Puppa, L
Cupelli, E
Fornasin, A
D'Elia, AV
Dolcetti, R
Damante, G
Bertok, S
Miolo, G
Maestro, R
de Paoli, P
Amoroso, A
Viel, A

February 2016

BACKGROUND: About 20 % of hereditary breast cancers are caused by mutations in BRCA1 and BRCA2 genes...

Mutational spectrum in a worldwide study of 29,700 families with BRCA1 or BRCA2 mutations

Rebbeck, Timothy R.
Friebel, Tara M.
Friedman, Eitan
Hamann, Ute
Huo, Dezheng
Kwong, Ava
Olah, Edith
Olopade, Olufunmilayo I.
Solano, Angela R.
Teo, Soo-Hwang
Thomassen, Mads
Rashid, Muhammad Usman
Rhiem, Kerstin
Robson, Mark
Rodriguez, Gustavo C.
Rogers, Mark T.
Rudaitis, Vilius
Schmidt, Ane Y.
Schmutzler, Rita Katharina
Senter, Leigha
van Rensburg, Elizabeth J.
Gronwald, Jacek
Shah, Payal D.
Sharma, Priyanka
Side, Lucy E.
Simard, Jacques
Singer, Christian F.
Skytte, Anne-Bine
Slavin, Thomas P.
Snape, Katie
Sobol, Hagay
Southey, Melissa
Gutierrez-Barrera, Angelica
McGuffog, Lesley
Steele, Linda
Steinemann, Doris
Sukiennicki, Grzegorz
Sutter, Christian
Szabo, Csilla I.
Tan, Yen Y.
Teixeira, Manuel R.
Terry, Mary Beth
Teulé, Alex
Hahnen, Eric
Thomas, Abigail
Parsons, Michael T.
Thull, Darcy L.
Tischkowitz, Marc
Tognazzo, Silvia
Toland, Amanda Ewart
Topka, Sabine
Trainer, Alison H
Tung, Nadine
van Asperen, Christi J.
Hauke, Jan
van der Hout, Annemieke H.
van der Kolk, Lizet E.
Leslie, Goska
van der Luijt, Rob B.
Van Heetvelde, Mattias
Varesco, Liliana
Varon-Mateeva, Raymonda
Vega, Ana
Villarreal-Garza, Cynthia
von Wachenfeldt, Anna
Henderson, Alex
Walker, Lisa
Wang-Gohrke, Shan
Wappenschmidt, Barbara
Aalfs, Cora M.
Weber, Bernhard H. F.
Yannoukakos, Drakoulis
Yoon, Sook-Yee
Zanzottera, Cristina
Zidan, Jamal
Zorn, Kristin K.
Hentschel, Julia
Hutten Selkirk, Christina G.
Hulick, Peter J.
Chenevix-Trench, Georgia
Spurdle, Amanda B.
Abugattas, Julio
Antoniou, Antonis C.
Nathanson, Katherine L.
Adlard, Julian
Agata, Simona
Aittomäki, Kristiina
Hogervorst, Frans B.L.
Andrews, Lesley
Andrulis, Irene L.
Arason, Adalgeir
Arnold, Norbert
Arun, Banu K.
Asseryanis, Ella
Auerbach, Leo
Azzollini, Jacopo
Balmaña, Judith
Barile, Monica
Honisch, Ellen
Barkardottir, Rosa B.
Barrowdale, Daniel
Benitez, Javier
Berger, Andreas
Berger, Raanan
Blanco, Amie M.
Blazer, Kathleen R.
Blok, Marinus J.
Bonadona, Valérie
Bonanni, Bernardo
Imyanitov, Evgeny N.
Bradbury, Angela R.
Brewer, Carole
Buecher, Bruno
Buys, Saundra S.
Caldes, Trinidad
Caliebe, Almuth
Caligo, Maria A.
Campbell, Ian
Caputo, Sandrine M.
Chiquette, Jocelyne
Isaacs, Claudine
Chung, Wendy K.
Claes, Kathleen B.M.
Collée, J. Margriet
Cook, Jackie
Davidson, Rosemarie
de la Hoya, Miguel
De Leeneer, Kim
de Pauw, Antoine
Delnatte, Capucine
Diez, Orland
Weitzel, Jeffrey N.
Ding, Yuan Chun
Ditsch, Nina
Domchek, Susan M.
Dorfling, Cecilia M.
Velazquez, Carolina
Dworniczak, Bernd
Eason, Jacqueline
Easton, Douglas F.
Eeles, Ros
Ehrencrona, Hans
Izatt, Louise
Ejlertsen, Bent
Engel, Christoph
Engert, Stefanie
Evans, D. Gareth
Faivre, Laurence
Feliubadaló, Lidia
Ferrer, Sandra Fert
Foretova, Lenka
Fowler, Jeffrey
Frost, Debra
Izquierdo, Angel
Galvão, Henrique C. R.
Ganz, Patricia A.
Garber, Judy
Gauthier-Villars, Marion
Gehrig, Andrea
Gerdes, Anne-Marie
Gesta, Paul
Giannini, Giuseppe
Giraud, Sophie
Glendon, Gord
Jakubowska, Anna
Godwin, Andrew K.
Greene, Mark H.
James, Paul
Janavicius, Ramunas
Jensen, Uffe Birk
John, Esther M.
Vijai, Joseph
Kaczmarek, Katarzyna
Karlan, Beth Y.
Chan, TL
Kast, Karin
Investigators, KConFab
Kim, Sung-Won
Konstantopoulou, Irene
Korach, Jacob
Laitman, Yael
Lasa, Adriana
Lasset, Christine
Lázaro, Conxi
Lee, Annette
Couch, Fergus J.
Lee, Min Hyuk
Lester, Jenny
Lesueur, Fabienne
Liljegren, Annelie
Lindor, Noralane M.
Longy, Michel
Loud, Jennifer T.
Lu, Karen H.
Lubinski, Jan
Machackova, Eva
Goldgar, David E.
Manoukian, Siranoush
Mari, Véronique
Martínez-Bouzas, Cristina
Matrai, Zoltan
Mebirouk, Noura
Meijers-Heijboer, Hanne E.J.
Meindl, Alfons
Mensenkamp, Arjen R.
Mickys, Ugnius
Miller, Austin
Kruse, Torben A.
Montagna, Marco
Moysich, Kirsten B.
Mulligan, Anna Marie
Musinsky, Jacob
Neuhausen, Susan L.
Nevanlinna, Heli
Ngeow, Joanne
Nguyen, Huu Phuc
Niederacher, Dieter
Nielsen, Henriette Roed
Palmero, Edenir Inêz
Nielsen, Finn Cilius
Nussbaum, Robert L.
Offit, Kenneth
Öfverholm, Anna
Ong, Kai-ren
Osorio, Ana
Papi, Laura
Papp, Janos
Pasini, Barbara
Pedersen, Inge Sokilde
Park, Sue Kyung
Peixoto, Ana
Peruga, Nina
Peterlongo, Paolo
Pohl, Esther
Pradhan, Nisha
Prajzendanc, Karolina
Prieur, Fabienne
Pujol, Pascal
Radice, Paolo
Ramus, Susan J.
Torres, Diana
Rantala, Johanna

May 2018

To access publisher's full text version of this article click on the hyperlink belowThe prevalence a...

Proportion of pathogenic mutations detected in BRCA1/2 and non-BRCA1/2 genes by Ethnicity (N = 419).

Samuel Guan Wei Ow (3204204)
Pei Yi Ong (6470513)
Soo-Chin Lee (132913)

March 2019

(Excluding n = 41 probands who underwent predictive testing) Proportion of Pathogenic Mutations by E...

Frequency of typical mutations observed among the 2,610 M2 individuals screened.

Liang Chen (73736)
Linzhou Huang (314974)
Donghong Min (138113)
Andy Phillips (11704)
Shiqiang Wang (314975)
Pippa J. Madgwick (314976)
Martin A. J. Parry (95209)
Yin-Gang Hu (138123)

February 2013

Frequency of typical mutations observed among the 2,610 M2 individuals screened.</p

BRCA1 founder mutations and beyond in the Polish population: A single-institution BRCA1/2 next-generation sequencing study

Artur Kowalik (4164751)
Monika Siołek (5549693)
Janusz Kopczyński (4164760)
Kamila Krawiec (5549687)
Joanna Kalisz (5549690)
Sebastian Zięba (5549699)
Beata Kozak-Klonowska (5549678)
Elżbieta Wypiórkiewicz (4164754)
Jowita Furmańczyk (5549681)
Ewelina Nowak-Ozimek (5549696)
Małgorzata Chłopek (4164769)
Paweł Macek (5549684)
Jolanta Smok-Kalwat (5549702)
Stanisław Góźdź (778173)

July 2018

<div>Hereditary mutations in BRCA1/2 genes increase the risk of breast cancer by 60–80% an...

Frequency of BRCA1 dysfunction in ovarian cancer

John P. Geisler
Melanie A. Hatterman-zogg
Jennifer A. Rathe
Richard E. Buller

January 2002

Background: Ovarian cancer is one of the most common hereditary cancers in women. Mutations in the B...

BRCA1 and BRCA2 mutational profile and prevalence in hereditary breast and ovarian cancer (HBOC) probands from Southern Brazil: Are international testing criteria appropriate for this specific population?

Bárbara Alemar (4607857)
Cleandra Gregório (4607863)
Josef Herzog (395277)
Camila Matzenbacher Bittar (4607851)
Cristina Brinckmann Oliveira Netto (4484374)
Osvaldo Artigalas (4607854)
Ida Vanessa D. Schwartz (4607860)
Jordy Coffa (4607866)
Suzi Alves Camey (4607848)
Jeffrey Weitzel (269835)
Patricia Ashton-Prolla (128262)

November 2017

<div>BackgroundGermline pathogenic variants in BRCA1 and BRCA2 (BRCA)...

Cancer Incidence in BRCA1 Mutation Carriers

Thompson, D.
Easton, D. F.
Breast Cancer Linkage Consortium, .

January 2002

Background: Germline BRCA1 mutations confer a substantial lifetime risk of breast and ovarian cancer...

Frequencies of mutations detected with the screening test targeting founder and recurrent <i>loci</i> in <i>BRCA1</i> per year and total.

Abstract

Extracted data

Frequencies of mutations detected with the screening test targeting founder and recurrent <i>loci</i> in <i>BRCA1</i> per year and total.

Abstract

Extracted data

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