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genome-wide association (11) 11
breast cancer (10) 10
oncology (10) 10
susceptibility loci (8) 8
humans (7) 7
ovarian-cancer (7) 7
population (7) 7
common variants (6) 6
female (6) 6
genetic modifiers (6) 6
life sciences & biomedicine (6) 6
mutation (6) 6
science & technology (6) 6
skin and connective tissue diseases (6) 6
breast neoplasms - genetics (5) 5
consortium (5) 5
disease (5) 5
risk (5) 5
brca1 (4) 4
brca1 and brca2 mutation carriers (4) 4
brca2 (4) 4
brca2 mutation carriers (4) 4
cis-regulatory variants (4) 4
differential allelic expression (4) 4
epidemiology (4) 4
expression (4) 4
genes (4) 4
genes, brca1 (4) 4
genes, brca2 (4) 4
genetic predisposition to disease (4) 4
genetic susceptibility (4) 4
genetics (4) 4
mutations (4) 4
ovarian cancer (4) 4
association (3) 3
biological and medical sciences (3) 3
breast (3) 3
breast-cancer (3) 3
cancer (3) 3
cancer research (3) 3
confer susceptibility (3) 3
endocrine system diseases (3) 3
endometriosis (3) 3
estrogen-receptor (3) 3
functional variants (3) 3
germline mutations (3) 3
identification (3) 3
medical sciences (3) 3
medicin och hälsovetenskap (3) 3
metaanalysis (3) 3
modifiers (3) 3
ovarian neoplasms - genetics (3) 3
polymorphism (3) 3
yes (3) 3
alleles (2) 2
brca1 protein (2) 2
breast neoplasms (2) 2
cancer and oncology (2) 2
cancer och onkologi (2) 2
cell (2) 2
chip-seq (2) 2
clear-cell carcinoma (2) 2
clinical medicine (2) 2
elements (2) 2
expression signature (2) 2
family (2) 2
fanconi-anemia (2) 2
female genital diseases (2) 2
gene-expression (2) 2
genetic interaction networks (2) 2
genetic linkage (2) 2
genetic testing (2) 2
genetic-variants (2) 2
genetics and genomics (2) 2
gynecology. andrology. obstetrics (2) 2
heterozygote (2) 2
investigators (2) 2
klinisk medicin (2) 2
lod score (2) 2
medical and health sciences (2) 2
obesity (2) 2
ovarian cancers (2) 2
polymorphism, single nucleotide (2) 2
reveals (2) 2
risk factors (2) 2
sequence variants (2) 2
subtypes (2) 2
survival (2) 2
susceptibility alleles (2) 2
telomere length (2) 2
tumors (2) 2
umcg approved (2) 2
unclassified variants (2) 2
unknown clinical-significance (2) 2
variants (2) 2
znf365 (2) 2
185delag mutation (1) 1
2 mutation carriers (1) 1
2q35 (1) 1
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1. Risks of breast, ovarian, and contralateral breast cancer for BRCA1 and BRCA2 mutation carriers
by Kuchenbaecker, Karoline B and Hopper, John L and Barnes, Daniel R and Phillips, Kelly-Anne and Mooij, Thea M and Roos-Blom, Marie-José and Jervis, Sarah and Van Leeuwen, Flora E and Milne, Roger L and Andrieu, Nadine and Goldgar, David E and Terry, Mary Beth and Rookus, Matti A and Easton, Douglas F and Antoniou, Antonis C and BRCA1 BRCA2 Cohort Consortium and BRCA1 and BRCA2 Cohort Consortium
JAMA : the journal of the American Medical Association, ISSN 0098-7484, 06/2017, Volume 317, Issue 23, pp. 2402 - 2416
Medicine, General & Internal | Life Sciences & Biomedicine | General & Internal Medicine | Science & Technology | Age Distribution | Prospective Studies | Age Factors | Risk Assessment | Humans | Middle Aged | Incidence | Neoplasms, Second Primary - epidemiology | Ovarian Neoplasms - epidemiology | Ovarian Neoplasms - genetics | Breast Neoplasms - genetics | Time Factors | Aged, 80 and over | Genes, BRCA2 | Adult | Family | Female | Aged | Genes, BRCA1 | Mutation | Neoplasms, Second Primary - genetics | Breast Neoplasms - epidemiology | BRCA2 protein | Ovarian carcinoma | BRCA1 protein | Health risks | Oncology | Population studies | Breast cancer | Estimates | Ovarian cancer | Carriers | Consortia | Design modifications | Risk assessment | Data collection | Genetics | Diagnosis | Genetic testing | Position (location) | Age | Cancer
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2. Full Text A Transcriptome-Wide Association Study Among 97,898 Women to Identify Candidate Susceptibility Genes for Epithelial Ovarian Cancer Risk
by Lu, Yingchang and Beeghly-Fadiel, Alicia and Wu, Lang and Guo, Xingyi and Li, Bingshan and Schildkraut, Joellen M and Im, Hae Kyung and Permuth, Jennifer B and Reid, Brett M and Moysich, Kirsten B and Anton-Culver, Hoda and Bandera, Elisa V and Barkardottir, Rosa B and Barnes, Daniel R and Benitez, Javier and Bjorge, Line and Brenton, James and Caldes, Trinidad and Caligo, Maria A and Campbell, Ian and Chang-Claude, Jenny and Claes, Kathleen B M and Cramer, Daniel W and Daly, Mary B and Diez, Orland and Domchek, Susan M and Easton, Douglas F and Eccles, Diana M and Fasching, Peter A and Fortner, Renée T and Friedman, Eitan and Ganz, Patricia A and Garber, Judy and Godwin, Anew K and Goldgar, David E and Greene, Mark H and Gronwald, Jacek and Hamann, Ute and Heitz, Florian and Høgdall, Claus K and Huntsman, David G and Imyanitov, Evgeny N and Isaacs, Claudine and Jakubowska, Anna and James, Paul and Karlan, Beth Y and Kelemen, Linda E and Kiemeney, Lambertus A and Kjaer, Susanne K and Kwong, Ava and Leslie, Goska and Lesueur, Fabienne and Levine, Douglas A and Mattiello, Amalia and May, Taymaa and McNeish, Iain A and Modugno, Francesmary and Montagna, Marco and Nielsen, Finn C and Nikitina-Zake, Liene and Nussbaum, Robert L and Offit, Kenneth and Olopade, Olufunmilayo I and Olson, Sara H and Osorio, Ana and Park, Sue K and Peeters, Petra H M and Pejovic, Tanja and Peterlongo, Paolo and Phelan, Catherine M and Pujana, Miquel Angel and Ramus, Susan J and Risch, Harvey and Roiguez, Gustavo C and Romieu, Isabelle and Rookus, Matti A and Rossing, Mary Anne and Sieh, Weiva and Simard, Jacques and Song, Honglin and Southey, Melissa C and Sutphen, Rebecca and Swerdlow, Anthony J and Teo, Soo H and Thomassen, Mads and Tischkowitz, Marc and Tworoger, Shelley S and van Rensburg, Elizabeth J and Vega, Ana and Edwards, Digna Velez and Webb, Penelope M and Weitzel, Jeffrey N and Wentzensen, Nicolas and White, Emily and Wolk, Alicja and Zorn, Kristin K and Gayther, Simon A and Berchuck, Anew and Goode, Ellen L and Pharoah, Paul D P
Cancer research (Chicago, Ill.), ISSN 0008-5472, 09/2018, Volume 78, Issue 18, p. 5419
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3. Full Text The BRCA2 c.68-7T > A variant is not pathogenic: A model for clinical calibration of spliceogenicity
by Colombo, Mara and Lopez-Perolio, Irene and Meeks, Huong D and Caleca, Laura and Parsons, Michael T and Li, Hongyan and De Vecchi, Giovanna and Tudini, Emma and Foglia, Claudia and Mondini, Patrizia and Manoukian, Siranoush and Behar, Raquel and Garcia, Encarna B. Gomez and Meindl, Alfons and Montagna, Marco and Niederacher, Dieter and Schmidt, Ane Y and Varesco, Liliana and Wappenschmidt, Barbara and Bolla, Manjeet K and Dennis, Joe and Michailidou, Kyriaki and Wang, Qin and Aittomaki, Kristiina and Anulis, Irene L and Anton-Culver, Hoda and Arndt, Volker and Beckmann, Matthias W and Beeghly-Fadel, Alicia and Benitez, Javier and Boeckx, Bram and Bogdanova, Natalia V and Bojesen, Stig E and Bonanni, Bernardo and Brauch, Hiltrud and Brenner, Hermann and Burwinkel, Barbara and Chang-Claude, Jenny and Conroy, Don M and Couch, Fergus J and Cox, Angela and Cross, Simon S and Czene, Kamila and Devilee, Peter and Dork, Thilo and Eriksson, Mikael and Fasching, Peter A and Figueroa, Jonine and Fletcher, Olivia and Flyger, Henrik
Human mutation, ISSN 1059-7794, 05/2018, Volume 39, Issue 5, pp. 729 - 741
digital PCR | RNA | multifactorial likelihood analysis | SEQUENCE VARIANTS | RISK | UNCLASSIFIED VARIANTS | BRCA2 | quantitative real-time PCR | FANCONI-ANEMIA | CANCER | BREAST | INTEGRATED EVALUATION | spliceogenic variants | GENES | MUTATIONS
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4. Full Text The Influence of Number and Timing of Pregnancies on Breast Cancer Risk for Women With BRCA1 or BRCA2 Mutations
by Terry, Mary Beth and Liao, Yuyan and Kast, Karin and Antoniou, Antonis C and McDonald, Jasmine A and Mooij, Thea M and Engel, Christoph and Nogues, Catherine and Buecher, Bruno and Mari, Véronique and Moretta-Serra, Jessica and Gladieff, Laurence and Luporsi, Elisabeth and Barrowdale, Daniel and Frost, Debra and Henderson, Alex and Brewer, Carole and Evans, D Gareth and Eccles, Diana and Cook, Jackie and Ong, Kai-Ren and Izatt, Louise and Ahmed, Munaza and Morrison, Patrick J and Dommering, Charlotte J and Oosterwijk, Jan C and Ausems, Margreet G E M and Kriege, Mieke and Buys, Sauna S and Anulis, Irene L and John, Esther M and Daly, Mary and Friedlander, Michael and McLachlan, Sue Anne and Osorio, Ana and Caldes, Trinidad and Jakubowska, Anna and Simard, Jacques and Singer, Christian F and Tan, Yen and Olah, Edith and Navratilova, Marie and Foretova, Lenka and Gerdes, Anne-Marie and Roos-Blom, Marie-José and Arver, Brita and Olsson, Håkan and Schmutzler, Rita K and Hopper, John L and van Leeuwen, Flora E and EMBRACE, GENEPSO, BCFR, HEBON, kConFab and IBCCS
JNCI cancer spectrum, ISSN 2515-5091, 12/2018, Volume 2, Issue 4, pp. pky078 - pky078
Life Sciences | Santé publique et épidémiologie | Genetics | Cancer
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5. Full Text Association of the Variants CASP8 D302H and CASP10 V410I with Breast and Ovarian Cancer Risk in BRCA1 and BRCA2 Mutation Carriers
by Engel, Christoph and Versmold, Beatrix and Wappenschmidt, Barbara and Simard, Jacques and Easton, Douglas F and Peock, Susan and Cook, Margaret and Oliver, Clare and Frost, Debra and Mayes, Rebecca and Evans, D. Gareth and Eeles, Rosalind and Paterson, Joan and Brewer, Carole and McGuffog, Lesley and Antoniou, Antonis C and Stoppa-Lyonnet, Dominique and Sinilnikova, Olga M and Barjhoux, Laure and Frenay, Marc and Michel, Cécile and Leroux, Dominique and yfus, Helene and Toulas, Christine and Gladieff, Laurence and Uhrhammer, Nancy and Bignon, Yves-Jean and Meindl, Alfons and Arnold, Norbert and Varon-Mateeva, Raymonda and Niederacher, Dieter and Preisler-Adams, Sabine and Kast, Karin and Deissler, Helmut and Sutter, Christian and Gadzicki, Dorothea and Chenevix-Trench, Georgia and Spurdle, Amanda B and Chen, Xiaoqing and Beesley, Jonathan and Olsson, Håkan and Kristoffersson, Ulf and Ehrencrona, Hans and Liljegren, Annelie and van der Luijt, Rob B and van Os, Theo A and van Leeuwen, Flora E and Domchek, Susan M and Rebbeck, Timothy R and Nathanson, Katherine L and Osorio, Ana and Ramón Y Cajal, Teresa and Konstantopoulou, Irene and Benítez, Javier and Friedman, Eitan and Kaufman, Bella and Laitman, Yael and Mai, Phuong L and Greene, Mark H and Nevanlinna, Heli and Aittomäki, Kristiina and Szabo, Csilla I and Caldes, Trinidad and Couch, Fergus J and Anulis, Irene L and Godwin, Anew K and Hamann, Ute and Schmutzler, Rita K and Kathleen Cuningham Fdn Consortium and Consortium Investigators Modifiers and Sweden SWE-BRCA and Epidemiological Study Familial Bre and Hereditary Breast Ovarian Canc Grp and Hereditary Breast and Ovarian cancer group Netherlands (HEBON) and Epidemiological Study of Familial Breast Cancer (EMBRACE) and Swedish Breast Cancer Study, Sweden (SWE-BRCA) and Kathleen Cuningham Foundation Consortium for Research into Familial Breast Cancer (kConFab) and Consortium of Investigators of Modifiers of BRCA1/2 (CIMBA) and on behalf of the Consortium of Investigators of Modifiers of BRCA1/2 (CIMBA) and for the Kathleen Cuningham Foundation Consortium for Research into Familial Breast Cancer (kConFab) and for the Hereditary Breast and Ovarian cancer group Netherlands (HEBON) and for the Swedish Breast Cancer Study, Sweden (SWE-BRCA) and for the Epidemiological Study of Familial Breast Cancer (EMBRACE) and Institutionen för biomedicin, avdelningen för medicinsk genetik och klinisk genetik and Göteborgs universitet and Gothenburg University and Institute of Biomedicine, Department of Medical and Clinical Genetics and Sahlgrenska Academy and Institute of Clinical Sciences, Department of Oncology and Sahlgrenska akademin and Institutionen för kliniska vetenskaper, Avdelningen för onkologi
Cancer epidemiology, biomarkers & prevention, ISSN 1055-9965, 2010, Volume 19, Issue 11, pp. 2859 - 2868
Oncology | Public, Environmental & Occupational Health | Life Sciences & Biomedicine | Science & Technology | Gynecology. Andrology. Obstetrics | Biological and medical sciences | Medical sciences | Tumors | Female genital diseases | Genetic Predisposition to Disease - genetics | Humans | Risk Factors | Genotype | Ovarian Neoplasms - enzymology | Caspase 8 - genetics | Ovarian Neoplasms - genetics | Breast Neoplasms - enzymology | Breast Neoplasms - genetics | Polymerase Chain Reaction | Caspase 10 - genetics | Genes, BRCA2 | Female | Polymorphism, Single Nucleotide | Genes, BRCA1 | Mutation | Index Medicus | Genetic Predisposition to Disease | Caspase 8 | Genes | Cell and Molecular Biology | BRCA1 | Breast Neoplasms | BRCA2 | enzymology | Single Nucleotide | genetics | Caspase 10 | Ovarian Neoplasms | Cell- och molekylärbiologi | Polymorphism | Clinical Medicine | Medical and Health Sciences | Klinisk medicin | Cancer and Oncology | Medicin och hälsovetenskap | Cancer och onkologi
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6. Full Text Fine-mapping of 150 breast cancer risk regions identifies 191 likely target genes
by Fachal, Laura and Aschard, Hugues and Beesley, Jonathan and Barnes, Daniel R and Allen, Jamie and Kar, Siddhartha and Pooley, Karen A and Dennis, Joe and Michailidou, Kyriaki and Turman, Constance and Soucy, Penny and Lemacon, Auey and Lush, Michael and Tyrer, Jonathan P and Ghoussaini, Maya and Marjaneh, Mahdi Moradi and Jiang, Xia and Agata, Simona and Aittomaki, Kristiina and Rosario Alonso, M and Anulis, Irene L and Anton-Culver, Hoda and Antonenkova, Natalia N and Arason, Adalgeir and Arndt, Volker and Aronson, Kristan J and Arun, Banu K and Auber, Bernd and Auer, Paul L and Azzollini, Jacopo and Balmana, Judith and Barkardottir, Rosa B and Barrowdale, Daniel and Beeghly-Fadiel, Alicia and Benitez, Javier and Bermisheva, Marina and Bialkowska, Katarzyna and Blanco, Amie M and Blomqvist, Carl and Blot, William and Bogdanova, Natalia and Bojesen, Stig E and Bolla, Manjeet K and Bonanni, Bernardo and Borg, Ake and Bosse, Kristin and Brauch, Hiltrud and Brenner, Hermann and de Boer, Maaike and Garcia, Encarna Gomez and Blok, Marinus
Nature genetics, ISSN 1061-4036, 01/2020, Volume 52, Issue 1
COMPREHENSIVE MOLECULAR PORTRAITS | FUNCTIONAL VARIANTS | CHROMATIN | INTEGRATIVE ANALYSIS | SUSCEPTIBILITY LOCI | ENHANCER | PROTEIN FUNCTION | ESTROGEN-RECEPTOR | GENOME-WIDE ASSOCIATION | REVEALS
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7. Full Text Genome-wide association and transcriptome studies identify target genes and risk loci for breast cancer
by Ferreira, Manuel A and Gamazon, Eric R and Al-Ejeh, Fares and Aittomäki, Kristiina and Anulis, Irene L and Anton-Culver, Hoda and Arason, Adalgeir and Arndt, Volker and Aronson, Kristan J and Arun, Banu K and Asseryanis, Ella and Azzollini, Jacopo and Balmaña, Judith and Barnes, Daniel R and Barrowdale, Daniel and Beckmann, Matthias W and Behrens, Sabine and Benitez, Javier and Bermisheva, Marina and Białkowska, Katarzyna and Blomqvist, Carl and Bogdanova, Natalia V and Bojesen, Stig E and Bolla, Manjeet K and Borg, Ake and Brauch, Hiltrud and Brenner, Hermann and Broeks, Annegien and Burwinkel, Barbara and Caldés, Trinidad and Caligo, Maria A and Campa, Daniele and Campbell, Ian and Canzian, Federico and Carter, Jonathan and Carter, Brian D and Castelao, Jose E and Chang-Claude, Jenny and Chanock, Stephen J and Christiansen, Hans and Chung, Wendy K and Claes, Kathleen B. M and Clarke, Christine L and Adlard, Julian and van Engelen, Klaartje and van Hest, Liselotte and van Os, Theo A. M
Nature communications, ISSN 2041-1723, 12/2019, Volume 10, Issue 1
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8. Full Text Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer
by Milne, Roger L and Kuchenbaecker, Karoline B and Michailidou, Kyriaki and Beesley, Jonathan and Kar, Siddhartha and Lindstrom, Sara and Hui, Shirley and Lemacon, Auey and Soucy, Penny and Dennis, Joe and Jiang, Xia and Rostamianfar, Asha and Finucane, Hilary and Bolla, Manjeet K and McGuffog, Lesley and Wang, Qin and Aalfs, Cora M and Adams, Marcia and Adlard, Julian and Agata, Simona and Ahmed, Shahana and Ahsan, Habibul and Aittomaki, Kristiina and Al-Ejeh, Fares and Allen, Jamie and Ambrosone, Christine B and Amos, Christopher I and Anulis, Irene L and Anton-Culver, Hoda and Antonenkova, Natalia N and Arndt, Volker and Arnold, Norbert and Aronson, Kristan J and Auber, Bernd and Auer, Paul L and Ausems, Margreet G. E. M and Azzollini, Jacopo and Bacot, Francois and Balmana, Judith and Barile, Monica and Barjhoux, Laure and Barkardottir, Rosa B and Barrdahl, Myrto and Barnes, Daniel and Barrowdale, Daniel and Baynes, Caroline and Beckmann, Matthias W and Benitez, Javier and Bermisheva, Marina and Oosterwijk, Jan C
Nature genetics, ISSN 1061-4036, 12/2017, Volume 49, Issue 12, pp. 1767 - 1778
BRCA2 MUTATION CARRIERS | CONSORTIUM | FUNCTIONAL VARIANTS | COMMON VARIANTS | OVARIAN CANCERS | DISEASE | SUSCEPTIBILITY LOCI | CONFER SUSCEPTIBILITY | EXPRESSION | GENOME-WIDE ASSOCIATION
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9. Full Text Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer
by Milne, Roger L and Kuchenbaecker, Karoline B and Michailidou, Kyriaki and Beesley, Jonathan and Kar, Siddhartha and Lindström, Sara and Hui, Shirley and Lemaçon, Auey and Soucy, Penny and Dennis, Joe and Jiang, Xia and Rostamianfar, Asha and Finucane, Hilary K and Bolla, Manjeet K and McGuffog, Lesley and Wang, Qin and Aalfs, Cora M and Adams, Marcia and Adlard, Julian and Agata, Simona and Ahmed, Shahana and Ahsan, Habibul and Aittomäki, Kristiina and Al-Ejeh, Fares and Allen, Jamie and Ambrosone, Christine B and Amos, Christopher I and Anulis, Irene L and Anton-Culver, Hoda and Antonenkova, Natalia N and Arndt, Volker and Arnold, Norbert and Aronson, Kristan J and Auber, Bernd and Auer, Paul L and Ausems, Margreet G E M and Azzollini, Jacopo and Bacot, François and Balmaña, Judith and Barile, Monica and Barjhoux, Laure and Barkardottir, Rosa B and Barrdahl, Myrto and Barnes, Daniel R and Barrowdale, Daniel and Baynes, Caroline and Beckmann, Matthias W and Benitez, Javier and Bermisheva, Marina and Bernstein, Leslie
Nature genetics, ISSN 1061-4036, 12/2017, Volume 49, Issue 12, p. 1767
Genetic Predisposition to Disease | Genome-Wide Association Study | Receptors, Estrogen | Humans | Risk Factors | European Continental Ancestry Group | Breast Neoplasms | Journal Article | Female | Heterozygote | Polymorphism, Single Nucleotide | Mutation | BRCA1 Protein
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10. Full Text Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer
by Milne, Roger L and Kuchenbaecker, Karoline B and Michailidou, Kyriaki and Beesley, Jonathan and Kar, Siddhartha and Lindstrom, Sara and Hui, Shirley and Lemacon, Auey and Soucy, Penny and Dennis, Joe and Jiang, Xia and Rostamianfar, Asha and Finucane, Hilary and Bolla, Manjeet K and McGuffog, Lesley and Wang, Qin and Aalfs, Cora M and Adams, Marcia and Adlard, Julian and Agata, Simona and Ahmed, Shahana and Ahsan, Habibul and Aittomaki, Kristiina and Al-Ejeh, Fares and Allen, Jamie and Ambrosone, Christine B and Amos, Christopher I and Anulis, Irene L and Anton-Culver, Hoda and Antonenkova, Natalia N and Arndt, Volker and Arnold, Norbert and Aronson, Kristan J and Auber, Bernd and Auer, Paul L and Ausems, Margreet G. E. M and Azzollini, Jacopo and Bacot, Francois and Balmana, Judith and Barile, Monica and Barjhoux, Laure and Barkardottir, Rosa B and Barrdahl, Myrto and Barnes, Daniel and Barrowdale, Daniel and Baynes, Caroline and Beckmann, Matthias W and Benitez, Javier and Bermisheva, Marina and Blok, Marinus J
Nature genetics, ISSN 1061-4036, 12/2017, Volume 49, Issue 12, pp. 1767 - 1778
BRCA2 MUTATION CARRIERS | CONSORTIUM | FUNCTIONAL VARIANTS | COMMON VARIANTS | OVARIAN CANCERS | DISEASE | SUSCEPTIBILITY LOCI | CONFER SUSCEPTIBILITY | EXPRESSION | GENOME-WIDE ASSOCIATION
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11. Full Text A genome wide linkage search for breast cancer susceptibility genes
by Smith, Paula and McGuffog, Lesley and Easton, Douglas F and Mann, Graham J and Pupo, Gulietta M and Newman, Beth and Chenevix-Trench, Georgia and Szabo, Csilla and Southey, Melissa and Renard, Hélène and Odefrey, Fabrice and Lynch, Henry and Stoppa-Lyonnet, Dominique and Couch, Fergus and Hopper, John L and Giles, Graham G and McCredie, Margaret R. E and Buys, Sauna and Anulis, Irene and Senie, Ruby and Goldgar, David E and Oldenburg, Rogier and Kroeze-Jansema, Karin and Kraan, Jaennelle and Meijers-Heijboer, Hanne and Klijn, Jan G. M and van Asperen, Christi and van Leeuwen, Inge and Vasen, Hans F. A and Cornelisse, Cees J and Devilee, Peter and Baskcomb, Linda and Seal, Sheila and Barfoot, Rita and Mangion, Jon and Hall, Anita and Edkins, Sarah and Rapley, Elizabeth and Wooster, Richard and Chang-Claude, Jenny and Eccles, Diana and Evans, D. Gareth and Futreal, P. Anew and Nathanson, Katherine L and Weber, Barbara L and Rahman, Nazneen and Stratton, Michael R and kConFab Investigators and IARC Grp and Breast Canc Susceptibility Collabo and United Kingdom Grp and Cambridge Group and BCFS and Australia Grp and BRCAX Collaborators Grp and Netherlands Grp and Breast Cancer Susceptibility Collaboration (UK) and BCFS, BRCAX Collaborators Group and Australia Group and IARC Group and the Breast Cancer Susceptibility Collaboration (UK) and Netherlands Group and United Kingdom Group
Genes chromosomes & cancer, ISSN 1045-2257, 2006, Volume 45, Issue 7, pp. 646 - 655
Oncology | Genetics & Heredity | Life Sciences & Biomedicine | Science & Technology | Genetic Predisposition to Disease | Breast Neoplasms - genetics | Genetic Testing | Humans | Genes, BRCA2 | Female | Male | Genes, BRCA1 | Models, Statistical | Genome, Human | Lod Score | Genetic Linkage | Index Medicus
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12. Full Text Mendelian randomisation study of height and body mass index as modifiers of ovarian cancer risk in 22,588 BRCA1 and BRCA2 mutation carriers
by Qian, Frank and Rookus, Matti A and Leslie, Goska and Risch, Harvey A and Greene, Mark H and Aalfs, Cora M and Adank, Muriel A and Adlard, Julian and Agnarsson, Bjarni A and Ahmed, Munaza and Aittomaki, Kristiina and Anulis, Irene L and Arnold, Norbert and Arun, Banu K and Ausems, Margreet G. E. M and Azzollini, Jacopo and Barrowdale, Daniel and Barwell, Julian and Benitez, Javier and Bialkowska, Katarzyna and Bonadona, Valerie and Borde, Julika and Borg, Ake and Bradbury, Angela R and Brunet, Joan and Buys, Sauna S and Caldes, Trinidad and Caligo, Maria A and Campbell, Ian and Carter, Jonathan and Chiquette, Jocelyne and Chung, Wendy K and Claes, Kathleen B. M and Collee, J. Margriet and Collonge-Rame, Marie-Agnes and Couch, Fergus J and Daly, Mary B and Delnatte, Capucine and Diez, Orland and Domchek, Susan M and Dorfling, Cecilia M and Eason, Jacqueline and Easton, Douglas F and Eeles, Ros and Engel, Christoph and Evans, D. Gareth and Faivre, Laurence and Feliubado, Lidia and Foretova, Lenka and Friedman, Eitan and Gomez Garcia, Encarna
British journal of cancer, ISSN 0007-0920, 07/2019, Volume 121, Issue 2, pp. 180 - 192
MORTALITY | PATHWAYS | APOPTOSIS | OBESITY | INFERTILITY | ANTHROPOMETRIC MEASURES | COHORT | PROGESTIN | ASSOCIATION | BREAST
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13. Full Text Mendelian randomisation study of height and body mass index as modifiers of ovarian cancer risk in 22,588 BRCA1 and BRCA2 mutation carriers
by Qian, Frank and Rookus, Matti A and Leslie, Goska and Risch, Harvey A and Greene, Mark H and Aalfs, Cora M and Adank, Muriel A and Adlard, Julian and Agnarsson, Bjarni A and Ahmed, Munaza and Aittomäki, Kristiina and Anulis, Irene L and Arnold, Norbert and Arun, Banu K and Ausems, Margreet G. E. M and Azzollini, Jacopo and Barrowdale, Daniel and Barwell, Julian and Benitez, Javier and Białkowska, Katarzyna and Bonadona, Valérie and Borde, Julika and Borg, Ake and Bradbury, Angela R and Brunet, Joan and Buys, Sauna S and Caldés, Trinidad and Caligo, Maria A and Campbell, Ian and Carter, Jonathan and Chiquette, Jocelyne and Chung, Wendy K and Claes, Kathleen B. M and Collée, J. Margriet and Collonge-Rame, Marie-Agnès and Couch, Fergus J and Daly, Mary B and Delnatte, Capucine and Diez, Orland and Domchek, Susan M and Dorfling, Cecilia M and Eason, Jacqueline and Easton, Douglas F and Eeles, Ros and Engel, Christoph and Evans, D. Gareth and Faivre, Laurence and Meijers-Heijboer, Hanne E. J and Oosterwijk, Jan C and van Engelen, Klaartje
British journal of cancer, ISSN 0007-0920, 07/2019, Volume 121
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14. Full Text Mutational spectrum in a worldwide study of 29,700 families with BRCA1 or BRCA2 mutations
by Rebbeck, Timothy R and Friebel, Tara M and Friedman, Eitan and Hamann, Ute and Huo, Dezheng and Kwong, Ava and Olah, Edith and Olopade, Olufunmilayo I and Solano, Angela R and Teo, Soo-Hwang and Thomassen, Mads and Weitzel, Jeffrey N and Chan, T. L and Fergus, Fergus J and Goldgar, David E and Kruse, Torben A and Edenir, Edenir Inez and Park, Sue Kyung and Torres, Diana and van Rensburg, Elizabeth J and McGuffog, Lesley and Parsons, Michael T and Leslie, Goska and Aalfs, Cora M and Abugattas, Julio and Adlard, Julian and Agata, Simona and Aittomaki, Kristiina and Anews, Lesley and Anulis, Irene L and Arason, Adalgeir and Arnold, Norbert and Arun, Banu K and Asseryanis, Ella and Auerbach, Leo and Azzollini, Jacopo and Balmana, Judith and Barile, Monica and Barkardottir, Rosa B and Barrowdale, Daniel and Benitez, Javier and Berger, Aneas and Berger, Raanan and Blanco, Amie M and Blazer, Kathleen R and Blok, Marinus J and Bonadona, Valerie and Bonanni, Bernardo and Bradbury, Angela R and Brewer, Carole
Human mutation, ISSN 1059-7794, 05/2018, Volume 39, Issue 5, pp. 593 - 620
ethnicity | ovarian cancer | HEREDITARY BREAST | breast cancer | 185DELAG MUTATION | BRCA1 | OVARIAN-CANCER | BRCA2 | FOUNDER MUTATIONS | mutation | HAPLOTYPE ANALYSIS | PHENOTYPE ANALYSIS | geography | RISK HISPANIC FAMILIES | PROSTATE-CANCER | BREAST-CANCER PATIENTS | GERMLINE MUTATIONS
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15. Full Text Genomic analyses identify hundreds of variants associated with age at menarche and support a role for puberty timing in cancer risk
by Day, Felix R and Thompson, Deborah J and Helgason, Hannes and Chasman, Daniel I and Finucane, Hilary and Sulem, Patrick and Ruth, Katherine S and Whalen, Sean and Sarkar, Abhishek K and Albrecht, Eva and Altmaier, Elisabeth and Amini, Marzyeh and Barbieri, Caterina M and Boutin, Thibaud and Campbell, Archie and Demerath, Ellen and Giri, Ayush and He, Chunyan and Hottenga, Jouke J and Karlsson, Robert and Kolcic, Ivana and Loh, Po-Ru and Lunetta, Kathryn L and Mangino, Massimo and Marco, Brumat and McMahon, George and Medland, Sarah E and Nolte, Ilja M and Noordam, Raymond and Nutile, Teresa and Paternoster, Lavinia and Perjakova, Natalia and Porcu, Eleonora and Rose, Lynda M and Schraut, Katharina E and Segrè, Ayellet V and Smith, Albert V and Stolk, Lisette and Teumer, Alexander and Anulis, Irene L and Bandinelli, Stefania and Beckmann, Matthias W and Benitez, Javier and Bergmann, Sven and Bochud, Murielle and de Geus, Eco J C N and Mbarek, Hamdi and Willemsen, Gonneke and Boomsma, Dorret I and Visser, Jenny A
Nature genetics, ISSN 1061-4036, 06/2017, Volume 49, Issue 6, pp. 834 - 841
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16. Full Text Association of breast cancer risk in BRCA1 and BRCA2 mutation carriers with genetic variants showing differential allelic expression: identification of a modifier of breast cancer risk at locus 11q22.3
by Soucy, Penny and Kuchenbaeker, Karoline B and Pastinen, Tomi and Aittomaki, Kristiina and Arnold, Norbert and Arun, Banu K and Azzollini, Jacopo and Barjhoux, Laure and Barrowdale, Daniel and Berthet, Pascaline and Blok, Marinus J and Bonadona, Valerie and Bonanni, Bernardo and Bradbury, Angela R and Buecher, Bruno and Caligo, Maria A and Chung, Wendy K and Davidson, Rosemarie and De Leeneer, Kim and Diez, Orland and Dolcetti, Riccardo and Eccles, Diana and Eeles, Ros and Ejlertsen, Bent and Engel, Christoph and Evans, D. Gareth and Foulkes, William D and Fountzilas, George and Friedman, Eitan and Frost, Debra and Ganschow, Pamela and Garber, Judy and Gerdes, Anne-Marie and Glendon, Gord and Goldgar, David E and Greene, Mark H and Hahnen, Eric and Hulick, Peter J and Imyanitov, Evgeny N and Isaacs, Claudine and Izatt, Louise and Janavicius, Ramunas and John, Esther M and Joseph, Vijai and Just, Walter and Kaczmarek, Katarzyna and Karlan, Beth Y and Kirk, Judy and Kriege, Mieke and Laitman, Yael and Laurent, Maite and Lazaro, Conxi and Leslie, Goska and Lester, Jenny and Lesueur, Fabienne and Loman, Niklas and Loud, Jennifer T and Manoukian, Siranoush and Mariani, Milena and Mazoyer, Sylvie and McGuffog, Lesley and Meijers-Heijboer, Hanne E. J and Mulligan, Anna Marie and Nathanson, Katherine L and Olopade, Olufunmilayo I and Osorio, Ana and Papi, Laura and Park, Sue Kyung and Pedersen, Inge Sokilde and Peterlongo, Paolo and Radice, Paolo and Rantala, Johanna and Rennert, Gad and Robson, Mark and Roiguez, Gustavo C and Schmutzler, Rita Katharina and Sevenet, Nicolas and Shah, Payal D and Singer, Christian F and Slavin, Thomas P and Sokolowska, Johanna and Southey, Melissa and Spurdle, Amanda B and Stadler, Zsofia and Stoppa-Lyonnet, Dominique and Tea, Muy-Kheng and Teixeira, Manuel R and Teo, Soo-Hwang and Terry, Mary Beth and Thomassen, Mads and Tihomirova, Laima and Tognazzo, Silvia and Toland, Amanda Ewart and van den Ouweland, Ans M. W and van Rensburg, Elizabeth J and Varon-Mateeva, Raymonda and Wijnen, Juul T and Couch, Fergus J and Nord, Silje and Simard, Jacques
Breast cancer research and treatment, ISSN 0167-6806, 01/2017, Volume 161, Issue 1, pp. 117 - 134
Differential allelic expression | Genetic susceptibility | BRCA1 and BRCA2 mutation carriers | Cis-regulatory variants | Genetic modifiers | Breast cancer
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17. Full Text BRCA2 Hypomorphic Missense Variants Confer Moderate Risks of Breast Cancer
by Shimelis, Hermela and Mesman, Romy L. S and Von Nicolai, Catharina and Ehlen, Asa and Guidugli, Lucia and Martin, Charlotte and Calleja, Fabienne M. G. R and Meeks, Huong and Hallberg, Emily and Hinton, Jamie and Lilyquist, Jenna and Hu, Chunling and Aalfs, Cora M and Aittomaki, Kristiina and Anulis, Irene and Anton-Culver, Hoda and Arndt, Volker and Beckmann, Matthias W and Benitez, Javier and Bogdanova, Natalia V and Bojesen, Stig E and Bolla, Manjeet K and Borresen-Dale, Anne-Lise and Brauch, Hiltrud and Brennan, Paul and Brenner, Hermann and Broeks, Annegien and Brouwers, Barbara and Bruning, Thomas and Burwinkel, Barbara and Chang-Claude, Jenny and Chenevix-Trench, Georgia and Cheng, Ching-Yu and Choi, Ji-Yeob and Collee, J. Margriet and Cox, Angela and Cross, Simon S and Czene, Kamila and Darabi, Hatef and Dennis, Joe and Dork, Thilo and dos-Santos-Silva, Isabel and Dunning, Alison M and Fasching, Peter A and Figueroa, Jonine and Flyger, Henrik and Garcia-Closas, Montserrat and Giles, Graham G and Glendon, Gord and Oosterwijk, Jan J. C
Cancer research (Chicago, Ill.), ISSN 0008-5472, 06/2017, Volume 77, Issue 11, pp. 2789 - 2799
CELL-BASED ASSAY | DNA-BINDING | UNKNOWN CLINICAL-SIGNIFICANCE | FUNCTIONAL-EVALUATION | GENES | SEQUENCE VARIANTS | CLASSIFICATION | UNCLASSIFIED VARIANTS | UNCERTAIN SIGNIFICANCE | OVARIAN-CANCER
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18. Full Text Identification of 12 new susceptibility loci for different histotypes of epithelial ovarian cancer
by Phelan, Catherine M and Kuchenbaecker, Karoline B and Tyrer, Jonathan P and Kar, Siddhartha P and Lawrenson, Kate and Winham, Stacey J and Dennis, Joe and Pirie, Ailith and Riggan, Marjorie J and Chornokur, Ganna and Earp, Madalene A and Lyra, Paulo C and Lee, Janet M and Coetzee, Simon and Beesley, Jonathan and McGuffog, Lesley and Soucy, Penny and Dicks, Ed and Lee, Anew and Barrowdale, Daniel and Lecarpentier, Julie and Leslie, Goska and Aalfs, Cora M and Aben, Katja K. H and Adams, Marcia and Adlard, Julian and Anulis, Irene L and Anton-Culver, Hoda and Antonenkova, Natalia and Aravantinos, Gerasimos and Arnold, Norbert and Arun, Banu K and Arver, Brita and Azzollini, Jacopo and Balmana, Judith and Banerjee, Susana N and Barjhoux, Laure and Barkardottir, Rosa B and Bean, Yukie and Beckmann, Matthias W and Beeghly-Fadiel, Alicia and Benitez, Javier and Bermisheva, Marina and Bernardini, Marcus Q and Birrer, Michael J and Bjorge, Line and Black, Amanda and Blankstein, Kenneth and Mensenkamp, Arjen R and van der Hout, Annemarie H
Nature genetics, ISSN 1061-4036, 05/2017, Volume 49, Issue 5, pp. 680 - 691
BREAST-CANCER | COMMON VARIANTS | POPULATION | METAANALYSIS | RISK | MUTATIONS | CLEAR-CELL CARCINOMA | ASSOCIATION | ENDOMETRIOSIS | TELOMERE LENGTH
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19. Full Text Identification of 12 new susceptibility loci for different histotypes of epithelial ovarian cancer
by Phelan, Catherine M and Kuchenbaecker, Karoline B and Tyrer, Jonathan P and Kar, Siddhartha P and Lawrenson, Kate and Winham, Stacey J and Dennis, Joe and Pirie, Ailith and Riggan, Marjorie J and Chornokur, Ganna and Earp, Madalene A and Lyra, Paulo C and Lee, Janet M and Coetzee, Simon and Beesley, Jonathan and McGuffog, Lesley and Soucy, Penny and Dicks, Ed and Lee, Anew and Barrowdale, Daniel and Lecarpentier, Julie and Leslie, Goska and Aalfs, Cora M and Aben, Katja K. H and Adams, Marcia and Adlard, Julian and Anulis, Irene L and Anton-Culver, Hoda and Antonenkova, Natalia and Aravantinos, Gerasimos and Arnold, Norbert and Arun, Banu K and Arver, Brita and Azzollini, Jacopo and Balmana, Judith and Banerjee, Susana N and Barjhoux, Laure and Barkardottir, Rosa B and Bean, Yukie and Beckmann, Matthias W and Beeghly-Fadiel, Alicia and Benitez, Javier and Bermisheva, Marina and Bernardini, Marcus Q and Birrer, Michael J and Bjorge, Line and Black, Amanda and Blankstein, Kenneth and Blok, Marinus J and Bodelon, Clara
Nature genetics, ISSN 1061-4036, 05/2017, Volume 49, Issue 5, pp. 680 - 691
BREAST-CANCER | COMMON VARIANTS | POPULATION | METAANALYSIS | RISK | MUTATIONS | CLEAR-CELL CARCINOMA | ASSOCIATION | ENDOMETRIOSIS | TELOMERE LENGTH
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