HuGE Literature Finder
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Records 1-38
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The rate of the recurrent MSH6 mutations in Ashkenazi Jewish breast cancer patients.
Cancer causes & control : CCC 2019 Jan 30 (1): 97-101. Bernstein-Molho Rinat, Laitman Yael, Schayek Hagit, Iomdin Sarah, Friedman Eit |
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Breast cancer patients suggestive of Li-Fraumeni syndrome: mutational spectrum, candidate genes, and unexplained heredity.
Breast cancer research : BCR 2018 Aug 20 (1): 87. Penkert Judith, Schmidt Gunnar, Hofmann Winfried, Schubert Stephanie, Schieck Maximilian, Auber Bernd, Ripperger Tim, Hackmann Karl, Sturm Marc, Prokisch Holger, Hille-Betz Ursula, Mark Dorothea, Illig Thomas, Schlegelberger Brigitte, Steinemann Dor |
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Racial/ethnic differences in multiple-gene sequencing results for hereditary cancer risk.
Genetics in medicine : official journal of the American College of Medical Genetics 2018 02 20 (2): 234-239. Caswell-Jin Jennifer L, Gupta Tanya, Hall Evan, Petrovchich Iva M, Mills Meredith A, Kingham Kerry E, Koff Rachel, Chun Nicolette M, Levonian Peter, Lebensohn Alexandra P, Ford James M, Kurian Allison |
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Panel sequencing of 264 candidate susceptibility genes and segregation analysis in a cohort of non-BRCA1, non-BRCA2 breast cancer families.
Breast cancer research and treatment 2017 Aug . Li Jun, Li Hongyan, Makunin Igor, , Thompson Bryony A, Tao Kayoko, Young Erin L, Lopez Jacqueline, Camp Nicola J, Tavtigian Sean V, John Esther M, Andrulis Irene L, Khanna Kum Kum, Goldgar David, Chenevix-Trench Georg |
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Novel BRCA1 splice-site mutation in ovarian cancer patients of Slavic origin.
Familial cancer 2017 Jul . Krivokuca Ana, Dragos Vita Setrajcic, Stamatovic Ljiljana, Blatnik Ana, Boljevic Ivana, Stegel Vida, Rakobradovic Jelena, Skerl Petra, Jovandic Stevo, Krajc Mateja, Magic Mirjana Brankovic, Novakovic Srdj |
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The Prevalence of Founder Mutations among Individuals from Families with Familial Pancreatic Cancer Syndrome.
Cancer research and treatment : official journal of Korean Cancer Association 2017 Apr 49 (2): 430-436. Lener Marcin R, Kashyap Aniruddh, Kluzniak Wojciech, Cybulski Cezary, Soluch Agnieszka, Pietrzak Sandra, Huzarski Tomasz, Gronwald Jacek, Lubinski J |
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BARD1 Gene Polymorphisms Confer Nephroblastoma Susceptibility.
EBioMedicine 2017 Feb 16 101-105. Fu Wen, Zhu Jinhong, Xiong Si-Wei, Jia Wei, Zhao Zhang, Zhu Shi-Bo, Hu Jin-Hua, Wang Feng-Hua, Xia Huimin, He Jing, Liu Guo-Cha |
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Mismatch Repair Polymorphisms as Markers of Breast Cancer Prevalence in the Breast Cancer Family Registry.
Anticancer research 2016 Sep 36 (9): 4437-41. Kappil Maya, Terry Mary Beth, Delgado-Cruzata Lissette, Liao Yuyan, Santella Regina |
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Reevaluation of RINT1 as a breast cancer predisposition gene.
Breast cancer research and treatment 2016 Sep 159 (2): 385-92. Li Na, Thompson Ella R, Rowley Simone M, McInerny Simone, Devereux Lisa, Goode David, Investigators LifePool, Wong-Brown Michelle W, Scott Rodney J, Trainer Alison H, Gorringe Kylie L, James Paul A, Campbell Ian |
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The Fanconi anemia DNA damage repair pathway in the spotlight for germline predisposition to colorectal cancer.
European journal of human genetics : EJHG 2016 May . Esteban-Jurado Clara, Franch-Expósito Sebastià, Muñoz Jenifer, Ocaña Teresa, Carballal Sabela, López-Cerón Maria, Cuatrecasas Miriam, Vila-Casadesús Maria, Lozano Juan José, Serra Enric, Beltran Sergi, Brea-Fernández Alejandro, Ruiz-Ponte Clara, Castells Antoni, Bujanda Luis, Garre Pilar, Caldés Trinidad, Cubiella Joaquín, Balaguer Francesc, Castellví-Bel Ser |
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A cohort analysis of men with a family history of BRCA1/2 and Lynch mutations for prostate cancer.
BMC cancer 2016 16 (1): 529. Kerr Lynne, Rewhorn Matthew J, Longmuir Mark, Fraser Sioban, Walsh Shaun, Andrew Nicola, Leung Hing |
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[Germline mutations of TP53 gene among Chinese families with high risk for breast cancer].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2015 Dec 32 (6): 761-5. Yang Xiaochen, Hu Zhen, Wu Jiong, Liu Guangyu, Di Genhong, Chen Canming, Hou Yifeng, Huang Xiaoyan, Liu Zhebin, Shen Zhenzhou, Shao Zhim |
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Identification of germline genetic mutations in patients with pancreatic cancer.
Cancer 2015 Oct . Salo-Mullen Erin E, O'Reilly Eileen M, Kelsen David P, Ashraf Asad M, Lowery Maeve A, Yu Kenneth H, Reidy Diane L, Epstein Andrew S, Lincoln Anne, Saldia Amethyst, Jacobs Lauren M, Rau-Murthy Rohini, Zhang Liying, Kurtz Robert C, Saltz Leonard, Offit Kenneth, Robson Mark E, Stadler Zsofia |
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Identification of a Variety of Mutations in Cancer Predisposition Genes in Patients With Suspected Lynch Syndrome.
Gastroenterology 2015 Sep 149 (3): 604-613.e20. Yurgelun Matthew B, Allen Brian, Kaldate Rajesh R, Bowles Karla R, Judkins Thaddeus, Kaushik Praveen, Roa Benjamin B, Wenstrup Richard J, Hartman Anne-Renee, Syngal Sap |
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Development and analytical validation of a 25-gene next generation sequencing panel that includes the BRCA1 and BRCA2 genes to assess hereditary cancer risk.
BMC cancer 2015 15 215. Judkins Thaddeus, Leclair Benoît, Bowles Karla, Gutin Natalia, Trost Jeff, McCulloch James, Bhatnagar Satish, Murray Adam, Craft Jonathan, Wardell Bryan, Bastian Mark, Mitchell Jeffrey, Chen Jian, Tran Thanh, Williams Deborah, Potter Jennifer, Jammulapati Srikanth, Perry Michael, Morris Brian, Roa Benjamin, Timms Kirst |
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Utilization of multigene panels in hereditary cancer predisposition testing: analysis of more than 2,000 patients.
Genetics in medicine : official journal of the American College of Medical Genetics 2014 Nov 16 (11): 830-7. LaDuca Holly, Stuenkel A J, Dolinsky Jill S, Keiles Steven, Tandy Stephany, Pesaran Tina, Chen Elaine, Gau Chia-Ling, Palmaer Erika, Shoaepour Kamelia, Shah Divya, Speare Virginia, Gandomi Stephanie, Chao Elizabe |
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Design and validation of an oligonucleotide microarray for the detection of genomic rearrangements associated with common hereditary cancer syndromes.
Journal of experimental & clinical cancer research : CR 2014 33 74. Mancini-DiNardo Debora, Judkins Thaddeus, Woolstenhulme Nick, Burton Collin, Schoenberger Jeremy, Ryder Matthew, Murray Adam, Gutin Natalia, Theisen Aaron, Holladay Jayson, Craft Jonathan, Arnell Christopher, Moyes Kelsey, Roa Benjam |
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Phenotypic heterogeneity of hereditary gynecologic cancers: a report from the Creighton hereditary cancer registry.
Familial cancer 2013 Dec 12 (4): 719-40. Casey Murray Joseph, Bewtra Chhanda, Lynch Henry T, Snyder Carrie, Stacy Mark, Watson Patri |
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Low prevalence of SLX4 loss-of-function mutations in non-BRCA1/2 breast and/or ovarian cancer families.
European journal of human genetics : EJHG 2012 Dec . de Garibay GR, Díaz A, Gaviña B, Romero A, Garre P, Vega A, Blanco A, Tosar A, Díez O, Pérez-Segura P, Díaz-Rubio E, Caldés T, de la Hoya M |
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Comparable frequency of BRCA1, BRCA2 and TP53 germline mutations in a multi-ethnic Asian cohort suggests TP53 screening should be offered together with BRCA1/2 screening to early-onset breast cancer patients.
Breast cancer research : BCR 2012 14 (2): R66. Lee Daphne S C, Yoon Sook-Yee, Looi Lai Meng, Kang Peter, Kang In Nee, Sivanandan Kavitta, Ariffin Hany, Thong Meow Keong, Chin Kin Fah, Mohd Taib Nur Aishah, Yip Cheng-Har, Teo Soo-Hwa |
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[Ovarian epithelial dysplasia: Description of a dysplasia scoring scheme].
Annales de pathologie 2011 Feb 31 (1): 3-10. Chene Gautier, Dauplat Jacques, Raoelfils Ines, Bignon Yves-Jean, Cayre Anne, Jaffeux Patricia, Aublet-Cuvelier Bruno, Pomel Christophe, Penault-Llorca Frédériq |
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PALB2 mutations 1592delT and 229delT are not present in Korean breast cancer patients negative for BRCA1 and BRCA2 mutations.
Breast cancer research and treatment 2010 Jul 122 (1): 303-6. Kim Jin Ho, Choi Doo Ho, Cho Dae Yeon, Ahn Sei Hyun, Son Byung Ho, Haffty Bruce |
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Pooled analysis indicates that the GSTT1 deletion, GSTM1 deletion, and GSTP1 Ile105Val polymorphisms do not modify breast cancer risk in BRCA1 and BRCA2 mutation carriers.
Breast cancer research and treatment 2010 Jul 122 (1): 281-5. Spurdle Amanda B, Fahey Paul, Chen Xiaoqing, McGuffog Lesley, , Easton Douglas, Peock Susan, Cook Margaret, , Simard Jacques, , Rebbeck Tim R, , Antoniou Antonis C, Chenevix-Trench Georg |
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A polymorphism in Werner syndrome gene is associated with breast cancer susceptibility in Chinese women.
Breast cancer research and treatment 2009 Nov 118 (1): 169-75. Wang Zhanwei, Xu Yan, Tang Jinhai, Ma Hongxia, Qin Jianwei, Lu Chen, Wang Xuechen, Hu Zhibin, Wang Xinru, Shen Hongbi |
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Age-dependent penetrance of different germline mutations in the BRCA1 gene.
Journal of clinical pathology 2009 Apr 62 (4): 350-6. Al-Mulla F, Bland J M, Serratt D, Miller J, Chu C, Taylor G |
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Analysis of FANCB and FANCN/PALB2 fanconi anemia genes in BRCA1/2-negative Spanish breast cancer families.
Breast cancer research and treatment 2009 Feb 113 (3): 545-51. García María J, Fernández Victoria, Osorio Ana, Barroso Alicia, Llort Gemma, Lázaro Conxi, Blanco Ignacio, Caldés Trinidad, de la Hoya Miguel, Ramón Y Cajal Teresa, Alonso Carmen, Tejada María-Isabel, San Román Carlos, Robles-Díaz Luis, Urioste Miguel, Benítez Javi |
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Evaluation of the BRCA1 interacting genes RAP80 and CCDC98 in familial breast cancer susceptibility.
Breast cancer research and treatment 2009 Jan 113 (2): 371-6. Osorio Ana, Barroso Alicia, García Maria J, Martínez-Delgado Beatriz, Urioste Miguel, Benítez Javi |
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Germline RAP80 mutations and susceptibility to breast cancer.
Breast cancer research and treatment 2009 Jan 113 (2): 377-81. Akbari Mohammad Reza, Ghadirian Parviz, Robidoux Andre, Foumani Maryam, Sun Yulong, Royer Robert, Zandvakili Inuk, Lynch Henry, Narod Steven |
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Potential excess mortality in BRCA1/2 mutation carriers beyond breast, ovarian, prostate, and pancreatic cancers, and melanoma.
PloS one 2009 4 (3): e4812. Mai Phuong L, Chatterjee Nilanjan, Hartge Patricia, Tucker Margaret, Brody Lawrence, Struewing Jeffery P, Wacholder Shol |
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Coinheritance of BRCA1 and BRCA2 mutations with Fanconi anemia and Bloom syndrome mutations in Ashkenazi Jewish population: possible role in risk modification for cancer development.
American journal of hematology 2005 Mar 78 (3): 203-6. Koren-Michowitz M, Friedman E, Gershoni-Baruch R, Brok-Simoni F, Patael Y, Rechavi G, Amariglio |
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Familial breast cancer: characteristics and outcome of BRCA 1-2 positive and negative cases.
BMC cancer 2005 5 (): 70. Veronesi Andrea, de Giacomi Clelia, Magri Maria D, Lombardi Davide, Zanetti Martina, Scuderi Cristina, Dolcetti Riccardo, Viel Alessandra, Crivellari Diana, Bidoli Ettore, Boiocchi Mau |
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Analyses of p53 expression pattern and BRCA mutations in patients with double primary breast and ovarian cancer.
International journal of gynecological cancer : official journal of the International Gynecological Cancer Society 2004 14 (2): 251-8. Bruchim I, Fishman A, Friedman E, Goldberg I, Chetrit A, Barshack I, Dekel E, Hirsh-Yechezkel G, Modan B, Kopolovic J |
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Frequency of the ATM IVS10-6T-->G variant in Australian multiple-case breast cancer families.
Breast cancer research : BCR 2004 6 (4): R401-7. Lindeman Geoffrey J, Hiew Melody, Visvader Jane E, Leary Jennifer, Field Michael, Gaff Clara L, Gardner R J McKinlay, Trainor Kevin, Cheetham Glenice, Suthers Graeme, Kirk Ju |
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Characterization of 458 single nucleotide polymorphisms of disease candidate genes in the Korean population.
Journal of human genetics 2003 48 (5): 213-6. Lee Jong-Keuk, Kim Hung-Tae, Cho Sung-Mi, Kim Kyung-Hee, Jin Hee-Jeong, Ryu Gil-Mi, Oh Bermseok, Park Chan, Kimm Kuchan, Jo Sangmee Ahn, Jung Sung-Chul, Kim Sook, In Sun Mi, Lee Jong-Eun, Jo In |
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Genes other than BRCA1 and BRCA2 involved in breast cancer susceptibility.
Journal of medical genetics 2002 Apr 39 (4): 225-42. de Jong M M, Nolte I M, te Meerman G J, van der Graaf W T A, Oosterwijk J C, Kleibeuker J H, Schaapveld M, de Vries E G |
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Association between BRCA1 and BRCA2 mutations and cancer phenotype in Spanish breast/ovarian cancer families: implications for genetic testing.
International journal of cancer. Journal international du cancer 2002 Feb 97 (4): 466-71. de la Hoya Miguel, Osorio Ana, Godino Javier, Sulleiro Sara, Tosar Alicia, Perez-Segura Pedro, Fernandez Cristina, Rodríguez Raquel, Díaz-Rubio Eduardo, Benítez Javier, Devilee Peter, Caldés Trinid |
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Comprehensive analysis of 989 patients with breast or ovarian cancer provides BRCA1 and BRCA2 mutation profiles and frequencies for the German population.
International journal of cancer. Journal international du cancer 2002 Feb 97 (4): 472-80. Meindl A, |
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Novel mutations in the BRCA1 and BRCA2 genes in Iranian women with early-onset breast cancer.
Breast cancer research : BCR 2002 4 (4): R6. Yassaee Vahid R, Zeinali Sirous, Harirchi Iraj, Jarvandi Soghra, Mohagheghi Mohammad A, Hornby David P, Dalton A |
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- Page last updated:Dec 12, 2019
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