Human Genome Epidemiology Literature Finder
Records 1 - 12 (of 12 Records) |
Query Trace: TOPBP1[original query] |
---|
Identification of a common polymorphism in the TopBP1 gene associated with hereditary susceptibility to breast and ovarian cancer. European journal of cancer (Oxford, England : 1990) 2006 Oct 42 (15): 2647-52. Karppinen Sanna-Maria, Erkko Hannele, Reini Kaarina, Pospiech Helmut, Heikkinen Katri, Rapakko Katrin, Syväoja Juhani E, Winqvist Robe |
Scan of 977 nonsynonymous SNPs in CLL4 trial patients for the identification of genetic variants influencing prognosis. Blood 2008 Feb 111 (3): 1625-33. Sellick Gabrielle S, Wade Rachel, Richards Susan, Oscier David G, Catovsky Daniel, Houlston Richard |
Modification of ovarian cancer risk by BRCA1/2-interacting genes in a multicenter cohort of BRCA1/2 mutation carriers. Cancer research 2009 Jul 69 (14): 14. Rebbeck TR, Mitra N, Domchek SM, Wan F, Chuai S, Friebel TM, Panossian S, Spurdle A, Chenevix-Trench G, Singer CF, Pfeiler G, Neuhausen SL, Lynch HT, Garber JE, Weitzel JN, Isaacs C, Couch F, Narod SA, Rubinstein WS, Tomlinson GE, Ganz PA, Olopade OI, Tung N, Blum JL, Greenberg R, Nathanson KL, Daly MB |
TOPBP1 missense variant Arg309Cys and breast cancer in a German hospital-based case-control study. Journal of negative results in biomedicine 2010 9 (1): 9. Blaut Magda A, Bogdanova Natalia V, Bremer Michael, Karstens Johann H, Hillemanns Peter, Dörk Thi |
A two-phase case-control study for colorectal cancer genetic susceptibility: candidate genes from chromosomal regions 9q22 and 3q22. British journal of cancer 2011 Sep 105 (6): 870-5. Abulí A, Fernández-Rozadilla C, Giráldez M D, Muñoz J, Gonzalo V, Bessa X, Bujanda L, Reñé J M, Lanas A, García A M, Saló J, Argüello L, Vilella A, Carreño R, Jover R, Xicola R M, Llor X, Carvajal-Carmona L, Tomlinson I P M, Kerr D J, Houlston R S, Piqué J M, Carracedo A, Castells A, Andreu M, Ruiz-Ponte C, Castellví-Bel S, |
Modification of BRCA1-Associated Breast and Ovarian Cancer Risk by BRCA1-Interacting Genes. Cancer research 2011 Sep 71 (17): 5792-805. Rebbeck Timothy R, Mitra Nandita, Domchek Susan M, Wan Fei, Friebel Tara M, Tran Teo V, Singer Christian F, Tea Muy-Kheng Maria, Blum Joanne L, Tung Nadine, Olopade Olufunmilayo I, Weitzel Jeffrey N, Lynch Henry T, Snyder Carrie L, Garber Judy E, Antoniou Antonis C, Peock Susan, Evans D Gareth, Paterson Joan, Kennedy M John, Donaldson Alan, Dorkins Huw, Easton Douglas F, , Rubinstein Wendy S, Daly Mary B, Isaacs Claudine, Nevanlinna Heli, Couch Fergus J, Andrulis Irene L, Freidman Eitan, Laitman Yael, Ganz Patricia A, Tomlinson Gail E, Neuhausen Susan L, Narod Steven A, Phelan Catherine M, Greenberg Roger, Nathanson Katherine |
Novel somatic frameshift mutations of genes related to cell cycle and DNA damage response in gastric and colorectal cancers with microsatellite instability. Tumori 0 96 (6): 1004-9. Kim Yoo Ri, Chung Nak Gyun, Kang Mi Ran, Yoo Nam Jin, Lee Sug Hyu |
Interaction of polymorphisms in mitotic regulator genes with cigarette smoking and pancreatic cancer risk. Molecular carcinogenesis 2013 Nov 52 Suppl 1 E103-9. Jang Ji-Hyun, Cotterchio Michelle, Borgida Ayelet, Liu Geoffrey, Gallinger Steven, Cleary Sean |
Topoisomerase IIß binding protein 1 c.*229C>T (rs115160714) gene polymorphism and endometrial cancer risk. Pathology oncology research : POR 2014 Jul 20 (3): 597-602. Forma Ewa, Wójcik-Krowiranda Katarzyna, Jó?wiak Pawe?, Szymczyk Agnieszka, Bie?kiewicz Andrzej, Bry? Magdalena, Krze?lak An |
Association between the c.*229C>T polymorphism of the topoisomerase IIß binding protein 1 (TopBP1) gene and breast cancer. Molecular biology reports 2013 Jan . Forma E, Brzezia?ska E, Krze?lak A, Chwatko G, Jó?wiak P, Szymczyk A, Smolarz B, Romanowicz-Makowska H, Ró?a?ski W, Bry? M |
Evaluation of the RHINO gene for breast cancer predisposition in Finnish breast cancer families. Breast cancer research and treatment 2014 Apr 144 (2): 437-41. Heikkinen Tuomas, Khan Sofia, Huovari Elina, Vilske Sara, Schleutker Johanna, Kallioniemi Anne, Blomqvist Carl, Aittomäki Kristiina, Nevanlinna He |
Exome data clouds the pathogenicity of genetic variants in Pulmonary Arterial Hypertension. Molecular genetics & genomic medicine 2018 Aug . Abbasi Yeganeh, Jabbari Javad, Jabbari Reza, Glinge Charlotte, Izadyar Seyed Bahador, Spiekerkoetter Edda, Zamanian Roham T, Carlsen Jørn, Tfelt-Hansen Jac |
- Page last reviewed:Feb 1, 2024
- Page last updated:Apr 22, 2024
- Content source: