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Molecular and genealogical characterization of the R1443X BRCA1 mutation in high-risk French-Canadian breast/ovarian cancer familiesVEZINA, Hélène; DUROCHER, Francine; NEVANLINNA, Heli et al.Human genetics. 2005, Vol 117, Num 2-3, pp 119-132, issn 0340-6717, 14 p.Article

Increased power for case-control studies of single nucleotide polymorphisms through incorporation of family history and genetic constraintsTHOMPSON, Deborah; WITTE, John S; SLATTERY, Martha et al.Genetic epidemiology. 2004, Vol 27, Num 3, pp 215-224, issn 0741-0395, 10 p.Article

Pathology of Breast and Ovarian Cancers among BRCA1 and BRCA2 Mutation Carriers: Results from the Consortium of Investigators of Modifiers of BRCA1/2 (CIMBA)MAVADDAT, Nasim; BARROWDALE, Daniel; MULLIGAN, Anna Marie et al.Cancer epidemiology, biomarkers & prevention. 2012, Vol 21, Num 1, pp 134-147, issn 1055-9965, 14 p.Article

G1738R is a BRCA1 founder mutation in Greek breast/ovarian cancer patients : evaluation of its pathogenicity and inferences on its genealogical historyANAGNOSTOPOULOS, Theodore; PERTESI, Maroulio; FOUNTZILAS, George et al.Breast cancer research and treatment. 2008, Vol 110, Num 2, pp 377-385, issn 0167-6806, 9 p.Article

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Evaluation of BRCA1 and BRCA2 mutation prevalence, risk prediction models and a multi step testing approach in French-Canadian families with high risk of breast and ovarian cancerSIMARD, Jacques; DUMONT, Martine; BROUSSEAU, Claire et al.Journal of medical genetics. 2007, Vol 44, Num 2, pp 107-121, issn 0022-2593, 15 p.Article

Genetic and histopathologic evaluation of BRCA1 and BRCA2 DNA sequence variants of unknown clinical significanceCHENEVIX-TRENCH, Georgia; HEALEY, Sue; SCHOLL, Tom et al.Cancer research (Baltimore). 2006, Vol 66, Num 4, pp 2019-2027, issn 0008-5472, 9 p.Article

Role of CHEK2*1100delc in unselected series of non-brca1/2 male breast cancersNEUHAUSEN, Susan; DUNNING, Alison; EASTON, Doug et al.International journal of cancer. 2004, Vol 108, Num 3, pp 477-478, issn 0020-7136, 2 p.Article

Likelihood ratios to assess genetic evidence for clinical significance of uncertain variants : Hereditary hemorrhagic telangiectasia as a modelBAYRAK-TOYDEMIR, Pinar; MCDONALD, Jamie; RONG MAO et al.Experimental and molecular pathology. 2008, Vol 85, Num 1, pp 45-49, issn 0014-4800, 5 p.Article

Determination of cancer risk associated with germ line BRCA1 missense variants by functional analysisCARVALHO, Marcelo A; MARSILLAC, Sylvia M; BAUMBACH, Lisa et al.Cancer research (Baltimore). 2007, Vol 67, Num 4, pp 1494-1501, issn 0008-5472, 8 p.Article

Functional evaluation and cancer risk assessment of BRCA2 unclassified variantsKANGJIAN WU; HINSON, Shannon R; OHASHI, Akihiro et al.Cancer research (Baltimore). 2005, Vol 65, Num 2, pp 417-426, issn 0008-5472, 10 p.Article

CGH-targeted linkage analysis reveals a possible BRCA1 modifier locus on chromosome 5qNATHANSON, Katherine L; SHUGART, Yin Y; OMARUDDIN, Romaica et al.Human molecular genetics (Print). 2002, Vol 11, Num 11, pp 1327-1332, issn 0964-6906Article

Rare and Common Variants in CARD 14, Encoding an Epidermal Regulator of NF-kappaB, in PsoriasisJORDAN, Catherine T; LI CAO; OLFSON, Emily H et al.American journal of human genetics. 2012, Vol 90, Num 5, pp 796-808, issn 0002-9297, 13 p.Article

The Role of KRAS rs61764370 in Invasive Epithelial Ovarian Cancer: Implications for Clinical TestingPHAROAH, Paul D. P; PALMIERI, Rachel T; BECKMANN, Matthias W et al.Clinical cancer research (Print). 2011, Vol 17, Num 11, pp 3742-3750, issn 1078-0432, 9 p.Article

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Genome-wide scan reveals association of psoriasis with IL-23 and NF-κB pathwaysNAIR, Rajan P; CALLIS DUFFIN, Kristina; RUETHER, Andreas et al.Nature genetics. 2009, Vol 41, Num 2, pp 199-204, issn 1061-4036, 6 p.Article

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BRCA1 wild-type allele modifies risk of ovarian cancer in carriers of BRCA1 germ-line mutationsGINOLHAC, Sophie M; GAD, Sophie; MULLER, Danièle et al.Cancer epidemiology, biomarkers & prevention. 2003, Vol 12, Num 2, pp 90-95, issn 1055-9965, 6 p.Article

Immunohistochemical Staining with Melan-A of Uninvolved Sun-Damaged Skin Shows Features Characteristic of Lentigo MalignaBOWEN, Anneli R; PERRY THACKER, Betsy N; GOLDGAR, David E et al.Dermatologic surgery. 2011, Vol 37, Num 5, pp 657-663, issn 1076-0512, 7 p.Article

Prevalence of the BRCA2 6174 del T mutation in Israeli uveal melanoma patientsISCOVICH, Jose; ABDULRAZIK, Mohammed; COUR, Carol et al.International journal of cancer. 2002, Vol 98, Num 1, pp 42-44, issn 0020-7136Article

A Computational Method to Classify Variants of Uncertain Significance Using Functional Assay Data with Application to BRCA1IVERSEN, Edwin S; COUCH, Fergus J; GOLDGAR, David E et al.Cancer epidemiology, biomarkers & prevention. 2011, Vol 20, Num 6, pp 1078-1088, issn 1055-9965, 11 p.Article

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Li-Fraumeni and related syndromes: Correlation between tumor type, family structure, and TP53 genotypeOLIVIER, Magali; GOLDGAR, David E; SODHA, Nayanta et al.Cancer research (Baltimore). 2003, Vol 63, Num 20, pp 6643-6650, issn 0008-5472, 8 p.Article