The genotype of the original wiskott phenotypeBINDER, Vera; ALBERT, Michael H; KABUS, Maria et al.The New England journal of medicine. 2006, Vol 355, Num 17, pp 1790-1793, issn 0028-4793, 4 p.Article

A novel mutation in the interleukin-2 receptor γ gene as the cause of lymphopenia in a neonate vertically exposed to human immunodeficiency virusNEUBERT, Jennifer; MEINDL, Alfons; THEISEN, Albert et al.The Pediatric infectious disease journal. 2005, Vol 24, Num 2, pp 187-189, issn 0891-3668, 3 p.Article

9q31.2-rs865686 as a Susceptibility Locus for Estrogen Receptor-Positive Breast Cancer: Evidence from the Breast Cancer Association ConsortiumWARREN, Helen; DUDBRIDGE, Frank; BROEKS, Annegien et al.Cancer epidemiology, biomarkers & prevention. 2012, Vol 21, Num 10, pp 1783-1791, issn 1055-9965, 9 p.Article

Genetic variants within miR-126 and miR-335 are not associated with breast cancer riskRONGXI YANG; DICK, Michelle; SCHOTT, Sarah et al.Breast cancer research and treatment. 2011, Vol 127, Num 2, pp 549-554, issn 0167-6806, 6 p.Article

Missense Variants in ATM in 26,101 Breast Cancer Cases and 29,842 ControlsFLETCHER, Olivia; JOHNSON, Nichola; BARTRAM, Claus R et al.Cancer epidemiology, biomarkers & prevention. 2010, Vol 19, Num 9, pp 2143-2151, issn 1055-9965, 9 p.Article

A two base pair deletion in the PQBP1 gene is associated with microphthalmia, microcephaly, and mental retardationMARTINEZ-GARAY, Isabel; TOMAS, Miguel; OLTRA, Silvestre et al.European journal of human genetics. 2007, Vol 15, Num 1, pp 29-34, issn 1018-4813, 6 p.Article

AURKA F31I polymorphism and breast cancer risk in BRCA1 and BRCA2 mutation carriers : A consortium of investigators of modifiers of BRCA1/2 studyCOUCH, Fergus J; SINILNIKOVA, Olga; PEOCK, Susan et al.Cancer epidemiology, biomarkers & prevention. 2007, Vol 16, Num 7, pp 1416-1421, issn 1055-9965, 6 p.Article

Associations of genetic variants in the estrogen receptor coactivators PPARGC1A, PPARGC1B and EP300 with familial breast cancerWIRTENBERGER, Michael; TCHATCHOU, Sandrine; WEBER, Bernhard H. F et al.Carcinogenesis (New York. Print). 2006, Vol 27, Num 11, pp 2201-2208, issn 0143-3334, 8 p.Article

Immunohistochemical demonstration of the zinc metalloprotease insulin-degrading enzyme in normal and malignant human breast : Correlation with tissue insulin levelsRADULESCU, Razvan T; HUFNAGEL, Carla; WEIRICH, Gregor et al.International journal of oncology. 2006, Vol 30, Num 1, pp 73-80, issn 1019-6439, 8 p.Article

A variant affecting miRNAs binding in the circadian gene Neuronal PAS domain protein 2 (NPAS2) is not associated with breast cancer riskFURU WANG; ZHIBIN HU; MEINDL, Alfons et al.Breast cancer research and treatment. 2011, Vol 127, Num 3, pp 769-775, issn 0167-6806, 7 p.Article

Association of the Variants CASP8 D302H and CASP10 V410I with Breast and Ovarian Cancer Risk in BRCA1 and BRCA2 Mutation CarriersENGEL, Christoph; VERSMOLD, Beatrix; GARETH EVANS, D et al.Cancer epidemiology, biomarkers & prevention. 2010, Vol 19, Num 11, pp 2859-2868, issn 1055-9965, 10 p.Article

Common Breast Cancer-Predisposition Alleles Are Associated with Breast Cancer Risk in BRCA1 and BRCA2 Mutation CarriersANTONIOU, Antonis C; SPURDLE, Amanda B; HOFMANN, Wera et al.American journal of human genetics. 2008, Vol 82, Num 4, pp 937-948, issn 0002-9297, 12 p.Article

The functional genetic variant Ile646Val located in the kinase binding domain of the A-kinase anchoring protein 10 is associated with familial breast cancerWIRTENBERGER, Michael; SCHMUTZHARD, Julia; NIEDERACHER, Dieter et al.Carcinogenesis (New York. Print). 2007, Vol 28, Num 2, pp 423-426, issn 0143-3334, 4 p.Article

Genetic variation in the major mitotic checkpoint genes does not affect familial breast cancer riskVACLAVICEK, Annika; LORENZO BERMEJO, Justo; HEMMINKI, Kari et al.Breast cancer research and treatment. 2007, Vol 106, Num 2, pp 205-213, issn 0167-6806, 9 p.Article

Interaction of Werner and Bloom syndrome genes with p53 in familial breast cancerWIRTENBERGER, Michael; FRANK, Bernd; NIEDERACHER, Dieter et al.Carcinogenesis (New York. Print). 2006, Vol 27, Num 8, pp 1655-1660, issn 0143-3334, 6 p.Article

19p13.1 Is a Triple-Negative―Specific Breast Cancer Susceptibility LocusSTEVENS, Kristen N; FREDERICKSEN, Zachary; CHANG-CLAUDE, Jenny et al.Cancer research (Chicago, Ill.). 2012, Vol 72, Num 7, pp 1795-1803, issn 0008-5472, 9 p.Article

Two new families with X-linked inhibitor of apoptosis deficiency and a review of all 26 published casesHORN, Peter C; BELOHRADSKY, Bernd H; URBAN, Christian et al.Journal of allergy and clinical immunology. 2011, Vol 127, Num 2, pp 544-546, issn 0091-6749, 3 p.Article

A genetic variant in the pre-miR-27a oncogene is associated with a reduced familial breast cancer riskRONGXI YANG; SCHLEHE, Bettina; ARNOLD, Norbert et al.Breast cancer research and treatment. 2010, Vol 121, Num 3, pp 693-702, issn 0167-6806, 10 p.Article

X-linked thrombocytopenia (XLT) due to WAS mutations: clinical characteristics, long-term outcome, and treatment optionsALBERT, Michael H; BITTNER, Tanja C; MORIO, Tomohiro et al.Blood. 2010, Vol 115, Num 16, pp 3231-3238, issn 0006-4971, 8 p.Article

No association of TGFB1 L10P genotypes and breast cancer risk in BRCA1 and BRCA2 mutation carriers: a multi-center cohort studyREBBECK, Timothy R; ANTONIOU, Antonis C; GREENE, Mark H et al.Breast cancer research and treatment. 2009, Vol 115, Num 1, pp 185-192, issn 0167-6806, 8 p.Article

Association of a Common AKAP9 Variant With Breast Cancer Risk : A Collaborative AnalysisFRANK, Bernd; WIESTLER, Miriam; MEINDL, Alfons et al.Journal of the National Cancer Institute. 2008, Vol 100, Num 6, pp 437-442, issn 0027-8874, 6 p.Article

SNPs in ultraconserved elements and familial breast cancer riskRONGXI YANG; FRANK, Bernd; WEBER, Bernhard H. F et al.Carcinogenesis (New York. Print). 2008, Vol 29, Num 2, pp 351-355, issn 0143-3334, 5 p.Article

Comparison of gene expression data from human and mouse breast cancers : Identification of a conserved breast tumor gene setKLEIN, Andreas; WESSEL, Ralf; SEITZ, Susanne et al.International journal of cancer. 2007, Vol 121, Num 3, pp 683-688, issn 0020-7136, 6 p.Article

A male infant with a 9.6 Mb terminal Xp deletion including the OA1 locus : Limit of viability of Xp deletions in malesMELICHAR, Volker O; GUTH, Sabine; HELLEBRAND, Heide et al.American journal of medical genetics. Part A. 2007, Vol 143, Num 2, pp 135-141, issn 1552-4825, 7 p.Article

Limited relevance of the CHEK2 gene in hereditary breast cancerDUFAULT, Michael R; BETZ, Beate; VON LINDERN, Celia et al.International journal of cancer. 2004, Vol 110, Num 3, pp 320-325, issn 0020-7136, 6 p.Article