MicroRNA Signatures: Novel Biomarker for Colorectal Cancer?XIAOYA LUO; BURWINKEL, Barbara; SHA TAO et al.Cancer epidemiology, biomarkers & prevention. 2011, Vol 20, Num 7, pp 1272-1286, issn 1055-9965, 15 p.Article

SNP microarray analysis for genome-wide detection of crossover regionsWIRTENBERGER, Michael; HEMMINKI, Kari; BOWANG CHEN et al.Human genetics. 2005, Vol 117, Num 4, pp 389-397, issn 0340-6717, 9 p.Article

Targeting Id1 and Id3 by a specific peptide aptamer induces E-box promoter activity, cell cycle arrest, and apoptosis in breast cancer cellsMERN, Demissew S; HOPPE-SEYLER, Karin; HOPPE-SEYLER, Felix et al.Breast cancer research and treatment. 2010, Vol 124, Num 3, pp 623-633, issn 0167-6806, 11 p.Article

The functional genetic variant Arg324Gly of frizzled-related protein is associated with colorectal cancer riskSHANMUGAM, Kalai S; BRENNER, Hermann; HOFFMEISTER, Michael et al.Carcinogenesis (New York. Print). 2007, Vol 28, Num 9, pp 1914-1917, issn 0143-3334, 4 p.Article

Smoking, F2RL3 methylation, and prognosis in stable coronary heart diseaseBREITLING, Lutz Philipp; SALZMANN, Katrin; ROTHENBACHER, Dietrich et al.European heart journal. 2012, Vol 33, Num 22, pp 2841-2848, issn 0195-668X, 8 p.Article

Tobacco-Smoking-Related Differential DNA Methylation: 27K Discovery and ReplicationBREITLING, Lutz P; RONGXI YANG; KORN, Bernhard et al.American journal of human genetics. 2011, Vol 88, Num 4, pp 450-457, issn 0002-9297, 8 p.Article

Severe phenotype of phosphorylase kinase-deficient liver glycogenosis with mutations in the PHKG2 geneBURWINKEL, Barbara; ROOTWELT, Terje; KVITTINGEN, Eli. Anne et al.Pediatric research. 2003, Vol 54, Num 6, pp 834-839, issn 0031-3998, 6 p.Article

Germline variants of base excision repair genes and breast cancer: a polymorphism in DNA polymerase gamma modifies gene expression and breast cancer riskPOPANDA, Odilia; SEIBOLD, Petra; NIKOLOV, Ivaylo et al.International journal of cancer (Print). 2013, Vol 132, Num 1, pp 55-62, issn 0020-7136, 8 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

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

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

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

Mutations in ROGDI Cause Kohlschütter-Tönz SyndromeSCHOSSIG, Anna; WOLF, Nicole I; HABERLANDT, Edda et al.American journal of human genetics. 2012, Vol 90, Num 4, pp 701-707, issn 0002-9297, 7 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

First evidence for an association of a functional variant in the microRNA-510 target site of the serotonin receptor-type 3E gene with diarrhea predominant irritable bowel syndromeKAPELLER, Johannes; HOUGHTON, Lesley A; GASSLER, Nikolaus et al.Human molecular genetics (Print). 2008, Vol 17, Num 19, pp 2967-2977, issn 0964-6906, 11 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

CD24 polymorphisms in breast cancer: impact on prognosis and riskBUCK, Katharina; HUG, Sarah; CHANG-CLAUDE, Jenny et al.Breast cancer research and treatment. 2013, Vol 137, Num 3, pp 927-937, issn 0167-6806, 11 p.Article

Circulating miRNAs as Surrogate Markers for Circulating Tumor Cells and Prognostic Markers in Metastatic Breast CancerMADHAVAN, Dharanija; ZUCKNICK, Manuela; BENNER, Axel et al.Clinical cancer research (Print). 2012, Vol 18, Num 21, pp 5972-5982, issn 1078-0432, 11 p.Article

The CASP8 -652 6N del promoter polymorphism and breast cancer risk : a multicenter studyFRANK, Bernd; RIGAS, Sushila H; MEINDL, Alfons et al.Breast cancer research and treatment. 2008, Vol 111, Num 1, pp 139-144, issn 0167-6806, 6 p.Article

Association analyses of GIP and GIPR polymorphisms with traits of the metabolic syndromeNITZ, Inke; FISHER, Eva; WEIKERT, Cornelia et al.Molecular nutrition & food research (Print). 2007, Vol 51, Num 8, pp 1046-1052, issn 1613-4125, 7 p.Article

ARLTS1 variants and melanoma riskFRANK, Bernd; MEYER, Peter; BOETTGER, Melanie Barbara et al.International journal of cancer. 2006, Vol 119, Num 7, pp 1736-1737, issn 0020-7136, 2 p.Article

Association of prolactin and its receptor gene regions with familial breast cancerVACLAVICEK, Annika; HEMMINKI, Kari; FÖRSTI, Asta et al.The Journal of clinical endocrinology and metabolism. 2006, Vol 91, Num 4, pp 1513-1519, issn 0021-972X, 7 p.Article

Arthrogryposis multiplex with deafness, inguinal hernias, and early death : A family report of a probably autosomal recessive traitTIEMANN, Christian; BÜHRER, Christoph; BURWINKEL, Barbara et al.American journal of medical genetics. 2005, Vol 137A, Num 2, pp 125-129, issn 0148-7299, 5 p.Article