Hilmi Ozcelik

发表

SNP-SNP interactions in breast cancer susceptibility

Laurent Briollais, Irene L Andrulis, Julia A Knight, 2006, BMC Cancer.

Biological implications of SNPs in signal peptide domains of human proteins

J. Dennis, H. Ozçelik, H. Jarjanazi, 2007, Proteins.

Human SNPs resulting in premature stop codons and protein truncation

Sukru Tuzmen, H. Ozçelik, S. Savas, 2006, Human Genomics.

Common alleles at 6q25.1 and 1p11.2 are associated with breast cancer risk for BRCA1 and BRCA2 mutation carriers.

Christiana Kartsonaki, Mads Thomassen, Etienne Rouleau, 2011, Human molecular genetics.

Common variants at 12p11, 12q24, 9p21, 9q31.2 and in ZNF365 are associated with breast cancer risk for BRCA1 and/or BRCA2 mutation carriers

Mads Thomassen, Nina Ditsch, Vijai Joseph, 2012, Breast Cancer Research.

Common variants in LSP1, 2q35 and 8q24 and breast cancer risk for BRCA1 and BRCA2 mutation carriers.

Mads Thomassen, Nina Ditsch, Dieter Niederacher, 2009, Human molecular genetics.

Nonsense-mediated decay microarray analysis identifies mutations of EPHB2 in human prostate cancer

Tony Pawson, Sampsa Hautaniemi, Spyro Mousses, 2004, Nature Genetics.

A locus on 19p13 modifies risk of breast cancer in BRCA1 mutation carriers and is associated with hormone receptor–negative breast cancer in the general population

Christiana Kartsonaki, Mads Thomassen, Julian Peto, 2010, Nature Genetics.

Correction: Common Genetic Variants and Modification of Penetrance of BRCA2-Associated Breast Cancer

Joshua M. Korn, Christiana Kartsonaki, Amanda B. Spurdle, 2010, PLoS Genetics.

MADR2 Maps to 18q21 and Encodes a TGFβ–Regulated MAD–Related Protein That Is Functionally Mutated in Colorectal Carcinoma

Irene L Andrulis, Stephen W Scherer, Steven Gallinger, 1996, Cell.

Mutational analysis of BRCA1 and BRCA2 genes in Chinese ovarian cancer identifies 6 novel germline mutations

Jing Lu, I. Andrulis, H. Ozçelik, 2000, Human mutation.

Methodological issues in detecting gene-gene interactions in breast cancer susceptibility: a population-based study in Ontario

Laurent Briollais, Julia Knight, J. Knight, 2007, BMC medicine.

Homologous recombination and prostate cancer: a model for novel DNA repair targets and therapies.

Danny Vesprini, R. Bristow, F. Jalali, 2007, Radiotherapy and oncology : journal of the European Society for Therapeutic Radiology and Oncology.

Common breast cancer susceptibility alleles and the risk of breast cancer for BRCA1 and BRCA2 mutation carriers: implications for risk prediction.

Mads Thomassen, Etienne Rouleau, Dieter Niederacher, 2010, Cancer research.

Common breast cancer susceptibility alleles are associated with tumour subtypes in BRCA1 and BRCA2 mutation carriers: results from the Consortium of Investigators of Modifiers of BRCA1/2

Mads Thomassen, Stephen Fox, Dieter Niederacher, 2011, Breast Cancer Research.

Long-range PCR and next-generation sequencing of BRCA1 and BRCA2 in breast cancer.

Aaron Goldman, K. Siminovitch, R. Kandel, 2012, The Journal of molecular diagnostics : JMD.

A BAYESIAN GRAPHICAL MODEL FOR GENOME-WIDE ASSOCIATION STUDIES (GWAS).

Adrian Dobra, Laurent Briollais, Hélène Massam, 2016, The annals of applied statistics.

Bioinformatic analyses identifies novel protein-coding pharmacogenomic markers associated with paclitaxel sensitivity in NCI60 cancer cell lines

H. Ozçelik, K. Pritchard, H. Jarjanazi, 2011, BMC Medical Genomics.

Common breast cancer-predisposition alleles are associated with breast cancer risk in BRCA1 and BRCA2 mutation carriers.

Dieter Niederacher, Ute Hamann, Alfons Meindl, 2008, American journal of human genetics.