Phosphorylation states of cell cycle and DNA repair proteins can be altered by the nsSNPs

Autor Savas, Sevtap, Ozcelik, Hilmi
Vydáno 2005

Human SNPs resulting in premature stop codons and protein truncation

Autor Savas, Sevtap, Tuzmen, Sukru, Ozcelik, Hilmi
Vydáno 2006

Missense Variants of Uncertain Significance (VUS) Altering the Phosphorylation Patterns of BRCA1 and BRCA2

Autor Tram, Eric, Savas, Sevtap, Ozcelik, Hilmi
Vydáno 2013

Functional nsSNPs from carcinogenesis-related genes expressed in breast tissue: Potential breast cancer risk alleles and their distribution across human populations

Autor Savas, Sevtap, Schmidt, Steffen, Jarjanazi, Hamdi, Ozcelik, Hilmi
Vydáno 2006

Genome Wide Screening of CAG Trinucleotide Repeat Lengths in Breast Cancer

Autor Jarjanazi, Hamdi, Li, Hong, Andrulis, Irene L., Ozcelik, Hilmi
Vydáno 2006

Menopausal Status Modifies Breast Cancer Risk Associated with the Myeloperoxidase (MPO) G463A Polymorphism in Caucasian Women: A Meta-Analysis

Autor Pabalan, Noel, Jarjanazi, Hamdi, Sung, Lillian, Li, Hong, Ozcelik, Hilmi
Vydáno 2012

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

Autor Briollais, Laurent, Dobra, Adrian, Liu, Jinnan, Friedlander, Matt, Ozcelik, Hilmi, Massam, Hélène
Vydáno v Ann Appl Stat (2016)

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

Autor Briollais, Laurent, Wang, Yuanyuan, Rajendram, Isaac, Onay, Venus, Shi, Ellen, Knight, Julia, Ozcelik, Hilmi
Vydáno 2007

Identification of germline alterations of the mad homology 2 domain of SMAD3 and SMAD4 from the Ontario site of the breast cancer family registry (CFR)

Autor Tram, Eric, Ibrahim-zada, Irada, Briollais, Laurent, Knight, Julia A, Andrulis, Irene L, Ozcelik, Hilmi
Vydáno 2011

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

Autor Eng, Lawson, Ibrahim-zada, Irada, Jarjanazi, Hamdi, Savas, Sevtap, Meschian, Mehran, Pritchard, Kathleen I, Ozcelik, Hilmi
Vydáno 2011

A Whole-Genome SNP Association Study of NCI60 Cell Line Panel Indicates a Role of Ca(2+) Signaling in Selenium Resistance

Autor Savas, Sevtap, Briollais, Laurent, Ibrahim-zada, Irada, Jarjanazi, Hamdi, Choi, Yun Hee, Musquera, Mireia, Fleshner, Neil, Venkateswaran, Vasundara, Ozcelik, Hilmi
Vydáno 2010

SNP-SNP interactions in breast cancer susceptibility

Autor Wang Yuanyuan, Shi Ellen, Knight Julia A, Briollais Laurent, Onay Venüs, Wells Sean, Li Hong, Rajendram Isaac, Andrulis Irene L, Ozcelik Hilmi
Vydáno 2006-05-01

Discovery, Validation and Characterization of Erbb4 and Nrg1 Haplotypes Using Data from Three Genome-Wide Association Studies of Schizophrenia

Autor Agim, Zeynep Sena, Esendal, Melda, Briollais, Laurent, Uyan, Ozgun, Meschian, Mehran, Martinez, Luis Antonio Mendoza, Ding, Yongmei, Basak, A. Nazli, Ozcelik, Hilmi
Vydáno 2013

SNP-SNP interactions in breast cancer susceptibility

Autor Onay, Venüs Ümmiye, Briollais, Laurent, Knight, Julia A, Shi, Ellen, Wang, Yuanyuan, Wells, Sean, Li, Hong, Rajendram, Isaac, Andrulis, Irene L, Ozcelik, Hilmi
Vydáno 2006

Combined effect of CCND1 and COMT polymorphisms and increased breast cancer risk

Autor Onay, Ummiye V, Aaltonen, Kirsimari, Briollais, Laurent, Knight, Julia A, Pabalan, Noel, Kilpivaara, Outi, Andrulis, Irene L, Blomqvist, Carl, Nevanlinna, Heli, Ozcelik, Hilmi
Vydáno 2008

Discovery of Novel Hypermethylated Genes in Prostate Cancer Using Genomic CpG Island Microarrays

Autor Kron, Ken, Pethe, Vaijayanti, Briollais, Laurent, Sadikovic, Bekim, Ozcelik, Hilmi, Sunderji, Alia, Venkateswaran, Vasundara, Pinthus, Jehonathan, Fleshner, Neil, van der Kwast, Theodorus, Bapat, Bharati
Vydáno 2009

ATXN2 and Its Neighbouring Gene SH2B3 Are Associated with Increased ALS Risk in the Turkish Population

Autor Lahut, Suna, Ömür, Özgür, Uyan, Özgün, Ağım, Zeynep Sena, Özoğuz, Aslihan, Parman, Yeşim, Deymeer, Feza, Oflazer, Piraye, Koç, Filiz, Özçelik, Hilmi, Auburger, Georg, Başak, A. Nazlı
Vydáno 2012

Genome-Wide Copy Number Variation in Sporadic Amyotrophic Lateral Sclerosis in the Turkish Population: Deletion of EPHA3 Is a Possible Protective Factor

Autor Uyan, Özgün, Ömür, Özgür, Ağım, Zeynep Sena, Özoğuz, Aslıhan, Li, Hong, Parman, Yeşim, Deymeer, Feza, Oflazer, Piraye, Koç, Filiz, Tan, Ersin, Özçelik, Hilmi, Başak, A. Nazlı
Vydáno 2013

Polymorphisms cMyc-N11S and p27-V109G and breast cancer risk and prognosis

Autor Figueiredo, Jane C, Knight, Julia A, Cho, Stewart, Savas, Sevtap, Onay, U Venus, Briollais, Laurent, Goodwin, Pamela J, McLaughlin, John R, Andrulis, Irene L, Ozcelik, Hilmi
Vydáno 2007

NCI60 Cancer Cell Line Panel Data and RNAi Analysis Help Identify EAF2 as a Modulator of Simvastatin and Lovastatin Response in HCT-116 Cells

Autor Savas, Sevtap, Azorsa, David O., Jarjanazi, Hamdi, Ibrahim-Zada, Irada, Gonzales, Irma M., Arora, Shilpi, Henderson, Meredith C., Choi, Yun Hee, Briollais, Laurent, Ozcelik, Hilmi, Tuzmen, Sukru
Vydáno 2011