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ATXN2 and its neighbouring gene SH2B3 are associated with increased ALS risk in the Turkish population

PloS one, 2012-08, Vol.7 (8), p.e42956-e42956

2012

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Genome-wide copy number variation in sporadic amyotrophic lateral sclerosis in the Turkish population: deletion of EPHA3 is a possible protective factor

PloS one, 2013-08, Vol.8 (8), p.e72381

2013

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The distinct genetic pattern of ALS in Turkey and novel mutations

Neurobiology of aging, 2015-04, Vol.36 (4), p.1764.e9-1764.e18

2015

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Missense variants of uncertain significance (VUS) altering the phosphorylation patterns of BRCA1 and BRCA2

PloS one, 2013-05, Vol.8 (5), p.e62468-e62468

2013

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Menopausal status modifies breast cancer risk associated with the myeloperoxidase (MPO) G463A polymorphism in Caucasian women: a meta-analysis

PloS one, 2012-03, Vol.7 (3), p.e32389-e32389

2012

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SNP-SNP interactions in breast cancer susceptibility

BMC cancer, 2006-05, Vol.6 (1), p.114-114, Article 114

2006

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Discovery, validation and characterization of Erbb4 and Nrg1 haplotypes using data from three genome-wide association studies of schizophrenia

PloS one, 2013-01, Vol.8 (1), p.e53042-e53042

2013

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p53 protein accumulation in non-invasive lesions surrounding p53 mutation positive invasive breast cancers

Breast cancer research and treatment, 2001, Vol.65 (2), p.111-118

2001

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Long-Range PCR and Next-Generation Sequencing of BRCA1 and BRCA2 in Breast Cancer

The Journal of molecular diagnostics : JMD, 2012-09, Vol.14 (5), p.467-475

2012

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Discovery of novel hypermethylated genes in prostate cancer using genomic CpG island microarrays

PloS one, 2009-03, Vol.4 (3), p.e4830

2009

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Genetic epidemiologic studies of preterm birth: guidelines for research

American journal of obstetrics and gynecology, 2007-02, Vol.196 (2), p.107-118

2007

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Breast Cancer Risk for Noncarriers of Family-Specific BRCA1 and BRCA2 Mutations: Findings From the Breast Cancer Family Registry

Journal of clinical oncology, 2011-12, Vol.29 (34), p.4505-4509

2011

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

Radiotherapy and oncology, 2007-06, Vol.83 (3), p.220-230

2007

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

Nature genetics, 2004-09, Vol.36 (9), p.979-983

2004

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Identifying Functional Genetic Variants in DNA Repair Pathway Using Protein Conservation Analysis

Cancer epidemiology, biomarkers & prevention, 2004-05, Vol.13 (5), p.801-807

2004

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Quantitative DNA methylation analysis of genes coding for kallikrein-related peptidases 6 and 10 as biomarkers for prostate cancer

Epigenetics, 2012-09, Vol.7 (9), p.1037-1045

2012

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Epigenetic factors controlling the BRCA1 and BRCA2 genes in sporadic ovarian cancer

Cancer research (Chicago, Ill.), 2002-07, Vol.62 (14), p.4151-4156

2002

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BRCA1 and BRCA2 mutation carriers in the Breast Cancer Family Registry: an open resource for collaborative research

Breast cancer research and treatment, 2009-07, Vol.116 (2), p.379-386

2009

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Polymorphisms XRCC1-R399Q and XRCC3-T241M and the Risk of Breast Cancer at the Ontario Site of the Breast Cancer Family Registry

Cancer epidemiology, biomarkers & prevention, 2004-04, Vol.13 (4), p.583-591

2004

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

BMC medicine, 2007-08, Vol.5 (1), p.22-22, Article 22

2007

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A whole-genome SNP association study of NCI60 cell line panel indicates a role of Ca2+ signaling in selenium resistance

PloS one, 2010-09, Vol.5 (9), p.e12601

2010

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NCI60 cancer cell line panel data and RNAi analysis help identify EAF2 as a modulator of simvastatin and lovastatin response in HCT-116 cells

PloS one, 2011-04, Vol.6 (4), p.e18306-e18306

2011

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Genetic Variants of GPX1 and SOD2 and Breast Cancer Risk at the Ontario Site of the Breast Cancer Family Registry

Cancer epidemiology, biomarkers & prevention, 2004-01, Vol.13 (1), p.146-149

2004

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

BMC cancer, 2005-08, Vol.5 (1), p.107-107, Article 107

2005

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

BMC medical genomics, 2011-02, Vol.4 (1), p.18-18, Article 18

2011

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ATXN2 and its neighbouring gene SH2B3 are associated with increased ALS risk in the Turkish population

Genome-wide copy number variation in sporadic amyotrophic lateral sclerosis in the Turkish population: deletion of EPHA3 is a possible protective factor

The distinct genetic pattern of ALS in Turkey and novel mutations

Missense variants of uncertain significance (VUS) altering the phosphorylation patterns of BRCA1 and BRCA2

Menopausal status modifies breast cancer risk associated with the myeloperoxidase (MPO) G463A polymorphism in Caucasian women: a meta-analysis

SNP-SNP interactions in breast cancer susceptibility

Discovery, validation and characterization of Erbb4 and Nrg1 haplotypes using data from three genome-wide association studies of schizophrenia

p53 protein accumulation in non-invasive lesions surrounding p53 mutation positive invasive breast cancers

Long-Range PCR and Next-Generation Sequencing of BRCA1 and BRCA2 in Breast Cancer

Discovery of novel hypermethylated genes in prostate cancer using genomic CpG island microarrays

Genetic epidemiologic studies of preterm birth: guidelines for research

Breast Cancer Risk for Noncarriers of Family-Specific BRCA1 and BRCA2 Mutations: Findings From the Breast Cancer Family Registry

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

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

Identifying Functional Genetic Variants in DNA Repair Pathway Using Protein Conservation Analysis

Quantitative DNA methylation analysis of genes coding for kallikrein-related peptidases 6 and 10 as biomarkers for prostate cancer

Epigenetic factors controlling the BRCA1 and BRCA2 genes in sporadic ovarian cancer

BRCA1 and BRCA2 mutation carriers in the Breast Cancer Family Registry: an open resource for collaborative research

Polymorphisms XRCC1-R399Q and XRCC3-T241M and the Risk of Breast Cancer at the Ontario Site of the Breast Cancer Family Registry

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

A whole-genome SNP association study of NCI60 cell line panel indicates a role of Ca2+ signaling in selenium resistance

NCI60 cancer cell line panel data and RNAi analysis help identify EAF2 as a modulator of simvastatin and lovastatin response in HCT-116 cells

Genetic Variants of GPX1 and SOD2 and Breast Cancer Risk at the Ontario Site of the Breast Cancer Family Registry

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

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

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