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Biology and Biochemistry

D-Index
47
Citations
8306
World Ranking
18695
National Ranking
655

Overview

Hilmi Ozcelik is affiliated with the University of Toronto in Canada and conducts research primarily within the fields of biochemistry, genetics, and molecular biology. Their work focuses significantly on genetics, with a particular emphasis on BRCA gene mutations related to cancer.

The scientist has several recent publications, all from the year 2020, which are hosted by UNC Libraries. These publications include the following:

  • Common Breast Cancer Susceptibility Alleles and the Risk of Breast Cancer for BRCA1 and BRCA2 Mutation Carriers: Implications for Risk Prediction (2020, UNC Libraries)
  • Common Variants at the 19p13.1 and ZNF365 Loci Are Associated with ER Subtypes of Breast Cancer and Ovarian Cancer Risk in BRCA1 and BRCA2 Mutation Carriers (2020, UNC Libraries)
  • Common alleles at 6q25.1 and 1p11.2 are associated with breast cancer risk for BRCA1 and BRCA2 mutation carriers (2020, UNC Libraries)
  • Common variants in LSP1, 2q35 and 8q24 and breast cancer risk for BRCA1 and BRCA2 mutation carriers (2020, UNC Libraries)

Their research explicitly contributes to the understanding of breast cancer risk in mutation carriers of BRCA1 and BRCA2 genes.

Frequent co-authors in Hilmi Ozcelik's publications include:

  • Antonis C. Antoniou
  • Lesley McGuffog
  • Olga M. Sinilnikova
  • Sue Healey
  • Irene L. Andrulis

Most of their scholarly articles have been published through UNC Libraries, which serves as the main venue for their research dissemination.

The main topics of their work are centered particularly on:

  • BRCA gene mutations in cancer

Best Publications

  • MADR2 maps to 18q21 and encodes a TGFβ-regulated MAD-related protein that is functionally mutated in colorectal carcinoma

    Kolja Eppert;Stephen W Scherer;Hilmi Ozcelik;Rosa Pirone

  • Prevalence and Penetrance of BRCA1 and BRCA2 Gene Mutations in Unselected Ashkenazi Jewish Women With Breast Cancer

    Ellen Warner;William Foulkes;Pamela Goodwin;Wendy Meschino

  • 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

    Antonis C. Antoniou;Xianshu Wang;Zachary S. Fredericksen;Lesley McGuffog

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

    Antonis C. Antoniou;Antonis C. Antoniou;Amanda B. Spurdle;Amanda B. Spurdle;Olga M. Sinilnikova;Olga M. Sinilnikova;Sue Healey;Sue Healey

  • Genome-wide association study in BRCA1 mutation carriers identifies novel loci associated with breast and ovarian cancer risk

    Fergus J. Couch;Xianshu Wang;Lesley McGuffog;Andrew Lee

  • Inherited predisposition to pancreatic adenocarcinoma: role of family history and germ-line p16, BRCA1, and BRCA2 mutations.

    Geeta Lal;Geoffrey Liu;Beverley Schmocker;Pardeep Kaurah

  • RAD51 135G→C Modifies Breast Cancer Risk among BRCA2 Mutation Carriers: Results from a Combined Analysis of 19 Studies

    Antonis C. Antoniou;Olga M. Sinilnikova;Jacques Simard;Mélanie Léoné

  • Germline BRCA2 6174delT mutations in Ashkenazi Jewish pancreatic cancer patients.

    Ozçelik H;Schmocker B;Di Nicola N;Shi Xh

  • Methylation of the BRCA1 promoter is associated with decreased BRCA1 mRNA levels in clinical breast cancer specimens

    Judd C. Rice;Hilmi Ozcelik;Hilmi Ozcelik;Patrick Maxeiner;Irene Andrulis;Irene Andrulis

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

    Pia Huusko;Damaris Ponciano-Jackson;Maija Wolf;Jeff A. Kiefer

  • Common Breast Cancer Susceptibility Alleles and the Risk of Breast Cancer for BRCA1 and BRCA2 Mutation Carriers: Implications for Risk Prediction

    Antonis C. Antoniou;Jonathan Beesley;Lesley McGuffog;Olga M. Sinilnikova

  • SNP-SNP interactions in breast cancer susceptibility

    Venüs Ümmiye Onay;Laurent Briollais;Laurent Briollais;Julia A Knight;Julia A Knight;Ellen Shi

  • Genetic epidemiologic studies of preterm birth: guidelines for research.

    Craig E. Pennell;Craig E. Pennell;Bo Jacobsson;Bo Jacobsson;Scott M. Williams;Rebecca M. Buus

  • Epigenetic Factors Controlling the BRCA1 and BRCA2 Genes in Sporadic Ovarian Cancer

    Kelvin Y. K. Chan;Hilmi Ozçelik;Annie N. Y. Cheung;Hextan Y. S. Ngan

  • Two variants of the CIP1/WAF1 gene occur together and are associated with human cancer

    Spyro Mousses;Hilmi Özçelik;Peter D.Lee;Peter D.Lee;David Malkin

  • Hereditary haemorrhagic telangiectasia: mutation detection, test sensitivity and novel mutations

    N L Prigoda;S Savas;S A Abdalla;B Piovesan

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

    Mia M. Gaudet;Tomas Kirchhoff;Todd Green;Joseph Vijai

  • The Combination of p53 Mutation and neu/erbB-2 Amplification Is Associated With Poor Survival in Node-Negative Breast Cancer

    Shelley B. Bull;Hilmi Ozcelik;Dushanthi Pinnaduwage;Martin E. Blackstein

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

    Antonis C. Antoniou;Olga M. Sinilnikova;Lesley McGuffog;Sue Healey

  • Frequency of p53 mutations in breast carcinomas from Ashkenazi Jewish carriers of BRCA1 mutations.

    Kelly-Anne Phillips;Kerrie Nichol;Hilmi Ozcelik;Julia Knight

Frequent Co-Authors

Irene L. Andrulis
Irene L. Andrulis University of Toronto
Esther M. John
Esther M. John Stanford University
Julia A. Knight
Julia A. Knight Lunenfeld-Tanenbaum Research Institute
Douglas F. Easton
Douglas F. Easton University of Cambridge
Heli Nevanlinna
Heli Nevanlinna University of Helsinki
Georgia Chenevix-Trench
Georgia Chenevix-Trench QIMR Berghofer Medical Research Institute
Susan L. Neuhausen
Susan L. Neuhausen City Of Hope National Medical Center
Mary B. Daly
Mary B. Daly Fox Chase Cancer Center
Fergus J. Couch
Fergus J. Couch Mayo Clinic

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