Marc Tischkowitz


Ontology type: schema:Person     


Person Info

NAME

Marc

SURNAME

Tischkowitz

Publications in SciGraph latest 50 shown

  • 2019-12 Shared heritability and functional enrichment across six solid cancers in NATURE COMMUNICATIONS
  • 2019-04 Clinical implications of germline mutations in breast cancer genes: RECQL in BREAST CANCER RESEARCH AND TREATMENT
  • 2018-12 Risks of breast or ovarian cancer in BRCA1 or BRCA2 predictive test negatives: findings from the EMBRACE study in GENETICS IN MEDICINE
  • 2018-01 Clinical implications of germline mutations in breast cancer: TP53 in BREAST CANCER RESEARCH AND TREATMENT
  • 2017-12 When to Consider Risk-Reducing Mastectomy in BRCA1/BRCA2 Mutation Carriers with Advanced Stage Ovarian Cancer: a Case Study Illustrating the Genetic Counseling Challenges in JOURNAL OF GENETIC COUNSELING
  • 2017-07 Compromised BRCA1–PALB2 interaction is associated with breast cancer risk in ONCOGENE
  • 2017-05 Identification of 12 new susceptibility loci for different histotypes of epithelial ovarian cancer in NATURE GENETICS
  • 2016-12 Incorporating truncating variants in PALB2, CHEK2, and ATM into the BOADICEA breast cancer risk model in GENETICS IN MEDICINE
  • 2016-12 Inheritance of deleterious mutations at both BRCA1 and BRCA2 in an international sample of 32,295 women in BREAST CANCER RESEARCH
  • 2016-06 An international survey of surveillance schemes for unaffected BRCA1 and BRCA2 mutation carriers in BREAST CANCER RESEARCH AND TREATMENT
  • 2015-12 An original phylogenetic approach identified mitochondrial haplogroup T1a1 as inversely associated with breast cancer risk in BRCA2 mutation carriers in BREAST CANCER RESEARCH
  • 2015-02 Identification of six new susceptibility loci for invasive epithelial ovarian cancer in NATURE GENETICS
  • 2014-12 Mutation analysis of PALB2 in BRCA1 and BRCA2-negative breast and/or ovarian cancer families from Eastern Ontario, Canada in HEREDITARY CANCER IN CLINICAL PRACTICE
  • 2014-12 Associations of common breast cancer susceptibility alleles with risk of breast cancer subtypes in BRCA1 and BRCA2 mutation carriers in BREAST CANCER RESEARCH
  • 2014-05 Germline and somatic SMARCA4 mutations characterize small cell carcinoma of the ovary, hypercalcemic type in NATURE GENETICS
  • 2014-02 Serum levels of mature microRNAs in DICER1-mutated pleuropulmonary blastoma in ONCOGENESIS
  • 2013-12 Germ-line DICER1 mutations do not make a major contribution to the etiology of familial testicular germ cell tumours in BMC RESEARCH NOTES
  • 2012-01 Erratum to: The BRCA2 c.9004G>A (E3002K) variant is likely pathogenic and recurs in breast and/or ovarian cancer families of French Canadian descent in BREAST CANCER RESEARCH AND TREATMENT
  • 2012-01 The BRCA2 c.9004G>A (E2003K) variant is likely pathogenic and recurs in breast and/or ovarian cancer families of French Canadian descent in BREAST CANCER RESEARCH AND TREATMENT
  • 2011-12 A survey of APC mutations in Quebec in FAMILIAL CANCER
  • 2011-06 Mutation analysis of the PALB2 cancer predisposition gene in familial melanoma in FAMILIAL CANCER
  • 2010-12 Mutation analysis of the gene encoding the PALB2-binding protein MRG15 in BRCA1/2-negative breast cancer families in JOURNAL OF HUMAN GENETICS
  • 2010-08 RAD51C germline mutations in breast and ovarian cancer patients in BREAST CANCER RESEARCH
  • 2009-09 Analysis of the genes coding for the BRCA1-interacting proteins, RAP80 and Abraxas (CCDC98), in high-risk, non-BRCA1/2, multiethnic breast cancer cases in BREAST CANCER RESEARCH AND TREATMENT
  • 2008-12 Cancer incidence in relatives of British Fanconi Anaemia patients in BMC CANCER
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