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Author Details

William D Foulkes
Segal Cancer Centre, Jewish General Hospital
1962
679
105
PMIDPaper TitleJournal TitlePublished Year
38030749Risk-reducing mastectomy and breast cancer mortality in women with a BRCA1 or BRCA2 pathogenic variant: an international analysis.Br J Cancer2024
38030749Risk-reducing mastectomy and breast cancer mortality in women with a BRCA1 or BRCA2 pathogenic variant: an international analysis.Br J Cancer2024
37838650Surgical Decision Making in Genetically High-Risk Women: Quantifying Postoperative Complications and Long-Term Risks of Supplemental Surgery After Risk-Reducing Mastectomy.Ann Surg Oncol2024
37925057Dedifferentiated and Undifferentiated Ovarian Carcinoma: An Aggressive and Molecularly Distinct Ovarian Tumor Characterized by Frequent SWI/SNF Complex Inactivation.Mod Pathol2024
37973648Awareness and Candidacy for Endocrine Prevention and Risk Reducing Mastectomy in Unaffected High-Risk Women Referred for Breast Cancer Risk Assessment.Ann Surg Oncol2024
38050371Fetal Type Morphologies Suggest the Presence of DICER1 Hotspot Mutations in Non-small Cell Lung Cancer.Am J Surg Pathol2024
37957483Functional and phenotypic consequences of an unusual inversion in MSH2.Fam Cancer2024
37957483Functional and phenotypic consequences of an unusual inversion in MSH2.Fam Cancer2024
37838650Surgical Decision Making in Genetically High-Risk Women: Quantifying Postoperative Complications and Long-Term Risks of Supplemental Surgery After Risk-Reducing Mastectomy.Ann Surg Oncol2024
38050371Fetal Type Morphologies Suggest the Presence of DICER1 Hotspot Mutations in Non-small Cell Lung Cancer.Am J Surg Pathol2024
37973648Awareness and Candidacy for Endocrine Prevention and Risk Reducing Mastectomy in Unaffected High-Risk Women Referred for Breast Cancer Risk Assessment.Ann Surg Oncol2024
37925057Dedifferentiated and Undifferentiated Ovarian Carcinoma: An Aggressive and Molecularly Distinct Ovarian Tumor Characterized by Frequent SWI/SNF Complex Inactivation.Mod Pathol2024
35039446Long-term tumour dormancy in a <i>BRCA1</i> heterozygote.J Med Genet2023
36240479Genomic Microsatellite Signatures Identify Germline Mismatch Repair Deficiency and Risk of Cancer Onset.J Clin Oncol2023
38019076Physical Activity During Adolescence and Early-adulthood and Ovarian Cancer Among Women with a BRCA1 or BRCA2 Mutation.Cancer Res Commun2023
37638828A systematic review of the prevalence of pathogenic or likely pathogenic germline variants in individuals with FOXO1 fusion-positive rhabdomyosarcoma.Pediatr Blood Cancer2023
38084291Specifications of the ACMG/AMP Variant Classification Guidelines for Germline <i>DICER1</i> Variant Curation.Hum Mutat2023
37345679Unusual Aspects of Small Cell Carcinoma of the Ovary of Hypercalcaemic Type: Retained SMARCA4 Immunohistochemical Staining and Positive Staining With TLE1.Am J Surg Pathol2023
36969007Genetic analyses of DNA repair pathway associated genes implicate new candidate cancer predisposing genes in ancestrally defined ovarian cancer cases.Front Oncol2023
36833203Molecular Genetic Characteristics of <i>FANCI</i>, a Proposed New Ovarian Cancer Predisposing Gene.Genes (Basel)2023
36586540Constitutional Microsatellite Instability, Genotype, and Phenotype Correlations in Constitutional Mismatch Repair Deficiency.Gastroenterology2023
37210563Alanine supplementation exploits glutamine dependency induced by SMARCA4/2-loss.Nat Commun2023
37209596Germline EGFR c.2527G &gt; A (p.V843I) variant and familial lung cancer.Lung Cancer2023
36966138Genomic characterization of DICER1-associated neoplasms uncovers molecular classes.Nat Commun2023
36583307Well-differentiated Sertoli-Leydig Cell Tumors (SLCTs) Are Not Associated With DICER1 Pathogenic Variants and Represent a Different Tumor Type to Moderately and Poorly Differentiated SLCTs.Am J Surg Pathol2023
37333613DICER1 platform domain missense variants inhibit miRNA biogenesis and lead to tumor susceptibility.NAR Cancer2023
37460202Performance of the eHealth decision support tool, MIPOGG, for recognising children with Li-Fraumeni, DICER1, Constitutional mismatch repair deficiency and Gorlin syndromes.J Med Genet2023
37015678Moving breast cancer susceptibility gene testing into the mainstream.Med J Aust2023
36813544Germline pathogenic <i>SMARCA4</i> variants in neuroblastoma.J Med Genet2023
36571512The risks of cancer in older women with BRCA pathogenic variants: How far have we come?Cancer2023
36944611Author Correction: SMARCA4/2 loss inhibits chemotherapy-induced apoptosis by restricting IP3R3-mediated Ca<sup>2+</sup> flux to mitochondria.Nat Commun2023
37248399Reclassification of two germline DICER1 splicing variants leads to DICER1 syndrome diagnosis.Fam Cancer2023
36863945miRNA biogenesis and inherited disorders: clinico-molecular insights.Trends Genet2023
37114246Germline Platelet-derived growth factor receptor beta p.R987W pathogenic variant in 2 children with brain tumors.Neurooncol Adv2023
36786840SMARCA4-associated schwannomatosis.Acta Neuropathol2023
37490054Management of individuals with germline pathogenic/likely pathogenic variants in CHEK2: A clinical practice resource of the American College of Medical Genetics and Genomics (ACMG).Genet Med2023
35039446Long-term tumour dormancy in a <i>BRCA1</i> heterozygote.J Med Genet2023
38084291Specifications of the ACMG/AMP Variant Classification Guidelines for Germline <i>DICER1</i> Variant Curation.Hum Mutat2023
38019076Physical Activity During Adolescence and Early-adulthood and Ovarian Cancer Among Women with a BRCA1 or BRCA2 Mutation.Cancer Res Commun2023
37490054Management of individuals with germline pathogenic/likely pathogenic variants in CHEK2: A clinical practice resource of the American College of Medical Genetics and Genomics (ACMG).Genet Med2023
37638828A systematic review of the prevalence of pathogenic or likely pathogenic germline variants in individuals with FOXO1 fusion-positive rhabdomyosarcoma.Pediatr Blood Cancer2023
37460202Performance of the eHealth decision support tool, MIPOGG, for recognising children with Li-Fraumeni, DICER1, Constitutional mismatch repair deficiency and Gorlin syndromes.J Med Genet2023
37345679Unusual Aspects of Small Cell Carcinoma of the Ovary of Hypercalcaemic Type: Retained SMARCA4 Immunohistochemical Staining and Positive Staining With TLE1.Am J Surg Pathol2023
37248399Reclassification of two germline DICER1 splicing variants leads to DICER1 syndrome diagnosis.Fam Cancer2023
37015678Moving breast cancer susceptibility gene testing into the mainstream.Med J Aust2023
37210563Alanine supplementation exploits glutamine dependency induced by SMARCA4/2-loss.Nat Commun2023
37114246Germline Platelet-derived growth factor receptor beta p.R987W pathogenic variant in 2 children with brain tumors.Neurooncol Adv2023
36944611Author Correction: SMARCA4/2 loss inhibits chemotherapy-induced apoptosis by restricting IP3R3-mediated Ca<sup>2+</sup> flux to mitochondria.Nat Commun2023
37209596Germline EGFR c.2527G &gt; A (p.V843I) variant and familial lung cancer.Lung Cancer2023
37333613DICER1 platform domain missense variants inhibit miRNA biogenesis and lead to tumor susceptibility.NAR Cancer2023
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Collaborators

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Co-authored papers 41
David Geffen School of Medicine, University of California los angeles
Co-authored papers 35
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Co-authored papers 35
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University of Utah
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The Institute of Cancer Research
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National Cancer Institute
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University of Toronto.
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Duke University School of Medicine, and the Duke Cancer Institute
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University of British Columbia
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Institute of Biomedicine, University of Turku
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McGill University
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QIMR Berghofer Medical Research Institute
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Karolinska Institute
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