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Risk-Reducing Bilateral Salpingo-Oophorectomy for Ovarian Cancer: A Review and Clinical Guide for Hereditary Predisposition Genes

JCO oncology practice, 2022-03, Vol.18 (3), p.201-209

2022

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Genetics healthcare providers' experiences counseling patients with results from consumer genomic testing

Molecular genetics & genomic medicine, 2024-08, Vol.12 (8), p.e2508-n/a

2024

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The RAD51D c.82GA

Breast cancer research and treatment, 2021-02, Vol.185 (3), p.869

2021

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The RAD51D c.82GA variant disrupts normal splicing and is associated with hereditary ovarian cancer

Breast cancer research and treatment, 2021-02, Vol.185 (3), p.869

2021

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NBN Pathogenic Germline Variants are Associated with Pan-Cancer Susceptibility and In Vitro DNA Damage Response Defects

Clinical cancer research, 2023-01, Vol.29 (2), p.422-431

2023

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Uptake and acceptability of a mainstreaming model of hereditary cancer multigene panel testing among patients with ovarian, pancreatic, and prostate cancer

Genetics in medicine, 2021-11, Vol.23 (11), p.2105-2113

2021

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An updated counseling framework for moderate-penetrance colorectal cancer susceptibility genes

Genetics in medicine, 2022-12, Vol.24 (12), p.2587-2590

2022

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Factors associated with detection of hereditary diffuse gastric cancer on endoscopy in individuals with germline CDH1 mutations

Gastrointestinal endoscopy, 2023-09, Vol.98 (3), p.326-336.e3

2023

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The RAD51D c.82G>A (p.Val28Met) variant disrupts normal splicing and is associated with hereditary ovarian cancer

Breast cancer research and treatment, 2021-02, Vol.185 (3), p.869-877

2021

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ATM Germline-Mutated Gastroesophageal Junction Adenocarcinomas: Clinical Descriptors, Molecular Characteristics, and Potential Therapeutic Implications

JNCI : Journal of the National Cancer Institute, 2022-05, Vol.114 (5), p.761-770

2022

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A synonymous germline variant PALB2 c.18GT disrupts normal splicing in a family with pancreatic and breast cancers

Breast cancer research and treatment, 2019-01, Vol.173 (1), p.79

2019

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A synonymous germline variant PALB2 c.18GT

Breast cancer research and treatment, 2019-01, Vol.173 (1), p.79

2019

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Comprehensive analysis of germline drivers in endometrial cancer

JNCI : Journal of the National Cancer Institute, 2023-05, Vol.115 (5), p.560-569

2023

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Gastric-type adenocarcinoma of the cervix in patients with Peutz-Jeghers syndrome: a systematic review of the literature with proposed screening guidelines

International journal of gynecological cancer, 2022-01, Vol.32 (1), p.79-88

2022

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Early age of onset and broad cancer spectrum persist in MSH6- and PMS2-associated Lynch syndrome

Genetics in medicine, 2022-06, Vol.24 (6), p.1187-1195

2022

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Outcomes of incidentally detected ovarian cancers diagnosed at time of risk-reducing salpingo-oophorectomy in BRCA mutation carriers

Gynecologic oncology, 2021-05, Vol.161 (2), p.521-526

2021

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Early age of onset and broad cancer spectrum persist in MSH6 and PMS2 -associated Lynch syndrome

Journal of clinical oncology, 2021-05, Vol.39 (15_suppl), p.10516-10516

2021

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O017/#479 Germline pathogenic variants in DNA repair genes and endometrial cancer risk

International journal of gynecological cancer, 2022-12, Vol.32 (Suppl 3), p.A10-A11

2022

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Prevalence and clinical characterization of MMR-D/MSI extra-colonic cancers among germline PMS2 mutation carriers

Journal of clinical oncology, 2020-05, Vol.38 (15_suppl), p.1527-1527

2020

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A synonymous germline variant PALB2 c.18G>T (p.Gly6=) disrupts normal splicing in a family with pancreatic and breast cancers

Breast cancer research and treatment, 2019-01, Vol.173 (1), p.79-86

2019

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Consideration of a Novel Surgical Approach in the Management of Gastric Adenocarcinoma and Proximal Polyposis Syndrome

JCO precision oncology, 2024-06, Vol.8 (8), p.e2400175

2024

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Abstract B042: Clinical and molecular characterization of Lynch syndrome-associated pancreas adenocarcinoma (PDAC)

Cancer research (Chicago, Ill.), 2024-01, Vol.84 (2_Supplement), p.B042-B042

2024

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Risk-Reducing Bilateral Salpingo-Oophorectomy for Ovarian Cancer: A Review and Clinical Guide for Hereditary Predisposition Genes

Genetics healthcare providers' experiences counseling patients with results from consumer genomic testing

The RAD51D c.82GA

The RAD51D c.82GA variant disrupts normal splicing and is associated with hereditary ovarian cancer

NBN Pathogenic Germline Variants are Associated with Pan-Cancer Susceptibility and In Vitro DNA Damage Response Defects

Uptake and acceptability of a mainstreaming model of hereditary cancer multigene panel testing among patients with ovarian, pancreatic, and prostate cancer

An updated counseling framework for moderate-penetrance colorectal cancer susceptibility genes

Factors associated with detection of hereditary diffuse gastric cancer on endoscopy in individuals with germline CDH1 mutations

The RAD51D c.82G>A (p.Val28Met) variant disrupts normal splicing and is associated with hereditary ovarian cancer

ATM Germline-Mutated Gastroesophageal Junction Adenocarcinomas: Clinical Descriptors, Molecular Characteristics, and Potential Therapeutic Implications

A synonymous germline variant PALB2 c.18GT disrupts normal splicing in a family with pancreatic and breast cancers

A synonymous germline variant PALB2 c.18GT

Pathogenic germline variants in patients with endometrial cancer of diverse ancestry

Comprehensive analysis of germline drivers in endometrial cancer

Gastric-type adenocarcinoma of the cervix in patients with Peutz-Jeghers syndrome: a systematic review of the literature with proposed screening guidelines

Early age of onset and broad cancer spectrum persist in MSH6- and PMS2-associated Lynch syndrome

Outcomes of incidentally detected ovarian cancers diagnosed at time of risk-reducing salpingo-oophorectomy in BRCA mutation carriers

Early age of onset and broad cancer spectrum persist in MSH6 and PMS2 -associated Lynch syndrome

O017/#479 Germline pathogenic variants in DNA repair genes and endometrial cancer risk

Prevalence and clinical characterization of MMR-D/MSI extra-colonic cancers among germline PMS2 mutation carriers

A synonymous germline variant PALB2 c.18G>T (p.Gly6=) disrupts normal splicing in a family with pancreatic and breast cancers

Consideration of a Novel Surgical Approach in the Management of Gastric Adenocarcinoma and Proximal Polyposis Syndrome

Abstract B042: Clinical and molecular characterization of Lynch syndrome-associated pancreas adenocarcinoma (PDAC)

Prevalence and Clinical Implications of Mismatch Repair-Proficient Colorectal Cancer in Patients With Lynch Syndrome

Prevalence and Characterization of Biallelic and Monoallelic NTHL1 and MSH3 Variant Carriers From a Pan-Cancer Patient Population

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