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IL-6 variant is associated with metastasis in breast cancer patients

PloS one, 2017-07, Vol.12 (7), p.e0181725-e0181725

2017

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The prevalence of BRCA1 mutations among young women with triple-negative breast cancer

BMC cancer, 2009-03, Vol.9 (1), p.86-86, Article 86

2009

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Large Germline Deletions of Mitochondrial Complex II Subunits SDHB and SDHD in Hereditary Paraganglioma

The journal of clinical endocrinology and metabolism, 2004-11, Vol.89 (11), p.5694-5699

2004

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Atypical choroidal nevus in a subject with a germline PALB2 pathogenic variant

Familial cancer, 2022-01, Vol.21 (1), p.1-5

2022

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KIAA0101 interacts with BRCA1 and regulates centrosome number

Molecular cancer research, 2011-08, Vol.9 (8), p.1091-1099

2011

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Aberrant expression of DNA damage response proteins is associated with breast cancer subtype and clinical features

Breast cancer research and treatment, 2011-09, Vol.129 (2), p.421-432

2011

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Low cancer incidence rates in Ohio Amish

Cancer causes & control, 2010-01, Vol.21 (1), p.69-75

2010

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Abstract P2-09-19: Inequitable access to genetic testing leads to missed screening and prevention opportunities for individuals at risk for hereditary breast and ovarian cancer

Cancer research (Chicago, Ill.), 2022-02, Vol.82 (4_Supplement), p.P2-P2-09-19

2022

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Fragile histidine triad protein, WW domain‐containing oxidoreductase protein Wwox, and activator protein 2γ expression levels correlate with basal phenotype in breast cancer

Cancer, 2009-02, Vol.115 (4), p.899-908

2009

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Significant upregulation of small heat shock protein αA-crystallin in retinal detachment

Experimental eye research, 2019-12, Vol.189, p.107811-107811, Article 107811

2019

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A large-scale assessment of two-way SNP interactions in breast cancer susceptibility using 46,450 cases and 42,461 controls from the breast cancer association consortium

Human molecular genetics, 2014-04, Vol.23 (7), p.1934-1946

2014

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Fragile histidine triad protein, WW domain-containing oxidoreductase protein Wwox, and activator protein 2gamma expression levels correlate with basal phenotype in breast cancer

Cancer, 2009-02, Vol.115 (4), p.899-908

2009

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Fhit, Wwox and AP2γ expression levels correlate with basal phenotype in breast cancer

Cancer, 2009-02, Vol.115 (4), p.899-908

2009

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Fragile Histidine Triad Protein, WW Domain-containing Oxidoreductase Protein Wwox, and Activator Protein 2y Expression Levels Correlate With Basal Phenotype in Breast Cancer

Cancer, 2009, Vol.115 (4), p.899-908

2009

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Hand-Reduction Malformations: Genetic and Syndromic Analysis

Journal of pediatric orthopaedics, 1985-05, Vol.5 (3), p.274-280

1985

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Developing a Role for Genetics within a Cancer Program

Annals of the New York Academy of Sciences, 1995-09, Vol.768 (1), p.258-258

1995

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Attenuated familial adenomatous polyposis in a man with an interstitial deletion of chromosome arm 5q

American journal of medical genetics, 1999-10, Vol.86 (4), p.321-324

1999

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Karsch-Neugebauer syndrome: split foot/split hand and congenital nystagmus

Clinical genetics, 1985-01, Vol.27 (1), p.97-101

1985

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PTEN Hamartoma Tumor Syndrome: A Clinical Overview

Cancers, 2019-06, Vol.11 (6), p.844

Pilarski, Robert

2019

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How Have Multigene Panels Changed the Clinical Practice of Genetic Counseling and Testing

Journal of the National Comprehensive Cancer Network, 2021-01, Vol.19 (1), p.103-108

Pilarski, Robert

2021

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Cowden Syndrome: A Critical Review of the Clinical Literature

Journal of genetic counseling, 2009-02, Vol.18 (1), p.13-27

Pilarski, Robert

2009

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Cowden Syndrome and the PTEN Hamartoma Tumor Syndrome: Systematic Review and Revised Diagnostic Criteria

JNCI : Journal of the National Cancer Institute, 2013-11, Vol.105 (21), p.1607-1616

2013

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Germline BAP1 mutation predisposes to uveal melanoma, lung adenocarcinoma, meningioma, and other cancers

Journal of medical genetics, 2011-12, Vol.48 (12), p.856-859

2011

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The Role of BRCA Testing in Hereditary Pancreatic and Prostate Cancer Families

American Society of Clinical Oncology educational book, 2019-05, Vol.39 (39), p.79-86

Pilarski, Robert

2019

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Predicting PTEN mutations: an evaluation of Cowden syndrome and Bannayan–Riley–Ruvalcaba syndrome clinical features

Journal of medical genetics, 2011-08, Vol.48 (8), p.505-512

2011

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IL-6 variant is associated with metastasis in breast cancer patients

The prevalence of BRCA1 mutations among young women with triple-negative breast cancer

Large Germline Deletions of Mitochondrial Complex II Subunits SDHB and SDHD in Hereditary Paraganglioma

Atypical choroidal nevus in a subject with a germline PALB2 pathogenic variant

KIAA0101 interacts with BRCA1 and regulates centrosome number

Aberrant expression of DNA damage response proteins is associated with breast cancer subtype and clinical features

Low cancer incidence rates in Ohio Amish

Abstract P2-09-19: Inequitable access to genetic testing leads to missed screening and prevention opportunities for individuals at risk for hereditary breast and ovarian cancer

Fragile histidine triad protein, WW domain‐containing oxidoreductase protein Wwox, and activator protein 2γ expression levels correlate with basal phenotype in breast cancer

Significant upregulation of small heat shock protein αA-crystallin in retinal detachment

A large-scale assessment of two-way SNP interactions in breast cancer susceptibility using 46,450 cases and 42,461 controls from the breast cancer association consortium

Fragile histidine triad protein, WW domain-containing oxidoreductase protein Wwox, and activator protein 2gamma expression levels correlate with basal phenotype in breast cancer

Fhit, Wwox and AP2γ expression levels correlate with basal phenotype in breast cancer

Fragile Histidine Triad Protein, WW Domain-containing Oxidoreductase Protein Wwox, and Activator Protein 2y Expression Levels Correlate With Basal Phenotype in Breast Cancer

Hand-Reduction Malformations: Genetic and Syndromic Analysis

Developing a Role for Genetics within a Cancer Program

Attenuated familial adenomatous polyposis in a man with an interstitial deletion of chromosome arm 5q

Karsch-Neugebauer syndrome: split foot/split hand and congenital nystagmus

PTEN Hamartoma Tumor Syndrome: A Clinical Overview

How Have Multigene Panels Changed the Clinical Practice of Genetic Counseling and Testing

Cowden Syndrome: A Critical Review of the Clinical Literature

Cowden Syndrome and the PTEN Hamartoma Tumor Syndrome: Systematic Review and Revised Diagnostic Criteria

Germline BAP1 mutation predisposes to uveal melanoma, lung adenocarcinoma, meningioma, and other cancers

The Role of BRCA Testing in Hereditary Pancreatic and Prostate Cancer Families

Predicting PTEN mutations: an evaluation of Cowden syndrome and Bannayan–Riley–Ruvalcaba syndrome clinical features

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