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Early onset prostate cancer has a significant genetic component

The Prostate, 2012-02, Vol.72 (2), p.147-156

2012

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Optimizing Hemodynamic Management in the Neonatal Intensive Care Unit: Leveraging Neonatal Echocardiography

Journal of cardiothoracic and vascular anesthesia, 2024-08, Vol.38 (8), p.1630-1633

2024

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Double‐blind, randomized crossover study of intravenous infusion of magnesium sulfate versus 5% dextrose on depressive symptoms in adults with treatment‐resistant depression

Psychiatry and clinical neurosciences, 2017-03, Vol.71 (3), p.204-211

2017

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Germline Mutations in HOXB13 and Prostate-Cancer Risk

The New England journal of medicine, 2012-01, Vol.366 (2), p.141-149

2012

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Developing a Real-Time Electroencephalogram-Guided Anesthesia-Management Curriculum for Educating Residents: A Single-Center Randomized Controlled Trial

Anesthesia and analgesia, 2022-01, Vol.134 (1), p.159-170

2022

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Common Variation in the BRCA1 Gene and Prostate Cancer Risk

Cancer epidemiology, biomarkers & prevention, 2007-07, Vol.16 (7), p.1510-1516

2007

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The experiences of socially vulnerable groups in England during the COVID-19 pandemic: A rapid health needs assessment

Public health in practice (Oxford, England), 2021-11, Vol.2, p.100192-100192, Article 100192

2021

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Association between Germline Variation in the FHIT Gene and Prostate Cancer in Caucasians and African Americans

Cancer epidemiology, biomarkers & prevention, 2007-06, Vol.16 (6), p.1294-1297

2007

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Chromosome 17q12 variants contribute to risk of early-onset prostate cancer

Cancer research (Chicago, Ill.), 2008-08, Vol.68 (16), p.6492-6495

2008

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Evidence for an association between prostate cancer and chromosome 8q24 and 10q11 genetic variants in African American men: The flint men's health study

The Prostate, 2011-02, Vol.71 (3), p.225-231

2011

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Hereditary prostate cancer as a feature of Lynch Syndrome

Familial cancer, 2011-03, Vol.10 (1), p.37-42

2011

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Analysis of the gene coding for the BRCA2-Interacting protein PALB2 in hereditary prostate cancer

The Prostate, 2008-05, Vol.68 (6), p.675-678

2008

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Sequence variation in the mitochondrial gene cytochrome c oxidase subunit I and prostate cancer in African American men

The Prostate, 2009-06, Vol.69 (9), p.956-960

2009

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Genome-wide linkage scan for prostate cancer susceptibility from the university of michigan prostate cancer genetics project: Suggestive evidence for linkage at 16q23

The Prostate, 2009-03, Vol.69 (4), p.385-391

2009

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Anti-cancer effects of aloe-emodin: a systematic review

Journal of clinical and translational research, 2018-01, Vol.3 (3), p.283-296

Lewis, John

2018

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Chromosome 8q24 markers: Risk of early‐onset and familial prostate cancer

International journal of cancer, 2008-06, Vol.122 (12), p.2876-2879

2008

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Sequence variation in α-methylacyl-CoA racemase and risk of early-onset and familial prostate cancer

The Prostate, 2007-10, Vol.67 (14), p.1507-1513

2007

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The effect of exercise training on disease progression, fitness, quality of life, and mental health in people living with HIV on antiretroviral therapy: a systematic review

Journal of clinical and translational research, 2015-12, Vol.1 (3), p.129-139

2015

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Genome-wide association of familial prostate cancer cases identifies evidence for a rare segregating haplotype at 8q24.21

Human genetics, 2016-08, Vol.135 (8), p.923-938

2016

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The experiences of socially vulnerable groups in England during the COVID-19 pandemic: A rapid health needs assessmentBox 1: Urgent actions

Public health in practice (Oxford, England), 2021-11, Vol.2, p.100192

2021

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Genetic variation in adiponectin ( ) and the type 1 receptor ( ), obesity and prostate cancer in African Americans

Prostate cancer and prostatic diseases, 2010-12, Vol.13 (4), p.362-368

2010

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Association analysis of 9,560 prostate cancer cases from the International Consortium of Prostate Cancer Genetics confirms the role of reported prostate cancer associated SNPs for familial disease

Human genetics, 2014-03, Vol.133 (3), p.347-356

2014

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Abstract 1642: Rare missense variants in MAP3K14 and ARHGAP27 in men with hereditary prostate cancer

Cancer research (Chicago, Ill.), 2012-04, Vol.72 (8_Supplement), p.1642-1642

2012

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Identification of a novel NBN truncating mutation in a family with hereditary prostate cancer

Familial cancer, 2012-12, Vol.11 (4), p.595-600

2012

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Validation of prostate cancer risk-related loci identified from genome-wide association studies using family-based association analysis: evidence from the International Consortium for Prostate Cancer Genetics (ICPCG)

Human genetics, 2012-07, Vol.131 (7), p.1095-1103

2012

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Early onset prostate cancer has a significant genetic component

Optimizing Hemodynamic Management in the Neonatal Intensive Care Unit: Leveraging Neonatal Echocardiography

Double‐blind, randomized crossover study of intravenous infusion of magnesium sulfate versus 5% dextrose on depressive symptoms in adults with treatment‐resistant depression

Germline Mutations in HOXB13 and Prostate-Cancer Risk

Developing a Real-Time Electroencephalogram-Guided Anesthesia-Management Curriculum for Educating Residents: A Single-Center Randomized Controlled Trial

Common Variation in the BRCA1 Gene and Prostate Cancer Risk

The experiences of socially vulnerable groups in England during the COVID-19 pandemic: A rapid health needs assessment

Association between Germline Variation in the FHIT Gene and Prostate Cancer in Caucasians and African Americans

Chromosome 17q12 variants contribute to risk of early-onset prostate cancer

Evidence for an association between prostate cancer and chromosome 8q24 and 10q11 genetic variants in African American men: The flint men's health study

Hereditary prostate cancer as a feature of Lynch Syndrome

Analysis of the gene coding for the BRCA2-Interacting protein PALB2 in hereditary prostate cancer

Sequence variation in the mitochondrial gene cytochrome c oxidase subunit I and prostate cancer in African American men

Genome-wide linkage scan for prostate cancer susceptibility from the university of michigan prostate cancer genetics project: Suggestive evidence for linkage at 16q23

Anti-cancer effects of aloe-emodin: a systematic review

Chromosome 8q24 markers: Risk of early‐onset and familial prostate cancer

Sequence variation in α-methylacyl-CoA racemase and risk of early-onset and familial prostate cancer

The effect of exercise training on disease progression, fitness, quality of life, and mental health in people living with HIV on antiretroviral therapy: a systematic review

Genome-wide association of familial prostate cancer cases identifies evidence for a rare segregating haplotype at 8q24.21

The experiences of socially vulnerable groups in England during the COVID-19 pandemic: A rapid health needs assessmentBox 1: Urgent actions

Genetic variation in adiponectin ( ) and the type 1 receptor ( ), obesity and prostate cancer in African Americans

Association analysis of 9,560 prostate cancer cases from the International Consortium of Prostate Cancer Genetics confirms the role of reported prostate cancer associated SNPs for familial disease

Abstract 1642: Rare missense variants in MAP3K14 and ARHGAP27 in men with hereditary prostate cancer

Identification of a novel NBN truncating mutation in a family with hereditary prostate cancer

Validation of prostate cancer risk-related loci identified from genome-wide association studies using family-based association analysis: evidence from the International Consortium for Prostate Cancer Genetics (ICPCG)

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