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Author Details

Peter J Hulick
Neaman Center for Personalized Medicine, NorthShore University HealthSystem
2000
65
28
PMIDPaper TitleJournal TitlePublished Year
36781323Association of Reported Candidate Monogenic Genes With Lung Cancer Risk.Clin Lung Cancer2023
37560999Utility of Polygenic Scores for Differentiating Diabetes Diagnosis Among Patients With Atypical Phenotypes of Diabetes.J Clin Endocrinol Metab2023
37334598Refining Risk for Alzheimer's Disease Among Heterozygous APOEÉ¿4 Carriers.J Alzheimers Dis2023
37419004Cancer-associated thrombosis by cancer sites and inherited factors in a prospective population-based cohort.Thromb Res2023
36781323Association of Reported Candidate Monogenic Genes With Lung Cancer Risk.Clin Lung Cancer2023
37560999Utility of Polygenic Scores for Differentiating Diabetes Diagnosis Among Patients With Atypical Phenotypes of Diabetes.J Clin Endocrinol Metab2023
37419004Cancer-associated thrombosis by cancer sites and inherited factors in a prospective population-based cohort.Thromb Res2023
37334598Refining Risk for Alzheimer's Disease Among Heterozygous APOEÉ¿4 Carriers.J Alzheimers Dis2023
33443076Calibration of polygenic risk scores is required prior to clinical implementation: results of three common cancers in UKB.J Med Genet2022
36353656Reliability of Ancestry-specific Prostate Cancer Genetic Risk Score in Four Racial and Ethnic Populations.Eur Urol Open Sci2022
35887642Effect Modification by Social Determinants of Pharmacogenetic Medication Interactions on 90-Day Hospital Readmissions within an Integrated U.S. Healthcare System.J Pers Med2022
36275420Reclassification of coronary artery disease risk using genetic risk score among subjects with borderline or intermediate clinical risk.Int J Cardiol Heart Vasc2022
33443076Calibration of polygenic risk scores is required prior to clinical implementation: results of three common cancers in UKB.J Med Genet2022
35347252Inherited risk assessment and its clinical utility for predicting prostate cancer from diagnostic prostate biopsies.Prostate Cancer Prostatic Dis2022
35347252Inherited risk assessment and its clinical utility for predicting prostate cancer from diagnostic prostate biopsies.Prostate Cancer Prostatic Dis2022
36275420Reclassification of coronary artery disease risk using genetic risk score among subjects with borderline or intermediate clinical risk.Int J Cardiol Heart Vasc2022
36353656Reliability of Ancestry-specific Prostate Cancer Genetic Risk Score in Four Racial and Ethnic Populations.Eur Urol Open Sci2022
35887642Effect Modification by Social Determinants of Pharmacogenetic Medication Interactions on 90-Day Hospital Readmissions within an Integrated U.S. Healthcare System.J Pers Med2022
33270363Flype: Software for enabling personalized medicine.Am J Med Genet C Semin Med Genet2021
33990587Author Correction: A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers.Nat Commun2021
34254341Observed evidence for guideline-recommended genes in predicting prostate cancer risk from a large population-based cohort.Prostate2021
34312282Implementing Primary Care Mediated Population Genetic Screening Within an Integrated Health System.J Am Board Fam Med2021
33596141Patient-Reported Outcomes and Experiences with Population Genetic Testing Offered Through a Primary Care Network.Genet Test Mol Biomarkers2021
33257031Performance of Three Inherited Risk Measures for Predicting Prostate Cancer Incidence and Mortality: A Population-based Prospective Analysis.Eur Urol2021
33300603Cystic fibrosis F508del carriers and cancer risk: Results from the UK Biobank.Int J Cancer2021
33270363Flype: Software for enabling personalized medicine.Am J Med Genet C Semin Med Genet2021
34404389Physician-directed genetic screening to evaluate personal risk for medically actionable disorders: a large multi-center cohort study.BMC Med2021
34732190Correction to: Physician-directed genetic screening to evaluate personal risk for medically actionable disorders: a large multi-center cohort study.BMC Med2021
34672204The integration of personalized medicine into health systems: progress and a path forward.Per Med2021
34945714The Contribution of Pharmacogenetic Drug Interactions to 90-Day Hospital Readmissions: Preliminary Results from a Real-World Healthcare System.J Pers Med2021
33596141Patient-Reported Outcomes and Experiences with Population Genetic Testing Offered Through a Primary Care Network.Genet Test Mol Biomarkers2021
34945714The Contribution of Pharmacogenetic Drug Interactions to 90-Day Hospital Readmissions: Preliminary Results from a Real-World Healthcare System.J Pers Med2021
34672204The integration of personalized medicine into health systems: progress and a path forward.Per Med2021
34732190Correction to: Physician-directed genetic screening to evaluate personal risk for medically actionable disorders: a large multi-center cohort study.BMC Med2021
34404389Physician-directed genetic screening to evaluate personal risk for medically actionable disorders: a large multi-center cohort study.BMC Med2021
33990587Author Correction: A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers.Nat Commun2021
34312282Implementing Primary Care Mediated Population Genetic Screening Within an Integrated Health System.J Am Board Fam Med2021
34254341Observed evidence for guideline-recommended genes in predicting prostate cancer risk from a large population-based cohort.Prostate2021
33257031Performance of Three Inherited Risk Measures for Predicting Prostate Cancer Incidence and Mortality: A Population-based Prospective Analysis.Eur Urol2021
33300603Cystic fibrosis F508del carriers and cancer risk: Results from the UK Biobank.Int J Cancer2021
32830201Germline HOXB13 G84E mutation carriers and risk to twenty common types of cancer: results from the UK Biobank.Br J Cancer2020
32020508Primary care physician experiences utilizing a family health history tool with electronic health record-integrated clinical decision support: an implementation process assessment.J Community Genet2020
31723001Association of Genomic Domains in <i>BRCA1</i> and <i>BRCA2</i> with Prostate Cancer Risk and Aggressiveness.Cancer Res2020
33066060Primary Care Physician Experiences with Integrated Population-Scale Genetic Testing: A Mixed-Methods Assessment.J Pers Med2020
32891193Mutations of the Transcriptional Corepressor ZMYM2 Cause Syndromic Urinary Tract Malformations.Am J Hum Genet2020
33409458Prevalence of Germline Pathogenic and Likely Pathogenic Variants in Patients With Second Breast Cancers.JNCI Cancer Spectr2020
32830201Germline HOXB13 G84E mutation carriers and risk to twenty common types of cancer: results from the UK Biobank.Br J Cancer2020
31723001Association of Genomic Domains in <i>BRCA1</i> and <i>BRCA2</i> with Prostate Cancer Risk and Aggressiveness.Cancer Res2020
32020508Primary care physician experiences utilizing a family health history tool with electronic health record-integrated clinical decision support: an implementation process assessment.J Community Genet2020
33066060Primary Care Physician Experiences with Integrated Population-Scale Genetic Testing: A Mixed-Methods Assessment.J Pers Med2020
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Co-authored papers 20
Irene L Andrulis
University of Toronto
Co-authored papers 20
Paolo Radice
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University of Cambridge
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Perelman School of Medicine, University of Pennsylvania, USA Abramson Cancer Center
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Judy E Garber
Dana-Farber Cancer Institute
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Familial Cancer Clinical Unit, Spanish National Cancer Research Centre
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Mary Beth Terry
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Pomeranian Medical University
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Amanda B Spurdle
QIMR Berghofer Medical Research Institute
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Jianfeng Xu
Co-authored papers 13
Jenny Lester
David Geffen School of Medicine, University of California at Los Angeles
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Rosalind A Eeles
The Institute of Cancer Research
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Siranoush Manoukian
Fondazione IRCCS Istituto Nazionale dei Tumori
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Ian G Campbell
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Jacek Gronwald
International Hereditary Cancer Center, Pomeranian Medical University
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Jenny Chang-Claude
German Cancer Research Center (DKFZ)
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Graham G Giles
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Susan J Ramus
School of Clinical Medicine, University of NSW Sydney, Lowy Cancer Research Centre
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Release 1.2