Skip to Main Content

Author Details

Adam S Gordon
Northwestern University Feinberg School of Medicine.
2008
46
19
PMIDPaper TitleJournal TitlePublished Year
36621880Returning integrated genomic risk and clinical recommendations: The eMERGE study.Genet Med2023
37790445Genetic Sex Validation for Sample Tracking in Clinical Testing.Res Sq2023
37883979Prospective, multi-site study of healthcare utilization after actionable monogenic findings from clinical sequencing.Am J Hum Genet2023
37347242ACMG SF v3.2 list for reporting of secondary findings in clinical exome and genome sequencing: A policy statement of the American College of Medical Genetics and Genomics (ACMG).Genet Med2023
34380996Genetic association of primary nonresponse to anti-TNFα therapy in patients with inflammatory bowel disease.Pharmacogenet Genomics2022
35802134ACMG SF v3.1 list for reporting of secondary findings in clinical exome and genome sequencing: A policy statement of the American College of Medical Genetics and Genomics (ACMG).Genet Med2022
36721401Anti-racist strategies for clinical and translational research: Design, implementation, and lessons learned from a new course.J Clin Transl Sci2022
36372681Quantifying the phenome-wide disease burden of obesity using electronic health records and genomics.Obesity (Silver Spring)2022
35915156Large-scale genome-wide association study of coronary artery disease in genetically diverse populations.Nat Med2022
35216901The reckoning: The return of genomic results to 1444 participants across the eMERGE3 Network.Genet Med2022
34906521Response to McGurk et al.Genet Med2022
34930020Arrhythmia Variant Associations and Reclassifications in the eMERGE-III Sequencing Study.Circulation2022
35322684Practitioners' Confidence and Desires for Education in Cardiovascular and Sudden Cardiac Death Genetics.J Am Heart Assoc2022
32964493Loci identified by a genome-wide association study of carotid artery stenosis in the eMERGE network.Genet Epidemiol2021
33850243Medical records-based chronic kidney disease phenotype for clinical care and "big data" observational and genetic studies.NPJ Digit Med2021
33848333Multiplexing mutation rate assessment: determining pathogenicity of Msh2 variants in Saccharomyces cerevisiae.Genetics2021
34377931Penetrance of Breast Cancer Susceptibility Genes From the eMERGE III Network.JNCI Cancer Spectr2021
34302027Quantitative disease risk scores from EHR with applications to clinical risk stratification and genetic studies.NPJ Digit Med2021
34345026Correction to: ACMG SF v3.0 list for reporting of secondary findings in clinical exome and genome sequencing: a policy statement of the American College of Medical Genetics and Genomics (ACMG).Genet Med2021
34151428Genome-Wide Approach to Measure Variant-Based Heritability of Drug Outcome Phenotypes.Clin Pharmacol Ther2021
34012069Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2021 update: a policy statement of the American College of Medical Genetics and Genomics (ACMG).Genet Med2021
34012068ACMG SF v3.0 list for reporting of secondary findings in clinical exome and genome sequencing: a policy statement of the American College of Medical Genetics and Genomics (ACMG).Genet Med2021
33977795Pleiotropy of systemic lupus erythematosus risk alleles and cardiometabolic disorders: A phenome-wide association study and inverse-variance weighted meta-analysis.Lupus2021
33951936Practice Patterns After Return of Rare Variants Associated With Cardiomyopathy in the Electronic Medical Records and Genomics Network.Circ Heart Fail2021
33407432Association between triglycerides, known risk SNVs and conserved rare variation in SLC25A40 in a multi-ancestry cohort.BMC Med Genomics2021
32307929Pleiotropy in the Genetic Predisposition to Rheumatoid Arthritis: A Phenome-Wide Association Study and Inverse Variance-Weighted Meta-Analysis.Arthritis Rheumatol2020
35047832Hemochromatosis risk genotype is not associated with colorectal cancer or age at its diagnosis.HGG Adv2020
30298529The eMERGE genotype set of 83,717 subjects imputed to ~40â¿¿million variants genome wide and association with the herpes zoster medical record phenotype.Genet Epidemiol2019
31422818Rates of Actionable Genetic Findings in Individuals with Colorectal Cancer or Polyps Ascertained from a Community Medical Setting.Am J Hum Genet2019
30988330Heritability and genome-wide association study of benign prostatic hyperplasia (BPH) in the eMERGE network.Sci Rep2019
30166544A study paradigm integrating prospective epidemiologic cohorts and electronic health records to identify disease biomarkers.Nat Commun2018
28502727Concordance between Research Sequencing and Clinical Pharmacogenetic Genotyping in the eMERGE-PGx Study.J Mol Diagn2017
26736087PGRNseq: a targeted capture sequencing panel for pharmacogenetic research and implementation.Pharmacogenet Genomics2016
28361098Building a family network from genetic testing.Mol Genet Genomic Med2016
26746457Association of Arrhythmia-Related Genetic Variants With Phenotypes Documented in Electronic Medical Records.JAMA2016
26857349Genetic variation among 82 pharmacogenes: The PGRNseq data from the eMERGE network.Clin Pharmacol Ther2016
25946405Variation in genes controlling warfarin disposition and response in American Indian and Alaska Native people: CYP2C9, VKORC1, CYP4F2, CYP4F11, GGCX.Pharmacogenet Genomics2015
26221186Prospective participant selection and ranking to maximize actionable pharmacogenetic variants and discovery in the eMERGE Network.Genome Med2015
24282029Quantifying rare, deleterious variation in 12 human cytochrome P450 drug-metabolism genes in a large-scale exome dataset.Hum Mol Genet2014
25087612Pathogenic variants for Mendelian and complex traits in exomes of 6,517 European and African Americans: implications for the return of incidental results.Am J Hum Genet2014
24960519Design and anticipated outcomes of the eMERGE-PGx project: a multicenter pilot for preemptive pharmacogenomics in electronic health record systems.Clin Pharmacol Ther2014
24616401Refining the structure and content of clinical genomic reports.Am J Med Genet C Semin Med Genet2014
24711634Rare coding variation in paraoxonase-1 is associated with ischemic stroke in the NHLBI Exome Sequencing Project.J Lipid Res2014
23778323Pharmacogenetics in American Indian populations: analysis of CYP2D6, CYP3A4, CYP3A5, and CYP2C9 in the Confederated Salish and Kootenai Tribes.Pharmacogenet Genomics2013
24013571Exome sequencing reveals novel rare variants in the ryanodine receptor and calcium channel genes in malignant hyperthermia families.Anesthesiology2013
18282109Adaptations to climate in candidate genes for common metabolic disorders.PLoS Genet2008
  • 1 - 46 of 46

Recommended Authors

Invitae Corporation
Career Start Year 2018
Number of shared co-authors 12
Stanford University
Career Start Year 2018
Number of shared co-authors 10
SD Sanford School of Medicine, University of South Dakota
Career Start Year 2016
Number of shared co-authors 4
Mayo Clinic
Career Start Year 2012
Number of shared co-authors 35
Invitae Corporation
Career Start Year 2012
Number of shared co-authors 6
Stanford Medicine Clinical Genomics Program
Career Start Year 2011
Number of shared co-authors 4
Vanderbilt University Medical Center
Career Start Year 2010
Number of shared co-authors 71
Broad Institute of MIT and Harvard
Career Start Year 2010
Number of shared co-authors 22
Corporal Michael J Crescenz VA Medical Center Philadelphia
Career Start Year 2010
Number of shared co-authors 60
Nationwide Children's Hospital, The Ohio State University College of Medicine
Career Start Year 2010
Number of shared co-authors 27
Regeneron Pharmaceuticals
Career Start Year 2008
Number of shared co-authors 29
Scripps Research Translational Institute, The Scripps Research Institute
Career Start Year 2008
Number of shared co-authors 3
Stanford University School of Medicine
Career Start Year 2008
Number of shared co-authors 29
Regeneron Pharmaceuticals, Inc.
Career Start Year 2007
Number of shared co-authors 33
Center for Inherited Disease Research, Johns Hopkins School of Medicine
Career Start Year 2007
Number of shared co-authors 17
Duke University
Career Start Year 2007
Number of shared co-authors 4
Icahn School of Medicine at Mount Sinai
Career Start Year 2005
Number of shared co-authors 6
Scripps Science Institute
Career Start Year 2005
Number of shared co-authors 18
Boston University School of Public Health
Career Start Year 2004
Number of shared co-authors 2
University of California San Diego Health System
Career Start Year 2004
Number of shared co-authors 22
National Human Genome Research Institute
Career Start Year 2004
Number of shared co-authors 41
Coriell Institute for Medical Research
Career Start Year 2003
Number of shared co-authors 2
Broad Institute of MIT and Harvard
Career Start Year 2001
Number of shared co-authors 70
University of Pennsylvania
Career Start Year 2001
Number of shared co-authors 86
National Human Genome Research Institute, National Institutes of Health
Career Start Year 2001
Number of shared co-authors 113
Neaman Center for Personalized Medicine, NorthShore University HealthSystem
Career Start Year 2000
Number of shared co-authors 20
Yale School of Medicine
Career Start Year 1999
Number of shared co-authors 39
University of North Carolina
Career Start Year 1999
Number of shared co-authors 53
Mayo Clinic
Career Start Year 1999
Number of shared co-authors 15
University of Washington
Career Start Year 1994
Number of shared co-authors 94

Collaborators

University of Washington Medical Center
Co-authored papers 27
University of Washington Medical Center
Co-authored papers 19
Mayo Clinic
Co-authored papers 17
University of Washington
Co-authored papers 16
Vanderbilt University
Co-authored papers 13
Vanderbilt University Medical Center
Co-authored papers 12
The Center for Applied Genomics, Children's Hospital of Philadelphia
Co-authored papers 12
Kaiser Permanente Washington Health Research Institute
Co-authored papers 11
Northwestern University, Center for Genetic Medicine
Co-authored papers 11
Center for Systems Genomics, Pennsylvania State University, University Park
Co-authored papers 11
Vanderbilt University Medical Center
Co-authored papers 10
Kaiser Permanente Washington
Co-authored papers 9
Kidney Research Institute and Division of Nephrology, University of Washington
Co-authored papers 9
Boston Children's Hospital, Harvard Medical School
Co-authored papers 9
Center for Genetic Medicine, Feinberg School of Medicine, Northwestern University
Co-authored papers 9
University of Washington
Co-authored papers 9
University of Washington.
Co-authored papers 9
University of Washington Medical Center
Co-authored papers 8
National Human Genome Research Institute
Co-authored papers 8
University of Washington Medical Center
Co-authored papers 8
Center for Applied Genomics, Children's Hospital of Philadelphia
Co-authored papers 8
Cincinnati Children's Hospital Medical Center
Co-authored papers 7
Illumina Inc.
Co-authored papers 7
Cincinnati Children's Hospital
Co-authored papers 7
Vanderbilt University Medical Center
Co-authored papers 6
Center for Genetic Medicine, Feinberg School of Medicine, Northwestern University
Co-authored papers 6
Boston Children's Hospital
Co-authored papers 6
Brown University, Brown University Warren Alpert Medical School, Dartmouth-Hitchcock Medical Center, Harvard School of Public Health, Johns Hopkins Medicine, Mayo Clinic Minnesota
Co-authored papers 6
University of Pennsylvania
Co-authored papers 6
Marshfield Clinic Research Institute
Co-authored papers 6