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Author Details

David R Crosslin
University of Washington Medical Center
2000
136
45
PMIDPaper TitleJournal TitlePublished Year
36302597Genomic Disorders in CKD across the Lifespan.J Am Soc Nephrol2023
36302597Genomic Disorders in CKD across the Lifespan.J Am Soc Nephrol2023
37898691Genetic variation in the human leukocyte antigen region confers susceptibility to Clostridioides difficile infection.Sci Rep2023
37968452Author Correction: Genetic variation in the human leukocyte antigen region confers susceptibility to Clostridioides difficile infection.Sci Rep2023
37783704Combining Asian and European genome-wide association studies of colorectal cancer improves risk prediction across racial and ethnic populations.Nat Commun2023
37559024Evaluating construct validity of computable acute respiratory distress syndrome definitions in adults hospitalized with COVID-19: an electronic health records based approach.BMC Pulm Med2023
36746961Author Correction: Genetic regulation of serum IgA levels and susceptibility to common immune, infectious, kidney, and cardio-metabolic traits.Nat Commun2023
36621880Returning integrated genomic risk and clinical recommendations: The eMERGE study.Genet Med2023
37181728A metadata framework for computational phenotypes.JAMIA Open2023
36789420Combining Asian-European Genome-Wide Association Studies of Colorectal Cancer Improves Risk Prediction Across Race and Ethnicity.medRxiv2023
37559024Evaluating construct validity of computable acute respiratory distress syndrome definitions in adults hospitalized with COVID-19: an electronic health records based approach.BMC Pulm Med2023
37898691Genetic variation in the human leukocyte antigen region confers susceptibility to Clostridioides difficile infection.Sci Rep2023
37783704Combining Asian and European genome-wide association studies of colorectal cancer improves risk prediction across racial and ethnic populations.Nat Commun2023
37968452Author Correction: Genetic variation in the human leukocyte antigen region confers susceptibility to Clostridioides difficile infection.Sci Rep2023
37181728A metadata framework for computational phenotypes.JAMIA Open2023
36789420Combining Asian-European Genome-Wide Association Studies of Colorectal Cancer Improves Risk Prediction Across Race and Ethnicity.medRxiv2023
36621880Returning integrated genomic risk and clinical recommendations: The eMERGE study.Genet Med2023
36746961Author Correction: Genetic regulation of serum IgA levels and susceptibility to common immune, infectious, kidney, and cardio-metabolic traits.Nat Commun2023
35216901The reckoning: The return of genomic results to 1444 participants across the eMERGE3 Network.Genet Med2022
36372681Quantifying the phenome-wide disease burden of obesity using electronic health records and genomics.Obesity (Silver Spring)2022
35710995Genome-wide polygenic score to predict chronic kidney disease across ancestries.Nat Med2022
35707062Lessons learned and recommendations for data coordination in collaborative research: The CSER consortium experience.HGG Adv2022
35701404Large-scale genomic analyses reveal insights into pleiotropy across circulatory system diseases and nervous system disorders.Nat Commun2022
35446370Association of Pathogenic Variants in Hereditary Cancer Genes With Multiple Diseases.JAMA Oncol2022
36600780Angiopoietin-Like4 Is a Novel Marker of COVID-19 Severity.Crit Care Explor2022
35216901The reckoning: The return of genomic results to 1444 participants across the eMERGE3 Network.Genet Med2022
35226188Uterine fibroid polygenic risk score (PRS) associates and predicts risk for uterine fibroid.Hum Genet2022
35710995Genome-wide polygenic score to predict chronic kidney disease across ancestries.Nat Med2022
35707062Lessons learned and recommendations for data coordination in collaborative research: The CSER consortium experience.HGG Adv2022
35701404Large-scale genomic analyses reveal insights into pleiotropy across circulatory system diseases and nervous system disorders.Nat Commun2022
35446370Association of Pathogenic Variants in Hereditary Cancer Genes With Multiple Diseases.JAMA Oncol2022
36600780Angiopoietin-Like4 Is a Novel Marker of COVID-19 Severity.Crit Care Explor2022
36372681Quantifying the phenome-wide disease burden of obesity using electronic health records and genomics.Obesity (Silver Spring)2022
35226188Uterine fibroid polygenic risk score (PRS) associates and predicts risk for uterine fibroid.Hum Genet2022
32952152Evaluation of the MC4R gene across eMERGE network identifies many unreported obesity-associated variants.Int J Obes (Lond)2021
33591484The FamilyTalk randomized controlled trial: patient-reported outcomes in clinical genetic sequencing for colorectal cancer.Cancer Causes Control2021
33850243Medical records-based chronic kidney disease phenotype for clinical care and "big data" observational and genetic studies.NPJ Digit Med2021
33951936Practice Patterns After Return of Rare Variants Associated With Cardiomyopathy in the Electronic Medical Records and Genomics Network.Circ Heart Fail2021
33729212Genome-wide association studies of low back pain and lumbar spinal disorders using electronic health record data identify a locus associated with lumbar spinal stenosis.Pain2021
33941608Medical Records-Based Genetic Studies of the Complement System.J Am Soc Nephrol2021
33667396Response to Li and Hopper.Am J Hum Genet2021
33455827What improves the likelihood of people receiving genetic test results communicating to their families about genetic risk?Patient Educ Couns2021
33930535Genomic considerations for FHIR®; eMERGE implementation lessons.J Biomed Inform2021
33597122Copy Number Variant Analysis and Genome-wide Association Study Identify Loci with Large Effect for Vesicoureteral Reflux.J Am Soc Nephrol2021
32579152Relationship between genetic knowledge and familial communication of CRC risk and intent to communicate CRCP genetic information: insights from FamilyTalk eMERGE III.Transl Behav Med2021
32964493Loci identified by a genome-wide association study of carotid artery stenosis in the eMERGE network.Genet Epidemiol2021
32952152Evaluation of the MC4R gene across eMERGE network identifies many unreported obesity-associated variants.Int J Obes (Lond)2021
33407432Association between triglycerides, known risk SNVs and conserved rare variation in SLC25A40 in a multi-ancestry cohort.BMC Med Genomics2021
34377931Penetrance of Breast Cancer Susceptibility Genes From the eMERGE III Network.JNCI Cancer Spectr2021
33850243Medical records-based chronic kidney disease phenotype for clinical care and "big data" observational and genetic studies.NPJ Digit Med2021
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Collaborators

Gail P Jarvik
University of Washington Medical Center
Co-authored papers 92
Joshua C Denny
Vanderbilt University
Co-authored papers 52
Eric B Larson
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Iftikhar J Kullo
Mayo Clinic
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Marylyn D Ritchie
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Hakon Hakonarson
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David S Carrell
Kaiser Permanente Washington Health Research Institute
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Dan M Roden
Vanderbilt University Medical Center
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Catherine A McCarty
University of Minnesota Medical School, 1035 University Drive duluth
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Ian B Stanaway
Kidney Research Institute and Division of Nephrology, University of Washington
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Marshfield Clinic Research Institute
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Laura J Rasmussen-Torvik
Northwestern University, Center for Genetic Medicine
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Adam S Gordon
Northwestern University Feinberg School of Medicine.
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Helena Kuivaniemi
Biomedical Research Institute, Stellenbosch University.
Co-authored papers 18
Shefali S Verma
University of Pennsylvania
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Elisabeth A Rosenthal
University of Washington Medical Center
Co-authored papers 18
Dana C Crawford
Cleveland Institute for Computational Biology, Case Western Reserve University
Co-authored papers 17
Marc S Williams
University of Washington Medical Center
Co-authored papers 17
John J Connolly
Center for Applied Genomics, Children's Hospital of Philadelphia
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Svati H Shah
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Lisa Bastarache
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Rex L Chisholm
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