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Author Details

Ian B Stanaway
Kidney Research Institute and Division of Nephrology, University of Washington
2006
57
20
PMIDPaper TitleJournal TitlePublished Year
37949747Identification of prognostic biomarkers for antibiotic associated nephrotoxicity in cystic fibrosis.J Cyst Fibros2024
36824881Genetic Predictors of Blood Pressure Traits are Associated with Preeclampsia.medRxiv2023
37248708Mitochondrial N-formyl methionine peptides contribute to exaggerated neutrophil activation in patients with COVID-19.Virulence2023
37011698A dynamic in vitro developing testis model reflects structures and functions of testicular development in vivo.Reprod Toxicol2023
37099286Association of Trauma Molecular Endotypes With Differential Response to Transfusion Resuscitation Strategies.JAMA Surg2023
36516690Alteration of oral microbiome composition in children living with pesticide-exposed farm workers.Int J Hyg Environ Health2023
36746961Author Correction: Genetic regulation of serum IgA levels and susceptibility to common immune, infectious, kidney, and cardio-metabolic traits.Nat Commun2023
35017169Angiopoietins as Prognostic Markers for Future Kidney Disease and Heart Failure Events after Acute Kidney Injury.J Am Soc Nephrol2022
35377938ABO O blood group as a risk factor for platelet reactivity in heparin-induced thrombocytopenia.Blood2022
35701404Large-scale genomic analyses reveal insights into pleiotropy across circulatory system diseases and nervous system disorders.Nat Commun2022
35594287Mendelian randomization analysis of plasma levels of CD209 and MICB proteins and the risk of varicose veins of lower extremities.PLoS One2022
35590255Psychiatric manifestations of rare variation in medically actionable genes: a PheWAS approach.BMC Genomics2022
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
35915156Large-scale genome-wide association study of coronary artery disease in genetically diverse populations.Nat Med2022
32952152Evaluation of the MC4R gene across eMERGE network identifies many unreported obesity-associated variants.Int J Obes (Lond)2021
33850243Medical records-based chronic kidney disease phenotype for clinical care and "big data" observational and genetic studies.NPJ Digit Med2021
33597122Copy Number Variant Analysis and Genome-wide Association Study Identify Loci with Large Effect for Vesicoureteral Reflux.J Am Soc Nephrol2021
33667396Response to Li and Hopper.Am J Hum Genet2021
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
34377931Penetrance of Breast Cancer Susceptibility Genes From the eMERGE III Network.JNCI Cancer Spectr2021
34536346Genomic and functional characterization of a mucosal symbiont involved in early-stage colorectal cancer.Cell Host Microbe2021
34767537Cross-validation of SARS-CoV-2 responses in kidney organoids and clinical populations.JCI Insight2021
33941608Medical Records-Based Genetic Studies of the Complement System.J Am Soc Nephrol2021
34341450The genetic architecture of plasma kynurenine includes cardiometabolic disease mechanisms associated with the SH2B3 gene.Sci Rep2021
34197840A genome-wide association study suggests correlations of common genetic variants with peritoneal solute transfer rates in patients with kidney failure receiving peritoneal dialysis.Kidney Int2021
33407432Association between triglycerides, known risk SNVs and conserved rare variation in SLC25A40 in a multi-ancestry cohort.BMC Med Genomics2021
32964493Loci identified by a genome-wide association study of carotid artery stenosis in the eMERGE network.Genet Epidemiol2021
32289280A genome-wide association study of polycystic ovary syndrome identified from electronic health records.Am J Obstet Gynecol2020
35047832Hemochromatosis risk genotype is not associated with colorectal cancer or age at its diagnosis.HGG Adv2020
31740287Anchoring a dynamic in vitro model of human neuronal differentiation to key processes of early brain development in vivo.Reprod Toxicol2020
32758450Genome-wide Modeling of Polygenic Risk Score in Colorectal Cancer Risk.Am J Hum Genet2020
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
31311600GWAS and enrichment analyses of non-alcoholic fatty liver disease identify new trait-associated genes and pathways across eMERGE Network.BMC Med2019
31422818Rates of Actionable Genetic Findings in Individuals with Colorectal Cancer or Polyps Ascertained from a Community Medical Setting.Am J Hum Genet2019
30864329Detecting potential pleiotropy across cardiovascular and neurological diseases using univariate, bivariate, and multivariate methods on 43,870 individuals from the eMERGE network.Pac Symp Biocomput2019
30890783Atlas-CNV: a validated approach to call single-exon CNVs in the eMERGESeq gene panel.Genet Med2019
30459343Unfolding of hidden white blood cell count phenotypes for gene discovery using latent class mixed modeling.Genes Immun2019
27956748Association of rare missense variants in the second intracellular loop of Na<sub>V</sub>1.7 sodium channels with familial autism.Mol Psychiatry2018
30092202An Atlas of Genetic Variation Linking Pathogen-Induced Cellular Traits to Human Disease.Cell Host Microbe2018
30267214Rare loss of function variants in candidate genes and risk of colorectal cancer.Hum Genet2018
28927471A vascular endothelial growth factor A genetic variant is associated with improved ventricular function and transplant-free survival after surgery for non-syndromic CHD.Cardiol Young2018
26704054Burden of potentially pathologic copy number variants is higher in children with isolated congenital heart disease and significantly impairs covariate-adjusted transplant-free survival.J Thorac Cardiovasc Surg2016
27836847Human Oral Buccal Microbiomes Are Associated with Farmworker Status and Azinphos-Methyl Agricultural Pesticide Exposure.Appl Environ Microbiol2016
27120335Genetic Candidate Variants in Two Multigenerational Families with Childhood Apraxia of Speech.PLoS One2016
24811984Patient genotypes impact survival after surgery for isolated congenital heart disease.Ann Thorac Surg2014
22495309Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations.Nature2012
23594493Identification of rare variants from exome sequence in a large pedigree with autism.Hum Hered2012
23160955Multiplex targeted sequencing identifies recurrently mutated genes in autism spectrum disorders.Science2012
23049896Results of genome-wide analyses on neurodevelopmental phenotypes at four-year follow-up following cardiac surgery in infancy.PLoS One2012
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Ning Shang
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Laura J Rasmussen-Torvik
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John B Harley
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Daniel J Schaid
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Shefali S Verma
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Krzysztof Kiryluk
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