Author details

Full Name

Matthew Zawistowski

Affiliation

ORCID

Career Start Year

2010

Papers

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
37934784	Whole genome sequencing of 4,787 individuals identifies gene-based rare variants in age-related macular degeneration.	Hum Mol Genet	2024
37034792	The Mediating Role of Systemic Inflammation and Moderating Role of Race/Ethnicity in Racialized Disparities in Incident Dementia: A Decomposition Analysis.		2023
37607538	The phenotype-genotype reference map: Improving biobank data science through replication.	Am J Hum Genet	2023
37945903	Characterizing prostate cancer risk through multi-ancestry genome-wide discovery of 187 novel risk variants.	Nat Genet	2023
37662324	Clinical consequences of a polygenic predisposition to benign lower white blood cell counts: Consequences of benign WBC count genetics.	medRxiv	2023
37688361	A pilot genome-wide association study meta-analysis of gastroparesis.	United European Gastroenterol J	2023
37034649	Multi-ancestry genome-wide study in >2.5 million individuals reveals heterogeneity in mechanistic pathways of type 2 diabetes and complications.	medRxiv	2023
37323925	Decomposing interaction and mediating effects of race/ethnicity and circulating blood levels of cystatin C on cognitive status in the United States health and retirement study.	Front Hum Neurosci	2023
37188560	Cardiometabolic disease and obesity patterns differentially predict acute kidney injury after total joint replacement: a retrospective analysis.		2023
37066239	The Mediating Role of Systemic Inflammation and Moderating Role of Race/Ethnicity in Racialized Disparities in Incident Dementia: A Decomposition Analysis.		2023
37300819	Sex-specific DNA methylation in saliva from the multi-ethnic Future of Families and Child Wellbeing Study.		2023
37422323	Federal Food Program Participation and Beverage Intake Among Families With Low Household Income.		2023
34378841	A survey of functional dyspepsia in 361,360 individuals: Phenotypic and genetic cross-disease analyses.	Neurogastroenterol Motil	2022
36374587	Fibromuscular Dysplasia and Abdominal Aortic Aneurysms Are Dimorphic Sex-Specific Diseases With Shared Complex Genetic Architecture.	Circ Genom Precis Med	2022
36271344	Limited clinical utility for GWAS or polygenic risk score for postoperative acute kidney injury in non-cardiac surgery in European-ancestry patients.	BMC Nephrol	2022
35606478	Lack of association of CYP2B6 pharmacogenetics with cyclophosphamide toxicity in patients with cancer.	Support Care Cancer	2022
34916535	Author Correction: GWAS of thyroid stimulating hormone highlights the pleiotropic effects and inverse association with thyroid cancer.	Nat Commun	2021
33674754	Correction: Investigating rare pathogenic/likely pathogenic exonic variation in bipolar disorder.	Mol Psychiatry	2021
33888516	Genome-wide analysis of 944 133 individuals provides insights into the etiology of haemorrhoidal disease.	Gut	2021
34027909	Genome-Wide Association Study of Pelvic Organ Prolapse Using the Michigan Genomics Initiative.	Female Pelvic Med Reconstr Surg	2021
32938213	A Novel Recurrent <i>COL5A1</i> Genetic Variant Is Associated With a Dysplasia-Associated Arterial Disease Exhibiting Dissections and Fibromuscular Dysplasia.	Arterioscler Thromb Vasc Biol	2020
32341527	Genome-wide association meta-analyses combining multiple risk phenotypes provide insights into the genetic architecture of cutaneous melanoma susceptibility.	Nat Genet	2020
32887874	Chromosome 1q21.2 and additional loci influence risk of spontaneous coronary artery dissection and myocardial infarction.	Nat Commun	2020
32769997	GWAS of thyroid stimulating hormone highlights pleiotropic effects and inverse association with thyroid cancer.	Nat Commun	2020
33339817	Loss-of-function genomic variants highlight potential therapeutic targets for cardiovascular disease.	Nat Commun	2020
33175840	LabWAS: Novel findings and study design recommendations from a meta-analysis of clinical labs in two independent biobanks.	PLoS Genet	2020
31194742	Exploring various polygenic risk scores for skin cancer in the phenomes of the Michigan genomics initiative and the UK Biobank with a visual catalog: PRSWeb.	PLoS Genet	2019
30963077	Leveraging summary statistics to make inferences about complex phenotypes in large biobanks.	Pac Symp Biocomput	2019
31433078	Meta-MultiSKAT: Multiple phenotype meta-analysis for region-based association test.	Genet Epidemiol	2019
31015462	Sex-specific and pleiotropic effects underlying kidney function identified from GWAS meta-analysis.	Nat Commun	2019
29779563	Association of Polygenic Risk Scores for Multiple Cancers in a Phenome-wide Study: Results from The Michigan Genomics Initiative.	Am J Hum Genet	2018
30218074	Extremely rare variants reveal patterns of germline mutation rate heterogeneity in humans.	Nat Commun	2018
29279374	Evaluating the contribution of rare variants to type 2 diabetes and related traits using pedigrees.	Proc Natl Acad Sci U S A	2018
29728633	The psoriasis-protective TYK2 I684S variant impairs IL-12 stimulated pSTAT4 response in skin-homing CD4+ and CD8+ memory T-cells.	Scientific Reports	2018
27984508	Characterization of ADME gene variation in 21 populations by exome sequencing.	Pharmacogenet Genomics	2017
28501801	A rare coding allele in <i>IFIH1</i> is protective for psoriatic arthritis.	Ann Rheum Dis	2017
28763374	The Veterans Affairs Cardiac Risk Score: Recalibrating the Atherosclerotic Cardiovascular Disease Score for Applied Use.	Medical Care	2017
28537254	Large scale meta-analysis characterizes genetic architecture for common psoriasis associated variants.	Nat Commun	2017
28973304	Exome-wide association study reveals novel psoriasis susceptibility locus at TNFSF15 and rare protective alleles in genes contributing to type I IFN signalling.	Hum Mol Genet	2017
28245528	Corrected ROC analysis for misclassified binary outcomes.	Statistics in Medicine	2017
25740221	Methods for association analysis and meta-analysis of rare variants in families.	Genet Epidemiol	2015
24336170	Meta-analysis of gene-level tests for rare variant association.	Nat Genet	2014
24398795	Analysis of rare variant population structure in Europeans explains differential stratification of gene-based tests.	Eur J Hum Genet	2014
23526307	A geometric framework for evaluating rare variant tests of association.	Genet Epidemiol	2013
23990608	The influence of genomic context on mutation patterns in the human genome inferred from rare variants.	Genome Res	2013
22604722	An abundance of rare functional variants in 202 drug target genes sequenced in 14,002 people.	Science	2012
22595242	A coalescent model for genotype imputation.	Genetics	2012
21070896	Extending rare-variant testing strategies: analysis of noncoding sequence and imputed genotypes.	Am J Hum Genet	2010