Josyf C. Mychaleckyj

University of Virginia — United States

Biochemistry, Genetics and Molecular Biology · Life Sciences

62h-index22.3kcitations281works2.62yr avg
OpenAlex↗ORCID↗Google Scholar↗Lab page↗

Accepting Students?

No reports yet. Know if this professor is taking students?

Research Topics

Genetic Associations and Epidemiology(71), Pancreatic function and diabetes(32), Diabetes and associated disorders(31), Epigenetics and DNA Methylation(26), Diabetes Treatment and Management(25)

Publications248 total

Cross-ancestry comparison of aptamer and antibody protein measures
Nature Communications·2026· 1 citedOpen Access
Figure S1 from Associations between Ambient Air Pollutants and Clonal Hematopoiesis of Indeterminate Potential
2025Open Access
Table S1 from Associations between Ambient Air Pollutants and Clonal Hematopoiesis of Indeterminate Potential
2025Open Access
Table S2 from Associations between Ambient Air Pollutants and Clonal Hematopoiesis of Indeterminate Potential
2025Open Access
Exome-Wide Analysis Identifies a Rare EXD3 Missense Variant Associated With Diabetic Kidney Disease
Kidney International Reports·2025Open Access
Genomic and phenotypic correlates of mosaic loss of chromosome Y in blood
UNC Libraries·2025Open Access
Genome-wide study investigating effector genes and polygenic prediction for kidney function in persons with ancestry from Africa and the Americas
UNC Libraries·2025Open Access
Mosaic chromosomal alterations in blood across ancestries using whole-genome sequencing
UNC Libraries·2025Open Access
Associations between Ambient Air Pollutants and Clonal Hematopoiesis of Indeterminate Potential.
UNC Libraries·2025Open Access
DNA Methylation and 28-Year Incidence of Kidney Disease in Type 1 Diabetes
Kidney360·2025Open Access
Associations of interstitial lung disease subtype and CT pattern with lung function and survival
Thorax·2025· 3 citedOpen Access
Creating and Integrating TelSeq Telomere Length Nomograms from Topmed for Survival Assessment in PFF-PR IPF Patients
American Journal of Respiratory and Critical Care Medicine·2025
Rare variants and survival of patients with idiopathic pulmonary fibrosis: analysis of a multicentre, observational cohort study with independent validation
The Lancet Respiratory Medicine·2025· 10 citedOpen Access
cellSTAAR: Incorporating single-cell-sequencing-based functional data to boost power in rare variant association testing of non-coding regions
2025· 2 citedOpen Access
DNA methylation and 28 year incidence of two neuropathy phenotypes in type 1 diabetes: the Pittsburgh Epidemiology of Diabetes Complications cohort study
Diabetologia·2025· 1 citedOpen Access
Alterations in DNA Methylation, Proteomic, and Metabolomic Profiles in African Ancestry Populations with APOL1 Risk Alleles
Journal of the American Society of Nephrology·2025Open Access
Cross-Ancestry Comparison of Aptamer and Antibody Proteomics Measures
2025· 1 citedOpen Access
Genomic and phenotypic correlates of mosaic loss of chromosome Y in blood
The American Journal of Human Genetics·2025· 6 citedOpen Access
Metabolomic profiles of infants classified as sudden infant death syndrome: a case-control analysis
EBioMedicine·2024· 3 citedOpen Access
X-chromosome and kidney function: evidence from a multi-trait genetic analysis of 908,697 individuals reveals sex-specific and sex-differential findings in genes regulated by androgen response elements
UNC Libraries·2024Open Access
page 1 of 13Next →

Frequent Co-authors

Stephen S. Rich(17), Ching‐Ti Liu(10), Jerome I. Rotter(10), Uma Nayak(10), Kurt Lohman(8), Bruce M. Psaty(8), Carl D. Langefeld(8), Donald W. Bowden(8), Michèle M. Sale(7), Kent D. Taylor(7), Eric Boerwinkle(7), Barry I. Freedman(7), Tamara B. Harris(6), Lisa R. Yanek(6), Ani Manichaikul(5), Wei‐Min Chen(5), M Kellis(5), David S. Siscovick(5), Yingchang Lu(5), Erwin P. Böttinger(5)