National Human Genome Research Institute

An Open-Label Phase 2 Study of N-Acetyl-D-Mannosamine (ManNAc) in Subjects With Podocyte Diseases

Phase 2Recruiting202630 people30 Oct 2024clinicaltrials.gov

NCT03952637

Phase 1/2Recruiting201954 people16 May 2019clinicaltrials.gov

NCT02428296

Phase 2Completed201539 people28 Apr 2015clinicaltrials.gov

NCT00975689

CollaboratorPhase 1/2Completed200935 people11 Sept 2009clinicaltrials.gov

NCT00467831

Phase 1/2Terminated20073 people1 May 2007clinicaltrials.gov

Mark Chaisson

R01Computational methods to discover, annotate, and genotype complex variation using long-read and biobank dataR01HG0116492021–203017 Sept 2026reporter.nih.gov

University of Southern California

R01Computational methods to discover, annotate, and genotype complex variation using long-read and biobank dataR01HG011649US$409.8k2021–203017 Sept 2026reporter.nih.gov

Mark Douglas Yandell

U01Empowering Interoperable Genomics-Enabled Learning Health Systems at ScaleU01HG0137842024–20294 Sept 2026reporter.nih.gov

Martin Tristani-firouzi

U01Empowering Interoperable Genomics-Enabled Learning Health Systems at ScaleU01HG0137842024–20294 Sept 2026reporter.nih.gov

Kensaku Kawamoto

U01Empowering Interoperable Genomics-Enabled Learning Health Systems at ScaleU01HG0137842024–20294 Sept 2026reporter.nih.gov

University of Utah

U01Empowering Interoperable Genomics-Enabled Learning Health Systems at ScaleU01HG013784US$636.8k2024–20294 Sept 2026reporter.nih.gov

Mylynda Massart

R01Leveraging a Card Study Methodology to Promote Integration of Genetics in Primary CareR01HG0151022026–20304 Sept 2026reporter.nih.gov

Charles Lee

R01Leveraging a Card Study Methodology to Promote Integration of Genetics in Primary CareR01HG0151022026–20304 Sept 2026reporter.nih.gov

University of Connecticut Sch of Med/dnt

R01Leveraging a Card Study Methodology to Promote Integration of Genetics in Primary CareR01HG015102US$849.3k2026–20304 Sept 2026reporter.nih.gov

Margarita Hernandez

K00Noventa Millas: Migration history, genomic ancestry, and health disparities among Cuban immigrants and Cuban-Americans in the United StatesK00HG0127112022–20273 Sept 2026reporter.nih.gov

Dartmouth College

K00Noventa Millas: Migration history, genomic ancestry, and health disparities among Cuban immigrants and Cuban-Americans in the United StatesK00HG012711US$105.9k2022–20273 Sept 2026reporter.nih.gov

Siyu He

K99Modeling Cell Fate and Perturbation Dynamics with Generative AI using Single-cell and Spatial Omics DataK99HG0151282026–20283 Sept 2026reporter.nih.gov

Stanford University

K99Modeling Cell Fate and Perturbation Dynamics with Generative AI using Single-cell and Spatial Omics DataK99HG015128US$146.8k2026–20283 Sept 2026reporter.nih.gov

Dan M Roden

U01Vanderbilt Genomic Learning Health System Clinical SiteU01HG0137762024–202921 Aug 2026reporter.nih.gov

Sunil Kripalani

U01Vanderbilt Genomic Learning Health System Clinical SiteU01HG0137762024–202921 Aug 2026reporter.nih.gov

Alexander Bick

U01Vanderbilt Genomic Learning Health System Clinical SiteU01HG0137762024–202921 Aug 2026reporter.nih.gov

Vanderbilt University Medical Center

U01Vanderbilt Genomic Learning Health System Clinical SiteU01HG013776US$711.3k2024–202921 Aug 2026reporter.nih.gov

Yusuph Mavura

K00Genetic and Environmental Determinants of Antihypertensive Response in a Real-World Longitudinal CohortK00HG0134372025–202818 Aug 2026reporter.nih.gov

Stanford University

K00Genetic and Environmental Determinants of Antihypertensive Response in a Real-World Longitudinal CohortK00HG013437US$104k2025–202818 Aug 2026reporter.nih.gov

Moran Snir

R42Closing the GAPS: Guideline Adherence, Prevention and Surveillance in Hereditary CancerR42HG0139082024–202718 Aug 2026reporter.nih.gov

Generalizability of proteomic risk prediction across biobanks reveals dependence on phenotype definitions

UG3HG0143792 Oct 2026api.crossref.org

Prevalence and significance of family history of kidney disease in the electronic health record in three United States health systems

R01HG01179928 Sept 2026api.crossref.org

Somatic mutations and single-nucleus transcriptomics reveal uniquely human properties of neuronal aging

R01HG01164124 Sept 2026api.crossref.org

Privacy-Preserving Distilled Large Language Models Enhance Multimorbidity Scoring

HG011052, HG011052-03S121 Sept 2026api.crossref.org

Blood-based emerging biomarkers in early detection and diagnosis of Alzheimer's disease

3 Feb 2026api.crossref.org