Publications
52
Citations
7,168
Est. group size
~1
Recurring co-author estimate
Active years
16
Publishing since 2010
Typically publishes in teams of ~12 · 13% small-team papers (≤3 authors) · across 10 venues
- Contribution of genetic variants to nephrolithiasis
Kidney International · 2025
- Genome-Wide Association Study (GWAS) of Serum Galactose-Deficient IgA1 Uncovers Shared Genetic Determinants with IgAN
Journal of the American Society of Nephrology · 2025
- #1899 Cardiorenal outcomes and long-term kidney function decline in IgA nephropathy compared with chronic kidney disease patients with and without diabetes—FinnGen study
Nephrology Dialysis Transplantation · 2025
- Genetic screens of imaging-derived kidney volumes identify genes linked to kidney function
Kidney International · 2025
- WCN25-318 FELZARTAMAB DURABLY REDUCES DISEASE RELEVANT BIOMARKERS THROUGH TARGETING OF CD38+ PLASMA CELLS AND PLASMABLASTS, THE UPSTREAM DRIVERS OF IgA NEPHROPATHY (IgAN)
Kidney International Reports · 2025
- From GWAS to Translational Insights: Comprehensive Genetic Analysis of Nephrotic Syndrome from Multiple Populations
Research Square · 2025
- Advancing Genetic Testing in Kidney Diseases: Report From a National Kidney Foundation Working Group
American Journal of Kidney Diseases · 2024
- Bridging the Gap in Genomic Implementation: Identifying User Needs for Precision Nephrology
Kidney International Reports · 2024
- Cross‐Phenotype Genome‐Wide Association Study on the Shared Genetic Susceptibility to Systemic Sclerosis and Primary Biliary Cholangitis
Arthritis & Rheumatology · 2024
- Noninvasive Diagnostic Strategies for Membranous Nephropathy in the NEPTUNE Study
Journal of the American Society of Nephrology · 2024
- Felzartamab Durably Reduces Disease-Relevant Biomarkers through Targeting of CD38+ Plasma Cells and Plasmablasts, the Upstream Drivers of IgAN
Journal of the American Society of Nephrology · 2024
- Cross-Phenotype GWAS Supports Shared Genetic Susceptibility to Systemic Sclerosis and Primary Biliary Cholangitis
medRxiv · 2024
- Exome-wide analysis of congenital kidney anomalies reveals new genes and shared architecture with developmental disorders
medRxiv · 2024
- PheW2P2V: a phenome-wide prediction framework with weighted patient representations using electronic health records
JAMIA Open · 2024
- Value of Genetic Testing in a Glomerular Disease Center
Journal of the American Society of Nephrology · 2024
- Journal of the American Society of Nephrology×22
- medRxiv×7
- Kidney International Reports×3
- Kidney International×3
- bioRxiv (Cold Spring Harbor Laboratory)×2
- Felix Eichinger
Medicine · University of Michigan
- Damian Fermin
Medicine · University of Michigan
- Chrysta Lienczewski
Medicine · University of Michigan
- Christopher L. O’Connor
Medicine · University of Michigan
- Jamal El Saghir
Medicine · University of Michigan
This profile was generated automatically from public scholarly data (OpenAlex). Group size and activity levels are estimates derived from co-authorship patterns.
Last updated Jul 25, 2026.
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