Posters
Integrative Genomics and Multi-Omics in Noncystic Genetic Kidney Disease
October 22, 2026 | 10:00 AM - 12:00 PM
Location: Exhibit Hall A, Convention Center
Session Description
Poster Session
Posters
Multiancestry Genome-Wide Association Study Meta-Analysis Reveals Hundreds of Genetic Loci Related to Serum Calcium and Phosphate Levels
Genome-Wide Association Study of Diabetic Kidney Disease in Stroke Survivors
Genetic Landscape of Kidney Failure in a Korean Transplant Cohort: Genome-Wide Association and Multipolygenic Risk Score Analyses
Conditional Logistic Ancestry-Inclusive Regression Analysis (CLAIRA) Enables Ancestry-Inclusive Rare Disease Genome-Wide Association Study Using UK Biobank Controls
Linkage Analysis of Families with Mesoamerican Nephropathy Identifies BICC1 as a Potential Susceptibility Gene
Integrated Genomic Analyses Implicate GCC2 in Kidney Disease Susceptibility
Genetic Underpinning of Diabetic Kidney Disease
Whole-Genome Sequencing Identifies a Recessive Loss-of-Function Ret Variant Underlying Congenital Anomalies of the Kidney and Urinary Tract in an N-Ethyl-N-Nitrosourea (ENU)-Induced Mouse Line
Rapid Long-Read Sequencing in Thrombotic Microangiopathy to Triage Therapy in a Low-Resource Setting
Long-Read Genome Sequencing Improves Diagnostic Yield in Nephronophthisis and Steroid-Resistant Nephrotic Syndrome Cohorts
Proteomic Discovery of Urinary Myoglobin as a Noninvasive Biomarker for Chronic Benign Proteinuria Caused by CUBN Variants
Proteomic Analysis of FSGS Protein NOS1AP Identifies Mutation-Impaired PTPN14 Interaction That Modulates YAP1 Activity
Proteome-Wide Mendelian Randomization Nominates Complement and Adipocyte-Derived Mediators of Adiposity-Driven ESKD
Proximity Labeling Proteomics Identifies Epigenetic and Chromatin Regulatory Complexes Associated with WT1
Genetic Spectrum of Proteinuria-Associated Variants in Patients with Nephrotic Syndrome: A Large-Scale Targeted Sequencing Study
Single-Cell Multi-Omic Analysis for Building Cell-Type-Specific Gene-Enhancer Maps in the Kidneys
Cross-Tissue Multi-Omic Discovery of Biomarkers Associated with Kidney Function in a High-Risk Population
A Functional Promoter Connectivity Map of Human Kidney Cortex
Spatial Metabolomic Mapping of Fibrosis-Associated Metabolites in a Unilateral Ureteral Obstruction Mouse Model
Structure-Guided Prediction of SLC26A1 Variant Effects Prioritizes Functionally Impaired Alleles for Clinical Investigation
Heterozygous Variants in Autosomal Recessive Kidney Disease Genes Confer Clinically Relevant Kidney Phenotypes
Identification of 15 Independent Loci Associated with the Variance of eGFR in 359,677 Adults
A Broad Panel as the Perfect Complement: Unexpected Genetic Findings in Patients at Risk for Complement-Mediated Disease
Clinical and Genetic Characterization of an Autosomal Dominant Tubulointerstitial Kidney Disease Brazilian Cohort
Precision Nephrology in Practice: Genetic Testing in a Predominantly Hispanic/Latino Population
Evidence of Reduced Penetrance in Complement Gene-Positive Patients from a Large Renal Cohort
MRI Radiomics-Based Assessment of Mayo Imaging Classification (MIC) and Longitudinal Radiomic Changes in ADPKD
Defective Tubular Albumin Reabsorption in CUBN Variants Disrupts Tubuloglomerular Feedback and Promotes Hyperfiltration Injury
Megalin as a Mediator of Diet-Induced Kidney Injury and Urate Handling Dysfunction
MANF Clears Mutant Uromodulin in Human Kidney Organoids of Autosomal Dominant Tubulointerstitial Kidney Disease
Early Profibrotic Remodeling Precedes Functional Decline in Male Townes Mice with Sickle Cell Trait and Disease
Functional Kidney Disease Predominates in PTPN11-Associated Noonan Syndrome Identified Through Nephrology Practice
Molecular Dynamics Analysis for Intramolecular Autoinhibitory Interactions of INF2 Variants
Expanding the Spectrum of FOXI1-Related Distal Renal Tubular Acidosis
From Assumption to Precision with Genetic Testing
Transmembrane Emp24 Protein Transport Domain-Containing (TMED) Entrapment Complex Is a Therapeutic Node for Mucin 1 Kidney Disease and Other Proteinopathies
Sibling Cases of Isolated Asymptomatic Proteinuria Without Megaloblastic Anemia Caused by Novel Homozygous AMN Variants
Progressive Kidney Failure in 22q11.2 Duplication and SEMA3E Deletion: A Case Report
The Triple Hit: Mitochondrial Podocytopathy and Peritoneal Dialysis-Associated Type B Lactic Acidosis
Human Kidney Organoid Platform to Systematically Evaluate Adeno-Associated Virus Serotype Tropism and Podocyte Gene Delivery Efficiency
YOLT-203, an In Vivo Gene-Editing Therapy for Primary Hyperoxaluria Type 1: Interim Efficacy Results from Two Investigator-Initiated Trials