- Genome-Wide Association Study of GFR Slope Decline in a Diverse Cohort from the Million Veteran Program
10:00 AM - 12:00 PM
Genome-Wide Association Study of GFR Slope Decline in a Diverse Cohort from the Million Veteran Program
October 25, 2024 | 10:00 AM - 12:00 PM
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- Genetic GLP1R Gene Expression and Kidney Disease Progression: A Mechanistic Proteome-Wide Analysis in the Million Veteran Program
10:00 AM - 12:00 PM
Genetic GLP1R Gene Expression and Kidney Disease Progression: A Mechanistic Proteome-Wide Analysis in the Million Veteran Program
October 25, 2024 | 10:00 AM - 12:00 PM
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- Canonical Correlation Analysis Identifies Single Nucleotide Polymorphisms and Gene Expression Associated with CKD Subtypes
10:00 AM - 12:00 PM
Canonical Correlation Analysis Identifies Single Nucleotide Polymorphisms and Gene Expression Associated with CKD Subtypes
October 25, 2024 | 10:00 AM - 12:00 PM
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- UMOD p.Thr62Pro Pathogenicity Is Modified by Polygenic CKD Risk
10:00 AM - 12:00 PM
UMOD p.Thr62Pro Pathogenicity Is Modified by Polygenic CKD Risk
October 25, 2024 | 10:00 AM - 12:00 PM
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- Individuals Heterozygous for SLC34A3 Predicted Pathogenic Variants Are at Increased Risk of Nephrolithiasis
10:00 AM - 12:00 PM
Individuals Heterozygous for SLC34A3 Predicted Pathogenic Variants Are at Increased Risk of Nephrolithiasis
October 25, 2024 | 10:00 AM - 12:00 PM
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- Predicted Pathogenic Missense Variants in CLDN10 Are Associated with CKD
10:00 AM - 12:00 PM
Predicted Pathogenic Missense Variants in CLDN10 Are Associated with CKD
October 25, 2024 | 10:00 AM - 12:00 PM
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- Association of Heterozygous CLDN10 Protein-Truncating Variants with CKD, Proteinuria, and Gout: Insights from the Geisinger MyCode/DiscovEHR Study
10:00 AM - 12:00 PM
Association of Heterozygous CLDN10 Protein-Truncating Variants with CKD, Proteinuria, and Gout: Insights from the Geisinger MyCode/DiscovEHR Study
October 25, 2024 | 10:00 AM - 12:00 PM
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- Phenome-Wide Association Study of APOL1 Risk Genotypes in the Mass General Brigham Biobank Using Data-Driven Disease Association Clustering
10:00 AM - 12:00 PM
Phenome-Wide Association Study of APOL1 Risk Genotypes in the Mass General Brigham Biobank Using Data-Driven Disease Association Clustering
October 25, 2024 | 10:00 AM - 12:00 PM
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- Kidney Outcomes in APOL1 High-Risk and Mendelian Variant in Patients with Adult Nephrotic Syndrome in Mass General Brigham Biobank
10:00 AM - 12:00 PM
Kidney Outcomes in APOL1 High-Risk and Mendelian Variant in Patients with Adult Nephrotic Syndrome in Mass General Brigham Biobank
October 25, 2024 | 10:00 AM - 12:00 PM
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- Challenges and Results of ClinGen Gene-Disease Clinical Validity Curation for Complement-Mediated Kidney Disease
10:00 AM - 12:00 PM
Challenges and Results of ClinGen Gene-Disease Clinical Validity Curation for Complement-Mediated Kidney Disease
October 25, 2024 | 10:00 AM - 12:00 PM
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- Genome-Wide Association Studies of Pediatric Nephrotic Syndrome Identify Variants Associated with Corticosteroid Response
10:00 AM - 12:00 PM
Genome-Wide Association Studies of Pediatric Nephrotic Syndrome Identify Variants Associated with Corticosteroid Response
October 25, 2024 | 10:00 AM - 12:00 PM
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- Genetic Causal Relationship and Risk Factors Associated with Type 2 Diabetes and CKD
10:00 AM - 12:00 PM
Genetic Causal Relationship and Risk Factors Associated with Type 2 Diabetes and CKD
October 25, 2024 | 10:00 AM - 12:00 PM
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- Multiancestry Genome-Wide Association Meta-Analyses of Kidney Function Traits: The CKDGen Consortium R5 Project
10:00 AM - 12:00 PM
Multiancestry Genome-Wide Association Meta-Analyses of Kidney Function Traits: The CKDGen Consortium R5 Project
October 25, 2024 | 10:00 AM - 12:00 PM
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- Insights into Kidney Protein Handling through a Genome-Wide Association Study (GWAS) of the Urine Proteome
10:00 AM - 12:00 PM
Insights into Kidney Protein Handling through a Genome-Wide Association Study (GWAS) of the Urine Proteome
October 25, 2024 | 10:00 AM - 12:00 PM
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- Causal Association between Plasma Oxalate and Kidney Disease: Mendelian Randomization Analysis
10:00 AM - 12:00 PM
Causal Association between Plasma Oxalate and Kidney Disease: Mendelian Randomization Analysis
October 25, 2024 | 10:00 AM - 12:00 PM
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- Building a Biobank for Genetic Studies on Primary and Recurrent Focal Segmental Glomerulosclerosis
10:00 AM - 12:00 PM
Building a Biobank for Genetic Studies on Primary and Recurrent Focal Segmental Glomerulosclerosis
October 25, 2024 | 10:00 AM - 12:00 PM
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- Importance of Copy Number Variant Analysis in Patients with Monogenic Kidney Diseases: Insights from 8 Years of Experience in an Expert Centre's Genome Diagnostic Laboratory
10:00 AM - 12:00 PM
Importance of Copy Number Variant Analysis in Patients with Monogenic Kidney Diseases: Insights from 8 Years of Experience in an Expert Centre's Genome Diagnostic Laboratory
October 25, 2024 | 10:00 AM - 12:00 PM
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- Results of Genetic Testing with a 385-Gene Panel in African American Patients with Kidney Diseases
10:00 AM - 12:00 PM
Results of Genetic Testing with a 385-Gene Panel in African American Patients with Kidney Diseases
October 25, 2024 | 10:00 AM - 12:00 PM
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- Exome Sequencing Reveals a Monogenic Cause of Kidney Disease in 34% of Pediatric Patients at a Single Saudi Arabian Center
10:00 AM - 12:00 PM
Exome Sequencing Reveals a Monogenic Cause of Kidney Disease in 34% of Pediatric Patients at a Single Saudi Arabian Center
October 25, 2024 | 10:00 AM - 12:00 PM
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- Genetic Testing in Biopsy-Confirmed Kidney Disease
10:00 AM - 12:00 PM
Genetic Testing in Biopsy-Confirmed Kidney Disease
October 25, 2024 | 10:00 AM - 12:00 PM
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- Genotype-Phenotype Correlations in Combined Kidney Histopathology and Genetic Testing on a 385-Gene Kidney Disease Panel
10:00 AM - 12:00 PM
Genotype-Phenotype Correlations in Combined Kidney Histopathology and Genetic Testing on a 385-Gene Kidney Disease Panel
October 25, 2024 | 10:00 AM - 12:00 PM
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- Utility of Genetic Testing in Patients with CKD of Uncertain Etiology: Results from an Underserved, Predominantly African American, Urban Population
10:00 AM - 12:00 PM
Utility of Genetic Testing in Patients with CKD of Uncertain Etiology: Results from an Underserved, Predominantly African American, Urban Population
October 25, 2024 | 10:00 AM - 12:00 PM
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- The RenaCARE Study: Updating Genetic Testing Results in Response to New Gene-Disease Association and Variant Upgrade
10:00 AM - 12:00 PM
The RenaCARE Study: Updating Genetic Testing Results in Response to New Gene-Disease Association and Variant Upgrade
October 25, 2024 | 10:00 AM - 12:00 PM
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- Fabry Disease Genetic Diagnosis in a Large CKD Population Tested with a Broad Kidney Gene Panel
10:00 AM - 12:00 PM
Fabry Disease Genetic Diagnosis in a Large CKD Population Tested with a Broad Kidney Gene Panel
October 25, 2024 | 10:00 AM - 12:00 PM
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- Importance of 3-Year-Old Urinalysis in Diagnosing Alport Syndrome
10:00 AM - 12:00 PM
Importance of 3-Year-Old Urinalysis in Diagnosing Alport Syndrome
October 25, 2024 | 10:00 AM - 12:00 PM
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- Familial Variability of Disease Progression in Autosomal Dominant Alport Syndrome: Results from SHRAS
10:00 AM - 12:00 PM
Familial Variability of Disease Progression in Autosomal Dominant Alport Syndrome: Results from SHRAS
October 25, 2024 | 10:00 AM - 12:00 PM
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- The ClinGen Alport Syndrome Variant Curation Expert Panel: Guiding Variant Classification in COL4A3, COL4A4, and COL4A5
10:00 AM - 12:00 PM
The ClinGen Alport Syndrome Variant Curation Expert Panel: Guiding Variant Classification in COL4A3, COL4A4, and COL4A5
October 25, 2024 | 10:00 AM - 12:00 PM
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- Increased Odds of Nephrotic Syndrome and ESKD in Fin-Major Heterozygotes
10:00 AM - 12:00 PM
Increased Odds of Nephrotic Syndrome and ESKD in Fin-Major Heterozygotes
October 25, 2024 | 10:00 AM - 12:00 PM
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- A Novel Pattern of Mutations in Northern Indian Children with Steroid-Resistant Nephrotic Syndrome
10:00 AM - 12:00 PM
A Novel Pattern of Mutations in Northern Indian Children with Steroid-Resistant Nephrotic Syndrome
October 25, 2024 | 10:00 AM - 12:00 PM
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- Population Frequency of Genetic Causes of Autosomal Dominant FSGS
10:00 AM - 12:00 PM
Population Frequency of Genetic Causes of Autosomal Dominant FSGS
October 25, 2024 | 10:00 AM - 12:00 PM
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- Population Frequency of Common Genetic Causes of Congenital Anomalies of the Kidney and Urinary Tract (CAKUT)
10:00 AM - 12:00 PM
Population Frequency of Common Genetic Causes of Congenital Anomalies of the Kidney and Urinary Tract (CAKUT)
October 25, 2024 | 10:00 AM - 12:00 PM
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- Genetic Landscape of Glomerular Diseases and FSGS among More than 50,000 People Genetically Tested for CKD
10:00 AM - 12:00 PM
Genetic Landscape of Glomerular Diseases and FSGS among More than 50,000 People Genetically Tested for CKD
October 25, 2024 | 10:00 AM - 12:00 PM
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- Diagnostic Yield and Clinical Utility of Genomic Testing in Patients with Suspected Genetic Kidney Disease: Singapore's First-Year Experience
10:00 AM - 12:00 PM
Diagnostic Yield and Clinical Utility of Genomic Testing in Patients with Suspected Genetic Kidney Disease: Singapore's First-Year Experience
October 25, 2024 | 10:00 AM - 12:00 PM
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- Trio Exome Sequencing Implicates Wnt Signaling in the Pathogenesis of Bladder-Exstrophy-Epispadias Complex
10:00 AM - 12:00 PM
Trio Exome Sequencing Implicates Wnt Signaling in the Pathogenesis of Bladder-Exstrophy-Epispadias Complex
October 25, 2024 | 10:00 AM - 12:00 PM
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- Systematic Screening of ADTKD-MUC1 27dupC Variant through Exome Sequencing
10:00 AM - 12:00 PM
Systematic Screening of ADTKD-MUC1 27dupC Variant through Exome Sequencing
October 25, 2024 | 10:00 AM - 12:00 PM
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- Autosomal Dominant Tubulointerstitial Kidney Diseases
10:00 AM - 12:00 PM
Autosomal Dominant Tubulointerstitial Kidney Diseases
October 25, 2024 | 10:00 AM - 12:00 PM
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- Assessment of Combined α-Galactosidase (α-GAL) Enzyme Activity and Lyso-GL3 for Fabry Disease Screening in Women
10:00 AM - 12:00 PM
Assessment of Combined α-Galactosidase (α-GAL) Enzyme Activity and Lyso-GL3 for Fabry Disease Screening in Women
October 25, 2024 | 10:00 AM - 12:00 PM
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- Screening for Fabry Disease in Haemodialysis Population (SoFAH) Study
10:00 AM - 12:00 PM
Screening for Fabry Disease in Haemodialysis Population (SoFAH) Study
October 25, 2024 | 10:00 AM - 12:00 PM
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- A Real-World Study on the Clinical Characteristics and Treatments of Complement-Mediated Kidney Diseases in China
10:00 AM - 12:00 PM
A Real-World Study on the Clinical Characteristics and Treatments of Complement-Mediated Kidney Diseases in China
October 25, 2024 | 10:00 AM - 12:00 PM
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- Rare Diseases: Significance of Molecular Genetic Analyses in Finding a Diagnosis
10:00 AM - 12:00 PM
Rare Diseases: Significance of Molecular Genetic Analyses in Finding a Diagnosis
October 25, 2024 | 10:00 AM - 12:00 PM
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- Pathogenic Mutations in Ras-MAPK Pathway Genes in Patients with Lupus Nephritis
10:00 AM - 12:00 PM
Pathogenic Mutations in Ras-MAPK Pathway Genes in Patients with Lupus Nephritis
October 25, 2024 | 10:00 AM - 12:00 PM
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- Genetic Analysis of Familial Mediterranean Fever in an ESKD Cohort
10:00 AM - 12:00 PM
Genetic Analysis of Familial Mediterranean Fever in an ESKD Cohort
October 25, 2024 | 10:00 AM - 12:00 PM
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- Exome Sequencing in Patients with Loin Pain Hematuria Syndrome
10:00 AM - 12:00 PM
Exome Sequencing in Patients with Loin Pain Hematuria Syndrome
October 25, 2024 | 10:00 AM - 12:00 PM
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- Founder Effect for the APOE Tokyo-Maebashi Variant in the Northern Chinese Population
10:00 AM - 12:00 PM
Founder Effect for the APOE Tokyo-Maebashi Variant in the Northern Chinese Population
October 25, 2024 | 10:00 AM - 12:00 PM
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