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| 36920755 | Inaxaplin for Proteinuric Kidney Disease in Persons with Two <i>APOL1</i> Variants. | N Engl J Med | 2023 |
| 36449077 | Apolipoprotein L1 (APOL1) cation current in HEK-293 cells and in human podocytes. | Pflugers Arch | 2023 |
| 38036523 | Strong protective effect of the APOL1 p.N264K variant against G2-associated focal segmental glomerulosclerosis and kidney disease. | Nat Commun | 2023 |
| 37873196 | Exome copy number variant detection, analysis and classification in a large cohort of families with undiagnosed rare genetic disease. | medRxiv | 2023 |
| 37120605 | Multi-population genome-wide association study implicates immune and non-immune factors in pediatric steroid-sensitive nephrotic syndrome. | Nat Commun | 2023 |
| 37113494 | APOL1 and APOL1-Associated Kidney Disease: A Common Disease, an Unusual Disease Gene - Proceedings of the Henry Shavelle Professorship. | | 2023 |
| 34541902 | Bioengineering Strategies to Develop Podocyte Culture Systems. | Tissue Engineering - Part B: Reviews | 2022 |
| 36282916 | ADAR regulates APOL1 via A-to-I RNA editing by inhibition of MDA5 activation in a paradoxical biological circuit. | Proc Natl Acad Sci U S A | 2022 |
| 36144007 | Disease Modeling with Kidney Organoids. | Micromachines | 2022 |
| 35489216 | Apolipoprotein L1 Opinions of African American Living Kidney Donors, Kidney Transplant Patients, and Nonpatients. | Journal of Surgical Research | 2022 |
| 36137753 | Nephrotic Syndrome Gene Is Required for Endosomal Maturation and Nephrin Endocytosis in . | Journal of the American Society of Nephrology : JASN | 2022 |
| 36506246 | Clinical and Pathological Heterogeneity in FSGS due to Mutations. | | 2022 |
| 34929253 | A glomerular transcriptomic landscape of apolipoprotein L1 in Black patients with focal segmental glomerulosclerosis. | Kidney Int | 2022 |
| 35244702 | Effects of Testing and Disclosing Ancestry-Specific Genetic Risk for Kidney Failure on Patients and Health Care Professionals: A Randomized Clinical Trial. | JAMA Netw Open | 2022 |
| 35232775 | DGAT2 Inhibition Potentiates Lipid Droplet Formation To Reduce Cytotoxicity in APOL1 Kidney Risk Variants. | J Am Soc Nephrol | 2022 |
| 34766590 | APOL1 renal risk variants are associated with obesity and body composition in African ancestry adults: An observational genotype-phenotype association study. | Medicine (Baltimore) | 2021 |
| 33784256 | Aberrantly glycosylated IgG elicits pathogenic signaling in podocytes and signifies lupus nephritis. | JCI Insight | 2021 |
| 33508234 | De novo TRIM8 variants impair its protein localization to nuclear bodies and cause developmental delay, epilepsy, and focal segmental glomerulosclerosis. | Am J Hum Genet | 2021 |
| 33443052 | Dysregulated Dynein-Mediated Trafficking of Nephrin Causes INF2-related Podocytopathy. | Journal of the American Society of Nephrology : JASN | 2021 |
| 34350953 | Recessive, gain-of-function toxicity in an APOL1 BAC transgenic mouse model mirrors human APOL1 kidney disease. | Dis Model Mech | 2021 |
| 33863784 | A Rare Autosomal Dominant Variant in Regulator of Calcineurin Type 1 (<i>RCAN1</i>) Gene Confers Enhanced Calcineurin Activity and May Cause FSGS. | J Am Soc Nephrol | 2021 |
| 33350326 | Mutations in do Not Confer a Dominant Phenotype Manifesting as Kidney Stone Disease. | Journal of Urology | 2021 |
| 32616495 | APOL1 Nephropathy: From Genetics to Clinical Applications. | Clinical journal of the American Society of Nephrology : CJASN | 2021 |
| 32659871 | Opinions of African American adults about the use of apolipoprotein L1 (ApoL1) genetic testing in living kidney donation and transplantation. | American Journal of Transplantation | 2021 |
| 32675303 | Kidney Disease-Associated Variants Have Dose-Dependent, Dominant Toxic Gain-of-Function. | Journal of the American Society of Nephrology : JASN | 2020 |
| 31992573 | The Genetic Architecture of Kidney Disease. | Clinical journal of the American Society of Nephrology : CJASN | 2020 |
| 31710572 | and Kidney Disease: From Genetics to Biology. | Annual Review of Physiology | 2020 |
| 31924668 | FSGS-Causing INF2 Mutation Impairs Cleaved INF2 N-Fragment Functions in Podocytes. | J Am Soc Nephrol | 2020 |
| 32274456 | Autosomal Dominant Tubulointerstitial Kidney Disease-Uromodulin Misclassified as Focal Segmental Glomerulosclerosis or Hereditary Glomerular Disease. | Kidney International Reports | 2020 |
| 32540856 | Phosphorylation of ACTN4 Leads to Podocyte Vulnerability and Proteinuric Glomerulosclerosis. | J Am Soc Nephrol | 2020 |
| 32958645 | Circulating testican-2 is a podocyte-derived marker of kidney health. | Proc Natl Acad Sci U S A | 2020 |
| 31408864 | Autosomal Recessive Alport Syndrome Unveiled by Pregnancy. | Nephron | 2019 |
| 31580460 | APOL1 gene variants and kidney disease in whites: the cardiovascular health study. | Nephrol Dial Transplant | 2019 |
| 31993563 | Genome-wide Association Study of 24-Hour Urinary Excretion of Calcium, Magnesium, and Uric Acid. | Mayo Clin Proc Innov Qual Outcomes | 2019 |
| 31664084 | Focal segmental glomerulosclerosis ACTN4 mutants binding to actin: regulation by phosphomimetic mutations. | Sci Rep | 2019 |
| 31558683 | APOL1 Kidney Risk Variants Induce Cell Death <i>via</i> Mitochondrial Translocation and Opening of the Mitochondrial Permeability Transition Pore. | J Am Soc Nephrol | 2019 |
| 31611067 | Apolipoprotein L1 (APOL1) risk variant toxicity depends on the haplotype background. | Kidney Int | 2019 |
| 30733285 | Recruitment of APOL1 kidney disease risk variants to lipid droplets attenuates cell toxicity. | Proc Natl Acad Sci U S A | 2019 |
| 31317114 | APOL1-Associated Kidney Disease in Brazil. | Kidney International Reports | 2019 |
| 31308072 | Contributions of Rare Gene Variants to Familial and Sporadic FSGS. | J Am Soc Nephrol | 2019 |
| 29363327 | Mechanical challenges and cytoskeletal impairments in focal segmental glomerulosclerosis. | Am J Physiol Renal Physiol | 2018 |
| 28339911 | A null variant in the apolipoprotein L3 gene is associated with non-diabetic nephropathy. | Nephrol Dial Transplant | 2018 |
| 30596165 | The Glomerular Disease Study and Trial Consortium: A Grassroots Initiative to Foster Collaboration and Innovation. | Kidney Int Rep | 2018 |
| 29971324 | Association of APOL1 With Heart Failure With Preserved Ejection Fraction in Postmenopausal African American Women. | JAMA Cardiol | 2018 |
| 30189357 | Guided tissue organization and disease modeling in a kidney tubule array. | Biomaterials | 2018 |
| 29531077 | <i>UBD</i> modifies <i>APOL1</i>-induced kidney disease risk. | Proc Natl Acad Sci U S A | 2018 |
| 29618612 | Interrelated role of Klotho and calcium-sensing receptor in parathyroid hormone synthesis and parathyroid hyperplasia. | Proceedings of the National Academy of Sciences of the United States of America | 2018 |
| 29378953 | Disease-causing mutation in α-actinin-4 promotes podocyte detachment through maladaptation to periodic stretch. | Proceedings of the National Academy of Sciences of the United States of America | 2018 |
| 27932478 | Most ApoL1 Is Secreted by the Liver. | J Am Soc Nephrol | 2017 |
| 28373577 | Parathyroid hormone controls paracellular Ca transport in the thick ascending limb by regulating the tight-junction protein Claudin14. | Proceedings of the National Academy of Sciences of the United States of America | 2017 |