APOL1 genotype-associated morphologic changes among patients with focal segmental glomerulosclerosis
-
Published:2021-03-01
Issue:9
Volume:36
Page:2747-2757
-
ISSN:0931-041X
-
Container-title:Pediatric Nephrology
-
language:en
-
Short-container-title:Pediatr Nephrol
Author:
Zee JarcyORCID, McNulty Michelle T., Hodgin Jeffrey B., Zhdanova Olga, Hingorani Sangeeta, Jefferson Jonathan Ashley, Gibson Keisha L., Trachtman Howard, Fornoni Alessia, Dell Katherine M., Reich Heather N., Bagnasco Serena, Greenbaum Larry A., Lafayette Richard A., Gipson Debbie S., Brown Elizabeth, Kretzler Matthias, Appel Gerald, Sambandam Kamalanathan K., Tuttle Katherine R., Chen Dhruti, Atkinson Meredith A., Hogan Marie C., Kaskel Frederick J., Meyers Kevin E., O’Toole John, Srivastava Tarak, Sethna Christine B., Hladunewich Michelle A., Lin JJ, Nast Cynthia C., Derebail Vimal K., Patel Jiten, Vento Suzanne, Holzman Lawrence B., Athavale Ambarish M., Adler Sharon G., Lemley Kevin V., Lieske John C., Hogan Jonathan J., Gadegbeku Crystal A., Fervenza Fernando C., Wang Chia-Shi, Matar Raed Bou, Singer Pamela, Kopp Jeffrey B., Barisoni Laura, Sampson Matthew G.ORCID
Publisher
Springer Science and Business Media LLC
Subject
Nephrology,Pediatrics, Perinatology, and Child Health
Reference38 articles.
1. Genovese G, Friedman DJ, Ross MD, Lecordier L, Uzureau P, Freedman BI, Bowden DW, Langefeld CD, Oleksyk TK, Uscinski Knob AL, Bernhardy AJ, Hicks PJ, Nelson GW, Vanhollebeke B, Winkler CA, Kopp JB, Pays E, Pollak MR (2010) Association of trypanolytic ApoL1 variants with kidney disease in African Americans. Science 329:841–845 2. Tzur S, Rosset S, Shemer R, Yudkovsky G, Selig S, Tarekegn A, Bekele E, Bradman N, Wasser WG, Behar DM, Skorecki K (2010) Missense mutations in the APOL1 gene are highly associated with end stage kidney disease risk previously attributed to the MYH9 gene. Hum Genet 128:345–350 3. Kopp JB, Nelson GW, Sampath K, Johnson RC, Genovese G, An P, Friedman D, Briggs W, Dart R, Korbet S, Mokrzycki MH, Kimmel PL, Limou S, Ahuja TS, Berns JS, Fryc J, Simon EE, Smith MC, Trachtman H, Michel DM, Schelling JR, Vlahov D, Pollak M, Winkler CA (2011) APOL1 genetic variants in focal segmental glomerulosclerosis and HIV-associated nephropathy. J Am Soc Nephrol 22:2129–2137 4. Ng DK, Robertson CC, Woroniecki RP, Limou S, Gillies CE, Reidy KJ, Winkler CA, Hingorani S, Gibson KL, Hjorten R, Sethna CB, Kopp JB, Moxey-Mims M, Furth SL, Warady BA, Kretzler M, Sedor JR, Kaskel FJ, Sampson MG (2017) APOL1-associated glomerular disease among African-American children: a collaboration of the Chronic Kidney Disease in Children (CKiD) and Nephrotic Syndrome Study Network (NEPTUNE) cohorts. Nephrol Dial Transplant 32:983–990 5. Sampson MG, Robertson CC, Martini S, Mariani LH, Lemley KV, Gillies CE, Otto EA, Kopp JB, Randolph A, Vega-Warner V, Eichinger F, Nair V, Gipson DS, Cattran DC, Johnstone DB, O'Toole JF, Bagnasco SM, Song PX, Barisoni L, Troost JP, Kretzler M, Sedor JR, Nephrotic Syndrome Study Network (2016) Integrative genomics identifies novel associations with APOL1 risk genotypes in Black NEPTUNE subjects. J Am Soc Nephrol 27:814–823
Cited by
3 articles.
订阅此论文施引文献
订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
|
|