Barua M - Search Results

1

Association of Genetically Predicted Skipping of COL4A4 Exon 27 with Hematuria and Albuminuria.

Lona-Durazo F, Omachi K, Fermin D, Eichinger F, Troost JP, Lin MH, Dinsmore IR, Mirshahi T, Chang AR, Miner JH, Paterson AD, Barua M, Gagliano Taliun SA. Lona-Durazo F, et al. Among authors: barua m. J Am Soc Nephrol. 2025 Jan 1;36(1):48-59. doi: 10.1681/ASN.0000000000000480. Epub 2024 Aug 27. J Am Soc Nephrol. 2025. PMID: 39190490

2

Mutations in the INF2 gene account for a significant proportion of familial but not sporadic focal and segmental glomerulosclerosis.

Barua M, Brown EJ, Charoonratana VT, Genovese G, Sun H, Pollak MR. Barua M, et al. Kidney Int. 2013 Feb;83(2):316-22. doi: 10.1038/ki.2012.349. Epub 2012 Sep 26. Kidney Int. 2013. PMID: 23014460 Free PMC article.

3

Explainable Biomarkers for Automated Glomerular and Patient-Level Disease Classification.

Basso MN, Barua M, John R, Khademi A. Basso MN, et al. Among authors: barua m. Kidney360. 2021 Dec 9;3(3):534-545. doi: 10.34067/KID.0005102021. eCollection 2022 Mar 31. Kidney360. 2021. PMID: 35582169 Free PMC article.

4

Genetic testing for nephrotic syndrome and FSGS in the era of next-generation sequencing.

Brown EJ, Pollak MR, Barua M. Brown EJ, et al. Among authors: barua m. Kidney Int. 2014 May;85(5):1030-8. doi: 10.1038/ki.2014.48. Epub 2014 Mar 5. Kidney Int. 2014. PMID: 24599252 Free PMC article. Review.

5

Exome sequencing and in vitro studies identified podocalyxin as a candidate gene for focal and segmental glomerulosclerosis.

Barua M, Shieh E, Schlondorff J, Genovese G, Kaplan BS, Pollak MR. Barua M, et al. Kidney Int. 2014 Jan;85(1):124-33. doi: 10.1038/ki.2013.354. Epub 2013 Sep 18. Kidney Int. 2014. PMID: 24048372 Free PMC article.

6

Family history of renal disease severity predicts the mutated gene in ADPKD.

Barua M, Cil O, Paterson AD, Wang K, He N, Dicks E, Parfrey P, Pei Y. Barua M, et al. J Am Soc Nephrol. 2009 Aug;20(8):1833-8. doi: 10.1681/ASN.2009020162. Epub 2009 May 14. J Am Soc Nephrol. 2009. PMID: 19443633 Free PMC article.

7

X-Linked Glomerulopathy Due to COL4A5 Founder Variant.

Barua M, John R, Stella L, Li W, Roslin NM, Sharif B, Hack S, Lajoie-Starkell G, Schwaderer AL, Becknell B, Wuttke M, Köttgen A, Cattran D, Paterson AD, Pei Y. Barua M, et al. Am J Kidney Dis. 2018 Mar;71(3):441-445. doi: 10.1053/j.ajkd.2017.09.005. Epub 2017 Dec 1. Am J Kidney Dis. 2018. PMID: 29198386 Review.

8

Integration of Genetic Testing and Pathology for the Diagnosis of Adults with FSGS.

Yao T, Udwan K, John R, Rana A, Haghighi A, Xu L, Hack S, Reich HN, Hladunewich MA, Cattran DC, Paterson AD, Pei Y, Barua M. Yao T, et al. Among authors: barua m. Clin J Am Soc Nephrol. 2019 Feb 7;14(2):213-223. doi: 10.2215/CJN.08750718. Epub 2019 Jan 15. Clin J Am Soc Nephrol. 2019. PMID: 30647093 Free PMC article.

9

Evaluation of the Genetic Association Between Adult Obesity and Neuropsychiatric Disease.

Stahel P, Nahmias A, Sud SK, Lee SJ, Pucci A, Yousseif A, Youseff A, Jackson T, Urbach DR, Okrainec A, Allard JP, Sockalingam S, Yao T, Barua M, Jiao H, Magi R, Bassett AS, Paterson AD, Dahlman I, Batterham RL, Dash S. Stahel P, et al. Among authors: barua m. Diabetes. 2019 Dec;68(12):2235-2246. doi: 10.2337/db18-1254. Epub 2019 Sep 10. Diabetes. 2019. PMID: 31506345

10

Population-based studies reveal an additive role of type IV collagen variants in hematuria and albuminuria.

Barua M, Paterson AD. Barua M, et al. Pediatr Nephrol. 2022 Feb;37(2):253-262. doi: 10.1007/s00467-021-04934-y. Epub 2021 Feb 26. Pediatr Nephrol. 2022. PMID: 33635378 Review.

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