Pei Y - Search Results

1

Functional analysis of a novel GATA3 mutation in a family with the hypoparathyroidism, deafness, and renal dysplasia syndrome.

Zahirieh A, Nesbit MA, Ali A, Wang K, He N, Stangou M, Bamichas G, Sombolos K, Thakker RV, Pei Y. Zahirieh A, et al. Among authors: pei y. J Clin Endocrinol Metab. 2005 Apr;90(4):2445-50. doi: 10.1210/jc.2004-1969. Epub 2005 Feb 10. J Clin Endocrinol Metab. 2005. PMID: 15705923

2

Genotype-renal function correlation in type 2 autosomal dominant polycystic kidney disease.

Magistroni R, He N, Wang K, Andrew R, Johnson A, Gabow P, Dicks E, Parfrey P, Torra R, San-Millan JL, Coto E, Van Dijk M, Breuning M, Peters D, Bogdanova N, Ligabue G, Albertazzi A, Hateboer N, Demetriou K, Pierides A, Deltas C, St George-Hyslop P, Ravine D, Pei Y. Magistroni R, et al. Among authors: pei y. J Am Soc Nephrol. 2003 May;14(5):1164-74. doi: 10.1097/01.asn.0000061774.90975.25. J Am Soc Nephrol. 2003. PMID: 12707387 Free article.

3

Progressive loss of renal function is an age-dependent heritable trait in type 1 autosomal dominant polycystic kidney disease.

Paterson AD, Magistroni R, He N, Wang K, Johnson A, Fain PR, Dicks E, Parfrey P, St George-Hyslop P, Pei Y. Paterson AD, et al. Among authors: pei y. J Am Soc Nephrol. 2005 Mar;16(3):755-62. doi: 10.1681/ASN.2004090758. Epub 2005 Jan 26. J Am Soc Nephrol. 2005. PMID: 15677307

4

Genome-wide linkage scan of a large family with IgA nephropathy localizes a novel susceptibility locus to chromosome 2q36.

Paterson AD, Liu XQ, Wang K, Magistroni R, Song X, Kappel J, Klassen J, Cattran D, St George-Hyslop P, Pei Y. Paterson AD, et al. Among authors: pei y. J Am Soc Nephrol. 2007 Aug;18(8):2408-15. doi: 10.1681/ASN.2007020241. Epub 2007 Jul 18. J Am Soc Nephrol. 2007. PMID: 17634434

5

Recessive NPHS2 (Podocin) mutations are rare in adult-onset idiopathic focal segmental glomerulosclerosis.

He N, Zahirieh A, Mei Y, Lee B, Senthilnathan S, Wong B, Mucha B, Hildebrandt F, Cole DE, Cattran D, Pei Y. He N, et al. Among authors: pei y. Clin J Am Soc Nephrol. 2007 Jan;2(1):31-7. doi: 10.2215/CJN.02690806. Epub 2006 Oct 25. Clin J Am Soc Nephrol. 2007. PMID: 17699384

6

Molecular diagnostics in autosomal dominant polycystic kidney disease: utility and limitations.

Zhao X, Paterson AD, Zahirieh A, He N, Wang K, Pei Y. Zhao X, et al. Among authors: pei y. Clin J Am Soc Nephrol. 2008 Jan;3(1):146-52. doi: 10.2215/CJN.03430807. Epub 2007 Dec 12. Clin J Am Soc Nephrol. 2008. PMID: 18077784 Free PMC article. Clinical Trial.

7

IL5RA and TNFRSF6B gene variants are associated with sporadic IgA nephropathy.

Liu XQ, Paterson AD, He N, St George-Hyslop P, Rauta V, Gronhagen-Riska C, Laakso M, Thibaudin L, Berthoux F, Cattran D, Pei Y. Liu XQ, et al. Among authors: pei y. J Am Soc Nephrol. 2008 May;19(5):1025-33. doi: 10.1681/ASN.2007091013. Epub 2008 Feb 6. J Am Soc Nephrol. 2008. PMID: 18256354 Free PMC article.

8

Evidence for pathogenicity of atypical splice mutations in autosomal dominant polycystic kidney disease.

Wang K, Zhao X, Chan S, Cil O, He N, Song X, Paterson AD, Pei Y. Wang K, et al. Among authors: pei y. Clin J Am Soc Nephrol. 2009 Feb;4(2):442-9. doi: 10.2215/CJN.00980208. Epub 2009 Jan 21. Clin J Am Soc Nephrol. 2009. PMID: 19158373 Free PMC article.

9

Systems biology of autosomal dominant polycystic kidney disease (ADPKD): computational identification of gene expression pathways and integrated regulatory networks.

Song X, Di Giovanni V, He N, Wang K, Ingram A, Rosenblum ND, Pei Y. Song X, et al. Among authors: pei y. Hum Mol Genet. 2009 Jul 1;18(13):2328-43. doi: 10.1093/hmg/ddp165. Epub 2009 Apr 3. Hum Mol Genet. 2009. PMID: 19346236

10

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. Among authors: pei y. 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.

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