Pei Y - Search Results

1

Refining Genotype-Phenotype Correlation in Autosomal Dominant Polycystic Kidney Disease.

Hwang YH, Conklin J, Chan W, Roslin NM, Liu J, He N, Wang K, Sundsbak JL, Heyer CM, Haider M, Paterson AD, Harris PC, Pei Y. Hwang YH, et al. Among authors: pei y. J Am Soc Nephrol. 2016 Jun;27(6):1861-8. doi: 10.1681/ASN.2015060648. Epub 2015 Oct 9. J Am Soc Nephrol. 2016. PMID: 26453610 Free PMC article.

2

Recurrent fetal loss associated with bilineal inheritance of type 1 autosomal dominant polycystic kidney disease.

Paterson AD, Wang KR, Lupea D, St George-Hyslop P, Pei Y. Paterson AD, et al. Among authors: pei y. Am J Kidney Dis. 2002 Jul;40(1):16-20. doi: 10.1053/ajkd.2002.33908. Am J Kidney Dis. 2002. PMID: 12087556

3

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.

4

Molecular genetics of autosomal dominant polycystic kidney disease.

Pei Y. Pei Y. Clin Invest Med. 2003 Oct;26(5):252-8. Clin Invest Med. 2003. PMID: 14596487 Review.

5

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

6

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

7

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

8

Incident renal events and risk factors in autosomal dominant polycystic kidney disease: a population and family-based cohort followed for 22 years.

Dicks E, Ravani P, Langman D, Davidson WS, Pei Y, Parfrey PS. Dicks E, et al. Among authors: pei y. Clin J Am Soc Nephrol. 2006 Jul;1(4):710-7. doi: 10.2215/CJN.01581105. Epub 2006 Jun 8. Clin J Am Soc Nephrol. 2006. PMID: 17699277

9

Diagnostic approach in autosomal dominant polycystic kidney disease.

Pei Y. Pei Y. Clin J Am Soc Nephrol. 2006 Sep;1(5):1108-14. doi: 10.2215/CJN.02190606. Epub 2006 Aug 9. Clin J Am Soc Nephrol. 2006. PMID: 17699332 Review.

10

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

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