Paterson AD - Search Results

1

Bilineal disease and trans-heterozygotes in autosomal dominant polycystic kidney disease.

Pei Y, Paterson AD, Wang KR, He N, Hefferton D, Watnick T, Germino GG, Parfrey P, Somlo S, St George-Hyslop P. Pei Y, et al. Among authors: paterson ad. Am J Hum Genet. 2001 Feb;68(2):355-63. doi: 10.1086/318188. Epub 2001 Jan 10. Am J Hum Genet. 2001. PMID: 11156533 Free PMC article.

2

A novel frameshift mutation induced by an adenosine insertion in the polycystic kidney disease 2 (PKD2) gene.

Pei Y, Wang K, Kasenda M, Paterson AD, Liang Y, Huang E, Lian J, Rogovea E, Somlo S, St George-Hyslop P. Pei Y, et al. Among authors: paterson ad. Kidney Int. 1998 May;53(5):1127-32. doi: 10.1046/j.1523-1755.1998.00890.x. Kidney Int. 1998. PMID: 9573526 Free article.

3

A spectrum of mutations in the polycystic kidney disease-2 (PKD2) gene from eight Canadian kindreds.

Pei Y, He N, Wang K, Kasenda M, Paterson AD, Chan G, Liang Y, Roscoe J, Brissenden J, Hefferton D, Parfrey P, Somlo S, St George-Hyslop P. Pei Y, et al. Among authors: paterson ad. J Am Soc Nephrol. 1998 Oct;9(10):1853-60. doi: 10.1681/ASN.V9101853. J Am Soc Nephrol. 1998. PMID: 9773786 Clinical Trial.

4

Is there a third gene for autosomal dominant polycystic kidney disease?

Paterson AD, Pei Y. Paterson AD, et al. Kidney Int. 1998 Nov;54(5):1759-61. doi: 10.1046/j.1523-1755.1998.00166.x. Kidney Int. 1998. PMID: 9844156 Free article. No abstract available.

5

PKD3-to be or not to be?

Paterson AD, Pei Y. Paterson AD, et al. Nephrol Dial Transplant. 1999 Dec;14(12):2965-6. doi: 10.1093/ndt/14.12.2965. Nephrol Dial Transplant. 1999. PMID: 10570111 No abstract available.

6

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. Am J Kidney Dis. 2002 Jul;40(1):16-20. doi: 10.1053/ajkd.2002.33908. Am J Kidney Dis. 2002. PMID: 12087556

7

Clinical and genetic study of a large Italian family linked to SPG12 locus.

Orlacchio A, Kawarai T, Rogaeva E, Song YQ, Paterson AD, Bernardi G, St George-Hyslop PH. Orlacchio A, et al. Among authors: paterson ad. Neurology. 2002 Nov 12;59(9):1395-401. doi: 10.1212/01.wnl.0000031423.43482.19. Neurology. 2002. PMID: 12427890

8

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. 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

9

CRYBA4, a novel human cataract gene, is also involved in microphthalmia.

Billingsley G, Santhiya ST, Paterson AD, Ogata K, Wodak S, Hosseini SM, Manisastry SM, Vijayalakshmi P, Gopinath PM, Graw J, Héon E. Billingsley G, et al. Among authors: paterson ad. Am J Hum Genet. 2006 Oct;79(4):702-9. doi: 10.1086/507712. Epub 2006 Aug 17. Am J Hum Genet. 2006. PMID: 16960806 Free PMC article.

10

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. 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

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