Similar articles for PMID: 10966492

Year	Number of Results
1988	1
1994	1
1995	6
1996	4
1997	2
1998	6
1999	6
2000	8
2001	5
2002	3
2003	10
2004	3
2005	3
2006	2
2007	4
2008	5
2009	1
2010	3
2011	2
2012	2
2013	6
2014	3
2015	1
2016	1
2017	2
2018	1
2019	2
2020	1
2021	2
2022	2
2024	0

1

A locus for adolescent and adult onset familial focal segmental glomerulosclerosis on chromosome 1q25-31.

Tsukaguchi H, Yager H, Dawborn J, Jost L, Cohlmia J, Abreu PF, Pereira AB, Pollak MR. Tsukaguchi H, et al. J Am Soc Nephrol. 2000 Sep;11(9):1674-1680. doi: 10.1681/ASN.V1191674. J Am Soc Nephrol. 2000. PMID: 10966492

2

Clinical, histopathologic, and genetic studies in nine families with focal segmental glomerulosclerosis.

Rana K, Isbel N, Buzza M, Dagher H, Henning P, Kainer G, Savige J. Rana K, et al. Am J Kidney Dis. 2003 Jun;41(6):1170-8. doi: 10.1016/s0272-6386(03)00347-0. Am J Kidney Dis. 2003. PMID: 12776268

3

Linkage of a gene causing familial focal segmental glomerulosclerosis to chromosome 11 and further evidence of genetic heterogeneity.

Winn MP, Conlon PJ, Lynn KL, Howell DN, Slotterbeck BD, Smith AH, Graham FL, Bembe M, Quarles LD, Pericak-Vance MA, Vance JM. Winn MP, et al. Genomics. 1999 Jun 1;58(2):113-20. doi: 10.1006/geno.1999.5828. Genomics. 1999. PMID: 10368108

4

Clinical and genetic heterogeneity in familial focal segmental glomerulosclerosis. International Collaborative Group for the Study of Familial Focal Segmental Glomerulosclerosis.

Winn MP, Conlon PJ, Lynn KL, Howell DN, Gross DA, Rogala AR, Smith AH, Graham FL, Bembe M, Quarles LD, Pericak-Vance MA, Vance JM. Winn MP, et al. Kidney Int. 1999 Apr;55(4):1241-6. doi: 10.1046/j.1523-1755.1999.00384.x. Kidney Int. 1999. PMID: 10200986 Free article.

5

Autosomal dominant progressive nephropathy with deafness: linkage to a new locus on chromosome 11q24.

Prakash S, Chung KW, Sinha S, Barmada M, Ellis D, Ferrell RE, Finegold DN, Randhawa PS, Dinda A, Vats A. Prakash S, et al. J Am Soc Nephrol. 2003 Jul;14(7):1794-803. doi: 10.1097/01.asn.0000071513.73427.97. J Am Soc Nephrol. 2003. PMID: 12819239

6

A locus for inherited focal segmental glomerulosclerosis maps to chromosome 19q13.

Mathis BJ, Kim SH, Calabrese K, Haas M, Seidman JG, Seidman CE, Pollak MR. Mathis BJ, et al. Kidney Int. 1998 Feb;53(2):282-6. doi: 10.1046/j.1523-1755.1998.00828.x. Kidney Int. 1998. PMID: 9461087 Free article.

7

Familial nephrotic syndrome: clinical spectrum and linkage to chromosome 19q13.

Vats A, Nayak A, Ellis D, Randhawa PS, Finegold DN, Levinson KL, Ferrell RE. Vats A, et al. Kidney Int. 2000 Mar;57(3):875-81. doi: 10.1046/j.1523-1755.2000.057003875.x. Kidney Int. 2000. PMID: 10720940 Free article.

8

MYH9 is a major-effect risk gene for focal segmental glomerulosclerosis.

Kopp JB, Smith MW, Nelson GW, Johnson RC, Freedman BI, Bowden DW, Oleksyk T, McKenzie LM, Kajiyama H, Ahuja TS, Berns JS, Briggs W, Cho ME, Dart RA, Kimmel PL, Korbet SM, Michel DM, Mokrzycki MH, Schelling JR, Simon E, Trachtman H, Vlahov D, Winkler CA. Kopp JB, et al. Nat Genet. 2008 Oct;40(10):1175-84. doi: 10.1038/ng.226. Epub 2008 Sep 14. Nat Genet. 2008. PMID: 18794856 Free PMC article.

9

Primary autosomal recessive microcephaly: MCPH5 maps to 1q25-q32.

Jamieson CR, Fryns JP, Jacobs J, Matthijs G, Abramowicz MJ. Jamieson CR, et al. Am J Hum Genet. 2000 Dec;67(6):1575-7. doi: 10.1086/316909. Epub 2000 Nov 6. Am J Hum Genet. 2000. PMID: 11067780 Free PMC article.

10

A new locus for inherited nuclear cataract mapped to the long arm of chromosome 1.

Wang L, Lin H, Shen Y, Huang S, Gu J, Su H, Qi Y. Wang L, et al. Mol Vis. 2007 Aug 1;13:1357-62. Mol Vis. 2007. PMID: 17768382

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