Haider NB - Search Results

1

A Bedouin kindred with infantile nephronophthisis demonstrates linkage to chromosome 9 by homozygosity mapping.

Haider NB, Carmi R, Shalev H, Sheffield VC, Landau D. Haider NB, et al. Am J Hum Genet. 1998 Nov;63(5):1404-10. doi: 10.1086/302108. Am J Hum Genet. 1998. PMID: 9792867 Free PMC article.

2

Positional cloning of a novel gene on chromosome 16q causing Bardet-Biedl syndrome (BBS2).

Nishimura DY, Searby CC, Carmi R, Elbedour K, Van Maldergem L, Fulton AB, Lam BL, Powell BR, Swiderski RE, Bugge KE, Haider NB, Kwitek-Black AE, Ying L, Duhl DM, Gorman SW, Heon E, Iannaccone A, Bonneau D, Biesecker LG, Jacobson SG, Stone EM, Sheffield VC. Nishimura DY, et al. Among authors: haider nb. Hum Mol Genet. 2001 Apr 1;10(8):865-74. doi: 10.1093/hmg/10.8.865. Hum Mol Genet. 2001. PMID: 11285252

3

Iraqi-Jewish kindreds with optic atrophy plus (3-methylglutaconic aciduria type 3) demonstrate linkage disequilibrium with the CTG repeat in the 3' untranslated region of the myotonic dystrophy protein kinase gene.

Nystuen A, Costeff H, Elpeleg ON, Apter N, Bonné-Tamir B, Mohrenweiser H, Haider N, Stone EM, Sheffield VC. Nystuen A, et al. Hum Mol Genet. 1997 Apr;6(4):563-9. doi: 10.1093/hmg/6.4.563. Hum Mol Genet. 1997. PMID: 9097959

4

Complement factor H gene mutation associated with autosomal recessive atypical hemolytic uremic syndrome.

Ying L, Katz Y, Schlesinger M, Carmi R, Shalev H, Haider N, Beck G, Sheffield VC, Landau D. Ying L, et al. Am J Hum Genet. 1999 Dec;65(6):1538-46. doi: 10.1086/302673. Am J Hum Genet. 1999. PMID: 10577907 Free PMC article.

5

Pitfalls in homozygosity mapping.

Miano MG, Jacobson SG, Carothers A, Hanson I, Teague P, Lovell J, Cideciyan AV, Haider N, Stone EM, Sheffield VC, Wright AF. Miano MG, et al. Am J Hum Genet. 2000 Nov;67(5):1348-51. doi: 10.1016/S0002-9297(07)62966-8. Epub 2000 Sep 27. Am J Hum Genet. 2000. PMID: 11007652 Free PMC article.

6

Evaluation and molecular characterization of EHD1, a candidate gene for Bardet-Biedl syndrome 1 (BBS1).

Haider NB, Searby C, Galperin E, Mintz L, Horowitz M, Stone EM, Sheffield VC. Haider NB, et al. Gene. 1999 Nov 15;240(1):227-32. doi: 10.1016/s0378-1119(99)00395-9. Gene. 1999. PMID: 10564830

7

Mutation of a nuclear receptor gene, NR2E3, causes enhanced S cone syndrome, a disorder of retinal cell fate.

Haider NB, Jacobson SG, Cideciyan AV, Swiderski R, Streb LM, Searby C, Beck G, Hockey R, Hanna DB, Gorman S, Duhl D, Carmi R, Bennett J, Weleber RG, Fishman GA, Wright AF, Stone EM, Sheffield VC. Haider NB, et al. Nat Genet. 2000 Feb;24(2):127-31. doi: 10.1038/72777. Nat Genet. 2000. PMID: 10655056

8

Identification of the gene that, when mutated, causes the human obesity syndrome BBS4.

Mykytyn K, Braun T, Carmi R, Haider NB, Searby CC, Shastri M, Beck G, Wright AF, Iannaccone A, Elbedour K, Riise R, Baldi A, Raas-Rothschild A, Gorman SW, Duhl DM, Jacobson SG, Casavant T, Stone EM, Sheffield VC. Mykytyn K, et al. Among authors: haider nb. Nat Genet. 2001 Jun;28(2):188-91. doi: 10.1038/88925. Nat Genet. 2001. PMID: 11381270

9

The cloning and developmental expression of unconventional myosin IXA (MYO9A) a gene in the Bardet-Biedl syndrome (BBS4) region at chromosome 15q22-q23.

Gorman SW, Haider NB, Grieshammer U, Swiderski RE, Kim E, Welch JW, Searby C, Leng S, Carmi R, Sheffield VC, Duhl DM. Gorman SW, et al. Among authors: haider nb. Genomics. 1999 Jul 15;59(2):150-60. doi: 10.1006/geno.1999.5867. Genomics. 1999. PMID: 10409426

10

Excess cone cell proliferation due to lack of a functional NR2E3 causes retinal dysplasia and degeneration in rd7/rd7 mice.

Haider NB, Naggert JK, Nishina PM. Haider NB, et al. Hum Mol Genet. 2001 Aug 1;10(16):1619-26. doi: 10.1093/hmg/10.16.1619. Hum Mol Genet. 2001. PMID: 11487564

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