Heckenlively JR - Search Results

1

Long-term follow-up of a family with dominant X-linked retinitis pigmentosa.

Wu DM, Khanna H, Atmaca-Sonmez P, Sieving PA, Branham K, Othman M, Swaroop A, Daiger SP, Heckenlively JR. Wu DM, et al. Among authors: heckenlively jr. Eye (Lond). 2010 May;24(5):764-74. doi: 10.1038/eye.2009.270. Epub 2009 Nov 6. Eye (Lond). 2010. PMID: 19893586 Free PMC article.

2

Mutations in a novel retina-specific gene cause autosomal dominant retinitis pigmentosa.

Sullivan LS, Heckenlively JR, Bowne SJ, Zuo J, Hide WA, Gal A, Denton M, Inglehearn CF, Blanton SH, Daiger SP. Sullivan LS, et al. Among authors: heckenlively jr. Nat Genet. 1999 Jul;22(3):255-9. doi: 10.1038/10314. Nat Genet. 1999. PMID: 10391212 Free PMC article.

3

Mutations in the RP1 gene causing autosomal dominant retinitis pigmentosa.

Bowne SJ, Daiger SP, Hims MM, Sohocki MM, Malone KA, McKie AB, Heckenlively JR, Birch DG, Inglehearn CF, Bhattacharya SS, Bird A, Sullivan LS. Bowne SJ, et al. Among authors: heckenlively jr. Hum Mol Genet. 1999 Oct;8(11):2121-8. doi: 10.1093/hmg/8.11.2121. Hum Mol Genet. 1999. PMID: 10484783 Free PMC article.

4

Remapping of the RP15 locus for X-linked cone-rod degeneration to Xp11.4-p21.1, and identification of a de novo insertion in the RPGR exon ORF15.

Mears AJ, Hiriyanna S, Vervoort R, Yashar B, Gieser L, Fahrner S, Daiger SP, Heckenlively JR, Sieving PA, Wright AF, Swaroop A. Mears AJ, et al. Among authors: heckenlively jr. Am J Hum Genet. 2000 Oct;67(4):1000-3. doi: 10.1086/303091. Epub 2000 Sep 1. Am J Hum Genet. 2000. PMID: 10970770 Free PMC article.

5

Autosomal dominant sectoral retinitis pigmentosa. Two families with transversion mutation in codon 23 of rhodopsin.

Heckenlively JR, Rodriguez JA, Daiger SP. Heckenlively JR, et al. Arch Ophthalmol. 1991 Jan;109(1):84-91. doi: 10.1001/archopht.1991.01080010086038. Arch Ophthalmol. 1991. PMID: 1987955

6

Further evidence of exclusion of linkage between type II autosomal dominant retinitis pigmentosa (ADRP) and D3S47 on 3q.

Blanton SH, Cottingham AW, Giesenschlag N, Heckenlively JR, Humphries P, Daiger SP. Blanton SH, et al. Among authors: heckenlively jr. Genomics. 1990 Sep;8(1):179-81. doi: 10.1016/0888-7543(90)90243-n. Genomics. 1990. PMID: 2081594

7

Establishing baseline rod electroretinogram values in achromatopsia and cone dystrophy.

Wang I, Khan NW, Branham K, Wissinger B, Kohl S, Heckenlively JR. Wang I, et al. Among authors: heckenlively jr. Doc Ophthalmol. 2012 Dec;125(3):229-33. doi: 10.1007/s10633-012-9350-1. Epub 2012 Aug 19. Doc Ophthalmol. 2012. PMID: 22903242

8

X-linked dominant cone-rod degeneration: linkage mapping of a new locus for retinitis pigmentosa (RP 15) to Xp22.13-p22.11.

McGuire RE, Sullivan LS, Blanton SH, Church MW, Heckenlively JR, Daiger SP. McGuire RE, et al. Among authors: heckenlively jr. Am J Hum Genet. 1995 Jul;57(1):87-94. Am J Hum Genet. 1995. PMID: 7611300 Free PMC article.

9

Linkage mapping of autosomal dominant retinitis pigmentosa (RP1) to the pericentric region of human chromosome 8.

Blanton SH, Heckenlively JR, Cottingham AW, Friedman J, Sadler LA, Wagner M, Friedman LH, Daiger SP. Blanton SH, et al. Among authors: heckenlively jr. Genomics. 1991 Dec;11(4):857-69. doi: 10.1016/0888-7543(91)90008-3. Genomics. 1991. PMID: 1783394

10

DNA linkage studies of degenerative retinal diseases.

Daiger SP, Heckenlively JR, Lewis RA, Pelias MZ. Daiger SP, et al. Among authors: heckenlively jr. Prog Clin Biol Res. 1987;247:147-62. Prog Clin Biol Res. 1987. PMID: 3317443 Review.

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