EY07142/EY/NEI NIH HHS/United States[Grants and Funding] - Search Results

Year	Number of Results
1990	2
1991	5
1992	3
1993	1
1996	1
1997	3
1999	4
2000	5
2001	3
2002	2
2003	3
2006	3
2007	1
2010	1
2024	0

1

Genetic factors modifying clinical expression of autosomal dominant RP.

Daiger SP, Shankar SP, Schindler AB, Sullivan LS, Bowne SJ, King TM, Daw EW, Stone EM, Heckenlively JR. Daiger SP, et al. Adv Exp Med Biol. 2006;572:3-8. doi: 10.1007/0-387-32442-9_1. Adv Exp Med Biol. 2006. PMID: 17249547 Free PMC article. Review. No abstract available.

2

Identification of the RP1 and RP10 (IMPDH1) genes causing autosomal dominant RP.

Daiger SP, Sullivan LS, Bowne SJ, Kennan A, Humphries P, Birch DG, Heckenlively JR; RP1 Consortium. Daiger SP, et al. Adv Exp Med Biol. 2003;533:1-11. doi: 10.1007/978-1-4615-0067-4_1. Adv Exp Med Biol. 2003. PMID: 15180241 Free PMC article. Review. No abstract available.

3

Prevalence of mutations causing retinitis pigmentosa and other inherited retinopathies.

Sohocki MM, Daiger SP, Bowne SJ, Rodriquez JA, Northrup H, Heckenlively JR, Birch DG, Mintz-Hittner H, Ruiz RS, Lewis RA, Saperstein DA, Sullivan LS. Sohocki MM, et al. Hum Mutat. 2001;17(1):42-51. doi: 10.1002/1098-1004(2001)17:1<42::AID-HUMU5>3.0.CO;2-K. Hum Mutat. 2001. PMID: 11139241 Free PMC article.

4

Genetic mapping of RP1 on 8q11-q21 in an Australian family with autosomal dominant retinitis pigmentosa reduces the critical region to 4 cM between D8S601 and D8S285.

Xu SY, Denton M, Sullivan L, Daiger SP, Gal A. Xu SY, et al. Hum Genet. 1996 Dec;98(6):741-3. doi: 10.1007/s004390050296. Hum Genet. 1996. PMID: 8931712

5

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. Nat Genet. 1999 Jul;22(3):255-9. doi: 10.1038/10314. Nat Genet. 1999. PMID: 10391212 Free PMC article.

6

Cleft lip and palate: no evidence of linkage to transforming growth factor alpha.

Hecht JT, Wang YP, Blanton SH, Michels VV, Daiger SP. Hecht JT, et al. Am J Hum Genet. 1991 Sep;49(3):682-6. Am J Hum Genet. 1991. PMID: 1679292 Free PMC article.

7

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. 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.

8

Prevalence of AIPL1 mutations in inherited retinal degenerative disease.

Sohocki MM, Perrault I, Leroy BP, Payne AM, Dharmaraj S, Bhattacharya SS, Kaplan J, Maumenee IH, Koenekoop R, Meire FM, Birch DG, Heckenlively JR, Daiger SP. Sohocki MM, et al. Mol Genet Metab. 2000 Jun;70(2):142-50. doi: 10.1006/mgme.2000.3001. Mol Genet Metab. 2000. PMID: 10873396

9

Localization and characterization of the human ADP-ribosylation factor 5 (ARF5) gene.

McGuire RE, Daiger SP, Green ED. McGuire RE, et al. Genomics. 1997 May 1;41(3):481-4. doi: 10.1006/geno.1997.4689. Genomics. 1997. PMID: 9169151

10

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. Genomics. 1991 Dec;11(4):857-69. doi: 10.1016/0888-7543(91)90008-3. Genomics. 1991. PMID: 1783394

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