Black GC - Search Results

1

Global prevalence of congenital heart disease in school-age children: a meta-analysis and systematic review.

Liu Y, Chen S, Zühlke L, Babu-Narayan SV, Black GC, Choy MK, Li N, Keavney BD. Liu Y, et al. Among authors: black gc. BMC Cardiovasc Disord. 2020 Nov 19;20(1):488. doi: 10.1186/s12872-020-01781-x. BMC Cardiovasc Disord. 2020. PMID: 33213369 Free PMC article.

2

Whole Exome Sequencing Reveals the Major Genetic Contributors to Nonsyndromic Tetralogy of Fallot.

Page DJ, Miossec MJ, Williams SG, Monaghan RM, Fotiou E, Cordell HJ, Sutcliffe L, Topf A, Bourgey M, Bourque G, Eveleigh R, Dunwoodie SL, Winlaw DS, Bhattacharya S, Breckpot J, Devriendt K, Gewillig M, Brook JD, Setchfield KJ, Bu'Lock FA, O'Sullivan J, Stuart G, Bezzina CR, Mulder BJM, Postma AV, Bentham JR, Baron M, Bhaskar SS, Black GC, Newman WG, Hentges KE, Lathrop GM, Santibanez-Koref M, Keavney BD. Page DJ, et al. Among authors: black gc. Circ Res. 2019 Feb 15;124(4):553-563. doi: 10.1161/CIRCRESAHA.118.313250. Circ Res. 2019. PMID: 30582441 Free PMC article.

3

Global birth prevalence of congenital heart defects 1970-2017: updated systematic review and meta-analysis of 260 studies.

Liu Y, Chen S, Zühlke L, Black GC, Choy MK, Li N, Keavney BD. Liu Y, et al. Among authors: black gc. Int J Epidemiol. 2019 Apr 1;48(2):455-463. doi: 10.1093/ije/dyz009. Int J Epidemiol. 2019. PMID: 30783674 Free PMC article.

4

Hearing Loss in Enlarged Vestibular Aqueduct: A Prognostic Factor Systematic Review of the Literature.

Saeed HS, Kenth J, Black G, Saeed SR, Stivaros S, Bruce IA. Saeed HS, et al. Otol Neurotol. 2021 Jan;42(1):99-107. doi: 10.1097/MAO.0000000000002843. Otol Neurotol. 2021. PMID: 33026783

5

A Review of Genetic and Physiological Disease Mechanisms Associated With Cav1 Channels: Implications for Incomplete Congenital Stationary Night Blindness Treatment.

Sadeh TT, Black GC, Manson F. Sadeh TT, et al. Among authors: black gc. Front Genet. 2021 Jan 28;12:637780. doi: 10.3389/fgene.2021.637780. eCollection 2021. Front Genet. 2021. PMID: 33584831 Free PMC article.

6

Enlarged Vestibular Aqueduct: Disease Characterization and Exploration of Potential Prognostic Factors for Cochlear Implantation.

Saeed HS, Rajai A, Nash R, Saeed SR, Stivaros SM, Black G, Bruce IA. Saeed HS, et al. Otol Neurotol. 2022 Jun 1;43(5):e563-e570. doi: 10.1097/MAO.0000000000003518. Epub 2022 Mar 8. Otol Neurotol. 2022. PMID: 35261386

7

Personalized diagnosis and management of congenital cataract by next-generation sequencing.

Gillespie RL, O'Sullivan J, Ashworth J, Bhaskar S, Williams S, Biswas S, Kehdi E, Ramsden SC, Clayton-Smith J, Black GC, Lloyd IC. Gillespie RL, et al. Among authors: black gc. Ophthalmology. 2014 Nov;121(11):2124-37.e1-2. doi: 10.1016/j.ophtha.2014.06.006. Epub 2014 Aug 19. Ophthalmology. 2014. PMID: 25148791

8

Genome sequencing identifies a large deletion at 13q32.1 as the cause of microcoria and childhood-onset glaucoma.

Sergouniotis PI, Ellingford JM, O'Sullivan J, Fenerty CH, Black GC. Sergouniotis PI, et al. Among authors: black gc. Acta Ophthalmol. 2017 May;95(3):e249-e250. doi: 10.1111/aos.13246. Epub 2016 Sep 28. Acta Ophthalmol. 2017. PMID: 27678338 Free article. No abstract available.

9

Panel-Based Clinical Genetic Testing in 85 Children with Inherited Retinal Disease.

Taylor RL, Parry NRA, Barton SJ, Campbell C, Delaney CM, Ellingford JM, Hall G, Hardcastle C, Morarji J, Nichol EJ, Williams LC, Douzgou S, Clayton-Smith J, Ramsden SC, Sharma V, Biswas S, Lloyd IC, Ashworth JL, Black GC, Sergouniotis PI. Taylor RL, et al. Among authors: black gc. Ophthalmology. 2017 Jul;124(7):985-991. doi: 10.1016/j.ophtha.2017.02.005. Epub 2017 Mar 22. Ophthalmology. 2017. PMID: 28341476

10

Clinical and genetic findings in TRPM1-related congenital stationary night blindness.

Iosifidis C, Liu J, Gale T, Ellingford JM, Campbell C, Ingram S, Chandler K, Parry NRA, Black GC, Sergouniotis PI. Iosifidis C, et al. Among authors: black gc. Acta Ophthalmol. 2022 Sep;100(6):e1332-e1339. doi: 10.1111/aos.15186. Epub 2022 May 28. Acta Ophthalmol. 2022. PMID: 35633130 Free article.

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