Vernon Long - Concepedia

Author

Vernon Long

St James's University Hospital

Also Known As

A. Lobo, Long,Vu, Lucilla Butler, V Long, V. Long, Vernon Long, Vernon W Long, Vernon W. Long, Vernon W. Long

Publications

715

Citations

H-Index

Concepts

All Affiliations

St James's University Hospital University College London Leeds General Infirmary University of Pennsylvania

About

Vernon Long is an author at St James's University Hospital specializing in medicine, ophthalmology, and genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	6	6	266
2	Molecular Genetics	1	1	19
3	Neurology	1	1	67
4	Orthopaedics	1	1	25
5	Plastic Surgery	1	1	25

Vernon Long

Publications

571

Citations

H-Index

Page 1

	Year	Citations
Whole-Exome Sequencing Identifies Mutations in GPR179 Leading to Autosomal-Recessive Complete Congenital Stationary Night Blindness Isabelle Audo, Kinga M. Bujakowska, Elise Orhan, The American Journal of Human Genetics Ocular DiseaseDevelopmental BiologyMendelian DisorderOphthalmologyGenetic Disorder	2012	132
Treatment trends for retinopathy of prematurity in the UK: active surveillance study of infants at risk Gillian Adams, Catey Bunce, Wen Xing, BMJ Open	2017	82
Recessive Mutations in<i>TSPAN12</i>Cause Retinal Dysplasia and Severe Familial Exudative Vitreoretinopathy (FEVR) James A. Poulter, Alice E. Davidson, Manir Ali, Investigative Ophthalmology & Visual Science	2012	71
Visual impairment, severe visual impairment, and blindness in children in Britain (BCVIS2): a national observational study Lucinda Teoh, Ameenat Lola Solebo, Jugnoo S. Rahi, The Lancet Child & Adolescent Health OphthalmologyNational Observational StudyMedicinePediatricsSevere Visual Impairment	2021	67
Outcome of zone 1 retinopathy of prematurity Michael O’Keefe, Bernadette Lanigan, Vernon Long Acta Ophthalmologica Scandinavica	2003	46
Prognosis for splicing factor PRPF8 retinitis pigmentosa, novel mutations and correlation between human and yeast phenotypes Katherine V. Towns, Athina Kipioti, Vernon Long, Human Mutation	2010	40
An endoscopically implantable device stimulates the lower esophageal sphincter on demand by remote control: a study using a canine model John O. Clarke, Sundar Jagannath, Anthony N. Kalloo, Endoscopy	2007	32
A proposal for a new classification of complications in craniosynostosis surgery Dmitri Shastin, Sharron Peacock, Velu Guruswamy, Journal of Neurosurgery Pediatrics Craniosynostosis SurgerySurgeryOutpatient ComplicationsOrthopaedic SurgeryCraniofacial Anomalies	2017	25
Pseudo-Foster Kennedy Syndrome due to unilateral optic nerve hypoplasia: a case report Shveta Bansal, T R Dabbs, Vernon Long Journal of Medical Case Reports	2008	19
X‐linked retinoschisis in a female with a heterozygous <i>RS1</i> missense mutation Manuel Saldaña, Jenny Thompson, Elizabeth Monk, American Journal of Medical Genetics Part A Mendelian DisorderOphthalmologyGenetic DisorderGeneticsCraniofacial Development	2007	19

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