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Vernon Long
ResearcherPublications, citations & collaboration network
Vernon Long is a researcher indexed in ScholarIQ from OpenAlex & ORCID. ScholarIQ records 43 works, 741 citations, an h-index of 14 and an i10-index of 16.
43
Works
741
Citations
14
h-index
16
i10-index
IDs:OpenAlex
How has Vernon Long's publication output changed over time?
ScholarIQpublication output · 2003–2022
Output grew0% over the shown period — from 1 works in 2003 to 1 in 2022.
1
1
1
1
2
2
1
1
20032006200720102012201720212022
What are the most-cited papers on Vernon Long?
ScholarIQmost cited works
Whole-Exome Sequencing Identifies Mutations in GPR179 Leading to Autosomal-Recessive Complete Congenital Stationary Night Blindness
Isabelle Audo, Kinga M. Bujakowska, Elise Orhan, Charlotte M. Poloschek, Sabine Defoort‐Dhellemmes, Isabelle Drumare, Susanne Kohl, Tien Dao Luu, Odile Lecompte, Eberhart Zrenner, Marie‐Elise Lancelot, Aline Antonio, Aurore Germain, Christelle Michiels, Claire Audier, Mélanie Letexier, Jean‐Paul Saraiva, Bart P. Leroy, Francis L. Munier, Saddek Mohand‐Saïd, Birgit Lorenz, Christoph Friedburg, Markus N. Preising, Ulrich Kellner, Agnes B. Renner, Veselina Moskova‐Doumanova, Wolfgang Berger, Bernd Wissinger, Christian Hamel, Daniel F. Schorderet, Elfride De Baere, Dror Sharon, Eyal Banin, Samuel G. Jacobson, Dominique Bonneau, Xavier Zanlonghi, Guylène Le Meur, Ingele Casteels, Robert K. Koenekoop, Vernon Long, Françoise Meire, Katrina Prescott, Thomy de Ravel, Ian Simmons, Hoan Nguyen, Hélène Dollfus, Olivier Poch, Thierry Léveillard, Kim T. Nguyen-Ba-Charvet, José‐Alain Sahel, Shomi S. Bhattacharya, Christina Zeitz
S134425043. 2012136 CitationsOPEN ACCESS
Treatment trends for retinopathy of prematurity in the UK: active surveillance study of infants at risk
Gillian Adams, Catey Bunce, Wen Xing, Lucilla Butler, Vernon Long, Aravind Reddy, Annegret Dahlmann‐Noor
BMJ Open. 201783 CitationsOPEN ACCESS
Visual impairment, severe visual impairment, and blindness in children in Britain (BCVIS2): a national observational study
Lucinda Teoh, Ameenat Lola Solebo, Jugnoo S. Rahi, Joe Abbott, Wajda Abdullah, Gill Adams, Louise Allen, Christopher M. Anderson, Karen Ansell, Samira Anwar, Isabel M Ash, Jane Ashworth, Sher A. Aslam, Majunath Astagi, Colin Ball, Rajesh Balu, Victoria Barrett, Z. Bassi, Adam Bates, Dushyant Batra, Sarah Bell, Linda Belmour, James Benzimra, Ginny Birrell, Susmito Biswas, Andrew Blaikie, M S J Blundell, Kate Bolton, Ewoud Bos, Pamela G. Bowen, Richard Bowman, Natalie Boyle, John Bradbury, Maria Bredow, Marsel Bregu, Nicholas Brennan, Rosie Brennan, Paul Brittain, Charles Buchanan, Catey Bunce, Howard Bunting, Priscilla Burgess, Cathie Burke, Alexandra Kate Bush, Jeremy Butcher, Lucilla Butler, Clare Cane, Cathryn Chadwick, Ruth Charlton, Anne‐Marie Childs, Jessy Choi, Vivi Choleva, A Churchill, Michael W. Clarke, Peter Clayton, Luke Clifford, Alan Connor, Rachel Cox, Lyn Cresswell, Annegret Dahlmann‐Noor, Angela D’Amore, Mehul Dattani, Fiona Dean, Anita Devlin, Luna Dhir, Cora Doherty, S E Dorey, Fiona Drimmie, Tina Duke, Gordon N. Dutton, F.B. Eaton, Megan Eaton, Danielle Eckersley, Clive Edelsten, Rachel Elderkin, Julia Ennis, J A Escardó-Paton, Ziad Estephen, Onajite Etuwewe, Anthony Evans, Adjoa Ezekwe, Jenny Fairfield, Kevin Falzon, Allison Ferguson, Brian W. Fleck, Mary Gainsborough, Alexandra Galloway, Naomi Gerson-Sofer, Caspar Gibbon, Patricia Gibson, Kevin C. W. Goss, Katherine Graham-Evans, Judith Gray, Anna Gregory, Arun Gulati, Deniz Gurtin-Zorkun, Emma Guy, Diab Haddad, Helen R. Haggerty, P M Haigh
The Lancet Child & Adolescent Health. 202178 CitationsOPEN ACCESS
Recessive Mutations in<i>TSPAN12</i>Cause Retinal Dysplasia and Severe Familial Exudative Vitreoretinopathy (FEVR)
James A. Poulter, Alice E. Davidson, Manir Ali, David F. Gilmour, David Parry, Helen A. Mintz-Hittner, Ian Carr, H.M. Bottomley, Vernon Long, Louise Downey, Panagiotis I. Sergouniotis, Genevieve Wright, Robert E. MacLaren, Anthony T. Moore, Andrew R. Webster, Chris F. Inglehearn, Carmel Toomes
S76304953. 201273 Citations
Outcome of zone 1 retinopathy of prematurity
Michael O’Keefe, Bernadette Lanigan, Vernon Long
S195714098. 200346 CitationsOPEN ACCESS
Related on ScholarIQ
Whole-Exome Sequencing Identifies Mutations in GPR179 Leading to Autosomal-Recessive Complete Congenital Stationary Night Blindness
Paper
Treatment trends for retinopathy of prematurity in the UK: active surveillance study of infants at risk
Paper
Visual impairment, severe visual impairment, and blindness in children in Britain (BCVIS2): a national observational study
Paper
Recessive Mutations in<i>TSPAN12</i>Cause Retinal Dysplasia and Severe Familial Exudative Vitreoretinopathy (FEVR)
Paper
Outcome of zone 1 retinopathy of prematurity
Paper
Prognosis for splicing factor PRPF8 retinitis pigmentosa, novel mutations and correlation between human and yeast phenotypes
Paper