Veronica van Heyningen

Author

Also Known As

Andrew R Webster, Crowley, William F., David Allsup, Heyningen, Veronica Van, K. D. Bagshawe, Stephanie Halford, V VANHEYNINGEN, V Van Heyningen, V van Heyningen, V. VAN HEYNINGEN

334

Publications

23.6K

Citations

H-Index

213

Concepts

All Affiliations

Western General Hospital University of Edinburgh University College London Medical Research Council Institute of Genetics and Cancer

About

Veronica van Heyningen is an author at Western General Hospital specializing in medicine, genetics, and molecular genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	51	107	12.7K
2	Natural Sciences	16	18	2.7K
3	Health Sciences	4	4	448
4	Arts	1	1	27
5	Engineering	1	1	20

Veronica van Heyningen

161

Publications

18.4K

Citations

H-Index

Page 1

	Year	Citations
Mouse Small eye results from mutations in a paired-like homeobox-containing gene Robert E. Hill, Jack Favor, Brigid L.M. Hogan, Nature Knockout MouseOcular DiseaseDevelopmental BiologyOphthalmologyExperimental Ophthalmology	1991	1.2K
Pax6 Controls Progenitor Cell Identity and Neuronal Fate in Response to Graded Shh Signaling Johan Ericson, Penny Rashbass, Andreas Schedl, Cell	1997	1K
The candidate Wilms' tumour gene is involved in genitourinary development Kathy Pritchard‐Jones, Stewart Fleming, Duncan Davidson, Nature Developmental BiologyCancer PathologySomatic VariantGenetic DisorderGenetics	1990	876
Positional cloning and characterization of a paired box- and homeobox-containing gene from the aniridia region Carl C.T. Ton, Harri Hirvonen, Hiroshi Miwa, Cell BiologyComparative GenomicsGeneticsNatural SciencesGenome Structure	1991	870
The human PAX6 gene is mutated in two patients with aniridia Tim Jordan, Isabel M. Hanson, Dmitri Zaletayev, Nature Genetics Genetic DisorderGeneticsPathogenesisPathologyMolecular Genetics	1992	567
Mutations in SOX2 cause anophthalmia Judy Fantes, Nicola Ragge, Sally Ann Lynch, Nature Genetics Ocular DiseaseOphthalmologyGeneticsSox2 Cause AnophthalmiaMolecular Genetics	2003	538
Subnuclear localization of WT1 in splicing or transcription factor domains is regulated by alternative splicing Stefan Larsson, Jean-Paul Charlieu, Kiyoshi Miyagawa, Cell ChromatinTranscriptional RegulationNatural SciencesGeneticsRna Splicing	1995	506
Mutations at the PAX6 locus are found in heterogeneous anterior segment malformations including Peters' anomaly Isabel M. Hanson, Judy Fletcher, Tim Jordan, Nature Genetics Developmental AnomalyDevelopmental BiologyMendelian DisorderGenetic DisorderGenetics	1994	494
Influence of PAX6 Gene Dosage on Development: Overexpression Causes Severe Eye Abnormalities Andreas Schedl, Allyson Ross, Muriel Lee, Cell Ocular DiseaseDevelopmental BiologyOphthalmologyGenetic DisorderGenetics	1996	436
Advances in genetics M. Demerec, Ernst Caspari, J. M. Thoday, Advances in genetics	1947	413

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