David I. Wilson - Concepedia

Author

David I. Wilson

Also Known As

D I Wilson, D WILSON, D Wilson, D. I. Wilson, D. Wilson, D.I Wilson, D.I. Wilson, DAVID I WILSON, DAVID I. WILSON, DI Wilson

167

Publications

10.8K

Citations

H-Index

159

Concepts

All Affiliations

University of Southampton Newcastle University Southampton General Hospital University of Edinburgh Imperial College London

About

David I. Wilson is an author at University of Southampton specializing in medicine, genetics, and developmental biology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	32	43	7.6K
2	Health Sciences	6	6	1.3K
3	Business	1	1	15
4	Management	1	1	15
5	Natural Sciences	1	1	121

David I. Wilson

Publications

9.7K

Citations

H-Index

Page 1

	Year	Citations
Spectrum of clinical features associated with interstitial chromosome 22q11 deletions: a European collaborative study. A K Ryan, Judith A. Goodship, David I. Wilson, Journal of Medical Genetics CytogeneticsGeneticsGenetic EpidemiologyEuropean Collaborative StudyPathology	1997	1.2K
Holt-Oram syndrome is caused by mutations in TBX5, a member of the Brachyury (T) gene family Newbury-Ecob Ra, David I. Wilson, T Strachan, Nature Genetics Developmental AnomalyGenetic DisorderGeneticsPathogenesisPathology	1997	925
DiGeorge syndrome: part of CATCH 22. David I. Wilson, John Burn, Peter Scambler, Journal of Medical Genetics GeneticsPathologyCongenital Heart AnomalyClinical GeneticsMendelian Disorder	1993	511
Endoglin, an Ancillary TGFβ Receptor, Is Required for Extraembryonic Angiogenesis and Plays a Key Role in Heart Development Helen M. Arthur, Jan Ure, Andrew J. H. Smith, Developmental Biology AngiogenesisDevelopmental BiologyExtraembryonic AngiogenesisPhysiologyMorphogenesis	2000	435
Velo-cardio-facial syndrome associated with chromosome 22 deletions encompassing the DiGeorge locus Peter Scambler, David A. Kelly, Elizabeth Lindsay, The Lancet Genetic DisorderGeneticsPathologyCongenital Heart DefectDigeorge Locus	1992	418
Mutations in a new gene in Ellis-van Creveld syndrome and Weyers acrodental dysostosis Víctor L. Ruiz‐Pérez, Susan Ide, Tim M. Strom, Nature Genetics Developmental AnomalyMendelian DisorderGenetic DisorderGeneticsNew Gene	2000	350
SRY, SOX9, and DAX1 expression patterns during human sex determination and gonadal development Neil A. Hanley, D.M. Hagan, Mark Clement-Jones, Mechanisms of Development Developmental BiologyGerm Cell FateSex DeterminationDevelopmental GeneticsGenetics	2000	329
Mutation of ALMS1, a large gene with a tandem repeat encoding 47 amino acids, causes Alström syndrome Tom Hearn, Glenn L. Renforth, C. Mirella Spalluto, Nature Genetics Alström SyndromeLarge GeneTandem RepeatAmyotrophic Lateral SclerosisMendelian Disorder	2002	312
A homeobox gene, HLXB9, is the major locus for dominantly inherited sacral agenesis Alison Ross, Víctor L. Ruiz‐Pérez, Yiming Wang, Nature Genetics BiologyDevelopmental BiologyGenetic DisorderGeneticsMajor Locus	1998	289
Conotruncal anomaly face syndrome is associated with a deletion within chromosome 22q11. John Burn, Atsuyoshi Takao, David I. Wilson, Journal of Medical Genetics Probe Do832Developmental AnomalyGenetic DisorderPathologyCraniofacial Anomalies	1993	269

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