Peter Beighton - Concepedia

Author

Peter Beighton

Also Known As

P Beighton, P H Beighton, P. BEIGHTON, P. Beighton, P. H. BEIGHTON, P. H. Beighton, P.H. Beighton, PETER BEIGHTON, PETER H. BEIGHTON, Peter Beighton

720

Publications

24.6K

Citations

H-Index

247

Concepts

All Affiliations

University of Cape Town Groote Schuur Hospital University of the Witwatersrand Red Cross War Memorial Children's Hospital

About

Peter Beighton is an author at University of Cape Town specializing in medicine, orthopaedics, and pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	43	137	12.1K
2	Health Sciences	5	5	120
3	Arts	4	4	61
4	Language Studies	2	2	27
5	Engineering	1	1	16

Peter Beighton

236

Publications

18.5K

Citations

H-Index

Page 1

	Year	Citations
LDL Receptor-Related Protein 5 (LRP5) Affects Bone Accrual and Eye Development Yaoqin Gong, Roger B. Slee, N Fukai, Cell Bone AccrualSclerostinSignal TransductionMolecular PhysiologyDevelopmental Biology	2001	2.2K
Ehlers-Danlos syndromes: Revised nosology, Villefranche, 1997 Peter Beighton, Anne De Paepe, Beat Steinmann, American Journal of Medical Genetics	1998	1.7K
Articular mobility in an African population. Peter Beighton, Louis Solomon, Colin L. Soskolne Annals of the Rheumatic Diseases OsteoarthritisAfrican DiasporaSocial SciencesDemographyHuman Movement	1973	1.7K
Bone Dysplasia Sclerosteosis Results from Loss of the SOST Gene Product, a Novel Cystine Knot–Containing Protein Mary E. Brunkow, Jessica C. Gardner, Jeff Van Ness, The American Journal of Human Genetics Bone DiseaseSclerostinBone Morphogenic ProteinGeneticsPathology	2001	999
International nosology of heritable disorders of connective tissue, Berlin, 1986 Peter Beighton, A. De Paepe, D. M. Danks, American Journal of Medical Genetics Gross AnatomyMendelian DisorderHistopathologyInternational NosologyPathology	1988	729
ORTHOPAEDIC ASPECTS OF THE EHLERS. DANLOS SYNDROME Peter Beighton, Frank Horan Journal of Bone and Joint Surgery - British Volume Ehlers-danlos SyndromeRheumatologyDiagnosisPathologyOrthopaedics	1969	628
A 52‐kb deletion in the <i>SOST‐MEOX1</i> intergenic region on 17q12‐q21 is associated with van Buchem disease in the Dutch population Karen Staehling-Hampton, Sean Proll, Bryan Paeper, American Journal of Medical Genetics SclerostinGeneticsGenetic EpidemiologyPathologyMolecular Genetics	2002	299
Perlecan, the major proteoglycan of basement membranes, is altered in patients with Schwartz-Jampel syndrome (chondrodystrophic myotonia) Sophie Nicole, Claire-Sophie Davoine, Haluk Topaloğlu, Nature Genetics Schwartz-jampel SyndromeSurgical PathologyHistopathologyMajor ProteoglycanPathology	2000	296
Split-Hand/Split-Foot Malformation Is Caused by Mutations in the p63 Gene on 3q27 Peter Ianakiev, Michael W. Kilpatrick, Iva Toudjarska, The American Journal of Human Genetics Split-hand/split-foot Malformation IsThumb HypoplasiaDevelopmental AnomalyDevelopmental BiologyMendelian Disorder	2000	293
Osteoporosis-pseudoglioma syndrome, a disorder affecting skeletal strength and vision, is assigned to chromosome region 11q12-13. Yaoqin Gong, Miikka Vikkula, Laurence M. Boon, PubMed	1996	247

Page 1