John A. Crolla - Concepedia

Author

John A. Crolla

Also Known As

J A Crolla, J Crolla, J. A. CROLLA, J. A. Crolla, J. Crolla, J.A Crolla, J.A. Crolla, JOHN A. CROLLA, John A Crolla, John A. Crolla

175

Publications

11.7K

Citations

H-Index

135

Concepts

All Affiliations

Wessex Regional Genetics Laboratory Salisbury District Hospital Princess Anne Hospital University of Southampton Salisbury University

About

John A. Crolla is an author at Wessex Regional Genetics Laboratory specializing in medicine, genetics, and molecular genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	38	56	4.1K
2	Public Health	9	9	567
3	Engineering	2	2	85
4	Education	1	1	128
5	Health Sciences	1	1	51

John A. Crolla

Publications

8.2K

Citations

H-Index

Page 1

	Year	Citations
Recurrent Rearrangements of Chromosome 1q21.1 and Variable Pediatric Phenotypes Heather C. Mefford, Andrew J. Sharp, Carl Baker, New England Journal of Medicine	2008	803
An evidence-based approach to establish the functional and clinical significance of copy number variants in intellectual and developmental disabilities Erin B. Kaminsky, Vineith Kaul, Justin Paschall, Genetics in Medicine Intellectual ImpairmentPsychiatryGenetic DisorderGeneticsDisability	2011	444
Further delineation of the 15q13 microdeletion and duplication syndromes: a clinical spectrum varying from non-pathogenic to a severe outcome Bregje W.M. van Bon, Heather C. Mefford, Björn Menten, Journal of Medical Genetics	2009	366
Deletion 17q12 Is a Recurrent Copy Number Variant that Confers High Risk of Autism and Schizophrenia Daniel Moreno‐De‐Luca, Jennifer G. Mullé, Erin B. Kaminsky, The American Journal of Human Genetics	2010	331
A cytogenetic study of human spontaneous abortions using banding techniques M. R. Creasy, John A. Crolla, Eva Alberman Human Genetics Human Spontaneous AbortionsInfertilityDevelopmental BiologyFertilityAbortion	1976	254
Breakpoint Mapping and Array CGH in Translocations: Comparison of a Phenotypically Normal and an Abnormal Cohort Júlia Baptista, Catherine Mercer, Elena Prigmore, The American Journal of Human Genetics Array CghBiostatisticsBreakpoint MappingAbnormal Cohort	2008	237
Frequent Chromosome Aberrations Revealed by Molecular Cytogenetic Studies in Patients with Aniridia John A. Crolla, Veronica van Heyningen The American Journal of Human Genetics CytogeneticsGenetic DisorderGeneticsPathologyAneuploidy	2002	222
SOX2 Plays a Critical Role in the Pituitary, Forebrain, and Eye during Human Embryonic Development Daniel Kelberman, Sandra C. de Castro, Shuwen Huang, The Journal of Clinical Endocrinology & Metabolism	2008	179
Genetic abnormalities detected in ependymomas by comparative genomic hybridisation M Carter, James C. Nicholson, F. Ross, British Journal of Cancer	2002	172
Clinical and molecular stratification of disease risk in medulloblastoma Richard J. Gilbertson, Chanaka D. Wickramasinghe, Roberto Hernán, British Journal of Cancer	2001	168

Page 1