Regina Regan - Concepedia

Concepedia

Author

Regina Regan

Centre for Human Genetics

Also Known As

Cali, Phil, Chung, Brian H.Y., Klei, Lambertus, R J Regan, R Regan, R. Regan, Regan, R, Regina Regan

54

Publications

11.2K

Citations

27

H-Index

78

Concepts

All Affiliations

Centre for Human Genetics University of Washington University of Oxford University College Dublin Trinity College Dublin

RR

About

Regina Regan is an author at Centre for Human Genetics specializing in medicine, genetics, and neurogenetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	14	15	5K
2	Engineering	2	2	319
3	Health Sciences	2	2	45
4	Public Health	2	2	2K
5	Natural Sciences	1	1	292

Regina Regan

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32

Publications

11.2K

Citations

27

H-Index

	Year	Citations
Functional impact of global rare copy number variation in autism spectrum disorders Dalila Pinto, Alistair T. Pagnamenta, Lambertus Klei, Nature Autism Spectrum DisordersSyndromic AutismGeneticsPsychiatric GeneticsAutism	2010	2K
Analysis of shared heritability in common disorders of the brain Verneri Anttila, Brendan Bulik‐Sullivan, Hilary K. Finucane, Science Brain FunctionPsychiatric DisordersGeneticsGenetic EpidemiologyNeuropsychiatry	2018	2K
Convergence of Genes and Cellular Pathways Dysregulated in Autism Spectrum Disorders Dalila Pinto, Elsa Delaby, Daniele Merico, The American Journal of Human Genetics	2014	1K
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
Discovery of previously unidentified genomic disorders from the duplication architecture of the human genome Andrew J. Sharp, S.K. Hansen, Rebecca R. Selzer, Nature Genetics Mendelian DisorderGenetic DisorderUnidentified Genomic DisordersGeneticsMedicine	2006	663
A recurrent 15q13.3 microdeletion syndrome associated with mental retardation and seizures Andrew J. Sharp, Heather C. Mefford, Kelly Li, Nature Genetics Mendelian DisorderGenetic DisorderPsychiatric GeneticsRecurrent 15Q13.3Mental Retardation	2008	588
A genome-wide scan for common alleles affecting risk for autism Richard Anney, Lambertus Klei, Dalila Pinto, Human Molecular Genetics	2010	585
A new chromosome 17q21.31 microdeletion syndrome associated with a common inversion polymorphism David A. Koolen, Lisenka E.L.M. Vissers, Rolph Pfundt, Nature Genetics Genetic DisorderGeneticsCommon Inversion PolymorphismHuman PolymorphismPathology	2006	466
Subtle chromosomal rearrangements in children with unexplained mental retardation Samantha J.L. Knight, Regina Regan, A Nicod, The Lancet Down SyndromeDevelopmental AnomalySubtle Chromosomal RearrangementsGenetic DisorderGenetics	1999	453
Individual common variants exert weak effects on the risk for autism spectrum disorders Richard Anney, Lambertus Klei, Dalila Pinto, Human Molecular Genetics	2012	372

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