Andrea K. Vaags - Concepedia

Author

Andrea K. Vaags

University of Toronto

Also Known As

A Vaags, A. K. Vaags, A. Vaags, Andrea K Vaags, Andrea K. Vaags, Andrea Vaags, Andrea K. Vaags, Raymond H. Kim

Publications

Citations

H-Index

Concepts

All Affiliations

University of Toronto Hospital for Sick Children SickKids Foundation University of Alberta Mayo Clinic

About

Andrea K. Vaags is an author at University of Toronto specializing in medicine, autism, and genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	4	4	470
2	Health Sciences	1	1	27
3	Social Sciences	1	1	58
4	Biomedical Engineering	1	1	27
5	Cell Biology	1	1	27

Andrea K. Vaags

Publications

968

Citations

H-Index

Page 1

	Year	Citations
Rare Deletions at the Neurexin 3 Locus in Autism Spectrum Disorder Andrea K. Vaags, Anath C. Lionel, Daisuke Sato, The American Journal of Human Genetics Rare DeletionsSyndromic AutismGeneticsPsychiatric GeneticsAutism	2011	213
Disruption of the ASTN2/TRIM32 locus at 9q33.1 is a risk factor in males for autism spectrum disorders, ADHD and other neurodevelopmental phenotypes A. C. Lionel, Kristiina Tammimies, Andrea K. Vaags, Human Molecular Genetics Astn2/trim32 LocusBrain DevelopmentAutism Spectrum DisordersGeneticsMolecular Biology	2013	172
Rare exonic deletions implicate the synaptic organizer Gephyrin (GPHN) in risk for autism, schizophrenia and seizures Anath C. Lionel, Andrea K. Vaags, Daisuke Sato, Human Molecular Genetics	2013	151
CHD2 haploinsufficiency is associated with developmental delay, intellectual disability, epilepsy and neurobehavioural problems Sébastien Chénier, Grace Yoon, Bob Argiropoulos, Journal of Neurodevelopmental Disorders	2014	93
Derivation and Characterization of Canine Embryonic Stem Cell Lines with In Vitro and In Vivo Differentiation Potential Andrea K. Vaags, Suzana Rosic-Kablar, Cathy Gartley, Stem Cells	2008	81
Deletions in 16q24.2 are associated with autism spectrum disorder, intellectual disability and congenital renal malformation Gregory R. Handrigan, David Chitayat, Anath C. Lionel, Journal of Medical Genetics	2013	79
Microdeletions of<i>ELP4</i>Are Associated with Language Impairment, Autism Spectrum Disorder, and Mental Retardation Laura Addis, Joo Wook Ahn, Richard Dobson, Human Mutation Copy-number VariationsGeneticsSmall CnvsSocial SciencesAutism Spectrum Disorder	2015	58
Absent <scp>CNKSR</scp>2 causes seizures and intellectual, attention, and language deficits Andrea K. Vaags, Sarah Bowdin, Mary‐Lou Smith, Annals of Neurology	2014	52
Data sharing to improve concordance in variant interpretation across laboratories: results from the Canadian Open Genetics Repository Chloe Mighton, Amanda Smith, Justin Mayers, Journal of Medical Genetics	2021	30
Long-term tracking of bone marrow progenitor cells following intracoronary injection post-myocardial infarction in swine using MRI John Graham, Warren D. Foltz, Andrea K. Vaags, American Journal of Physiology-Heart and Circulatory Physiology Cell TherapyBmc DeliveryBiomedical EngineeringMagnetic Resonance ImagingLong-term Tracking	2010	27

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