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Concordance of genetic variation that increases risk for To..:

Mufford, Mary ; Cheung, Josh ; Jahanshad, Neda...
qt60x1f9cd. , 2019

Link: https://escholarship.org/uc/item/60x1f9cd

RT Journal
T1 <Title>Concordance of genetic variation that increases risk for Tourette Syndrome and that influences its underlying neurocircuitry</Title>

UL https://suche.suub.uni-bremen.de/peid=base-ftcdlib:oai:escholarship.org:ark:_13030_qt60x1f9cd&Exemplar=1&LAN=DE
				
A1 Mufford, Mary
A1 Cheung, Josh
A1 Jahanshad, Neda
A1 van der Merwe, Celia
A1 Ding, Linda
A1 Groenewold, Nynke
A1 Koen, Nastassja
A1 Chimusa, Emile R
A1 Dalvie, Shareefa
A1 Ramesar, Raj
A1 Knowles, James A
A1 Lochner, Christine
A1 Hibar, Derrek P
A1 Paschou, Peristera
A1 van den Heuvel, Odile A
A1 Medland, Sarah E
A1 Scharf, Jeremiah M
A1 Mathews, Carol A
A1 Thompson, Paul M
A1 Stein, Dan J
PB eScholarship, University of California
YR 2019
K1 Biological Psychology
K1 Psychology
K1 Tourette Syndrome
K1 Neurodegenerative
K1 Genetics
K1 Brain Disorders
K1 Serious Mental Illness
K1 Mental Health
K1 Neurosciences
K1 Human Genome
K1 2.1 Biological and endogenous factors
K1 Aetiology
K1 Case-Control Studies
K1 DNA Mutational Analysis
K1 Genetic Pleiotropy
K1 Genetic Predisposition to Disease
K1 Genome-Wide Association Study
K1 Hippocampus
K1 Humans
K1 Linkage Disequilibrium
K1 Magnetic Resonance Imaging
K1 Neural Pathways
K1 Polymorphism
K1 Single Nucleotide
K1 Putamen
K1 Psychiatric Genomics Consortium - Tourette Syndrome working group
K1 Clinical Sciences
K1 Public Health and Health Services
JF qt60x1f9cd
LK http://dx.doi.org/https://escholarship.org/uc/item/60x1f9cd
DO https://escholarship.org/uc/item/60x1f9cd
SF ELIB - SuUB Bremen

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