about
Analysis of protein-coding genetic variation in 60,706 humansGenetic association signal near NTN4 in Tourette syndromeCNV analysis in Tourette syndrome implicates large genomic rearrangements in COL8A1 and NRXN1.Cross-disorder genome-wide analyses suggest a complex genetic relationship between Tourette's syndrome and OCD.The genetics of Tourette syndrome: a review.Joint oligogenic segregation and linkage analysis using bayesian Markov chain Monte Carlo methods.Involvement of astrocyte metabolic coupling in Tourette syndrome pathogenesisRare Copy Number Variants in NRXN1 and CNTN6 Increase Risk for Tourette Syndrome.Social disinhibition is a heritable subphenotype of tics in Tourette syndromeIdentification of Two Heritable Cross-Disorder Endophenotypes for Tourette Syndrome.De Novo Coding Variants Are Strongly Associated with Tourette Disorder.Analysis of shared heritability in common disorders of the brainSex differences in the genetic architecture of obsessive-compulsive disorderPolygenic Risk Scores Derived From a Tourette Syndrome Genome-wide Association Study Predict Presence of Tics in the Avon Longitudinal Study of Parents and Children CohortExamination of the shared genetic basis of anorexia nervosa and obsessive-compulsive disorder.De Novo Sequence and Copy Number Variants Are Strongly Associated with Tourette Disorder and Implicate Cell Polarity in Pathogenesis
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description
onderzoeker
@nl
researcher ORCID ID = 0000-0001-7901-4365
@en
name
Dongmei Yu
@ast
Dongmei Yu
@en
Dongmei Yu
@nl
type
label
Dongmei Yu
@ast
Dongmei Yu
@en
Dongmei Yu
@nl
prefLabel
Dongmei Yu
@ast
Dongmei Yu
@en
Dongmei Yu
@nl
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P31
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0000-0001-7901-4365