Detalhe da pesquisa
1.
Epigenome-Wide Association Study of Tic Disorders.
Twin Res Hum Genet
; 18(6): 699-709, 2015 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-26499864
2.
Genome-wide Association Study Points to Novel Locus for Gilles de la Tourette Syndrome.
Biol Psychiatry
; 2023 Feb 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-36738982
3.
De Novo Sequence and Copy Number Variants Are Strongly Associated with Tourette Disorder and Implicate Cell Polarity in Pathogenesis.
Cell Rep
; 24(13): 3441-3454.e12, 2018 09 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-30257206
4.
Investigation of SNP rs2060546 Immediately Upstream to NTN4 in a Danish Gilles de la Tourette Syndrome Cohort.
Front Neurosci
; 10: 531, 2016.
Artigo
em Inglês
| MEDLINE | ID: mdl-27920664
5.
Meta-Analysis of Tourette Syndrome and Attention Deficit Hyperactivity Disorder Provides Support for a Shared Genetic Basis.
Front Neurosci
; 10: 340, 2016.
Artigo
em Inglês
| MEDLINE | ID: mdl-27499730
6.
TS-EUROTRAIN: A European-Wide Investigation and Training Network on the Etiology and Pathophysiology of Gilles de la Tourette Syndrome.
Front Neurosci
; 10: 384, 2016.
Artigo
em Inglês
| MEDLINE | ID: mdl-27601976
7.
TopFed: TCGA tailored federated query processing and linking to LOD.
J Biomed Semantics
; 5: 47, 2014.
Artigo
em Inglês
| MEDLINE | ID: mdl-25937882
8.
Combining evidence of preferential gene-tissue relationships from multiple sources.
PLoS One
; 8(8): e70568, 2013.
Artigo
em Inglês
| MEDLINE | ID: mdl-23950964
9.
De Novo Sequence and Copy Number Variants Are Strongly Associated with Tourette Disorder and Implicate Cell Polarity in Pathogenesis.
Cell Rep
; 25(12): 3544, 2018 Dec 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-30566877