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Cathy L. Barr · Study
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Author
Cathy L. Barr
25 works
· latest 2022
· 3 institutions
cluster: provisional
ORCID 0000-0003-0361-0106
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Citations
2,813
Works here
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Most cited in this library
Interrogating the Genetic Determinants of Tourette’s Syndrome and Other Tic Disorders Through Genome-Wide Association Studies
2019 · 408 citations
Partitioning the Heritability of Tourette Syndrome and Obsessive Compulsive Disorder Reveals Differences in Genetic Architecture
2013 · 332 citations
Genome-wide association study of Tourette's syndrome
2012 · 211 citations
Rare Copy Number Variants in NRXN1 and CNTN6 Increase Risk for Tourette Syndrome
2017 · 181 citations
Cross-Disorder Genome-Wide Analyses Suggest a Complex Genetic Relationship Between Tourette’s Syndrome and OCD
2014 · 148 citations
Works
25 shown
Discovery of 42 genome-wide significant loci associated with dyslexia
Nature Genetics
·
2022
·
99 authors
·
Open access
141
citations
Genome-wide analyses of individual differences in quantitatively assessed reading- and language-related skills in up to 34,000 people
Proceedings of the National Academy of Sciences
·
2022
·
94 authors
·
Open access
133
citations
Language Difficulties in School-Age Children With Developmental Dyslexia
Journal of Learning Disabilities
·
2021
·
10 authors
·
Open access
31
citations
Synaptic processes and immune-related pathways implicated in Tourette syndrome
Translational Psychiatry
·
2021
·
56 authors
·
Open access
63
citations
Genome‐wide association study of word reading: Overlap with risk genes for neurodevelopmental disorders
Genes Brain & Behavior
·
2020
·
11 authors
56
citations
Interrogating the Genetic Determinants of Tourette’s Syndrome and Other Tic Disorders Through Genome-Wide Association Studies
American Journal of Psychiatry
·
2019
·
82 authors
·
Open access
408
citations
Rare Copy Number Variants in NRXN1 and CNTN6 Increase Risk for Tourette Syndrome
Neuron
·
2017
·
66 authors
·
Open access
181
citations
Cross-Disorder Genome-Wide Analyses Suggest a Complex Genetic Relationship Between Tourette’s Syndrome and OCD
American Journal of Psychiatry
·
2014
·
99 authors
·
Open access
148
citations
Genetic association signal near NTN 4 in T ourette syndrome
Annals of Neurology
·
2014
·
38 authors
·
Open access
62
citations
Copy Number Variation in Obsessive-Compulsive Disorder and Tourette Syndrome: A Cross-Disorder Study
Journal of the American Academy of Child & Adolescent Psychiatry
·
2014
·
99 authors
·
Open access
141
citations
Association of the ROBO1 gene with reading disabilities in a family‐based analysis
Genes Brain & Behavior
·
2014
·
8 authors
·
Open access
36
citations
Partitioning the Heritability of Tourette Syndrome and Obsessive Compulsive Disorder Reveals Differences in Genetic Architecture
PLoS Genetics
·
2013
·
100 authors
·
Open access
332
citations
Support of the histaminergic hypothesis in Tourette Syndrome: association of the histamine decarboxylase gene in a large sample of families
Journal of Medical Genetics
·
2013
·
24 authors
·
Open access
111
citations
Genome-wide association study of Tourette's syndrome
Molecular Psychiatry
·
2012
·
93 authors
·
Open access
211
citations
Arginine vasopressin 1a receptor gene and maternal behavior: evidence of association and moderation
Genes Brain & Behavior
·
2012
·
6 authors
·
Open access
53
citations
Replication of association between a SLITRK1 haplotype and Tourette Syndrome in a large sample of families
Molecular Psychiatry
·
2011
·
16 authors
63
citations
Genetic Variation in the KIAA0319 5′ Region as a Possible Contributor to Dyslexia
Behavior Genetics
·
2011
·
6 authors
·
Open access
35
citations
Association of reading disabilities with regions marked by acetylated H3 histones in KIAA0319
American Journal of Medical Genetics Part B Neuropsychiatric Genetics
·
2009
·
12 authors
·
Open access
51
citations
The KIAA0319-Like(KIAA0319L)Gene on Chromosome 1p34 as a Candidate for Reading Disabilities
Journal of Neurogenetics
·
2008
·
11 authors
·
Open access
55
citations
Association of SLITRK1 to Gilles de la Tourette Syndrome
American Journal of Medical Genetics Part B Neuropsychiatric Genetics
·
2008
·
6 authors
69
citations
Evidence for the gamma‐amino‐butyric acid type B receptor 1 (GABBR1) gene as a susceptibility factor in obsessive‐compulsive disorder
American Journal of Medical Genetics Part B Neuropsychiatric Genetics
·
2005
·
6 authors
68
citations
Indications of Linkage and Association of Gilles de la Tourette Syndrome in Two Independent Family Samples: 17q25 Is a Putative Susceptibility Region
The American Journal of Human Genetics
·
2004
·
11 authors
·
Open access
70
citations
Support for EKN1 as the susceptibility locus for dyslexia on 15q21
Molecular Psychiatry
·
2004
·
9 authors
127
citations
Myelin oligodendrocyte glycoprotein (MOG) gene is associated with obsessive‐compulsive disorder
American Journal of Medical Genetics Part B Neuropsychiatric Genetics
·
2004
·
7 authors
74
citations
Genome scan for linkage to Gilles de la Tourette syndrome
American Journal of Medical Genetics
·
1999
·
8 authors
94
citations