ADGRL 3 ( LPHN 3) variants are associated with a refined phenotype of ADHD in the MTA study-Reference-Cited by-同舟云学术

ADGRL 3 ( LPHN 3) variants are associated with a refined phenotype of ADHD in the MTA study

Published:2016-07-18 Issue:5 Volume:4 Page:540-547
ISSN:2324-9269
Container-title:Molecular Genetics & Genomic Medicine
language:en
Short-container-title:Mol Genet Genomic Med

Author:

Acosta Maria T.¹²,Swanson James³⁴,Stehli Annamarie⁴,Molina Brooke S. G.⁵,Martinez Ariel F.¹,Arcos‐Burgos Mauricio⁶,Muenke Maximilian¹,

Affiliation:

1. Medical Genetics Branch National Human Genome Research Institute National Institutes of Health Bethesda Maryland

2. Department of Pediatric and Neurology George Washington University Children's National Medical Center Washington District of Columbia

3. Department of Psychiatry Florida International University Miami Florida

4. Department of Pediatrics University of California at Irvine Irvine California

5. Departments of Psychiatry and Psychology University of Pittsburgh Pittsburgh Pennsylvania

6. Genomics and Predictive Medicine Genome Biology Department John Curtin School of Medical Research ANU College of Medicine, Biology and Environment The Australian National University Canberra ACT Australia

Publisher

Wiley

Subject

Genetics(clinical),Genetics,Molecular Biology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/mgg3.230

Reference31 articles.

1. A two-locus genetic interaction between LPHN3 and 11q predicts ADHD severity and long-term outcome

2. Toward a better understanding of ADHD: LPHN3 gene variants and the susceptibility to develop ADHD

3. Attention-Deficit/Hyperactivity Disorder in a Population Isolate: Linkage to Loci at 4q13.2, 5q33.3, 11q22, and 17p11

4. A common variant of the latrophilin 3 gene, LPHN3, confers susceptibility to ADHD and predicts effectiveness of stimulant medication

5. A common genetic network underlies substance use disorders and disruptive or externalizing disorders

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