Association between AVPR1A, DRD2, and ASPM and endophenotypes of communication disorders-Reference-Cited by-同舟云学术

Association between AVPR1A, DRD2, and ASPM and endophenotypes of communication disorders

Published:2014-10 Issue:5 Volume:24 Page:191-200
ISSN:0955-8829
Container-title:Psychiatric Genetics
language:en
Short-container-title:

Author:

Stein Catherine M.,Truitt Barbara,Deng Fenghua,Ciesla Allison Avrich,Qiu Feiyou,Joseph Peronne,Raghavendra Rekha,Fondran Jeremy,Igo Robert P.,Tag Jessica,Freebairn Lisa,Taylor H. Gerry,Lewis Barbara A.,Iyengar Sudha K.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Biological Psychiatry,Psychiatry and Mental health,Genetics(clinical),Genetics

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1. Contributions of common genetic variants to specific languages and to when a language is learned;Scientific Reports;2022-01-12

2. ASPM -lexical tone association in speakers of a tone language: Direct evidence for the genetic-biasing hypothesis of language evolution;Science Advances;2020-05-29

3. A truncating Aspm allele leads to a complex cognitive phenotype and region-specific reductions in parvalbuminergic neurons;Translational Psychiatry;2020-02-13

4. Emotion recognition associated with polymorphism in oxytocinergic pathway gene ARNT2;Social Cognitive and Affective Neuroscience;2017-11-28

5. The DYX2 locus and neurochemical signaling genes contribute to speech sound disorder and related neurocognitive domains;Genes, Brain and Behavior;2015-04