Varaico: Literature-Extracted Genetic Variants

Gene:OXTR
Variant:p.A218T
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OXTR

NM_000916.4:p.A218T

Associated Papers

Functional significance of some common oxytocin receptor SNPs involved in complex human traits.

Ma SL et al.

Bmc Molecular and Cell Biology, 2025

Predicting oxytocin binding dynamics in receptor genetic variants through computational modeling.

Dubey P et al.

Npj Women's Health, 2025

R150S mutation in the human oxytocin receptor: Gain-of-function effects and implication in autism spectrum disorder.

Liu X et al.

Peptides, 2024

Single nucleotide variations encoding missense mutations in G protein-coupled receptors may contribute to autism.

van der Westhuizen ET

British Journal of Pharmacology, 2024

Association of verbal and non-verbal theory of mind abilities with non-coding variants of OXTR in youth with autism spectrum disorder and typically developing individuals: a case-control study.

Ghamari R et al.

Bmc Psychiatry, 2024

Structure-function relationships of the disease-linked A218T oxytocin receptor variant.

Meyer M et al.

Molecular Psychiatry, 2022

Naturally Occurring Genetic Variants in the Oxytocin Receptor Alter Receptor Signaling Profiles.

Malik M et al.

Acs Pharmacology & Translational Science, 2021

Prioritization of candidate genes for a South African family with Parkinson's disease using in-silico tools.

Sebate B et al.

Plos One, 2021

33770142 (PubMed )
Supplement: pone.0249324.s003.xlsx › 8772__III-8__

The repertoire of family A-peptide GPCRs in archaic hominins.

Mata X et al.

Peptides, 2019

Influence of oxytocin receptor single nucleotide sequence variants on contractility of human myometrium: an in vitro functional study.

Füeg F et al.

Bmc Medical Genetics, 2019

Novel oxytocin receptor variants in laboring women requiring high doses of oxytocin.

Reinl EL et al.

American Journal of Obstetrics and Gynecology, 2017

Resequencing and association analysis of OXTR with autism spectrum disorder in a Japanese population.

Egawa J et al.

Psychiatry and Clinical Neurosciences, 2015

Novel rare variations of the oxytocin receptor (OXTR) gene in autism spectrum disorder individuals.

Liu X et al.

Human Genome Variation, 2015

27081536 (PubMed )
Supplement: hgv201524-s2.xls › Supplenmentary_Table_2

Large-scale polymorphism discovery in macaque G-protein coupled receptors.

Goswami DB et al.

Bmc Genomics, 2013

Sequence variants in oxytocin pathway genes and preterm birth: a candidate gene association study.

Kim J et al.

Bmc Medical Genetics, 2013

Variation in the oxytocin receptor gene is associated with pair-bonding and social behavior.

Walum H et al.

Biological Psychiatry, 2012

Oxytocin receptor genetic variation promotes human trust behavior.

Krueger F et al.

Frontiers in Human Neuroscience, 2012

No association between oxytocin receptor (OXTR) gene polymorphisms and experimentally elicited social preferences.

Apicella CL et al.

Plos One, 2010

Search for autism loci by combined analysis of Autism Genetic Resource Exchange and Finnish families.

Ylisaukko-oja T et al.

Annals of Neurology, 2006

[Polymorphism of exon 4 in the CANP-3 gene in patients with primary myopathies].

Lipatova NA et al.

Genetika, 1999

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Regarding the variants extracted from papers and shown text snippets from research papers, the following holds: "Some rights reserved. This work permits non-commercial use, distribution and reproduction in any medium, provided the original author and source are credited."