Associated Papers
Naturally Occurring Genetic Variants in the Oxytocin Receptor Alter Receptor Signaling Profiles.
Malik M et al.
Acs Pharmacology & Translational Science, 2021
Sequence variants in ESR1 and OXTR are associated with Mayer-Rokitansky-Küster-Hauser syndrome.
Brucker SY et al.
Acta Obstetricia Et Gynecologica Scandinavica, 2017
Novel oxytocin receptor variants in laboring women requiring high doses of oxytocin.
Reinl EL et al.
American Journal of Obstetrics and Gynecology, 2017
Sequence variants in oxytocin pathway genes and preterm birth: a candidate gene association study.
Kim J et al.
Bmc Medical Genetics, 2013
Evidence for the involvement of genetic variation in the oxytocin receptor gene (OXTR) in the etiology of autistic disorders on high-functioning level.
Wermter AK et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics, 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
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