Publications:

Relationship of a common OXTR gene variant to brain structure and default mode network function in healthy humans.

Neuroimage

Wang, Junping J; Braskie, Meredith N MN; Hafzalla, George W GW; Faskowitz, Joshua J; McMahon, Katie L KL; de Zubicaray, Greig I GI; Wright, Margaret J MJ; Yu, Chunshui C; Thompson, Paul M PM

Publication Date: 2017-02-15

Variant appearance in text: rs237875

PubMed Link: 28017919

Variant Present in the following documents:

• Main text

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Association of oxytocin receptor (OXTR) gene variants with multiple phenotype domains of autism spectrum disorder.

Journal Of Neurodevelopmental Disorders

Campbell, Daniel B DB; Datta, Dibyadeep D; Jones, Shaine T ST; Batey Lee, Evon E; Sutcliffe, James S JS; Hammock, Elizabeth A D EA; Levitt, Pat P

Publication Date: 2011-06

Variant appearance in text: rs237875

PubMed Link: 21484202

Variant Present in the following documents:

• Main text
• 11689_2010_Article_9071.pdf

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Genetic risk factors for hepatopulmonary syndrome in patients with advanced liver disease.

Gastroenterology

Roberts, Kari E KE; Kawut, Steven M SM; Krowka, Michael J MJ; Brown, Robert S RS; Trotter, James F JF; Shah, Vijay V; Peter, Inga I; Tighiouart, Hocine H; Mitra, Nandita N; Handorf, Elizabeth E; Knowles, James A JA; Zacks, Steven S; Fallon, Michael B MB; ,

Publication Date: 2010-07

Variant appearance in text: rs237875

PubMed Link: 20346360

Variant Present in the following documents:

• Main text

View BVdb publication page