Publications by authors named "Ryan Chao"

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Regional Anesthesia as an Alternative to Moderate Sedation for Perioperative Pain Control for Percutaneous Gastrostomy Tube Placement.
Dalen Kuang, Ryan Chao, Jiwon Youm, Stephen Hugdal, Brett Miller

J Vasc Interv Radiol· November 2022

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F-18 FDG perfusion PET: intraprocedural assessment of the liver tumor ablation margin.
Paul B Shyn, Alan J Cubre, Paul J Catalano, Leslie K Lee, Hyewon Hyun, Ryan T Chao

Abdom Radiol (NY)· July 2021

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Developing a mHealth Routine Outcome Monitoring and Feedback App ("SMART Track") to Support Self-Management of Addictive Behaviours.
Alison K Beck, Peter J Kelly, Frank P Deane, Amanda L Baker, Leanne Hides, Ryan Chao

Front Psychiatry· June 2021

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Healthy beginnings: a system of care for children in Atlanta.
Ryan Chao, Susan Bertonaschi, Julie Gazmararian

Health Aff (Millwood)· December 2014

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VAX1 mutation associated with microphthalmia, corpus callosum agenesis, and orofacial clefting: the first description of a VAX1 phenotype in humans.
Anne M Slavotinek, Ryan Chao, Tomas Vacik, Mani Yahyavi, Hana Abouzeid

Hum Mutat· February 2012

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Manitoba-oculo-tricho-anal (MOTA) syndrome is caused by mutations in FREM1.
Anne M Slavotinek, Sergio E Baranzini, Denny Schanze, Cassandre Labelle-Dumais, Kieran M Short, Ryan Chao

J Med Genet· June 2011

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A de novo deletion of CALN1 in a male with a bilateral diaphragmatic defect does not definitely cause this malformation.
Anne M Slavotinek, Jill A Rosenfeld, Ryan Chao, Dimitry Niyazov, Marthand Eswara

Am J Med Genet A· May 2011

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A male with unilateral microphthalmia reveals a role for TMX3 in eye development.
Ryan Chao, Linda Nevin, Pooja Agarwal, Jan Riemer, Xiaoyang Bai

PLoS One· May 2010

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A maternally inherited chromosome 18q22.1 deletion in a male with late-presenting diaphragmatic hernia and microphthalmia-evaluation of DSEL as a candidate gene for the diaphragmatic defect.
Hatem Zayed, Ryan Chao, Ali Moshrefi, Nelson Lopezjimenez, Allen Delaney

Am J Med Genet A· April 2010

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