Publications by authors named "Samantha Ayres"

5Publications

NCKAP1 Disruptive Variants Lead to a Neurodevelopmental Disorder with Core Features of Autism.

Am J Hum Genet 2020 11;107(5):963-976

Center for Medical Genetics, School of Life Sciences, Central South University, Changsha, Hunan 410078, China; Hunan Key Laboratory of Animal Models for Human Diseases, Changsha, Hunan 410078, China; CAS Center for Excellence in Brain Science and Intelligences Technology (CEBSIT), Chinese Academy of Sciences, Shanghai 200000, China. Electronic address:

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http://dx.doi.org/10.1016/j.ajhg.2020.10.002DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7674997PMC
November 2020

Human Genetics Society of Australasia Position Statement: Predictive and Presymptomatic Genetic Testing in Adults and Children.

Twin Res Hum Genet 2020 06;23(3):184-189

Faculty of Medicine and Health, Sydney School of Public Health, Sydney Health Ethics, The University of Sydney, Sydney, NSW, Australia.

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http://dx.doi.org/10.1017/thg.2020.51DOI Listing
June 2020

Genetic counseling in pediatric acute care: Reflections on ultra-rapid genomic diagnoses in neonates.

J Genet Couns 2019 04 21;28(2):273-282. Epub 2019 Jan 21.

Australian Genomics Health Alliance, Melbourne, Australia.

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http://dx.doi.org/10.1002/jgc4.1086DOI Listing
April 2019