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Clinical Genetics|December 8, 1998
Genetic variation in paraoxonase-2 is associated with variation in plasma lipoproteins in Canadian Oji-CreeR A Hegele, S B Harris, P W Connelly, et al.Plos One|June 24, 2014
Novel population specific autosomal copy number variation and its functional analysis amongst Negritos from Peninsular MalaysiaSiti Shuhada Mokhtar, Christian R Marshall, Maude E Phipps, et al.Journal of Autism and Developmental Disorders|July 12, 2012
Parents' perspectives on participating in genetic research in autismMagan Trottier, Wendy Roberts, Irene Drmic, et al.BMC Medical Genomics|May 9, 2015
Individualized medicine enabled by genomics in Saudi ArabiaMuhammad Abu-Elmagd, Mourad Assidi, Hans-Juergen Schulten, et al.Neurology. Genetics|May 31, 2018
Chorea-acanthocytosis: Homozygous 1-kb deletion in VPS13A detected by whole-genome sequencingSusan Walker, Rubina Dad, Bhooma Thiruvahindrapuram, et al.Annals of Clinical and Translational Neurology|April 26, 2019
Dominant LMAN2L mutation causes intellectual disability with remitting epilepsyReem A Alkhater, Peixiang Wang, Alessandra Ruggieri, et al.Gene|August 26, 1998
Human PON2 gene at 7q21.3: cloning, multiple mRNA forms, and missense polymorphisms in the coding sequenceH Mochizuki, S W Scherer, T Xi, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 29, 2012
1q21.1 Microduplication expression in adultsAlessia Dolcetti, Candice K Silversides, Christian R Marshall, et al.Elife|August 9, 2022
Temporal analysis of enhancers during mouse cerebellar development reveals dynamic and novel regulatory functionsMiguel Ramirez, Yuliya Badayeva, Joanna Yeung, et al.Molecular Autism|May 14, 2020
Modeling neuronal consequences of autism-associated gene regulatory variants with human induced pluripotent stem cellsP Joel Ross, Rebecca S F Mok, Brandon S Smith, et al.Pageof 88