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International Psychogeriatrics|February 2, 2025
Genome-wide screen to identify genetic loci associated with cognitive decline in late-life depressionD C Steffens, M E Garrett, K L Soldano, et al.
International Psychogeriatrics|July 10, 2020
Genome-wide screen to identify genetic loci associated with cognitive decline in late-life depressionD C Steffens, M E Garrett, K L Soldano, et al.
Genetic Epidemiology|September 5, 1998
Testing for contributions of mitochondrial DNA mutations to complex diseasesF Sun, A E Ashley-Koch, L K Durham, et al.
American Journal of Human Genetics|August 27, 1998
Examination of factors associated with instability of the FMR1 CGG repeatA E Ashley-Koch, H Robinson, A E Glicksman, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|September 30, 2008
SNPs in dopamine D2 receptor gene (DRD2) and norepinephrine transporter gene (NET) are associated with continuous performance task (CPT) phenotypes in ADHD children and their familiesS H Kollins, A D Anastopoulos, A M Lachiewicz, et al.
Frontiers in Cell and Developmental Biology|June 28, 2023
Gene-nutrient interactions that impact magnesium homeostasis increase risk for neural tube defects in mice exposed to dolutegravirJ Gelineau-van Waes, M A van Waes, J Hallgren, et al.
Neuroscience Letters|April 22, 2005
An autosomal genomic screen for dementia in an extended Amish familyA E Ashley-Koch, Y Shao, J B Rimmler, et al.
American Journal of Human Genetics|April 20, 2001
Identification and expression analysis of spastin gene mutations in hereditary spastic paraplegiaI K Svenson, A E Ashley-Koch, P C Gaskell, et al.
Annals of Human Genetics|May 6, 2006
An analysis paradigm for investigating multi-locus effects in complex disease: examination of three GABA receptor subunit genes on 15q11-q13 as risk factors for autistic disorderA E Ashley-Koch, H Mei, J Jaworski, et al.
American Journal of Human Genetics|August 5, 2005
Identification of significant association and gene-gene interaction of GABA receptor subunit genes in autismD Q Ma, P L Whitehead, M M Menold, et al.
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