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Medrxiv : the Preprint Server for Health Sciences|July 29, 2024
AD plasma biomarkers are stable for an extended period at -20°C: implications for resource-constrained environmentsBiniyam A Ayele, Patrice L Whitehead, Julianna Pascual, et al.Autism Research : Official Journal of the International Society for Autism Research|October 31, 2009
Identification of chromosome 7 inversion breakpoints in an autistic family narrows candidate region for autism susceptibilityHolly N Cukier, David A Skaar, Melissa Y Rayner-Evans, et al.Autism Research : Official Journal of the International Society for Autism Research|February 18, 2020
Three Brothers With Autism Carry a Stop-Gain Mutation in the HPA-Axis Gene NR3C2Holly N Cukier, Anthony J Griswold, Natalia K Hofmann, et al.Journal of Alzheimer'S Disease : JAD|August 4, 2025
Exploring the stability of Alzheimer's disease plasma biomarkers stored for extended periods at -20°C: Implications for resource-constrained environmentsBiniyam A Ayele, Patrice L Whitehead, Julianna Pascual, et al.Neurology. Genetics|November 9, 2016
SORL1 mutations in early- and late-onset Alzheimer diseaseMichael L Cuccaro, Regina M Carney, Yalun Zhang, et al.Annals of Human Genetics|April 9, 2010
Analysis of single nucleotide polymorphisms in the NOS2A gene and interaction with smoking in age-related macular degenerationJuan A Ayala-Haedo, Paul J Gallins, Patrice L Whitehead, et al.Neurogenetics|June 14, 2006
Investigation of autism and GABA receptor subunit genes in multiple ethnic groupsAnn L Collins, Deqiong Ma, Patrice L Whitehead, et al.Molecular Autism|January 21, 2011
A noise-reduction GWAS analysis implicates altered regulation of neurite outgrowth and guidance in autismJohn P Hussman, Ren-Hua Chung, Anthony J Griswold, et al.Annals of Human Genetics|November 8, 2012
Evaluating mitochondrial DNA variation in autism spectrum disordersAthena Hadjixenofontos, Michael A Schmidt, Patrice L Whitehead, et al.Molecular Autism|November 5, 2011
An X chromosome-wide association study in autism families identifies TBL1X as a novel autism spectrum disorder candidate gene in malesRen-Hua Chung, Deqiong Ma, Kai Wang, et al.Pageof 5