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American Journal on Intellectual and Developmental Disabilities|March 4, 2017
Efficacy and Social Validity of Peer Network Interventions for High School Students With Severe DisabilitiesJennifer M Asmus, Erik W Carter, Colleen K Moss, et al.
Translational Psychiatry|October 17, 2022
Wide spectrum of neuronal and network phenotypes in human stem cell-derived excitatory neurons with Rett syndrome-associated MECP2 mutationsRebecca S F Mok, Wenbo Zhang, Taimoor I Sheikh, et al.
Translational Psychiatry|January 8, 2021
Biallelic mutations in the death domain of PIDD1 impair caspase-2 activation and are associated with intellectual disabilityTaimoor I Sheikh, Nasim Vasli, Stephen Pastore, et al.
Nature Genetics|January 19, 2010
Meta-analysis of genome-wide association data identifies a risk locus for major mood disorders on 3p21.1Francis J McMahon, Nirmala Akula, Thomas G Schulze, et al.
The World Journal of Biological Psychiatry : the Official Journal of the World Federation of Societies of Biological Psychiatry|September 30, 2014
Investigation of the genetic interaction between BDNF and DRD3 genes in suicidical behaviour in psychiatric disordersClement C Zai, Mirko Manchia, Ida Elken Sønderby, et al.
American Journal of Human Genetics|October 13, 2006
Absence of a paternally inherited FOXP2 gene in developmental verbal dyspraxiaLars Feuk, Aino Kalervo, Marita Lipsanen-Nyman, et al.
Human Molecular Genetics|February 22, 2015
Mutations in DCPS and EDC3 in autosomal recessive intellectual disability indicate a crucial role for mRNA decapping in neurodevelopmentIltaf Ahmed, Rebecca Buchert, Mi Zhou, et al.
American Journal of Human Genetics|December 7, 2014
Biallelic truncating mutations in FMN2, encoding the actin-regulatory protein Formin 2, cause nonsyndromic autosomal-recessive intellectual disabilityRosalind Law, Tracy Dixon-Salazar, Julie Jerber, et al.
Plos Genetics|March 4, 2021
Genome-wide association study of resistance to Mycobacterium tuberculosis infection identifies a locus at 10q26.2 in three distinct populationsJocelyn Quistrebert, Marianna Orlova, Gaspard Kerner, et al.
American Journal of Human Genetics|July 19, 2011
Mutations in the alpha 1,2-mannosidase gene, MAN1B1, cause autosomal-recessive intellectual disabilityMuhammad Arshad Rafiq, Andreas W Kuss, Lucia Puettmann, et al.
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