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American Journal of Human Genetics|November 1, 2019
The Human-Specific BOLA2 Duplication Modifies Iron Homeostasis and Anemia Predisposition in Chromosome 16p11.2 Autism IndividualsGiuliana Giannuzzi, Paul J Schmidt, Eleonora Porcu, et al.
Frontiers in Psychiatry|May 26, 2022
Identifying Age Based Maturation in the ERP Response to Faces in Children With Autism: Implications for Developing Biomarkers for Use in Clinical TrialsSara Jane Webb, Iris Emerman, Catherine Sugar, et al.
Translational Psychiatry|March 7, 2019
Correction: Psychiatric disorders in children with 16p11.2 deletion and duplicationMaria Niarchou, Samuel J R A Chawner, Joanne L Doherty, et al.
Translational Psychiatry|January 22, 2019
Psychiatric disorders in children with 16p11.2 deletion and duplicationMaria Niarchou, Samuel J R A Chawner, Joanne L Doherty, et al.
Translational Psychiatry|March 5, 2020
Imaging-genetics of sex differences in ASD: distinct effects of OXTR variants on brain connectivityLeanna M Hernandez, Katherine E Lawrence, N Tanya Padgaonkar, et al.
Autism Research : Official Journal of the International Society for Autism Research|March 17, 2023
Evaluation of clinical assessments of social abilities for use in autism clinical trials by the autism biomarkers consortium for clinical trialsSusan Faja, Maura Sabatos-DeVito, Aksheya Sridhar, et al.
Human Genetics|November 17, 2016
Identification of new TRIP12 variants and detailed clinical evaluation of individuals with non-syndromic intellectual disability with or without autismNuria C Bramswig, H-J Lüdecke, M Pettersson, et al.
Brain : a Journal of Neurology|May 29, 2021
Impact of autism genetic risk on brain connectivity: a mechanism for the female protective effectKatherine E Lawrence, Leanna M Hernandez, Emily Fuster, et al.
Frontiers in Integrative Neuroscience|April 30, 2020
The Autism Biomarkers Consortium for Clinical Trials (ABC-CT): Scientific Context, Study Design, and Progress Toward Biomarker QualificationJames C McPartland, Raphael A Bernier, Shafali S Jeste, et al.
Science Advances|June 5, 2021
The CHD8/CHD7/Kismet family links blood-brain barrier glia and serotonin to ASD-associated sleep defectsMireia Coll-Tané, Naihua N Gong, Samuel J Belfer, et al.
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