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The Lancet. Neurology|December 3, 2013
The genetic basis of DOORS syndrome: an exome-sequencing studyPhilippe M Campeau, Dalia Kasperaviciute, James T Lu, et al.
Research Square|April 10, 2023
Unraveling Neuro-Proteogenomic Landscape and Therapeutic Implications for Human Behaviors and Psychiatric DisordersLinda Repetto, Jiantao Chen, Zhijian Yang, et al.
Medrxiv : the Preprint Server for Health Sciences|February 24, 2023
Genetic mechanisms of 184 neuro-related proteins in human plasmaLinda Repetto, Jiantao Chen, Zhijian Yang, et al.
Archives of Pathology & Laboratory Medicine|February 10, 2022
Placental Tissue Destruction and Insufficiency From COVID-19 Causes Stillbirth and Neonatal Death From Hypoxic-Ischemic InjuryDavid A Schwartz, Elyzabeth Avvad-Portari, Pavel Babál, et al.
The American Journal of Psychiatry|July 29, 2017
Rare Genome-Wide Copy Number Variation and Expression of Schizophrenia in 22q11.2 Deletion SyndromeAnne S Bassett, Chelsea Lowther, Daniele Merico, et al.
Circulation. Cardiovascular Genetics|October 14, 2017
Genome-Wide Association Study to Find Modifiers for Tetralogy of Fallot in the 22q11.2 Deletion Syndrome Identifies Variants in the GPR98 Locus on 5q14.3Tingwei Guo, Gabriela M Repetto, Donna M McDonald McGinn, et al.
Archives of Toxicology|May 3, 2011
Alternative (non-animal) methods for cosmetics testing: current status and future prospects-2010Sarah Adler, David Basketter, Stuart Creton, et al.
Nature Human Behaviour|August 29, 2024
The genetic landscape of neuro-related proteins in human plasmaLinda Repetto, Jiantao Chen, Zhijian Yang, et al.
Human Mutation|April 13, 2021
Clinical, neuroimaging, and molecular spectrum of TECPR2-associated hereditary sensory and autonomic neuropathy with intellectual disabilitySonja Neuser, Barbara Brechmann, Gali Heimer, et al.
American Journal of Human Genetics|December 25, 2019
Complete Sequence of the 22q11.2 Allele in 1,053 Subjects with 22q11.2 Deletion Syndrome Reveals Modifiers of Conotruncal Heart DefectsYingjie Zhao, Alexander Diacou, H Richard Johnston, et al.
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