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Systemic Proteome Phenotypes Reveal Defective Metabolic Flexibility in Mecp2 Mutants.
Zlatic SA, Werner E, Surapaneni V, Lee CE, Gokhale A, Singleton K, Duong D, Crocker A, Gentile K, Middleton F, Dalloul JM, Liu WL, Patgiri A, Tarquinio D, Carpenter R, Faundez V. Zlatic SA, et al. Among authors: gentile k. bioRxiv [Preprint]. 2023 Sep 1:2023.04.03.535431. doi: 10.1101/2023.04.03.535431. bioRxiv. 2023. PMID: 37066332 Free PMC article. Updated. Preprint.
Systemic proteome phenotypes reveal defective metabolic flexibility in Mecp2 mutants.
Zlatic SA, Werner E, Surapaneni V, Lee CE, Gokhale A, Singleton K, Duong D, Crocker A, Gentile K, Middleton F, Dalloul JM, Liu WL, Patgiri A, Tarquinio D, Carpenter R, Faundez V. Zlatic SA, et al. Among authors: gentile k. Hum Mol Genet. 2023 Dec 12;33(1):12-32. doi: 10.1093/hmg/ddad154. Hum Mol Genet. 2023. PMID: 37712894
Associations between neurodevelopmental genes, neuroanatomy, and ultra high risk symptoms of psychosis in 22q11.2 deletion syndrome.
Thompson CA, Karelis J, Middleton FA, Gentile K, Coman IL, Radoeva PD, Mehta R, Fremont WP, Antshel KM, Faraone SV, Kates WR. Thompson CA, et al. Among authors: gentile k. Am J Med Genet B Neuropsychiatr Genet. 2017 Apr;174(3):295-314. doi: 10.1002/ajmg.b.32515. Epub 2017 Jan 31. Am J Med Genet B Neuropsychiatr Genet. 2017. PMID: 28139055
Deletion at the SLC1A1 glutamate transporter gene co-segregates with schizophrenia and bipolar schizoaffective disorder in a 5-generation family.
Myles-Worsley M, Tiobech J, Browning SR, Korn J, Goodman S, Gentile K, Melhem N, Byerley W, Faraone SV, Middleton FA. Myles-Worsley M, et al. Among authors: gentile k. Am J Med Genet B Neuropsychiatr Genet. 2013 Mar;162B(2):87-95. doi: 10.1002/ajmg.b.32125. Epub 2013 Jan 22. Am J Med Genet B Neuropsychiatr Genet. 2013. PMID: 23341099
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