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Page 1
Large 22q13.3 deletions perturb peripheral transcriptomic and metabolomic profiles in Phelan-McDermid syndrome.
Breen MS, Fan X, Levy T, Pollak RM, Collins B, Osman A, Tocheva AS, Sahin M, Berry-Kravis E, Soorya L, Thurm A, Powell CM, Bernstein JA, Kolevzon A, Buxbaum JD; Developmental Synaptopathies Consortium. Breen MS, et al. Among authors: soorya l. HGG Adv. 2022 Sep 26;4(1):100145. doi: 10.1016/j.xhgg.2022.100145. eCollection 2023 Jan 12. HGG Adv. 2022. PMID: 36276299 Free PMC article.
Atypical Functional Connectivity During Unfamiliar Music Listening in Children With Autism.
Freitas C, Hunt BAE, Wong SM, Ristic L, Fragiadakis S, Chow S, Iaboni A, Brian J, Soorya L, Chen JL, Schachar R, Dunkley BT, Taylor MJ, Lerch JP, Anagnostou E. Freitas C, et al. Among authors: soorya l. Front Neurosci. 2022 Apr 19;16:829415. doi: 10.3389/fnins.2022.829415. eCollection 2022. Front Neurosci. 2022. PMID: 35516796 Free PMC article.
Multiplex ligation-dependent probe amplification for genetic screening in autism spectrum disorders: efficient identification of known microduplications and identification of a novel microduplication in ASMT.
Cai G, Edelmann L, Goldsmith JE, Cohen N, Nakamine A, Reichert JG, Hoffman EJ, Zurawiecki DM, Silverman JM, Hollander E, Soorya L, Anagnostou E, Betancur C, Buxbaum JD. Cai G, et al. Among authors: soorya l. BMC Med Genomics. 2008 Oct 16;1:50. doi: 10.1186/1755-8794-1-50. BMC Med Genomics. 2008. PMID: 18925931 Free PMC article.
76 results