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Page 1
Motor phenotypes associated with genetic neurodevelopmental disorders.
Santana Almansa A, Snyder LG, Chung WK, Bain JM, Srivastava S. Santana Almansa A, et al. Among authors: snyder lg. Ann Clin Transl Neurol. 2024 Dec;11(12):3238-3245. doi: 10.1002/acn3.52231. Epub 2024 Nov 2. Ann Clin Transl Neurol. 2024. PMID: 39487960 Free PMC article.
Return of genetic research results in 21,532 individuals with autism.
Wright JR, Astrovskaya I, Barns SD, Goler A, Zhou X, Shu C, Snyder LG, Han B; SPARK Consortium; Shen Y, Volfovsky N, Hall JB, Feliciano P, Chung WK. Wright JR, et al. Among authors: snyder lg. Genet Med. 2024 Oct;26(10):101202. doi: 10.1016/j.gim.2024.101202. Epub 2024 Jun 29. Genet Med. 2024. PMID: 38958063 Free article.
Integrating de novo and inherited variants in 42,607 autism cases identifies mutations in new moderate-risk genes.
Zhou X, Feliciano P, Shu C, Wang T, Astrovskaya I, Hall JB, Obiajulu JU, Wright JR, Murali SC, Xu SX, Brueggeman L, Thomas TR, Marchenko O, Fleisch C, Barns SD, Snyder LG, Han B, Chang TS, Turner TN, Harvey WT, Nishida A, O'Roak BJ, Geschwind DH; SPARK Consortium; Michaelson JJ, Volfovsky N, Eichler EE, Shen Y, Chung WK. Zhou X, et al. Among authors: snyder lg. Nat Genet. 2022 Sep;54(9):1305-1319. doi: 10.1038/s41588-022-01148-2. Epub 2022 Aug 18. Nat Genet. 2022. PMID: 35982159 Free PMC article.
Neurodevelopmental profile of HIVEP2-related disorder.
Mo A, Snyder LG, Babington O, Chung WK, Sahin M, Srivastava S. Mo A, et al. Among authors: snyder lg. Dev Med Child Neurol. 2022 May;64(5):654-661. doi: 10.1111/dmcn.15100. Epub 2021 Oct 26. Dev Med Child Neurol. 2022. PMID: 34704275 Free PMC article.
Recent ultra-rare inherited variants implicate new autism candidate risk genes.
Wilfert AB, Turner TN, Murali SC, Hsieh P, Sulovari A, Wang T, Coe BP, Guo H, Hoekzema K, Bakken TE, Winterkorn LH, Evani US, Byrska-Bishop M, Earl RK, Bernier RA; SPARK Consortium; Zody MC, Eichler EE. Wilfert AB, et al. Nat Genet. 2021 Aug;53(8):1125-1134. doi: 10.1038/s41588-021-00899-8. Epub 2021 Jul 26. Nat Genet. 2021. PMID: 34312540 Free PMC article.
Availability of Services and Caregiver Burden: Supporting Individuals With Neurogenetic Conditions During the COVID-19 Pandemic.
Kowanda M, Cartner L, Kentros C, Geltzeiler AR, Singer KE, Weaver WC, Lehman CD, Smith S, Smith RS, Walsh LK, Diehl K, Nagpal N, Brooks E, Mebane CM, Wilson AL, Marvin AR, White LC, Law JK, Jensen W, Daniels AM, Tjernagel J, Snyder LG, Taylor CM, Chung WK. Kowanda M, et al. Among authors: snyder lg. J Child Neurol. 2021 Aug;36(9):760-767. doi: 10.1177/08830738211001209. Epub 2021 Apr 8. J Child Neurol. 2021. PMID: 33829918 Free PMC article.
16p11.2 deletion syndrome.
Chung WK, Roberts TP, Sherr EH, Snyder LG, Spiro JE. Chung WK, et al. Among authors: snyder lg. Curr Opin Genet Dev. 2021 Jun;68:49-56. doi: 10.1016/j.gde.2021.01.011. Epub 2021 Mar 2. Curr Opin Genet Dev. 2021. PMID: 33667823 Free PMC article. Review.
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