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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2022 | 2 |
2023 | 4 |
2024 | 1 |
Search Results
6 results
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Page 1
Rare coding variation provides insight into the genetic architecture and phenotypic context of autism.
Nat Genet. 2022 Sep;54(9):1320-1331. doi: 10.1038/s41588-022-01104-0. Epub 2022 Aug 18.
Nat Genet. 2022.
PMID: 35982160
Free PMC article.
In Search of Biomarkers to Guide Interventions in Autism Spectrum Disorder: A Systematic Review.
Parellada M, Andreu-Bernabeu Á, Burdeus M, San José Cáceres A, Urbiola E, Carpenter LL, Kraguljac NV, McDonald WM, Nemeroff CB, Rodriguez CI, Widge AS, State MW, Sanders SJ.
Parellada M, et al.
Am J Psychiatry. 2023 Jan 1;180(1):23-40. doi: 10.1176/appi.ajp.21100992. Epub 2022 Dec 7.
Am J Psychiatry. 2023.
PMID: 36475375
Free PMC article.
Review.
Item in Clipboard
Neuropsychiatric biomarker discovery: go big or go home.
Ljungdahl A, Sanders SJ.
Ljungdahl A, et al.
Trends Mol Med. 2023 Nov;29(11):878-879. doi: 10.1016/j.molmed.2023.09.002. Epub 2023 Sep 14.
Trends Mol Med. 2023.
PMID: 37714797
Free PMC article.
Item in Clipboard
AlphaMissense is better correlated with functional assays of missense impact than earlier prediction algorithms.
Ljungdahl A, Kohani S, Page NF, Wells ES, Wigdor EM, Dong S, Sanders SJ.
Ljungdahl A, et al.
bioRxiv [Preprint]. 2023 Oct 27:2023.10.24.562294. doi: 10.1101/2023.10.24.562294.
bioRxiv. 2023.
PMID: 37961354
Free PMC article.
Preprint.
Item in Clipboard
Characterization of De Novo Promoter Variants in Autism Spectrum Disorder with Massively Parallel Reporter Assays.
Koesterich J, An JY, Inoue F, Sohota A, Ahituv N, Sanders SJ, Kreimer A.
Koesterich J, et al.
Int J Mol Sci. 2023 Feb 9;24(4):3509. doi: 10.3390/ijms24043509.
Int J Mol Sci. 2023.
PMID: 36834916
Free PMC article.
Item in Clipboard
De novo variants in the non-coding spliceosomal snRNA gene RNU4-2 are a frequent cause of syndromic neurodevelopmental disorders.
Chen Y, Dawes R, Kim HC, Stenton SL, Walker S, Ljungdahl A, Lord J, Ganesh VS, Ma J, Martin-Geary AC, Lemire G, D'Souza EN, Dong S, Ellingford JM, Adams DR, Allan K, Bakshi M, Baldwin EE, Berger SI, Bernstein JA, Brown NJ, Burrage LC, Chapman K, Compton AG, Cunningham CA, D'Souza P, Délot EC, Dias KR, Elias ER, Evans CA, Ewans L, Ezell K, Fraser JL, Gallacher L, Genetti CA, Grant CL, Haack T, Kuechler A, Lalani SR, Leitão E, Fevre AL, Leventer RJ, Liebelt JE, Lockhart PJ, Ma AS, Macnamara EF, Maurer TM, Mendez HR, Montgomery SB, Nassogne MC, Neumann S, O'Leary M, Palmer EE, Phillips J, Pitsava G, Pysar R, Rehm HL, Reuter CM, Revencu N, Riess A, Rius R, Rodan L, Roscioli T, Rosenfeld JA, Sachdev R, Simons C, Sisodiya SM, Snell P, Clair L, Stark Z, Tan TY, Tan NB, Temple SE, Thorburn DR, Tifft CJ, Uebergang E, VanNoy GE, Vilain E, Viskochil DH, Wedd L, Wheeler MT, White SM, Wojcik M, Wolfe LA, Wolfenson Z, Xiao C, Zocche D, Rubenstein JL, Markenscoff-Papadimitriou E, Fica SM, Baralle D, Depienne C, MacArthur DG, Howson JM, Sanders SJ, O'Donnell-Luria A, Whiffin N.
Chen Y, et al.
medRxiv [Preprint]. 2024 Apr 9:2024.04.07.24305438. doi: 10.1101/2024.04.07.24305438.
medRxiv. 2024.
PMID: 38645094
Free PMC article.
Preprint.
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