Alicia Ljungdahl

Title(s)	Junior Specialist, Psychiatry
School	School of Medicine
Phone	--
ORCID	0000-0002-3742-7003
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Publications

Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Researchers can login to make corrections and additions, or contact us for help. to make corrections and additions.

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PMC Citations indicate the number of times the publication was cited by articles in PubMed Central, and the Altmetric score represents citations in news articles and social media. (Note that publications are often cited in additional ways that are not shown here.) Fields are based on how the National Library of Medicine (NLM) classifies the publication's journal and might not represent the specific topic of the publication. Translation tags are based on the publication type and the MeSH terms NLM assigns to the publication. Some publications (especially newer ones and publications not in PubMed) might not yet be assigned Field or Translation tags.) Click a Field or Translation tag to filter the publications.

Haploinsufficiency underlies the neurodevelopmental consequences of SLC6A1 variants. Am J Hum Genet [forthcoming]. 2023. Silva DB, Trinidad M, Ljungdahl A, Revalde JL, Berguig GY, Wallace W, Patrick CS, Bomba L, Arkin M, Dong S, Estrada K, Hutchinson K, LeBowitz JH, Schlessinger A, Johannesen KM, Møller RS, Giacomini KM, Froelich S, Sanders SJ, & Wuster S. View Publication.
AlphaMissense is better correlated with functional assays of missense impact than earlier prediction algorithms. bioRxiv. 2023 Oct 27. Ljungdahl A, Kohani S, Page NF, Wells ES, Wigdor EM, Dong S, Sanders SJ. PMID: 37961354; PMCID: PMC10634779.

View in: PubMed Mentions:
Gordon JA & Binder EB (eds.), Exploring and Exploiting Genetic Risk for Psychiatric Disorders. Data Collection: Next Steps in Psychiatric Genetics. 2023; 31:11. Robinson E, Kim H, Weiner D, Ljungdahl A, & Sanders SJ. View Publication.
Neuropsychiatric biomarker discovery: go big or go home. Trends Mol Med. 2023 Nov; 29(11):878-879. Ljungdahl A, Sanders SJ. PMID: 37714797; PMCID: PMC10879988.

View in: PubMed Mentions: Fields:
Mol Molecular Biology
Translation:Humans
Rare coding variation provides insight into the genetic architecture and phenotypic context of autism. Nat Genet. 2022 09; 54(9):1320-1331. Fu JM, Satterstrom FK, Peng M, Brand H, Collins RL, Dong S, Wamsley B, Klei L, Wang L, Hao SP, Stevens CR, Cusick C, Babadi M, Banks E, Collins B, Dodge S, Gabriel SB, Gauthier L, Lee SK, Liang L, Ljungdahl A, Mahjani B, Sloofman L, Smirnov AN, Barbosa M, Betancur C, Brusco A, Chung BHY, Cook EH, Cuccaro ML, Domenici E, Ferrero GB, Gargus JJ, Herman GE, Hertz-Picciotto I, Maciel P, Manoach DS, Passos-Bueno MR, Persico AM, Renieri A, Sutcliffe JS, Tassone F, Trabetti E, Campos G, Cardaropoli S, Carli D, Chan MCY, Fallerini C, Giorgio E, Girardi AC, Hansen-Kiss E, Lee SL, Lintas C, Ludena Y, Nguyen R, Pavinato L, Pericak-Vance M, Pessah IN, Schmidt RJ, Smith M, Costa CIS, Trajkova S, Wang JYT, Yu MHC, Autism Sequencing Consortium (ASC), Broad Institute Center for Common Disease Genomics (Broad-CCDG), iPSYCH-BROAD Consortium, Cutler DJ, De Rubeis S, Buxbaum JD, Daly MJ, Devlin B, Roeder K, Sanders SJ, Talkowski ME. PMID: 35982160; PMCID: PMC9653013.

View in: PubMed Mentions: 85 Fields:
Gen Genetics
Translation:Humans