Alicia Ljungdahl
Jr. Specialist
Psychiatry
School of Medicine

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• Posts on X ljungdahlalicia (X.com)

Publications (11)

Top publication keywords:
Autistic DisorderNeurodevelopmental DisordersMutation, MissenseGABA Plasma Membrane Transport Proteinsbeta CateninBrain-Derived Neurotrophic FactorHaploinsufficiencyCodon, InitiatorProteomicsOpen Reading FramesSynapsesUp-RegulationRNA, Small NuclearHigh-Throughput Screening AssaysBiomedical Research

• Targeted BDNF upregulation via upstream open reading frame disruption.
  Molecular therapy : the journal of the American Society of Gene Therapy 2025 Feng N, Goedert T, Svrzikapa N, Yan D, Friedrichsen HJ, Hanson B, Ljungdahl A, Dafinca R, Talbot K, Sanders SJ, Gupta D, Wood MJA, Roberts TC
• Genotypic, functional, and phenotypic characterization in CTNNB1 neurodevelopmental syndrome.
  HGG advances 2025 Žakelj N, Gosar D, Miroševic Š, Sanders SJ, Ljungdahl A, Kohani S, Huang S, Leong LI, An Y, Teo MJ, Moultrie F, Jerala R, Lainšcek D, Forstneric V, Sušjan P, Lisowski L, Perez-Iturralde A, Mrak JO, …
• Minding the synapse: A multi-omic approach reveals hidden regulators of neurodevelopment.
  Cell systems 2025 Ljungdahl A, Dhindsa RS
• De novo variants in the RNU4-2 snRNA cause a frequent neurodevelopmental syndrome.
  Nature 2024 Chen Y, Dawes R, Kim HC, Ljungdahl A, Stenton SL, Walker S, Lord J, Lemire G, Martin-Geary AC, Ganesh VS, Ma J, Ellingford JM, Delage E, D'Souza EN, Dong S, Adams DR, Allan K, Bakshi M, Baldwin EE, …
• Haploinsufficiency underlies the neurodevelopmental consequences of SLC6A1 variants.
  American journal of human genetics 2024 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…

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• De novo variants in the non-coding spliceosomal snRNA gene RNU4-2 are a frequent cause of syndromic neurodevelopmental disorders.
  medRxiv : the preprint server for health sciences 2024 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, …
• 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…
• AlphaMissense is better correlated with functional assays of missense impact than earlier prediction algorithms.
  bioRxiv : the preprint server for biology 2023 Ljungdahl A, Kohani S, Page NF, Wells ES, Wigdor EM, Dong S, Sanders SJ
• Gordon JA & Binder EB (eds.), Exploring and Exploiting Genetic Risk for Psychiatric Disorders
  Data Collection: Next Steps in Psychiatric Genetics 2023 Robinson E, Kim H, Weiner D, Ljungdahl A, & Sanders SJ
• Neuropsychiatric biomarker discovery: go big or go home.
  Trends in molecular medicine 2023 Ljungdahl A, Sanders SJ
• Rare coding variation provides insight into the genetic architecture and phenotypic context of autism.
  Nature genetics 2022 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, …