Publications Niklas Dahl

Publications in DiVA (Niklas Dahl)

Publications in PubMed (Niklas Dahl)

Selected publications

  1. Schuster J, Klar J, Khalfallah A, Laan L, Hoeber J, Fatima A, Sequeira VM, Jin Z, Korol SV, Huss M, Nordgren A, Anderlid BM, Gallant C, Birnir B, Dahl N. ZEB2 haploinsufficient Mowat-Wilson syndrome iPSCs show disrupted GABAergic transcriptional regulation and function. Front Mol Neurosci. 2022, 15:988993. eCollection 2022.
  2. Schuster J, de Guidi C, Tripathi R, Klar J, Dahl N. Generation of a human iPSC line (UUIGPi015-A) from a patient with Dravet Syndrome and a 2.9 Mb deletion spanning SCN1A on chromosome 2. Stem Cell Res. 2022, 60:102712.
  3. Fineschi S, Klar S, Ayoola Gustafsson K, Jonsson K, Karlsson B, Dahl N. Inflammation and interferon signatures in peripheral B-lymphocytes and sera of individuals with fibromyalgia. Front Immunol. 2022, 13:874490
  4. Fatima A, Hoeber J, Schuster J, Koshimizu E, Maya-Gonzalez C, Keren B, Mignot C, Akram T, Ali Z, Miyatake S, Tanigawa J, Koike T, Kato M, Murakami Y, Abdullah U, Akhtar Ali M, Fadoul R, Laan L, Castillejo-López C, Liik M, Jin Z, Birnir B, Matsumoto N, Baig S, Klar J, Dahl N (2021) Mono-allelic and Bi-allelic Variants in NCDN Cause Neurodevelopmental Delay, Intellectual Disability and Epilepsy. Am J Hum Genet. 2021, S0002-9297(21)00057-4.
  5. Klar J, Engstrand-Lilja H, Maqbool K, Mattisson J, Feuk L, Dahl N (2020) Whole genome sequencing of familial isolated oesophagus atresia uncover shared structural variants. BMC Med Genomics. 2020, 13(1):85.
  6. Fatima A, Schuster J, Akram T, González CM, Hoeber J, Dahl N (2020) Generation of a human Neurochondrin deficient iPSC line KICRi002-A-3 using CRISPR/Cas9. Stem Cell Res. 2020, 101758.
  7. Laan L, Klar J, Sobol M, Hoeber J, Shahsavani M, Kele M, Fatima A, Zakaria M, Annerén G, Falk A, Schuster J, Dahl N (2020) DNA methylation changes in Down syndrome derived neural iPSCs uncover co-dysregulation of ZNF and HOX3 families of transcription factors. Clin Epigenetics. 2020, 12(1):9.
  8. Kvarnung M, Shahsavani M, Taylan F, Breeuwsma N, Laan L, Schuster J, Jin Z, Nilsson D, Lieden A, Edvardsson S, Anderlid BM, Nordenskjöld M, Syk Lundberg E, Birnir B, Dahl N, Nordgren A, Lindstrand A, Falk A. Absence of NFASC isoform NF186 causes an autosomal recessive ataxia syndrome. Front Genet. 2019, 10:896.
  9. Schuster J, Laan L, Klar J, Jin Z, Huss M, Korol M, Noraddin FH, Sobol M, Birnir B, Dahl N. Transcriptomes of Dravet syndrome iPSC derived GABAergic cells reveal dysregulation of pathways for chromatin remodeling and neurodevelopment. Neurobiol Dis 2019, 132:104583.
  10. Sobol M, Klar J, Laan L, Mansoureh S, Schuster J, Annerén G, Berquist J, Nordlund J, Hoeber J, Huss M, Falk A, Dahl N. Transcriptome and proteome profiling of neural induced pluripotent stem cells from individuals with Down syndrome discloses dynamic dysregulations of key pathways and cellular functions. Mol Neurobiol. 2019, 56(10):7113-7127.

Last modified: 2023-01-27
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