Niklas Dahl

Publication Activity (10 Years)

Years Active: 2017-2024
Publications (10 Years): 10

Top Topics

Intellectual Disability

Neural Stem Cells

Top Venues

Clinical epigenetics

BMC medical genetics

This page only lists publications with an associated author ORCID identifier.

Publications

Jens Schuster, Xi Lu, Yonglong Dang, Joakim Klar, Amelie Wenz, Niklas Dahl, Xingqi Chen
Epigenetic insights into GABAergic development in Dravet Syndrome iPSC and therapeutic implications. eLife 12 (2024)
Jens Schuster, Xi Lu, Yonglong Dang, Joakim Klar, Amelie Wenz, Niklas Dahl, Xingqi Chen
Epigenetic insights into GABAergic development in Dravet Syndrome iPSC and therapeutic implications. eLife 12 (2024)
Jens Schuster, Xi Lu, Yonglong Dang, Joakim Klar, Amelie Wenz, Niklas Dahl, Xingqi Chen
Epigenetic insights into GABAergic development in Dravet Syndrome iPSC and therapeutic implications. eLife 12 (2024)
Johan Reimegård, Marcel Tarbier, Marcus Danielsson, Jens Schuster, Sathishkumar Baskaran, Styliani Panagiotou, Niklas Dahl, Marc R Friedländer, Caroline J Gallant
A combined approach for single-cell mRNA and intracellular protein expression analysis. Communications biology 4 (1) (2021)
Talia Akram, Ambrin Fatima, Joakim Klar, Jan Hoeber, Muhammad Zakaria, Muhammad Tariq, Shahid M Baig, Jens Schuster, Niklas Dahl
Aberrant splicing due to a novel RPS7 variant causes Diamond-Blackfan Anemia associated with spontaneous remission and meningocele. International journal of hematology 112 (6) (2020)
Loora Laan, Joakim Klar, Maria Sobol, Jan Hoeber, Mansoureh Shahsavani, Malin Kele, Ambrin Fatima, Muhammad Zakaria, Göran Annerén, Anna Falk, Jens Schuster, Niklas Dahl
DNA methylation changes in Down syndrome derived neural iPSCs uncover co-dysregulation of ZNF and HOX3 families of transcription factors. Clinical epigenetics 12 (1) (2020)
Maria Sobol, Joakim Klar, Loora Laan, Mansoureh Shahsavani, Jens Schuster, Göran Annerén, Anne Konzer, Jia Mi, Jonas Bergquist, Jessica Nordlund, Jan Hoeber, Mikael Huss, Anna Falk, Niklas Dahl
Transcriptome and Proteome Profiling of Neural Induced Pluripotent Stem Cells from Individuals with Down Syndrome Disclose Dynamic Dysregulations of Key Pathways and Cellular Functions. Molecular neurobiology 56 (10) (2019)
Muhammad Zakaria, Ambrin Fatima, Joakim Klar, Johan Wikström, Uzma Abdullah, Zafar Ali, Talia Akram, Muhammad Tariq, Habib Ahmad, Jens Schuster, Shahid M Baig, Niklas Dahl
Primary microcephaly, primordial dwarfism, and brachydactyly in adult cases with biallelic skipping of RTTN exon 42. Human mutation 40 (7) (2019)
Ida Höijer, Yu-Chih Tsai, Tyson A Clark, Paul Kotturi, Niklas Dahl, Eva-Lena Stattin, Marie-Louise Bondeson, Lars Feuk, Ulf Gyllensten, Adam Ameur
Detailed analysis of HTT repeat elements in human blood using targeted amplification-free long-read sequencing. Human mutation 39 (9) (2018)
Zafar Ali, Shumaila Zulfiqar, Joakim Klar, Johan Wikström, Farid Ullah, Ayaz Khan, Uzma Abdullah, Shahid Baig, Niklas Dahl
Homozygous GRID2 missense mutation predicts a shift in the D-serine binding domain of GluD2 in a case with generalized brain atrophy and unusual clinical features. BMC medical genetics 18 (1) (2017)