Niklas Dahl

Uppsala, C 75185, Sweden

Last Updated: 09/26/2026

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Found 84 publications

Clinical and Molecular Characterization of Pakistani Mucopolysaccharidosis Families with SGSH and GALNS Deficiencies.

Clinical and Molecular Characterization of Pakistani Mucopolysaccharidosis Families with SGSH and GALNS Deficiencies.

Journal: Genes

Published: March 16, 2026

Plasma proteomic profile reveals persistent immune activation in post-acute sequelae of SARS-CoV-2 infection.

Plasma proteomic profile reveals persistent immune activation in post-acute sequelae of SARS-CoV-2 infection.

Journal: Frontiers in immunology

Published: December 24, 2025

Abnormalities in the functional activity of neural networks in a human iPSC model of Dravet syndrome.

Abnormalities in the functional activity of neural networks in a human iPSC model of Dravet syndrome.

Journal: Neuroscience research

Published: June 26, 2025

Comprehensive transcriptome assessment in PBMCs of post-COVID patients at a median follow-up of 28 months after a mild COVID infection reveals upregulation of JAK/STAT signaling and a prolonged immune response.

Comprehensive transcriptome assessment in PBMCs of post-COVID patients at a median follow-up of 28 months after a mild COVID infection reveals upregulation of JAK/STAT signaling and a prolonged immune response.

Journal: Frontiers in immunology

Published: March 11, 2025

Epigenetic insights into GABAergic development in Dravet Syndrome iPSC and therapeutic implications.

Epigenetic insights into GABAergic development in Dravet Syndrome iPSC and therapeutic implications.

Journal: eLife

Published: August 27, 2024

KRIT1 heterozygous mutations are sufficient to induce a pathological phenotype in patient-derived iPSC models of cerebral cavernous malformation.

KRIT1 heterozygous mutations are sufficient to induce a pathological phenotype in patient-derived iPSC models of cerebral cavernous malformation.

Journal: Cell reports

Published: December 09, 2023

Generation of a ZEB2 deficient human iPSC line (KICRi002A-4).

Generation of a ZEB2 deficient human iPSC line (KICRi002A-4).

Journal: Stem cell research

Published: December 06, 2023

Genetic Investigation of Consanguineous Pakistani Families Segregating Rare Spinocerebellar Disorders.

Genetic Investigation of Consanguineous Pakistani Families Segregating Rare Spinocerebellar Disorders.

Journal: Genes

Published: June 08, 2023

Mutations in human DNA methyltransferase DNMT1 induce specific genome-wide epigenomic and transcriptomic changes in neurodevelopment.

Mutations in human DNA methyltransferase DNMT1 induce specific genome-wide epigenomic and transcriptomic changes in neurodevelopment.

Journal: Human molecular genetics

Published: March 20, 2023

Novel PNKP mutations associated with reduced DNA single-strand break repair and severe microcephaly, seizures, and developmental delay.

Novel PNKP mutations associated with reduced DNA single-strand break repair and severe microcephaly, seizures, and developmental delay.

Journal: Molecular genetics & genomic medicine

Published: March 16, 2023

Early-onset hereditary isolated non-neurogenic orthostatic hypotension in a Swedish family.

Early-onset hereditary isolated non-neurogenic orthostatic hypotension in a Swedish family.

Journal: Clinical autonomic research : official journal of the Clinical Autonomic Research Society

Published: March 05, 2023

Heredity of pregnancy-related pelvic girdle pain in Sweden.

Heredity of pregnancy-related pelvic girdle pain in Sweden.

Journal: Acta obstetricia et gynecologica Scandinavica

Published: February 14, 2023

Showing 1-12 of 84

Last Updated: 09/26/2026