Jussi-pekka Tolonen
Oulu, Finland
Last Updated: 09/26/2026
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Found 8 publications
Clinical and genetic characterization of intellectual disability.
Journal: Developmental medicine and child neurology
Published: June 04, 2025
A Novel Homozygous KIF1C Variant in 2 Cases of Spastic Ataxia Type 2.
Journal: Neurology. Genetics
Published: March 25, 2025
Phenotypic Heterogeneity in Genetic and Acquired Pediatric Cerebellar Disorders.
Journal: Movement disorders : official journal of the Movement Disorder Society
Published: November 27, 2024
Optical Genome Mapping Identifies a Second Xq27.1 Rearrangement Associated With Charcot-Marie-Tooth Neuropathy CMTX3.
Journal: Molecular genetics & genomic medicine
Published: April 25, 2024
Reduced Bone Mass in Collagen Prolyl 4-Hydroxylase P4ha1 +/-; P4ha2 -/- Compound Mutant Mice.
Journal: JBMR plus
Published: February 23, 2022
Medulloblastoma, macrocephaly, and a pathogenic germline PTEN variant: Cause or coincidence?
Journal: Molecular genetics & genomic medicine
Published: March 13, 2020
A long hypoxia-inducible factor 3 isoform 2 is a transcription activator that regulates erythropoietin.
Journal: Cellular and molecular life sciences : CMLS
Published: April 16, 2019
Use of psychiatric medications in schizophrenia and other psychoses in a general population sample.
Journal: Psychiatry research
Published: January 11, 2015
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Last Updated: 09/26/2026