Asbjorn Holmgren

Oslo, 0450, Norway

Last Updated: 09/26/2026

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Found 23 publications

Novel Loss of Function Variants in CENPF Including a Large Intragenic Deletion in Patients with Strømme Syndrome.

Novel Loss of Function Variants in CENPF Including a Large Intragenic Deletion in Patients with Strømme Syndrome.

Journal: Genes

Published: September 28, 2023

Bipolar patients display stoichiometric imbalance of gene expression in post-mortem brain samples.

Bipolar patients display stoichiometric imbalance of gene expression in post-mortem brain samples.

Journal: Molecular psychiatry

Published: May 11, 2023

A single amino acid deletion in the ER Ca2+ sensor STIM1 reverses the in vitro and in vivo effects of the Stormorken syndrome-causing R304W mutation.

A single amino acid deletion in the ER Ca2+ sensor STIM1 reverses the in vitro and in vivo effects of the Stormorken syndrome-causing R304W mutation.

Journal: Science signaling

Published: February 07, 2023

Mapping the expression of an ANK3 isoform associated with bipolar disorder in the human brain.

Mapping the expression of an ANK3 isoform associated with bipolar disorder in the human brain.

Journal: Translational psychiatry

Published: September 03, 2021

Exploring lithium's transcriptional mechanisms of action in bipolar disorder: a multi-step study.

Exploring lithium's transcriptional mechanisms of action in bipolar disorder: a multi-step study.

Journal: Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology

Published: August 01, 2019

STIM1 R304W in mice causes subgingival hair growth and an increased fraction of trabecular bone.

STIM1 R304W in mice causes subgingival hair growth and an increased fraction of trabecular bone.

Journal: Cell calcium

Published: July 13, 2019

Loss of CBY1 results in a ciliopathy characterized by features of Joubert syndrome.

Loss of CBY1 results in a ciliopathy characterized by features of Joubert syndrome.

Journal: Human mutation

Published: June 20, 2019

Mutated Thyroid Hormone Transporter OATP1C1 Associates with Severe Brain Hypometabolism and Juvenile Neurodegeneration.

Mutated Thyroid Hormone Transporter OATP1C1 Associates with Severe Brain Hypometabolism and Juvenile Neurodegeneration.

Journal: Thyroid : official journal of the American Thyroid Association

Published: October 10, 2018

STIM1 R304W causes muscle degeneration and impaired platelet activation in mice.

STIM1 R304W causes muscle degeneration and impaired platelet activation in mice.

Journal: Cell calcium

Published: September 11, 2018

Elevated expression of a minor isoform of ANK3 is a risk factor for bipolar disorder.

Elevated expression of a minor isoform of ANK3 is a risk factor for bipolar disorder.

Journal: Translational psychiatry

Published: April 16, 2018

Relationship Between Postmortem Urine and Blood Concentrations of GHB Furnishes Useful Information to Help Interpret Drug Intoxication Deaths.

Relationship Between Postmortem Urine and Blood Concentrations of GHB Furnishes Useful Information to Help Interpret Drug Intoxication Deaths.

Journal: Journal of analytical toxicology

Published: March 23, 2018

Biallelic variants in LINGO1 are associated with autosomal recessive intellectual disability, microcephaly, speech and motor delay.

Biallelic variants in LINGO1 are associated with autosomal recessive intellectual disability, microcephaly, speech and motor delay.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics

Published: March 13, 2017

Showing 1-12 of 23

Last Updated: 09/26/2026