Brynjar O. Jensson

Reykjavik, Iceland

Last Updated: 09/26/2026

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Found 47 publications

Congenital insensitivity to pain caused by a novel SCN9A-genotype

Congenital insensitivity to pain caused by a novel SCN9A-genotype

Journal: Laeknabladid
Published: May 27, 2026

WDTC1 Haploinsufficiency as a Cause of Neurodevelopmental Phenotypes.

WDTC1 Haploinsufficiency as a Cause of Neurodevelopmental Phenotypes.

Journal: Clinical genetics
Published: January 06, 2026

Sequence Diversity Lost in Early Pregnancy.

Sequence Diversity Lost in Early Pregnancy.

Journal: Obstetrical & gynecological survey
Published: November 25, 2025

De novo and inherited dominant variants in U4 and U6 snRNA genes cause retinitis pigmentosa.

De novo and inherited dominant variants in U4 and U6 snRNA genes cause retinitis pigmentosa.

Journal: Nature genetics
Published: June 02, 2025

Mutations in the small nuclear RNA gene RNU2-2 cause a severe neurodevelopmental disorder with prominent epilepsy.

Mutations in the small nuclear RNA gene RNU2-2 cause a severe neurodevelopmental disorder with prominent epilepsy.

Journal: Nature genetics
Published: September 13, 2024

Sequence diversity lost in early pregnancy.

Sequence diversity lost in early pregnancy.

Journal: Nature
Published: July 16, 2024

Actionable Genotypes and Life Span in Iceland. Reply.

Actionable Genotypes and Life Span in Iceland. Reply.

Journal: The New England journal of medicine
Published: March 06, 2024

Homozygosity for a stop-gain variant in CCDC201 causes primary ovarian insufficiency.

Homozygosity for a stop-gain variant in CCDC201 causes primary ovarian insufficiency.

Journal: Nature genetics
Published: February 01, 2024

Loss-of-function variants in ITSN1 confer high risk of Parkinson's disease.

Loss-of-function variants in ITSN1 confer high risk of Parkinson's disease.

Journal: NPJ Parkinson's disease
Published: January 29, 2024

Rare loss-of-function variants in HECTD2 and AKAP11 confer risk of bipolar disorder.

Rare loss-of-function variants in HECTD2 and AKAP11 confer risk of bipolar disorder.

Journal: Nature genetics
Published: January 18, 2024

Actionable Genotypes and Their Association with Life Span in Iceland.

Actionable Genotypes and Their Association with Life Span in Iceland.

Journal: The New England journal of medicine
Published: November 08, 2023

Screening for Rare Coding Variants That Associate With the QTc Interval in Iceland.

Screening for Rare Coding Variants That Associate With the QTc Interval in Iceland.

Journal: Journal of the American Heart Association
Published: July 14, 2023
Showing 1-12 of 47

Last Updated: 09/26/2026