Kristin L. Eiklid

Nydalen, 4950, Norway

Last Updated: 09/26/2026

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Found 10 publications

Aagenaes syndrome/lymphedema cholestasis syndrome 1 is caused by a founder variant in the 5'-untranslated region of UNC45A.

Aagenaes syndrome/lymphedema cholestasis syndrome 1 is caused by a founder variant in the 5'-untranslated region of UNC45A.

Journal: Journal of hepatology
Published: May 25, 2022

APOE-ε4 Is Associated With Reduced Verbal Memory Performance and Higher Emotional, Cognitive, and Everyday Executive Function Symptoms Two Months After Mild Traumatic Brain Injury.

APOE-ε4 Is Associated With Reduced Verbal Memory Performance and Higher Emotional, Cognitive, and Everyday Executive Function Symptoms Two Months After Mild Traumatic Brain Injury.

Journal: Frontiers in neurology
Published: July 02, 2021

Apolipoprotein ɛ4 Status and Brain Structure 12 Months after Mild Traumatic Injury: Brain Age Prediction Using Brain Morphometry and Diffusion Tensor Imaging.

Apolipoprotein ɛ4 Status and Brain Structure 12 Months after Mild Traumatic Injury: Brain Age Prediction Using Brain Morphometry and Diffusion Tensor Imaging.

Journal: Journal of clinical medicine
Published: December 11, 2020

Whole exome sequencing of sporadic patients with Currarino Syndrome: A report of three trios.

Whole exome sequencing of sporadic patients with Currarino Syndrome: A report of three trios.

Journal: Gene
Published: November 01, 2016

Mutation analysis in Norwegian families with hereditary hemorrhagic telangiectasia: founder mutations in ACVRL1.

Mutation analysis in Norwegian families with hereditary hemorrhagic telangiectasia: founder mutations in ACVRL1.

Journal: Clinical genetics
Published: February 09, 2015

Familial globotriaosylceramide-associated cardiomyopathy mimicking Fabry disease.

Familial globotriaosylceramide-associated cardiomyopathy mimicking Fabry disease.

Journal: Heart (British Cardiac Society)
Published: July 18, 2014

CCBE1 mutation in two siblings, one manifesting lymphedema-cholestasis syndrome, and the other, fetal hydrops.

CCBE1 mutation in two siblings, one manifesting lymphedema-cholestasis syndrome, and the other, fetal hydrops.

Journal: PloS one
Published: March 20, 2013

Copy number variation findings among 50 children and adolescents with autism spectrum disorder.

Copy number variation findings among 50 children and adolescents with autism spectrum disorder.

Journal: Psychiatric genetics
Published: January 02, 2013

A 5.8 kb deletion removing the entire MNX1 gene in a Norwegian family with Currarino syndrome.

A 5.8 kb deletion removing the entire MNX1 gene in a Norwegian family with Currarino syndrome.

Journal: Gene
Published: October 19, 2012

Characterization of a Norwegian cherubism cohort; molecular genetic findings, oral manifestations and quality of life.

Characterization of a Norwegian cherubism cohort; molecular genetic findings, oral manifestations and quality of life.

Journal: European journal of medical genetics
Published: October 17, 2012
Showing 1-10 of 10

Last Updated: 09/26/2026