Henrik Okkels
Aalborg, Denmark
Last Updated: 09/26/2026
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Found 17 publications
Possible explanations for the common clinical familial hypercholesterolemia phenotypes in the Faroe Islands.
Journal: Journal of clinical lipidology
Published: December 08, 2022
Genetic predisposition and evolutionary traces of pediatric cancer risk: a prospective 5-year population-based genome sequencing study of children with CNS tumors.
Journal: Neuro-oncology
Published: July 28, 2022
Colorectal cancer incidences in Lynch syndrome: a comparison of results from the prospective lynch syndrome database and the international mismatch repair consortium.
Journal: Hereditary cancer in clinical practice
Published: December 03, 2021
Cell-based non-invasive prenatal testing for monogenic disorders: confirmation of unaffected fetuses following preimplantation genetic testing.
Journal: Journal of assisted reproduction and genetics
Published: October 06, 2020
First reported case of Doyne honeycomb retinal dystrophy (Malattia Leventinese/autosomal dominant drusen) in Scandinavia.
Journal: Molecular genetics & genomic medicine
Published: August 25, 2020
Correction: Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome Database.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: July 22, 2020
First reported CABP2-related non-syndromic hearing loss in Northern Europe.
Journal: Molecular genetics & genomic medicine
Published: June 11, 2020
Risk-reducing hysterectomy and bilateral salpingo-oophorectomy in female heterozygotes of pathogenic mismatch repair variants: a Prospective Lynch Syndrome Database report.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: June 02, 2020
New Pathogenic Germline Variants in Very Early Onset and Familial Colorectal Cancer Patients.
Journal: Frontiers in genetics
Published: May 27, 2020
A systematic review on concurrent aneuploidy screening and preimplantation genetic testing for hereditary disorders: What is the prevalence of aneuploidy and is there a clinical effect from aneuploidy screening?
Journal: Acta obstetricia et gynecologica Scandinavica
Published: October 15, 2019
Detection of PMS2 Mutations by Screening Hereditary Nonpolyposis Colon Cancer Families from Denmark and Sweden.
Journal: Genetic testing and molecular biomarkers
Published: August 22, 2019
Whole-exome sequencing identifies a GREB1L variant in a three-generation family with Müllerian and renal agenesis: a novel candidate gene in Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome. A case report.
Journal: Human reproduction (Oxford, England)
Published: March 26, 2019
Last Updated: 09/26/2026