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Karen Grønskov

Publication Activity (10 Years)

Years Active: 2019-2021
Publications (10 Years): 4

Top Topics

Staphylococcus Aureus

Dna Methylation

Knee Osteoarthritis

Top Venues

Scientific reports

European journal of human genetics : EJHG

Ophthalmic genetics

Rigshospitalet

Novo Nordisk AS Hagedorn Research Institute (PHD)

This page only lists publications with an associated author ORCID identifier.

Affiliation History

Rigshospitalet Mar 15o 1995

Denmark

Senior Scientist :: Clinical Genetic Clinic, Kennedy Center

Education History

Novo Nordisk AS Hagedorn Research Institute Sep 1o 1991 - Mar 14o 1995

Denmark

PHD

Publications

Kessel Line, Birgit Kjer, Ulrikke Lei, Morten Duno, Karen Grønskov
Genotype-phenotype associations in Danish patients with ocular and oculocutaneous albinism. Ophthalmic genetics 42 (3) (2021)
Abdullah Aamir, Helen J Kuht, Karen Grønskov, Brian P Brooks, Mervyn G Thomas
Clinical utility gene card for oculocutaneous (OCA) and ocular albinism (OA)-an update. European journal of human genetics : EJHG 29 (10) (2021)
Cathrine Jespersgaard, Mingyan Fang, Mette Bertelsen, Xiao Dang, Hanne Jensen, Yulan Chen, Niels Bech, Lanlan Dai, Thomas Rosenberg, Jianguo Zhang, Lisbeth Birk Møller, Zeynep Tümer, Karen Brøndum-Nielsen, Karen Grønskov
Molecular genetic analysis using targeted NGS analysis of 677 individuals with retinal dystrophy. Scientific reports 9 (1) (2019)
Karen Grønskov, Cathrine Jespersgaard, Gitte Hoffmann Bruun, Pernille Harris, Karen Brøndum-Nielsen, Brage Storstein Andresen, Thomas Rosenberg
A pathogenic haplotype, common in Europeans, causes autosomal recessive albinism and uncovers missing heritability in OCA1. Scientific reports 9 (1) (2019)