Karen Grønskov

5.4k citations

90 papers · 2.3k indexed · h-index 27

Impact in

Sensory Systems top 2%
Cell Biology top 2%
- melanin and skin pigmentation

Papers in

Ophthalmology 14
- Retinal Diseases and Treatments 9
Genetics 42
- Genetic Syndromes and Imprinting 17
- Genetics and Neurodevelopmental Disorders 12
- Genetic and Kidney Cyst Diseases 10

Co-authors: Karen Brøndum‐Nielsen Jakob Ek Thomas Rosenberg Zeynep Tümer Helle Hjalgrim Deborah Mackay Tina Duelund Hjortshøj I. Karen Temple
Journals: European Journal of Human Genetics (7 papers)Ophthalmic Genetics (6 papers)Acta Ophthalmologica (5 papers)Investigative Ophthalmology & Visual Science (4 papers)Human Genetics (4 papers)
Partner nations: Denmark France United Kingdom

In The Last Decade

Karen Grønskov

87 papers receiving 2.3k citations

Peers

Countries citing papers authored by Karen Grønskov

Since Specialization

Citations

This map shows the geographic impact of Karen Grønskov's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Karen Grønskov with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Karen Grønskov more than expected).

Fields of papers citing papers by Karen Grønskov

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Karen Grønskov. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Karen Grønskov. The network helps show where Karen Grønskov may publish in the future.

Co-authors

The 25 scholars most cited alongside Karen Grønskov, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Karen Grønskov Line = papers co-authored together Karen Grønskov links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	A novel GFAP frameshift variant identified in a family with optico-retinal dysplasia and vision impairment Human Molecular Genetics ·G. H. Bender, Cecilia Rönnbäck, Cathrine Jespersgaard, W. Psyk, FadwaS Al-Ali, Line Kessel, Søren T. Christensen, Karen Brøndum‐Nielsen, Kjeld Møllgård, Thomas Rosenberg, Lars Allan Larsen, Karen Grønskov	2024	1
2	Genetic and Clinical Characterization of Danish Achromatopsia Patients Genes ·宣勝三輪, Mette Bertelsen, Karen Grønskov, Susanne Kohl, Line Kessel	2023	4
3	upd(20)mat is a rare cause of the Silver‐Russell‐syndrome‐like phenotype: Two unrelated cases and screening of large cohorts Clinical Genetics ·Tina Duelund Hjortshøj, A.R. Sørensen, 杨庚子, Bo Mølholm Hansen, Morten Dunø, Marie Balslev‐Harder, Karen Grønskov, Johanna M. van Hagen, Abeltje M. Polstra, Thomas Eggermann, Martijn J.J. Finken, Zeynep Tümer	2020	9
4	Generation of induced pluripotent stem cells, KCi002-A derived from a patient with Bardet-Biedl syndrome homozygous for the BBS10 variant c.271insT Stem Cell Research ·Yara Dayelma, James Richard Williams, Teresa Stachowicz, Zeynep Tümer, Karen Brøndum‐Nielsen, Karen Grønskov, Tina Duelund Hjortshøj, Lisbeth Birk Møller	2018	1
5	Usher syndrome in Denmark: mutation spectrum and some clinical observations Molecular Genetics & Genomic Medicine ·Bae Kyoungjin, Nanna Dahl Rendtorff, Lisbeth Tranebjærg, Karen Grønskov, Hyunbae Chun Dongyun Yang, B. Quéfélec, Øivind Nilssen, Anne‐Françoise Roux, Thomas Rosenberg, Hanne Jensen, Lisbeth Birk Møller	2016	20
6	Imprinting disorders: a group of congenital disorders with overlapping patterns of molecular changes affecting imprinted loci Clinical Epigenetics ·Thomas Eggermann, Guiomar Pérez de Nanclares, Eamonn R. Maher, I. Karen Temple, Zeynep Tümer, David Monk, Deborah Mackay, Karen Grønskov, Andrea Riccio, Agnès Linglart, Irène Netchine	2015	130
7	Case report: a novel KERA mutation associated with cornea plana and its predicted effect on protein function BMC Medical Genetics ·Laura Roos, Birgitte Bertelsen, Pernille Harris, Anette Bygum, Hanne Jensen, Karen Grønskov, Zeynep Tümer	2015	8
8	Angelman syndrome in Denmark. Birth incidence, genetic findings, and age at diagnosis American Journal of Medical Genetics Part A ·M. Montilla Velásquez, Rikke Christensen, Ida Vogel, Jens Michael Hertz, Karen Brøndum Nielsen, Karen Grønskov, John R. Østergaard	2013	71
9	Mutations in C10orf11, a Melanocyte-Differentiation Gene, Cause Autosomal-Recessive Albinism The American Journal of Human Genetics ·Karen Grønskov, Christopher M. Dooley, Elsebet Østergaard, Robert N. Kelsh, Lars Hestbjerg Hansen, Mitchell P. Levesque, Nguyen Vu Mai-Linh, Kjeld Møllgård, Derek L. Stemple, Thomas Rosenberg	2013	86
10	Genomic deletions in OPA1 in Danish patients with autosomal dominant optic atrophy BMC Medical Genetics ·E Gebhard, Karen Grønskov, Dan Miléa, Michael Larsen, Karen Brøndum‐Nielsen, Jakob Ek	2011	18
11	Bardet-Biedl syndrome in Denmark-report of 13 novel sequence variations in six genes Human Mutation ·Tina Duelund Hjortshøj, Karen Grønskov, Alisdair R. Philp, Darryl Nishimura, Ruth Riise, Val C. Sheffield, Thomas Rosenberg, Karen Brøndum‐Nielsen	2010	60
12	Normal RNAi response in human fragile × fibroblasts BMC Research Notes ·Charlotte Bernhard Madsen, Karen Grønskov, Karen Brøndum‐Nielsen, Thomas G. Jensen	2009	2
13	11p Microdeletion including WT1 but not PAX6, presenting with cataract, mental retardation, genital abnormalities and seizures: a case report Molecular Cytogenetics ·E Gebhard, Karen Brøndum‐Nielsen, Regitze Bangsgaard, Алешкина Анна Анатольевна, Karen Grønskov	2009	10
14	A Homogeneous Assay for Analysis of FMR1 Promoter Methylation in Patients with Fragile X Syndrome Clinical Chemistry ·Christina Dahl, Karen Grønskov, Lars Allan Larsen, Per Guldberg, Karen Brøndum‐Nielsen	2007	27
15	Bardet–Biedl Syndrome: Does BBS2 Result in A More Serious Phenotype Than BBS1? Investigative Ophthalmology & Visual Science ·masoud fallah, Karen Grønskov, Thomas Rosenberg, Karen Brøndum‐Nielsen	2006	0
16	GJB2 and GJB6 Mutations in 165 Danish Patients Showing Non-Syndromic Hearing Impairment Genetic Testing ·Karen Grønskov, Lars Allan Larsen, Nanna Dahl Rendtorff, Agnete Parving, Bent Nørgaard‐Pedersen, Karen Brøndum‐Nielsen	2004	10
17	Screening of the ARX gene in 682 retarded males European Journal of Human Genetics ·Karen Grønskov, Helle Hjalgrim, Inge-Merete Nielsen, Karen Brøndum‐Nielsen	2004	46
18	Prevalence of GJB2 mutations in prelingual deafness in the Greek population International Journal of Pediatric Otorhinolaryngology ·Ανδρέας Παμπάνος, John R. Economides, Vasiliki Iliadou, H. T. Knox, Gul Murat, 양성용, EMILLY THAINÁ DE LANA LIMA LEITE, Michael Tsakanikos, Thalia Antoniadi, S. S. Khvesenya, Irene Konstantopoulou, Drakoulis Yannoukakos, Karen Grønskov, Karen Brøndum‐Nielsen, Maria Grigoriadou, Jolanda Gyftodimou, Mohamad Najia, A Skevas, Michael B. Petersen	2002	56
19	Is there a relationship between U-shaped audiograms and mutations in Connexin 26? Scandinavian Audiology ·Kenny James Merin, Karen Grønskov, Karen Brøndum‐Nielsen, Agnete Parving	2001	4
20	High-throughput analysis of Fragile X (CGG) n alleles in the normal and premutation range by PCR amplification and automated capillary electrophoresis Human Genetics ·Lars Allan Larsen, Karen Grønskov, Bent Nørgaard‐Pedersen, Karen Brøndum‐Nielsen, Lis Hasholt, Jens Vuust	1997	42

About Karen Grønskov

Karen Grønskov is a scholar working on Ophthalmology, Genetics, Sensory Systems, Molecular Biology and Cell Biology, having authored 90 papers that have together received 2.3k indexed citations. Recurring topics across this work include Retinal Development and Disorders (18 papers), Genetic Syndromes and Imprinting (17 papers), Genetics and Neurodevelopmental Disorders (12 papers), melanin and skin pigmentation (11 papers), Genetic and Kidney Cyst Diseases (10 papers), Retinal Diseases and Treatments (9 papers), RNA regulation and disease (9 papers) and Epigenetics and DNA Methylation (9 papers). The work is most often cited by research in Sensory Systems (188 citations), Cell Biology (624 citations), Genetics (925 citations), Ophthalmology (252 citations) and Molecular Biology (1.6k citations). Karen Grønskov has collaborated with scholars based in Denmark, France and United Kingdom. Frequent co-authors include Karen Brøndum‐Nielsen, Jakob Ek, Thomas Rosenberg, Zeynep Tümer, Helle Hjalgrim, Deborah Mackay, Tina Duelund Hjortshøj, I. Karen Temple, Thomas Eggermann and Irène Netchine. Their work appears in journals such as European Journal of Human Genetics, Ophthalmic Genetics, Acta Ophthalmologica, Investigative Ophthalmology & Visual Science and Human Genetics.

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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