Katrien Storm

1.0k citations

24 papers · 701 indexed · h-index 12

Impact in

Sensory Systems top 5%
- Hearing, Cochlea, Tinnitus, Genetics
Genetics top 5%
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities

Papers in ⓘ

Sensory Systems 2
Genetics 10
- Genetics and Neurodevelopmental Disorders 7

Co-authors: Edwin Reyniers (11 shared papers)R. Frank Kooy (8 shared papers)Patrick J. Willems (6 shared papers)Guy Nagels (2 shared papers)Guy Van Camp (2 shared papers)Wim Wuyts (6 shared papers)Kris Flothmann (1 shared paper)B. A. Oostra (2 shared papers)
Journals: Journal of Cystic Fibrosis (2 papers)Clinical Genetics (2 papers)Pigment Cell & Melanoma Research (1 paper)Neuroscience (1 paper)Movement Disorders (1 paper)
Partner nations: Belgium Netherlands Germany

In The Last Decade

Katrien Storm

22 papers receiving 687 citations

Peers

Countries citing papers authored by Katrien Storm

Since Specialization

Citations

This map shows the geographic impact of Katrien Storm'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 Katrien Storm with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Katrien Storm more than expected).

Fields of papers citing papers by Katrien Storm

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Katrien Storm. 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 Katrien Storm. The network helps show where Katrien Storm may publish in the future.

Co-authors

The 25 scholars most cited alongside Katrien Storm, 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 Katrien Storm Line = papers co-authored together Katrien Storm links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 24 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Mildly impaired water maze performance in maleFmr1 knockout mice Neuroscience ·Rudi D’Hooge, Guy Nagels, F. Franck, C.E. Bakker, Edwin Reyniers, Katrien Storm, R. Frank Kooy, B. A. Oostra, Patrick J. Willems, Peter Paul De Deyn	1997	164
2	Transgenic mouse model for the fragile X syndrome American Journal of Medical Genetics ·R. Frank Kooy, Rudi D’Hooge, Edwin Reyniers, Cathy E. Bakker, Guy Nagels, Kristel De Boulle, Katrien Storm, Gilbert Clincke, Peter P. De Deyn, Ben A. Oostra, Patrick J. Willems	1996	141
3	Determination of the carrier frequency of the common GJB2 (connexin-26) 35delG mutation in the Belgian population using an easy and reliable screening method Human Mutation ·Katrien Storm, Sandra Willocx, Kris Flothmann, Guy Van Camp	1999	79
4	Multiplex ligation‐dependent probe amplification to detect subtelomeric rearrangements in routine diagnostics Clinical Genetics ·Liesbeth Rooms, Edwin Reyniers, Wim Wuyts, Katrien Storm, Rob van Luijk, Stefaan Scheers, J. Wauters, Jenneke van den Ende, Martine Biervliet, François Eyskens, G. Van Goethem, Annick Laridon, Berten Ceulemans, Winnie Courtens, R. Frank Kooy	2005	51
5	The M34T Allele Variant of Connexin 26 Genetic Testing ·Robert A. Cucci, Sai Prasad, Philip M. Kelley, Glenn E. Green, Katrien Storm, Sandra Willocx, Edward Cohn, Guy Van Camp, Richard J. Smith	2000	43
6	An optimized DHPLC protocol for molecular testing of the EXT1 and EXT2 genes in hereditary multiple osteochondromas Clinical Genetics ·Wim Wuyts, Reinder Radersma, Katrien Storm, Lieve Vits	2005	31
7	Myopathy and phosphorylase kinase deficiency caused by a mutation in thePHKA1 gene American Journal of Medical Genetics Part A ·Wim Wuyts, Edwin Reyniers, C. Ceuterick, Katrien Storm, Thierry de Barsy, Jean‐Jacques Martin	2005	29
8	Somatic and gonadal mosaicism in Hutchinson–Gilford progeria American Journal of Medical Genetics Part A ·Wim Wuyts, Martine Biervliet, Edwin Reyniers, Maria Rosaria D’Apice, Giuseppe Novelli, Katrien Storm	2005	27
9	Increased chromosomal radiosensitivity in asymptomatic carriers of a heterozygous BRCA1 mutation Breast Cancer Research ·Annelot Baert, Julie Depuydt, Tom Van Maerken, Bruce Poppe, Fransiska Malfait, Katrien Storm, Jenneke van den Ende, Tim Van Damme, Sylvia De Nobele, Gianpaolo Perletti, Kim De Leeneer, Kathleen Claes, Anne Vral	2016	25
10	Analysis of FOXG1 Is Highly Recommended in Male and Female Patients with Rett Syndrome Molecular Syndromology ·Nathalie Van der Aa, M. Van den Bergh, N. Ponomarenko, Lieve Verstraete, Berten Ceulemans, Katrien Storm	2010	18
11	An interstitial deletion of chromosome 7 at band q21: A case report and review American Journal of Medical Genetics Part A ·Winnie Courtens, Stefan Vermeulen, Wim Wuyts, Ludwine Messiaen, J. Wauters, Lieve Nuytinck, Nils Peeters, Katrien Storm, Frank Speleman, Markus M. Nöthen	2005	17
12	CAG repeat contraction in the androgen receptor gene in three brothers with mental retardation American Journal of Medical Genetics ·R. Frank Kooy, Edwin Reyniers, Katrien Storm, Lieve Vits, D�sir�e van Velzen, Petra E. de Ruiter, Albert O. Brinkmann, Anne De Paepe, Patrick J. Willems	1999	12
13	Muscle Pain as the Only Presenting Symptom in a Girl With Dystrophinopathy Pediatric Neurology ·Berten Ceulemans, Katrien Storm, Edwin Reyniers, Luc Callewaert, J. J. Martin	2007	10
14	Oculocutaneous albinism type IV: A boy of Moroccan descent with a novel mutation in SLC45A2 American Journal of Medical Genetics Part A ·Takayuki Konno, Yuko Abe, Masakazu Kawaguchi, Katrien Storm, Martine Biervliet, Winnie Courtens, Michihiro Kono, Yasushi Tomita, Tamio Suzuki	2009	10
15	Absence of constitutional Y chromosome AZF deletions in patients with testicular germ cell tumors Urology ·Martijn F. Lutke Holzik, Katrien Storm, Rolf H. Sijmons, Maria D'Hollander, Jos Arts, M.L. Verstraaten, Dirk Th. Sleijfer, Harald J. Hoekstra	2005	9
16	N1303K and IVS8-5T, clinical presentation within a family with atypical cystic fibrosis Journal of Cystic Fibrosis ·Kim Van Hoorenbeeck, Katrien Storm, Jenneke van den Ende, Martine Biervliet, Kristine Desager	2006	8
17	Severe mental retardation and macroorchidism without mutation in the FMR1 gene American Journal of Medical Genetics ·Edwin Reyniers, G. Wolff, Gholamali Tariverdian, Kristel De Boulle, Katrien Storm, R. Frank Kooy, Patrick J. Willems	1996	7
18	High incidence of the CFTR mutations 3272-26A→G and L927P in Belgian cystic fibrosis patients, and identification of three new CFTR mutations (186-2A→G, E588V, and 1671insTATCA) Journal of Cystic Fibrosis ·Katrien Storm, Els Moens, Lieve Vits, Haike De Vlieger, Gino Delaere, Maria D'Hollander, Wim Wuyts, Martine Biervliet, L. Van Schil, Kristine Desager, Markus M. Nöthen	2007	5
19	Incomplete Eco RI digestion may lead to false diagnosis of fragile X syndrome Human Genetics ·Katrien Storm, Ingrid Handig, Edwin Reyniers, B. A. Oostra, R. Frank Kooy, Patrick J. Willems	1998	5
20	Oculocutaneous albinism type IV: a boy of Moroccan descent with a novel mutation in SLC45A2 Pigment Cell & Melanoma Research ·Takayuki Konno, Yuichi Abe, Masakazu Kawaguchi, Katrien Storm, Martine Biervliet, Winnie Courtens, Yasushi Tomita, Taichi A. Suzuki	2009	4

About Katrien Storm

Katrien Storm is a scholar working on Sensory Systems, Genetics, Cognitive Neuroscience, Molecular Biology and Endocrinology, Diabetes and Metabolism, having authored 24 papers that have together received 701 indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (7 papers), Autism Spectrum Disorder Research (4 papers), Genetic Neurodegenerative Diseases (3 papers), Cystic Fibrosis Research Advances (2 papers), Hormonal and reproductive studies (2 papers), RNA regulation and disease (2 papers), Connexins and lens biology (2 papers) and RNA modifications and cancer (2 papers). The work is most often cited by research in Sensory Systems (121 citations), Genetics (395 citations), Cognitive Neuroscience (247 citations), Developmental Neuroscience (37 citations) and Endocrine and Autonomic Systems (47 citations). Katrien Storm has collaborated with scholars based in Belgium, Netherlands and Germany. Frequent co-authors include Edwin Reyniers, R. Frank Kooy, Patrick J. Willems, Guy Nagels, Guy Van Camp, Wim Wuyts, Kris Flothmann, B. A. Oostra, Rudi D’Hooge and F. Franck. Their work appears in journals such as Journal of Cystic Fibrosis, Clinical Genetics, Pigment Cell & Melanoma Research, Neuroscience and Movement Disorders.

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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