Katrien Storm

1.0k total citations
24 papers, 701 citations indexed

About

Katrien Storm is a scholar working on Molecular Biology, Genetics and Cognitive Neuroscience. According to data from OpenAlex, Katrien Storm has authored 24 papers receiving a total of 701 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 10 papers in Genetics and 4 papers in Cognitive Neuroscience. Recurrent topics in Katrien Storm's work include Genetics and Neurodevelopmental Disorders (7 papers), Autism Spectrum Disorder Research (4 papers) and Genetic Neurodegenerative Diseases (3 papers). Katrien Storm is often cited by papers focused on Genetics and Neurodevelopmental Disorders (7 papers), Autism Spectrum Disorder Research (4 papers) and Genetic Neurodegenerative Diseases (3 papers). Katrien Storm collaborates with scholars based in Belgium, Netherlands and Germany. Katrien Storm's co-authors include Edwin Reyniers, R. Frank Kooy, Patrick J. Willems, Guy Nagels, Guy Van Camp, Wim Wuyts, Kris Flothmann, B. A. Oostra, C.E. Bakker and Peter Paul De Deyn and has published in prestigious journals such as Neuroscience, Movement Disorders and Urology.

In The Last Decade

Katrien Storm

22 papers receiving 687 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Katrien Storm Belgium 12 437 395 247 121 69 24 701
Roberta Polli Italy 15 470 1.1× 508 1.3× 204 0.8× 164 1.4× 47 0.7× 32 868
Britt‐Marie Anderlid Sweden 22 607 1.4× 813 2.1× 200 0.8× 33 0.3× 51 0.7× 56 1.3k
Bruno Delobel France 19 366 0.8× 481 1.2× 92 0.4× 47 0.4× 28 0.4× 37 804
Jan E. Dumon Belgium 14 498 1.1× 240 0.6× 140 0.6× 389 3.2× 42 0.6× 31 944
Shigeyasu Nakai Japan 6 764 1.7× 156 0.4× 65 0.3× 153 1.3× 113 1.6× 7 1.0k
Moritz Meins Germany 17 615 1.4× 394 1.0× 168 0.7× 105 0.9× 93 1.3× 27 894
Marie-Louise Bondeson Sweden 15 372 0.9× 133 0.3× 121 0.5× 229 1.9× 35 0.5× 26 711
Haibo Zhou China 12 583 1.3× 184 0.5× 168 0.7× 106 0.9× 176 2.6× 14 921
Heping Yu United States 19 376 0.9× 82 0.2× 123 0.5× 518 4.3× 48 0.7× 37 909
Ken‐Shiung Chen United States 13 435 1.0× 417 1.1× 31 0.1× 62 0.5× 81 1.2× 15 749

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-authorship network of co-authors of Katrien Storm

This figure shows the co-authorship network connecting the top 25 collaborators of Katrien Storm. A scholar is included among the top collaborators of Katrien Storm based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Katrien Storm. Katrien Storm is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Schil, Kristof Van, Tine Deconinck, Katrien Storm, et al.. (2025). TBP Repeat Expansion Analysis in Patients Carrying Heterozygous STUB1 Variants. Movement Disorders. 40(5). 980–985.
2.
Depuydt, Julie, Tom Van Maerken, Bruce Poppe, et al.. (2016). Increased chromosomal radiosensitivity in asymptomatic carriers of a heterozygous BRCA1 mutation. Breast Cancer Research. 18(1). 52–52. 25 indexed citations
3.
Aa, Nathalie Van der, et al.. (2010). Analysis of FOXG1 Is Highly Recommended in Male and Female Patients with Rett Syndrome. Molecular Syndromology. 1(6). 290–293. 18 indexed citations
4.
Konno, Takayuki, Yuichi Abe, Masakazu Kawaguchi, et al.. (2009). Oculocutaneous albinism type IV: a boy of Moroccan descent with a novel mutation in SLC45A2. Pigment Cell & Melanoma Research. 22(6). 916. 4 indexed citations
5.
Konno, Takayuki, Yuko Abe, Masakazu Kawaguchi, et al.. (2009). Oculocutaneous albinism type IV: A boy of Moroccan descent with a novel mutation in SLC45A2. American Journal of Medical Genetics Part A. 149A(8). 1773–1776. 10 indexed citations
6.
Ceulemans, Berten, et al.. (2007). Muscle Pain as the Only Presenting Symptom in a Girl With Dystrophinopathy. Pediatric Neurology. 38(1). 64–66. 10 indexed citations
7.
Storm, Katrien, Lieve Vits, Wim Wuyts, et al.. (2007). 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. 6(6). 371–375. 5 indexed citations
8.
Hoorenbeeck, Kim Van, Katrien Storm, Jenneke van den Ende, Martine Biervliet, & Kristine Desager. (2006). N1303K and IVS8-5T, clinical presentation within a family with atypical cystic fibrosis. Journal of Cystic Fibrosis. 6(3). 220–222. 8 indexed citations
9.
Wuyts, Wim, Martine Biervliet, Edwin Reyniers, et al.. (2005). Somatic and gonadal mosaicism in Hutchinson–Gilford progeria. American Journal of Medical Genetics Part A. 135A(1). 66–68. 27 indexed citations
10.
Courtens, Winnie, Stefan Vermeulen, Wim Wuyts, et al.. (2005). An interstitial deletion of chromosome 7 at band q21: A case report and review. American Journal of Medical Genetics Part A. 134A(1). 12–23. 17 indexed citations
11.
Rooms, Liesbeth, Edwin Reyniers, Wim Wuyts, et al.. (2005). Multiplex ligation‐dependent probe amplification to detect subtelomeric rearrangements in routine diagnostics. Clinical Genetics. 69(1). 58–64. 51 indexed citations
12.
Wuyts, Wim, Reinder Radersma, Katrien Storm, & Lieve Vits. (2005). An optimized DHPLC protocol for molecular testing of the EXT1 and EXT2 genes in hereditary multiple osteochondromas. Clinical Genetics. 68(6). 542–547. 31 indexed citations
13.
Holzik, Martijn F. Lutke, Katrien Storm, Rolf H. Sijmons, et al.. (2005). Absence of constitutional Y chromosome AZF deletions in patients with testicular germ cell tumors. Urology. 65(1). 196–201. 9 indexed citations
14.
Cucci, Robert A., Sai Prasad, Philip M. Kelley, et al.. (2000). The M34T Allele Variant of Connexin 26. Genetic Testing. 4(4). 335–344. 43 indexed citations
15.
16.
Storm, Katrien, et al.. (1998). Incomplete Eco RI digestion may lead to false diagnosis of fragile X syndrome. Human Genetics. 102(1). 54–56. 5 indexed citations
17.
D’Hooge, Rudi, Guy Nagels, F. Franck, et al.. (1997). Mildly impaired water maze performance in maleFmr1 knockout mice. Neuroscience. 76(2). 367–376. 164 indexed citations
18.
Reyniers, Edwin, G. Wolff, Gholamali Tariverdian, et al.. (1996). Severe mental retardation and macroorchidism without mutation in the FMR1 gene. American Journal of Medical Genetics. 64(2). 408–412. 7 indexed citations
19.
Kooy, R. Frank, Rudi D’Hooge, Edwin Reyniers, et al.. (1996). Transgenic mouse model for the fragile X syndrome. American Journal of Medical Genetics. 64(2). 241–245. 141 indexed citations
20.
Reyniers, Edwin, G. Wolff, Gholamali Tariverdian, et al.. (1996). Severe mental retardation and macroorchidism without mutation in the FMR1 gene. American Journal of Medical Genetics. 64(2). 408–412. 2 indexed citations

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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