Marleen Simon

3.0k total citations
21 papers, 611 citations indexed

About

Marleen Simon is a scholar working on Molecular Biology, Genetics and Cell Biology. According to data from OpenAlex, Marleen Simon has authored 21 papers receiving a total of 611 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 12 papers in Genetics and 4 papers in Cell Biology. Recurrent topics in Marleen Simon's work include Connective tissue disorders research (5 papers), Bone Metabolism and Diseases (3 papers) and Bone health and treatments (3 papers). Marleen Simon is often cited by papers focused on Connective tissue disorders research (5 papers), Bone Metabolism and Diseases (3 papers) and Bone health and treatments (3 papers). Marleen Simon collaborates with scholars based in Netherlands, Belgium and United Kingdom. Marleen Simon's co-authors include Marcel M. A. M. Mannens, Pauline Terhal, Jet Bliek, Saskia M. Maas, Tom G.W. Letteboer, Georgette B. Salieb–Beugelaar, Ben C.J. Hamel, Jasper van der Smagt, Lies H. Hoefsloot and Valérie Cormier‐Daire and has published in prestigious journals such as Nature Communications, Nature Genetics and The Journal of Clinical Endocrinology & Metabolism.

In The Last Decade

Marleen Simon

21 papers receiving 598 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Marleen Simon Netherlands 12 359 336 155 82 55 21 611
James Tepperberg United States 15 362 1.0× 532 1.6× 284 1.8× 67 0.8× 84 1.5× 28 889
Aleksander Jamsheer Poland 16 433 1.2× 397 1.2× 112 0.7× 48 0.6× 36 0.7× 77 731
Maia V. Ouspenskaia United States 14 622 1.7× 267 0.8× 99 0.6× 77 0.9× 33 0.6× 16 876
Muriel Rigolet France 12 662 1.8× 347 1.0× 170 1.1× 76 0.9× 54 1.0× 24 948
Alberto Sensi Italy 15 247 0.7× 205 0.6× 129 0.8× 104 1.3× 29 0.5× 56 676
Laurence Taine France 21 428 1.2× 398 1.2× 274 1.8× 53 0.6× 57 1.0× 46 924
M Shohat Israel 15 329 0.9× 387 1.2× 134 0.9× 64 0.8× 65 1.2× 29 911
Elisena Morizio Italy 20 410 1.1× 396 1.2× 186 1.2× 61 0.7× 31 0.6× 53 907
Gabriele Gillessen-Kaesbach Germany 5 349 1.0× 265 0.8× 64 0.4× 42 0.5× 37 0.7× 5 506
Valérie Layet France 13 506 1.4× 513 1.5× 67 0.4× 113 1.4× 165 3.0× 22 925

Countries citing papers authored by Marleen Simon

Since Specialization
Citations

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

Fields of papers citing papers by Marleen Simon

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Marleen Simon

This figure shows the co-authorship network connecting the top 25 collaborators of Marleen Simon. A scholar is included among the top collaborators of Marleen Simon 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 Marleen Simon. Marleen Simon 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.
Muijnck, Cansu de, Lonneke Haer‐Wigman, Marieke F. van Dooren, et al.. (2024). Characteristics of autosomal dominant WFS1-associated optic neuropathy and its comparability to OPA1-associated autosomal dominant optic atrophy. Scientific Reports. 14(1). 22956–22956. 1 indexed citations
2.
Asmar, Anthony J., Shaun R. Abrams, Jason C. Collins, et al.. (2023). A ubiquitin-based effector-to-inhibitor switch coordinates early brain, craniofacial, and skin development. Nature Communications. 14(1). 4499–4499. 2 indexed citations
3.
Tsujita, Maki, Marlène Rio, Céline Huber, et al.. (2022). Clinical diversity and molecular mechanism of VPS35L-associated Ritscher-Schinzel syndrome. Journal of Medical Genetics. 60(4). 359–367. 9 indexed citations
4.
Gripp, Karen W., Sarah Smithson, Ingrid Scurr, et al.. (2021). Syndromic disorders caused by gain-of-function variants in KCNH1, KCNK4, and KCNN3—a subgroup of K+ channelopathies. European Journal of Human Genetics. 29(9). 1384–1395. 25 indexed citations
5.
Reilly, Madeline Louise, Noor Ul Ain, Céline Huber, et al.. (2020). Biallelic KIF24 Variants Are Responsible for a Spectrum of Skeletal Disorders Ranging From Lethal Skeletal Ciliopathy to Severe Acromesomelic Dysplasia. Journal of Bone and Mineral Research. 37(9). 1642–1652. 7 indexed citations
6.
Bolling, Maria C., Marlies de Graaf, Peter C. van den Akker, et al.. (2020). Collodion babies: A 15-year retrospective multicenter study in The Netherlands—Evaluation of severity scores to predict the underlying disease. Journal of the American Academy of Dermatology. 84(4). 1111–1113. 3 indexed citations
7.
Bogaard, Ellen H. van den, Michel van Geel, Ivonne M.J.J. van Vlijmen‐Willems, et al.. (2018). Deficiency of the human cysteine protease inhibitor cystatin M/E causes hypotrichosis and dry skin. Genetics in Medicine. 21(7). 1559–1567. 11 indexed citations
8.
Cameron‐Christie, Sophia, Constance Wells, Marleen Simon, et al.. (2018). Recessive Spondylocarpotarsal Synostosis Syndrome Due to Compound Heterozygosity for Variants in MYH3. The American Journal of Human Genetics. 102(6). 1115–1125. 22 indexed citations
9.
Campos‐Obando, Natalia, Ling Oei, Lies H. Hoefsloot, et al.. (2014). Osteoporotic Vertebral Fractures During Pregnancy: Be Aware of a Potential Underlying Genetic Cause. The Journal of Clinical Endocrinology & Metabolism. 99(4). 1107–1111. 39 indexed citations
10.
Simon, Marleen, Belinda Campos‐Xavier, Eugênia Ribeiro Valadares, et al.. (2012). Severe neurologic manifestations from cervical spine instability in spondylo‐megaepiphyseal‐metaphyseal dysplasia. American Journal of Medical Genetics Part C Seminars in Medical Genetics. 160C(3). 230–237. 7 indexed citations
11.
Nikopoulos, Konstantinos, Isabelle Schrauwen, Marleen Simon, et al.. (2011). Autosomal Recessive Stickler Syndrome in Two Families Is Caused by Mutations in theCOL9A1Gene. Investigative Ophthalmology & Visual Science. 52(7). 4774–4774. 37 indexed citations
12.
Oudesluijs, Grétel, et al.. (2011). Abnormal facial appearance, body asymmetry, limb deformities, and internal malformations. American Journal of Medical Genetics Part A. 158A(2). 292–297. 1 indexed citations
13.
Goff, Carine Le, Clémentine Mahaut, Avinash Abhyankar, et al.. (2011). Mutations at a single codon in Mad homology 2 domain of SMAD4 cause Myhre syndrome. Nature Genetics. 44(1). 85–88. 117 indexed citations
14.
Vergult, Sarah, Andrew Dauber, Barbara Delle Chiaie, et al.. (2011). 17q24.2 microdeletions: a new syndromal entity with intellectual disability, truncal obesity, mood swings and hallucinations. European Journal of Human Genetics. 20(5). 534–539. 27 indexed citations
15.
Ott, Claus‐Eric, Gundula Leschik, Louise Brueton, et al.. (2010). Deletions of the RUNX2 gene are present in about 10% of individuals with cleidocranial dysplasia. Human Mutation. 31(8). E1587–E1593. 58 indexed citations
16.
Hellemans, Jan, Marleen Simon, Annelies Dheedene, et al.. (2009). Homozygous Inactivating Mutations in the NKX3-2 Gene Result in Spondylo-Megaepiphyseal-Metaphyseal Dysplasia. The American Journal of Human Genetics. 85(6). 916–922. 28 indexed citations
17.
18.
Laar, Ingrid M.B.H. van de, et al.. (2007). Limb anomalies in patients with CHARGE syndrome: An expansion of the phenotype. American Journal of Medical Genetics Part A. 143A(22). 2712–2715. 27 indexed citations
19.
Bliek, Jet, Pauline Terhal, Saskia M. Maas, et al.. (2006). Hypomethylation of the H19 Gene Causes Not Only Silver-Russell Syndrome (SRS) but Also Isolated Asymmetry or an SRS-Like Phenotype. The American Journal of Human Genetics. 78(4). 604–614. 151 indexed citations
20.
Simon, Marleen, et al.. (1986). Congenital varicella syndrome. Infection. 14(4). 177–180. 18 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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