Tim Van Damme

2.9k total citations
16 papers, 569 citations indexed

About

Tim Van Damme is a scholar working on Genetics, Molecular Biology and Cell Biology. According to data from OpenAlex, Tim Van Damme has authored 16 papers receiving a total of 569 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Genetics, 9 papers in Molecular Biology and 7 papers in Cell Biology. Recurrent topics in Tim Van Damme's work include Connective tissue disorders research (12 papers), Proteoglycans and glycosaminoglycans research (6 papers) and Dermatological and Skeletal Disorders (4 papers). Tim Van Damme is often cited by papers focused on Connective tissue disorders research (12 papers), Proteoglycans and glycosaminoglycans research (6 papers) and Dermatological and Skeletal Disorders (4 papers). Tim Van Damme collaborates with scholars based in Belgium, Netherlands and France. Tim Van Damme's co-authors include Fransiska Malfait, Delfien Syx, Anne De Paepe, Sofie Symoens, Sylvie Fournel‐Gigleux, Andy Willaert, Marianne Rohrbach, Cecilia Giunta, Ingrid Haußer and Johannes Zschocke and has published in prestigious journals such as Neurology, The American Journal of Human Genetics and PLoS Genetics.

In The Last Decade

Tim Van Damme

15 papers receiving 559 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Tim Van Damme Belgium	11	402	263	158	83	81	16	569
Fatema Alzahrani Saudi Arabia	14	386 1.0×	430 1.6×	62 0.4×	85 1.0×	43 0.5×	25	724
Belinda Campos‐Xavier Switzerland	17	475 1.2×	647 2.5×	161 1.0×	138 1.7×	122 1.5×	42	1.0k
Kristen C. Hart United States	6	233 0.6×	584 2.2×	96 0.6×	32 0.4×	113 1.4×	8	731
Elisabeth Castellanos Spain	13	139 0.3×	319 1.2×	188 1.2×	41 0.5×	78 1.0×	26	620
Siddharth R. Vora United States	11	107 0.3×	340 1.3×	43 0.3×	48 0.6×	43 0.5×	21	527
Kiminori Hasegawa Japan	13	240 0.6×	511 1.9×	31 0.2×	54 0.7×	73 0.9×	19	776
Greg B. Peters Australia	14	385 1.0×	382 1.5×	52 0.3×	15 0.2×	262 3.2×	22	785
Prasanthi Govindraj United States	9	147 0.4×	270 1.0×	330 2.1×	123 1.5×	33 0.4×	9	517
Lindsay B. Alcaraz France	12	68 0.2×	204 0.8×	53 0.3×	42 0.5×	89 1.1×	15	484
Shuyi Nie United States	15	121 0.3×	764 2.9×	122 0.8×	25 0.3×	189 2.3×	27	914

Countries citing papers authored by Tim Van Damme

Since Specialization

Citations

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

Fields of papers citing papers by Tim Van Damme

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Tim Van Damme. 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 Tim Van Damme. The network helps show where Tim Van Damme may publish in the future.

Co-authorship network of co-authors of Tim Van Damme

This figure shows the co-authorship network connecting the top 25 collaborators of Tim Van Damme. A scholar is included among the top collaborators of Tim Van Damme 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 Tim Van Damme. Tim Van Damme is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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16 of 16 papers shown

Damme, Tim Van, et al.. (2022). Shunt Nephritis: A Case of Mistaken Identity. Acta Clinica Belgica. 78(3). 248–253.

Damme, Tim Van, et al.. (2022). The Ehlers–Danlos Syndromes against the Backdrop of Inborn Errors of Metabolism. Genes. 13(2). 265–265. 6 indexed citations

Noborn, Fredrik, Jonas Nilsson, Tim Van Damme, et al.. (2022). Glycosaminoglycan linkage region of urinary bikunin as a potentially useful biomarker for β3GalT6‐deficient spondylodysplastic Ehlers–Danlos syndrome. JIMD Reports. 63(5). 462–467. 5 indexed citations

Damme, Tim Van, Delfien Syx, Laura Muiño Mosquera, et al.. (2021). More than meets the eye: Expanding and reviewing the clinical and mutational spectrum of brittle cornea syndrome. Human Mutation. 42(6). 711–730. 18 indexed citations

Syx, Delfien, Yoshihiro Ishikawa, Jan M. Gebauer, et al.. (2021). Aberrant binding of mutant HSP47 affects posttranslational modification of type I collagen and leads to osteogenesis imperfecta. PLoS Genetics. 17(2). e1009339–e1009339. 10 indexed citations

Damme, Tim Van, Delfien Syx, Sofie Symoens, et al.. (2019). Hypomorphic zebrafish models mimic the musculoskeletal phenotype of β4GalT7-deficient Ehlers-Danlos syndrome. Matrix Biology. 89. 59–75. 16 indexed citations

Damme, Tim Van, Elisabeth Steichen‐Gersdorf, Franco Laccone, et al.. (2019). The clinical and mutational spectrum of B3GAT3 linkeropathy: two case reports and literature review. Orphanet Journal of Rare Diseases. 14(1). 138–138. 12 indexed citations

Damme, Tim Van, et al.. (2017). Vascular phenotypes in nonvascular subtypes of the Ehlers-Danlos syndrome: a systematic review. Genetics in Medicine. 20(6). 562–573. 54 indexed citations

Depuydt, Julie, Tom Van Maerken, Bruce Poppe, et al.. (2017). Analysis of chromosomal radiosensitivity of healthy BRCA2 mutation carriers and non-carriers in BRCA families with the G2 micronucleus assay. Oncology Reports. 37(3). 1379–1386. 23 indexed citations

10.

Brady, Angela F., Serwet Demirdas, Sylvie Fournel‐Gigleux, et al.. (2017). The Ehlers–Danlos syndromes, rare types. American Journal of Medical Genetics Part C Seminars in Medical Genetics. 175(1). 70–115. 163 indexed citations

11.

Damme, Tim Van, Alain Colige, Delfien Syx, et al.. (2016). Expanding the clinical and mutational spectrum of the Ehlers–Danlos syndrome, dermatosparaxis type. Genetics in Medicine. 18(9). 882–891. 34 indexed citations

12.

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

13.

Syx, Delfien, Tim Van Damme, Sofie Symoens, et al.. (2015). Genetic Heterogeneity and Clinical Variability in Musculocontractural Ehlers-Danlos Syndrome Caused by Impaired Dermatan Sulfate Biosynthesis. Human Mutation. 36(5). 535–547. 63 indexed citations

14.

Santens, Patrick, Tim Van Damme, Wouter Steyaert, et al.. (2015). RNF216 mutations as a novel cause of autosomal recessive Huntington-like disorder. Neurology. 84(17). 1760–1766. 38 indexed citations

15.

Damme, Tim Van, Delfien Syx, Paul Coucke, et al.. (2015). Genetics of the Ehlers–Danlos syndrome: more than collagen disorders. Expert Opinion on Orphan Drugs. 3(4). 379–392. 4 indexed citations

16.

Malfait, Fransiska, Ariana Kariminejad, Tim Van Damme, et al.. (2013). Defective Initiation of Glycosaminoglycan Synthesis due to B3GALT6 Mutations Causes a Pleiotropic Ehlers-Danlos-Syndrome-like Connective Tissue Disorder. The American Journal of Human Genetics. 92(6). 935–945. 98 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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