Els Van Hul

1.0k total citations
15 papers, 739 citations indexed

About

Els Van Hul is a scholar working on Molecular Biology, Oncology and Genetics. According to data from OpenAlex, Els Van Hul has authored 15 papers receiving a total of 739 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 6 papers in Oncology and 4 papers in Genetics. Recurrent topics in Els Van Hul's work include Bone health and treatments (5 papers), Bone Metabolism and Diseases (4 papers) and interferon and immune responses (2 papers). Els Van Hul is often cited by papers focused on Bone health and treatments (5 papers), Bone Metabolism and Diseases (4 papers) and interferon and immune responses (2 papers). Els Van Hul collaborates with scholars based in Belgium, United States and France. Els Van Hul's co-authors include Wim Van Hul, Filip Vanhoenacker, Liesbeth Van Wesenbeeck, Patrick J. Willems, Wim Wuyts, Jeppe Gram, Jens Bollerslev, Matthew L. Warman, Sultan Bahabri and Andrea Superti‐Furga and has published in prestigious journals such as Journal of Clinical Investigation, Nature Genetics and The American Journal of Human Genetics.

In The Last Decade

Els Van Hul

14 papers receiving 723 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Els Van Hul Belgium	9	536	251	222	153	69	15	739
Ming-Ming Jiang United States	12	470 0.9×	233 0.9×	131 0.6×	127 0.8×	69 1.0×	13	713
MaryAnn Weis United States	10	331 0.6×	581 2.3×	131 0.6×	324 2.1×	98 1.4×	11	841
Shawna M. Pyott United States	9	263 0.5×	546 2.2×	121 0.5×	295 1.9×	52 0.8×	9	789
Blair Hopwood Australia	11	473 0.9×	89 0.4×	149 0.7×	170 1.1×	106 1.5×	14	692
Rosa Isela Ortiz De Luna United States	8	808 1.5×	732 2.9×	151 0.7×	113 0.7×	23 0.3×	8	1.2k
Philip Sohn United States	12	542 1.0×	162 0.6×	151 0.7×	235 1.5×	41 0.6×	13	791
Anna Smerdel‐Ramoya United States	13	558 1.0×	89 0.4×	103 0.5×	80 0.5×	44 0.6×	16	654
Lee‐Anne Stanton Canada	12	355 0.7×	80 0.3×	96 0.4×	299 2.0×	31 0.4×	15	686
Shawn A. Hallett United States	11	283 0.5×	97 0.4×	85 0.4×	107 0.7×	32 0.5×	16	506
Riikka E. Mäkitie Finland	16	386 0.7×	306 1.2×	134 0.6×	79 0.5×	125 1.8×	38	616

Countries citing papers authored by Els Van Hul

Since Specialization

Citations

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

Fields of papers citing papers by Els Van Hul

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Els Van Hul

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

All Works

Sort: Min cites: Since: Top N: Style:

15 of 15 papers shown

Hul, Els Van, et al.. (2025). Bone alterations in head and neck pleomorphic adenoma: Scoping review. Oral Radiology. 41(4). 439–448.

Oliver, Gavin R., Patrick R. Blackburn, Marissa S. Ellingson, et al.. (2019). RNA‐Seq detects a SAMD12‐EXT1 fusion transcript and leads to the discovery of an EXT1 deletion in a child with multiple osteochondromas. Molecular Genetics & Genomic Medicine. 7(3). e00560–e00560. 12 indexed citations

Borra, Vere, et al.. (2013). Localization of the gene for X-linked calvarial hyperostosis to chromosome Xq27.3–Xqter. Bone. 58. 67–71. 8 indexed citations

Wuyts, Wim, et al.. (2011). Clinical and molecular studies of EXT1/EXT2 in Bulgaria. Journal of Inherited Metabolic Disease. 34(4). 917–921. 6 indexed citations

Wesenbeeck, Liesbeth Van, Paul R. Odgren, Fraser P. Coxon, et al.. (2007). Involvement of PLEKHM1 in osteoclastic vesicular transport and osteopetrosis in incisors absent rats and humans. Journal of Clinical Investigation. 117(4). 919–930. 163 indexed citations

Entius, Mark M., et al.. (2007). Mutation Screening of EXT1 and EXT2 by Denaturing High-Performance Liquid Chromatography, Direct Sequencing Analysis, Fluorescence in Situ Hybridization, and a New Multiplex Ligation-Dependent Probe Amplification Probe Set in Patients with Multiple Osteochondromas. Journal of Molecular Diagnostics. 10(1). 85–92. 48 indexed citations

Declau, Frank, et al.. (2005). The facio-audio-symphalangism syndrome in a four generation family with a nonsense mutation in the NOG-gene. Clinical Dysmorphology. 14(2). 73–80. 17 indexed citations

Hul, Els Van, Erik Fransén, J. P. Devogelaer, et al.. (2004). Evaluation of the Role of the SQSTM1 Gene in Sporadic Belgian Patients with Paget’s Disease. Calcified Tissue International. 75(2). 144–152. 43 indexed citations

Hul, Els Van, Jeppe Gram, Jens Bollerslev, et al.. (2002). Localization of the Gene Causing Autosomal Dominant Osteopetrosis Type I to Chromosome 11q12-13. Journal of Bone and Mineral Research. 17(6). 1111–1117. 64 indexed citations

10.

Hul, Els Van, et al.. (2001). Exclusion of the chromosomal 1p21 region in a large pedigree with a phenotypic variant of type II autosomal dominant osteopetrosis. Joint Bone Spine. 68(4). 327–333. 6 indexed citations

11.

Hul, Wim Van, Hatem El‐Shanti, Andrea Superti‐Furga, et al.. (1999). Mutations in the CCN gene family member WISP3 cause progressive pseudorheumatoid dysplasia. Nature Genetics. 23(1). 94–98. 210 indexed citations

12.

Hul, Wim Van, Wendy Balemans, Els Van Hul, et al.. (1998). Van Buchem Disease (Hyperostosis Corticalis Generalisata) Maps to Chromosome 17q12-q21. The American Journal of Human Genetics. 62(2). 391–399. 107 indexed citations

13.

Balemans, Wendy, Wim Van Hul, Els Van Hul, et al.. (1997). Localisation of the gene for Van Buchem disease to a candidate region of less than 1 cM on chromosome 17.. Data Archiving and Networked Services (DANS). 1 indexed citations

14.

Hul, Wim Van, Jens Bollerslev, Jeppe Gram, et al.. (1997). Localization of a Gene for Autosomal Dominant Osteopetrosis (Albers-Schönberg Disease) to Chromosome 1p21. The American Journal of Human Genetics. 61(2). 363–369. 52 indexed citations

15.

Hul, Wim Van, J. Wauters, Els Van Hul, et al.. (1996). Assignment of the human Integral TransMembrane protein 1 gene (ITM1) to human chromosome band 11 q23.3 by in situ hybridization and YAC mapping. Cytogenetic and Genome Research. 74(3). 218–219. 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.

Explore authors with similar magnitude of impact