Eveline Boudin

1.7k total citations
43 papers, 920 citations indexed

About

Eveline Boudin is a scholar working on Molecular Biology, Genetics and Oncology. According to data from OpenAlex, Eveline Boudin has authored 43 papers receiving a total of 920 indexed citations (citations by other indexed papers that have themselves been cited), including 34 papers in Molecular Biology, 27 papers in Genetics and 13 papers in Oncology. Recurrent topics in Eveline Boudin's work include Wnt/β-catenin signaling in development and cancer (16 papers), Connective tissue disorders research (12 papers) and Bone Metabolism and Diseases (12 papers). Eveline Boudin is often cited by papers focused on Wnt/β-catenin signaling in development and cancer (16 papers), Connective tissue disorders research (12 papers) and Bone Metabolism and Diseases (12 papers). Eveline Boudin collaborates with scholars based in Belgium, Denmark and Netherlands. Eveline Boudin's co-authors include Wim Van Hul, Gretl Hendrickx, Elke Piters, Igor Fijałkowski, Geert Mortier, Kim Brixen, Torben Leo Nielsen, Marianne Andersen, Viviane Van Hoof and Feliciano J. Ramos and has published in prestigious journals such as The Journal of Clinical Endocrinology & Metabolism, The American Journal of Human Genetics and Journal of Bone and Mineral Research.

In The Last Decade

Eveline Boudin

40 papers receiving 912 citations

Peers

Countries citing papers authored by Eveline Boudin

Since Specialization

Citations

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

Fields of papers citing papers by Eveline Boudin

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Eveline Boudin

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

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Identification of Compound Heterozygous Variants in LRP4 Demonstrates That a Pathogenic Variant outside the Third β-Propeller Domain Can Cause Sclerosteosis 2021 ·Genes ·(unknown), Eveline Boudin, Gretl Hendrickx, (unknown), Neveen A. T. Hamdy, Geert Mortier, Guillermo Martínez Diaz‐Guerra, (unknown), Natasha M. Appelman‐Dijkstra, Wim Van Hul	3
2	A Panel-Based Sequencing Analysis of Patients with Paget’s Disease of Bone Suggests Enrichment of Rare Genetic Variation in regulators of NF-κB Signaling and Supports the Importance of the 7q33 Locus 2021 ·Calcified Tissue International ·R. de Ridder, Geert Vandeweyer, Eveline Boudin, Gretl Hendrickx, (unknown), (unknown), Jean‐Pierre Devogelaer, Geert Mortier, Erik Fransén, Wim Van Hul	1
3	A multi-omics approach expands the mutational spectrum of MAP2K1-related melorheostosis 2020 ·Bone ·R. de Ridder, Eveline Boudin, M. Carola Zillikens, Joe Ibrahim, Bram C. J. van der Eerden, Wim Van Hul, Geert Mortier	7
4	WNT Signaling and Bone: Lessons From Skeletal Dysplasias and Disorders 2020 ·Frontiers in Endocrinology ·(unknown), Geert Mortier, Eveline Boudin, Wim Van Hul	69
5	Genetic Variation in RIN3 in the Belgian Population Supports Its Involvement in the Pathogenesis of Paget’s Disease of Bone and Modifies the Age of Onset 2019 ·Calcified Tissue International ·R. de Ridder, Eveline Boudin, Geert Vandeweyer, Jean‐Pierre Devogelaer, Erik Fransén, Geert Mortier, Wim Van Hul	5
6	Camurati–Engelmann Disease 2019 ·Calcified Tissue International ·Wim Van Hul, Eveline Boudin, Filip Vanhoenacker, Geert Mortier	19
7	Bi-allelic Loss-of-Function Mutations in the NPR-C Receptor Result in Enhanced Growth and Connective Tissue Abnormalities 2018 ·The American Journal of Human Genetics ·Eveline Boudin, (unknown), Timothy C. R. Prickett, Bruno Lapauw, Kaatje Toye, Viviane Van Hoof, Ilse Luyckx, Aline Verstraeten, H. S. A. Heymans, (unknown), Lut Van Laer, Ian Berry, Angus Dobbie, Ed Blair, Bart Loeys, Eric A. Espiner, Jan M. Wit, Wim Van Hul, Peter Houpt, Geert Mortier	25
8	Human Genetics of Sclerosing Bone Disorders 2018 ·Current Osteoporosis Reports ·R. de Ridder, Eveline Boudin, Geert Mortier, Wim Van Hul	9
9	Sclerosing bone dysplasias 2018 ·Best Practice & Research Clinical Endocrinology & Metabolism ·Eveline Boudin, Wim Van Hul	17
10	Genetic Screening of WNT4 and WNT5B in Two Populations with Deviating Bone Mineral Densities 2017 ·Calcified Tissue International ·Gretl Hendrickx, Eveline Boudin, (unknown), Torben Leo Nielsen, Marianne Andersen, Kim Brixen, Wim Van Hul	6
11	Genetic control of bone mass 2015 ·Molecular and Cellular Endocrinology ·Eveline Boudin, Igor Fijałkowski, Gretl Hendrickx, Wim Van Hul	53
12	Sclerosing Bone Dysplasias: Leads Toward Novel Osteoporosis Treatments 2014 ·Current Osteoporosis Reports ·Igor Fijałkowski, Eveline Boudin, Geert Mortier, Wim Van Hul	11
13	Variation in the Kozak sequence of WNT16 results in an increased translation and is associated with osteoporosis related parameters 2013 ·Bone ·Gretl Hendrickx, Eveline Boudin, Igor Fijałkowski, Torben Leo Nielsen, Marianne Andersen, Kim Brixen, Wim Van Hul	35
14	A common LRP4 haplotype is associated with bone mineral density and hip geometry in men—Data from the Odense Androgen Study (OAS) 2013 ·Bone ·Eveline Boudin, (unknown), Fenna de Freitas, Torben Leo Nielsen, Marianne Andersen, Kim Brixen, Wim Van Hul, Elke Piters	18
15	No mutations in the serotonin related TPH1 and HTR1B genes in patients with monogenic sclerosing bone disorders 2013 ·Bone ·Eveline Boudin, Karen Jennes, Fenna de Freitas, David Tegay, Geert Mortier, Wim Van Hul	8
16	The role of extracellular modulators of canonical Wnt signaling in bone metabolism and diseases 2013 ·Seminars in Arthritis and Rheumatism ·Eveline Boudin, Igor Fijałkowski, Elke Piters, Wim Van Hul	62
17	Resistin polymorphisms show associations with obesity, but not with bone parameters in men: results from the Odense Androgen Study 2012 ·Molecular Biology Reports ·Sigri Beckers, Doreen Zegers, (unknown), Eveline Boudin, Torben Leo Nielsen, Kim Brixen, Marianne Andersen, Wim Van Hul	9
18	Mutations in sFRP1 or sFRP4 are not a common cause of craniotubular hyperostosis 2012 ·Bone ·Eveline Boudin, Elke Piters, Igor Fijałkowski, (unknown), (unknown), Outi Kuismin, Jukka S. Moilanen, Geert Mortier, Wim Van Hul	3
19	Identification of the first deletion in the LRP5 gene in a patient with Autosomal Dominant Osteopetrosis type I 2011 ·Bone ·Alessandra Pangrazio, Eveline Boudin, Elke Piters, Giuseppe Damante, Nadia Lo Iacono, Angela D’Elia, Paolo Vezzoni, Wim Van Hul, Anna Villa, Cristina Sobacchi	23
20	Common Genetic Variation in the DKK1 Gene is Associated with Hip Axis Length but not with Bone Mineral Density and Bone Turnover Markers in Young Adult Men: Results from the Odense Androgen Study 2010 ·Calcified Tissue International ·Elke Piters, Wendy Balemans, Torben Leo Nielsen, Marianne Andersen, Eveline Boudin, Kim Brixen, Wim Van Hul	19

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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