B Hamel

894 total citations
7 papers, 648 citations indexed

About

B Hamel is a scholar working on Genetics, Molecular Biology and Genetics. According to data from OpenAlex, B Hamel has authored 7 papers receiving a total of 648 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Genetics, 3 papers in Molecular Biology and 1 paper in Genetics. Recurrent topics in B Hamel's work include Genetics and Neurodevelopmental Disorders (3 papers), Genomics and Chromatin Dynamics (2 papers) and Genomic variations and chromosomal abnormalities (2 papers). B Hamel is often cited by papers focused on Genetics and Neurodevelopmental Disorders (3 papers), Genomics and Chromatin Dynamics (2 papers) and Genomic variations and chromosomal abnormalities (2 papers). B Hamel collaborates with scholars based in Netherlands, Germany and Australia. B Hamel's co-authors include Claude Moraine, Tjitske Kleefstra, Hans‐Hilger Ropers, Hilde Van Esch, Jozef Gécz, Ulf Gurok, Verena Gimmel, Gholamali Tariverdian, Andreas Janecke and Richard Reinhardt and has published in prestigious journals such as The American Journal of Human Genetics, Molecular Psychiatry and Journal of Medical Genetics.

In The Last Decade

B Hamel

7 papers receiving 637 citations

Peers

Countries citing papers authored by B Hamel

Since Specialization

Citations

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

Fields of papers citing papers by B Hamel

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of B Hamel

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

All Works

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7 of 7 papers shown

#	Work	Indexed citations
1	Recurrent and founder mutations in the Netherlands 2010 ·Netherlands Heart Journal ·Jan J.J. Aalberts, Agnes G. Schuurman, Gerard Pals, B Hamel, G. Bosman, Yvonne Hilhorst‐Hofstee, Daniela Q.C.M. Barge‐Schaapveld, Barbara J.M. Mulder, Maarten P. van den Berg, J. Peter van Tintelen	9
2	Genotype–phenotype correlations in L1 syndrome: a guide for genetic counselling and mutation analysis 2009 ·Journal of Medical Genetics ·Yvonne J. Vos, Hermien E. K. de Walle, (unknown), Arjan Stegeman, (unknown), Monique J. Bruining, Merel C. van Maarle, Mariet W. Elting, Nicolette S. den Hollander, B Hamel, Ana María Fortuna, Lone Sunde, Irene Stolte‐Dijkstra, C. T. R. M. Schrander‐Stumpel, Robert M.W. Hofstra	61
3	Mutations of the UPF3B gene, which encodes a protein widely expressed in neurons, are associated with nonspecific mental retardation with or without autism 2009 ·Molecular Psychiatry ·Frédéric Laumonnier, Cheryl Shoubridge, Catherine Antar, Lam Son Nguyen, Hilde Van Esch, Tjitske Kleefstra, Sylvain Briault, J. P. Fryns, B Hamel, Jamel Chelly, Hans‐Hilger Ropers, Nathalie Ronce, (unknown), Claude Moraine, Jozef Gécz, Martine Raynaud	89
4	Strategies for present and future mental retardation diagnosis 2006 ·Future Neurology ·Dorien Lugtenberg, B Hamel, Hans van Bokhoven, Arjan Pm de Brouwer	1
5	Mutations in the JARID1C Gene, Which Is Involved in Transcriptional Regulation and Chromatin Remodeling, Cause X-Linked Mental Retardation 2005 ·The American Journal of Human Genetics ·Lars Riff Jensen, (unknown), Ulf Gurok, Bettina A. Moser, Verena Gimmel, Andreas Tzschach, Andreas Janecke, Gholamali Tariverdian, Jamel Chelly, Jean‐Pierre Fryns, Hilde Van Esch, Tjitske Kleefstra, B Hamel, Claude Moraine, Jozef Gécz, Gillian Turner, Richard Reinhardt, Vera M. Kalscheuer, Hans‐Hilger Ropers, Steffen Lenzner	285
6	Interstitial 6q deletion with a Prader--Willi-like phenotype: a new case and review of the literature 2000 ·European Journal of Paediatric Neurology ·H. Jacobus Gilhuis, (unknown), B Hamel, F.J.M. Gabreëls	48
7	Mutations in the EXT1 and EXT2 Genes in Hereditary Multiple Exostoses 1998 ·The American Journal of Human Genetics ·Wim Wuyts, Wim Van Hul, Kristel De Boulle, Jan Hendrickx, Egbert Bakker, Filip Vanhoenacker, (unknown), Hermann‐Josef Lüdecke, Bekir Sıtkı Şaylı, Ugo E. Pazzaglia, Geert Mortier, B Hamel, (unknown), Mark Matsushita, (unknown), P J Willems	155

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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