Bram Perdu

536 total citations
10 papers, 288 citations indexed

About

Bram Perdu is a scholar working on Molecular Biology, Oncology and Genetics. According to data from OpenAlex, Bram Perdu has authored 10 papers receiving a total of 288 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 6 papers in Oncology and 5 papers in Genetics. Recurrent topics in Bram Perdu's work include Bone health and treatments (6 papers), Bone Metabolism and Diseases (5 papers) and Dermatological and Skeletal Disorders (4 papers). Bram Perdu is often cited by papers focused on Bone health and treatments (6 papers), Bone Metabolism and Diseases (5 papers) and Dermatological and Skeletal Disorders (4 papers). Bram Perdu collaborates with scholars based in Belgium, United States and United Kingdom. Bram Perdu's co-authors include Wim Van Hul, Liesbeth Van Wesenbeeck, Filip Vanhoenacker, Fraser P. Coxon, Miep Helfrich, Anna Teti, Jean‐Pierre Timmermans, Els Van Hul, Anna Villa and Reinhilde Jacobs and has published in prestigious journals such as Journal of Clinical Investigation, Brain and Journal of Bone and Mineral Research.

In The Last Decade

Bram Perdu

10 papers receiving 279 citations

Peers

Bram Perdu

MB

GENET

ONCOL

CB

RHEUM

Monica Pata Canada

Meilin Wu United States

Ei-ichi Takahashi Japan

H M Kronenberg United States

John D. Ansell United Kingdom

David S.W. Boam United Kingdom

Andrea V. Leisewitz Chile

Paul L. Woo United States

Michelle M. Thiaville United States

Monica Pata Canada

Bram Perdu

321 ×1.4

MB

55 ×0.5

GENET

133 ×1.4

ONCOL

52 ×0.9

CB

37 ×1.4

RHEUM

Citations per year, relative to Bram Perdu Bram Perdu (= 1×) peers Monica Pata

Countries citing papers authored by Bram Perdu

Since Specialization

Citations

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

Fields of papers citing papers by Bram Perdu

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Bram Perdu

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

All Works

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10 of 10 papers shown

1.

Bosley, Thomas M., Mustafa A. Salih, Ibrahim A. Alorainy, et al.. (2011). The neurology of carbonic anhydrase type II deficiency syndrome. Brain. 134(12). 3502–3515. 27 indexed citations

2.

Barbosa, Mafalda, et al.. (2011). [Osteopathia striata with cranial sclerosis].. PubMed. 23(6). 1147–50. 7 indexed citations

3.

Perdu, Bram & Wim Van Hul. (2010). Sclerosing Bone Disorders: Too Much of a Good Thing. Critical Reviews in Eukaryotic Gene Expression. 20(3). 195–212. 9 indexed citations

4.

Perdu, Bram, Phillis Lakeman, Geert Mortier, et al.. (2010). Two novel WTX mutations underscore the unpredictability of male survival in osteopathia striata with cranial sclerosis. Clinical Genetics. 80(4). 383–388. 22 indexed citations

5.

Perdu, Bram, et al.. (2009). Refined Genomic Localization of the Genetic Lesion in the Osteopetrosis (op) Rat and Exclusion of Three Positional and Functional Candidate Genes, Clcn7, Atp6v0c, and Slc9a3r2. Calcified Tissue International. 84(5). 355–360. 5 indexed citations

6.

Perdu, Bram, Fenna de Freitas, Suzanna G.M. Frints, et al.. (2009). Osteopathia striata with cranial sclerosis owing to WTX gene defect. Journal of Bone and Mineral Research. 25(1). 82–90. 50 indexed citations

7.

Perdu, Bram, Fraser P. Coxon, & Miep Helfrich. (2009). Human recessive osteopetrosis. Osteologie/Osteology. 18(4). 260–267. 3 indexed citations

8.

Wesenbeeck, Liesbeth Van, Bram Perdu, Wendy Balemans, & Wim Van Hul. (2008). Osteopetrosis. Drugs of the Future. 33(5). 447–447. 1 indexed citations

9.

Perdu, Bram, Wim Van Hul, & Liesbeth Van Wesenbeeck. (2008). Osteopetrosis: from Animal Models to Human Conditions. Clinical Reviews in Bone and Mineral Metabolism. 6(3-4). 71–81. 1 indexed citations

10.

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

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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