Eveline W Blom

432 total citations
8 papers, 156 citations indexed

About

Eveline W Blom is a scholar working on Molecular Biology, Genetics and Genetics. According to data from OpenAlex, Eveline W Blom has authored 8 papers receiving a total of 156 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Molecular Biology, 4 papers in Genetics and 1 paper in Genetics. Recurrent topics in Eveline W Blom's work include Genomic variations and chromosomal abnormalities (2 papers), Nuclear Structure and Function (1 paper) and Congenital limb and hand anomalies (1 paper). Eveline W Blom is often cited by papers focused on Genomic variations and chromosomal abnormalities (2 papers), Nuclear Structure and Function (1 paper) and Congenital limb and hand anomalies (1 paper). Eveline W Blom collaborates with scholars based in Netherlands, United States and Australia. Eveline W Blom's co-authors include Eva Klopocki, Randi Koll, Emiel Baten, Bianca P. Hennig, Thomy de Ravel, Johannes Weigel, Petra Seemann, Gabriele Krüger, Stefan Mundlos and Katarina Dathe and has published in prestigious journals such as The American Journal of Human Genetics, British Journal of Dermatology and European Journal of Human Genetics.

In The Last Decade

Eveline W Blom

8 papers receiving 141 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Eveline W Blom Netherlands 5 94 84 28 22 21 8 156
Emiel Baten Belgium 8 133 1.4× 147 1.8× 31 1.1× 11 0.5× 20 1.0× 8 234
Sonja A. de Munnik Netherlands 7 104 1.1× 121 1.4× 11 0.4× 20 0.9× 5 0.2× 9 209
Ellen Moran United States 4 193 2.1× 73 0.9× 23 0.8× 15 0.7× 7 0.3× 10 218
Jennie Murray United Kingdom 6 108 1.1× 77 0.9× 12 0.4× 13 0.6× 24 1.1× 13 158
Maha Faden Saudi Arabia 6 93 1.0× 100 1.2× 31 1.1× 9 0.4× 22 1.0× 9 178
Deirdre Cilliers United Kingdom 7 90 1.0× 122 1.5× 14 0.5× 11 0.5× 17 0.8× 11 181
Bita Bozorgmehr Iran 8 85 0.9× 63 0.8× 12 0.4× 10 0.5× 8 0.4× 14 135
Katalin Szakszon Hungary 10 178 1.9× 103 1.2× 14 0.5× 9 0.4× 13 0.6× 29 276
M E Oude Luttikhuis United Kingdom 8 221 2.4× 256 3.0× 38 1.4× 10 0.5× 22 1.0× 9 355
Magdalena Socha Poland 10 143 1.5× 113 1.3× 43 1.5× 8 0.4× 26 1.2× 24 260

Countries citing papers authored by Eveline W Blom

Since Specialization
Citations

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

Fields of papers citing papers by Eveline W Blom

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Eveline W Blom

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

All Works

8 of 8 papers shown
1.
Moghadasi, Setareh, Luc Janssen, Mar Rodríguez‐Girondo, et al.. (2017). Performance of BRCA1/2 mutation prediction models in male breast cancer patients. Clinical Genetics. 93(1). 52–59. 3 indexed citations
2.
Zaharieva, Irina, Emily C. Oates, Clara van Karnebeek, et al.. (2015). Recessive loss-of-function SCN4A mutations associated with a novel phenotype of congenital myopathy. Neuromuscular Disorders. 25. S275–S276. 2 indexed citations
3.
Mathijssen, Inge B., Frank Baas, Johanna I. de Vries, et al.. (2014). Identification of a Dutch founder mutation in MUSK causing fetal akinesia deformation sequence. European Journal of Human Genetics. 23(9). 1151–1157. 29 indexed citations
4.
Stevens, Servi J.C., et al.. (2014). A recurrent deletion syndrome at chromosome bands 2p11.2-2p12 flanked by segmental duplications at the breakpoints and including REEP1. European Journal of Human Genetics. 23(4). 543–546. 7 indexed citations
5.
Bakkers, Mayienne, et al.. (2012). [Small fibre neuropathy: knowledge is power].. PubMed. 156(7). A4224–A4224. 1 indexed citations
6.
Klopocki, Eva, Bianca P. Hennig, Katarina Dathe, et al.. (2010). Deletion and Point Mutations of PTHLH Cause Brachydactyly Type E. The American Journal of Human Genetics. 86(3). 434–439. 93 indexed citations
7.
Klaassens, Merel, Eveline W Blom, J. J. P. Schrander, et al.. (2009). Unique skin changes in a case of Albright hereditary osteodystrophy caused by a rare GNAS1 mutation. British Journal of Dermatology. 162(3). 690–694. 6 indexed citations
8.

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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