Eva Wohlleber

2.5k total citations
11 papers, 458 citations indexed

About

Eva Wohlleber is a scholar working on Genetics, Molecular Biology and Surgery. According to data from OpenAlex, Eva Wohlleber has authored 11 papers receiving a total of 458 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Genetics, 4 papers in Molecular Biology and 2 papers in Surgery. Recurrent topics in Eva Wohlleber's work include Genomic variations and chromosomal abnormalities (7 papers), Genetics and Neurodevelopmental Disorders (5 papers) and Genomics and Rare Diseases (4 papers). Eva Wohlleber is often cited by papers focused on Genomic variations and chromosomal abnormalities (7 papers), Genetics and Neurodevelopmental Disorders (5 papers) and Genomics and Rare Diseases (4 papers). Eva Wohlleber collaborates with scholars based in Germany, United Kingdom and Switzerland. Eva Wohlleber's co-authors include Hartmut Engels, Alexander M. Zink, Anita Rauch, Eva Rossier, Arif B. Ekici, Christiane Zweier, Markus Zweier, André Reis, Juliane Hoyer and Dagmar Wieczorek and has published in prestigious journals such as The American Journal of Human Genetics, Human Mutation and European Journal of Human Genetics.

In The Last Decade

Eva Wohlleber

11 papers receiving 420 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Eva Wohlleber Germany 9 298 286 61 45 33 11 458
Eva Rossier Germany 13 392 1.3× 406 1.4× 85 1.4× 74 1.6× 22 0.7× 21 644
Nara Sobreira United States 10 323 1.1× 325 1.1× 36 0.6× 27 0.6× 10 0.3× 27 550
Qixi Wu China 14 328 1.1× 290 1.0× 39 0.6× 79 1.8× 19 0.6× 28 568
Liesbeth Backx Belgium 10 196 0.7× 183 0.6× 18 0.3× 29 0.6× 16 0.5× 14 333
Anna Capalbo Italy 16 389 1.3× 244 0.9× 26 0.4× 59 1.3× 41 1.2× 29 579
Heidi A. Heilstedt United States 9 415 1.4× 307 1.1× 27 0.4× 27 0.6× 37 1.1× 9 568
Ton van Essen Netherlands 11 324 1.1× 474 1.7× 23 0.4× 39 0.9× 19 0.6× 13 726
Joanna Wiszniewska United States 12 360 1.2× 348 1.2× 15 0.2× 36 0.8× 43 1.3× 22 607
Muriel Holder France 9 185 0.6× 283 1.0× 19 0.3× 22 0.5× 25 0.8× 14 408
Viola Alesi Italy 13 309 1.0× 263 0.9× 12 0.2× 59 1.3× 72 2.2× 59 558

Countries citing papers authored by Eva Wohlleber

Since Specialization
Citations

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

Fields of papers citing papers by Eva Wohlleber

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Eva Wohlleber

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

All Works

11 of 11 papers shown
1.
Degenhardt, Franziska, Eva Wohlleber, Rami Abou Jamra, & Johannes Hebebrand. (2023). Genetische Diagnostik im klinischen Alltag der Kinder- und Jugendpsychiatrie – Indikationen, Rahmenbedingungen, Hürden und Lösungsvorschläge. Zeitschrift für Kinder- und Jugendpsychiatrie und Psychotherapie. 2 indexed citations
2.
Engels, Hartmut, Kirsten Cremer, Jessica Becker, et al.. (2016). De novo microdeletions and point mutations affecting SOX2 in three individuals with intellectual disability but without major eye malformations. American Journal of Medical Genetics Part A. 173(2). 435–443. 13 indexed citations
3.
Tawamie, Hasan, Eva Wohlleber, Steffen Uebe, et al.. (2015). Recurrent null mutation in SPG20 leads to Troyer syndrome. Molecular and Cellular Probes. 29(5). 315–318. 11 indexed citations
4.
Zink, Alexander M., Eva Wohlleber, Hartmut Engels, et al.. (2014). Microdeletions Including FMR1 in Three Female Patients with Intellectual Disability - Further Delineation of the Phenotype and Expression Studies. Molecular Syndromology. 5(2). 65–75. 6 indexed citations
5.
Bağcı, Soyhan, Eva Wohlleber, Anke Müller, et al.. (2012). Familial Translocation t(6;20)(p21;p13) Resulting in Partial Trisomy 6p and Partial Monosomy 20p: Report of a New Case and Review of the Literature. Cytogenetic and Genome Research. 136(4). 308–313. 15 indexed citations
6.
Hoyer, Juliane, Arif B. Ekici, Sabine Endele, et al.. (2012). Haploinsufficiency of ARID1B, a Member of the SWI/SNF-A Chromatin-Remodeling Complex, Is a Frequent Cause of Intellectual Disability. The American Journal of Human Genetics. 90(3). 565–572. 173 indexed citations
7.
Engels, Hartmut, Herdit M. Schüler, Alexander M. Zink, et al.. (2012). A phenotype map for 14q32.3 terminal deletions. American Journal of Medical Genetics Part A. 158A(4). 695–706. 24 indexed citations
8.
Zink, Alexander M., Jan Senderek, Elisabeth Mangold, et al.. (2012). 5q31 Microdeletions: Definition of a Critical Region and Analysis of <b><i>LRRTM2,</i></b> a Candidate Gene for Intellectual Disability. Molecular Syndromology. 3(2). 68–75. 22 indexed citations
9.
Wohlleber, Eva, Maria Kirchhoff, Alexander M. Zink, et al.. (2010). Clinical and molecular characterization of two patients with overlapping de novo microdeletions in 2p14-p15 and mild mental retardation. European Journal of Medical Genetics. 54(1). 67–72. 10 indexed citations
10.
Zweier, Markus, Anne Gregor, Christiane Zweier, et al.. (2010). Mutations in MEF2C from the 5q14.3q15 microdeletion syndrome region are a frequent cause of severe mental retardation and diminish MECP2 and CDKL5 expression. Human Mutation. 31(6). 722–733. 114 indexed citations
11.
Engels, Hartmut, Eva Wohlleber, Alexander M. Zink, et al.. (2009). A novel microdeletion syndrome involving 5q14.3-q15: clinical and molecular cytogenetic characterization of three patients. European Journal of Human Genetics. 17(12). 1592–1599. 68 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

Breakdown of academic impact, for papers by Eva Rossier Breakdown of academic impact, for papers by Nara Sobreira Breakdown of academic impact, for papers by Qixi Wu Breakdown of academic impact, for papers by Liesbeth Backx Breakdown of academic impact, for papers by Anna Capalbo Breakdown of academic impact, for papers by Heidi A. Heilstedt Breakdown of academic impact, for papers by Ton van Essen Breakdown of academic impact, for papers by Joanna Wiszniewska Breakdown of academic impact, for papers by Muriel Holder Breakdown of academic impact, for papers by Viola Alesi
Rankless by CCL
2026