Eva Wohlleber

2.5k citations
11 papers · 458 · h-index 9

Impact in

Papers in

  • Genetics 10
    • Genomic variations and chromosomal abnormalities 7
    • Genetics and Neurodevelopmental Disorders 5
    • Genomics and Rare Diseases 4
  • Molecular Biology 4
    • Chromatin Remodeling and Cancer 2
    • Congenital heart defects research 2
Co-authors
Hartmut Engels (8 shared papers)Anita Rauch (3 shared papers)Alexander M. Zink (7 shared papers)Arif B. Ekici (2 shared papers)André Reis (2 shared papers)Eva Rossier (2 shared papers)Christiane Zweier (2 shared papers)Markus Zweier (2 shared papers)
Journals
Human Mutation (1 paper)The American Journal of Human Genetics (1 paper)European Journal of Human Genetics (1 paper)European Journal of Medical Genetics (1 paper)Cytogenetic and Genome Research (1 paper)
Partner nations
GermanyUnited KingdomSwitzerland

In The Last Decade

Eva Wohlleber

11 papers receiving 420 citations

Peers

Eva Wohlleber
Comparison fields: 5 of 55
  • Genetics 298
  • Developmental Neuroscience 18
  • Molecular Biology 286
  • Pathology and Forensic Medicine 61
  • Genetics 33
Replace Eva Rossier with:
Eva Rossier Germany
M Bhattacharjee United States
Ton van Essen Netherlands
Anna Capalbo Italy
Heidi A. Heilstedt United States
Qixi Wu China
Viola Alesi Italy
Nara Sobreira United States
Bellinda van den Helm Netherlands
Maureen Holvoet Belgium
Eva Wohlleber relative to Eva Rossier Germany Eva Rossier's profile →
Citations per field
00.5×1.7×
Eva Rossier · 1×
Citations per year

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-authors

The 25 scholars most cited alongside Eva Wohlleber, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Eva Wohlleber Line = papers co-authored together Eva Wohlleber links everyone, so they are left out of the graph.

All Works

11 of 11 papers shown
#Work
1
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 ·Juliane Hoyer, Arif B. Ekici, Sabine Endele, Bernt Popp, Christiane Zweier, Antje Wiesener, Eva Wohlleber, Andreas Dufke, Eva Rossier, Corinna Petsch, Markus Zweier, Ina Göhring, Alexander M. Zink, Gudrun Rappold, Evelin Schröck, Dagmar Wieczorek, Olaf Rieß, Hartmut Engels, Anita Rauch, André Reis
2012173
2
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 ·Markus Zweier, Anne Gregor, Christiane Zweier, Hartmut Engels, Heinrich Sticht, Eva Wohlleber, Emilia K. Bijlsma, Susan Holder, Martin Zenker, Eva Rossier, Ute Grasshoff, Diana Johnson, Lisa Robertson, Helen V. Firth, Cornelia Kraus, Arif B. Ekici, André Reis, Anita Rauch
2010114
3
A novel microdeletion syndrome involving 5q14.3-q15: clinical and molecular cytogenetic characterization of three patients
European Journal of Human Genetics ·Hartmut Engels, Eva Wohlleber, Alexander M. Zink, Juliane Hoyer, Kerstin U. Ludwig, Felix F. Brockschmidt, Dagmar Wieczorek, Ute Moog, Birgit Hellmann-Mersch, Ruthild G. Weber, Lionel Willatt, Martina Kreiß‐Nachtsheim, Helen V. Firth, Anita Rauch
200968
4
A phenotype map for 14q32.3 terminal deletions
American Journal of Medical Genetics Part A ·Hartmut Engels, Herdit M. Schüler, Alexander M. Zink, Eva Wohlleber, Antje Brockschmidt, Alexander Hoischen, Matthias Drechsler, Jennifer A. Lee, Kerstin U. Ludwig, Christian Kubisch, Gesa Schwanitz, Ruthild G. Weber, Barbara Leube, Raoul C. M. Hennekam, Sabine Rudnik‐Schöneborn, Martina Kreiß‐Nachtsheim, Heiko Reutter
201224
5
5q31 Microdeletions: Definition of a Critical Region and Analysis of <b><i>LRRTM2,</i></b> a Candidate Gene for Intellectual Disability
Molecular Syndromology ·W. Kleffmann, Alexander M. Zink, J.A. Lee, Jan Senderek, Elisabeth Mangold, Ute Moog, Gudrun Rappold, Eva Wohlleber, Hartmut Engels
201222
6
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 ·A.L. Berner, Soyhan Bağcı, Eva Wohlleber, E. Engels, Anke Müller, Peter Bartmann, Ruthild G. Weber, Heiko Reutter
201215
7
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 ·Nicola Dennert, Hartmut Engels, Kirsten Cremer, Jessica Becker, Eva Wohlleber, Beate Albrecht, Julia K. Ehret, Hermann‐Josef Lüdecke, Mohnish Suri, Giulia Carignani, Alessandra Renieri, Guido Kukuk, Thomas Wieland, Joris Andrieux, Tim M. Strom, Dagmar Wieczorek, Anne Dieux‐Coëslier, Alexander M. Zink
201613
8
Recurrent null mutation in SPG20 leads to Troyer syndrome
Molecular and Cellular Probes ·Hasan Tawamie, Eva Wohlleber, Steffen Uebe, Christine Schmäl, Markus M. Nöthen, Rami Abou Jamra
201511
9
Clinical and molecular characterization of two patients with overlapping de novo microdeletions in 2p14-p15 and mild mental retardation
European Journal of Medical Genetics ·Eva Wohlleber, Maria Kirchhoff, Alexander M. Zink, Martina Kreiß‐Nachtsheim, Alma Küchler, Birgit Jepsen, Susanne Kjærgaard, Hartmut Engels
201010
10
Microdeletions Including FMR1 in Three Female Patients with Intellectual Disability - Further Delineation of the Phenotype and Expression Studies
Molecular Syndromology ·Alexander M. Zink, Eva Wohlleber, Hartmut Engels, Olaug K. Rødningen, Kirstine Ravn, Stefanie Heilmann‐Heimbach, Julia Rehnitz, N. Katzorke, Cornelia Kraus, Susanne Blichfeldt, Per Hoffmann, Heiko Reutter, F.F. Brockschmidt, Martina Kreiß‐Nachtsheim, P. H. Vogt, Trine Prescott, Zeynep Tümer, J.A. Lee
20146
11
Genetische Diagnostik im klinischen Alltag der Kinder- und Jugendpsychiatrie – Indikationen, Rahmenbedingungen, Hürden und Lösungsvorschläge
Zeitschrift für Kinder- und Jugendpsychiatrie und Psychotherapie ·Franziska Degenhardt, Eva Wohlleber, Rami Abou Jamra, Johannes Hebebrand
20232

About Eva Wohlleber

Eva Wohlleber is a scholar working on Genetics, Molecular Biology, Surgery, Genetics and Cellular and Molecular Neuroscience, having authored 11 papers that have together received 458 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (7 papers), Genetics and Neurodevelopmental Disorders (5 papers), Genomics and Rare Diseases (4 papers), Chromatin Remodeling and Cancer (2 papers), Congenital heart defects research (2 papers), Neurological diseases and metabolism (1 paper), Reconstructive Facial Surgery Techniques (1 paper) and Hereditary Neurological Disorders (1 paper). The work is most often cited by research in Genetics (298 citations), Developmental Neuroscience (18 citations), Molecular Biology (286 citations), Pathology and Forensic Medicine (61 citations) and Genetics (33 citations). Eva Wohlleber has collaborated with scholars based in Germany, United Kingdom and Switzerland. Frequent co-authors include Hartmut Engels, Anita Rauch, Alexander M. Zink, Arif B. Ekici, André Reis, Eva Rossier, Christiane Zweier, Markus Zweier, Juliane Hoyer and Dagmar Wieczorek. Their work appears in journals such as Human Mutation, The American Journal of Human Genetics, European Journal of Human Genetics, European Journal of Medical Genetics and Cytogenetic and Genome Research.

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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