Michael Wittig

6.3k citations
29 papers · 1.3k · h-index 15

Impact in

  • Aging top 5%
  • Genetics top 5%
    • Genomic variations and chromosomal abnormalities
    • Genomics and Rare Diseases
    • Forensic and Genetic Research
    • Genetics and Neurodevelopmental Disorders

Papers in

    • Genomic variations and chromosomal abnormalities 4
    • Genetic Mapping and Diversity in Plants and Animals 4
    • Genetic diversity and population structure 4
    • Genetic and phenotypic traits in livestock 3
    • Genetic Associations and Epidemiology 3
    • Genetics and Neurodevelopmental Disorders 2
    • RNA regulation and disease 3
    • RNA modifications and cancer 3

Michael Wittig

29 papers receiving 1.2k citations

Peers

Michael Wittig
Comparison fields: 5 of 108
  • Aging 87
  • Genetics 458
  • Molecular Biology 609
  • Plant Science 204
  • Psychiatry and Mental health 69
Replace Corinna Menzel with:
Corinna Menzel Germany
Fernando Pardo-Manuel de Villena United States
D. Messina Italy
Alan Packer United States
Andrew Kirby United States
Jin Xue China
Abdul Karim Sesay United Kingdom
Takehito Kaneko Japan
H Katz United States
Jason A. Bubier United States
Michael Wittig relative to Corinna Menzel Germany Corinna Menzel's profile →
Citations per field
00.5×3.5×
Corinna Menzel · 1×
Citations per year

Countries citing papers authored by Michael Wittig

Since Specialization
Citations

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

Fields of papers citing papers by Michael Wittig

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Michael Wittig, 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 Michael Wittig Line = papers co-authored together Michael Wittig links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 29 papers — load more, or switch the sort, to bring in the rest.

#Work
1 2006273
2 2009167
3 2011162
4 2011155
5 2001110
6 201648
7 201539
8 201533
9 200226
10 200922
11 202120
12 201219
13 201118
14 202017
15 202215
16 201614
17 202214
18 200614
19 201712
20 200712

About Michael Wittig

Michael Wittig is a scholar working on Genetics, Molecular Biology, Cellular and Molecular Neuroscience, Neurology and Hematology, having authored 29 papers that have together received 1.3k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (4 papers), Genetic Mapping and Diversity in Plants and Animals (4 papers), Genetic diversity and population structure (4 papers), Genetic and phenotypic traits in livestock (3 papers), RNA regulation and disease (3 papers), Genetic Associations and Epidemiology (3 papers), RNA modifications and cancer (3 papers) and Genetics and Neurodevelopmental Disorders (2 papers). The work is most often cited by research in Aging (87 citations), Genetics (458 citations), Molecular Biology (609 citations), Plant Science (204 citations) and Psychiatry and Mental health (69 citations). Michael Wittig has collaborated with scholars based in Germany, United States and Australia. Frequent co-authors include Michael Krawczak, André Franke, Jochen Hampe, D.N. Cooper, Nick Thomas, Matthew Mort, H. Schmitter, Andreas Hellmann, Matthias Barann and Simon C. Griffith. Their work appears in journals such as Human Mutation, Nucleic Acids Research, Genome biology, Cell and Heredity.

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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