M. Winkelmann
Impact in
- Genetics top 2%
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Animal Genetics and Reproduction
- Developmental Biology top 10%
Papers in
-
- Ubiquitin and proteasome pathways 3
- Genomics and Chromatin Dynamics 2
- 14-3-3 protein interactions 1
- Mitochondrial Function and Pathology 1
- Genetics 3
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 3
- Co-authors
- Gudrun Rappold (5 shared papers)Annelyse Mertz (4 shared papers)Ercole Rao (2 shared papers)Andreas Rump (2 shared papers)André Rosenthal (2 shared papers)Michael B. Ranke (1 shared paper)Koji Muroya (1 shared paper)U. Heinrich (1 shared paper)
- Journals
- Human Molecular Genetics (2 papers)Cytogenetic and Genome Research (1 paper)Frontiers in Bioengineering and Biotechnology (1 paper)Nature Genetics (1 paper)Genomics (1 paper)
- Partner nations
- GermanyPolandUnited States
In The Last Decade
M. Winkelmann
7 papers receiving 891 citations
M. Winkelmann's Hit Papers
Peers
Comparison fields: 5 of 61
- Genetics 693
- Developmental Biology 23
- Gender Studies 96
- Reproductive Medicine 68
- Molecular Biology 537
Countries citing papers authored by M. Winkelmann
This map shows the geographic impact of M. Winkelmann'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 M. Winkelmann with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites M. Winkelmann more than expected).
Fields of papers citing papers by M. Winkelmann
This network shows the impact of papers produced by M. Winkelmann. 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 M. Winkelmann. The network helps show where M. Winkelmann may publish in the future.
Co-authors
The 25 scholars most cited alongside M. Winkelmann, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | Pseudoautosomal deletions encompassing a novel homeobox gene cause growth failure in idiopathic short stature and Turner syndrome Hit paper breakdown → | 1997 | 705 |
| 2 | 1997 | 95 | |
| 3 | 1995 | 52 | |
| 4 | 2023 | 27 | |
| 5 | 2000 | 22 | |
| 6 | 1994 | 13 | |
| 7 | 2008 | 5 |
About M. Winkelmann
M. Winkelmann is a scholar working on Molecular Biology, Genetics, Plant Science, Cancer Research and Genetics, having authored 7 papers that have together received 919 indexed citations. Recurring topics across this work include Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (3 papers), Ubiquitin and proteasome pathways (3 papers), Chromosomal and Genetic Variations (2 papers), Genomics and Chromatin Dynamics (2 papers), NF-κB Signaling Pathways (1 paper), 14-3-3 protein interactions (1 paper), Mitochondrial Function and Pathology (1 paper) and MicroRNA in disease regulation (1 paper). The work is most often cited by research in Genetics (693 citations), Developmental Biology (23 citations), Gender Studies (96 citations), Reproductive Medicine (68 citations) and Molecular Biology (537 citations). M. Winkelmann has collaborated with scholars based in Germany, Poland and United States. Frequent co-authors include Gudrun Rappold, Annelyse Mertz, Ercole Rao, Andreas Rump, André Rosenthal, Michael B. Ranke, Koji Muroya, U. Heinrich, Gabriele Nordsiek and Beate Niesler. Their work appears in journals such as Human Molecular Genetics, Cytogenetic and Genome Research, Frontiers in Bioengineering and Biotechnology, Nature Genetics and Genomics.
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.