Zeynep Tümer
Impact in
- Nutrition and Dietetics top 0.2%
- Trace Elements in Health
- Genetics top 0.5%
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Genetic Syndromes and Imprinting
Papers in
-
- RNA regulation and disease 19
- Genetics 88
- Genomic variations and chromosomal abnormalities 47
- Genetics and Neurodevelopmental Disorders 29
- Genetic Syndromes and Imprinting 18
- Co-authors
- Niels Tommerup (55 shared papers)Nina Horn (27 shared papers)Lisbeth Birk Møller (19 shared papers)T. Tønnesen (9 shared papers)Daniella Bach‐Holm (2 shared papers)Karen Brøndum‐Nielsen (31 shared papers)Anthony P. Monaco (4 shared papers)Jamel Chelly (2 shared papers)
- Journals
- Clinical Genetics (20 papers)European Journal of Human Genetics (11 papers)Journal of Medical Genetics (9 papers)Human Mutation (6 papers)Stem Cell Research (6 papers)
- Partner nations
- DenmarkGermanyUnited Kingdom
In The Last Decade
Zeynep Tümer
177 papers receiving 5.6k citations
Zeynep Tümer's Hit Papers
Peers
Comparison fields: 5 of 144
- Nutrition and Dietetics 1.5k
- Genetics 1.7k
- Molecular Biology 3.0k
- Health, Toxicology and Mutagenesis 479
- Hematology 360
Countries citing papers authored by Zeynep Tümer
This map shows the geographic impact of Zeynep Tümer'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 Zeynep Tümer with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Zeynep Tümer more than expected).
Fields of papers citing papers by Zeynep Tümer
This network shows the impact of papers produced by Zeynep Tümer. 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 Zeynep Tümer. The network helps show where Zeynep Tümer may publish in the future.
Co-authors
The 25 scholars most cited alongside Zeynep Tümer, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 179 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | A human phenome-interactome network of protein complexes implicated in genetic disorders Hit paper breakdown → | 2007 | 660 |
| 2 | Isolation of a candidate gene for Menkes disease that encodes a potential heavy metal binding protein Hit paper breakdown → | 1993 | 559 |
| 3 | 2009 | 273 | |
| 4 | 2009 | 193 | |
| 5 | 2015 | 132 | |
| 6 | 2014 | 128 | |
| 7 | 2008 | 116 | |
| 8 | 2014 | 102 | |
| 9 | 2012 | 101 | |
| 10 | Early treatment of Menkes disease with parenteral copper-histidine: long-term follow-up of four treated patients. | 1998 | 89 |
| 11 | 2019 | 88 | |
| 12 | 2008 | 86 | |
| 13 | 2016 | 85 | |
| 14 | 2000 | 85 | |
| 15 | Identification of point mutations in 41 unrelated patients affected with Menkes disease. | 1997 | 82 |
| 16 | 2010 | 73 | |
| 17 | 2016 | 71 | |
| 18 | 1995 | 67 | |
| 19 | 1998 | 66 | |
| 20 | 2006 | 64 |
About Zeynep Tümer
Zeynep Tümer is a scholar working on Molecular Biology, Genetics, Nutrition and Dietetics, Pediatrics, Perinatology and Child Health and Clinical Psychology, having authored 179 papers that have together received 5.8k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (47 papers), Trace Elements in Health (30 papers), Genetics and Neurodevelopmental Disorders (29 papers), RNA regulation and disease (19 papers), Genetic Syndromes and Imprinting (18 papers), Prenatal Screening and Diagnostics (15 papers), Obsessive-Compulsive Spectrum Disorders (12 papers) and Chromosomal and Genetic Variations (12 papers). The work is most often cited by research in Nutrition and Dietetics (1.5k citations), Genetics (1.7k citations), Molecular Biology (3.0k citations), Health, Toxicology and Mutagenesis (479 citations) and Hematology (360 citations). Zeynep Tümer has collaborated with scholars based in Denmark, Germany and United Kingdom. Frequent co-authors include Niels Tommerup, Nina Horn, Lisbeth Birk Møller, T. Tønnesen, Daniella Bach‐Holm, Karen Brøndum‐Nielsen, Anthony P. Monaco, Jamel Chelly, Yumiko Ishikawa-Brush and Yves Moreau. Their work appears in journals such as Clinical Genetics, European Journal of Human Genetics, Journal of Medical Genetics, Human Mutation and Stem Cell 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.