Thomas Meitinger
Impact in
- Nephrology top 0.2%
- Parathyroid Disorders and Treatments
- Clinical Biochemistry top 0.1%
- Metabolism and Genetic Disorders
Papers in
-
- Mitochondrial Function and Pathology 37
- Retinal Development and Disorders 17
- Genetics 101
- Genomic variations and chromosomal abnormalities 20
- Genetic Associations and Epidemiology 19
- Genetics and Neurodevelopmental Disorders 17
- Genomics and Rare Diseases 17
- Co-authors
- Tim M. Strom (73 shared papers)Holger Prokisch (60 shared papers)Peter Lichtner (46 shared papers)Michael J. Econs (5 shared papers)Bettina Lorenz‐Depiereux (9 shared papers)Monika Grabowski (3 shared papers)Alfons Meindl (10 shared papers)Kenneth E. White (3 shared papers)
- Journals
- European Journal of Human Genetics (16 papers)The American Journal of Human Genetics (15 papers)Nature Genetics (13 papers)Human Molecular Genetics (12 papers)Neuropediatrics (9 papers)
- Partner nations
- GermanyUnited StatesAustria
In The Last Decade
Thomas Meitinger
316 papers receiving 19.9k citations
Thomas Meitinger's Hit Papers
Peers
Comparison fields: 5 of 176
- Nephrology 1.9k
- Clinical Biochemistry 1.3k
- Genetics 5.3k
- Molecular Biology 10.9k
- Ophthalmology 1.2k
Countries citing papers authored by Thomas Meitinger
This map shows the geographic impact of Thomas Meitinger'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 Thomas Meitinger with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Thomas Meitinger more than expected).
Fields of papers citing papers by Thomas Meitinger
This network shows the impact of papers produced by Thomas Meitinger. 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 Thomas Meitinger. The network helps show where Thomas Meitinger may publish in the future.
Co-authors
The 25 scholars most cited alongside Thomas Meitinger, 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 321 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Autosomal dominant hypophosphataemic rickets is associated with mutations in FGF23 Hit paper breakdown → | 2000 | 1284 |
| 2 | An unusual member of the nuclear hormone receptor superfamily responsible for X-linked adrenal hypoplasia congenita Hit paper breakdown → | 1994 | 735 |
| 3 | Hypothetical LOC387715 is a second major susceptibility gene for age-related macular degeneration, contributing independently of complement factor H to disease risk Hit paper breakdown → | 2005 | 652 |
| 4 | Mutations in the DAX-1 gene give rise to both X-linked adrenal hypoplasia congenita and hypogonadotropic hypogonadism Hit paper breakdown → | 1994 | 640 |
| 5 | Genetics Meets Metabolomics: A Genome-Wide Association Study of Metabolite Profiles in Human Serum Hit paper breakdown → | 2008 | 552 |
| 6 | Mutations in the CEP290 (NPHP6) Gene Are a Frequent Cause of Leber Congenital Amaurosis Hit paper breakdown → | 2006 | 512 |
| 7 | A genome-wide perspective of genetic variation in human metabolism Hit paper breakdown → | 2009 | 510 |
| 8 | Mutations in the deubiquitinase gene USP8 cause Cushing's disease Hit paper breakdown → | 2014 | 440 |
| 9 | 1998 | 431 | |
| 10 | 1996 | 420 | |
| 11 | 1998 | 416 | |
| 12 | 2005 | 404 | |
| 13 | 2000 | 384 | |
| 14 | 2001 | 357 | |
| 15 | 2008 | 315 | |
| 16 | 2011 | 291 | |
| 17 | 2001 | 273 | |
| 18 | 2016 | 254 | |
| 19 | 2000 | 245 | |
| 20 | 2014 | 212 |
About Thomas Meitinger
Thomas Meitinger is a scholar working on Molecular Biology, Genetics, Clinical Biochemistry, Neurology and Neurology, having authored 321 papers that have together received 20.7k indexed citations. Recurring topics across this work include Mitochondrial Function and Pathology (37 papers), Metabolism and Genetic Disorders (27 papers), Neurological diseases and metabolism (21 papers), Genomic variations and chromosomal abnormalities (20 papers), Genetic Associations and Epidemiology (19 papers), Genetics and Neurodevelopmental Disorders (17 papers), Genomics and Rare Diseases (17 papers) and Retinal Development and Disorders (17 papers). The work is most often cited by research in Nephrology (1.9k citations), Clinical Biochemistry (1.3k citations), Genetics (5.3k citations), Molecular Biology (10.9k citations) and Ophthalmology (1.2k citations). Thomas Meitinger has collaborated with scholars based in Germany, United States and Austria. Frequent co-authors include Tim M. Strom, Holger Prokisch, Peter Lichtner, Michael J. Econs, Bettina Lorenz‐Depiereux, Monika Grabowski, Alfons Meindl, Kenneth E. White, W. Evans and Thomas Illig. Their work appears in journals such as European Journal of Human Genetics, The American Journal of Human Genetics, Nature Genetics, Human Molecular Genetics and Neuropediatrics.
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.