T. Grimm
Impact in
- Genetics top 2%
- Neurogenetic and Muscular Disorders Research
- Genomic variations and chromosomal abnormalities
- Molecular Biology top 5%
- Muscle Physiology and Disorders
- RNA modifications and cancer
- Ion channel regulation and function
- RNA Research and Splicing
Papers in
-
- Muscle Physiology and Disorders 21
- RNA Research and Splicing 8
- Genetics 36
- Neurogenetic and Muscular Disorders Research 17
- Genetics and Neurodevelopmental Disorders 7
- Genomic variations and chromosomal abnormalities 7
- BRCA gene mutations in cancer 6
- Co-authors
- Wolfram Kreß (9 shared papers)Michael Schmid (1 shared paper)Martina Guttenbach (1 shared paper)Birgit Koschorz (1 shared paper)Klaus Zerres (11 shared papers)C R Müller (5 shared papers)H Wesselhoeft (2 shared papers)Gerhard Meng (7 shared papers)
- Journals
- Human Genetics (13 papers)Journal of Medical Genetics (9 papers)Neuromuscular Disorders (8 papers)Genomics (5 papers)Clinical Genetics (3 papers)
- Partner nations
- GermanyUnited StatesItaly
In The Last Decade
T. Grimm
98 papers receiving 2.4k citations
Peers
Comparison fields: 5 of 102
- Genetics 478
- Genetics 637
- Molecular Biology 1.6k
- Developmental Neuroscience 79
- Cellular and Molecular Neuroscience 324
Countries citing papers authored by T. Grimm
This map shows the geographic impact of T. Grimm'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 T. Grimm with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites T. Grimm more than expected).
Fields of papers citing papers by T. Grimm
This network shows the impact of papers produced by T. Grimm. 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 T. Grimm. The network helps show where T. Grimm may publish in the future.
Co-authors
The 25 scholars most cited alongside T. Grimm, 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 103 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Sex chromosome loss and aging: in situ hybridization studies on human interphase nuclei. | 1995 | 188 |
| 2 | 2008 | 160 | |
| 3 | 2008 | 130 | |
| 4 | Characterization of the factor VIII defect in 147 patients with sporadic hemophilia A: family studies indicate a mutation type-dependent sex ratio of mutation frequencies. | 1996 | 114 |
| 5 | 1995 | 112 | |
| 6 | 1994 | 89 | |
| 7 | 2002 | 88 | |
| 8 | 1994 | 86 | |
| 9 | 1981 | 71 | |
| 10 | 1991 | 66 | |
| 11 | 1999 | 63 | |
| 12 | 2009 | 62 | |
| 13 | Survival in Duchenne muscular dystrophy. | 2012 | 61 |
| 14 | 1999 | 60 | |
| 15 | Discordance, in a malignant hyperthermia pedigree, between in vitro contracture-test phenotypes and haplotypes for the MHS1 region on chromosome 19q12-13.2, comprising the C1840T transition in the RYR1 gene. | 1995 | 58 |
| 16 | [The genetic aspects of Williams-Beuren syndrome and the isolated form of the supravalvular aortic stenosis. Investigation of 128 families (author's transl)]. | 1980 | 57 |
| 17 | 1991 | 51 | |
| 18 | 2000 | 47 | |
| 19 | 2000 | 41 | |
| 20 | 1999 | 38 |
About T. Grimm
T. Grimm is a scholar working on Molecular Biology, Genetics, Genetics, Cellular and Molecular Neuroscience and Cardiology and Cardiovascular Medicine, having authored 103 papers that have together received 2.6k indexed citations. Recurring topics across this work include Muscle Physiology and Disorders (21 papers), Neurogenetic and Muscular Disorders Research (17 papers), Genetic Neurodegenerative Diseases (11 papers), Cardiomyopathy and Myosin Studies (9 papers), RNA Research and Splicing (8 papers), Genetics and Neurodevelopmental Disorders (7 papers), Genomic variations and chromosomal abnormalities (7 papers) and BRCA gene mutations in cancer (6 papers). The work is most often cited by research in Genetics (478 citations), Genetics (637 citations), Molecular Biology (1.6k citations), Developmental Neuroscience (79 citations) and Cellular and Molecular Neuroscience (324 citations). T. Grimm has collaborated with scholars based in Germany, United States and Italy. Frequent co-authors include Wolfram Kreß, Michael Schmid, Martina Guttenbach, Birgit Koschorz, Klaus Zerres, C R Müller, H Wesselhoeft, Gerhard Meng, B. Müller and K. Ricker. Their work appears in journals such as Human Genetics, Journal of Medical Genetics, Neuromuscular Disorders, Genomics and Clinical Genetics.
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.