T. Grimm

3.9k total citations
100 papers, 2.3k citations indexed

About

T. Grimm is a scholar working on Molecular Biology, Genetics and Genetics. According to data from OpenAlex, T. Grimm has authored 100 papers receiving a total of 2.3k indexed citations (citations by other indexed papers that have themselves been cited), including 59 papers in Molecular Biology, 36 papers in Genetics and 18 papers in Genetics. Recurrent topics in T. Grimm's work include Muscle Physiology and Disorders (21 papers), Neurogenetic and Muscular Disorders Research (17 papers) and Genetic Neurodegenerative Diseases (12 papers). T. Grimm is often cited by papers focused on Muscle Physiology and Disorders (21 papers), Neurogenetic and Muscular Disorders Research (17 papers) and Genetic Neurodegenerative Diseases (12 papers). T. Grimm collaborates with scholars based in Germany, United States and Italy. T. Grimm's co-authors include Wolfram Kreß, Martina Guttenbach, Michael Schmid, Birgit Koschorz, C R Müller, Klaus Zerres, Gerhard Meng, H Wesselhoeft, B. Müller and C. R. Müller and has published in prestigious journals such as Nature, Neurology and Cancer Research.

In The Last Decade

T. Grimm

95 papers receiving 2.2k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
T. Grimm Germany 28 1.6k 618 441 317 312 100 2.3k
Francesca Gualandi Italy 32 2.1k 1.3× 531 0.9× 316 0.7× 513 1.6× 342 1.1× 115 2.8k
Dalil Hamroun France 24 2.1k 1.4× 976 1.6× 380 0.9× 414 1.3× 361 1.2× 60 3.5k
Jaakko Leisti Finland 27 1.1k 0.7× 873 1.4× 202 0.5× 99 0.3× 338 1.1× 82 2.1k
Giulio Piluso Italy 26 2.0k 1.2× 405 0.7× 316 0.7× 516 1.6× 484 1.6× 83 2.5k
Ruth Newbury‐Ecob United Kingdom 25 2.0k 1.3× 1.3k 2.0× 222 0.5× 257 0.8× 208 0.7× 64 3.2k
Anna Sárközy United Kingdom 30 2.4k 1.5× 449 0.7× 192 0.4× 503 1.6× 165 0.5× 91 2.9k
M A Patton United Kingdom 26 1.0k 0.7× 751 1.2× 151 0.3× 158 0.5× 150 0.5× 61 1.9k
Pamela J. Snyder United States 20 1.5k 0.9× 221 0.4× 674 1.5× 130 0.4× 194 0.6× 42 2.5k
Bruno Leheup France 29 1.1k 0.7× 758 1.2× 215 0.5× 145 0.5× 114 0.4× 97 2.2k
Rafaëlle Bernard France 20 2.3k 1.5× 274 0.4× 274 0.6× 237 0.7× 354 1.1× 54 2.8k

Countries citing papers authored by T. Grimm

Since Specialization
Citations

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

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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-authorship network of co-authors of T. Grimm

This figure shows the co-authorship network connecting the top 25 collaborators of T. Grimm. A scholar is included among the top collaborators of T. Grimm based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with T. Grimm. T. Grimm is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Stellzig‐Eisenhauer, Angelika, Eva L. Decker, Philipp Meyer‐Marcotty, et al.. (2013). [Primary failure of eruption (PFE). Clinical and molecular genetics analysis] Article in French. University of Regensburg Publication Server (University of Regensburg). 2 indexed citations
2.
Stellzig‐Eisenhauer, Angelika, Eva L. Decker, Philipp Meyer‐Marcotty, et al.. (2013). Défaut primaire d’éruption (DPE). Analyse génétique clinique et moléculaire. L Orthodontie Française. 84(3). 241–250. 17 indexed citations
3.
König, Inke R., Johannes Schumacher, Per Hoffmann, et al.. (2010). Mapping for dyslexia and related cognitive trait loci provides strong evidence for further risk genes on chromosome 6p21. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 156(1). 36–43. 25 indexed citations
4.
Zirn, Birgit, Wolfram Kreß, T. Grimm, et al.. (2008). Association of homozygous LMNA mutation R471C with new phenotype: Mandibuloacral dysplasia, progeria, and rigid spine muscular dystrophy. American Journal of Medical Genetics Part A. 146A(8). 1049–1054. 33 indexed citations
5.
Decker, Eva L., Angelika Stellzig‐Eisenhauer, Britta Fiebig, et al.. (2008). PTHR1 Loss-of-Function Mutations in Familial, Nonsyndromic Primary Failure of Tooth Eruption. The American Journal of Human Genetics. 83(6). 781–786. 112 indexed citations
6.
Frank, Valeska, Nadina Ortiz Brüchle, Suzanna G.M. Frints, et al.. (2007). Aberrant splicing is a common mutational mechanism inMKS1, a key player in Meckel-Gruber syndrome. Human Mutation. 28(6). 638–639. 17 indexed citations
7.
Felbor, Ute, Ulrich Sure, T. Grimm, & Helmut Bertalanffy. (2006). Genetics of Cerebral Cavernous Angioma. Central European Neurosurgery - Zentralblatt für Neurochirurgie. 67(3). 110–116. 25 indexed citations
8.
Giess, Ralf, Bettina Holtmann, M. Braga, et al.. (2002). Early Onset of Severe Familial Amyotrophic Lateral Sclerosis with a SOD-1 Mutation: Potential Impact of CNTF as a Candidate Modifier Gene. The American Journal of Human Genetics. 70(5). 1277–1286. 84 indexed citations
9.
Schneider, Carsten Q., Carsten Wessig, C. R. Müller, D. Brechtelsbauer, & T. Grimm. (2001). Proximal myotonic myopathy and proximal myotonic dystrophy: Two different entities? The phenotypic variability of proximal myotonic syndromes. Neuromuscular Disorders. 11(5). 485–488. 5 indexed citations
10.
Hofmann, U., Nicola Wagner, T. Grimm, E.‐B. Bröcker, & Henning Hamm. (1998). Streifen- und wirbelförmige nävoide Hypermelanose : Fallbeschreibung und Literaturübersicht. Der Hautarzt. 49(5). 408–412. 1 indexed citations
11.
Oldenburg, Johannes, R. Schwaab, T. Grimm, et al.. (1993). Direct and indirect estimation of the sex ratio of mutation frequencies in hemophilia A.. PubMed. 53(6). 1229–38. 19 indexed citations
12.
Schwemmle, Sabine, K. Wolff, L. Palmucci, et al.. (1993). Multipoint Mapping of the Central Core Disease Locus. Genomics. 17(1). 205–207. 11 indexed citations
13.
Koch, Manuela C., T. Grimm, H G Harley, & Peter S. Harper. (1992). Reply to Goodship et al.. The American Journal of Human Genetics. 50(6). 1341–1342. 2 indexed citations
14.
Kausch, Katrin, T. Grimm, K. Ricker, et al.. (1991). No evidence for linkage of autosomal dominant proximal spinal muscular atrophies to chromosome 5q markers. Human Genetics. 86(3). 317–8. 17 indexed citations
15.
Hejtmancik, J. Fielding, G. Romeo, Mikael Lindlöf, et al.. (1989). A genetic linkage map of five marker loci in and around the Duchenne muscular dystrophy locus. Genomics. 4(1). 105–109. 17 indexed citations
16.
Mostacciuolo, Maria Luisa, et al.. (1989). Problems in genetic counseling in a family with an “atypical” centronuclear myopathy. American Journal of Medical Genetics. 32(3). 417–419. 5 indexed citations
17.
18.
Schmid, Michael, et al.. (1986). Chromosome 7 short arm deletion, 7p21?pter. Human Genetics. 74(3). 323–5. 31 indexed citations
19.
Grimm, T.. (1982). The influence of half-chromatid mutations on the ratio of new mutations in lethal X-linked recessive disorders.. PubMed. 34(1). 142–5. 2 indexed citations
20.
Grimm, T.. (1981). [Newborn screening for Duchenne muscular dystrophy (author's transl)].. PubMed. 129(7). 414–7. 4 indexed citations

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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