T. Grimm

3.9k citations

100 papers · 2.3k indexed · h-index 28

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 ⓘ

Molecular Biology 59
- Muscle Physiology and Disorders 21
- RNA Research and Splicing 8
- RNA modifications and cancer 6
Genetics 36
- Neurogenetic and Muscular Disorders Research 17
- Genomic variations and chromosomal abnormalities 7
- Genetics and Neurodevelopmental Disorders 6

Co-authors: Wolfram Kreß (9 shared papers)Birgit Koschorz (1 shared paper)Martina Guttenbach (1 shared paper)Michael Schmid (1 shared paper)C R Müller (5 shared papers)Klaus Zerres (8 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)The American Journal of Human Genetics (3 papers)
Partner nations: Germany United States Italy

In The Last Decade

T. Grimm

95 papers receiving 2.2k citations

Peers

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-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.

Border = papers with T. Grimm Line = papers co-authored together T. Grimm links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 100 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. PubMed ·Martina Guttenbach, Birgit Koschorz, Ulrike Bernthaler, T. Grimm, Michael Schmid	1995	181
2	Congenital heart disease is a feature of severe infantile spinal muscular atrophy Journal of Medical Genetics ·Sabine Rudnik‐Schöneborn, Raoul Heller, C Berg, Christopher Betzler, T. Grimm, Thomas Eggermann, Katja Eggermann, Radu Wirth, Brunhilde Wirth, Klaus Zerres	2008	144
3	PTHR1 Loss-of-Function Mutations in Familial, Nonsyndromic Primary Failure of Tooth Eruption The American Journal of Human Genetics ·Eva L. Decker, Angelika Stellzig‐Eisenhauer, Britta Fiebig, Christiane Rau, Wolfram Kreß, Kathrin Saar, Franz Rüschendorf, Norbert Hübner, T. Grimm, Bernhard H. F. Weber	2008	112
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. PubMed ·Jéfferson Becker, R. Schwaab, A. Möller-Taube, U. Schwaab, W. Schmidt, Hans‐Hermann Brackmann, T. Grimm, K. Olek, Johannes Oldenburg	1996	102
5	The myotubular myopathies: differential diagnosis of the X linked recessive, autosomal dominant, and autosomal recessive forms and present state of DNA studies. Journal of Medical Genetics ·Carina Wallgren‐Pettersson, Angus Clarke, Françoise Samson, Michel Fardeau, Victor Dubowitz, H. Moser, T. Grimm, Richard J. Barohn, P. G. Barth	1995	97
6	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 ·Ralf Giess, Bettina Holtmann, M. Braga, T. Grimm, Bertram Müller‐Myhsok, Klaus V. Toyka, Michael Sendtner	2002	84
7	On the origin of deletions and point mutations in Duchenne muscular dystrophy: most deletions arise in oogenesis and most point mutations result from events in spermatogenesis. Journal of Medical Genetics ·T. Grimm, Gerhard Meng, Sabina Liechti‐Gallati, T. Bettecken, C R Müller, B. Müller	1994	84
8	The Human Gene for Alkaptonuria (AKU) Maps to Chromosome 3q Genomics ·S. Janocha, Werner Wolz, S Srseń, K Srsnová, Xavier Montagutelli, Jean‐Louis Guénet, T. Grimm, (unknown), C R Müller	1994	81
9	The dup(3q) syndrome: Report of eight cases and review of the literature American Journal of Medical Genetics ·Peter Steinbach, William N. Adkins, H. Caspar, Kenneth W. Dumars, J. Gebauer, Enid F. Gilbert, T. Grimm, M Habedank, I. Hansmann, J. Herrmann, Elisabeth G. Kaveggia, U. Langenbeck, L F Meisner, T. M. Najafzadeh, John M. Opitz, Catherine G. Palmer, Heiko Peters, W. Scholz, Adelci Tavares, C. Wiedeking	1981	69
10	Survival in Duchenne muscular dystrophy. PubMed ·Susanne Rall, T. Grimm	2012	60
11	Evidence for linkage of the central core disease locus to the proximal long arm of human chromosome 19 Genomics ·Katrin Kausch, F. Lehmann‐Horn, M. Janka, Bé Wieringa, T. Grimm, C. R. Müller	1991	59
12	Interleukin‐1 haplotype and periodontal disease progression following therapy Journal Of Clinical Periodontology ·Benjamin Ehmke, Wolfram Kreß, Helge Karch, T. Grimm, B Klaiber, Daniel S. Thoma	1999	58
13	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. PubMed ·Thomas Deufel, Ralf Sudbrak, Y Feist, B Rübsam, Ingrid Du Chesne, K L Schäfer, Norbert Roewer, T. Grimm, F. Lehmann‐Horn, E J Hartung	1995	56
14	Genotype–phenotype studies in infantile spinal muscular atrophy (SMA) type I in Germany: implications for clinical trials and genetic counselling Clinical Genetics ·Sabine Rudnik‐Schöneborn, C Berg, Klaus Zerres, Christopher Betzler, T. Grimm, Thomas Eggermann, Katja Eggermann, Radu Wirth, Brunhilde Wirth, Raoul Heller	2009	55
15	Linkage of proximal myotonic myopathy to chromosome 3q Neurology ·K. Ricker, T. Grimm, Manuela C. Koch, Carsten Q. Schneider, (unknown), C. D. Reimers, Wilhelm Schulte‐Mattler, B. Mueller-Myhsok, K. V. Toyka, C R Mueller	1999	55
16	[The genetic aspects of Williams-Beuren syndrome and the isolated form of the supravalvular aortic stenosis. Investigation of 128 families (author's transl)]. PubMed ·T. Grimm, H Wesselhoeft	1980	52
17	Linkage data suggesting allelic heterogeneity for paramyotonia congenita and hyperkalemic periodic paralysis on chromosome 17 Human Genetics ·ManuelaC. Koch, K. Ricker, Michaël Otto, T. Grimm, Klaus Bender, Barbara Zoll, PeterS. Harper, Frank Lehmann‐Horn, R. R�del, Eric P. Hoffman	1991	47
18	An unusual FGFR1 mutation (fibroblast growth factor receptor 1 mutation) in a girl with non-syndromic trigonocephaly Cytogenetic and Genome Research ·(unknown), Birgit Petersen, H. Collmann, T. Grimm	2000	42
19	Genetic linkage analysis with dyslexia: Evidence for linkage of spelling disability to chromosome 15 European Child & Adolescent Psychiatry ·Markus M. Nöthen, Gerd Schulte‐Körne, T. Grimm, Sven Cichon, Ina R. Vogt, Bertram Müller‐Myhsok, Peter Propping, Helmut Remschmidt	1999	36
20	Proximal myotonic myopathy Neurology ·Carsten Q. Schneider, Andreas Ziegler, K. Ricker, T. Grimm, (unknown), C. D. Reimers, H.‐M. Meinck, Karlheinz Reiners, K. V. Toyka	2000	35

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 100 papers that have together received 2.3k indexed citations. Recurring topics across this work include Muscle Physiology and Disorders (21 papers), Neurogenetic and Muscular Disorders Research (17 papers), Genetic Neurodegenerative Diseases (12 papers), Cardiomyopathy and Myosin Studies (9 papers), RNA Research and Splicing (8 papers), Genomic variations and chromosomal abnormalities (7 papers), RNA modifications and cancer (6 papers) and Genetics and Neurodevelopmental Disorders (6 papers). The work is most often cited by research in Genetics (441 citations), Molecular Biology (1.6k citations), Genetics (618 citations), Developmental Neuroscience (77 citations) and Cellular and Molecular Neuroscience (312 citations). T. Grimm has collaborated with scholars based in Germany, United States and Italy. Frequent co-authors include Wolfram Kreß, Birgit Koschorz, Martina Guttenbach, Michael Schmid, C R Müller, Klaus Zerres, H Wesselhoeft, Gerhard Meng, B. Müller and C. R. Müller. Their work appears in journals such as Human Genetics, Journal of Medical Genetics, Neuromuscular Disorders, Genomics and The American Journal of Human 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.

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