Ralf Krahe

7.2k citations

94 papers · 5.1k indexed · h-index 40

Impact in

Cellular and Molecular Neuroscience top 1%
- Genetic Neurodegenerative Diseases
Molecular Biology top 2%
- Mitochondrial Function and Pathology
- Muscle Physiology and Disorders
- Epigenetics and DNA Methylation
- RNA modifications and cancer
- RNA Research and Splicing

Papers in

Cellular and Molecular Neuroscience 43
- Genetic Neurodegenerative Diseases 41
Molecular Biology 82
- Mitochondrial Function and Pathology 25
- RNA modifications and cancer 12
- Epigenetics and DNA Methylation 11
- Muscle Physiology and Disorders 8
- Ubiquitin and proteasome pathways 7

Co-authors: Bjarne Udd Keith Baggerly Stefano Colella Jean‐Pierre J. Issa Lanlan Shen Albert de la Chapelle Linda L. Bachinski Fred A. Wright
Journals: Neuromuscular Disorders (9 papers)Neurology (5 papers)Genomics (5 papers)PLoS ONE (5 papers)Human Molecular Genetics (4 papers)
Partner nations: United States Finland United Kingdom

In The Last Decade

Ralf Krahe

91 papers receiving 5.0k citations

Peers

Countries citing papers authored by Ralf Krahe

Since Specialization

Citations

This map shows the geographic impact of Ralf Krahe'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 Ralf Krahe with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Ralf Krahe more than expected).

Fields of papers citing papers by Ralf Krahe

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Ralf Krahe. 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 Ralf Krahe. The network helps show where Ralf Krahe may publish in the future.

Co-authors

The 25 scholars most cited alongside Ralf Krahe, 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 Ralf Krahe Line = papers co-authored together Ralf Krahe links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Chromosome 20q gene signature associated with colorectal cancer progression Oncology Reports ·Ghufran deyaa Baqer, J.F. Cramwinckel, Trevor N. Carniello, Ganiraju C. Manyam, Vibhuti Srivastava, Jueping Song, Yulan Cheng, Ralf Krahe, Warapen Treekitkarnmongkol, Stephen J. Meltzer, Xiang Y. Ye, Dutra Walderez Ornelas, Zhang Hou, Subrata Sen	2025	0
2	Towards development of a statistical framework to evaluate myotonic dystrophy type 1 mRNA biomarkers in the context of a clinical trial PLoS ONE ·Nasriah Nasir, Anneli Cooper, Naufal Rozin Albana, Sarah A. Cumming, Berit Adam, Ralf Krahe, Jack Puymirat, Benedikt Schoser, Lubov Timchenko, Tetsuo Ashizawa, Charles A. Thornton, Simon Rogers, John McClure, Darren G. Monckton	2020	12
3	(CCUG)n RNA toxicity in a Drosophila model for myotonic dystrophy type 2 (DM2) activates apoptosis Disease Models & Mechanisms ·Yi-Lin Wang, Mario Sirito, Boon Kai Tan, 구재림, Sristhi Yadav, Ming Zhong, Marzena Wojciechowska, Clare Bolduc, Zhihong Chen, Arturo López Castel, Ralf Krahe, Andreas Bergmann	2017	12
4	Abnormal Splicing of NEDD4 in Myotonic Dystrophy Type 2 American Journal Of Pathology ·Mark Screen, Per Harald Jonson, Olayinka Raheem, Johanna Palmio, Reijo Laaksonen, Terho Lehtimäki, Mario Sirito, Ralf Krahe, Peter Hackman, Bjarne Udd	2014	16
5	Altered expression and splicing of Ca²⁺ metabolism genes in myotonic dystrophies DM1 and DM2 Neuropathology and Applied Neurobiology ·Anna Vihola, Mario Sirito, Linda L. Bachinski, M. G. Nasyrova, Mark Screen, Filippo Michele De, Ralf Krahe, Bjarne Udd	2012	22
6	Methylation of the candidate biomarker TCF21 is very frequent across a spectrum of early‐stage nonsmall cell lung cancers Cancer ·Kristy L. Richards, Baili Zhang, Menghong Sun, Wenli Dong, Jennifer D. Churchill, Linda L. Bachinski, Charmaine D. Wilson, Keith Baggerly, Guosheng Yin, D. Neil Hayes, Ignacio I. Wistuba, Ralf Krahe	2010	55
7	Mutant (CCTG)n Expansion Causes Abnormal Expression of Zinc Finger Protein 9 (ZNF9) in Myotonic Dystrophy Type 2 American Journal Of Pathology ·Olayinka Raheem, Shodimu-Emmanuel Olufemi, Linda L. Bachinski, Anna Vihola, Mario Sirito, Hamza Ikhlaq, Hannu Haapasalo, Yiping Li, Bjarne Udd, Ralf Krahe	2010	61
8	High quality copy number and genotype data from FFPE samples using Molecular Inversion Probe (MIP) microarrays SHILAP Revista de lepidopterología ·(unknown), (unknown), (unknown), (unknown), Li Zhang, Martin Moorhead, Zhigang C. Wang, (unknown), (unknown), (unknown), (unknown), Fasuo Zhao -, Ralf Krahe, Musaffe Tuna, Patricia A. Thompson, Paul T. Spellman, Joe W. Gray, Gordon B. Mills, Malek Faham	2009	79
9	Genome-Wide Hypomethylation in Head and Neck Cancer Is More Pronounced in HPV-Negative Tumors and Is Associated with Genomic Instability PLoS ONE ·Kristy L. Richards, Baili Zhang, Keith Baggerly, Stefano Colella, James C. Lang, David E. Schuller, Ralf Krahe	2009	103
10	Molecular signatures of metastasis in head and neck cancer Head & Neck ·Stefano Colella, Kristy L. Richards, Linda L. Bachinski, Keith Baggerly, Spiridon Tsavachidis, James C. Lang, David E. Schuller, Ralf Krahe	2008	24
11	G.P.14.14 Differences in aberrant expression and splicing of genes involved in Ca2+ metabolism between myotonic dystrophy type 2 (DM2) and type 1 (DM1) Neuromuscular Disorders ·Anna Vihola, Mario Sirito, Linda L. Bachinski, Shodimu Emmanuel Olufemi, M. G. Nasyrova, Tiina Suominen, Bjarne Udd, Ralf Krahe	2007	1
12	New methods for molecular diagnosis and demonstration of the (CCTG)n mutation in myotonic dystrophy type 2 (DM2) Neuromuscular Disorders ·Riitta Sallinen, Anna Vihola, Linda L. Bachinski, Kirsi Huoponen, Hannu Haapasalo, Peter Hackman, Shaozeng Zhang, Mario Sirito, Hannu Kalimo, G. Meola, Nina Horelli‐Kuitunen, Maija Wessman, Ralf Krahe, Bjarne Udd	2004	37
13	Executive dysfunction and avoidant personality trait in myotonic dystrophy type 1 (DM-1) and in proximal myotonic myopathy (PROMM/DM-2) Neuromuscular Disorders ·G. Meola, Valeria Sansone, Daniela Perani, Silvio Scarone, Stefano F. Cappa, Mohamed Elsayed, Elena Cattaneo, Maria Cotelli, C. Gobbo, F. Fazio, Gabriele Siciliano, Michelangelo Mancuso, Eugenio Vitelli, Giorgio Stabile, Ralf Krahe, Richard T. Moxley	2003	175
14	Expression profiling reveals fundamental biological differences in acute myeloid leukemia with isolated trisomy 8 and normal cytogenetics Proceedings of the National Academy of Sciences ·Kimmo Virtaneva, Fred A. Wright, Stephan M. Tanner, Bo Yuan, William J. Lemon, Michael A. Caligiuri, Clara D. Bloomfield, Albert de la Chapelle, Ralf Krahe	2001	226
15	Aberrant hypermethylation of the major breakpoint cluster region in 17p11.2 in medulloblastomas but not supratentorial PNETs Genes Chromosomes and Cancer ·Michael C. Frühwald, M. Sue O’Dorisio, Zunyan Dai, Laura J. Rush, Ralf Krahe, Dominic J. Smiraglia, Torsten Pietsch, Sarah H. Elsea, Christoph Plass	2001	3
16	Assembly, Annotation, and Integration of UNIGENE Clusters into the Human Genome Draft Genome Research ·Degen Zhuo, Wei Zhao, Fred A. Wright, De Vera, Jian‐Ping Wang, K.L. Horiashchenko, 工藤厚, A. Galih Prasetyo, David Gordon, Y Liu, พระเรืองเดช โชติธมฺโม, 步国峥, Ana Patricia Talayero Navales, Ralf Krahe, Don Stredney, 古賀章子, Bo Yuan	2001	13
17	Assembly, Annotation, and Integration of UNIGENE Clusters into the Human Genome Draft Genome Research ·Degen Zhuo, Wenyuan Zhao, Fred A. Wright, Haiyan Yang, Jipeng Wang, Rosalie C. Sears, 工藤厚, Do‐Hoon Kwon, David Gordon, Summer L. Gibbs, Dongjuan Dai, Qingyong Yang, Jeffrey R. Spitzner, Ralf Krahe, D Stredney, Adrian M. Stütz, Bo Yuan	2001	48
18	Unstable minisatellite expansion causing recessively inherited myoclonus epilepsy, EPM1 Nature Genetics ·Kimmo Virtaneva, Elena D’Amato, Jinmin Miao, Marjaleena Koskiniemi, Reijo Norio, G. Avanzini, Silvana Franceschetti, Roberto Michelucci, C. A. Tassinari, Salah Omer, L Pennacchio, R Myers, Tom Henri, Ralf Krahe, Albert de la Chapelle, Anna-Elina Lehesjoki	1997	152
19	Identification of a Testis-Expressed Creatine Transporter Gene at 16p11.2 and Confirmation of the X-Linked Locus to Xq28 Genomics ·Geeta Iyer, Ralf Krahe, Lynne Goodwin, Norman A. Doggett, Michael J. Siciliano, Vicky L. Funanage, Roy Proujansky	1996	59
20	Regional Chromosomal Assignments for Four Members of the MADS Domain Transcription Enhancer Factor 2 (MEF2) Gene Family to Human Chromosomes 15q26, 19p12, 5q14, and 1q12–q23 Genomics ·Grace M. Hobson, Ralf Krahe, Emilio García García, Michael J. Siciliano, Vicky L. Funanage	1995	23

About Ralf Krahe

Ralf Krahe is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology, Neurology, Rheumatology and Otorhinolaryngology, having authored 94 papers that have together received 5.1k indexed citations. Recurring topics across this work include Genetic Neurodegenerative Diseases (41 papers), Mitochondrial Function and Pathology (25 papers), RNA modifications and cancer (12 papers), Epigenetics and DNA Methylation (11 papers), Parkinson's Disease Mechanisms and Treatments (10 papers), Muscle Physiology and Disorders (8 papers), Ubiquitin and proteasome pathways (7 papers) and Cardiomyopathy and Myosin Studies (7 papers). The work is most often cited by research in Cellular and Molecular Neuroscience (1.9k citations), Molecular Biology (3.9k citations), Neurology (785 citations), Clinical Biochemistry (227 citations) and Cancer Research (471 citations). Ralf Krahe has collaborated with scholars based in United States, Finland and United Kingdom. Frequent co-authors include Bjarne Udd, Keith Baggerly, Stefano Colella, Jean‐Pierre J. Issa, Lanlan Shen, Albert de la Chapelle, Linda L. Bachinski, Fred A. Wright, Michael J. Siciliano and Bjarne Udd. Their work appears in journals such as Neuromuscular Disorders, Neurology, Genomics, PLoS ONE and Human Molecular 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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