Klaus Wrogemann

6.7k total citations · 1 hit paper
85 papers, 3.4k citations indexed

About

Klaus Wrogemann is a scholar working on Molecular Biology, Physiology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Klaus Wrogemann has authored 85 papers receiving a total of 3.4k indexed citations (citations by other indexed papers that have themselves been cited), including 74 papers in Molecular Biology, 17 papers in Physiology and 15 papers in Cellular and Molecular Neuroscience. Recurrent topics in Klaus Wrogemann's work include Muscle Physiology and Disorders (35 papers), Mitochondrial Function and Pathology (21 papers) and Genetic Neurodegenerative Diseases (15 papers). Klaus Wrogemann is often cited by papers focused on Muscle Physiology and Disorders (35 papers), Mitochondrial Function and Pathology (21 papers) and Genetic Neurodegenerative Diseases (15 papers). Klaus Wrogemann collaborates with scholars based in Canada, Germany and United Kingdom. Klaus Wrogemann's co-authors include Cheryl R. Greenberg, Edward Nylen, M. C. Blanchaer, Patrick Frosk, Tracey Weiler, Kenneth Morgan, Beryl Jacobson, Eduardo Rosenmann, Takuya Fujiwara and Jean‐Louis Mandel and has published in prestigious journals such as Nature, The Lancet and Nucleic Acids Research.

In The Last Decade

Klaus Wrogemann

85 papers receiving 3.2k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

MITOCHONDRIAL CALCIUM OVERLOAD: A GENERAL MECHANISM FOR CELL-NECROSIS IN MUSCLE DISEASES

1976 393 citations Klaus Wrogemann et al. The Lancet profile →

Peers

Countries citing papers authored by Klaus Wrogemann

Since Specialization

Citations

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

Fields of papers citing papers by Klaus Wrogemann

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Klaus Wrogemann

This figure shows the co-authorship network connecting the top 25 collaborators of Klaus Wrogemann. A scholar is included among the top collaborators of Klaus Wrogemann 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 Klaus Wrogemann. Klaus Wrogemann is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	TRIM32 Regulates Skeletal Muscle Stem Cell Differentiation and Is Necessary for Normal Adult Muscle Regeneration 2012 ·PLoS ONE ·Sarah Nicklas, Anthony Otto, Xiaoli Wu, Pamela S. Miller, Sandra Stelzer, Yefei Wen, Shihuan Kuang, Klaus Wrogemann, Ketan Patel, Hao Ding, Jens C. Schwamborn	65
2	Novel GDI1 mutation in a large family with nonsyndromic X‐linked intellectual disability 2011 ·American Journal of Medical Genetics Part A ·Gertrud Strobl‐Wildemann, Vera M. Kalscheuer, Hao Hu, Klaus Wrogemann, Hans‐Hilger Ropers, Andreas Tzschach	11
3	Mutation of a Gene Essential for Ribosome Biogenesis, EMG1, Causes Bowen-Conradi Syndrome 2009 ·The American Journal of Human Genetics ·Joy Armistead, (unknown), Britta Meyer, Brian L. Mark, Nehal Patel, Gail Coghlan, Ryan E. Lamont, Shuangbo Liu, (unknown), Peter A. Cattini, P. Koetter, Klaus Wrogemann, Cheryl R. Greenberg, Karl‐Dieter Entian, Teresa Zelinski, Barbara L. Triggs‐Raine	98
4	The Interaction of Piasy with Trim32, an E3-Ubiquitin Ligase Mutated in Limb-girdle Muscular Dystrophy Type 2H, Promotes Piasy Degradation and Regulates UVB-induced Keratinocyte Apoptosis through NFκB 2006 ·Journal of Biological Chemistry ·(unknown), (unknown), (unknown), Melanie B. Laederich, Patrick Frosk, Klaus Wrogemann, Molly Kulesz‐Martin	77
5	The most common mutation inFKRP causing limb girdle muscular dystrophy type 2I (LGMD2I) may have occurred only once and is present in Hutterites and other populations 2004 ·Human Mutation ·Patrick Frosk, Cheryl R. Greenberg, (unknown), Ryan E. Lamont, Edward Nylen, (unknown), Danielle Frappier, Nicole M. Roslin, (unknown), Kate Bushby, Volker Straub, Mayana Zatz, Flavia Paula, Kenneth Morgan, Takuya Fujiwara, Klaus Wrogemann	53
6	Cardiac and respiratory failure in limb‐girdle muscular dystrophy 2I 2004 ·Annals of Neurology ·Maja Poppe, John Bourke, Michelle Eagle, Patrick Frosk, Klaus Wrogemann, Cheryl R. Greenberg, Francesco Muntoni, Thomas Voit, Volker Straub, David Hilton‐Jones, Cheerag Shirodaria, Kate Bushby	81
7	Limb-Girdle Muscular Dystrophy Type 2H Associated with Mutation in TRIM32, a Putative E3-Ubiquitin–Ligase Gene 2002 ·The American Journal of Human Genetics ·Patrick Frosk, Tracey Weiler, Edward Nylen, Thangirala Sudha, Cheryl R. Greenberg, Kenneth Morgan, Takuya Fujiwara, Klaus Wrogemann	188
8	Identical Mutation in Patients with Limb Girdle Muscular Dystrophy Type 2B Or Miyoshi Myopathy Suggests a Role for Modifier Gene(s) 1999 ·Human Molecular Genetics ·Tracey Weiler, R. Bashir, Louise V.B. Anderson, Kenneth Davison, Jessica Moss, S. Britton, Edward Nylen, Sharon Keers, Elizabeth Vafiadaki, Cheryl R. Greenberg, Kate Bushby, Klaus Wrogemann	142
9	A Gene for Autosomal Recessive Limb-Girdle Muscular Dystrophy in Manitoba Hutterites Maps to Chromosome Region 9q31-q33: Evidence for Another Limb-Girdle Muscular Dystrophy Locus 1998 ·The American Journal of Human Genetics ·Tracey Weiler, Cheryl R. Greenberg, Teresa Zelinski, Edward Nylen, Gail Coghlan, M. JOYCE CRUMLEY, Takuya Fujiwara, Kenneth Morgan, Klaus Wrogemann	84
10	Limb girdle muscular dystrophy in Manitoba Hutterites does not map to any of the known LGMD loci 1997 ·American Journal of Medical Genetics ·Tracey Weiler, Cheryl R. Greenberg, Edward Nylen, Kenneth Morgan, Takuya Fujiwara, M. JOYCE CRUMLEY, Teresa Zelinski, W Halliday, Barbara E. Nickel, Barbara L. Triggs‐Raine, Klaus Wrogemann	11
11	Comparison of the Segregation of the RYR1 C1840T Mutation with Segregation of the Caffeine/Halothane Contracture Test Results for Malignant Hyperthermia Susceptibility in a Large Manitoba Mennonite Family 1996 ·Anesthesiology ·(unknown), D. Böse, (unknown), Klaus Wrogemann, Michael Phillips, David H. MacLennan, Cheryl R. Greenberg	27
12	Leu-676-Pro mutation of the androgen receptor causes complete androgen insensitivity syndrome in a large Hutterite kindred 1995 ·Human Mutation ·Denise D. Belsham, Fred A. Pereira, Cheryl R. Greenberg, Shutsung Liao, Klaus Wrogemann	8
13	Human Cytosolic Aldehyde Dehydrogenase in Androgen Insensitivity Syndrome 1993 ·Advances in experimental medicine and biology ·Fred A. Pereira, Eduardo Rosenmann, Edward Nylen, Klaus Wrogemann	4
14	Single-Blind Study of Dystrophin Staining in Carriers of Duchenne Muscular Dystrophy 1993 ·Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques ·François P. Bernier, Cheryl R. Greenberg, William Halliday, Klaus Wrogemann	4
15	Analysis of the CAG repeat region of the androgen receptor gene in a kindred with X-linked spinal and bulbar muscular atrophy 1992 ·Journal of the Neurological Sciences ·Denise D. Belsham, Woon-Chee Yee, (unknown), Klaus Wrogemann	27
16	The 56/58 kDa androgen-binding protein in male genital skin fibroblasts with a deleted androgen receptor gene 1991 ·Molecular and Cellular Endocrinology ·Mark Trifiro, Bruce Gottlieb, Leonard Pinsky, (unknown), (unknown), Denise D. Belsham, Klaus Wrogemann, Carolyn J. Brown, Huntington F. Willard, Jan Trapman, Albert O. Brinkmann, (unknown), (unknown), F. R. Sergovich, Jack H. Jung	39
17	A 63-kDa protein with androgen-binding activity is not from the androgen receptor 1991 ·Biochemistry and Cell Biology ·Klaus Wrogemann, (unknown), Jin Gu, Eduardo Rosenmann	3
18	GENE STUDIES IN NEWBORN MALES WITH DUCHENNE MUSCULAR DYSTROPHY DETECTED BY NEONATAL SCREENING 1988 ·The Lancet ·Cheryl R. Greenberg, Hans Jacobs, Edward Nylen, (unknown), Nuzhat Averill, G.J.B. van Ommen, Klaus Wrogemann	28
19	An abundant 56 kD protein with low affinity androgen binding: Another member of the steroid/thyroid receptor family? 1988 ·Biochemical and Biophysical Research Communications ·Klaus Wrogemann, Fred A. Pereira, Denise D. Belsham, Morris Kaufman, L. Pinsky, Eduardo Rosenmann	11
20	Abnormal oxidative phosphorylation in skeletal muscle mitochondria of the BIO 14.6 dystrophic Syrian hamster. 1972 ·PubMed ·Klaus Wrogemann, (unknown), (unknown)	1

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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