Klaus Wrogemann

6.7k citations

85 papers · 3.4k indexed · 1 hit paper · h-index 31

Molecular Biology top 2%
- Muscle Physiology and Disorders 35
- Mitochondrial Function and Pathology 21
- Sexual Differentiation and Disorders 9
- RNA Research and Splicing 7
Cellular and Molecular Neuroscience top 2%
- Genetic Neurodegenerative Diseases 15
Cell Biology top 2%
- Muscle metabolism and nutrition 10
Genetics top 5%
Cardiology and Cardiovascular Medicine top 5%
Endocrinology, Diabetes and Metabolism
- Hormonal and reproductive studies 11
Physiology
- Adipose Tissue and Metabolism 8

Co-authors: Cheryl R. Greenberg Edward Nylen M. C. Blanchaer Patrick Frosk Tracey Weiler Kenneth Morgan Beryl Jacobson Eduardo Rosenmann
Cited by: Molecular Biology Cellular and Molecular Neuroscience Cell Biology
Journals: Nature (2 papers)The Lancet (3 papers)Nucleic Acids Research (2 papers)
Partner nations: Canada Germany United Kingdom

In The Last Decade

Klaus Wrogemann

85 papers receiving 3.2k citations

Hit Papers

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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

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

All Works

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20 of 20 papers shown

#	Work
1	TRIM32 Regulates Skeletal Muscle Stem Cell Differentiation and Is Necessary for Normal Adult Muscle Regeneration 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	2012	65
2	Novel GDI1 mutation in a large family with nonsyndromic X‐linked intellectual disability American Journal of Medical Genetics Part A ·Gertrud Strobl‐Wildemann,Vera M. Kalscheuer,Hao Hu,Klaus Wrogemann,Hans‐Hilger Ropers,Andreas Tzschach	2011	11
3	Mutation of a Gene Essential for Ribosome Biogenesis, EMG1, Causes Bowen-Conradi Syndrome The American Journal of Human Genetics ·Joy Armistead,Sunita Khatkar,Britta Meyer,Brian L. Mark,Nehal Patel,Gail Coghlan,Ryan E. Lamont,Shuangbo Liu,Jill Wiechert,Peter A. Cattini,P. Koetter,Klaus Wrogemann,Cheryl R. Greenberg,Karl‐Dieter Entian,Teresa Zelinski,Barbara L. Triggs‐Raine	2009	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 Journal of Biological Chemistry ·Amador Albor,Sally El-Hizawi,Elizabeth J. Horn,Melanie B. Laederich,Patrick Frosk,Klaus Wrogemann,Molly Kulesz‐Martin	2006	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 Human Mutation ·Patrick Frosk,Cheryl R. Greenberg,Alysa A.P. Tennese,Ryan E. Lamont,Edward Nylen,Cheryl Hirst,Danielle Frappier,Nicole M. Roslin,M Zaik,Kate Bushby,Volker Straub,Mayana Zatz,Flavia Paula,Kenneth Morgan,Takuya Fujiwara,Klaus Wrogemann	2004	53
6	Cardiac and respiratory failure in limb‐girdle muscular dystrophy 2I 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	2004	81
7	Limb-Girdle Muscular Dystrophy Type 2H Associated with Mutation in TRIM32, a Putative E3-Ubiquitin–Ligase Gene The American Journal of Human Genetics ·Patrick Frosk,Tracey Weiler,Edward Nylen,Thangirala Sudha,Cheryl R. Greenberg,Kenneth Morgan,Takuya Fujiwara,Klaus Wrogemann	2002	188
8	Identical Mutation in Patients with Limb Girdle Muscular Dystrophy Type 2B Or Miyoshi Myopathy Suggests a Role for Modifier Gene(s) 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	1999	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 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	1998	84
10	Limb girdle muscular dystrophy in Manitoba Hutterites does not map to any of the known LGMD loci 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	1997	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 Anesthesiology ·Kimberly D. Serfas,D. Böse,Leena Patel,Klaus Wrogemann,Michael Phillips,David H. MacLennan,Cheryl R. Greenberg	1996	27
12	Leu-676-Pro mutation of the androgen receptor causes complete androgen insensitivity syndrome in a large Hutterite kindred Human Mutation ·Denise D. Belsham,Fred A. Pereira,Cheryl R. Greenberg,Shutsung Liao,Klaus Wrogemann	1995	8
13	Human Cytosolic Aldehyde Dehydrogenase in Androgen Insensitivity Syndrome Advances in experimental medicine and biology ·Fred A. Pereira,Eduardo Rosenmann,Edward Nylen,Klaus Wrogemann	1993	4
14	Single-Blind Study of Dystrophin Staining in Carriers of Duchenne Muscular Dystrophy Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques ·François P. Bernier,Cheryl R. Greenberg,William Halliday,Klaus Wrogemann	1993	4
15	Analysis of the CAG repeat region of the androgen receptor gene in a kindred with X-linked spinal and bulbar muscular atrophy Journal of the Neurological Sciences ·Denise D. Belsham,Woon-Chee Yee,Cheryl R. Greenberg,Klaus Wrogemann	1992	27
16	The 56/58 kDa androgen-binding protein in male genital skin fibroblasts with a deleted androgen receptor gene Molecular and Cellular Endocrinology ·Mark Trifiro,Bruce Gottlieb,Leonard Pinsky,Morris Kaufman,Lynn Prior,Denise D. Belsham,Klaus Wrogemann,Carolyn J. Brown,Huntington F. Willard,Jan Trapman,Albert O. Brinkmann,Chawnshang Chang,Shutsung Liao,F. R. Sergovich,Jack H. Jung	1991	39
17	A 63-kDa protein with androgen-binding activity is not from the androgen receptor Biochemistry and Cell Biology ·Klaus Wrogemann,G Podolsky,Jin Gu,Eduardo Rosenmann	1991	3
18	GENE STUDIES IN NEWBORN MALES WITH DUCHENNE MUSCULAR DYSTROPHY DETECTED BY NEONATAL SCREENING The Lancet ·Cheryl R. Greenberg,Hans Jacobs,Edward Nylen,Martin Rohringer,Nuzhat Averill,G.J.B. van Ommen,Klaus Wrogemann	1988	28
19	An abundant 56 kD protein with low affinity androgen binding: Another member of the steroid/thyroid receptor family? Biochemical and Biophysical Research Communications ·Klaus Wrogemann,Fred A. Pereira,Denise D. Belsham,Morris Kaufman,L. Pinsky,Eduardo Rosenmann	1988	11
20	Abnormal oxidative phosphorylation in skeletal muscle mitochondria of the BIO 14.6 dystrophic Syrian hamster. PubMed ·Klaus Wrogemann,Blanchaer Mc,Jacobson Be	1972	1

About Klaus Wrogemann

Klaus Wrogemann is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Cell Biology, having authored 85 papers that have together received 3.4k indexed citations. Recurring topics across this work include Muscle Physiology and Disorders (35 papers), Mitochondrial Function and Pathology (21 papers), Genetic Neurodegenerative Diseases (15 papers), Hormonal and reproductive studies (11 papers), Muscle metabolism and nutrition (10 papers), Sexual Differentiation and Disorders (9 papers), Adipose Tissue and Metabolism (8 papers) and RNA Research and Splicing (7 papers). The work is most often cited by research in Molecular Biology (2.6k citations), Cellular and Molecular Neuroscience (640 citations) and Cell Biology (474 citations). Klaus Wrogemann has collaborated with scholars based in Canada, Germany and United Kingdom. Frequent 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. Their work appears in journals such as Nature, The Lancet and Nucleic Acids Research.

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