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K. Wrogemann · SciRah

Researcher profile · Semantic Scholar

K. Wrogemann

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K. Wrogemann — researcher profile on SciRah

h-index: 30
Works: 86
Citations: 5,463

Most-cited papers

The molecular basis for Duchenne versus Becker muscular dystrophy: correlation of severity with type of deletion.
M. Koenig, A. Beggs, M. Moyer, S. Scherpf +32 more
1989American Journal of Human Genetics1,007 citations
Semantic Scholar
Deep sequencing reveals 50 novel genes for recessive cognitive disorders
H. Najmabadi, Hao Hu, M. Garshasbi, T. Żemojtel +41 more
2011Nature967 citations
Semantic Scholar
Mitochondrial calcium overload: A general mechanism for cell-necrosis in muscle diseases.
K. Wrogemann, S. D. Pena
1976The Lancet489 citations
Semantic Scholar
X-exome sequencing of 405 unresolved families identifies seven novel intellectual disability genes
H. Hu, S. Haas, J. Chelly, H. Van Esch +80 more
2015Molecular Psychiatry296 citations Open access
Semantic Scholar
Limb-girdle muscular dystrophy type 2H associated with mutation in TRIM32, a putative E3-ubiquitin-ligase gene.
P. Frosk, T. Weiler, E. Nylen, T. Sudha +4 more
2002American Journal of Human Genetics261 citations Open access
Semantic Scholar
Secondary reduction in calpain 3 expression in patients with limb girdle muscular dystrophy type 2B and Miyoshi myopathy (primary dysferlinopathies).
L. V. Anderson, Ruth Harrison, R. Pogue, E. Vafiadaki +15 more
2000Neuromuscular Disorders158 citations Open access
Semantic Scholar
Identical dysferlin mutation in limb-girdle muscular dystrophy type 2B and distal myopathy
S. Illarioshkin, I. Ivanova-Smolenskaya, C. R. Greenberg, E. Nylen +4 more
2000Neurology128 citations
Semantic Scholar
Mutation of a gene essential for ribosome biogenesis, EMG1, causes Bowen-Conradi syndrome.
J. Armistead, Sunita Khatkar, B. Meyer, B. Mark +12 more
2009American Journal of Human Genetics126 citations Open access
Semantic Scholar
ST3GAL3 mutations impair the development of higher cognitive functions.
Hao Hu, Katinka Eggers, Wei Chen, M. Garshasbi +12 more
2011American Journal of Human Genetics122 citations Open access
Semantic Scholar
Cardiac and respiratory failure in limb‐girdle muscular dystrophy 2I
M. Poppe, J. Bourke, M. Eagle, P. Frosk +8 more
2004Annals of Neurology118 citations Open access
Semantic Scholar
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.
T. Weiler, C. Greenberg, T. Zelinski, E. Nylen +5 more
1998American Journal of Human Genetics111 citations Open access
Semantic Scholar
Prostaglandin and thromboxane synthesis in a pure macrophage population and the inhibition, by E‐type prostaglandins, of chemiluminescence
Maurice J. Weidemann, B. Peskar, K. Wrogemann, Ernst Th. Rietschel +2 more
1978FEBS Letters108 citations Open access
Semantic Scholar
Serum CK, calcium, magnesium, and oxidative phosphorylation in mdx mouse muscular dystrophy
M. Glesby, E. Rosenmann, E. Nylen, K. Wrogemann
1988Muscle and Nerve96 citations
Semantic Scholar
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*
A. Albor, Sally El-Hizawi, Elizabeth J. Horn, Melanie B. Laederich +3 more
2006Journal of Biological Chemistry92 citations Open access
Semantic Scholar
Commonality of TRIM32 mutation in causing sarcotubular myopathy and LGMD2H
B. Schoser, P. Frosk, A. Engel, U. Klutzny +2 more
2005Annals of Neurology91 citations
Semantic Scholar
TRIM32 Regulates Skeletal Muscle Stem Cell Differentiation and Is Necessary for Normal Adult Muscle Regeneration
Sarah Nicklas, A. Otto, Xiaoli Wu, Pamela. Miller +7 more
2012PLoS ONE84 citations Open access
Semantic Scholar
The most common mutation in FKRP causing limb girdle muscular dystrophy type 2I (LGMD2I) may have occurred only once and is present in Hutterites and other populations
P. Frosk, C. Greenberg, Alysa A. P. Tennese, R. Lamont +12 more
2005Human Mutation83 citations
Semantic Scholar
On the mechanism of a calcium-associated defect of oxidative phosphorylation in progessive muscular dystrophy.
K. Wrogemann, B. Jacobson, M. Blanchaer
1973Archives of Biochemistry and Biophysics66 citations
Semantic Scholar
Mutation screening in 86 known X-linked mental retardation genes by droplet-based multiplex PCR and massive parallel sequencing
Hao Hu, K. Wrogemann, V. Kalscheuer, A. Tzschach +10 more
2009The HUGO Journal55 citations Open access
Semantic Scholar
The 56/58 kDa androgen-binding protein in male genital skin fibroblasts with a deleted androgen receptor gene.
M. Trifiro, B. Gottlieb, L. Pinsky, M. Kaufman +11 more
1991Molecular and Cellular Endocrinology54 citations
Semantic Scholar
Chemiluminescence and immune cell activation I. Early activation of rat thymocytes can be monitored by chemiluminescence measurements
K. Wrogemann, M. J. Weidemann, B. Peskar, H. Staudinger +2 more
1978European Journal of Immunology48 citations
Semantic Scholar
Liver morphology and enzyme release: further studies in the isolated perfused rat liver
E. Schmidt, Schmidt Fw, J. Möhr, P. Otto +3 more
197548 citations
Semantic Scholar
The Friedreich ataxia region: characterization of two novel genes and reduction of the critical region to 300 kb.
F. Duclos, F. Rodius, K. Wrogemann, Jean-Louis Mandel +1 more
1994Human Molecular Genetics46 citations
Semantic Scholar
Erratum to: Mutation screening in 86 known X-linked mental retardation genes by droplet-based multiplex PCR and massive parallel sequencing
Hao Hu, K. Wrogemann, V. Kalscheuer, A. Tzschach +10 more
2009The HUGO Journal45 citations Open access
Semantic Scholar
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
K. Serfas, D. Bose, Leena R. Patel, K. Wrogemann +3 more
1996Anesthesiology42 citations
Semantic Scholar
Intragenic deletion of TRIM32 in compound heterozygotes with sarcotubular myopathy/LGMD2H
K. Borg, R. Stucka, M. Locke, E. Melin +9 more
2009Human Mutation38 citations Open access
Semantic Scholar
BIOCHEMICAL ASPECTS OF MUSCLE NECROSIS IN HAMSTER DYSTROPHY *
K. Wrogemann, W. A. K. Hayward, M. Blanchaer
1979Annals of the New York Academy of Sciences38 citations
Semantic Scholar
Analysis of fibroblast proteins from patients with Duchenne muscular dystrophy by two-dimensional gel electrophoresis
E. Rosenmann, C. Kreis, R. Thompson, M. Dobbs +2 more
1982Nature35 citations
Semantic Scholar
Analysis of the CAG repeat region of the androgen receptor gene in a kindred with X-linked spinal and bulbar muscular atrophy.
D. Belsham, W. Yee, C. Greenberg, K. Wrogemann
1992Journal of Neurological Sciences33 citations
Semantic Scholar
Hutterite brothers both affected with two forms of limb girdle muscular dystrophy: LGMD2H and LGMD2I
P. Frosk, M. D. Del Bigio, K. Wrogemann, C. Greenberg
2005European Journal of Human Genetics31 citations
Semantic Scholar
Respiration and oxidative phosphorylation by muscle and heart mitochondria of hamsters with hereditary myocardiopathy and polymyopathy.
K. Wrogemann, M. Blanchaer
1968Canadian Journal of Biochemistry30 citations
Semantic Scholar
Amber mutation creates a diagnostic MaeI site in the androgen receptor gene of a family with complete androgen insensitivity.
M. Trifiro, R. Prior, N. Sabbaghian, L. Pinsky +5 more
1991American journal of medical genetics29 citations
Semantic Scholar
Differing populations of mitochondria isolated from the skeletal muscle of normal and dystrophic hamsters.
B. Mezon, K. Wrogemann, M. Blanchaer
1974Canadian Journal of Biochemistry29 citations
Semantic Scholar
A calcium-associated magnesium-responsive defect of respiration and oxidative phosphorylation by skeletal muscle mitochondria of BIO 14.6 dystrophic hamsters.
K. Wrogemann, M. Blanchaer, B. Jacobson
1970Life sciences. Pt. 2: Biochemistry, general and molecular biology29 citations
Semantic Scholar
Regional localization of 18 human X-linked DNA sequences.
D. Riddell, H.-S. Wang, J. Beckett, A. Chan +7 more
1986Cytogenetics and Cell Genetics26 citations
Semantic Scholar
Defective respiration and oxidative phosphorylation in muscle mitochondria of hamsters in the late stages of hereditary muscular dystrophy.
B. Jacobson, M. Blanchaer, K. Wrogemann
1970Canadian Journal of Biochemistry26 citations
Semantic Scholar
Effect of ruthenium red on oxidative phosphorylation and the calcium and magnesium content of skeletal muscle mitochondria of normal and BIO 14.6 dystrophic hamsters.
J. Thakar, K. Wrogemann, M. Blanchaer
1973Biochimica et Biophysica Acta25 citations
Semantic Scholar
A magnesium-responsive defect of respiration and oxidative phosphorylation in skeletal muscle mitochondria of dystrophic hamsters.
K. Wrogemann, M. Blanchaer, B. Jacobson
1970Canadian Journal of Biochemistry25 citations
Semantic Scholar
Mitochondrial calcium content and oxidative phosphorylation in heart and skeletal muscle of dystrophic mice.
E. Nylen, K. Wrogemann
1983Experimental Neurology23 citations
Semantic Scholar
Chemiluminescence and immune cell activation II. Enhancement of concanavalin A‐induced chemiluminescence following in vitro preincubation of rat thymocytes; dependency on macrophage‐ lymphocyte interaction
K. Wrogemann, Maurice J. Weidemann, U. Ketelsen, H. Wekerle +1 more
1980European Journal of Immunology22 citations
Semantic Scholar
Oxidative phosphorylation in smooth muscle.
N. Stephens, K. Wrogemann
1970American Journal of Physiology22 citations Open access
Semantic Scholar
Multipoint genetic mapping of the Xq26-q28 region in families with fragile X mental retardation and in normal families reveals tight linkage of markers in q26–q27
I. Oberlé, G. Camerino, K. Wrogemann, B. Arveiler +3 more
1987Human Genetics21 citations
Semantic Scholar
Oxidative phosphorylation by muscle mitochondria of dysstrophic mice.
K. Wrogemann, M. Blanchaer
1967Canadian Journal of Biochemistry20 citations
Semantic Scholar
Novel GDI1 mutation in a large family with nonsyndromic X‐linked intellectual disability
G. Strobl‐Wildemann, V. Kalscheuer, Hao Hu, K. Wrogemann +2 more
2011American Journal of Medical Genetics. Part A18 citations
Semantic Scholar
Segregation analysis of a marker localised Xp21.2-Xp21.3 in Duchenne and Becker muscular dystrophy families
Huw Dorkins, C. Iunien, Jean-Louis Mandel, K. Wrogemann +11 more
2004Human Genetics18 citations
Semantic Scholar
Concanavalin A-induced chemiluminescence in rat thymus lymphocytes. Its origin and role in mitogenesis.
David A. Hume, K. Wrogemann, Ernst Ferber, M. Kolbuch-Braddon +3 more
1981Biochemical Journal18 citations Open access
Semantic Scholar
Searching for Molecular Abnormalities in Genetic Diseases by the Use of a Double Labeling Technique. I. Rationale, Techniques, and Initial Evaluation
S. D. Pena, K. Wrogemann
1978Pediatric Research15 citations
Semantic Scholar
On the role of mitochondria in the hereditary cardiomyopathy of the Syrian hamster.
K. Wrogemann, M. Blanchaer, J. Thakar, B. Mezon
1975Recent advances in studies on cardiac structure and metabolism15 citations
Semantic Scholar
A locus for Bowen–Conradi syndrome maps to chromosome region 12p13.3
R. Lamont, J. Loredo-Osti, N. Roslin, Jill Mauthe +12 more
2005American Journal of Medical Genetics. Part A13 citations
Semantic Scholar
Leu‐676‐Pro mutation of the androgen receptor causes complete androgen insensitivity syndrome in a large Hutterite kindred
D. Belsham, Fred A. Pereira, C. Greenberg, S. Liao +1 more
1995Human Mutation13 citations Open access
Semantic Scholar

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