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R. Stucka · SciRah

Researcher profile · Semantic Scholar

R. Stucka

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R. Stucka — researcher profile on SciRah

h-index: 34
Works: 66
Citations: 2,895

Most-cited papers

Complete DNA sequence of yeast chromosome II.
H. Feldmann, M. Aigle, G. Aljinović, B. André +93 more
1994EMBO Journal253 citations Open access
Semantic Scholar
Transcriptional regulator PRDM12 is essential for human pain perception
Ya-Chun Chen, M. Auer-Grumbach, S. Matsukawa, M. Zitzelsberger +55 more
2015Nature Genetics166 citations Open access
Semantic Scholar
DIT101 (CSD2, CAL1), a cell cycle‐regulated yeast gene required for synthesis of chitin in cell walls and chitosan in spore walls
Manuela Pammer, P. Briza, A. Ellinger, T. Schuster +3 more
1992Yeast137 citations
Semantic Scholar
Cytochrome c oxidase deficiency due to mutations in SCO2, encoding a mitochondrial copper-binding protein, is rescued by copper in human myoblasts.
M. Jaksch, C. Paret, R. Stucka, N. Horn +11 more
2001Human Molecular Genetics121 citations Open access
Semantic Scholar
Identification of a set of yeast genes coding for a novel family of putative ATPases with high similarity to constituents of the 26S protease complex
Ralf Schnall, G. Mannhaupt, R. Stucka, Reimund Tauer +4 more
1994Yeast119 citations
Semantic Scholar
Loss of tubulin deglutamylase CCP1 causes infantile‐onset neurodegeneration
V. Shashi, M. Magiera, D. Klein, M. Zaki +56 more
2018EMBO Journal118 citations Open access
Semantic Scholar
Molecular cloning of CIF1, a yeast gene necessary for growth on glucose
M. I. González, M. Blázquez, C. Gancedo, R. Stucka +1 more
1992Yeast112 citations
Semantic Scholar
A common mutation (ε1267delG) in congenital myasthenic patients of Gypsy ethnic origin
A. Abicht, R. Stucka, V. Karcagi, Á. Herczegfalvi +13 more
199996 citations Open access
Semantic Scholar
Rapsyn N88K is a frequent cause of congenital myasthenic syndromes in European patients
J. Müller, G. Mildner, W. Müller-Felber, U. Schara +11 more
2003Neurology94 citations Open access
Semantic Scholar
FKRP (826C>A) frequently causes limb-girdle muscular dystrophy in German patients
M. Walter, J. Petersen, R. Stucka, D. Fischer +17 more
2004Journal of Medical Genetics87 citations Open access
Semantic Scholar
Characterization of human muscle type cofilin (CFL2) in normal and regenerating muscle.
C. Thirion, R. Stucka, B. Mendel, A. Gruhler +5 more
2001European Journal of Biochemistry82 citations
Semantic Scholar
Trehalose-6-P synthase is dispensable for growth on glucose but not for spore germination in Schizosaccharomyces pombe
M. Blázquez, R. Stucka, Horst Feldmann, Carlos Gancedo
1994Journal of Bacteriology82 citations Open access
Semantic Scholar
Targeted HIV-1 Latency Reversal Using CRISPR/Cas9-Derived Transcriptional Activator Systems
Julia K Bialek, G. Dunay, Maike Voges, Carola Schäfer +4 more
2016PLoS ONE78 citations Open access
Semantic Scholar
Highly Significant Antiviral Activity of HIV-1 LTR-Specific Tre-Recombinase in Humanized Mice
I. Hauber, H. Hofmann-Sieber, J. Chemnitz, D. Dubrau +14 more
2013PLoS Pathogens70 citations Open access
Semantic Scholar
Mutations in INPP5K, Encoding a Phosphoinositide 5-Phosphatase, Cause Congenital Muscular Dystrophy with Cataracts and Mild Cognitive Impairment
M. Wiessner, A. Roos, C. Munn, Ranjith Viswanathan +34 more
2017American Journal of Human Genetics64 citations Open access
Semantic Scholar
DNA sequences in chromosomes 11 and VII code for pyruvate carboxylase isoenzymes in Saccharomyces cerevisiae: analysis of pyruvate carboxylase-deficient strains
R. Stucka, S. Dequin, J. Salmon, C. Gancedo
1991Molecular and General Genetics MGG63 citations
Semantic Scholar
Molecular characterisation of congenital myasthenic syndromes in Southern Brazil
V. Mihaylova, R. Scola, B. Gervini, P. Lorenzoni +9 more
2010Journal of Neurology Neurosurgery & Psychiatry61 citations Open access
Semantic Scholar
Salbutamol-responsive limb-girdle congenital myasthenic syndrome due to a novel missense mutation and heteroallelic deletion in MUSK
C. Gallenmüller, W. Müller-Felber, M. Dusl, R. Stucka +7 more
2014Neuromuscular Disorders59 citations Open access
Semantic Scholar
Expression of dystrophin driven by the 1.35-kb MCK promoter ameliorates muscular dystrophy in fast, but not in slow muscles of transgenic mdx mice.
P. Dunant, N. Larochelle, C. Thirion, R. Stucka +4 more
2003Molecular Therapy53 citations Open access
Semantic Scholar
PRDM12 Is Required for Initiation of the Nociceptive Neuron Lineage during Neurogenesis
Luca Bartesaghi, Yiqiao Wang, P. Fontanet, Simone Wanderoy +23 more
2019Cell Reports47 citations Open access
Semantic Scholar
The congenital myasthenic syndrome mutation RAPSN N88K derives from an ancient Indo-European founder
J. Müller, G. Burke, J. Cossins, P. Richard +7 more
2004Journal of Medical Genetics47 citations Open access
Semantic Scholar
Long-Term Preservation of Cardiac Structure and Function After Adeno-Associated Virus Serotype 9-Mediated Microdystrophin Gene Transfer in mdx Mice
S. Schinkel, R. Bauer, R. Bekeredjian, R. Stucka +5 more
2012Human Gene Therapy46 citations Open access
Semantic Scholar
Characterization of the prephenate dehydrogenase-encoding gene, TYR1, from Saccharomyces cerevisiae.
G. Mannhaupt, R. Stucka, U. Pilz, C. Schwarzlose +1 more
1989Gene46 citations
Semantic Scholar
Biallelic variants in HPDL cause pure and complicated hereditary spastic paraplegia.
M. Wiessner, R. Maroofian, Meng-Yuan Ni, A. Pedroni +102 more
2021Brain : a journal of neurology45 citations Open access
Semantic Scholar
Clinical and neuropathological findings in patients with TACO1 mutations.
J. Seeger, B. Schrank, A. Pyle, R. Stucka +7 more
2010Neuromuscular Disorders44 citations Open access
Semantic Scholar
A newly identified chromosomal microdeletion and an N-box mutation of the AChR epsilon gene cause a congenital myasthenic syndrome.
A. Abicht, R. Stucka, C. Schmidt, Alexandre Briguet +6 more
2002Brain : a journal of neurology44 citations Open access
Semantic Scholar
A common mutation (epsilon1267delG) in congenital myasthenic patients of Gypsy ethnic origin.
A. Abicht, R. Stucka, V. Karcagi, Á. Herczegfalvi +13 more
1999Neurology44 citations
Semantic Scholar
Sequence of a cDNA clone encompassing the complete mature human prostate specific antigen (PSA) and an unspliced leader sequence
P. Schulz, R. Stucka, H. Feldmann, G. Combriato +2 more
1988Nucleic Acids Res.42 citations Open access
Semantic Scholar
Characterization of human SCO1 and COX17 genes in mitochondrial cytochrome-c-oxidase deficiency.
R. Horvath, Hanns Lochmüller, R. Stucka, Jian-Bo Yao +4 more
2000Biochemical and Biophysical Research Communications - BBRC40 citations Open access
Semantic Scholar
A 3'-UTR mutation creates a microRNA target site in the GFPT1 gene of patients with congenital myasthenic syndrome.
M. Dusl, J. Senderek, J. Müller, Johannes G Vogel +5 more
2015Human Molecular Genetics39 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
Nucleotide sequence of the phosphoenolpyruvate carboxykinase gene from Saccharomyces cerevisiae.
R. Stucka, M. D. Valdés-Hevia, C. Gancedo, C. Schwarzlose +1 more
1988Nucleic Acids Research38 citations Open access
Semantic Scholar
A newly identified chromosomal microdeletion of the rapsyn gene causes a congenital myasthenic syndrome.
J. Müller, A. Abicht, H. Christen, R. Stucka +4 more
2004Neuromuscular Disorders35 citations
Semantic Scholar
Ty4, a novel low-copy number element in Saccharomyces cerevisiae: one copy is located in a cluster of Ty elements and tRNA genes.
R. Stucka, Hanns Lochmüller, H. Feldmann
1989Nucleic Acids Research34 citations Open access
Semantic Scholar
Analysis of yeast chromosomal regions carrying members of the glutamate tRNA gene family: various transposable elements are associated with them.
Joachim Hauber, R. Stucka, Robert Krieg, Horst Feldmann
1988Nucleic Acids Research32 citations Open access
Semantic Scholar
Synaptic congenital myasthenic syndrome in three patients due to a novel missense mutation (T441A) of the COLQ gene.
J. Müller, S. Petrova, R. Kiefer, R. Stucka +5 more
2004Neuropediatrics30 citations Open access
Semantic Scholar
MPV17 mutations in juvenile‐ and adult‐onset axonal sensorimotor polyneuropathy
M. Baumann, H. Schreiber, B. Schlotter‐Weigel, W. Löscher +8 more
2018Clinical Genetics28 citations
Semantic Scholar
Genetic landscape of congenital insensitivity to pain and hereditary sensory and autonomic neuropathies
A. Lischka, K. Eggermann, C. Record, M. Dohrn +78 more
2023Brain : a journal of neurology23 citations Open access
Semantic Scholar
Isolation and Identification of PACE-Binding Protein Rpn4, a New Transcriptional Activator Regulating 26S-Proteasomal and Other Genes
A. Kapranov, M. V. Kuryatova, O. Preobrazhenskaya, V. Tutyaeva +3 more
2001Molecular Biology23 citations
Semantic Scholar
Molecular analysis of yeast chromosome II between CMD1 and LYS2: The excision repair gene RAD16 located in this region belongs to a novel group of double‐finger proteins
G. Mannhaupt, R. Stucka, S. Ehnle, I. Vetter +1 more
1992Yeast23 citations
Semantic Scholar
II. Yeast sequencing reports. Analysis of a 70kb region on the right arm of yeast chromosome II
G. Mannhaupt, R. Stucka, S. Ehnle, I. Vetter +1 more
199422 citations
Semantic Scholar
Molecular analysis of the yeast Ty4 element: homology with Ty1, copia, and plant retrotransposons.
R. Stucka, C. Schwarzlose, Hanns Lochmüller, U. Häcker +1 more
1992Gene21 citations
Semantic Scholar
Efficient and Fast Functional Screening of Microdystrophin Constructs In Vivo and In Vitro for Therapy of Duchenne Muscular Dystrophy
L. H. Jørgensen, N. Larochelle, K. Orlopp, P. Dunant +6 more
2009Human Gene Therapy18 citations
Semantic Scholar
Analysis of a 70 kb region on the right arm of yeast chromosome II.
G. Mannhaupt, R. Stucka, S. Ehnle, I. Vetter +1 more
1994Yeast17 citations
Semantic Scholar
Structure of a Saccharomyces cerevisiae gene encoding minor (AGY)tRNA(Ser).
R. Stucka, H. Feldmann
1988Nucleic Acids Research15 citations Open access
Semantic Scholar
An element of symmetry in yeast TATA‐box binding protein transcription factor IID
R. Stucka, H. Feldmann
1990FEBS Letters14 citations Open access
Semantic Scholar
An intronic base alteration of the CHRNE gene leading to a congenital myasthenic syndrome
J. Müller, R. Stucka, S. Neudecker, S. Zierz +4 more
2005Neurology13 citations Open access
Semantic Scholar
Congenital myasthenic syndrome (CMS) in three European kinships due to a novel splice mutation (IVS7 - 2 A/G) in the epsilon acetylcholine receptor (AChR) subunit gene.
N. Barišić, C. Schmidt, O. Sidorova, Á. Herczegfalvi +6 more
2002Neuropediatrics12 citations Open access
Semantic Scholar
The use of a synthetic tRNA gene as a novel approach to study in vivo transcription and chromatin structure in yeast.
Robert Krieg, R. Stucka, Shawna Clark, Horst Feldmann
1991Nucleic Acids Research11 citations Open access
Semantic Scholar
The fdp1 and cif1 mutations are caused by different single nucleotide changes in the yeast CIF1 gene.
R. Stucka, M. Blázquez
1993FEMS Microbiology Letters10 citations
Semantic Scholar

Frequent co-authors

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H. Feldmann×15
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H. Feldmann — researcher profile on SciRah
H. Lochmüller×13
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H. Lochmüller — researcher profile on SciRah
J. Müller×12
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J. Müller — researcher profile on SciRah
Hanns Lochmüller×11
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Hanns Lochmüller — researcher profile on SciRah

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J. Senderek — researcher profile on SciRah

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A. Abicht — researcher profile on SciRah

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A. Huebner — researcher profile on SciRah

W. Müller-Felber×7

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W. Müller-Felber — researcher profile on SciRah

G. Mannhaupt×6

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G. Mannhaupt — researcher profile on SciRah

C. Schwarzlose×5

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C. Schwarzlose — researcher profile on SciRah

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I. Vetter — researcher profile on SciRah

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T. Strom — researcher profile on SciRah