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W. Wolz · SciRah

Researcher profile · Semantic Scholar

W. Wolz

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W. Wolz — researcher profile on SciRah

h-index: 9
Works: 13
Citations: 714

Most-cited papers

Identification of novel mutations in the ryanodine-receptor gene (RYR1) in malignant hyperthermia: genotype-phenotype correlation.
B. M. Manning, K. Quane, H. Ording, Albert Urwyler +17 more
1998American Journal of Human Genetics121 citations Open access
Semantic Scholar
The human gene for alkaptonuria (AKU) maps to chromosome 3q.
S. Janocha, W. Wolz, Š. Sršeň, K. Srsnová +5 more
1994Genomics113 citations
Semantic Scholar
Congenital Deficiency of Vitamin K Dependent Coagulation Factors in Two Families Presents as a Genetic Defect of the Vitamin K-Epoxide-Reductase-Complex
J. Oldenburg, B. von Brederlow, A. Fregin, S. Rost +11 more
2000Thrombosis and Haemostasis111 citations
Semantic Scholar
A genome wide search for susceptibility loci in three European malignant hyperthermia pedigrees.
R. Robinson, N. Monnier, W. Wolz, Martin Jung +12 more
1997Human Molecular Genetics111 citations Open access
Semantic Scholar
Homozygosity mapping of a second gene locus for hereditary combined deficiency of vitamin K-dependent clotting factors to the centromeric region of chromosome 16.
A. Fregin, S. Rost, W. Wolz, A. Krebsova +2 more
2002Blood80 citations Open access
Semantic Scholar
Sorsby's fundus dystrophy is genetically linked to chromosome 22q13–qter
B. Weber, Gudrun Vogt, W. Wolz, E. Ives +1 more
1994Nature Genetics79 citations
Semantic Scholar
Novel mutations at a CpG dinucleotide in the ryanodine receptor in malignant hyperthermia
B. M. Manning, K. Quane, Patrick J. Lynch, A. Urwyler +9 more
1998Human Mutation48 citations Open access
Semantic Scholar
New mutations in the ataxia telangiectasia gene
A. Baumer, U. Bernthaler, W. Wolz, H. Hoehn +1 more
1996Human Genetics34 citations
Semantic Scholar
Genomic sequence and organization of the human gene for cytochrome c oxidase subunit (COX7A1) VIIa-M.
W. Wolz, Wolfram Kress, C. R. Mueller
1997Genomics15 citations
Semantic Scholar
Homozygosity Mapping of a Second Gene Locus for Hereditary Combined Deficiency of Vitamin K-Dependent Clotting Factors (FMFD) to Chromosome 16
A. Fregin, S. Rost, W. Wolz, A. Krebsova +2 more
20041 citations
Semantic Scholar
First Case of Compound Heterozygosity in the Gamma- Glutamyl Carboxylase Gene Causing Combined Deficiency of all Vitamin K-Dependent Blood Coagulation Factors
S. Rost, A. Fregin, D. Koch, M. Compés +3 more
20041 citations
Semantic Scholar
A complex satellite DNA polymorphism flanking the human ryanodine receptor gene (RYR1).
W. Wolz, U. Wendelmuth, S. Rouquier, D. Giorgi +1 more
1996Cytogenetics and Cell Genetics1 citations
Semantic Scholar
Congenital Deficiency of Vitamin K Dependent Coagulation Factors in Two Families: Evidence for a Defective Vitamin K-Epoxide-Reductase Complex
B. von Brederlow, A. Fregin, S. Rost, W. Wolz +11 more
20010 citations
Semantic Scholar

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