Werner Wolz

585 total citations
7 papers, 330 citations indexed

About

Werner Wolz is a scholar working on Molecular Biology, Hematology and Nutrition and Dietetics. According to data from OpenAlex, Werner Wolz has authored 7 papers receiving a total of 330 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Molecular Biology, 2 papers in Hematology and 2 papers in Nutrition and Dietetics. Recurrent topics in Werner Wolz's work include Ion channel regulation and function (2 papers), Vitamin K Research Studies (2 papers) and Blood Coagulation and Thrombosis Mechanisms (2 papers). Werner Wolz is often cited by papers focused on Ion channel regulation and function (2 papers), Vitamin K Research Studies (2 papers) and Blood Coagulation and Thrombosis Mechanisms (2 papers). Werner Wolz collaborates with scholars based in Germany, France and United States. Werner Wolz's co-authors include Andreas Fregin, Simone Rost, Johannes Oldenburg, Alice Krebsová, Clemens R. Müller, Jean‐Louis Guénet, T. Grimm, C R Müller, Xavier Montagutelli and Alessandra Baumer and has published in prestigious journals such as Blood, Human Molecular Genetics and Thrombosis and Haemostasis.

In The Last Decade

Werner Wolz

7 papers receiving 310 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Werner Wolz Germany	6	178	79	74	61	52	7	330
Carole R. Pritzker United States	7	208 1.2×	51 0.6×	42 0.6×	28 0.5×	7 0.1×	9	374
Eduard N. Lavrentyev United States	9	184 1.0×	12 0.2×	52 0.7×	141 2.3×	22 0.4×	11	427
Nicolas Godin Canada	7	185 1.0×	23 0.3×	63 0.9×	81 1.3×	4 0.1×	8	437
K Aida Japan	9	187 1.1×	66 0.8×	50 0.7×	34 0.6×	20 0.4×	18	427
N. Brust United States	9	376 2.1×	25 0.3×	54 0.7×	46 0.8×	37 0.7×	12	781
F Matsumoto Japan	12	114 0.6×	25 0.3×	34 0.5×	13 0.2×	8 0.2×	33	349
A. Herrero-San Martín Spain	5	207 1.2×	19 0.2×	48 0.6×	38 0.6×	19 0.4×	6	623
Masao Omata Japan	8	163 0.9×	23 0.3×	21 0.3×	145 2.4×	10 0.2×	9	448
H. Niederhoff Germany	10	135 0.8×	53 0.7×	118 1.6×	31 0.5×	3 0.1×	44	304
Mark M. Danney United States	7	137 0.8×	32 0.4×	93 1.3×	11 0.2×	5 0.1×	8	376

Countries citing papers authored by Werner Wolz

Since Specialization

Citations

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

Fields of papers citing papers by Werner Wolz

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Werner Wolz

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

All Works

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7 of 7 papers shown

1.

Fregin, Andreas, Simone Rost, Werner Wolz, et al.. (2002). Homozygosity mapping of a second gene locus for hereditary combined deficiency of vitamin K–dependent clotting factors to the centromeric region of chromosome 16. Blood. 100(9). 3229–3232. 57 indexed citations

2.

Fregin, Andreas, Simone Rost, Werner Wolz, et al.. (2000). Congenital Deficiency of Vitamin K Dependent Coagulation Factors in Two Families Presents as a Genetic Defect of the Vitamin K-Epoxide-Reductase-Complex. Thrombosis and Haemostasis. 84(12). 937–941. 67 indexed citations

3.

Robinson, Rachel L., Nicole Monnier, Werner Wolz, et al.. (1997). A Genome Wide Search for Susceptibility Loci in Three European Malignant Hyperthermia Pedigrees. Human Molecular Genetics. 6(6). 953–961. 85 indexed citations

4.

Wolz, Werner, et al.. (1997). Genomic Sequence and Organization of the Human Gene for Cytochrome c Oxidase Subunit (COX7A1) VIIa-M. Genomics. 45(2). 438–442. 10 indexed citations

5.

Baumer, Alessandra, et al.. (1996). New mutations in the ataxia telangiectasia gene. Human Genetics. 98(2). 246–249. 29 indexed citations

6.

Wolz, Werner, et al.. (1996). A complex satellite DNA polymorphism flanking the human ryanodine receptor gene (RYR1). Cytogenetic and Genome Research. 72(2-3). 215–216. 1 indexed citations

7.

Wolz, Werner, et al.. (1994). The Human Gene for Alkaptonuria (AKU) Maps to Chromosome 3q. Genomics. 19(1). 5–8. 81 indexed citations

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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