A. Rodewald

930 total citations
41 papers, 726 citations indexed

About

A. Rodewald is a scholar working on Genetics, Molecular Biology and Developmental Biology. According to data from OpenAlex, A. Rodewald has authored 41 papers receiving a total of 726 indexed citations (citations by other indexed papers that have themselves been cited), including 31 papers in Genetics, 13 papers in Molecular Biology and 7 papers in Developmental Biology. Recurrent topics in A. Rodewald's work include Dermatoglyphics and Human Traits (12 papers), Congenital limb and hand anomalies (7 papers) and Genomic variations and chromosomal abnormalities (7 papers). A. Rodewald is often cited by papers focused on Dermatoglyphics and Human Traits (12 papers), Congenital limb and hand anomalies (7 papers) and Genomic variations and chromosomal abnormalities (7 papers). A. Rodewald collaborates with scholars based in Germany, Poland and Denmark. A. Rodewald's co-authors include S. Stengel‐Rutkowski, K. D. Zang, Brigitte Pakendorf, Jan Murken, Hartwig Clevė, Spitsyn Va, Jon Stene, H. Zankl, Mark Stoneking and Larissa A. Tarskaia and has published in prestigious journals such as American Journal of Physical Anthropology, Journal of Medical Genetics and Diabetic Medicine.

In The Last Decade

A. Rodewald

40 papers receiving 674 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
A. Rodewald Germany	17	552	218	170	154	55	41	726
Ali Hellani Saudi Arabia	14	333 0.6×	286 1.3×	311 1.8×	46 0.3×	10 0.2×	39	787
G. I. Lazjuk Belarus	18	407 0.7×	336 1.5×	202 1.2×	91 0.6×	46 0.8×	34	732
Sarah F. Slaney United Kingdom	10	1.2k 2.2×	721 3.3×	111 0.7×	23 0.1×	63 1.1×	19	1.4k
Indira B. Taylor United Kingdom	12	422 0.8×	466 2.1×	46 0.3×	21 0.1×	62 1.1×	14	703
Kutay Taysi United States	17	440 0.8×	277 1.3×	221 1.3×	133 0.9×	49 0.9×	48	710
M. Ray Canada	15	731 1.3×	391 1.8×	377 2.2×	292 1.9×	39 0.7×	36	1.1k
J. B. Bijlsma Netherlands	17	335 0.6×	223 1.0×	151 0.9×	106 0.7×	25 0.5×	32	553
M. S. NEWTON United Kingdom	14	536 1.0×	363 1.7×	209 1.2×	310 2.0×	19 0.3×	23	793
Mary K. Kukolich United States	14	492 0.9×	374 1.7×	222 1.3×	96 0.6×	65 1.2×	28	680
H. Reinwein Germany	13	640 1.2×	377 1.7×	174 1.0×	216 1.4×	85 1.5×	54	782

Countries citing papers authored by A. Rodewald

Since Specialization

Citations

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

Fields of papers citing papers by A. Rodewald

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of A. Rodewald

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

All Works

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20 of 20 papers shown

Arghir, Aurora, et al.. (2008). Chromosome Y Isodicentrics in two Cases with Ambiguous genitalia and Features of Turner Syndrome. Balkan Journal of Medical Genetics. 11(2). 51–58. 2 indexed citations

Pakendorf, Brigitte, Victor Wiebe, Larissa A. Tarskaia, et al.. (2003). Mitochondrial DNA evidence for admixed origins of central Siberian populations. American Journal of Physical Anthropology. 120(3). 211–224. 74 indexed citations

Pakendorf, Brigitte, Bharti Morar, Larissa A. Tarskaia, et al.. (2002). Y-chromosomal evidence for a strong reduction in male population size of Yakuts. Human Genetics. 110(2). 198–200. 24 indexed citations

Pakendorf, Brigitte, Spitsyn Va, & A. Rodewald. (1999). Genetic structure of a Sakha population from Siberia and ethnic affinities.. PubMed. 71(2). 231–44. 15 indexed citations

Rodewald, A., et al.. (1994). Genetic Differentiation of Jordanian Moslems and Christians. Human Heredity. 44(6). 316–321. 4 indexed citations

Rodewald, A., Rainer Pankau, Angela Gosch, & Armin Wessel. (1994). Dermatoglyphic peculiarities in patients with Williams‐Beuren syndrome. American Journal of Medical Genetics. 53(3). 227–235.

Rodewald, A., et al.. (1993). Cytogenetic survey of 32 cancers of the prostate. Cancer Genetics and Cytogenetics. 66(2). 93–99. 66 indexed citations

Ziegler, Anette‐Gabriele, et al.. (1993). Dermatoglyphics in Type 1 Diabetes Mellitus. Diabetic Medicine. 10(8). 720–724. 18 indexed citations

Rodewald, A., et al.. (1989). Genetic differentiation among four groups of fishermen of the Eastern coast, India. Annals of Human Biology. 16(4). 321–333. 10 indexed citations

10.

Clevė, Hartwig, et al.. (1988). Genetic transferrin types and iron-binding: a comparative study of a European and an African population sample. Human Genetics. 78(1). 16–20. 10 indexed citations

11.

Meinecke, Peter, et al.. (1987). Smith‐Lemli‐Opitz syndrome. American Journal of Medical Genetics. 28(3). 735–739. 16 indexed citations

12.

Rodewald, A., U. Froster‐Iskenius, U. Langenbeck, et al.. (1986). Dermatoglyphic peculiarities in families with X‐linked mental retardation and fragile site Xq27: a collaborative study. Clinical Genetics. 30(1). 1–13. 12 indexed citations

13.

Rodewald, A., et al.. (1982). Moderate Down's syndrome in three siblings having partial trisomy 21q22.2?qter and therefore no SOD-1 excess. Human Genetics. 60(1). 74–77. 36 indexed citations

14.

Rodewald, A., et al.. (1981). Dermatoglyphic Peculiarities in Down’s Syndrome Detection of Mosaicism and Balanced Translocation Carriers. PubMed. 2. 41–56. 2 indexed citations

15.

Rodewald, A., Astrid Wirtz, Jan Murken, et al.. (1980). A (1;21) balanced translocation in a male with mucopolysaccharidosis type IIIA. Cytogenetic and Genome Research. 27(4). 267–267. 2 indexed citations

16.

Rodewald, A., et al.. (1980). Partial trisomie 5q: Three different phenotypes depending on different duplication segments. Human Genetics. 55(2). 191–198. 44 indexed citations

17.

Rodewald, A., et al.. (1980). Dermatoglyphs in carriers of a balanced 15;21 translocation.. Journal of Medical Genetics. 17(4). 301–305. 2 indexed citations

18.

Rodewald, A., S. Stengel‐Rutkowski, Petra Schulz, & Hartwig Clevė. (1977). New chromosomal malformation syndromes. European Journal of Pediatrics. 125(1). 45–57. 24 indexed citations

19.

Zankl, H. & A. Rodewald. (1977). [Diagnostic problems in mosaic-Downs-syndrome (author's transl)].. PubMed. 189(6). 430–9. 2 indexed citations

20.

Stengel‐Rutkowski, S., et al.. (1976). Aspermia, associated with a presumably balanced X/autosomal translocation. Human Genetics. 31(1). 97–106. 19 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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