R. Voss

1.9k total citations · 1 hit paper
37 papers, 1.5k citations indexed

About

R. Voss is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, R. Voss has authored 37 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 11 papers in Genetics and 9 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in R. Voss's work include Prenatal Screening and Diagnostics (8 papers), Genomic variations and chromosomal abnormalities (5 papers) and DNA Repair Mechanisms (4 papers). R. Voss is often cited by papers focused on Prenatal Screening and Diagnostics (8 papers), Genomic variations and chromosomal abnormalities (5 papers) and DNA Repair Mechanisms (4 papers). R. Voss collaborates with scholars based in Israel, United States and Germany. R. Voss's co-authors include E. Solomon, I. Patel, Victoria L. Hall, Walter F. Bodmer, Jeremy R. Jass, S.H. Rider, Frances C. Lucibello, A.J. Jeffreys, Israela Lerer and J. Wahrman and has published in prestigious journals such as Nature, Science and Proceedings of the National Academy of Sciences.

In The Last Decade

R. Voss

37 papers receiving 1.4k citations

Hit Papers

Chromosome 5 allele loss in human colorectal carcinomas 1987 2026 2000 2013 1987 100 200 300 400

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
R. Voss Israel 17 669 605 337 286 267 37 1.5k
J. L. M. Beck Netherlands 12 433 0.6× 292 0.5× 176 0.5× 120 0.4× 211 0.8× 17 934
Gregory B. Peters Australia 21 773 1.2× 420 0.7× 247 0.7× 70 0.2× 120 0.4× 33 1.3k
W. F. Benedict United States 9 998 1.5× 416 0.7× 828 2.5× 242 0.8× 443 1.7× 11 1.9k
Sabina Solinas‐Toldo Germany 12 786 1.2× 963 1.6× 249 0.7× 160 0.6× 369 1.4× 24 1.6k
Masahiro Muto Japan 18 1.4k 2.1× 405 0.7× 212 0.6× 85 0.3× 123 0.5× 54 1.9k
A. Thomas Look United States 27 1.2k 1.8× 242 0.4× 596 1.8× 295 1.0× 312 1.2× 40 2.3k
Edith Chevret France 18 695 1.0× 451 0.7× 152 0.5× 212 0.7× 77 0.3× 44 1.4k
Susan Pfeifer‐Ohlsson Sweden 16 1.1k 1.6× 519 0.9× 166 0.5× 57 0.2× 122 0.5× 23 1.6k
B. Kaiser McCaw United States 8 334 0.5× 198 0.3× 121 0.4× 114 0.4× 97 0.4× 18 775
Ian D. Dubé Canada 26 1.8k 2.7× 638 1.1× 391 1.2× 224 0.8× 157 0.6× 69 2.9k

Countries citing papers authored by R. Voss

Since Specialization
Citations

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

Fields of papers citing papers by R. Voss

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of R. Voss

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

All Works

20 of 20 papers shown
1.
Goodman, Richard M., Batsheva Bonné‐Tamir, A. Adam, et al.. (1989). Medical genetics in Israel.. Journal of Medical Genetics. 26(3). 179–189. 7 indexed citations
2.
Chemke, Juan, R. Voss, Z. Appelman, et al.. (1989). The dilemma of chromosomal mosaicism in chorionic villus sampling—‘direct’ versus long‐term cultures. Prenatal Diagnosis. 9(4). 223–226. 11 indexed citations
3.
Zlotogora, Joël, et al.. (1989). Anorectal malformations and Down syndrome. American Journal of Medical Genetics. 34(3). 330–331. 23 indexed citations
4.
Voss, R.. (1989). Isodisomy of chromosome 7 in a patient with cystic fibrosis: could uniparental disomy be common in humans?. Trends in Genetics. 5(3). 392–392. 170 indexed citations
5.
Yagel, Simcha, et al.. (1988). Fetal Duodenal Obstruction. Acta Obstetricia Et Gynecologica Scandinavica. 67(5). 465–466. 1 indexed citations
6.
Dormer, Peter G., Chaim Hershko, R. Voss, & W. Wilmanns. (1987). Myelodysplastic syndromes: evolution of overt leukaemia by one or several steps of transformation. British Journal of Haematology. 67(2). 141–146. 6 indexed citations
7.
Solomon, E., R. Voss, Victoria L. Hall, et al.. (1987). Chromosome 5 allele loss in human colorectal carcinomas. Nature. 328(6131). 616–619. 451 indexed citations breakdown →
8.
Rosenmann, Ada, et al.. (1985). Meiotic association between the XY chromosomes and unpaired autosomal elements as a cause of human male sterility. Cytogenetic and Genome Research. 39(1). 19–29. 106 indexed citations
9.
Voss, R., Eva Gross‐Kieselstein, Haggit Hurvitz, et al.. (1984). A complex three way translocation resulting in two sibs with partial trisomy 3p23----3pter.. Journal of Medical Genetics. 21(6). 454–459. 8 indexed citations
10.
Yahalom, Joachim, et al.. (1983). Secondary Leukemia Following Treatment of Hodgkin’s Disease: Ultrastructural and Cytogenetic Data in Two Cases with a Review of the Literature. American Journal of Clinical Pathology. 80(2). 231–236. 13 indexed citations
11.
Goodfellow, P.N., George Banting, Denise Sheer, et al.. (1983). Genetic evidence that a Y-linked gene in man is homologous to a gene on the X chromosome. Nature. 302(5906). 346–349. 145 indexed citations
12.
Laufer, Neri, et al.. (1983). In vitro fertilization and embryo transfer--legal and religious aspects in Israel, patient selection, and a modified technique for oocyte collection.. PubMed. 19(3). 218–24. 2 indexed citations
13.
Voss, R., et al.. (1982). Partial trisomy 15 in a male with severe psychomotor retardation (48,XY,+15q−, +mar(15)). American Journal of Medical Genetics. 12(2). 131–139. 7 indexed citations
14.
Voss, R., Genia Maftzir, & Shimon Slavin. (1980). Cytogenetic analysis of the spontaneous murine B-cell leukemia (BCL1. Leukemia Research. 4(3). 325–332. 7 indexed citations
15.
Cohen, Maimon M., M. Sagi, T. Schaap, et al.. (1979). Ataxia telangiectasia: chromosomal stability in continuous lymphoblastoid cell lines. Cytogenetic and Genome Research. 23(1-2). 44–52. 41 indexed citations
16.
Siegal, Frederick P., R. Voss, Hamid Al‐Mondhiry, et al.. (1976). Association of a chromosomal abnormality with lymphocytes having both T and B markers in a patient with lymphoproliferative disease. The American Journal of Medicine. 60(1). 157–166. 37 indexed citations
17.
Voss, R. & Raphael Falk. (1973). The nature of reverse mutations in Drosophila melanogaster. Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis. 20(2). 221–234. 9 indexed citations
18.
Wahrman, J., et al.. (1969). Mucocutaneous pigmentation and intestinal polyposis (Peutz-Jeghers syndrome) in a family of Iraqi jews with polycystic kidney disease. With a chromosome study.. PubMed. 5(1). 81–90. 5 indexed citations
19.
Bettge, S, et al.. (1963). [COMPARATIVE STUDIES OF THE GLYCOGEN CONTENT OF HEART, LIVER AND BRAIN BEFORE AND AFTER IODINE TREATMENT AND UNDER CONDITIONS OF ASPHYXIA].. PubMed. 17. 552–6. 2 indexed citations
20.
Voss, R., et al.. (1961). Der Einfluß von Jodgaben auf den Glykogengehalt des Herzmuskels und die Herzaktion1. The Thoracic and Cardiovascular Surgeon. 9(3). 372–375. 1 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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