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

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Chromosome 5 allele loss in human colorectal carcinomas

1987 451 citations E. Solomon, R. Voss et al. Nature profile →

Peers

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

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20 of 20 papers shown

#	Work	Indexed citations
1	Medical genetics in Israel. 1989 ·Journal of Medical Genetics ·Richard M. Goodman, Batsheva Bonné‐Tamir, A. Adam, R. Voss, Gideon Bach, Yosef Shiloh, M B Katznelson, (unknown), B. Goldman, B Padeh	7
2	The dilemma of chromosomal mosaicism in chorionic villus sampling—‘direct’ versus long‐term cultures 1989 ·Prenatal Diagnosis ·(unknown), Juan Chemke, R. Voss, Z. Appelman, B. Caspi, A. Lewin, Hanna Dar, Alex J. Reiter	11
3	Anorectal malformations and Down syndrome 1989 ·American Journal of Medical Genetics ·Joël Zlotogora, (unknown), O Lernau, M. Sagi, R. Voss, Tara Cohen	23
4	Isodisomy of chromosome 7 in a patient with cystic fibrosis: could uniparental disomy be common in humans? 1989 ·Trends in Genetics ·R. Voss	170
5	Fetal Duodenal Obstruction 1988 ·Acta Obstetricia Et Gynecologica Scandinavica ·Simcha Yagel, Joël Zlotogora, (unknown), R. Voss	1
6	Myelodysplastic syndromes: evolution of overt leukaemia by one or several steps of transformation 1987 ·British Journal of Haematology ·Peter G. Dormer, Chaim Hershko, R. Voss, W. Wilmanns	6
7	Chromosome 5 allele loss in human colorectal carcinomas breakdown → 1987 ·Nature ·E. Solomon, R. Voss, Victoria L. Hall, Walter F. Bodmer, Jeremy R. Jass, A.J. Jeffreys, Frances C. Lucibello, I. Patel, S.H. Rider	451
8	Meiotic association between the XY chromosomes and unpaired autosomal elements as a cause of human male sterility 1985 ·Cytogenetic and Genome Research ·Ada Rosenmann, J. Wahrman, Carmelit Richler, R. Voss, (unknown), B. Goldman	106
9	A complex three way translocation resulting in two sibs with partial trisomy 3p23----3pter. 1984 ·Journal of Medical Genetics ·R. Voss, Eva Gross‐Kieselstein, Haggit Hurvitz, Judith Dagan, Eitan Kerem, Joël Zlotogora	8
10	Secondary Leukemia Following Treatment of Hodgkin’s Disease: Ultrastructural and Cytogenetic Data in Two Cases with a Review of the Literature 1983 ·American Journal of Clinical Pathology ·Joachim Yahalom, R. Voss, (unknown), Zvi Fuks, Aaron Polliack	13
11	Genetic evidence that a Y-linked gene in man is homologous to a gene on the X chromosome 1983 ·Nature ·P.N. Goodfellow, George Banting, Denise Sheer, Hans‐Hilger Ropers, A. Caine, M.A. Ferguson‐Smith, S. Povey, R. Voss	145
12	In vitro fertilization and embryo transfer--legal and religious aspects in Israel, patient selection, and a modified technique for oocyte collection. 1983 ·PubMed ·(unknown), Neri Laufer, D. Navot, (unknown), Shai Yarkoni, Ron Rabinowitz, R. Voss	2
13	Partial trisomy 15 in a male with severe psychomotor retardation (48,XY,+15q−, +mar(15)) 1982 ·American Journal of Medical Genetics ·R. Voss, Israela Lerer, Genia Maftzir, (unknown), Maimon M. Cohen	7
14	Cytogenetic analysis of the spontaneous murine B-cell leukemia (BCL1 1980 ·Leukemia Research ·R. Voss, Genia Maftzir, Shimon Slavin	7
15	Ataxia telangiectasia: chromosomal stability in continuous lymphoblastoid cell lines 1979 ·Cytogenetic and Genome Research ·Maimon M. Cohen, M. Sagi, (unknown), T. Schaap, R. Voss, Gertrude Kohn, Hannah Ben‐Bassat	41
16	Association of a chromosomal abnormality with lymphocytes having both T and B markers in a patient with lymphoproliferative disease 1976 ·The American Journal of Medicine ·Frederick P. Siegal, R. Voss, Hamid Al‐Mondhiry, Aaron Polliack, John A. Hansen, Marta Siegal, Robert A. Good	37
17	The nature of reverse mutations in Drosophila melanogaster 1973 ·Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis ·R. Voss, Raphael Falk	9
18	Mucocutaneous pigmentation and intestinal polyposis (Peutz-Jeghers syndrome) in a family of Iraqi jews with polycystic kidney disease. With a chromosome study. 1969 ·PubMed ·(unknown), (unknown), J. Wahrman, R. Voss, (unknown), (unknown), (unknown)	5
19	[COMPARATIVE STUDIES OF THE GLYCOGEN CONTENT OF HEART, LIVER AND BRAIN BEFORE AND AFTER IODINE TREATMENT AND UNDER CONDITIONS OF ASPHYXIA]. 1963 ·PubMed ·(unknown), S Bettge, R. Voss	2
20	Der Einfluß von Jodgaben auf den Glykogengehalt des Herzmuskels und die Herzaktion¹ 1961 ·The Thoracic and Cardiovascular Surgeon ·(unknown), R. Voss	1

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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