S. A. Schonberg

2.4k total citations · 1 hit paper
14 papers, 1.8k citations indexed

About

S. A. Schonberg is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, S. A. Schonberg has authored 14 papers receiving a total of 1.8k indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Genetics, 7 papers in Molecular Biology and 6 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in S. A. Schonberg's work include Genomic variations and chromosomal abnormalities (9 papers), Prenatal Screening and Diagnostics (6 papers) and Chromosomal and Genetic Variations (5 papers). S. A. Schonberg is often cited by papers focused on Genomic variations and chromosomal abnormalities (9 papers), Prenatal Screening and Diagnostics (6 papers) and Chromosomal and Genetic Variations (5 papers). S. A. Schonberg collaborates with scholars based in United States, Hungary and Pakistan. S. A. Schonberg's co-authors include R. S. K. Chaganti, James German, Mitchell S. Golbus, W. Allen Hogge, J German, E. Louie, Leland Allen, Tatsuro Ikeuchi, Hiroko Kawashima and Naotaka Ogasawara and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Virology and American Journal of Obstetrics and Gynecology.

In The Last Decade

S. A. Schonberg

14 papers receiving 1.7k citations

Hit Papers

A Manyfold Increase in Sister Chromatid Exchanges in Bloo... 1974 2026 1991 2008 1974 250 500 750

Peers

S. A. Schonberg
Heinz-Ulrich Weier United States
Elise Rose United States
Annabelle Lewis United Kingdom
Heinz-Ulrich Weier United States
S. A. Schonberg
Citations per year, relative to S. A. Schonberg S. A. Schonberg (= 1×) peers Heinz-Ulrich Weier

Countries citing papers authored by S. A. Schonberg

Since Specialization
Citations

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

Fields of papers citing papers by S. A. Schonberg

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of S. A. Schonberg

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

All Works

14 of 14 papers shown
1.
Eggerding, Faye A., S. A. Schonberg, FF Chehab, et al.. (1994). Uniparental isodisomy for paternal 7p and maternal 7q in a child with growth retardation.. PubMed. 55(2). 253–65. 62 indexed citations
2.
Schonberg, S. A.. (1993). Cytogenetic analysis in prenatal diagnosis.. PubMed. 159(3). 360–5. 5 indexed citations
3.
Ledbetter, David H., Joe Leigh Simpson, Mitchell S. Golbus, et al.. (1992). Cytogenetic results from the U.S. collaborative study on CVS. Prenatal Diagnosis. 12(5). 317–345. 264 indexed citations
4.
Korenberg, Julie R., Hiroko Kawashima, Stefan M. Pulst, et al.. (1990). Molecular definition of a region of chromosome 21 that causes features of the Down syndrome phenotype.. PubMed. 47(2). 236–46. 194 indexed citations
5.
Brandriff, Brigitte, Laurie Gordon, S. A. Schonberg, et al.. (1988). Sperm chromosome analysis to assess potential germ cell mosaicism. Clinical Genetics. 34(2). 85–89. 9 indexed citations
6.
Trask, Barbara J., et al.. (1988). Application of flow karyotyping in prenatal detection of chromosome aberrations.. PubMed. 42(1). 49–59. 25 indexed citations
7.
Hogge, W. Allen, S. A. Schonberg, & Mitchell S. Golbus. (1986). Chorionic villus sampling: Experience of the first 1000 cases. American Journal of Obstetrics and Gynecology. 154(6). 1249–1252. 106 indexed citations
8.
Shaul, Yosef, Pablo D. García, S. A. Schonberg, & William J. Rutter. (1986). Integration of hepatitis B virus DNA in chromosome-specific satellite sequences. Journal of Virology. 59(3). 731–734. 44 indexed citations
9.
Overhauser, Joan, Mitchell S. Golbus, S. A. Schonberg, & John J. Wasmuth. (1986). Molecular analysis of an unbalanced deletion of the short arm of chromosome 5 that produces no phenotype.. PubMed. 39(1). 1–10. 54 indexed citations
10.
Hogge, W. Allen, S. A. Schonberg, & Mitchell S. Golbus. (1985). Prenatal diagnosis by chorionic villus sampling: Lessons of the first 600 cases. Prenatal Diagnosis. 5(6). 393–400. 57 indexed citations
11.
Schonberg, S. A., M. F. Niermeijer, D. Bootsma, Edward D. Henderson, & J German. (1984). Werner's syndrome: proliferation in vitro of clones of cells bearing chromosome translocations.. PubMed. 36(2). 387–97. 40 indexed citations
12.
Lau, Yun‐Fai Chris & S. A. Schonberg. (1984). A male-specific DNA probe detects heterochromatin sequences in a familial Yq- chromosome.. PubMed. 36(6). 1394–6. 21 indexed citations
13.
German, J, S. A. Schonberg, E. Louie, & R. S. K. Chaganti. (1977). Bloom's syndrome. IV. Sister-chromatid exchanges in lymphocytes.. PubMed. 29(3). 248–55. 125 indexed citations
14.
Chaganti, R. S. K., S. A. Schonberg, & James German. (1974). A Manyfold Increase in Sister Chromatid Exchanges in Bloom's Syndrome Lymphocytes. Proceedings of the National Academy of Sciences. 71(11). 4508–4512. 783 indexed citations breakdown →

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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