J.R. Korenberg

738 total citations
19 papers, 590 citations indexed

About

J.R. Korenberg is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, J.R. Korenberg has authored 19 papers receiving a total of 590 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 6 papers in Genetics and 4 papers in Surgery. Recurrent topics in J.R. Korenberg's work include Genomic variations and chromosomal abnormalities (3 papers), Inflammasome and immune disorders (3 papers) and RNA modifications and cancer (3 papers). J.R. Korenberg is often cited by papers focused on Genomic variations and chromosomal abnormalities (3 papers), Inflammasome and immune disorders (3 papers) and RNA modifications and cancer (3 papers). J.R. Korenberg collaborates with scholars based in United States and Israel. J.R. Korenberg's co-authors include Christine M. Distèche, Cynthia M. Bradley, V. Michael Whitehead, Timothy A. Garrow, Barry Shane, Michelle Croyle, David R. Cox, Afsane Arvand, Christopher T. Denny and Mordechai Shohat and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nucleic Acids Research and Journal of Biological Chemistry.

In The Last Decade

J.R. Korenberg

18 papers receiving 577 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
J.R. Korenberg United States 10 385 155 74 67 60 19 590
Dorota Piekutowska‐Abramczuk Poland 17 773 2.0× 181 1.2× 41 0.6× 33 0.5× 42 0.7× 59 1.0k
M.F. Rousseau-Merck France 15 377 1.0× 186 1.2× 81 1.1× 30 0.4× 90 1.5× 29 687
Pilar Magoulas United States 15 383 1.0× 290 1.9× 63 0.9× 71 1.1× 17 0.3× 24 727
Michela Barbaro Sweden 22 885 2.3× 596 3.8× 135 1.8× 56 0.8× 53 0.9× 47 1.3k
Giulietta Roël Netherlands 11 459 1.2× 66 0.4× 37 0.5× 63 0.9× 36 0.6× 13 694
Guy Helman United States 19 692 1.8× 108 0.7× 156 2.1× 63 0.9× 12 0.2× 41 1.0k
Adi Mory Israel 15 245 0.6× 147 0.9× 124 1.7× 34 0.5× 28 0.5× 40 592
Anikó Újfalusi Hungary 10 205 0.5× 71 0.5× 35 0.5× 17 0.3× 70 1.2× 48 395
Marjan M. Nezarati Canada 10 232 0.6× 198 1.3× 43 0.6× 40 0.6× 18 0.3× 17 447

Countries citing papers authored by J.R. Korenberg

Since Specialization
Citations

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

Fields of papers citing papers by J.R. Korenberg

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of J.R. Korenberg

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

All Works

19 of 19 papers shown
1.
Chen, Xiaofei, Jeffrey A. Knauf, Rivkah Gonsky, et al.. (1998). From Amplification to Gene in Thyroid Cancer: A High-Resolution Mapped Bacterial-Artificial-Chromosome Resource for Cancer Chromosome Aberrations Guides Gene Discovery after Comparative Genome Hybridization. The American Journal of Human Genetics. 63(2). 625–637. 51 indexed citations
2.
Korenberg, J.R., et al.. (1996). Localization of the humanRGR opsin gene to chromosome 10q23. Human Genetics. 97(6). 720–722. 14 indexed citations
3.
Yamakawa, Kazuhiro, et al.. (1996). A periodic tryptophan protein 2 gene homologue (PWP2H) in the candidate region of progressive myoclonus epilepsy on 21q22.3. Cytogenetic and Genome Research. 74(1-2). 140–145. 6 indexed citations
4.
Arvand, Afsane, et al.. (1996). EAT-2 is a novel SH2 domain containing protein that is up regulated by Ewing's sarcoma EWS/FLI1 fusion gene.. PubMed. 13(12). 2649–58. 90 indexed citations
5.
Antonarakis, Stylianos E., David Patterson, Christine Van Broeckhoven, et al.. (1995). Report of the committee on the genetic constitution of chromosome 21. 1060–1099. 6 indexed citations
6.
Mohandas, T., Lucy B. Rowe, E H Birkenmeier, et al.. (1995). Localization of the Tight Junction Protein Gene TJP1 to Human Chromosome 15q13, Distal to the Prader-Willi/Angelman Region, and to Mouse Chromosome 7. Genomics. 30(3). 594–597. 9 indexed citations
7.
8.
Korenberg, J.R.. (1995). Molecular and stochastic basis of congenital heart disease in Down syndrome. Medical Entomology and Zoology. 581–596. 2 indexed citations
9.
Chen, Xiaonan, et al.. (1995). Gene amplification in thyroid cancer: A new mechanism defined by CGH and A BAC map of the human genome. Cancer Genetics and Cytogenetics. 84(2). 134–134. 1 indexed citations
10.
Malo, Madhu S., Barbara J. Blanchard, J. Michael Andresen, et al.. (1994). Localization of a putative human brain sodium channel gene (SCN1A) to chromosome band 2q24. Cytogenetic and Genome Research. 67(3). 178–186. 23 indexed citations
11.
12.
Korenberg, J.R.. (1994). Corrections: Down Syndrome Phenotypes: The Consequences of Chromosomal Imbalance. Proceedings of the National Academy of Sciences. 91(23). 11281a–11281. 1 indexed citations
13.
Garrow, Timothy A., et al.. (1993). Cloning of human cDNAs encoding mitochondrial and cytosolic serine hydroxymethyltransferases and chromosomal localization. Journal of Biological Chemistry. 268(16). 11910–11916. 145 indexed citations
14.
Korenberg, J.R., Cynthia M. Bradley, & Christine M. Distèche. (1992). Down syndrome: molecular mapping of the congenital heart disease and duodenal stenosis.. PubMed. 50(2). 294–302. 134 indexed citations
15.
Shohat, Mordechai, Viorel Herman, Шломо Мелмед, et al.. (1991). Deletion of 20p 11.23→pter with normal growth hormone‐releasing hormone genes. American Journal of Medical Genetics. 39(1). 56–63. 17 indexed citations
16.
Shohat, Mordechai, Tami Shohat, Jerome I. Rotter, et al.. (1990). Serum amyloid A and P protein genes in familial Mediterranean fever. Genomics. 8(1). 83–89. 14 indexed citations
17.
Shohat, Tami, Gloria M. Petersen, R S Sparkes, et al.. (1990). Genetic marker family studies in familial Mediterranean fever (FMF) in Armenians. Clinical Genetics. 38(5). 332–339. 6 indexed citations
18.
Shohat, Mordechai, J.R. Korenberg, Arthur D. Schwabe, & JI Rotter. (1989). Hypothesis: Familial Mediterranean fever—A genetic disorder of the lipocortin family?. American Journal of Medical Genetics. 34(2). 163–167. 21 indexed citations
19.
Korenberg, J.R., Michelle Croyle, & David R. Cox. (1987). Isolation and regional mapping of DNA sequences unique to human chromosome 21.. PubMed. 41(6). 963–78. 44 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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