Eric Rappaport

9.6k total citations · 1 hit paper
108 papers, 4.3k citations indexed

About

Eric Rappaport is a scholar working on Molecular Biology, Genetics and Hematology. According to data from OpenAlex, Eric Rappaport has authored 108 papers receiving a total of 4.3k indexed citations (citations by other indexed papers that have themselves been cited), including 66 papers in Molecular Biology, 24 papers in Genetics and 21 papers in Hematology. Recurrent topics in Eric Rappaport's work include Hemoglobinopathies and Related Disorders (14 papers), Acute Myeloid Leukemia Research (11 papers) and Neuroblastoma Research and Treatments (11 papers). Eric Rappaport is often cited by papers focused on Hemoglobinopathies and Related Disorders (14 papers), Acute Myeloid Leukemia Research (11 papers) and Neuroblastoma Research and Treatments (11 papers). Eric Rappaport collaborates with scholars based in United States, Italy and Australia. Eric Rappaport's co-authors include Saul Surrey, Paolo Fortina, Carolyn A. Felix, Elaine Mansfield, Maureen D. Megonigal, Elias Schwartz, Paolo Gasparini, Leopoldo Zelante, Montserrat Milà and Salvatore Melchionda and has published in prestigious journals such as Science, Proceedings of the National Academy of Sciences and The Lancet.

In The Last Decade

Eric Rappaport

107 papers receiving 4.2k citations

Hit Papers

Connexin-26 mutations in sporadic and inherited sensorine... 1998 2026 2007 2016 1998 100 200 300 400 500
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.

  1. Connexin-26 mutations in sporadic and inherited sensorineural deafness
    1998 523 citations Xavier Estivill, Paolo Fortina et al. The Lancet profile →

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Eric Rappaport United States 37 2.6k 673 664 535 441 108 4.3k
Frank N. van Leeuwen Netherlands 45 3.3k 1.2× 353 0.5× 850 1.3× 428 0.8× 593 1.3× 112 6.7k
Gudrun Nürnberg Germany 44 2.9k 1.1× 1.6k 2.3× 335 0.5× 424 0.8× 171 0.4× 93 5.1k
Misao Suzuki Japan 41 2.8k 1.1× 672 1.0× 222 0.3× 979 1.8× 513 1.2× 91 6.4k
Andreas Janecke Austria 37 2.2k 0.8× 1.3k 1.9× 334 0.5× 309 0.6× 163 0.4× 132 4.4k
María L. Arbonés Spain 36 2.3k 0.9× 953 1.4× 205 0.3× 560 1.0× 359 0.8× 65 4.7k
Paul K. Goldsmith United States 46 4.2k 1.6× 492 0.7× 161 0.2× 117 0.2× 778 1.8× 102 6.4k
Akihiro Kume Japan 34 2.2k 0.8× 1.5k 2.2× 131 0.2× 128 0.2× 618 1.4× 135 4.1k
Mary Jean Sunshine United States 31 2.9k 1.1× 485 0.7× 468 0.7× 102 0.2× 2.2k 5.0× 34 9.6k
Jean‐Marie Vanderwinden Belgium 32 3.3k 1.3× 681 1.0× 166 0.3× 139 0.3× 342 0.8× 81 5.7k
Naoki Takeda Japan 38 4.8k 1.8× 946 1.4× 424 0.6× 56 0.1× 716 1.6× 97 7.4k

Countries citing papers authored by Eric Rappaport

Since Specialization
Citations

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

Fields of papers citing papers by Eric Rappaport

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Eric Rappaport

This figure shows the co-authorship network connecting the top 25 collaborators of Eric Rappaport. A scholar is included among the top collaborators of Eric Rappaport 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 Eric Rappaport. Eric Rappaport 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.
Yu, Xiang, J. W. Davenport, Karen Urtishak, et al.. (2017). Genome-wide TOP2A DNA cleavage is biased toward translocated and highly transcribed loci. Genome Research. 27(7). 1238–1249. 43 indexed citations
2.
Ng, Jessica M.Y., Daniel Martínez, Eric D. Marsh, et al.. (2015). Generation of a Mouse Model of Atypical Teratoid/Rhabdoid Tumor of the Central Nervous System through Combined Deletion of Snf5 and p53. Cancer Research. 75(21). 4629–4639. 30 indexed citations
3.
Wei, Zhi, Jane E. Minturn, Eric Rappaport, Garrett M. Brodeur, & Hongzhe Li. (2013). Network-Based Analysis of Multivariate Gene Expression Data. Methods in molecular biology. 972. 121–139. 7 indexed citations
4.
Busse, Tracy, John M. Graham, Gerald L. Feldman, et al.. (2010). High-Resolution genomic arrays identify CNVs that phenocopy the chromosome 22q11.2 deletion syndrome. Human Mutation. 32(1). 91–97. 15 indexed citations
5.
Teachey, David T., Robert Greiner, Alix E. Seif, et al.. (2009). Treatment with sirolimus results in complete responses in patients with autoimmune lymphoproliferative syndrome. British Journal of Haematology. 145(1). 101–106. 110 indexed citations
6.
Vorstman, Jacob, Bruce I. Turetsky, Bert Dorland, et al.. (2008). Proline Affects Brain Function in 22q11DS Children with the Low Activity COMT158 Allele. Neuropsychopharmacology. 34(3). 739–746. 80 indexed citations
7.
Markov, Vladimir, Kenro Kusumi, Mahlet G. Tadesse, et al.. (2007). Identification of Cord Blood-Derived Mesenchymal Stem/stromal Cell Populations with Distinct Growth Kinetics, Differentiation Potentials, and Gene Expression Profiles. Stem Cells and Development. 16(1). 53–74. 75 indexed citations
8.
William, Dilusha A., B. Saitta, Joshua D. Gibson, et al.. (2007). Identification of oscillatory genes in somitogenesis from functional genomic analysis of a human mesenchymal stem cell model. Developmental Biology. 305(1). 172–186. 48 indexed citations
9.
Ferraris, Alessandro, Eric Rappaport, Rosa Santacroce, et al.. (2002). Pyrosequencing for detection of mutations in the connexin 26 (GJB2) and mitochondrial 12S RNA (MTRNR1) genes associated with hereditary hearing loss. Human Mutation. 20(4). 312–320. 15 indexed citations
10.
11.
Lai, Jianping, Steven D. Douglas, Eric Rappaport, Jessie M. Wu, & Wen‐Zhe Ho. (1998). Identification of a δ isoform of preprotachykinin mRNA in human mononuclear phagocytes and lymphocytes. Journal of Neuroimmunology. 91(1-2). 121–128. 60 indexed citations
12.
Estivill, Xavier, Paolo Fortina, Saul Surrey, et al.. (1998). Connexin-26 mutations in sporadic and inherited sensorineural deafness. The Lancet. 351(9100). 394–398. 523 indexed citations breakdown →
13.
Mansfield, Elaine, et al.. (1996). Sensitivity, reproducibility, and accuracy in short tandem repeat genotyping using capillary array electrophoresis.. Genome Research. 6(9). 893–903. 35 indexed citations
14.
Kobayashi, Megumi, et al.. (1995). Fluorescence-based DNA minisequence analysis for detection of known single-base changes in genomic DNA. Molecular and Cellular Probes. 9(3). 175–182. 21 indexed citations
15.
Tamary, Hannah, Saul Surrey, Lea Shalmon, et al.. (1994). Systematic use of automated fluorescence‐based sequence analysis of amplified genomic DNA for rapid detection of point mutations. American Journal of Hematology. 46(2). 127–133. 8 indexed citations
16.
Keller, Michael A., Diana L. Cassel, Eric Rappaport, et al.. (1993). Fluorescence-based RT PCR analysis: determination of the ratio of soluble to membrane-bound forms of Fc gamma RIIA transcripts in hematopoietic cell lines.. Genome Research. 3(1). 32–38. 14 indexed citations
17.
Adachi, K., Saul Surrey, Hannah Tamary, et al.. (1993). HB Shelby [β131(H9)GLN→LYS] in Association with HB S [β6(A3)GLU→VAL]: Characterization, Stability, and Effects on HB S Polymerization. Hemoglobin. 17(4). 329–343. 8 indexed citations
18.
19.
Burk, Carol D., et al.. (1988). A Taq 1 polymorphism for the human platelet glycoprotein IIIa gene (GP3A). Nucleic Acids Research. 16(14). 7216–7216. 11 indexed citations
20.
Bayever, Eliel, et al.. (1988). Protection of uninfected human bone marrow cells in long-term culture from G418 toxicity after retroviral-mediated transfer of the NEOr gene. Experimental Cell Research. 179(1). 168–180. 9 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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