Steven L. Gersen

851 total citations
13 papers, 581 citations indexed

About

Steven L. Gersen is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Molecular Biology. According to data from OpenAlex, Steven L. Gersen has authored 13 papers receiving a total of 581 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Genetics, 6 papers in Pediatrics, Perinatology and Child Health and 4 papers in Molecular Biology. Recurrent topics in Steven L. Gersen's work include Prenatal Screening and Diagnostics (6 papers), Chromosomal and Genetic Variations (4 papers) and Genomic variations and chromosomal abnormalities (4 papers). Steven L. Gersen is often cited by papers focused on Prenatal Screening and Diagnostics (6 papers), Chromosomal and Genetic Variations (4 papers) and Genomic variations and chromosomal abnormalities (4 papers). Steven L. Gersen collaborates with scholars based in United States. Steven L. Gersen's co-authors include Dorothy Warburton, Stephen Brown, Kwame Anyane‐Yeboa, Brian E. Ward, K. Klinger, Constance J. Sandlin, Nancy M. McGuire, William R. Dackowski, Martha Weinstein and Richard J. Warren and has published in prestigious journals such as SHILAP Revista de lepidopterología, Blood and Genomics.

In The Last Decade

Steven L. Gersen

12 papers receiving 552 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Steven L. Gersen United States 9 410 337 193 158 95 13 581
E. J. Maher United Kingdom 8 440 1.1× 342 1.0× 173 0.9× 129 0.8× 66 0.7× 11 613
Chen‐Chi Lee Taiwan 17 673 1.6× 550 1.6× 285 1.5× 176 1.1× 185 1.9× 116 929
Yvonne K. Kwok China 13 285 0.7× 300 0.9× 216 1.1× 51 0.3× 51 0.5× 25 563
Shin-Wen Chen Taiwan 12 511 1.2× 548 1.6× 180 0.9× 77 0.5× 166 1.7× 152 747
Walter van der Vliet Netherlands 7 443 1.1× 127 0.4× 242 1.3× 153 1.0× 23 0.2× 8 623
Sugandhi A. Tharapel United States 10 215 0.5× 142 0.4× 83 0.4× 94 0.6× 31 0.3× 19 337
V. Cacheux France 8 129 0.3× 156 0.5× 165 0.9× 43 0.3× 135 1.4× 10 453
Dehua Cheng China 12 300 0.7× 307 0.9× 242 1.3× 67 0.4× 47 0.5× 44 618
Paolo Guanciali Franchi Italy 14 298 0.7× 80 0.2× 220 1.1× 71 0.4× 25 0.3× 31 484
Jiansheng Xie China 8 190 0.5× 142 0.4× 129 0.7× 29 0.2× 40 0.4× 33 341

Countries citing papers authored by Steven L. Gersen

Since Specialization
Citations

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

Fields of papers citing papers by Steven L. Gersen

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Steven L. Gersen. 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 Steven L. Gersen. The network helps show where Steven L. Gersen may publish in the future.

Co-authorship network of co-authors of Steven L. Gersen

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

All Works

13 of 13 papers shown
1.
2.
Wang, Yongbao, Russell L. Maiese, Kevin J. Arvai, et al.. (2014). Assessment of Mutation Status in a Large Series of Patients with Cytopenias with Normal Karyotypes and without Increased Blasts. Blood. 124(21). 4606–4606. 1 indexed citations
3.
Gersen, Steven L., et al.. (2013). The Principles of Clinical Cytogenetics. Digital Access to Libraries (Université catholique de Louvain (UCL), l'Université de Namur (UNamur) and the Université Saint-Louis (USL-B)). 28 indexed citations
4.
Meloni‐Ehrig, Aurelia, Jeanne Meck, JoAnn C. Kelly, et al.. (2009). Stimulation of B-Cell Mature Malignancies with the CpG-Oligonucleotide DSP30 and Interleukin-2 for Improved Detection of Chromosome Abnormalities.. Blood. 114(22). 1955–1955. 1 indexed citations
5.
Gersen, Steven L., et al.. (2003). I1307K Mutation Detection by Allele-Specific PCR in Familial Colorectal Cancer. PubMed. 50. 129–135. 2 indexed citations
6.
Tepperberg, James, Mark J. Pettenati, P. Nagesh Rao, et al.. (2001). Prenatal diagnosis using interphase fluorescence in situ hybridization (FISH): 2‐year multi‐center retrospective study and review of the literature. Prenatal Diagnosis. 21(4). 293–301. 89 indexed citations
7.
Gersen, Steven L., et al.. (1995). Rapid prenatal diagnosis of 14 cases of triploidy using fish with multiple probes. Prenatal Diagnosis. 15(1). 1–5. 12 indexed citations
8.
Ward, Brian E., Steven L. Gersen, Nancy M. McGuire, et al.. (1994). Rapid Prenatal Diagnosis of Chromosomal Aneuploidies by Fluorescence in Situ Hybridization: Clinical Experience With 4500 Specimens. Obstetrical & Gynecological Survey. 49(3). 163–165. 67 indexed citations
9.
Brown, Stephen, Steven L. Gersen, Kwame Anyane‐Yeboa, & Dorothy Warburton. (1993). Preliminary definition of a “critical region” of chromosome 13 in q32: Report of 14 cases with 13q deletions and review of the literature. American Journal of Medical Genetics. 45(1). 52–59. 130 indexed citations
10.
Ward, Brian E., Steven L. Gersen, Nancy M. McGuire, et al.. (1993). Rapid prenatal diagnosis of chromosomal aneuploidies by fluorescence in situ hybridization: clinical experience with 4,500 specimens.. PubMed. 52(5). 854–65. 165 indexed citations
11.
12.
Gersen, Steven L., et al.. (1987). The value of chromosome analysis in cases of neural tube defects: A case of anencephaly associated with fetal DUP(2) (p24→pter). Prenatal Diagnosis. 7(8). 567–571. 19 indexed citations
13.
Swayne, Lawrence C., et al.. (1986). Placental changes in fetal triploidy syndrome.. Journal of Ultrasound in Medicine. 5(10). 545–550. 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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