James Tepperberg

4.2k total citations
28 papers, 889 citations indexed

About

James Tepperberg is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, James Tepperberg has authored 28 papers receiving a total of 889 indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Genetics, 10 papers in Molecular Biology and 10 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in James Tepperberg's work include Genomic variations and chromosomal abnormalities (17 papers), Prenatal Screening and Diagnostics (10 papers) and Genomics and Rare Diseases (5 papers). James Tepperberg is often cited by papers focused on Genomic variations and chromosomal abnormalities (17 papers), Prenatal Screening and Diagnostics (10 papers) and Genomics and Rare Diseases (5 papers). James Tepperberg collaborates with scholars based in United States, Netherlands and Greece. James Tepperberg's co-authors include Peter Papenhausen, Stuart Schwartz, Inder Gadi, Rachel D. Burnside, Vikram Jaswaney, Romela Pasion, Hiba Risheg, Nathaniel H. Robin, Erin L. Youngs and Venkateswara R. Potluri and has published in prestigious journals such as American Journal of Obstetrics and Gynecology, The American Journal of Surgical Pathology and Urology.

In The Last Decade

James Tepperberg

27 papers receiving 850 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
James Tepperberg United States 15 532 362 284 149 86 28 889
Silvana Guerneri Italy 17 406 0.8× 357 1.0× 344 1.2× 121 0.8× 24 0.3× 50 902
Anita S. Kulharya United States 14 452 0.8× 509 1.4× 147 0.5× 106 0.7× 72 0.8× 31 843
Jacques C. Giltay Netherlands 23 760 1.4× 665 1.8× 306 1.1× 130 0.9× 82 1.0× 65 1.3k
Lukrecija Brečević Switzerland 17 479 0.9× 361 1.0× 174 0.6× 161 1.1× 35 0.4× 31 749
Anne W. Higgins United States 11 360 0.7× 529 1.5× 143 0.5× 409 2.7× 101 1.2× 17 885
E. Boyd United Kingdom 22 804 1.5× 623 1.7× 233 0.8× 304 2.0× 74 0.9× 55 1.3k
Stephen Laderman United States 4 541 1.0× 436 1.2× 126 0.4× 211 1.4× 26 0.3× 4 783
Nicole L. Hoppman United States 14 279 0.5× 279 0.8× 115 0.4× 47 0.3× 173 2.0× 62 704
Merete Bugge Denmark 10 584 1.1× 935 2.6× 146 0.5× 107 0.7× 31 0.4× 15 1.2k
Jiangzhen Li United States 8 751 1.4× 418 1.2× 294 1.0× 217 1.5× 14 0.2× 8 946

Countries citing papers authored by James Tepperberg

Since Specialization
Citations

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

Fields of papers citing papers by James Tepperberg

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of James Tepperberg

This figure shows the co-authorship network connecting the top 25 collaborators of James Tepperberg. A scholar is included among the top collaborators of James Tepperberg 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 James Tepperberg. James Tepperberg 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.
Papenhausen, Peter, et al.. (2018). Multidisciplinary analysis of pediatric T-ALL: 9q34 gene fusions. Cancer Genetics. 231-232. 1–13. 10 indexed citations
2.
Cherry, Athena M., Yassmine Akkari, Hutton M. Kearney, et al.. (2017). Diagnostic cytogenetic testing following positive noninvasive prenatal screening results: a clinical laboratory practice resource of the American College of Medical Genetics and Genomics (ACMG). Genetics in Medicine. 19(8). 845–850. 29 indexed citations
3.
Krishnamurthy, Savitri, Wendy A. Woodward, Wei Yang, et al.. (2013). Status of the anaplastic lymphoma kinase (ALK) gene in inflammatory breast carcinoma. SpringerPlus. 2(1). 409–409. 16 indexed citations
4.
Montgomery, Nathan D., et al.. (2012). A 137‐kb deletion within the Potocki–Shaffer syndrome interval on chromosome 11p11.2 associated with developmental delay and hypotonia. American Journal of Medical Genetics Part A. 161(1). 198–202. 7 indexed citations
5.
Levy, Brynn, David Tegay, Peter Papenhausen, et al.. (2012). Tetrasomy 15q26: a distinct syndrome or Shprintzen-Goldberg syndrome phenocopy?. Genetics in Medicine. 14(9). 811–818. 4 indexed citations
6.
Brothman, Arthur R., Michelle Dolan, Barbara K. Goodman, et al.. (2011). College of American Pathologists/American College of Medical Genetics proficiency testing for constitutional cytogenomic microarray analysis. Genetics in Medicine. 13(9). 765–769. 12 indexed citations
7.
8.
Weisfeld‐Adams, James D., et al.. (2011). Clinical and molecular characterization of chromosome 7p22.1 microduplication detected by array CGH. American Journal of Medical Genetics Part A. 155(10). 2508–2511. 18 indexed citations
9.
Burnside, Rachel D., Romela Pasion, Fady M. Mikhail, et al.. (2011). Microdeletion/microduplication of proximal 15q11.2 between BP1 and BP2: a susceptibility region for neurological dysfunction including developmental and language delay. Human Genetics. 130(4). 517–528. 182 indexed citations
10.
Mascarello, James T., Betsy Hirsch, Hutton M. Kearney, et al.. (2011). Section E9 of the American College of Medical Genetics technical standards and guidelines: Fluorescence in situ hybridization. Genetics in Medicine. 13(7). 667–675. 58 indexed citations
11.
Tsuchiya, Karen D., Lisa G. Shaffer, Swaroop Aradhya, et al.. (2009). Variability in interpreting and reporting copy number changes detected by array-based technology in clinical laboratories. Genetics in Medicine. 11(12). 866–873. 40 indexed citations
12.
Mehta, Lakshmi, et al.. (2008). Ovotesticular Disorder of Sexual Development (True Hermaphroditism). Urology. 73(2). 293–296. 17 indexed citations
13.
Wauters, J., Elvire Van Assche, A. Antsaklis, et al.. (2007). Fully automated FISH examination of amniotic fluid cells. Prenatal Diagnosis. 27(10). 951–955. 10 indexed citations
14.
Evans, Mark I., Michael Sharp, James Tepperberg, et al.. (2006). Automated Microscopy of Amniotic Fluid Cells: Detection of FISH Signals Using the <i>FastFISH</i>® Imaging System. Fetal Diagnosis and Therapy. 21(6). 523–527. 14 indexed citations
15.
Papenhausen, Peter, Sharon Griffin, & James Tepperberg. (2005). Oncogene amplification in transforming myelodysplasia. Experimental and Molecular Pathology. 79(2). 168–175. 17 indexed citations
16.
Gong, Jerald Z., Timothy T. Stenzel, Ellen Bennett, et al.. (2003). Burkitt Lymphoma Arising in Organ Transplant Recipients. The American Journal of Surgical Pathology. 27(6). 818–827. 39 indexed citations
17.
Tepperberg, James, et al.. (2002). Visual Diagnosis. Pediatrics in Review. 23(10). 365–367. 2 indexed citations
18.
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
19.
Levy, Brynn, Peter Papenhausen, James Tepperberg, et al.. (2000). Prenatal molecular cytogenetic diagnosis of partial tetrasomy 10p due to neocentromere formation in an inversion duplication analphoid marker chromosome. Cytogenetic and Genome Research. 91(1-4). 165–170. 25 indexed citations
20.
Hando, John C., James D. Tucker, Marsha L. Davenport, James Tepperberg, & J. Nath. (1997). X chromosome inactivation and micronuclei in normal and Turner individuals. Human Genetics. 100(5-6). 624–628. 40 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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