Peter Benn

8.6k total citations
192 papers, 5.5k citations indexed

About

Peter Benn is a scholar working on Pediatrics, Perinatology and Child Health, Infectious Diseases and Genetics. According to data from OpenAlex, Peter Benn has authored 192 papers receiving a total of 5.5k indexed citations (citations by other indexed papers that have themselves been cited), including 140 papers in Pediatrics, Perinatology and Child Health, 51 papers in Infectious Diseases and 44 papers in Genetics. Recurrent topics in Peter Benn's work include Prenatal Screening and Diagnostics (138 papers), Parvovirus B19 Infection Studies (51 papers) and Fetal and Pediatric Neurological Disorders (33 papers). Peter Benn is often cited by papers focused on Prenatal Screening and Diagnostics (138 papers), Parvovirus B19 Infection Studies (51 papers) and Fetal and Pediatric Neurological Disorders (33 papers). Peter Benn collaborates with scholars based in United States, United Kingdom and Italy. Peter Benn's co-authors include Howard Cuckle, Eugene Pergament, James Egan, Dave Wright, Audrey R. Chapman, Susan J. Gross, Zachary Demko, Mary E. Norton, Min Fang and Lillian Y. F. Hsu and has published in prestigious journals such as JAMA, Blood and PLoS ONE.

In The Last Decade

Peter Benn

186 papers receiving 5.2k citations

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author Last Decade Papers Cites
Peter Benn 4.2k 1.8k 1.5k 874 666 192 5.5k
Maurice J. Mahoney 2.6k 0.6× 760 0.4× 562 0.4× 980 1.1× 1.2k 1.8× 115 4.7k
J. M. Connor 1.4k 0.3× 1.3k 0.7× 417 0.3× 1.5k 1.7× 579 0.9× 105 5.8k
Eugene Pergament 2.8k 0.7× 1.1k 0.6× 661 0.4× 691 0.8× 635 1.0× 118 3.7k
Joanne Traeger‐Synodinos 2.4k 0.6× 1.0k 0.6× 461 0.3× 990 1.1× 412 0.6× 174 4.3k
Giuseppe Simoni 2.0k 0.5× 1.5k 0.8× 352 0.2× 727 0.8× 515 0.8× 112 3.3k
Karin J. Blakemore 1.3k 0.3× 565 0.3× 259 0.2× 299 0.3× 718 1.1× 162 2.7k
B. Brambati 2.3k 0.5× 545 0.3× 491 0.3× 352 0.4× 604 0.9× 97 2.8k
Humphrey H.H. Kanhai 1.6k 0.4× 485 0.3× 672 0.5× 744 0.9× 1.2k 1.8× 141 5.3k
Y. M. Dennis Lo 899 0.2× 318 0.2× 470 0.3× 972 1.1× 398 0.6× 54 2.9k
Monica Miozzo 669 0.2× 1.2k 0.7× 143 0.1× 1.9k 2.2× 466 0.7× 158 5.0k

Countries citing papers authored by Peter Benn

Since Specialization
Citations

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

Fields of papers citing papers by Peter Benn

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Peter Benn

This figure shows the co-authorship network connecting the top 25 collaborators of Peter Benn. A scholar is included among the top collaborators of Peter Benn 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 Peter Benn. Peter Benn 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.
Benn, Peter, et al.. (2024). Accuracy of fetal fraction measurements in a single‐nucleotide polymorphism‐based noninvasive prenatal test. Prenatal Diagnosis. 44(10). 1218–1224. 1 indexed citations
2.
Benn, Peter, et al.. (2024). Evaluating reproductive carrier screening using biotinidase deficiency as a model: Variants identified, variant rates, and management. Genetics in Medicine. 27(3). 101345–101345. 1 indexed citations
3.
Benn, Peter, et al.. (2024). Chromosome segregation of human nonhomologous Robertsonian translocations: insights from preimplantation genetic testing. European Journal of Human Genetics. 33(6). 711–717. 3 indexed citations
4.
Grati, Francesca Romana, José Carlos Ferreira, Peter Benn, et al.. (2020). Outcomes in Pregnancies With a Confined Placental Mosaicism and Implications for Prenatal Screening Using Cell-Free DNA. Obstetrical & Gynecological Survey. 75(7). 397–398. 1 indexed citations
5.
Grati, Francesca Romana, José Carlos Ferreira, Peter Benn, et al.. (2019). Outcomes in pregnancies with a confined placental mosaicism and implications for prenatal screening using cell-free DNA. Genetics in Medicine. 22(2). 309–316. 64 indexed citations
6.
Benn, Peter & Audrey R. Chapman. (2016). Ethical and practical challenges in providing noninvasive prenatal testing for chromosome abnormalities. Current Opinion in Obstetrics & Gynecology. Publish Ahead of Print(2). 119–24. 15 indexed citations
7.
Cuckle, Howard, Peter Benn, & Eugene Pergament. (2015). Cell-free DNA screening for fetal aneuploidy as a clinical service. Clinical Biochemistry. 48(15). 932–941. 64 indexed citations
8.
Wapner, Ronald J., Joshua Babiarz, Brynn Levy, et al.. (2014). Expanding the scope of noninvasive prenatal testing: detection of fetal microdeletion syndromes. American Journal of Obstetrics and Gynecology. 212(3). 332.e1–332.e9. 224 indexed citations
9.
Shamshirsaz, Alireza A., Alireza A. Shamshirsaz, Bahram Salmanian, et al.. (2013). Nuchal translucency and cardiac abnormalities in euploid singleton pregnancies. The Journal of Maternal-Fetal & Neonatal Medicine. 27(5). 495–499. 4 indexed citations
10.
Shamshirsaz, Alireza A., Alireza A. Shamshirsaz, Adam Borgida, et al.. (2013). Efficacy of the Genetic Sonogram in a Stepwise Sequential Protocol for Down Syndrome Screening. Journal of Ultrasound in Medicine. 32(9). 1607–1613. 5 indexed citations
11.
Benn, Peter, Howard Cuckle, & Eugene Pergament. (2013). Non‐invasive prenatal testing for aneuploidy: current status and future prospects. Ultrasound in Obstetrics and Gynecology. 42(1). 15–33. 234 indexed citations
12.
Benn, Peter, et al.. (2008). Human Lymphocyte Culture and Chromosome Analysis. Cold Spring Harbor Protocols. 2008(9). pdb.prot5035–pdb.prot5035. 12 indexed citations
13.
Wright, Dave, Ian Bradbury, Howard Cuckle, et al.. (2006). Three‐stage contingent screening for Down syndrome. Prenatal Diagnosis. 26(6). 528–534. 16 indexed citations
14.
Benn, Peter, Min Fang, & James Egan. (2005). Trends in the use of second trimester maternal serum screening from 1991 to 2003. Genetics in Medicine. 7(5). 328–331. 21 indexed citations
15.
Chen, Jieling, Dennis Heffley, Tryfon Beazoglou, & Peter Benn. (2000). Utilization of Amniocentesis by Women Screening Positive for Down Syndrome on the Second-Trimester Triple Test. Public Health Genomics. 3(1). 24–30. 19 indexed citations
16.
Benn, Peter. (1997). Aging chromosome telomeres: parallel studies with terminal repeat and telomere associated DNA probes. Mechanisms of Ageing and Development. 99(2). 153–166. 15 indexed citations
17.
Lu, Guohui, Arnold J. Altman, & Peter Benn. (1993). Review of the cytogenetic changes in acute megakaryoblastic leukemia: One disease or several?. Cancer Genetics and Cytogenetics. 67(2). 81–89. 39 indexed citations
18.
Verma, Ram S., Michael J. Macera, Peter Benn, & John Groffen. (1989). Molecular characterization of variant translocations in chronic myelogenous leukemia.. PubMed. 4(9). 1145–8. 5 indexed citations
19.
20.
Benn, Peter, et al.. (1977). Assignment of the genes for human β-glucuronidase and mitochondrial malate dehydrogenase to the region pter→q22 of chromosome 7. Cytogenetic and Genome Research. 19(5). 273–280. 5 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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