Peter Benn

8.7k citations

200 papers · 5.8k · h-index 44

Impact in

Pediatrics, Perinatology and Child Health top 0.05%
- Prenatal Screening and Diagnostics
- Fetal and Pediatric Neurological Disorders
Genetics top 1%
- Genomic variations and chromosomal abnormalities
- Genetic Syndromes and Imprinting
- Chronic Lymphocytic Leukemia Research

Papers in

Pediatrics, Perinatology and Child Health 136
- Prenatal Screening and Diagnostics 135
- Fetal and Pediatric Neurological Disorders 15
Genetics 38
- Genomic variations and chromosomal abnormalities 24
- Genetic Syndromes and Imprinting 15
- Chronic Lymphocytic Leukemia Research 12

Co-authors: Howard Cuckle (18 shared papers)Eugene Pergament (5 shared papers)James Egan (33 shared papers)Dave Wright (11 shared papers)Audrey R. Chapman (5 shared papers)Susan J. Gross (8 shared papers)Zachary Demko (15 shared papers)Lillian Y. F. Hsu (10 shared papers)
Journals: Prenatal Diagnosis (41 papers)Obstetrics and Gynecology (15 papers)American Journal of Obstetrics and Gynecology (14 papers)Ultrasound in Obstetrics and Gynecology (9 papers)Obstetrical & Gynecological Survey (6 papers)
Partner nations: United States United Kingdom Italy

In The Last Decade

Peter Benn

188 papers receiving 5.4k citations

Peers

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-authors

The 25 scholars most cited alongside Peter Benn, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Peter Benn Line = papers co-authored together Peter Benn links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 200 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Non‐invasive prenatal testing for aneuploidy: current status and future prospects Ultrasound in Obstetrics and Gynecology ·Peter Benn, Howard Cuckle, Eugene Pergament	2013	244
2	Expanding the scope of noninvasive prenatal testing: detection of fetal microdeletion syndromes American Journal of Obstetrics and Gynecology ·Ronald J. Wapner, Joshua Babiarz, Brynn Levy, Melissa Stosic, Bernhard Zimmermann, Styrmir Sigurjonsson, Nicholas Wayham, Allison Ryan, Milena Banjevic, Phil Lacroute, Jing Hu, Megan P. Hall, Zachary Demko, Asim Siddiqui, Matthew Rabinowitz, Susan J. Gross, Matthew D. Hill, Peter Benn	2014	234
3	Position statement from the Chromosome Abnormality Screening Committee on behalf of the Board of the International Society for Prenatal Diagnosis Prenatal Diagnosis ·Peter Benn, A. Borrell, Rossa W. K. Chiu, Howard Cuckle, Lorraine Dugoff, Brigitte H. W. Faas, Susan J. Gross, Tianhua Huang, Jo‐Ann Johnson, Ron Maymon, Mary E. Norton, Anthony Odibo, Peter C. J. I. Schielen, Kevin Spencer, Dave Wright, Yuval Yaron	2015	215
4	Clinical experience and follow-up with large scale single-nucleotide polymorphism–based noninvasive prenatal aneuploidy testing American Journal of Obstetrics and Gynecology ·P. Dar, Kirsten J. Curnow, Susan J. Gross, Megan P. Hall, Melissa Stosic, Zachary Demko, Bernhard Zimmermann, Matthew D. Hill, Styrmir Sigurjonsson, Allison Ryan, Milena Banjevic, Paula Kolacki, Susan W. Koch, Charles M. Strom, (unknown), Peter Benn	2014	191
5	Comparison of phenotype between patients with Prader-Willi syndrome due to deletion 15q and uniparental disomy 15 American Journal of Medical Genetics ·Suzanne B. Cassidy, Michele E. Forsythe, Shauna Heeger, Robert D. Nicholls, Nicholas J. Schork, Peter Benn, Stuart Schwartz	1997	183
6	Position statement from the Aneuploidy Screening Committee on behalf of the Board of the International Society for Prenatal Diagnosis Prenatal Diagnosis ·Peter Benn, Antoni Borell, Rossa W. K. Chiu, Howard Cuckle, Lorraine Dugoff, Brigitte H. W. Faas, Susan J. Gross, Jo‐Ann Johnson, Ron Maymon, Mary E. Norton, Anthony Odibo, Peter C. J. I. Schielen, Kevin Spencer, Tianhua Huang, Dave Wright, Yuval Yaron	2013	176
7	RARE TRISOMY MOSAICISM DIAGNOSED IN AMNIOCYTES, INVOLVING AN AUTOSOME OTHER THAN CHROMOSOMES 13, 18, 20, AND 21: KARYOTYPE/PHENOTYPE CORRELATIONS Prenatal Diagnosis ·Lillian Y. F. Hsu, Ming-Tsung Yu, Richard L. Neu, Daniel L. Van Dyke, Peter Benn, Christy Bradshaw, Lisa G. Shaffer, Rodney R. Higgins, Gabriel S. Khodr, Cynthia C. Morton, Hungshu Wang, Arthur R. Brothman, Dianne Chadwick, Christine M. Distèche, Lauren S. Jenkins, Dagmar K. Kalousek, TAPIO J. PANTZAR, Philip Wyatt	1997	149
8	Trisomy 16 and trisomy 16 mosaicism: A review American Journal of Medical Genetics ·Peter Benn	1998	137
9	Prenatal Detection of Down Syndrome using Massively Parallel Sequencing (MPS): a rapid response statement from a committee on behalf of the Board of the International Society for Prenatal Diagnosis, 24 October 2011 Prenatal Diagnosis ·Peter Benn, A. Borrell, Howard Cuckle, Lorraine Dugoff, Susan J. Gross, Jo-Ann Johnson, Ron Maymon, Anthony Odibo, Peter C. J. I. Schielen, Kevin Spencer, Dave Wright, Yuval Yaron	2012	130
10	Proposed guidelines for diagnosis of chromosome mosaicism in amniocytes based on data derived from chromosome mosaicism and pseudomosaicism studies Prenatal Diagnosis ·Lillian Y. F. Hsu, Sara Kaffe, Edmund C. Jenkins, Lita M. Alonso, Peter Benn, (unknown), Kurt Hirschhorn, Ernest Lieber, Alan Shanske, Lawrence R. Shapiro, Edward Schutta, Dorothy Warburton	1992	126
11	Clinical experience with single‐nucleotide polymorphism‐based non‐invasive prenatal screening for 22q11.2 deletion syndrome Ultrasound in Obstetrics and Gynecology ·Susan J. Gross, Melissa Stosic, Donna M. McDonald‐McGinn, Anne S. Bassett, Alain Norvez, Rupin Dhamankar, Kazukuni Kobara, Eser Kırkızlar, Bernhard Zimmermann, Nicholas Wayham, Joshua Babiarz, Allison Ryan, Kristine N. Jinnett, Zachary Demko, Peter Benn	2015	102
12	Down Syndrome Screening in the First and/or Second Trimester: Model Predicted Performance Using Meta-Analysis Parameters Seminars in Perinatology ·Howard Cuckle, Peter Benn, Dave Wright	2005	100
13	Maternal cfDNA screening for Down syndrome – a cost sensitivity analysis Prenatal Diagnosis ·Howard Cuckle, Peter Benn, Eugene Pergament	2013	92
14	Ethical challenges in providing noninvasive prenatal diagnosis Current Opinion in Obstetrics & Gynecology ·Peter Benn, Audrey R. Chapman	2010	91
15	Contingent screening for Down syndrome is an efficient alternative to non‐disclosure sequential screening Prenatal Diagnosis ·Dave Wright, Ian Bradbury, Peter Benn, Howard Cuckle, Karen Ritchie	2004	85
16	Clinical experience with a single‐nucleotide polymorphism‐based non‐invasive prenatal test for five clinically significant microdeletions Clinical Genetics ·Kimberly Martin, Shanto Iyengar, A. Kalyan, Cheng‐Che E. Lan, Alexander L. Simon, Melissa Stosic, Kenichi Kobara, Harini Ravi, Thérèse Truong, Allison Ryan, Zachary Demko, Peter Benn	2017	83
17	Noninvasive Prenatal Testing for Fetal Aneuploidy Obstetrics and Gynecology ·Mary E. Norton, Nancy C. Rose, Peter Benn	2013	80
18	Obstetricians and gynecologists' practice and opinions of expanded carrier testing and noninvasive prenatal testing Prenatal Diagnosis ·Peter Benn, Audrey R. Chapman, Kristine Erickson, Mark S. DeFrancesco, Louise Wilkins‐Haug, James Egan, Jay Schulkin	2013	76
19	Changes in the Utilization of Prenatal Diagnosis Obstetrics and Gynecology ·Peter Benn, James Egan, Min Fang, Rebecca Smith‐Bindman	2004	75
20	Outcomes in pregnancies with a confined placental mosaicism and implications for prenatal screening using cell-free DNA Genetics in Medicine ·Francesca Romana Grati, José Carlos Ferreira, Peter Benn, Claudia Izzi, Federica Verdi, E Vercellotti, Cristina Dalpiaz, Patrizia D’Ajello, Elisa Filippi, N. Volpe, Francesca Malvestiti, Federico Maggi, Giuseppe Simoni, T. Frusca, Gaetana Cirelli, Gabriella Bracalente, Antonino Lo Re, Daniela Surico, T. Ghi, Federico Prefumo	2019	70

About Peter Benn

Peter Benn is a scholar working on Pediatrics, Perinatology and Child Health, Genetics, Molecular Biology, Infectious Diseases and Genetics, having authored 200 papers that have together received 5.8k indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (135 papers), Parvovirus B19 Infection Studies (24 papers), Genomic variations and chromosomal abnormalities (24 papers), Fetal and Pediatric Neurological Disorders (15 papers), Genetic Syndromes and Imprinting (15 papers), Chronic Lymphocytic Leukemia Research (12 papers), Chronic Myeloid Leukemia Treatments (11 papers) and Congenital Anomalies and Fetal Surgery (10 papers). The work is most often cited by research in Pediatrics, Perinatology and Child Health (4.1k citations), Genetics (1.5k citations), Infectious Diseases (714 citations), Hematology (415 citations) and Genetics (360 citations). Peter Benn has collaborated with scholars based in United States, United Kingdom and Italy. Frequent co-authors include Howard Cuckle, Eugene Pergament, James Egan, Dave Wright, Audrey R. Chapman, Susan J. Gross, Zachary Demko, Lillian Y. F. Hsu, Mary E. Norton and Min Fang. Their work appears in journals such as Prenatal Diagnosis, Obstetrics and Gynecology, American Journal of Obstetrics and Gynecology, Ultrasound in Obstetrics and Gynecology and Obstetrical & Gynecological Survey.

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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