PETER A. BENN

8.6k citations
214 papers · 6.5k · h-index 44

Impact in

    • Prenatal Screening and Diagnostics
  • Genetics top 5%
    • Genomic variations and chromosomal abnormalities
    • Genetic Syndromes and Imprinting
    • Genomics and Rare Diseases
    • Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities

Papers in

PETER A. BENN

201 papers receiving 5.9k citations

Peers

PETER A. BENN
Comparison fields: 5 of 111
  • Pediatrics, Perinatology and Child Health 4.6k
  • Genetics 825
  • Hematology 344
  • Genetics 93
  • Obstetrics and Gynecology 92
Replace Giuseppe Simoni with:
Giuseppe Simoni Italy
Eugene Pergament United States
Norman D. Rosenblum Canada
Bruno Brambati Italy
Charles M. Strom United States
Valérie Anne Désilets Canada
Maurice J. Mahoney United States
Nico J. Leschot Netherlands
Joanne Traeger‐Synodinos Greece
Francesca Romana Grati Italy
PETER A. BENN relative to Giuseppe Simoni Italy Giuseppe Simoni's profile →
Citations per field
00.5×5×10×13.2×
Giuseppe Simoni · 1×
Citations per year

Countries citing papers authored by PETER A. BENN

Since Specialization
Citations

This map shows the geographic impact of PETER A. 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 A. 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 A. BENN more than expected).

Fields of papers citing papers by PETER A. BENN

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by PETER A. 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 A. BENN. The network helps show where PETER A. BENN may publish in the future.

Co-authors

The 25 scholars most cited alongside PETER A. 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 A. BENN Line = papers co-authored together PETER A. BENN links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 214 papers — load more, or switch the sort, to bring in the rest.

#Work
1 2013261
2 2014257
3 2015234
4 2014213
5 1997190
6 2013187
7 1997166
8 1998144
9 2012139
10 1992137
11 2015111
12 200599
13 201398
14 200494
15 201090
16 201788
17 200083
18 201383
19 201983
20 201377

About PETER A. BENN

PETER A. BENN is a scholar working on Pediatrics, Perinatology and Child Health, Hematology, Genetics, Clinical Biochemistry and Cancer Research, having authored 214 papers that have together received 6.5k indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (156 papers), Chronic Myeloid Leukemia Treatments (14 papers), Genomic variations and chromosomal abnormalities (10 papers), Down syndrome and intellectual disability research (8 papers), Metabolism and Genetic Disorders (5 papers), Genetic Syndromes and Imprinting (4 papers), Carcinogens and Genotoxicity Assessment (4 papers) and Telomeres, Telomerase, and Senescence (3 papers). The work is most often cited by research in Pediatrics, Perinatology and Child Health (4.6k citations), Genetics (825 citations), Hematology (344 citations), Genetics (93 citations) and Obstetrics and Gynecology (92 citations). PETER A. BENN has collaborated with scholars based in United States, United Kingdom and Italy. Frequent co-authors include Howard Cuckle, Eugene Pergament, JAMES F. X. EGAN, Donald S. Wright, Lillian Y. F. Hsu, Susan Joy Gross, Audrey R. Chapman, Zachary Demko, Mary E. Norton and Allison Ryan. Their work appears in journals such as Prenatal Diagnosis, American Journal of Obstetrics and Gynecology, Obstetrics and Gynecology, Ultrasound in Obstetrics and Gynecology and Genetics in Medicine.

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.

Explore authors with similar magnitude of impact