Brynn Levy

14.3k citations
160 papers · 10.6k · 4 hit papers · h-index 47

Impact in

    • Prenatal Screening and Diagnostics
    • Fetal and Pediatric Neurological Disorders
    • Assisted Reproductive Technology and Twin Pregnancy
  • Genetics top 0.5%
    • Genomic variations and chromosomal abnormalities
    • Genomics and Rare Diseases

Papers in

    • Prenatal Screening and Diagnostics 80
    • Fetal and Pediatric Neurological Disorders 19
    • Assisted Reproductive Technology and Twin Pregnancy 6
    • Genomic variations and chromosomal abnormalities 63
    • Genetic Syndromes and Imprinting 15

Brynn Levy

151 papers receiving 10.0k citations

Brynn Levy's Hit Papers

Whole-exome sequencing in the evaluation of fetal structural anomalies: a prospective cohort study 2019 · 447 citations
4470+7+14Years since publication50010001.5k

Peers

Brynn Levy
Comparison fields: 5 of 130
  • Pediatrics, Perinatology and Child Health 4.2k
  • Genetics 3.1k
  • Cancer Research 831
  • Molecular Biology 3.9k
  • Oncology 1.2k
Replace Gudrun E. Moore with:
Gudrun E. Moore United Kingdom
Kenichiro Hata Japan
Andrea Riccio Italy
Felix Beck United Kingdom
François Fuks Belgium
Rachel H. Giles Netherlands
Monica Rosa Miozzo Italy
Gerard Pals Netherlands
Daniel I. H. Linzer United States
JAMES L. GERMAN United States
Brynn Levy relative to Gudrun E. Moore United Kingdom Gudrun E. Moore's profile →
Citations per field
00.5×2×3×3.9×
Gudrun E. Moore · 1×
Citations per year

Countries citing papers authored by Brynn Levy

Since Specialization
Citations

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

Fields of papers citing papers by Brynn Levy

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

20 of 20 papers shown

Showing the 20 most-cited of 160 papers — load more, or switch the sort, to bring in the rest.

#Work
1
Activation of the DNA damage checkpoint and genomic instability in human precancerous lesions
Hit paper breakdown →
20051706
2
Chromosomal Microarray versus Karyotyping for Prenatal Diagnosis
Hit paper breakdown →
20121047
3
Whole-exome sequencing in the evaluation of fetal structural anomalies: a prospective cohort study
Hit paper breakdown →
2019447
4
In vitro fertilization with single euploid blastocyst transfer: a randomized controlled trial
Hit paper breakdown →
2013412
5 2017326
6 2012259
7 2014256
8 2016240
9 2018237
10 2005220
11 2010214
12 2010209
13 2012208
14 2000207
15 2002185
16 2007179
17 2014176
18 2018167
19 2010151
20 2010139

About Brynn Levy

Brynn Levy is a scholar working on Pediatrics, Perinatology and Child Health, Genetics, Cancer Research, Molecular Biology and Plant Science, having authored 160 papers that have together received 10.6k indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (80 papers), Genomic variations and chromosomal abnormalities (63 papers), Fetal and Pediatric Neurological Disorders (19 papers), Genetic Syndromes and Imprinting (15 papers), Chromosomal and Genetic Variations (14 papers), Cancer Genomics and Diagnostics (12 papers), Genomics and Chromatin Dynamics (7 papers) and Assisted Reproductive Technology and Twin Pregnancy (6 papers). The work is most often cited by research in Pediatrics, Perinatology and Child Health (4.2k citations), Genetics (3.1k citations), Cancer Research (831 citations), Molecular Biology (3.9k citations) and Oncology (1.2k citations). Brynn Levy has collaborated with scholars based in United States, United Kingdom and Canada. Frequent co-authors include Nathan R. Treff, Richard Thomas Scott, Ronald J. Wapner, Kurt Hirschhorn, Athanassios Kotsinas, Vassilis G. Gorgoulis, Christos N. Kittas, Xin Tao, Thanos D. Halazonetis and Dimitris Kletsas. Their work appears in journals such as Fertility and Sterility, Prenatal Diagnosis, American Journal of Obstetrics and Gynecology, Genetics in Medicine and Genomics.

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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