Brynn Levy

14.0k total citations · 2 hit papers
134 papers, 7.2k citations indexed

About

Brynn Levy is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Molecular Biology. According to data from OpenAlex, Brynn Levy has authored 134 papers receiving a total of 7.2k indexed citations (citations by other indexed papers that have themselves been cited), including 81 papers in Genetics, 77 papers in Pediatrics, Perinatology and Child Health and 41 papers in Molecular Biology. Recurrent topics in Brynn Levy's work include Prenatal Screening and Diagnostics (76 papers), Genomic variations and chromosomal abnormalities (69 papers) and Fetal and Pediatric Neurological Disorders (20 papers). Brynn Levy is often cited by papers focused on Prenatal Screening and Diagnostics (76 papers), Genomic variations and chromosomal abnormalities (69 papers) and Fetal and Pediatric Neurological Disorders (20 papers). Brynn Levy collaborates with scholars based in United States, United Kingdom and Canada. Brynn Levy's co-authors include Nathan R. Treff, Richard T. Scott, Ronald J. Wapner, Athanassios Kotsinas, Vassilis G. Gorgoulis, Kurt Hirschhorn, Christos Kittas, Thanos D. Halazonetis, Dimitris Kletsas and Triantafillos Liloglou and has published in prestigious journals such as Nature, New England Journal of Medicine and Proceedings of the National Academy of Sciences.

In The Last Decade

Brynn Levy

131 papers receiving 6.9k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Activation of the DNA damage checkpoint and genomic instability in human precancerous lesions

2005 1.6k citations Vassilis G. Gorgoulis, Leandros-Vassilios Vassiliou et al. Nature profile →
In vitro fertilization with single euploid blastocyst transfer: a randomized controlled trial

2013 379 citations Xin Tao, Brynn Levy et al. Fertility and Sterility profile →

Peers

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-authorship network of co-authors of Brynn Levy

This figure shows the co-authorship network connecting the top 25 collaborators of Brynn Levy. A scholar is included among the top collaborators of Brynn Levy 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 Brynn Levy. Brynn Levy is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Advances in Prenatal Cell‐Free DNA Screening for Dominant Monogenic Conditions: A Review of Current Progress and Future Directions in Clinical Implementation 2025 ·Prenatal Diagnosis ·Jun Liao, (unknown), (unknown), Tristan Hardy, Brynn Levy, Lakshmi Mehta, Kwong Wai Choy, Hefeng Huang, Jinglan Zhang	2
2	Prenatal Diagnosis of Tubulinopathy: Case Report of Neurosonographic Features and a Novel TUBA1A Variant 2025 ·Fetal Diagnosis and Therapy ·Eran Bornstein, Vaidehi Jobanputra, (unknown), Amanda Thomas‐Wilson, Caitlin Baptiste, Brynn Levy, G. Malinger	0
3	Conventional Cytogenetic Analysis of Solid Tumor Abnormalities: A 25-Year Review of Proficiency Test Results from the College of American Pathologists/American College of Medical Genetics and Genomics Cytogenetics Committee 2024 ·Genes ·(unknown), William R. Sukov, (unknown), Catherine Rehder, Brynn Levy, Gopalrao V.N. Velagaleti, Reha M. Toydemir, Guilin Tang, (unknown), (unknown), (unknown), Ying Zou, Caroline Astbury, Karen D. Tsuchiya, Jess F. Peterson	0
4	Detection of Constitutional Structural Variants by Optical Genome Mapping 2024 ·Journal of Molecular Diagnostics ·Ulrich Broeckel, M. Anwar Iqbal, Brynn Levy, Nikhil Sahajpal, Péter L. Nagy, Gunter Scharer, Vanessa Rodríguez‐Fanjul, Aaron Bossler, Aaron A. Stence, Cindy Skinner, Steven A. Skinner, Ravindra Kolhe, Roger E. Stevenson	8
5	Integration of a Cross-Ancestry Polygenic Model With Clinical Risk Factors Improves Breast Cancer Risk Stratification 2023 ·JCO Precision Oncology ·(unknown), (unknown), (unknown), (unknown), Brynn Levy, (unknown), Jeffrey N. Weitzel, Matthew Rabinowitz, Akash Kumar, (unknown)	5
6	Optical genome mapping in acute myeloid leukemia: a multicenter evaluation 2022 ·Blood Advances ·Brynn Levy, Linda B. Baughn, Yassmine Akkari, Scott Chartrand, (unknown), David F. Claxton, Patrick A. Lennon, (unknown), Ravindra Kolhe, (unknown), Beth A. Pitel, Nikhil Sahajpal, Malini Sathanoori, George Vlad, Lijun Zhang, Min Fang, Rashmi Kanagal‐Shamanna, James R. Broach	65
7	Guiding the global evolution of cytogenetic testing for hematologic malignancies 2022 ·Blood ·Yassmine Akkari, Linda B. Baughn, Adrian M. Dubuc, Adam C. Smith, Mar Mallo, Paola Dal Cin, María Díez‐Campelo, Marta S. Gallego, Isabel Granada, (unknown), Brigitte Schlegelberger, Irma Slavutsky, Cristina Mecucci, Ross L. Levine, Robert P. Hasserjian, Françesc Solé, Brynn Levy, Xinjie Xu	47
8	Chromosomal mosaicism: Origins and clinical implications in preimplantation and prenatal diagnosis 2021 ·Prenatal Diagnosis ·Brynn Levy, Eva R. Hoffmann, Rajiv C. McCoy, Francesca Romana Grati	32
9	A Rapid and Simple Bead-Bashing-Based Method for Genomic DNA Extraction from Mammalian Tissue 2020 ·BioTechniques ·Shan Wei, Brynn Levy, (unknown), (unknown), (unknown), Ronald J. Wapner, Mary E. D’Alton, Zev Williams	5
10	Right or wrong? Looking through the retrospectoscope to analyse predictions made a decade ago in prenatal diagnosis and fetal surgery 2020 ·Prenatal Diagnosis ·Lyn S. Chitty, Alessandro Ghidini, Jan Deprest, Tim Van Mieghem, Brynn Levy, Lisa Hui, Diana W. Bianchi	4
11	High‐resolution genomic alterations in Barrett's metaplasia of patients who progress to esophageal dysplasia and adenocarcinoma 2019 ·International Journal of Cancer ·Jorge L. Sepulveda, Elena V. Komissarova, (unknown), Richard A. Friedman, Jon M. Davison, Brynn Levy, (unknown), Vaidehi Jobanputra, Armando Del Portillo, Gary W. Falk, Joshua Sonett, Charles J. Lightdale, Julian A. Abrams, Timothy C. Wang, Antonia R. Sepulveda	10
12	Generation of induced pluripotent stem cells from revertant keratinocytes 2016 ·Journal of Dermatological Science ·Noriko Umegaki, (unknown), Anna M.G. Pasmooij, Munenari Itoh, Jane Cerise, Zongyou Guo, Brynn Levy, Antoni Gostyński, Lisa Rothman, Marcel F. Jonkman, Angela M. Christiano	1
13	Induced pluripotent stem cells (iPSC) created from skin fibroblasts of patients with Prader-Willi syndrome (PWS) retain the molecular signature of PWS 2016 ·Stem Cell Research ·Lisa C. Burnett, Charles A. LeDuc, Carlos R. Sulsona, Daniel Paull, Sanaa Eddiry, Brynn Levy, Jean‐Pierre Salles, M. Tauber, Daniel J. Driscoll, Dieter Egli, Rudolph L. Leibel	22
14	Rapid and concurrent comprehensive chromosome screening (CCS) and single gene disorder (SGD) PGD 2014 ·Fertility and Sterility ·Xin Tao, Chaim Jalas, Anastasia Fedick, (unknown), (unknown), (unknown), (unknown), Brynn Levy, Richard T. Scott, Nathan R. Treff	1
15	A novel single-cell DNA fingerprinting method successfully distinguishes sibling human embryos 2009 ·Fertility and Sterility ·Nathan R. Treff, Jing Su, Xin Tao, Kathleen A. Miller, Brynn Levy, Richard T. W. Scott	39
16	Deregulated Overexpression of hCdt1 and hCdc6 Promotes Malignant Behavior 2007 ·Cancer Research ·Michalis Liontos, (unknown), Maria Sideridou, Konstantinos Evangelou, Dimitris Kletsas, Brynn Levy, Athanassios Kotsinas, Odelia Nahum, Vassilis Zoumpourlis, Mirsini Kouloukoussa, Zoi Lygerou, Stavros Taraviras, Christos Kittas, Jiřina Bártková, Athanasios G. Papavassiliou, Jiří Bártek, Thanos D. Halazonetis, Vassilis G. Gorgoulis	160
17	Activation of the DNA damage checkpoint and genomic instability in human precancerous lesions breakdown → 2005 ·Nature ·Vassilis G. Gorgoulis, Leandros-Vassilios Vassiliou, Panagiotis Karakaidos, Panayotis Zacharatos, Athanassios Kotsinas, Triantafillos Liloglou, Monica Venere, Richard A. DiTullio, Nikolaos G. Kastrinakis, Brynn Levy, Dimitris Kletsas, (unknown), Meenhard Herlyn, Christos Kittas, Thanos D. Halazonetis	1598
18	Xenobiotic phenols in early pregnancy amniotic fluid 2005 ·Reproductive Toxicology ·Stephanie M. Engel, Brynn Levy, Zhisong Liu, (unknown), Mary S. Wolff	93
19	Molecular Cytogenetic Analysis of Uterine Leiomyoma and Leiomyosarcoma by Comparative Genomic Hybridization 2000 ·Cancer Genetics and Cytogenetics ·Brynn Levy, Tanmoy Mukherjee, Kurt Hirschhorn	75
20	Characterization of a de novo unbalanced chromosome rearrangement by comparative genomic hybridization and fluorescence in situ hybridization 1997 ·Cytogenetic and Genome Research ·Brynn Levy, (unknown), Robert J. Desnick, A. Babu, Bruce D. Gelb, Kurt Hirschhorn, (unknown)	25

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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