Andrew P. Feinberg

98.8k total citations · 21 hit papers
235 papers, 62.2k citations indexed

About

Andrew P. Feinberg is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Andrew P. Feinberg has authored 235 papers receiving a total of 62.2k indexed citations (citations by other indexed papers that have themselves been cited), including 193 papers in Molecular Biology, 119 papers in Genetics and 51 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Andrew P. Feinberg's work include Epigenetics and DNA Methylation (155 papers), Genetic Syndromes and Imprinting (92 papers) and Prenatal Screening and Diagnostics (39 papers). Andrew P. Feinberg is often cited by papers focused on Epigenetics and DNA Methylation (155 papers), Genetic Syndromes and Imprinting (92 papers) and Prenatal Screening and Diagnostics (39 papers). Andrew P. Feinberg collaborates with scholars based in United States, Sweden and United Kingdom. Andrew P. Feinberg's co-authors include Bert Vogelstein, Rafael A. Irizarry, Benjamin Tycko, Christine Ladd‐Acosta, Martin J. Aryee, Rolf Ohlsson, Kasper D. Hansen, Hengmi Cui, Andrew E. Jaffe and Steven Henikoff and has published in prestigious journals such as Nature, Science and New England Journal of Medicine.

In The Last Decade

Andrew P. Feinberg

229 papers receiving 60.6k citations

Hit Papers

A technique for radiolabeling DNA restriction endonucleas... 1983 2026 1997 2011 1983 2014 1983 2004 2009 5.0k 10.0k 15.0k 20.0k

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Andrew P. Feinberg United States 92 45.0k 15.5k 6.8k 5.9k 5.6k 235 62.2k
Stuart H. Orkin United States 157 51.2k 1.1× 10.2k 0.7× 6.0k 0.9× 5.8k 1.0× 3.9k 0.7× 539 76.4k
Peter A. Jones United States 112 48.9k 1.1× 8.9k 0.6× 10.9k 1.6× 8.3k 1.4× 2.5k 0.4× 352 61.5k
David Altshuler United States 80 29.7k 0.7× 30.5k 2.0× 7.1k 1.0× 3.5k 0.6× 1.6k 0.3× 150 63.8k
Adrian Bird United Kingdom 100 51.3k 1.1× 21.6k 1.4× 4.2k 0.6× 2.5k 0.4× 3.9k 0.7× 232 61.8k
Yi Zhang United States 110 52.9k 1.2× 9.3k 0.6× 5.6k 0.8× 3.5k 0.6× 2.7k 0.5× 420 60.2k
Jay Shendure United States 115 36.0k 0.8× 17.1k 1.1× 8.2k 1.2× 2.9k 0.5× 1.3k 0.2× 297 52.4k
Rudolf Jaenisch United States 179 107.3k 2.4× 33.2k 2.1× 14.1k 2.1× 7.6k 1.3× 5.4k 1.0× 590 136.9k
David E. Housman United States 104 32.2k 0.7× 9.2k 0.6× 3.8k 0.6× 9.8k 1.7× 2.9k 0.5× 329 47.8k
C. David Allis United States 143 77.5k 1.7× 9.7k 0.6× 5.1k 0.8× 5.7k 1.0× 1.6k 0.3× 344 87.9k
Stylianos E. Antonarakis Switzerland 102 21.9k 0.5× 13.3k 0.9× 3.4k 0.5× 1.9k 0.3× 3.1k 0.6× 602 40.8k

Countries citing papers authored by Andrew P. Feinberg

Since Specialization
Citations

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

Fields of papers citing papers by Andrew P. Feinberg

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Andrew P. Feinberg. 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 Andrew P. Feinberg. The network helps show where Andrew P. Feinberg may publish in the future.

Co-authorship network of co-authors of Andrew P. Feinberg

This figure shows the co-authorship network connecting the top 25 collaborators of Andrew P. Feinberg. A scholar is included among the top collaborators of Andrew P. Feinberg 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 Andrew P. Feinberg. Andrew P. Feinberg 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
2.
Maurer, H. Carlo, Adrian Idrizi, Kasper D. Hansen, et al.. (2023). Comprehensive DNA Methylation Analysis Indicates That Pancreatic Intraepithelial Neoplasia Lesions Are Acinar-Derived and Epigenetically Primed for Carcinogenesis. Cancer Research. 83(11). 1905–1916. 11 indexed citations
3.
Koldobskiy, Michael A., Garrett Jenkinson, Jordi Abante, et al.. (2021). Converging genetic and epigenetic drivers of paediatric acute lymphoblastic leukaemia identified by an information-theoretic analysis. Nature Biomedical Engineering. 5(4). 360–376. 13 indexed citations
4.
Koldobskiy, Michael A., Jordi Abante, Garrett Jenkinson, et al.. (2020). A Dysregulated DNA Methylation Landscape Linked to Gene Expression in MLL-Rearranged AML. Epigenetics. 15(8). 841–858. 12 indexed citations
5.
Wulfridge, Phillip, Ben Langmead, Andrew P. Feinberg, & Kasper D. Hansen. (2019). Analyzing whole genome bisulfite sequencing data from highly divergent genotypes. Nucleic Acids Research. 47(19). e117–e117. 18 indexed citations
6.
Wilton, Richard, Xin Li, Andrew P. Feinberg, & Alexander S. Szalay. (2018). Arioc: GPU-accelerated alignment of short bisulfite-treated reads. Bioinformatics. 34(15). 2673–2675. 12 indexed citations
7.
Jaffe, Andrew E., Peter Murakami, Hwa-Jin Lee, et al.. (2012). Bump hunting to identify differentially methylated regions in epigenetic epidemiology studies. International Journal of Epidemiology. 41(1). 200–209. 457 indexed citations breakdown →
8.
Lee, Hwa-Jin, Andrew E. Jaffe, Jason I. Feinberg, et al.. (2012). DNA methylation shows genome-wide association ofNFIX,RAPGEF2andMSRB3with gestational age at birth. International Journal of Epidemiology. 41(1). 188–199. 55 indexed citations
9.
Aryee, Martin J., Zhijin Wu, Christine Ladd‐Acosta, et al.. (2010). Accurate genome-scale percentage DNA methylation estimates from microarray data. Biostatistics. 12(2). 197–210. 58 indexed citations
10.
Nguyen, Phuongmai, Hengmi Cui, Kheem S. Bisht, et al.. (2008). CTCFL/BORIS Is a Methylation-Independent DNA-Binding Protein That Preferentially Binds to the Paternal H19 Differentially Methylated Region. Cancer Research. 68(14). 5546–5551. 39 indexed citations
11.
Sun, Lunching, Lei Huang, Phuongmai Nguyen, et al.. (2008). DNA Methyltransferase 1 and 3B Activate BAG-1 Expression via Recruitment of CTCFL/BORIS and Modulation of Promoter Histone Methylation. Cancer Research. 68(8). 2726–2735. 41 indexed citations
12.
Nguyen, Phuongmai, Gil Bar‐Sela, Lunching Sun, et al.. (2008). BAT3 and SET1A Form a Complex with CTCFL/BORIS To Modulate H3K4 Histone Dimethylation and Gene Expression. Molecular and Cellular Biology. 28(21). 6720–6729. 79 indexed citations
13.
Kaneda, Atsushi, Raymond Cheong, Winston Timp, et al.. (2007). Enhanced sensitivity to IGF-II signaling links loss of imprinting of IGF2 to increased cell proliferation and tumor risk. Proceedings of the National Academy of Sciences. 104(52). 20926–20931. 86 indexed citations
14.
Rivera, Miguel N., Woo‐Jae Kim, Julie Wells, et al.. (2007). An X Chromosome Gene, WTX , Is Commonly Inactivated in Wilms Tumor. Science. 315(5812). 642–645. 225 indexed citations
15.
Cui, Hengmi, Marcia Cruz‐Correa, Francis M. Giardiello, et al.. (2003). Loss of IGF2 Imprinting: A Potential Marker of Colorectal Cancer Risk. Science. 299(5613). 1753–1755. 551 indexed citations breakdown →
16.
Jouvenot, Yann, Vasudeva Ginjala, Mitsuo Oshimura, et al.. (2003). Targeted activation and repression of imprinted genes by synthetic zinc finger transcription factors.. Gene Therapy. 10. 1 indexed citations
17.
Onyango, Patrick, Ivana Celic, J. Michael McCaffery, Jef D. Boeke, & Andrew P. Feinberg. (2002). SIRT3, a human SIR2 homologue, is an NAD- dependent deacetylase localized to mitochondria. Proceedings of the National Academy of Sciences. 99(21). 13653–13658. 461 indexed citations
18.
Lee, Maxwell P., Lawrence R. Lustig, Gordon F. Tomaselli, et al.. (2000). Targeted disruption of the Kvlqt1 gene causes deafness and gastric hyperplasia in mice. Journal of Clinical Investigation. 106(12). 1447–1455. 241 indexed citations
19.
Garber, Alan M., W S Browner, Ernest L. Mazzaferri, et al.. (1996). Guidelines for using serum cholesterol, high-density lipoprotein cholesterol, and triglyceride levels as screening tests for preventing coronary heart disease in adults. Annals of Internal Medicine. 124(5). 515–517. 103 indexed citations
20.
Guba, Susan C., Andrew P. Feinberg, Moshe Talpaz, et al.. (1991). Interferon-alpha restores the deficient expression of the cytoadhesion molecule lymphocyte function antigen-3 by chronic myelogenous leukemia progenitor cells.. Journal of Clinical Investigation. 88(6). 2131–2136. 73 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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