David G. Peters

4.7k total citations
86 papers, 3.5k citations indexed

About

David G. Peters is a scholar working on Molecular Biology, Pediatrics, Perinatology and Child Health and Genetics. According to data from OpenAlex, David G. Peters has authored 86 papers receiving a total of 3.5k indexed citations (citations by other indexed papers that have themselves been cited), including 47 papers in Molecular Biology, 18 papers in Pediatrics, Perinatology and Child Health and 15 papers in Genetics. Recurrent topics in David G. Peters's work include Prenatal Screening and Diagnostics (15 papers), Epigenetics and DNA Methylation (10 papers) and Muscle Physiology and Disorders (9 papers). David G. Peters is often cited by papers focused on Prenatal Screening and Diagnostics (15 papers), Epigenetics and DNA Methylation (10 papers) and Muscle Physiology and Disorders (9 papers). David G. Peters collaborates with scholars based in United States, United Kingdom and Sweden. David G. Peters's co-authors include Robert E. Ferrell, Erkki Ruoslahti, Amin Kassam, Tianjiao Chu, Richard L. Lieber, Jan Fridén, Mark Kastantin, Matthew Tirrell, Venkata Ramana Kotamraju and Ilona A. Barash and has published in prestigious journals such as Science, Proceedings of the National Academy of Sciences and Nucleic Acids Research.

In The Last Decade

David G. Peters

86 papers receiving 3.4k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
David G. Peters United States 36 1.5k 426 358 347 316 86 3.5k
John D. Heiss United States 39 1.1k 0.8× 322 0.8× 315 0.9× 220 0.6× 265 0.8× 153 4.8k
François Berger France 33 1.9k 1.3× 223 0.5× 636 1.8× 225 0.6× 335 1.1× 122 4.6k
Didier Wion France 35 1.7k 1.2× 196 0.5× 375 1.0× 360 1.0× 241 0.8× 87 4.3k
Yan Chen China 34 1.5k 1.0× 214 0.5× 563 1.6× 206 0.6× 300 0.9× 187 3.7k
Emilio Ciusani Italy 36 2.1k 1.4× 348 0.8× 953 2.7× 169 0.5× 379 1.2× 152 4.7k
Tomohiro Matsuyama Japan 46 2.5k 1.7× 402 0.9× 419 1.2× 164 0.5× 197 0.6× 160 6.6k
Wen‐Ming Hsu Taiwan 47 1.7k 1.1× 678 1.6× 572 1.6× 200 0.6× 252 0.8× 306 7.7k
Manuel Ramı́rez Spain 39 1.5k 1.0× 426 1.0× 235 0.7× 698 2.0× 173 0.5× 243 6.1k
Rosalia Méndez‐Otero Brazil 37 1.8k 1.2× 236 0.6× 149 0.4× 102 0.3× 217 0.7× 140 4.1k
Spartaco Santi Italy 40 2.4k 1.6× 202 0.5× 436 1.2× 278 0.8× 695 2.2× 150 5.4k

Countries citing papers authored by David G. Peters

Since Specialization
Citations

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

Fields of papers citing papers by David G. Peters

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by David G. Peters. 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 David G. Peters. The network helps show where David G. Peters may publish in the future.

Co-authorship network of co-authors of David G. Peters

This figure shows the co-authorship network connecting the top 25 collaborators of David G. Peters. A scholar is included among the top collaborators of David G. Peters 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 David G. Peters. David G. Peters 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
1.
Lim, Joon Soo, et al.. (2024). Effects of AI versus human source attribution on trust and forgiveness in the identical corporate apology statement for a data breach scandal. Public Relations Review. 51(1). 102520–102520. 5 indexed citations
2.
Péter, Áron, Andrew P. Degnan, Megan A. Emmanuel, et al.. (2024). Simplifying Access to Targeted Protein Degraders via Nickel Electrocatalytic Cross‐Coupling. Angewandte Chemie International Edition. 63(16). e202319856–e202319856. 20 indexed citations
3.
Pan, Lisa, Jane C. Naviaux, Lin Wang, et al.. (2023). Metabolic features of treatment-refractory major depressive disorder with suicidal ideation. Translational Psychiatry. 13(1). 393–393. 18 indexed citations
4.
Luke, Cliff J., Lila S. Nolan, Qingqing Gong, et al.. (2023). Microfluidic device facilitates in vitro modeling of human neonatal necrotizing enterocolitis–on-a-chip. JCI Insight. 8(8). 21 indexed citations
5.
Pan, Lisa, Keith Hyland, Marion A. Hughes, et al.. (2022). Metabolomic disorders: confirmed presence of potentially treatable abnormalities in patients with treatment refractory depression and suicidal behavior. Psychological Medicine. 53(13). 6046–6054. 9 indexed citations
6.
Good, Misty, Tianjiao Chu, Patricia Shaw, et al.. (2021). Neonatal necrotizing enterocolitis-associated DNA methylation signatures in the colon are evident in stool samples of affected individuals. Epigenomics. 13(11). 829–844. 12 indexed citations
7.
Pan, Lisa, Lora McClain, Patricia Shaw, et al.. (2020). Non‐invasive epigenomic molecular phenotyping of the human brain via liquid biopsy of cerebrospinal fluid and next generation sequencing. European Journal of Neuroscience. 52(11). 4536–4545. 8 indexed citations
8.
Good, Misty, Tianjiao Chu, Patricia Shaw, et al.. (2020). Global hypermethylation of intestinal epithelial cells is a hallmark feature of neonatal surgical necrotizing enterocolitis. Clinical Epigenetics. 12(1). 190–190. 17 indexed citations
9.
McClain, Lora, et al.. (2019). Chromosome 15q13.3 microduplications are associated with treatment refractory major depressive disorder. Genes Brain & Behavior. 19(5). e12628–e12628. 1 indexed citations
10.
Rengasamy, Manivel, et al.. (2018). Associations of plasma interleukin-6 with plasma and cerebrospinal fluid monoamine biosynthetic pathway metabolites in treatment-resistant depression. Neurology Psychiatry and Brain Research. 30. 39–46. 8 indexed citations
11.
Chu, Tianjiao, et al.. (2017). Comparative evaluation of the Minimally-Invasive Karyotyping (MINK) algorithm for non-invasive prenatal testing. PLoS ONE. 12(3). e0171882–e0171882. 3 indexed citations
12.
Chu, Tianjiao, et al.. (2016). High Levels of Sample-to-Sample Variation Confound Data Analysis for Non-Invasive Prenatal Screening of Fetal Microdeletions. PLoS ONE. 11(6). e0153182–e0153182. 2 indexed citations
13.
Katz, Tiffany A., Serena G. Liao, Robert K. Dearth, et al.. (2015). Targeted DNA Methylation Screen in the Mouse Mammary Genome Reveals a Parity-Induced Hypermethylation of Igf1r That Persists Long after Parturition. Cancer Prevention Research. 8(10). 1000–1009. 18 indexed citations
14.
Yatsenko, Svetlana A., et al.. (2015). Maternal cell-free DNA–based screening for fetal microdeletion and the importance of careful diagnostic follow-up. Genetics in Medicine. 17(10). 836–838. 31 indexed citations
15.
Chu, Tianjiao, Brian Burke, Kimberly Bunce, et al.. (2009). A microarray‐based approach for the identification of epigenetic biomarkers for the noninvasive diagnosis of fetal disease. Prenatal Diagnosis. 29(11). 1020–1030. 35 indexed citations
16.
Peters, David G., Amin Kassam, & Yue-Fang Chang. (2005). A DNA Sequence Polymorphism in the Endoglin Gene Is Not Associated with Intracranial Aneurysm or Aneurysmal Subarachnoid Hemorrhage. Cerebrovascular Diseases. 20(2). 96–100. 10 indexed citations
17.
Ning, Wen, et al.. (2004). Genome-wide analysis of the endothelial transcriptome under short-term chronic hypoxia. Physiological Genomics. 18(1). 70–78. 36 indexed citations
18.
Serban, Nicoleta, Larry Wasserman, David G. Peters, et al.. (2002). Evidence of cross-hybridization artifact in expressed sequence tags (ESTs) on cDNA microarrays. 1 indexed citations
19.
Peters, David G.. (1999). Comprehensive transcript analysis in small quantities of mRNA by SAGE-Lite. Nucleic Acids Research. 27(24). 39e–39. 80 indexed citations
20.
Peters, David G., et al.. (1979). The oestrous cycle and basal body temperature in the common wombat ( Vombatus ursinus ). Reproduction. 57(2). 453–460. 28 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by John D. Heiss Breakdown of academic impact, for papers by François Berger Breakdown of academic impact, for papers by Didier Wion Breakdown of academic impact, for papers by Yan Chen Breakdown of academic impact, for papers by Emilio Ciusani Breakdown of academic impact, for papers by Tomohiro Matsuyama Breakdown of academic impact, for papers by Wen‐Ming Hsu Breakdown of academic impact, for papers by Manuel Ramı́rez Breakdown of academic impact, for papers by Rosalia Méndez‐Otero Breakdown of academic impact, for papers by Spartaco Santi
Rankless by CCL
2026