Peter S. Chines

7.5k total citations
16 papers, 900 citations indexed

About

Peter S. Chines is a scholar working on Molecular Biology, Genetics and Cancer Research. According to data from OpenAlex, Peter S. Chines has authored 16 papers receiving a total of 900 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 8 papers in Genetics and 4 papers in Cancer Research. Recurrent topics in Peter S. Chines's work include Genetic Associations and Epidemiology (4 papers), RNA Research and Splicing (3 papers) and Epigenetics and DNA Methylation (2 papers). Peter S. Chines is often cited by papers focused on Genetic Associations and Epidemiology (4 papers), RNA Research and Splicing (3 papers) and Epigenetics and DNA Methylation (2 papers). Peter S. Chines collaborates with scholars based in United States, Finland and United Kingdom. Peter S. Chines's co-authors include Francis S. Collins, Michael R. Erdos, Kan Cao, Ye Zhan, Haoyue Zhang, Job Dekker, Ashley Nazario-Toole, Rachel Patton McCord, Michael Boehnke and Michael L. Stitzel and has published in prestigious journals such as Nucleic Acids Research, Cell Metabolism and Diabetes.

In The Last Decade

Peter S. Chines

16 papers receiving 886 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Peter S. Chines United States 14 647 270 150 121 76 16 900
K Nelson United States 8 487 0.8× 168 0.6× 73 0.5× 81 0.7× 97 1.3× 10 776
Mark Strunk Spain 12 420 0.6× 114 0.4× 92 0.6× 163 1.3× 37 0.5× 23 643
M. Rivière Belgium 15 588 0.9× 238 0.9× 38 0.3× 69 0.6× 51 0.7× 42 775
Yousef G. Amaar United States 17 599 0.9× 121 0.4× 41 0.3× 155 1.3× 57 0.8× 22 821
Klaus-Peter Knoch Germany 14 370 0.6× 169 0.6× 270 1.8× 100 0.8× 84 1.1× 22 657
Melissa S. McNulty United States 13 470 0.7× 88 0.3× 38 0.3× 68 0.6× 98 1.3× 19 702
Joseph Jerry United States 2 619 1.0× 248 0.9× 132 0.9× 67 0.6× 60 0.8× 3 836
Jesse D. Riordan United States 16 484 0.7× 101 0.4× 40 0.3× 176 1.5× 90 1.2× 25 720
Kathryn E. Dickerson United States 10 602 0.9× 119 0.4× 52 0.3× 79 0.7× 41 0.5× 23 786
Greg Landes United States 9 258 0.4× 188 0.7× 61 0.4× 142 1.2× 46 0.6× 9 726

Countries citing papers authored by Peter S. Chines

Since Specialization
Citations

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

Fields of papers citing papers by Peter S. Chines

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Peter S. Chines. 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 S. Chines. The network helps show where Peter S. Chines may publish in the future.

Co-authorship network of co-authors of Peter S. Chines

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

All Works

16 of 16 papers shown
1.
Zou, Luli S., Michael R. Erdos, D. Leland Taylor, et al.. (2018). BoostMe accurately predicts DNA methylation values in whole-genome bisulfite sequencing of multiple human tissues. BMC Genomics. 19(1). 390–390. 35 indexed citations
2.
Davis, James P., Jeroen R. Huyghe, Adam E. Locke, et al.. (2017). Common, low-frequency, and rare genetic variants associated with lipoprotein subclasses and triglyceride measures in Finnish men from the METSIM study. PLoS Genetics. 13(10). e1007079–e1007079. 31 indexed citations
3.
Bar, Daniel Z., Martin F. Arlt, Joan F. Brazier, et al.. (2016). A novel somatic mutation achieves partial rescue in a child with Hutchinson-Gilford progeria syndrome. Journal of Medical Genetics. 54(3). 212–216. 23 indexed citations
4.
Baran‐Gale, Jeanette, C. Lisa Kurtz, Michael R. Erdos, et al.. (2015). Addressing Bias in Small RNA Library Preparation for Sequencing: A New Protocol Recovers MicroRNAs that Evade Capture by Current Methods. Frontiers in Genetics. 6. 352–352. 74 indexed citations
5.
Bu, Huajie, Narisu Narisu, Bettina Schlick, et al.. (2015). Putative Prostate Cancer Risk SNP in an Androgen Receptor‐Binding Site of the Melanophilin Gene Illustrates Enrichment of Risk SNPs in Androgen Receptor Target Sites. Human Mutation. 37(1). 52–64. 26 indexed citations
6.
Kelada, Samir N. P., David L. Aylor, Peter S. Chines, et al.. (2014). Integrative Genetic Analysis of Allergic Inflammation in the Murine Lung. American Journal of Respiratory Cell and Molecular Biology. 51(3). 436–445. 25 indexed citations
7.
Williams, Kendra A., Ying Hu, Jonathan Andreas, et al.. (2014). A Systems Genetics Approach Identifies CXCL14, ITGAX, and LPCAT2 as Novel Aggressive Prostate Cancer Susceptibility Genes. PLoS Genetics. 10(11). e1004809–e1004809. 61 indexed citations
8.
Aylor, David L., Bailey C. E. Peck, Peter S. Chines, et al.. (2014). Genetic Regulation ofZfp30, CXCL1, and Neutrophilic Inflammation in Murine Lung. Genetics. 198(2). 735–745. 33 indexed citations
9.
DuBose, Amanda J., Narisu Narisu, Lori L. Bonnycastle, et al.. (2013). Use of microarray hybrid capture and next-generation sequencing to identify the anatomy of a transgene. Nucleic Acids Research. 41(6). e70–e70. 35 indexed citations
10.
Bonnycastle, Lori L., Peter S. Chines, Takashi Hara, et al.. (2013). Autosomal Dominant Diabetes Arising From a Wolfram Syndrome 1 Mutation. Diabetes. 62(11). 3943–3950. 91 indexed citations
11.
McCord, Rachel Patton, Ashley Nazario-Toole, Haoyue Zhang, et al.. (2012). Correlated alterations in genome organization, histone methylation, and DNA–lamin A/C interactions in Hutchinson-Gilford progeria syndrome. Genome Research. 23(2). 260–269. 239 indexed citations
12.
Stitzel, Michael L., Praveen Sethupathy, Daniel S. Pearson, et al.. (2010). Global Epigenomic Analysis of Primary Human Pancreatic Islets Provides Insights into Type 2 Diabetes Susceptibility Loci. Cell Metabolism. 12(5). 443–455. 136 indexed citations
13.
14.
Willer, Cristen J., Laura J. Scott, Lori L. Bonnycastle, et al.. (2005). Tag SNP selection for Finnish individuals based on the CEPH Utah HapMap database. Genetic Epidemiology. 30(2). 180–190. 51 indexed citations
15.
Duggal, Priya, Elizabeth M. Gillanders, Rasika A. Mathias, et al.. (2005). Identification of tag single-nucleotide polymorphisms in regions with varying linkage disequilibrium. BMC Genetics. 6(S1). S73–S73. 7 indexed citations
16.
Brody, Lawrence C., Peter S. Chines, Anjene Musick, et al.. (1999). Methionine Synthase: High-Resolution Mapping of the Human Gene and Evaluation as a Candidate Locus for Neural Tube Defects. Molecular Genetics and Metabolism. 67(4). 324–333. 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.

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