Christopher N. Greene

450 total citations
13 papers, 384 citations indexed

About

Christopher N. Greene is a scholar working on Molecular Biology, Genetics and Pathology and Forensic Medicine. According to data from OpenAlex, Christopher N. Greene has authored 13 papers receiving a total of 384 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 6 papers in Genetics and 4 papers in Pathology and Forensic Medicine. Recurrent topics in Christopher N. Greene's work include DNA Repair Mechanisms (4 papers), Genetic factors in colorectal cancer (4 papers) and Diabetes and associated disorders (3 papers). Christopher N. Greene is often cited by papers focused on DNA Repair Mechanisms (4 papers), Genetic factors in colorectal cancer (4 papers) and Diabetes and associated disorders (3 papers). Christopher N. Greene collaborates with scholars based in United States and Uganda. Christopher N. Greene's co-authors include Sue Jinks-Robertson, Monika Wierdl, Thomas D. Petes, Abhijit Datta, Suzanne K. Cordovado, Patricia W. Mueller, Lisa M. Keong, Deborah Koontz, Carol Rubin and Mary V. Relling and has published in prestigious journals such as Molecular and Cellular Biology, The Journal of Clinical Endocrinology & Metabolism and Genetics.

In The Last Decade

Christopher N. Greene

13 papers receiving 371 citations

Peers

Christopher N. Greene
Hiromi Nagasaki Japan
Katsuyoshi Fujikawa Japan
Melvenia M. Martin United States
Midori Asano Japan
Elizabeth M. Boehm United States
M.A. Willington United Kingdom
Hideaki Chiyo Japan
Satoshi Imanishi Japan
Sang D. Park South Korea
Hong Mu United States
Hiromi Nagasaki Japan
Christopher N. Greene
Citations per year, relative to Christopher N. Greene Christopher N. Greene (= 1×) peers Hiromi Nagasaki

Countries citing papers authored by Christopher N. Greene

Since Specialization
Citations

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

Fields of papers citing papers by Christopher N. Greene

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Christopher N. Greene. 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 Christopher N. Greene. The network helps show where Christopher N. Greene may publish in the future.

Co-authorship network of co-authors of Christopher N. Greene

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

All Works

13 of 13 papers shown
1.
Sarafoglou, Kyriakie, Amy Gaviglio, Cindy Pham Lorentz, et al.. (2024). Can Incorporating Molecular Testing Improve the Accuracy of Newborn Screening for Congenital Adrenal Hyperplasia?. The Journal of Clinical Endocrinology & Metabolism. 110(4). e1194–e1203. 1 indexed citations
2.
Lee, Francis K., Christopher N. Greene, Kristina B. Mercer, et al.. (2024). CDC’s Laboratory Activities to Support Newborn Screening for Spinal Muscular Atrophy. International Journal of Neonatal Screening. 10(3). 51–51. 1 indexed citations
3.
Greene, Christopher N., et al.. (2014). Novel method to characterize CYP21A2 in Florida patients with congenital adrenal hyperplasia and commercially available cell lines. Molecular Genetics and Metabolism Reports. 1. 312–323. 14 indexed citations
4.
Cordovado, Suzanne K., Miyono Hendrix, Christopher N. Greene, et al.. (2011). CFTR mutation analysis and haplotype associations in CF patients. Molecular Genetics and Metabolism. 105(2). 249–254. 30 indexed citations
5.
Cordovado, Suzanne K., Laura Hancock, Miyono Hendrix, Christopher N. Greene, & Patricia W. Mueller. (2009). Novel human leukocyte antigen class I and class II alleles identified by sequence-based typing in the Genetics of Kidneys in Diabetes (GoKinD) study population. Human Immunology. 70(9). 747–749. 1 indexed citations
6.
Greene, Christopher N., Lisa M. Keong, Suzanne K. Cordovado, & Patricia W. Mueller. (2008). Sequence variants in the PLEKHH2 region are associated with diabetic nephropathy in the GoKinD study population. Human Genetics. 124(3). 255–262. 14 indexed citations
7.
Steinberg, Karen, Mary V. Relling, Margaret Gallagher, et al.. (2006). Genetic Studies of a Cluster of Acute Lymphoblastic Leukemia Cases in Churchill County, Nevada. Environmental Health Perspectives. 115(1). 158–164. 48 indexed citations
8.
Greene, Christopher N., Suzanne K. Cordovado, & Patricia W. Mueller. (2004). Polymorphism scan for differences between transmitted and nontransmitted DRB1*030101 alleles outside of exon 2 for type 1 diabetes: The frequency of polymorphisms is similar. Human Immunology. 65(7). 737–744. 1 indexed citations
9.
Greene, Christopher N. & Sue Jinks-Robertson. (2001). Spontaneous Frameshift Mutations in Saccharomyces cerevisiae: Accumulation During DNA Replication and Removal by Proofreading and Mismatch Repair Activities. Genetics. 159(1). 65–75. 40 indexed citations
10.
Greene, Christopher N., et al.. (2000). Genetic Analysis of Transcription-Associated Mutation in Saccharomyces cerevisiae. Genetics. 154(1). 109–120. 45 indexed citations
11.
Greene, Christopher N. & Sue Jinks-Robertson. (1999). Comparison of spontaneous and adaptive mutation spectra in yeast. Journal of Genetics. 78(1). 51–55. 10 indexed citations
12.
Greene, Christopher N. & Sue Jinks-Robertson. (1997). Frameshift Intermediates in Homopolymer Runs Are Removed Efficiently by Yeast Mismatch Repair Proteins. Molecular and Cellular Biology. 17(5). 2844–2850. 96 indexed citations
13.
Wierdl, Monika, Christopher N. Greene, Abhijit Datta, Sue Jinks-Robertson, & Thomas D. Petes. (1996). Destabilization of Simple Repetitive DNA Sequences by Transcription in Yeast. Genetics. 143(2). 713–721. 83 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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