Norman P. Gerry

44.6k total citations
39 papers, 2.6k citations indexed

About

Norman P. Gerry is a scholar working on Molecular Biology, Genetics and Cancer Research. According to data from OpenAlex, Norman P. Gerry has authored 39 papers receiving a total of 2.6k indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Molecular Biology, 16 papers in Genetics and 6 papers in Cancer Research. Recurrent topics in Norman P. Gerry's work include Genetic Associations and Epidemiology (11 papers), Gene expression and cancer classification (8 papers) and Molecular Biology Techniques and Applications (7 papers). Norman P. Gerry is often cited by papers focused on Genetic Associations and Epidemiology (11 papers), Gene expression and cancer classification (8 papers) and Molecular Biology Techniques and Applications (7 papers). Norman P. Gerry collaborates with scholars based in United States, Canada and United Kingdom. Norman P. Gerry's co-authors include Michael F. Christman, Marc E. Lenburg, Francis Barany, Garrett M. Frampton, Alan Herbert, Hanxia Huang, Ayo P. Doumatey, Adebowale Adeyemo, Jie Zhou and Guanjie Chen and has published in prestigious journals such as Journal of the American Chemical Society, Nature Medicine and Nature Biotechnology.

In The Last Decade

Norman P. Gerry

39 papers receiving 2.5k citations

Peers

Norman P. Gerry

GENET

PHYSI

PRM

Jennifer J. Johnston United States

Richard McIndoe United States

Nicole Endlich Germany

Brian Cox Canada

Brian H. Shirts United States

Jer‐Yuarn Wu Taiwan

Lasse Folkersen Sweden

Adelbert A. Roscher Germany

Bermseok Oh South Korea

Peng Wei United States

Jennifer J. Johnston United States

Norman P. Gerry

1.3k ×1.0

1.1k ×1.9

GENET

225 ×0.7

302 ×1.0

PHYSI

131 ×0.4

PRM

Citations per year, relative to Norman P. Gerry Norman P. Gerry (= 1×) peers Jennifer J. Johnston

Countries citing papers authored by Norman P. Gerry

Since Specialization

Citations

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

Fields of papers citing papers by Norman P. Gerry

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Norman P. Gerry

This figure shows the co-authorship network connecting the top 25 collaborators of Norman P. Gerry. A scholar is included among the top collaborators of Norman P. Gerry 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 Norman P. Gerry. Norman P. Gerry 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

Kusic, Dara, Stefan Zajic, Neda Gharani, et al.. (2023). Genome-wide Association Study of Caffeine Consumption Using Coriell Personalized Medicine Collaborative Data. 5(1). 1 indexed citations

Scheinfeldt, Laura, Kelly R. Hodges, Jonathan Pevsner, et al.. (2018). Genetic and genomic stability across lymphoblastoid cell line expansions. BMC Research Notes. 11(1). 558–558. 9 indexed citations

Shahabi, Payman, Laura Scheinfeldt, D.E. Lynch, et al.. (2016). An expanded pharmacogenomics warfarin dosing table with utility in generalised dosing guidance. Thrombosis and Haemostasis. 116(8). 337–348. 14 indexed citations

Scheinfeldt, Laura, Neda Gharani, Rachel Kasper, et al.. (2015). Using the Coriell Personalized Medicine Collaborative Data to conduct a genome‐wide association study of sleep duration. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 168(8). 697–705. 28 indexed citations

Shriner, Daniel, Alan Herbert, Ayo P. Doumatey, et al.. (2012). Multiple Loci Associated with Renal Function in African Americans. PLoS ONE. 7(9). e45112–e45112. 7 indexed citations

Adeyemo, Adebowale, Amy R. Bentley, Katherine G. Meilleur, et al.. (2012). Transferability and Fine Mapping of genome-wide associated loci for lipids in African Americans. BMC Medical Genetics. 13(1). 88–88. 28 indexed citations

Kalman, Lisa V., Jay Leonard, Norman P. Gerry, et al.. (2011). Quality Assurance for Duchenne and Becker Muscular Dystrophy Genetic Testing. Journal of Molecular Diagnostics. 13(2). 167–174. 18 indexed citations

Charles, Bashira A., Daniel Shriner, Ayo P. Doumatey, et al.. (2011). A genome-wide association study of serum uric acid in African Americans. BMC Medical Genomics. 4(1). 17–17. 73 indexed citations

Chen, Guanjie, Edward Ramos, Adebowale Adeyemo, et al.. (2011). UGT1A1 is a major locus influencing bilirubin levels in African Americans. European Journal of Human Genetics. 20(4). 463–468. 55 indexed citations

10.

Ramos, Edward, Guanghan Chen, Daniel Shriner, et al.. (2010). Replication of genome-wide association studies (GWAS) loci for fasting plasma glucose in African-Americans. Diabetologia. 54(4). 783–788. 59 indexed citations

11.

Chen, Guanjie, Daniel Shriner, Jie Zhou, et al.. (2010). Development of admixture mapping panels for African Americans from commercial high-density SNP arrays. BMC Genomics. 11(1). 417–417. 13 indexed citations

12.

Shriner, Daniel, Adebowale Adeyemo, Norman P. Gerry, et al.. (2009). Transferability and Fine-Mapping of Genome-Wide Associated Loci for Adult Height across Human Populations. PLoS ONE. 4(12). e8398–e8398. 39 indexed citations

13.

Adeyemo, Adebowale, Norman P. Gerry, Guanjie Chen, et al.. (2009). A Genome-Wide Association Study of Hypertension and Blood Pressure in African Americans. PLoS Genetics. 5(7). e1000564–e1000564. 286 indexed citations

14.

Bacolod, Manny D., Shuang Wang, Richard Shattock, et al.. (2008). The Signatures of Autozygosity among Patients with Colorectal Cancer. Cancer Research. 68(8). 2610–2621. 40 indexed citations

15.

Tripathi�, Anusri, Bohdana Burke, Erwin F. Hirsch, et al.. (2007). Gene expression abnormalities in histologically normal breast epithelium of breast cancer patients. International Journal of Cancer. 122(7). 1557–1566. 99 indexed citations

16.

Spira, Avrum, Jennifer Beane, Vishal Shah, et al.. (2007). Airway epithelial gene expression in the diagnostic evaluation of smokers with suspect lung cancer. Nature Medicine. 13(3). 361–366. 407 indexed citations

17.

Favis, Reyna, Norman P. Gerry, Yu‐Wei Cheng, & Francis Barany. (2005). Applications of the Universal DNA Microarray in Molecular Medicine. Humana Press eBooks. 114. 25–58. 11 indexed citations

18.

Lenburg, Marc E., Louis S. Liou, Norman P. Gerry, et al.. (2003). Previously unidentified changes in renal cell carcinoma gene expression identified by parametric analysis of microarray data. BMC Cancer. 3(1). 31–31. 221 indexed citations

19.

Favis, Reyna, Joseph Day, Norman P. Gerry, et al.. (2000). Universal DNA array detection of small insertions and deletions in BRCA1 and BRCA2. Nature Biotechnology. 18(5). 561–564. 172 indexed citations

20.

Gerry, Norman P., Nancy E. Witowski, Joseph Day, et al.. (1999). Universal DNA microarray method for multiplex detection of low abundance point mutations. Journal of Molecular Biology. 292(2). 251–262. 259 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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