Rodney T. Perry

2.7k total citations · 1 hit paper
28 papers, 1.6k citations indexed

About

Rodney T. Perry is a scholar working on Molecular Biology, Physiology and Genetics. According to data from OpenAlex, Rodney T. Perry has authored 28 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 10 papers in Physiology and 9 papers in Genetics. Recurrent topics in Rodney T. Perry's work include Alzheimer's disease research and treatments (9 papers), Genetic Associations and Epidemiology (6 papers) and Epigenetics and DNA Methylation (5 papers). Rodney T. Perry is often cited by papers focused on Alzheimer's disease research and treatments (9 papers), Genetic Associations and Epidemiology (6 papers) and Epigenetics and DNA Methylation (5 papers). Rodney T. Perry collaborates with scholars based in United States, Uganda and Venezuela. Rodney T. Perry's co-authors include Rodney C.P. Go, Susan Spear Bassett, Marilyn S. Albert, Bracie Watson, Deborah Blacker, Rudolph E. Tanzi, Melvin G. McInnis, Howard W. Wiener, L. E. Harrell and Lindy E. Harrell and has published in prestigious journals such as Nature Genetics, Circulation Research and Neurology.

In The Last Decade

Rodney T. Perry

28 papers receiving 1.5k citations

Hit Papers

1 papers align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Alpha-2 macroglobulin is genetically associated with Alzheimer disease

1998 518 citations Deborah Blacker, Marsha Wilcox et al. Nature Genetics profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Rodney T. Perry United States	15	903	612	270	222	202	28	1.6k
Alessandra Piccini Italy	21	1.0k 1.1×	914 1.5×	109 0.4×	220 1.0×	265 1.3×	39	2.2k
Vijay K. Ramanan United States	20	694 0.8×	574 0.9×	284 1.1×	475 2.1×	113 0.6×	62	1.5k
John Kauwe United States	24	834 0.9×	659 1.1×	359 1.3×	289 1.3×	111 0.5×	53	1.7k
Shea J. Andrews United States	21	567 0.6×	892 1.5×	331 1.2×	298 1.3×	114 0.6×	47	1.9k
R. Scacchi Italy	25	563 0.6×	451 0.7×	552 2.0×	205 0.9×	101 0.5×	78	2.0k
Shanker Swaminathan United States	16	657 0.7×	703 1.1×	420 1.6×	373 1.7×	93 0.5×	25	1.5k
Martina Chiappelli Italy	23	523 0.6×	519 0.8×	147 0.5×	101 0.5×	80 0.4×	43	1.6k
Yuan Lü United States	21	682 0.8×	685 1.1×	111 0.4×	180 0.8×	95 0.5×	93	2.0k
F. Coria Spain	25	852 0.9×	625 1.0×	115 0.4×	347 1.6×	332 1.6×	61	1.8k
Suk Ling Hong Kong	19	326 0.4×	443 0.7×	198 0.7×	137 0.6×	142 0.7×	65	1.1k

Countries citing papers authored by Rodney T. Perry

Since Specialization

Citations

This map shows the geographic impact of Rodney T. Perry'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 Rodney T. Perry with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Rodney T. Perry more than expected).

Fields of papers citing papers by Rodney T. Perry

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Rodney T. Perry. 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 Rodney T. Perry. The network helps show where Rodney T. Perry may publish in the future.

Co-authorship network of co-authors of Rodney T. Perry

This figure shows the co-authorship network connecting the top 25 collaborators of Rodney T. Perry. A scholar is included among the top collaborators of Rodney T. Perry 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 Rodney T. Perry. Rodney T. Perry 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

Aslibekyan, Stella, Marguerite R. Irvin, Bertha Hidalgo, et al.. (2017). Genome- and CD4 + T-cell methylome-wide association study of circulating trimethylamine-N-oxide in the Genetics of Lipid Lowering Drugs and Diet Network (GOLDN). Journal of Nutrition & Intermediary Metabolism. 8. 1–7. 10 indexed citations

Das, Mithun, Marguerite R. Irvin, Jin Sha, et al.. (2015). Lipid changes due to fenofibrate treatment are not associated with changes in DNA methylation patterns in the GOLDN study. Frontiers in Genetics. 6. 304–304. 19 indexed citations

Irvin, Marguerite R., Qunyuan Zhang, Edmond K. Kabagambe, et al.. (2012). Rare PPARA variants and extreme response to fenofibrate in the Genetics of Lipid-Lowering Drugs and Diet Network Study. Pharmacogenetics and Genomics. 22(5). 367–372. 12 indexed citations

Perry, Rodney T., et al.. (2012). A Simple PCR–RFLP Method for Genetic Phase Determination in Compound Heterozygotes. Frontiers in Genetics. 2. 108–108. 2 indexed citations

Perry, Rodney T., Howard W. Wiener, Lindy E. Harrell, & Rodney C.P. Go. (2008). P3‐249: Investigation for the presence of CNVs in SOD2 in the National Institute of Mental Health Alzheimer's Disease Genetics Initiative (NIMH‐ADGI) cohort. Alzheimer s & Dementia. 4(4S_Part_18). 1 indexed citations

Baye, Tesfaye M., et al.. (2008). Candidate Gene Discovery Procedure after Follow‐Up Confirmatory Analyses of Candidate Regions of Interests for Alzheimer’s Disease in the NIMH Sibling Dataset. Disease Markers. 24(6). 293–309. 7 indexed citations

Li, Jian, Janice King, Harry W. Schroeder, et al.. (2007). Effects of Chronic Stress and Interleukin-10 Gene Polymorphisms on Antibody Response to Tetanus Vaccine in Family Caregivers of Patients With Alzheimer’s Disease. Psychosomatic Medicine. 69(6). 551–559. 33 indexed citations

Wiener, Howard W., et al.. (2007). A polymorphism in SOD2 is associated with development of Alzheimer’s disease. Genes Brain & Behavior. 6(8). 770–776. 52 indexed citations

Simmons, Micah, et al.. (2007). Genetic Association of Neurotrophic Tyrosine Kinase Receptor Type 2 (NTRK2) With Alzheimer's Disease. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 147B(3). 363–369. 54 indexed citations

10.

Perry, Rodney T., Debra A. Gearhart, Howard W. Wiener, et al.. (2006). Hemoglobin binding to Aβ and HBG2 SNP association suggest a role in Alzheimer's disease. Neurobiology of Aging. 29(2). 185–193. 21 indexed citations

11.

Perry, Rodney T., Howard W. Wiener, Lindy E. Harrell, et al.. (2006). Follow‐up mapping supports the evidence for linkage in the candidate region at 9q22 in the NIMH Alzheimer's disease Genetics Initiative cohort. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 144B(2). 220–227. 11 indexed citations

12.

Bassett, Susan Spear, Dimitrios Avramopoulos, Rodney T. Perry, et al.. (2006). Further evidence of a maternal parent‐of‐origin effect on chromosome 10 in late‐onset Alzheimer's disease. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 141B(5). 537–540. 22 indexed citations

13.

Perry, Rodney T., et al.. (2005). Association studies of transforming growth factor‐β1 and Alzheimer's disease. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 139B(1). 38–41. 23 indexed citations

14.

Go, Rodney C.P., Rodney T. Perry, Howard W. Wiener, et al.. (2005). Neuregulin‐1 polymorphism in late onset Alzheimer's disease families with psychoses. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 139B(1). 28–32. 69 indexed citations

15.

Go, Rodney C.P., Rodney T. Perry, Howard W. Wiener, et al.. (2004). P4-053 Neuregulin-1 polymorphism in load with psychosis in the NIMH AD sibling families. Neurobiology of Aging. 25. S488–S488. 1 indexed citations

16.

Collins, Julianne S., Rodney T. Perry, Bracie Watson, et al.. (2000). Association of a haplotype for tumor necrosis factor in siblings with late-onset Alzheimer disease: The NIMH Alzheimer disease genetics initiative. American Journal of Medical Genetics. 96(6). 823–830. 106 indexed citations

17.

Alexander, Neâl, et al.. (1999). Acute disease episodes in a Wuchereria bancrofti-endemic area of Papua New Guinea.. American Journal of Tropical Medicine and Hygiene. 61(2). 319–324. 13 indexed citations

18.

Li, Ling, Rodney T. Perry, Jianming Wu, et al.. (1998). Polymorphic tetranucleotide repeat site within intron 7 of the β-amyloid precursor protein gene and its lack of association with Alzheimer's disease. Human Genetics. 103(1). 86–89. 12 indexed citations

19.

Blacker, Deborah, Marsha Wilcox, Nan M. Laird, et al.. (1998). Alpha-2 macroglobulin is genetically associated with Alzheimer disease. Nature Genetics. 19(4). 357–360. 518 indexed citations breakdown →

20.

Blacker, Deborah, Jonathan L. Haines, Henry Terwedow, et al.. (1997). ApoE-4 and Age at Onset of Alzheimer's Disease. Neurology. 48(1). 139–147. 380 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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