John B. Harley

9.3k total citations · 1 hit paper
57 papers, 2.3k citations indexed

About

John B. Harley is a scholar working on Molecular Biology, Immunology and Genetics. According to data from OpenAlex, John B. Harley has authored 57 papers receiving a total of 2.3k indexed citations (citations by other indexed papers that have themselves been cited), including 25 papers in Molecular Biology, 14 papers in Immunology and 11 papers in Genetics. Recurrent topics in John B. Harley's work include Systemic Lupus Erythematosus Research (8 papers), Lymphoma Diagnosis and Treatment (5 papers) and Multiple Myeloma Research and Treatments (4 papers). John B. Harley is often cited by papers focused on Systemic Lupus Erythematosus Research (8 papers), Lymphoma Diagnosis and Treatment (5 papers) and Multiple Myeloma Research and Treatments (4 papers). John B. Harley collaborates with scholars based in United States, Canada and China. John B. Harley's co-authors include Kenneth M. Kaufman, Swapan K. Nath, Young Ho Lee, Gwan Gyu Song, Y. H. Rho, Judith A. James, Sung Jae Choi, Jong Dae Ji, Yuanjia Tang and Nan Shen and has published in prestigious journals such as New England Journal of Medicine, Nature Medicine and Nature Genetics.

In The Last Decade

John B. Harley

54 papers receiving 2.2k citations

Hit Papers

The microRNA miR-23b suppresses IL-17-associated autoimmu... 2012 2026 2016 2021 2012 100 200 300

Peers

John B. Harley
John B. Harley
Citations per year, relative to John B. Harley John B. Harley (= 1×) peers George Vaiopoulos

Countries citing papers authored by John B. Harley

Since Specialization
Citations

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

Fields of papers citing papers by John B. Harley

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by John B. Harley. 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 John B. Harley. The network helps show where John B. Harley may publish in the future.

Co-authorship network of co-authors of John B. Harley

This figure shows the co-authorship network connecting the top 25 collaborators of John B. Harley. A scholar is included among the top collaborators of John B. Harley 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 John B. Harley. John B. Harley 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.
Sun, Celi, R. Hal Scofield, Kenneth M. Kaufman, et al.. (2024). 702 Comparative genome wide association studies (GWASs) of systemic lupus erythematosus (SLE) and multiple sclerosis (MS) from the million veteran program (MVP). SHILAP Revista de lepidopterología. A61–A62.
2.
Tripathi, Pulak, et al.. (2022). Haplotype-specific chromatin looping reveals genetic interactions of regulatory regions modulating gene expression in 8p23.1. Frontiers in Genetics. 13. 1008582–1008582. 5 indexed citations
3.
Zouk, Hana, Wanfeng Yu, Andrea M. Oza, et al.. (2021). Reanalysis of eMERGE phase III sequence variants in 10,500 participants and infrastructure to support the automated return of knowledge updates. Genetics in Medicine. 24(2). 454–462. 7 indexed citations
4.
Parameswaran, Sreeja, Xiaoting Chen, John B. Harley, et al.. (2020). Comprehensive Review of Steroid-Sensitive Nephrotic Syndrome Genetic Risk Loci and Transcriptional Regulation as a Possible Mechanistic Link to Disease Risk. Kidney International Reports. 6(1). 187–195. 4 indexed citations
5.
Sinner, Débora, Brenna Carey, Kenneth M. Kaufman, et al.. (2019). Complete Tracheal Ring Deformity. A Translational Genomics Approach to Pathogenesis. American Journal of Respiratory and Critical Care Medicine. 200(10). 1267–1281. 22 indexed citations
6.
Jog, Neelakshi R., Micah T. McClain, Latisha Heinlen, et al.. (2019). Epstein Barr virus nuclear antigen 1 (EBNA-1) peptides recognized by adult multiple sclerosis patient sera induce neurologic symptoms in a murine model. Journal of Autoimmunity. 106. 102332–102332. 62 indexed citations
7.
Glessner, Joseph, Jin Li, Melody R. Palmer, et al.. (2019). CNV Association of Diverse Clinical Phenotypes from eMERGE reveals novel disease biology underlying cardiovascular disease. International Journal of Cardiology. 298. 107–113. 6 indexed citations
8.
Harley, John B., Xiaoting Chen, Mario Pujato, et al.. (2018). Transcription factors operate across disease loci, with EBNA2 implicated in autoimmunity. Nature Genetics. 50(5). 699–707. 241 indexed citations
9.
Garbett, Nichola C., Guy Brock, Jonathan B. Chaires, et al.. (2017). Characterization and classification of lupus patients based on plasma thermograms. PLoS ONE. 12(11). e0186398–e0186398. 13 indexed citations
10.
Namjou, Bahram, Keith Marsolo, Todd Lingren, et al.. (2015). A GWAS Study on Liver Function Test Using eMERGE Network Participants. PLoS ONE. 10(9). e0138677–e0138677. 15 indexed citations
11.
Maiti, Amit K., Xana Kim-Howard, Vandana Pradhan, et al.. (2014). Combined protein- and nucleic acid-level effects of rs1143679 (R77H), a lupus-predisposing variant within ITGAM. Human Molecular Genetics. 23(15). 4161–4176. 20 indexed citations
12.
Namjou, Bahram, Mehdi Keddache, Keith Marsolo, et al.. (2013). EMR-linked GWAS study: investigation of variation landscape of loci for body mass index in children. Frontiers in Genetics. 4. 268–268. 39 indexed citations
13.
Zhu, Shu, Wen Pan, Xinyang Song, et al.. (2012). The microRNA miR-23b suppresses IL-17-associated autoimmune inflammation by targeting TAB2, TAB3 and IKK-α. Nature Medicine. 18(7). 1077–1086. 369 indexed citations breakdown →
14.
Uccellini, Lorenzo, Valeria De Giorgi, Yingdong Zhao, et al.. (2012). IRF5 gene polymorphisms in melanoma. Journal of Translational Medicine. 10(1). 170–170. 24 indexed citations
15.
Crowe, Sherry R., Lori Garman, Renata J.M. Engler, et al.. (2011). Anthrax vaccination induced anti-lethal factor IgG: Fine specificity and neutralizing capacity. Vaccine. 29(20). 3670–3678. 23 indexed citations
16.
Anaya, Juan‐Manuel, Xana Kim-Howard, Sampath Prahalad, et al.. (2011). Evaluation of genetic association between an ITGAM non-synonymous SNP (rs1143679) and multiple autoimmune diseases. Autoimmunity Reviews. 11(4). 276–280. 45 indexed citations
17.
Vladutiu, Georgirene D., Paul J. Isackson, Kenneth M. Kaufman, et al.. (2011). Genetic risk for malignant hyperthermia in non-anesthesia-induced myopathies. Molecular Genetics and Metabolism. 104(1-2). 167–173. 45 indexed citations
18.
Isackson, Paul J., Heather M. Ochs‐Balcom, Chang‐Xing Ma, et al.. (2011). Association of common variants in the human eyes shut ortholog (EYS) with statin‐induced myopathy: Evidence for additional functions of EYS. Muscle & Nerve. 44(4). 531–538. 36 indexed citations
19.
Thanou, Aikaterini, Amr H. Sawalha, A. Neil Crowson, & John B. Harley. (2010). Noodling and Mycobacterium marinum infection mimicking seronegative rheumatoid arthritis complicated by anti–tumor necrosis factor α therapy. Arthritis Care & Research. 63(1). 160–164. 6 indexed citations
20.
Sammalisto, Sampo, Tero Hiekkalinna, Karen Schwander, et al.. (2008). Genome-wide linkage screen for stature and body mass index in 3.032 families: evidence for sex- and population-specific genetic effects. European Journal of Human Genetics. 17(2). 258–266. 13 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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