Tushar Bhangale

18.0k total citations · 1 hit paper
30 papers, 2.6k citations indexed

About

Tushar Bhangale is a scholar working on Molecular Biology, Genetics and Immunology. According to data from OpenAlex, Tushar Bhangale has authored 30 papers receiving a total of 2.6k indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Molecular Biology, 13 papers in Genetics and 9 papers in Immunology. Recurrent topics in Tushar Bhangale's work include Genetic Associations and Epidemiology (8 papers), Immune Cell Function and Interaction (5 papers) and Genomic variations and chromosomal abnormalities (4 papers). Tushar Bhangale is often cited by papers focused on Genetic Associations and Epidemiology (8 papers), Immune Cell Function and Interaction (5 papers) and Genomic variations and chromosomal abnormalities (4 papers). Tushar Bhangale collaborates with scholars based in United States, France and United Kingdom. Tushar Bhangale's co-authors include Robert Graham, Timothy W. Behrens, Deborah A. Nickerson, Mark J. Rieder, Diana Chang, Marcel van der Brug, Baris Bingol, Morgan Sheng, Matthew Stephens and Ingileif B. Hallgrímsdóttir and has published in prestigious journals such as Science, Proceedings of the National Academy of Sciences and Nature Medicine.

In The Last Decade

Tushar Bhangale

30 papers receiving 2.5k citations

Hit 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.

A meta-analysis of genome-wide association studies identifies 17 new Parkinson's disease risk loci

2017 772 citations Diana Chang, Mike A. Nalls 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
Tushar Bhangale United States	20	1.0k	647	568	513	371	30	2.6k
Alexander G. Bassuk United States	37	2.4k 2.3×	1.0k 1.6×	505 0.9×	313 0.6×	152 0.4×	153	4.4k
Gudrun Nürnberg Germany	44	2.9k 2.8×	1.6k 2.4×	524 0.9×	154 0.3×	275 0.7×	93	5.1k
Hideki Garren United States	28	1.4k 1.4×	467 0.7×	1.9k 3.4×	552 1.1×	189 0.5×	59	4.6k
Eric Rappaport United States	37	2.6k 2.5×	673 1.0×	269 0.5×	319 0.6×	118 0.3×	108	4.3k
Maher Noureddine United States	15	1.3k 1.2×	372 0.6×	517 0.9×	292 0.6×	150 0.4×	19	3.0k
Ohad S. Birk Israel	33	2.1k 2.1×	1.2k 1.9×	508 0.9×	98 0.2×	175 0.5×	121	3.7k
Assumpció Bosch Spain	27	1.3k 1.3×	977 1.5×	137 0.2×	149 0.3×	320 0.9×	79	2.3k
Nathalie Drouot France	18	1.9k 1.8×	1.4k 2.2×	223 0.4×	188 0.4×	131 0.4×	36	3.5k
Christina A. Harrington United States	28	1.4k 1.4×	346 0.5×	343 0.6×	62 0.1×	318 0.9×	65	2.7k
Li He China	29	1.9k 1.9×	130 0.2×	420 0.7×	519 1.0×	212 0.6×	95	3.5k

Countries citing papers authored by Tushar Bhangale

Since Specialization

Citations

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

Fields of papers citing papers by Tushar Bhangale

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Tushar Bhangale. 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 Tushar Bhangale. The network helps show where Tushar Bhangale may publish in the future.

Co-authorship network of co-authors of Tushar Bhangale

This figure shows the co-authorship network connecting the top 25 collaborators of Tushar Bhangale. A scholar is included among the top collaborators of Tushar Bhangale 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 Tushar Bhangale. Tushar Bhangale 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

Huang, Yunfeng, Stephanie Loomis, Elizabeth Fisher, et al.. (2024). Adaptive and Innate Immunity Are Key Drivers of Age at Onset of Multiple Sclerosis. Neurology Genetics. 10(3). e200159–e200159. 2 indexed citations

Khan, Zia, Min Jung, Megan Crow, et al.. (2023). Whole genome sequencing across clinical trials identifies rare coding variants in GPR68 associated with chemotherapy-induced peripheral neuropathy. Genome Medicine. 15(1). 45–45. 6 indexed citations

Khan, Zia, Christian Hammer, Jonathan Carroll, et al.. (2021). Genetic variation associated with thyroid autoimmunity shapes the systemic immune response to PD-1 checkpoint blockade. Nature Communications. 12(1). 3355–3355. 50 indexed citations

Brendza, Robert P., Han Lin, Kimberly L. Stark, et al.. (2021). Genetic ablation of Gpnmb does not alter synuclein-related pathology. Neurobiology of Disease. 159. 105494–105494. 9 indexed citations

Orozco, Luz D., Hsu-Hsin Chen, Christian L. Cox, et al.. (2020). Integration of eQTL and a Single-Cell Atlas in the Human Eye Identifies Causal Genes for Age-Related Macular Degeneration. Cell Reports. 30(4). 1246–1259.e6. 138 indexed citations

Tom, Jennifer, Diana Chang, Arthur Wüster, et al.. (2018). Enabling genome-wide association testing with multiple diseases and no healthy controls. Gene. 684. 118–123. 3 indexed citations

Haug-Baltzell, Asher, Tushar Bhangale, Diana Chang, et al.. (2018). Previously reported placebo-response-associated variants do not predict patient outcomes in inflammatory disease Phase III trial placebo arms. Genes and Immunity. 20(2). 172–179. 2 indexed citations

Rathore, Nisha, Sree R. Ramani, Homer Pantua, et al.. (2018). Paired Immunoglobulin-like Type 2 Receptor Alpha G78R variant alters ligand binding and confers protection to Alzheimer's disease. PLoS Genetics. 14(11). e1007427–e1007427. 47 indexed citations

Yaspan, Brian L., David F. Williams, Frank G. Holz, et al.. (2017). Targeting factor D of the alternative complement pathway reduces geographic atrophy progression secondary to age-related macular degeneration. Science Translational Medicine. 9(395). 148 indexed citations

10.

Chang, Diana, Mike A. Nalls, Ingileif B. Hallgrímsdóttir, et al.. (2017). A meta-analysis of genome-wide association studies identifies 17 new Parkinson's disease risk loci. Nature Genetics. 49(10). 1511–1516. 772 indexed citations breakdown →

11.

Haddick, Patrick C. G., Jessica L. Larson, Nisha Rathore, et al.. (2017). A Common Variant of IL-6R is Associated with Elevated IL-6 Pathway Activity in Alzheimer’s Disease Brains. Journal of Alzheimer s Disease. 56(3). 1037–1054. 41 indexed citations

12.

Allen, E. Kaitlynn, Adrienne G. Randolph, Tushar Bhangale, et al.. (2017). SNP-mediated disruption of CTCF binding at the IFITM3 promoter is associated with risk of severe influenza in humans. Nature Medicine. 23(8). 975–983. 140 indexed citations

13.

Bronson, Paola G., Diana Chang, Tushar Bhangale, et al.. (2016). Common variants at PVT1, ATG13–AMBRA1, AHI1 and CLEC16A are associated with selective IgA deficiency. Nature Genetics. 48(11). 1425–1429. 48 indexed citations

14.

Yaspan, Brian L., Zhengrong Li, Amy Dressen, et al.. (2014). A Common SNP at the CFI Locus is Associated with Rapid Progression of Geographic Atrophy. Investigative Ophthalmology & Visual Science. 55(13). 2234–2234. 4 indexed citations

15.

Ho, Yen-Yi, Emily C. Baechler, Ward Ortmann, et al.. (2014). Using Gene Expression to Improve the Power of Genome-Wide Association Analysis. Human Heredity. 78(2). 94–103. 9 indexed citations

16.

Graham, Deborah S. Cunninghame, David Morris, Tushar Bhangale, et al.. (2011). Association of NCF2, IKZF1, IRF8, IFIH1, and TYK2 with Systemic Lupus Erythematosus. PLoS Genetics. 7(10). e1002341–e1002341. 218 indexed citations

17.

Bhangale, Tushar, Mark J. Rieder, & Deborah A. Nickerson. (2008). Estimating coverage and power for genetic association studies using near-complete variation data. Nature Genetics. 40(7). 841–843. 59 indexed citations

18.

Bhangale, Tushar, Matthew Stephens, & Deborah A. Nickerson. (2006). Automating resequencing-based detection of insertion-deletion polymorphisms. Nature Genetics. 38(12). 1457–1462. 65 indexed citations

19.

Bhangale, Tushar, Mark J. Rieder, Robert Livingston, & Deborah A. Nickerson. (2004). Comprehensive identification and characterization of diallelic insertion–deletion polymorphisms in 330 human candidate genes. Human Molecular Genetics. 14(1). 59–69. 103 indexed citations

20.

Crawford, Dana C., Tushar Bhangale, Na Li, et al.. (2004). Evidence for substantial fine-scale variation in recombination rates across the human genome. Nature Genetics. 36(7). 700–706. 214 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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