Angad Johar

548 total citations
14 papers, 245 citations indexed

About

Angad Johar is a scholar working on Genetics, Molecular Biology and Physiology. According to data from OpenAlex, Angad Johar has authored 14 papers receiving a total of 245 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Genetics, 6 papers in Molecular Biology and 3 papers in Physiology. Recurrent topics in Angad Johar's work include Genomics and Rare Diseases (2 papers), Genetic Associations and Epidemiology (2 papers) and Epigenetics and DNA Methylation (2 papers). Angad Johar is often cited by papers focused on Genomics and Rare Diseases (2 papers), Genetic Associations and Epidemiology (2 papers) and Epigenetics and DNA Methylation (2 papers). Angad Johar collaborates with scholars based in Australia, Colombia and United States. Angad Johar's co-authors include Mauricio Arcos‐Burgos, Claudio A. Mastronardi, Gilberto Paz-Filho, Ana Carolina Proença da Fonseca, Hardip R. Patel, Juan‐Manuel Anaya, Christian D. Huber, Raymond Tobler, Yassine Souilmi and David Enard and has published in prestigious journals such as Current Biology, Journal of Lipid Research and Autoimmunity Reviews.

In The Last Decade

Angad Johar

12 papers receiving 242 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Angad Johar Australia	9	91	83	46	35	26	14	245
Asude Durmaz Türkiye	11	92 1.0×	100 1.2×	32 0.7×	45 1.3×	13 0.5×	60	334
Tomislav Modric United States	8	75 0.8×	150 1.8×	55 1.2×	54 1.5×	51 2.0×	11	382
Ankur Singh India	11	77 0.8×	92 1.1×	28 0.6×	28 0.8×	7 0.3×	69	306
Apisadaporn Thambundit United States	7	84 0.9×	227 2.7×	19 0.4×	24 0.7×	14 0.5×	12	444
Emma L. Cambridge United Kingdom	7	22 0.2×	64 0.8×	44 1.0×	29 0.8×	12 0.5×	8	219
Osnat Admoni Israel	14	230 2.5×	245 3.0×	25 0.5×	15 0.4×	24 0.9×	22	555
Tomohiro Terasaka Japan	12	46 0.5×	105 1.3×	26 0.6×	24 0.7×	80 3.1×	37	365
Jose Chavez United States	10	30 0.3×	157 1.9×	50 1.1×	30 0.9×	12 0.5×	22	256
Josh Skorupski United States	11	61 0.7×	67 0.8×	26 0.6×	19 0.5×	35 1.3×	17	359
Keefe Chng Singapore	10	81 0.9×	157 1.9×	65 1.4×	13 0.4×	78 3.0×	21	400

Countries citing papers authored by Angad Johar

Since Specialization

Citations

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

Fields of papers citing papers by Angad Johar

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Angad Johar

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

All Works

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14 of 14 papers shown

Campbell, Peter M., et al.. (2025). A Pangenomic Approach to Improve Population Genetics Analysis and Reference Bias in Underrepresented Middle Eastern and Horn of Africa Populations. Biomolecules. 15(4). 582–582.

Norland, Kristján, et al.. (2023). Deep generative models of LDLR protein structure to predict variant pathogenicity. Journal of Lipid Research. 64(12). 100455–100455. 2 indexed citations

Zhou, Zhou, Wen Chen, Bo Ye, et al.. (2023). Rare loss-of-function variants in matrisome genes are enriched in Ebstein’s anomaly. Human Genetics and Genomics Advances. 5(1). 100258–100258. 1 indexed citations

Souilmi, Yassine, Raymond Tobler, Angad Johar, et al.. (2022). Admixture has obscured signals of historical hard sweeps in humans. Nature Ecology & Evolution. 6(12). 2003–2015. 13 indexed citations

Johar, Angad, et al.. (2022). The immunogenetic impact of European colonization in the Americas. Frontiers in Genetics. 13. 918227–918227. 3 indexed citations

Souilmi, Yassine, M. Elise Lauterbur, Raymond Tobler, et al.. (2021). An ancient viral epidemic involving host coronavirus interacting genes more than 20,000 years ago in East Asia. Current Biology. 31(16). 3504–3514.e9. 54 indexed citations

Fonseca, Ana Carolina Proença da, Claudio A. Mastronardi, Angad Johar, Mauricio Arcos‐Burgos, & Gilberto Paz-Filho. (2017). Genetics of non-syndromic childhood obesity and the use of high-throughput DNA sequencing technologies. Journal of Diabetes and its Complications. 31(10). 1549–1561. 58 indexed citations

Johar, Angad, Juan Camilo Sarmiento-Monroy, Adriana Rojas‐Villarraga, et al.. (2016). Definition of mutations in polyautoimmunity. Journal of Autoimmunity. 72. 65–72. 12 indexed citations

Vélez, Jorge I., Francisco Lopera, Hardip R. Patel, et al.. (2016). Mutations modifying sporadic Alzheimer's disease age of onset. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 171(8). 1116–1130. 15 indexed citations

10.

Johar, Angad, Claudio A. Mastronardi, Adriana Rojas‐Villarraga, et al.. (2015). Novel and rare functional genomic variants in multiple autoimmune syndrome and Sjögren’s syndrome. Journal of Translational Medicine. 13(1). 173–173. 27 indexed citations

11.

Johar, Angad, Juan‐Manuel Anaya, Hardip R. Patel, et al.. (2014). Candidate gene discovery in autoimmunity by using extreme phenotypes, next generation sequencing and whole exome capture. Autoimmunity Reviews. 14(3). 204–209. 27 indexed citations

12.

Johar, Angad, et al.. (2014). Image deblurring using saliency detection. 28. 1–4.

13.

Paz-Filho, Gilberto, Margaret Cristina da Silva Boguszewski, Claudio A. Mastronardi, et al.. (2014). Whole Exome Sequencing of Extreme Morbid Obesity Patients: Translational Implications for Obesity and Related Disorders. Genes. 5(3). 709–725. 18 indexed citations

14.

Latchney, Lisa R., Arthur R. Hand, Angad Johar, et al.. (2003). Thesldmutation is specific for sublingual salivary mucous cells and disrupts apomucin gene expression. Physiological Genomics. 14(2). 95–106. 15 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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