Vivek Appadurai

7.1k total citations
21 papers, 665 citations indexed

About

Vivek Appadurai is a scholar working on Genetics, Molecular Biology and Surgery. According to data from OpenAlex, Vivek Appadurai has authored 21 papers receiving a total of 665 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Genetics, 8 papers in Molecular Biology and 2 papers in Surgery. Recurrent topics in Vivek Appadurai's work include Genetic Associations and Epidemiology (8 papers), Genetics and Neurodevelopmental Disorders (5 papers) and Genomics and Rare Diseases (2 papers). Vivek Appadurai is often cited by papers focused on Genetic Associations and Epidemiology (8 papers), Genetics and Neurodevelopmental Disorders (5 papers) and Genomics and Rare Diseases (2 papers). Vivek Appadurai collaborates with scholars based in United States, Denmark and United Kingdom. Vivek Appadurai's co-authors include Thomas Werge, Penelope E. Bonnen, Andrew J. Schork, Alfonso Buil, Merete Nordentoft, Preben Bo Mortensen, Ron Nudel, David M. Hougaard, Ole Mors and Anders D. Børglum and has published in prestigious journals such as Nature Communications, Nature Genetics and Cancer Research.

In The Last Decade

Vivek Appadurai

20 papers receiving 659 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Vivek Appadurai United States	14	256	178	99	76	71	21	665
Sandra Leistner‐Segal Brazil	22	276 1.1×	190 1.1×	161 1.6×	71 0.9×	133 1.9×	88	1.6k
Laura Kananen Finland	19	509 2.0×	146 0.8×	81 0.8×	33 0.4×	44 0.6×	41	1.4k
Hidehiro Umehara Japan	12	421 1.6×	98 0.6×	62 0.6×	38 0.5×	112 1.6×	28	707
Michelle Stewart United Kingdom	14	204 0.8×	63 0.4×	45 0.5×	40 0.5×	121 1.7×	43	645
Stephen A. Haddad United States	17	207 0.8×	127 0.7×	217 2.2×	27 0.4×	48 0.7×	36	946
Jiewei Liu China	19	460 1.8×	347 1.9×	29 0.3×	49 0.6×	72 1.0×	91	1.1k
Laura Jackson United States	13	118 0.5×	137 0.8×	72 0.7×	141 1.9×	40 0.6×	24	606
Vassilios Zoumpourlis Greece	15	415 1.6×	58 0.3×	125 1.3×	63 0.8×	45 0.6×	35	1.0k
Aimin Hu China	16	116 0.5×	77 0.4×	120 1.2×	141 1.9×	125 1.8×	58	821
Vadlamudi Raghavendra Rao India	15	190 0.7×	223 1.3×	57 0.6×	30 0.4×	50 0.7×	60	812

Countries citing papers authored by Vivek Appadurai

Since Specialization

Citations

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

Fields of papers citing papers by Vivek Appadurai

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Vivek Appadurai

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Appadurai, Vivek, Richard Border, Noah Zaitlen, et al.. (2025). The relationship between genotype- and phenotype-based estimates of genetic liability to psychiatric disorders, in practice and in theory. The American Journal of Human Genetics. 113(1). 184–201.

Borbye‐Lorenzen, Nis, Filip Ottosson, Ron Nudel, et al.. (2024). High level of immunoglobulin G targeting mycoplasma or cytomegalovirus in the newborn increases risk of ADHD. Brain Behavior and Immunity. 123. 99–107. 2 indexed citations

Appadurai, Vivek, Jonas Bybjerg‐Grauholm, Morten Dybdahl Krebs, et al.. (2023). Accuracy of haplotype estimation and whole genome imputation affects complex trait analyses in complex biobanks. Communications Biology. 6(1). 101–101. 8 indexed citations

Appadurai, Vivek, Morten Dybdahl Krebs, Andrew J. Schork, et al.. (2023). Polygenic Analyses Show Important Differences Between Major Depressive Disorder Symptoms Measured Using Various Instruments. Biological Psychiatry. 95(12). 1110–1121. 3 indexed citations

Dahl, Andrew, Michael Thompson, Morten Dybdahl Krebs, et al.. (2023). Phenotype integration improves power and preserves specificity in biobank-based genetic studies of major depressive disorder. Nature Genetics. 55(12). 2082–2093. 23 indexed citations

Nudel, Ron, Vivek Appadurai, Alfonso Buil, Merete Nordentoft, & Thomas Werge. (2021). Pleiotropy between language impairment and broader behavioral disorders—an investigation of both common and rare genetic variants. Journal of Neurodevelopmental Disorders. 13(1). 54–54. 10 indexed citations

Aarøe, Lene, Vivek Appadurai, Kasper Møller Hansen, et al.. (2020). Genetic predictors of educational attainment and intelligence test performance predict voter turnout. Nature Human Behaviour. 5(2). 281–291. 21 indexed citations

Nudel, Ron, Vivek Appadurai, Andrew J. Schork, et al.. (2020). A large population-based investigation into the genetics of susceptibility to gastrointestinal infections and the link between gastrointestinal infections and mental illness. Human Genetics. 139(5). 593–604. 11 indexed citations

Eser, Hale Yapıcı, Vivek Appadurai, Dilek Yazıcı, et al.. (2020). Association between GLP-1 receptor gene polymorphisms with reward learning, anhedonia and depression diagnosis. Acta Neuropsychiatrica. 32(4). 218–225. 17 indexed citations

10.

Pagsberg, Anne Katrine, et al.. (2020). Copy Number Variants and Polygenic Risk Scores Predict Need of Care in Autism and/or ADHD Families. Journal of Autism and Developmental Disorders. 51(1). 276–285. 9 indexed citations

11.

Liu, Xueping, Ron Nudel, Wesley K. Thompson, et al.. (2020). Genetic factors underlying the bidirectional relationship between autoimmune and mental disorders – Findings from a Danish population-based study. Brain Behavior and Immunity. 91. 10–23. 14 indexed citations

12.

Nudel, Ron, Yunpeng Wang, Vivek Appadurai, et al.. (2019). A large-scale genomic investigation of susceptibility to infection and its association with mental disorders in the Danish population. Translational Psychiatry. 9(1). 283–283. 47 indexed citations

13.

Gandal, Michael J., Jillian R. Haney, Neelroop Parikshak, et al.. (2019). Shared Molecular Neuropathology Across Major Psychiatric Disorders Parallels Polygenic Overlap. FOCUS The Journal of Lifelong Learning in Psychiatry. 17(1). 66–72. 113 indexed citations

14.

Fan, Chun Chieh, John J. McGrath, Vivek Appadurai, et al.. (2018). Spatial fine-mapping for gene-by-environment effects identifies risk hot spots for schizophrenia. Nature Communications. 9(1). 5296–5296. 13 indexed citations

15.

Erlangsen, Annette, Vivek Appadurai, Yunpeng Wang, et al.. (2018). Genetics of suicide attempts in individuals with and without mental disorders: a population-based genome-wide association study. Molecular Psychiatry. 25(10). 2410–2421. 101 indexed citations

16.

Alaimo, Joseph T., Arnaud Besse, Charlotte L. Alston, et al.. (2018). Loss-of-function mutations inISCA2disrupt 4Fe-4S cluster machinery and cause a fatal leukodystrophy with hyperglycinemia and mtDNA depletion. Human Mutation. 39(4). 537–549. 21 indexed citations

17.

Besse, Arnaud, Andrea Petersen, Jill V. Hunter, et al.. (2016). Personalized medicine approach confirms a milder case of ABAT deficiency. Molecular Brain. 9(1). 93–93. 18 indexed citations

18.

Dogruluk, Turgut, Yiu Huen Tsang, Fengju Chen, et al.. (2015). Identification of Variant-Specific Functions of PIK3CA by Rapid Phenotyping of Rare Mutations. Cancer Research. 75(24). 5341–5354. 118 indexed citations

19.

Stiles, Ashlee R., Sacha Ferdinandusse, Arnaud Besse, et al.. (2015). Successful diagnosis of HIBCH deficiency from exome sequencing and positive retrospective analysis of newborn screening cards in two siblings presenting with Leigh's disease. Molecular Genetics and Metabolism. 115(4). 161–167. 29 indexed citations

20.

Appadurai, Vivek, Andrea E. DeBarber, Pei-Wen Chiang, et al.. (2015). Apparent underdiagnosis of Cerebrotendinous Xanthomatosis revealed by analysis of ~60,000 human exomes. Molecular Genetics and Metabolism. 116(4). 298–304. 71 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.

Explore authors with similar magnitude of impact