Vinay Puri

2.8k total citations
10 papers, 250 citations indexed

About

Vinay Puri is a scholar working on Genetics, Molecular Biology and Cognitive Neuroscience. According to data from OpenAlex, Vinay Puri has authored 10 papers receiving a total of 250 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Genetics, 5 papers in Molecular Biology and 3 papers in Cognitive Neuroscience. Recurrent topics in Vinay Puri's work include Genetic Associations and Epidemiology (6 papers), Genetics and Neurodevelopmental Disorders (4 papers) and Autism Spectrum Disorder Research (3 papers). Vinay Puri is often cited by papers focused on Genetic Associations and Epidemiology (6 papers), Genetics and Neurodevelopmental Disorders (4 papers) and Autism Spectrum Disorder Research (3 papers). Vinay Puri collaborates with scholars based in United Kingdom, United States and Gibraltar. Vinay Puri's co-authors include Jacob Lawrence, Andrew McQuillin, David Curtis, Nicholas Bass, Khalid Choudhury, Digby Quested, Jonathan Pimm, Srinivasa Thirumalai, Hugh Gurling and Susmita Datta and has published in prestigious journals such as American Journal of Psychiatry, Biological Psychiatry and The American Journal of Human Genetics.

In The Last Decade

Vinay Puri

9 papers receiving 246 citations

Peers

Vinay Puri
Srinivasa Thirumalai United Kingdom
Emily Moon United States
Núria Villalmanzo Spain
Dora Steel United Kingdom
Mizue Kametani Japan
An‐a Kazuno Japan
Ranjana Verma United States
Trine Bjørg Hammer Denmark
Stephanie L. Ciarlone United States
Kin Po Siu Canada
Srinivasa Thirumalai United Kingdom
Vinay Puri
Citations per year, relative to Vinay Puri Vinay Puri (= 1×) peers Srinivasa Thirumalai

Countries citing papers authored by Vinay Puri

Since Specialization
Citations

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

Fields of papers citing papers by Vinay Puri

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Vinay Puri

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

All Works

10 of 10 papers shown
1.
Pereira, Ana Carla, Andrew McQuillin, Vinay Puri, et al.. (2011). Genetic association and sequencing of the insulin-like growth factor 1 gene in bipolar affective disorder. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 156(2). 177–187. 29 indexed citations
2.
Curtis, David, Andrew McQuillin, Nicholas Bass, et al.. (2010). Case–case genome-wide association analysis shows markers differentially associated with schizophrenia and bipolar disorder and implicates calcium channel genes. Psychiatric Genetics. 21(1). 1–4. 58 indexed citations
3.
Bass, Nicholas, Susmita Datta, Andrew McQuillin, et al.. (2009). Evidence for the association of the DAOA (G72) gene with schizophrenia and bipolar disorder but not for the association of the DAO gene with schizophrenia. Behavioral and Brain Functions. 5(1). 28–28. 32 indexed citations
4.
Puri, Vinay, Andrew McQuillin, Susmita Datta, et al.. (2008). Confirmation of the genetic association between the U2AF homology motif (UHM) kinase 1 (UHMK1) gene and schizophrenia on chromosome 1q23.3. European Journal of Human Genetics. 16(10). 1275–1282. 16 indexed citations
5.
Choudhury, Khalid, Andrew McQuillin, Vinay Puri, et al.. (2007). A Genetic Association Study of Chromosome 11q22-24 in Two Different Samples Implicates the FXYD6 Gene, Encoding Phosphohippolin, in Susceptibility to Schizophrenia. The American Journal of Human Genetics. 80(4). 664–672. 31 indexed citations
6.
Datta, Susmita, Andrew McQuillin, Vinay Puri, et al.. (2007). Failure to confirm allelic and haplotypic association between markers at the chromosome 6p22.3 dystrobrevin-binding protein 1 (DTNBP1) locus and schizophrenia. Behavioral and Brain Functions. 3(1). 50–50. 17 indexed citations
7.
Puri, Vinay. (2007). Automated Alerting for Black Hole Routing. Calhoun: The Naval Postgraduate School Institutional Archive (Naval Postgraduate School). 1 indexed citations
8.
9.
Rizig, Mie, Andrew McQuillin, Vinay Puri, et al.. (2006). Failure to confirm genetic association between schizophrenia and markers on chromosome 1q23.3 in the region of the gene encoding the regulator of G‐protein signaling 4 protein (RGS4). American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 141B(3). 296–300. 27 indexed citations
10.
Puri, Vinay, Andrew McQuillin, Khalid Choudhury, et al.. (2006). Fine Mapping by Genetic Association Implicates the Chromosome 1q23.3 Gene UHMK1, Encoding a Serine/Threonine Protein Kinase, as a Novel Schizophrenia Susceptibility Gene. Biological Psychiatry. 61(7). 873–879. 28 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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