Khalid Choudhury

10.7k total citations
11 papers, 435 citations indexed

About

Khalid Choudhury is a scholar working on Genetics, Molecular Biology and Cognitive Neuroscience. According to data from OpenAlex, Khalid Choudhury has authored 11 papers receiving a total of 435 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 Cognitive Neuroscience. Recurrent topics in Khalid Choudhury's work include Genetic Associations and Epidemiology (6 papers), Genetics and Neurodevelopmental Disorders (4 papers) and Phosphodiesterase function and regulation (3 papers). Khalid Choudhury is often cited by papers focused on Genetic Associations and Epidemiology (6 papers), Genetics and Neurodevelopmental Disorders (4 papers) and Phosphodiesterase function and regulation (3 papers). Khalid Choudhury collaborates with scholars based in United Kingdom, United States and Gibraltar. Khalid Choudhury's co-authors include Jacob Lawrence, Andrew McQuillin, David Curtis, Nicholas Bass, Hugh Gurling, Vinita Puri, Srinivasa Thirumalai, Vinay Puri, Digby Quested and Jonathan Pimm 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

Khalid Choudhury

11 papers receiving 427 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Khalid Choudhury United Kingdom 11 199 171 110 78 66 11 435
Carola J. Maturana United States 10 200 1.0× 55 0.3× 29 0.3× 62 0.8× 52 0.8× 16 395
Fumika Sakaue Japan 10 254 1.3× 40 0.2× 35 0.3× 91 1.2× 222 3.4× 17 623
Gang Zhu China 9 170 0.9× 22 0.1× 122 1.1× 57 0.7× 23 0.3× 24 403
Daniel C. Maddison United Kingdom 9 247 1.2× 20 0.1× 72 0.7× 27 0.3× 219 3.3× 16 580
Xiaoxia Li United States 7 137 0.7× 61 0.4× 88 0.8× 7 0.1× 61 0.9× 11 323
Aitor Palomino Spain 8 80 0.4× 24 0.1× 66 0.6× 75 1.0× 71 1.1× 9 425
Eladia Ballmann Switzerland 6 209 1.1× 114 0.7× 110 1.0× 6 0.1× 122 1.8× 6 449
Amanda Crider United States 10 104 0.5× 139 0.8× 43 0.4× 13 0.2× 89 1.3× 12 431
Katsutoshi Ido Japan 11 177 0.9× 19 0.1× 156 1.4× 197 2.5× 21 0.3× 14 601
Andrew D. Benson United States 12 178 0.9× 143 0.8× 36 0.3× 5 0.1× 13 0.2× 17 420

Countries citing papers authored by Khalid Choudhury

Since Specialization
Citations

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

Fields of papers citing papers by Khalid Choudhury

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Khalid Choudhury

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

All Works

11 of 11 papers shown
1.
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
2.
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
3.
Datta, Susmita, Andrew McQuillin, Mie Rizig, et al.. (2008). A threonine to isoleucine missense mutation in the pericentriolar material 1 gene is strongly associated with schizophrenia. Molecular Psychiatry. 15(6). 615–628. 45 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.
6.
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
7.
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
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
11.
McQuillin, Andrew, Nicholas Bass, Gursharan Kalsi, et al.. (2005). Fine mapping of a susceptibility locus for bipolar and genetically related unipolar affective disorders, to a region containing the C21ORF29 and TRPM2 genes on chromosome 21q22.3. Molecular Psychiatry. 11(2). 134–142. 74 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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