G. Kalsi

628 total citations
7 papers, 80 citations indexed

About

G. Kalsi is a scholar working on Molecular Biology, Clinical Psychology and Cognitive Neuroscience. According to data from OpenAlex, G. Kalsi has authored 7 papers receiving a total of 80 indexed citations (citations by other indexed papers that have themselves been cited), including 2 papers in Molecular Biology, 2 papers in Clinical Psychology and 2 papers in Cognitive Neuroscience. Recurrent topics in G. Kalsi's work include Autism Spectrum Disorder Research (2 papers), Bipolar Disorder and Treatment (2 papers) and Obsessive-Compulsive Spectrum Disorders (1 paper). G. Kalsi is often cited by papers focused on Autism Spectrum Disorder Research (2 papers), Bipolar Disorder and Treatment (2 papers) and Obsessive-Compulsive Spectrum Disorders (1 paper). G. Kalsi collaborates with scholars based in United Kingdom, India and Iceland. G. Kalsi's co-authors include David Curtis, Andrew McQuillin, Mary Robertson, Peter Brett, Hmd Gurling, Jon Brynjolfsson, Hannes Pétursson, Robin Sherrington, Larry Rifkin and Joseph O’Neill and has published in prestigious journals such as American Journal of Psychiatry, Psychological Medicine and American Journal of Medical Genetics Part B Neuropsychiatric Genetics.

In The Last Decade

G. Kalsi

7 papers receiving 77 citations

Peers

G. Kalsi

GENET

CP

CN

MB

CMN

Hmd Gurling United Kingdom

Ravi Kumar Nadella India

S Meier Germany

I. Coelho Portugal

Mary S. Mufford South Africa

D. Rühl Germany

Cesar Ochoa‐Lubinoff United States

Paul A. Mulder Netherlands

Stacey Saenz de Viteri United States

A. I. Trandafir France

Hmd Gurling United Kingdom

G. Kalsi

69 ×2.1

GENET

49 ×1.6

CP

50 ×2.0

CN

32 ×1.9

MB

23 ×2.1

CMN

Citations per year, relative to G. Kalsi G. Kalsi (= 1×) peers Hmd Gurling

Countries citing papers authored by G. Kalsi

Since Specialization

Citations

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

Fields of papers citing papers by G. Kalsi

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of G. Kalsi

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

All Works

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7 of 7 papers shown

1.

Curtis, David, Peter Brett, Andrew McQuillin, et al.. (2004). Genome scan of Tourette syndrome in a single large pedigree shows some support for linkage to regions of chromosomes 5, 10 and 13. Psychiatric Genetics. 14(2). 83–87. 35 indexed citations

2.

Gurling, Hugh, David Curtis, G. Kalsi, et al.. (2000). Genome wide linkage anlaysis supports the presence of two separate susceptibility loci on chromosome 1q32 for biopolar disorder and 1q21-22.3 for schizophrenia. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 96(4). 1 indexed citations

3.

McQuillin, Andrew, et al.. (1999). Adjacent genetic markers on chromosome 11p15.5 at or near the tyrosine hydroxylase locus that show population linkage disequilibrium with each other do not show allelic association with bipolar affective disorder. Psychological Medicine. 29(6). 1449–1454. 8 indexed citations

4.

Kalsi, G., David Curtis, Jon Brynjolfsson, et al.. (1999). No evidence for linkage of schizophrenia to DXS7 at chromosome Xp11. Psychiatric Genetics. 9(4). 197–200. 2 indexed citations

5.

Kalsi, G., David Curtis, Jon Brynjolfsson, et al.. (1996). Exclusion of linkage between schizophrenia and the putative chromosome 3p24-p26 susceptibility locus. Psychiatric Genetics. 6(3). 148–148. 2 indexed citations

6.

Smyth, Cyril J., G. Kalsi, Jon Brynjolfsson, et al.. (1996). Further tests for linkage of bipolar affective disorder to the tyrosine hydroxylase gene locus on chromosome 11p15 in a new series of multiplex British affective disorder pedigrees [published erratum appears in Am J Psychiatry 1997 Jan;154(1):139]. American Journal of Psychiatry. 153(2). 271–274. 24 indexed citations

7.

Chen, Andrew C. H., G. Kalsi, Jon Brynjolfsson, et al.. (1996). Lack of evidence for close linkage of the glutamate GluR6 receptor gene with schizophrenia. American Journal of Psychiatry. 153(12). 1634–1636. 8 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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