Hugh Gurling

14.7k total citations
58 papers, 2.1k citations indexed

About

Hugh Gurling is a scholar working on Genetics, Molecular Biology and Psychiatry and Mental health. According to data from OpenAlex, Hugh Gurling has authored 58 papers receiving a total of 2.1k indexed citations (citations by other indexed papers that have themselves been cited), including 36 papers in Genetics, 26 papers in Molecular Biology and 17 papers in Psychiatry and Mental health. Recurrent topics in Hugh Gurling's work include Genetics and Neurodevelopmental Disorders (22 papers), Bipolar Disorder and Treatment (15 papers) and Genetic Associations and Epidemiology (14 papers). Hugh Gurling is often cited by papers focused on Genetics and Neurodevelopmental Disorders (22 papers), Bipolar Disorder and Treatment (15 papers) and Genetic Associations and Epidemiology (14 papers). Hugh Gurling collaborates with scholars based in United Kingdom, United States and Canada. Hugh Gurling's co-authors include Andrew McQuillin, David Curtis, Jacob Lawrence, Nicholas Bass, John B. Vincent, Mie Rizig, Gursharan Kalsi, Sally I. Sharp, Hannes Pétursson and Radhika Kandaswamy 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

Hugh Gurling

57 papers receiving 2.0k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Hugh Gurling United Kingdom 26 1.0k 834 573 417 389 58 2.1k
Detelina Grozeva United Kingdom 21 1.2k 1.2× 857 1.0× 575 1.0× 264 0.6× 305 0.8× 40 2.2k
Rami Abou Jamra Germany 29 1.1k 1.1× 1.4k 1.6× 407 0.7× 544 1.3× 244 0.6× 99 2.8k
Yoko Kinoshita Japan 28 571 0.6× 715 0.9× 395 0.7× 616 1.5× 224 0.6× 73 2.1k
Elaine Green United Kingdom 19 568 0.6× 492 0.6× 423 0.7× 165 0.4× 170 0.4× 33 1.3k
Hugh Gurling United Kingdom 24 681 0.7× 531 0.6× 318 0.6× 251 0.6× 221 0.6× 64 1.6k
Eiji Hattori Japan 24 568 0.6× 778 0.9× 298 0.5× 398 1.0× 151 0.4× 41 1.6k
Russell L. Margolis United States 17 521 0.5× 1.2k 1.5× 232 0.4× 972 2.3× 261 0.7× 37 2.7k
Thomas Sander Germany 28 565 0.6× 961 1.2× 560 1.0× 843 2.0× 369 0.9× 52 2.2k
Nirmala Akula United States 19 904 0.9× 603 0.7× 574 1.0× 183 0.4× 153 0.4× 42 1.6k
Gursharan Kalsi United Kingdom 20 637 0.6× 660 0.8× 203 0.4× 280 0.7× 110 0.3× 56 1.4k

Countries citing papers authored by Hugh Gurling

Since Specialization
Citations

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

Fields of papers citing papers by Hugh Gurling

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Hugh Gurling

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

All Works

20 of 20 papers shown
1.
Fiorentino, Alessia, Niamh L. O’Brien, Devin P. Locke, et al.. (2014). Analysis of ANK3 and CACNA1C variants identified in bipolar disorder whole genome sequence data. Bipolar Disorders. 16(6). 583–591. 36 indexed citations
2.
Kandaswamy, Radhika, Andrew McQuillin, David Curtis, & Hugh Gurling. (2014). Allelic association, DNA resequencing and copy number variation at the metabotropic glutamate receptor GRM7 gene locus in bipolar disorder. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 165(4). 365–372. 32 indexed citations
3.
Lydall, Gregory, Nicholas Bass, Andrew McQuillin, et al.. (2011). Confirmation of prior evidence of genetic susceptibility to alcoholism in a genome-wide association study of comorbid alcoholism and bipolar disorder. Psychiatric Genetics. 21(6). 294–306. 51 indexed citations
4.
Montagnese, Sara, Andrew McQuillin, Irene Guerrini, et al.. (2011). Genetic association study of GABRA2 single nucleotide polymorphisms and electroencephalography in alcohol dependence. Neuroscience Letters. 500(3). 162–166. 23 indexed citations
5.
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
6.
Perlis, Roy H., Jordan W. Smoller, Manuel A. R. Ferreira, et al.. (2009). A Genomewide Association Study of Response to Lithium for Prevention of Recurrence in Bipolar Disorder. American Journal of Psychiatry. 166(6). 718–725. 105 indexed citations
7.
Sharp, Sally I., Andrew McQuillin, & Hugh Gurling. (2009). Genetics of attention-deficit hyperactivity disorder (ADHD). Neuropharmacology. 57(7-8). 590–600. 99 indexed citations
8.
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
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.
11.
Vincent, John B., Georg Melmer, Patrick Bolton, et al.. (2005). Genetic linkage analysis of the X chromosome in autism, with emphasis on the fragile X region. Psychiatric Genetics. 15(2). 83–90. 22 indexed citations
12.
Vincent, John B., et al.. (2004). Mutation screening of X‐chromosomal neuroligin genes: No mutations in 196 autism probands. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 129B(1). 82–84. 85 indexed citations
13.
McQuillin, Andrew, Gursharan Kalsi, Soraya Mayet, et al.. (2002). A novel polymorphism in exon 11 of the WKL1 gene, shows no association with schizophrenia. European Journal of Human Genetics. 10(8). 491–494. 13 indexed citations
14.
Curtis, David, et al.. (2002). A quick and simple method for detecting subjects with abnormal genetic background in case‐control samples. Annals of Human Genetics. 66(3). 235–244. 13 indexed citations
15.
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
16.
Vincent, John B., Mario Masellis, Jacob Lawrence, et al.. (1999). Genetic Association Analysis of Serotonin System Genes in Bipolar Affective Disorder. American Journal of Psychiatry. 156(1). 136–138. 67 indexed citations
17.
Brett, Peter, David Curtis, Mary Robertson, & Hugh Gurling. (1997). Neuroreceptor subunit genes and the genetic susceptibility to gilles de la tourette syndrome. Biological Psychiatry. 42(10). 941–947. 18 indexed citations
18.
Turner, Adrian, Jacob Lawrence, Andrew C. H. Chen, Christopher L. Cook, & Hugh Gurling. (1997). Frequency of the A1/A2 alleles of the D2 dopamine receptor (DRD2) gene in a British, Caucasian control group screened to exclude alcoholism and heavy drinking. Addiction Biology. 2(2). 207–213. 10 indexed citations
19.
Konecki, David, Ewald Münstermann, PF Bolton, et al.. (1996). Point mutation analysis of the FMR-1 gene in autism.. PubMed. 1(3). 227–31. 16 indexed citations
20.
Sherrington, Robin, Baljinder S. Mankoo, M F Dixon, et al.. (1993). Microsatellite Polymorphisms for Chromosome 5 Bands q11.2-q13.3. Human Heredity. 43(3). 197–202. 9 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

Breakdown of academic impact, for papers by Detelina Grozeva Breakdown of academic impact, for papers by Rami Abou Jamra Breakdown of academic impact, for papers by Yoko Kinoshita Breakdown of academic impact, for papers by Elaine Green Breakdown of academic impact, for papers by Hugh Gurling Breakdown of academic impact, for papers by Eiji Hattori Breakdown of academic impact, for papers by Russell L. Margolis Breakdown of academic impact, for papers by Thomas Sander Breakdown of academic impact, for papers by Nirmala Akula Breakdown of academic impact, for papers by Gursharan Kalsi
Rankless by CCL
2026