Hugh Gurling

14.7k citations
58 papers · 2.1k indexed · h-index 26
Topics
Genetics and Neurodevelopmental Disorders (22 papers)Bipolar Disorder and Treatment (15 papers)Genetic Associations and Epidemiology (14 papers)

In The Last Decade

Hugh Gurling

57 papers receiving 2.0k citations

Peers

Hugh Gurling
Comparison fields: 5 of 96
  • Genetics 1.0k
  • Molecular Biology 834
  • Psychiatry and Mental health 573
  • Cellular and Molecular Neuroscience 417
  • Cognitive Neuroscience 389
Replace Detelina Grozeva with:
Detelina Grozeva United Kingdom
Robin Sherrington United Kingdom
Shuji Iritani Japan
Rami Abou Jamra Germany
D M Chuang United States
Gursharan Kalsi United Kingdom
Hugh Gurling United Kingdom
Russell L. Margolis United States
Li‐Dong Huang China
Eiji Hattori Japan
Hugh Gurling relative to Detelina Grozeva United Kingdom Detelina Grozeva's profile →
Citations per field
00.5×1.6×
Detelina Grozeva · 1×
Citations per year

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
#WorkIndexed citations
1 32
2 51
3 29
4 58
5 99
6 105
7 30
8 45
9 16
10 11
11 46
12 27
13 24
14 85
15 13
16
Genome wide linkage anlaysis supports the presence of two separate susceptibility loci on chromosome 1q32 for biopolar disorder and 1q21-22.3 for schizophrenia
1
17 17
18 18
19
Point mutation analysis of the FMR-1 gene in autism.
16
20 5

About Hugh Gurling

Hugh Gurling is a scholar working on Genetics, Psychiatry and Mental health and Cognitive Neuroscience, having authored 58 papers that have together received 2.1k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (22 papers), Bipolar Disorder and Treatment (15 papers) and Genetic Associations and Epidemiology (14 papers). The work is most often cited by research in Biological Psychiatry (142 citations), Psychiatry and Mental health (573 citations) and Genetics (1.0k citations). Hugh Gurling has collaborated with scholars based in United Kingdom, United States and Canada. Frequent 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. Their work appears in journals such as American Journal of Psychiatry, Biological Psychiatry and The American Journal of Human Genetics.

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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