Hmd Gurling

460 total citations
8 papers, 132 citations indexed

About

Hmd Gurling is a scholar working on Genetics, Molecular Biology and Cognitive Neuroscience. According to data from OpenAlex, Hmd Gurling has authored 8 papers receiving a total of 132 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Genetics, 4 papers in Molecular Biology and 4 papers in Cognitive Neuroscience. Recurrent topics in Hmd Gurling's work include Autism Spectrum Disorder Research (4 papers), Genetic Associations and Epidemiology (2 papers) and Obsessive-Compulsive Spectrum Disorders (2 papers). Hmd Gurling is often cited by papers focused on Autism Spectrum Disorder Research (4 papers), Genetic Associations and Epidemiology (2 papers) and Obsessive-Compulsive Spectrum Disorders (2 papers). Hmd Gurling collaborates with scholars based in United Kingdom, Iceland and United States. Hmd Gurling's co-authors include David Curtis, Mary Robertson, Hannes Pétursson, Jon Brynjolfsson, Gursharan Kalsi, G. Kalsi, Peter Brett, P. Murphy, Andrew McQuillin and Robin Sherrington and has published in prestigious journals such as Psychological Medicine, Human Genetics and American Journal of Medical Genetics.

In The Last Decade

Hmd Gurling

8 papers receiving 125 citations

Peers

Hmd Gurling

GENET

CN

CP

MB

CMN

N. Williams United Kingdom

Allan L. Naarden United States

Cathy L. Budman United States

G. Kalsi United Kingdom

Ravi Kumar Nadella India

David P. Lennon Australia

Marylin Lepleux France

Tanjala Gipson United States

Nawei Sun United States

Mary S. Mufford South Africa

N. Williams United Kingdom

Hmd Gurling

33 ×0.5

GENET

31 ×0.6

CN

33 ×0.7

CP

49 ×1.5

MB

35 ×1.5

CMN

Citations per year, relative to Hmd Gurling Hmd Gurling (= 1×) peers N. Williams

Countries citing papers authored by Hmd Gurling

Since Specialization

Citations

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

Fields of papers citing papers by Hmd Gurling

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Hmd Gurling

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

All Works

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8 of 8 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.

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

3.

Kalsi, Gursharan, Timothy A. Klempan, T. Breschel, et al.. (1998). No evidence of expansion of CAG or GAA repeats in schizophrenia families and monozygotic twins. Human Genetics. 103(1). 41–47. 26 indexed citations

4.

Kalsi, Gursharan, David Curtis, Jon Brynjolfsson, et al.. (1998). Tests of linkage, allelic and genotypic association between schizophrenia and the gene for the D3 dopamine receptor, DRD3. Psychiatric Genetics. 8(3). 187–190. 3 indexed citations

5.

Curtis, David, et al.. (1996). Linkage analysis and exclusion of regions of chromosomes 3 and 8 in Gilles de la Tourette syndrome following the identification of a balanced reciprocal translocation 46 XY, t(3. Psychiatric Genetics. 6(3). 99–106. 17 indexed citations

6.

Kalsi, Gursharan, Jon Brynjolfsson, Robert J. Butler, et al.. (1995). Linkage analysis of chromosome 22q12–13 in a United Kingdom/Icelandic sample of 23 multiplex schizophrenia families. American Journal of Medical Genetics. 60(4). 298–301. 32 indexed citations

7.

Kalsi, Gursharan, David Curtis, Jon Brynjolfsson, et al.. (1995). Exclusion of linkage of schizophrenia to the gene for the dopamine D2 receptor (DRD2) and chromosome 11q translocation sites. Psychological Medicine. 25(3). 531–537. 12 indexed citations

8.

Mankoo, Baljinder S., Robin Sherrington, Gursharan Kalsi, et al.. (1991). Analysis of Polymorphic Microsatellite DNA Sequences by PCR Amplification of Paraffin-embedded Tissue. Psychiatric Genetics. 2(2). 161–166. 5 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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