G.G. Govan

1.3k total citations
9 papers, 721 citations indexed

About

G.G. Govan is a scholar working on Molecular Biology, Pathology and Forensic Medicine and Clinical Biochemistry. According to data from OpenAlex, G.G. Govan has authored 9 papers receiving a total of 721 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 2 papers in Pathology and Forensic Medicine and 2 papers in Clinical Biochemistry. Recurrent topics in G.G. Govan's work include Mitochondrial Function and Pathology (9 papers), ATP Synthase and ATPases Research (4 papers) and interferon and immune responses (2 papers). G.G. Govan is often cited by papers focused on Mitochondrial Function and Pathology (9 papers), ATP Synthase and ATPases Research (4 papers) and interferon and immune responses (2 papers). G.G. Govan collaborates with scholars based in United Kingdom. G.G. Govan's co-authors include Paul Riordan‐Eva, A. E. Harding, Mary G. Sweeney, M D Sanders, A E Harding, Anthony H.V. Schapira, Jonathan M. Cooper, P.R. Smith, H. Kellar-Wood and Neil P. Robertson and has published in prestigious journals such as Brain, Annals of Neurology and Journal of Neurology Neurosurgery & Psychiatry.

In The Last Decade

G.G. Govan

9 papers receiving 697 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
G.G. Govan United Kingdom	9	607	170	162	111	69	9	721
Patrick Yu Wai Man United Kingdom	5	543 0.9×	223 1.3×	122 0.8×	17 0.2×	18 0.3×	6	592
Birgit Kjer Denmark	11	359 0.6×	56 0.3×	126 0.8×	8 0.1×	34 0.5×	14	483
Virginie Guillet France	10	483 0.8×	139 0.8×	44 0.3×	9 0.1×	36 0.5×	11	581
Sindhu Saraswathy United States	16	260 0.4×	32 0.2×	413 2.5×	25 0.2×	23 0.3×	36	666
A. De Negri Italy	5	489 0.8×	206 1.2×	88 0.5×	7 0.1×	22 0.3×	5	555
Yanchun Ji China	20	896 1.5×	280 1.6×	68 0.4×	8 0.1×	7 0.1×	45	938
Ghizlane Elachouri France	5	450 0.7×	160 0.9×	28 0.2×	10 0.1×	18 0.3×	6	474
Patrick Yu‐Wai‐Man United Kingdom	7	402 0.7×	188 1.1×	71 0.4×	14 0.1×	64 0.9×	16	513
Takuro Fujimaki Japan	14	335 0.6×	29 0.2×	183 1.1×	14 0.1×	7 0.1×	26	462
Guazzi Gc Italy	12	158 0.3×	40 0.2×	11 0.1×	29 0.3×	72 1.0×	58	359

Countries citing papers authored by G.G. Govan

Since Specialization

Citations

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

Fields of papers citing papers by G.G. Govan

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

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

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

All Works

Sort: Min cites: Since: Top N: Style:

9 of 9 papers shown

1.

Chalmers, R. M., G.G. Govan, Anthony H.V. Schapira, & A. E. Harding. (1996). HLA class I genotypes in Leber's hereditary optic neuropathy. Journal of the Neurological Sciences. 135(2). 173–175. 8 indexed citations

2.

Harding, A E, Paul Riordan‐Eva, & G.G. Govan. (1995). Mitochondrial DNA diseases: Genotype and phenotype in leber's hereditary optic neuropathy. Muscle & Nerve. 18(S14). S82–S84. 38 indexed citations

3.

Smith, P.R., Jonathan M. Cooper, G.G. Govan, et al.. (1995). Antibodies to human optic nerve in Leber's hereditary optic neuropathy. Journal of the Neurological Sciences. 130(2). 134–138. 23 indexed citations

4.

Riordan‐Eva, Paul, et al.. (1995). The clinical features of Leber's hereditary optic neuropathy defined by the presence of a pathogenic mitochondrial DNA mutation. Brain. 118(2). 319–337. 374 indexed citations

5.

Morrissey, Sean, David H. Miller, I. F. Moseley, et al.. (1995). Bilateral simultaneous optic neuropathy in adults: clinical, imaging, serological, and genetic studies.. Journal of Neurology Neurosurgery & Psychiatry. 58(1). 70–74. 33 indexed citations

6.

Kellar-Wood, H., Neil P. Robertson, G.G. Govan, D. A. S. Compston, & A E Harding. (1994). Leber's hereditary optic neuropathy mitochondrial DNA mutations in multiple sclerosis. Annals of Neurology. 36(1). 109–112. 107 indexed citations

7.

Govan, G.G., PR Smith, H. Kellar-Wood, Anthony H.V. Schapira, & A E Harding. (1994). HLA class II genotypes in Leber's hereditary optic neuropathy. Journal of the Neurological Sciences. 126(2). 193–196. 11 indexed citations

8.

Smith, P.R., Jonathan M. Cooper, G.G. Govan, A E Harding, & Anthony H.V. Schapira. (1994). Platelet mitochondrial function in Leber's hereditary optic neuropathy. Journal of the Neurological Sciences. 122(1). 80–83. 63 indexed citations

9.

Smith, P.R., Jonathan M. Cooper, G.G. Govan, A. E. Harding, & Anthony H.V. Schapira. (1993). Smoking and mitochondrial function: a model for environmental toxins. QJM. 86(10). 657–660. 64 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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