G.R. Sutherland

938 total citations
22 papers, 703 citations indexed

About

G.R. Sutherland is a scholar working on Molecular Biology, Genetics and Oncology. According to data from OpenAlex, G.R. Sutherland has authored 22 papers receiving a total of 703 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Molecular Biology, 13 papers in Genetics and 4 papers in Oncology. Recurrent topics in G.R. Sutherland's work include Genetics and Neurodevelopmental Disorders (9 papers), Genomic variations and chromosomal abnormalities (6 papers) and Cell Adhesion Molecules Research (3 papers). G.R. Sutherland is often cited by papers focused on Genetics and Neurodevelopmental Disorders (9 papers), Genomic variations and chromosomal abnormalities (6 papers) and Cell Adhesion Molecules Research (3 papers). G.R. Sutherland collaborates with scholars based in Australia, France and United Kingdom. G.R. Sutherland's co-authors include David F. Callen, John C. Mulley, V.J. Hyland, Ági K. Gedeon, Robert I. Richards, Danuta Z. Loesch, John Shine, H.M. Kozman, Elizabeth Baker and Richard Huggins and has published in prestigious journals such as Science, Nucleic Acids Research and Human Molecular Genetics.

In The Last Decade

G.R. Sutherland

22 papers receiving 679 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
G.R. Sutherland Australia	16	396	355	110	110	78	22	703
Julia Parrish United States	13	414 1.0×	348 1.0×	36 0.3×	71 0.6×	49 0.6×	19	695
David B. Everman United States	20	657 1.7×	466 1.3×	49 0.4×	25 0.2×	51 0.7×	39	1.1k
Rosangela Artuso Italy	14	447 1.1×	606 1.7×	210 1.9×	43 0.4×	32 0.4×	23	900
Nathalie Roëckel France	15	592 1.5×	422 1.2×	23 0.2×	35 0.3×	95 1.2×	21	946
Carlo Arduino Italy	11	230 0.6×	158 0.4×	77 0.7×	33 0.3×	79 1.0×	25	490
Pauline Terhal Netherlands	18	574 1.4×	632 1.8×	28 0.3×	33 0.3×	31 0.4×	28	1.0k
Thomas Schwarzbraun Austria	14	517 1.3×	252 0.7×	74 0.7×	30 0.3×	51 0.7×	26	852
Anne Puech United States	15	604 1.5×	351 1.0×	21 0.2×	31 0.3×	62 0.8×	25	851
Lysanne Patry Canada	14	671 1.7×	480 1.4×	58 0.5×	47 0.4×	138 1.8×	16	1.0k
Jiong Tao China	9	643 1.6×	583 1.6×	107 1.0×	32 0.3×	59 0.8×	14	1.0k

Countries citing papers authored by G.R. Sutherland

Since Specialization

Citations

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

Fields of papers citing papers by G.R. Sutherland

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of G.R. Sutherland

This figure shows the co-authorship network connecting the top 25 collaborators of G.R. Sutherland. A scholar is included among the top collaborators of G.R. Sutherland 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.R. Sutherland. G.R. Sutherland 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:

20 of 20 papers shown

Dibbens, Leanne M., Jenny Ekberg, I Taylor, et al.. (2007). NEDD4‐2 as a potential candidate susceptibility gene for epileptic photosensitivity. Genes Brain & Behavior. 6(8). 750–755. 44 indexed citations

Lower, Karen M., Rajeev Kumar, Erica Woollatt, et al.. (2004). Partial Androgen Insensitivity Syndrome and t(X;5): Are There Upstream Regulatory Elements of the Androgen Receptor Gene?. Hormone Research in Paediatrics. 62(4). 208–214. 13 indexed citations

Sutherland, G.R.. (2003). Rare fragile sites. Cytogenetic and Genome Research. 100(1-4). 77–84. 73 indexed citations

Friend, Kathryn, Denis Crimmins, Thanh G. Phan, et al.. (1999). Detection of a novel missense mutation and second recurrent mutation in the CACNA1A gene in individuals with EA-2 and FHM. Human Genetics. 105(3). 261–265. 20 indexed citations

Herzog, Herbert, Jillian Nicholl, Yvonne Hort, G.R. Sutherland, & John Shine. (1996). Molecular Cloning and Assignment of FAK2, a Novel Human Focal Adhesion Kinase, to 8p11.2–p22 by Nonisotopicin SituHybridization. Genomics. 32(3). 484–486. 49 indexed citations

Iismaa, Tiina P., et al.. (1994). Isolation and Chromosomal Localization of a Novel Human G-Protein-Coupled Receptor (GPR3) Expressed Predominantly in the Central Nervous System. Genomics. 24(2). 391–394. 28 indexed citations

Shen, Yang, H.M. Kozman, Andrew Thompson, et al.. (1994). A PCR-Based Genetic Linkage Map of Human Chromosome 16. Genomics. 22(1). 68–76. 28 indexed citations

Mulley, J.C. & G.R. Sutherland. (1993). Integrating maps of chromosome 16. Current Opinion in Genetics & Development. 3(3). 425–431. 4 indexed citations

Shen, Yang, Katherine Holman, Norman A. Doggett, et al.. (1993). Five dinucleotide repeat polymorphisms on human chromosome 16q24.2 – q24.3. Human Molecular Genetics. 2(9). 1504–1504. 1 indexed citations

10.

Loesch, Danuta Z., Richard Huggins, David Hay, et al.. (1993). Genotype-phenotype relationships in fragile X syndrome: a family study.. PubMed. 53(5). 1064–73. 68 indexed citations

11.

Tuypens, T, Geert Plaetinck, Elizabeth Baker, et al.. (1993). Organization and chromosomal localization of the human interleukin 5 receptor alpha-chain gene.. PubMed. 3(5). 451–9. 23 indexed citations

12.

Baker, Elizabeth, et al.. (1992). Mapping of the human integrin ?7 gene (ITG?7) to 12q13.13 by non-isotopic in situ hybridization. Mammalian Genome. 2(4). 272–273. 7 indexed citations

13.

Shen, Yang, K. Holman, Andrew Thompson, et al.. (1991). An STS at the D16S290 locus. Nucleic Acids Research. 19(20). 5793–5793. 3 indexed citations

14.

Harris, Peter C., Sinoula Apostolou, Elizabeth Baker, et al.. (1991). A refined physical map of the long arm of human chromosome 16. Genomics. 10(2). 308–312. 13 indexed citations

15.

Suthers, G K, I. Oberlé, J.K. Nancarrow, et al.. (1991). Genetic mapping of new RFLPs at Xq27–q28. Genomics. 9(1). 37–43. 35 indexed citations

16.

Hirst, Mark C., A. Roche, Tracey Flint, et al.. (1991). Linear order of new and established DNA markers around the fragile site at Xq27.3. Genomics. 10(1). 243–249. 23 indexed citations

17.

Baker, Elizabeth, et al.. (1991). Chromosomal location of the human tumor necrosis factor receptor genes. Cytogenetic and Genome Research. 57(2-3). 117–118. 33 indexed citations

18.

Richards, Robert I., Yang Shen, K. Holman, et al.. (1991). Fragile X syndrome: diagnosis using highly polymorphic microsatellite markers.. PubMed. 48(6). 1051–7. 38 indexed citations

19.

Scott, Hamish S., Helen J. Eyre, Elizabeth Baker, et al.. (1990). Chromosomal localization of the human alpha-L-iduronidase gene (IDUA) to 4p16.3.. PubMed. 47(5). 802–7. 59 indexed citations

20.

Suthers, G K, David F. Callen, V.J. Hyland, et al.. (1989). A New DNA Marker Tightly Linked to the Fragile X Locus ( FRAXA ). Science. 246(4935). 1298–1300. 54 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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