Scott Gurd

1.8k total citations
12 papers, 1.4k citations indexed

About

Scott Gurd is a scholar working on Molecular Biology, Genetics and Pathology and Forensic Medicine. According to data from OpenAlex, Scott Gurd has authored 12 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 6 papers in Genetics and 1 paper in Pathology and Forensic Medicine. Recurrent topics in Scott Gurd's work include Genomics and Chromatin Dynamics (5 papers), Genetic Associations and Epidemiology (4 papers) and Epigenetics and DNA Methylation (4 papers). Scott Gurd is often cited by papers focused on Genomics and Chromatin Dynamics (5 papers), Genetic Associations and Epidemiology (4 papers) and Epigenetics and DNA Methylation (4 papers). Scott Gurd collaborates with scholars based in Canada, Sweden and United States. Scott Gurd's co-authors include Thomas J. Hudson, Robert Sladek, Eef Harmsen, Bing Ge, Tomi Pastinen, Marie‐Claude Vohl, Tony Kwan, André Tchernof, Denis Richard and Julie Robitaille and has published in prestigious journals such as Nature Genetics, Genome Research and Human Molecular Genetics.

In The Last Decade

Scott Gurd

12 papers receiving 1.4k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Scott Gurd Canada	11	918	439	202	181	154	12	1.4k
Yu Sun China	24	925 1.0×	617 1.4×	136 0.7×	134 0.7×	69 0.4×	103	1.9k
Avinash Abhyankar United States	20	959 1.0×	650 1.5×	116 0.6×	186 1.0×	44 0.3×	30	1.9k
Elżbieta Ciara Poland	17	647 0.7×	278 0.6×	103 0.5×	72 0.4×	95 0.6×	88	1.1k
M C Postel-Vinay France	23	434 0.5×	325 0.7×	237 1.2×	163 0.9×	34 0.2×	40	1.5k
Omar Albagha United Kingdom	24	1.0k 1.1×	606 1.4×	131 0.6×	144 0.8×	206 1.3×	77	1.9k
Kristina Forsman‐Semb Sweden	18	766 0.8×	190 0.4×	151 0.7×	139 0.8×	132 0.9×	24	1.4k
Amal Alhashem Saudi Arabia	19	616 0.7×	447 1.0×	62 0.3×	84 0.5×	67 0.4×	76	1.1k
Marina Katerelos Australia	21	601 0.7×	312 0.7×	115 0.6×	92 0.5×	25 0.2×	44	1.4k
Louisa M. Villeneuve United States	11	1.2k 1.3×	209 0.5×	116 0.6×	78 0.4×	19 0.1×	11	1.6k
D B Thompson United States	17	635 0.7×	617 1.4×	585 2.9×	293 1.6×	37 0.2×	26	1.7k

Countries citing papers authored by Scott Gurd

Since Specialization

Citations

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

Fields of papers citing papers by Scott Gurd

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Scott Gurd

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

All Works

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12 of 12 papers shown

Lerner‐Ellis, Jordan, Natascia Anastasio, Junhui Liu, et al.. (2009). Spectrum of mutations inMMACHC, allelic expression, and evidence for genotypeâphenotype correlations. Human Mutation. 30(7). 1072–1081. 145 indexed citations

Kwan, Tony, David Benovoy, Christel Dias, et al.. (2008). Genome-wide analysis of transcript isoform variation in humans. Nature Genetics. 40(2). 225–231. 231 indexed citations

Verlaan, Dominique J., Bing Ge, Elin Grundberg, et al.. (2008). Targeted screening of cis- regulatory variation in human haplotypes. Genome Research. 19(1). 118–127. 61 indexed citations

Serre, David, Scott Gurd, Bing Ge, et al.. (2008). Differential Allelic Expression in the Human Genome: A Robust Approach To Identify Genetic and Epigenetic Cis-Acting Mechanisms Regulating Gene Expression. PLoS Genetics. 4(2). e1000006–e1000006. 179 indexed citations

Grundberg, Elin, Helena Brändström, Kevin C. L. Lam, et al.. (2008). Systematic assessment of the human osteoblast transcriptome in resting and induced primary cells. Physiological Genomics. 33(3). 301–311. 26 indexed citations

Kwan, Tony, David Benovoy, Christel Dias, et al.. (2007). Heritability of alternative splicing in the human genome. Genome Research. 17(8). 1210–1218. 91 indexed citations

Grundberg, Elin, E. M. C. Lau, Tomi Pastinen, et al.. (2007). Vitamin D Receptor 3′ Haplotypes Are Unequally Expressed in Primary Human Bone Cells and Associated With Increased Fracture Risk: The MrOS Study in Sweden and Hong Kong. Journal of Bone and Mineral Research. 22(6). 832–840. 30 indexed citations

Ge, Bing, Scott Gurd, Carole Doré, et al.. (2005). Survey of allelic expression using EST mining. Genome Research. 15(11). 1584–1591. 103 indexed citations

Pastinen, Tomi, Bing Ge, Scott Gurd, et al.. (2005). Mapping common regulatory variants to human haplotypes. Human Molecular Genetics. 14(24). 3963–3971. 77 indexed citations

10.

Serre, David, Scott Gurd, Bing Ge, et al.. (2005). Differential Allelic Expression in the Human Genome: A Robust Approach to Identify Genetic and Epigenetic Cis-Acting Mechanisms Regulating Gene Expression. PLoS Genetics. preprint(2008). e6–e6. 5 indexed citations

11.

Vohl, Marie‐Claude, Robert Sladek, Julie Robitaille, et al.. (2004). A Survey of Genes Differentially Expressed in Subcutaneous and Visceral Adipose Tissue in Men*. Obesity Research. 12(8). 1217–1222. 262 indexed citations

12.

Pastinen, Tomi, Robert Sladek, Scott Gurd, et al.. (2004). A survey of genetic and epigenetic variation affecting human gene expression. Physiological Genomics. 16(2). 184–193. 209 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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