Gregory McInnes

991 total citations
12 papers, 414 citations indexed

About

Gregory McInnes is a scholar working on Genetics, Pharmacology and Molecular Biology. According to data from OpenAlex, Gregory McInnes has authored 12 papers receiving a total of 414 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Genetics, 6 papers in Pharmacology and 5 papers in Molecular Biology. Recurrent topics in Gregory McInnes's work include Genetic Associations and Epidemiology (6 papers), Pharmacogenetics and Drug Metabolism (6 papers) and Genomics and Rare Diseases (5 papers). Gregory McInnes is often cited by papers focused on Genetic Associations and Epidemiology (6 papers), Pharmacogenetics and Drug Metabolism (6 papers) and Genomics and Rare Diseases (5 papers). Gregory McInnes collaborates with scholars based in United States and Italy. Gregory McInnes's co-authors include Russ B. Altman, Adam Lavertu, Michelle Whirl‐Carrillo, Katrin Sangkuhl, Teri E. Klein, Manuel A. Rivas, Yosuke Tanigawa, Sook Wah Yee, Yash Pershad and Matthew Aguirre and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Communications and Bioinformatics.

In The Last Decade

Gregory McInnes

12 papers receiving 412 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Gregory McInnes United States	10	193	159	150	54	42	12	414
Adam Lavertu United States	11	185 1.0×	157 1.0×	197 1.3×	51 0.9×	41 1.0×	15	510
Christina Mitropoulou Greece	15	208 1.1×	237 1.5×	145 1.0×	86 1.6×	43 1.0×	42	562
Kristi Krebs Estonia	10	109 0.6×	185 1.2×	106 0.7×	70 1.3×	49 1.2×	20	418
Seung‐been Lee United States	10	136 0.7×	263 1.7×	132 0.9×	60 1.1×	80 1.9×	17	408
Nina Gonzaludo United States	9	135 0.7×	98 0.6×	111 0.7×	48 0.9×	21 0.5×	11	307
Ryan Whaley United States	6	143 0.7×	268 1.7×	237 1.6×	92 1.7×	57 1.4×	9	606
Jennifer Hockings United States	9	118 0.6×	132 0.8×	233 1.6×	51 0.9×	86 2.0×	19	512
Maaike van der Lee Netherlands	10	73 0.4×	157 1.0×	77 0.5×	29 0.5×	42 1.0×	22	293
Reynold C. Ly United States	12	104 0.5×	222 1.4×	131 0.9×	105 1.9×	77 1.8×	23	394
Greyson P Twist United States	6	82 0.4×	219 1.4×	88 0.6×	62 1.1×	65 1.5×	7	316

Countries citing papers authored by Gregory McInnes

Since Specialization

Citations

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

Fields of papers citing papers by Gregory McInnes

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Gregory McInnes

This figure shows the co-authorship network connecting the top 25 collaborators of Gregory McInnes. A scholar is included among the top collaborators of Gregory McInnes 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 Gregory McInnes. Gregory McInnes 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

McInnes, Gregory, Julia E. H. Brown, Neil Thomas, et al.. (2022). Functional genomics of OCTN2 variants informs protein-specific variant effect predictor for Carnitine Transporter Deficiency. Proceedings of the National Academy of Sciences. 119(46). e2210247119–e2210247119. 12 indexed citations

Idda, Maria Laura, Magdalena Żołędziewska, Silvana Anna Maria Urru, et al.. (2022). Genetic Variation among Pharmacogenes in the Sardinian Population. International Journal of Molecular Sciences. 23(17). 10058–10058. 8 indexed citations

McInnes, Gregory, Andrew G. Sharo, Julia E. H. Brown, et al.. (2021). Opportunities and challenges for the computational interpretation of rare variation in clinically important genes. The American Journal of Human Genetics. 108(4). 535–548. 38 indexed citations

McInnes, Gregory, Sook Wah Yee, Yash Pershad, & Russ B. Altman. (2021). Genomewide Association Studies in Pharmacogenomics. Clinical Pharmacology & Therapeutics. 110(3). 637–648. 48 indexed citations

McInnes, Gregory, Rachel Dalton, Katrin Sangkuhl, et al.. (2020). Transfer learning enables prediction of CYP2D6 haplotype function. PLoS Computational Biology. 16(11). e1008399–e1008399. 35 indexed citations

McInnes, Gregory & Russ B. Altman. (2020). Drug Response Pharmacogenetics for 200,000 UK Biobank Participants. PubMed. 26. 184–195. 16 indexed citations

DeBoever, Christopher, Yosuke Tanigawa, Matthew Aguirre, et al.. (2020). Assessing Digital Phenotyping to Enhance Genetic Studies of Human Diseases. The American Journal of Human Genetics. 106(5). 611–622. 28 indexed citations

McInnes, Gregory, Adam Lavertu, Katrin Sangkuhl, et al.. (2020). Pharmacogenetics at Scale: An Analysis of the UK Biobank. Clinical Pharmacology & Therapeutics. 109(6). 1528–1537. 97 indexed citations

DeBoever, Christopher, Yosuke Tanigawa, Maléne E. Lindholm, et al.. (2018). Medical relevance of protein-truncating variants across 337,205 individuals in the UK Biobank study. Nature Communications. 9(1). 1612–1612. 61 indexed citations

10.

McInnes, Gregory, Yosuke Tanigawa, Adam Lavertu, et al.. (2018). Global Biobank Engine: enabling genotype-phenotype browsing for biobank summary statistics. Bioinformatics. 35(14). 2495–2497. 44 indexed citations

11.

Lavertu, Adam, Gregory McInnes, Roxana Daneshjou, et al.. (2018). Pharmacogenomics and big genomic data: from lab to clinic and back again. Human Molecular Genetics. 27(R1). R72–R78. 19 indexed citations

12.

Pan, Cuiping, Gregory McInnes, Nicole Deflaux, et al.. (2017). Cloud-based interactive analytics for terabytes of genomic variants data. Bioinformatics. 33(23). 3709–3715. 8 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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