Andrew D. Paterson

37.0k total citations · 2 hit papers
329 papers, 12.9k citations indexed

About

Andrew D. Paterson is a scholar working on Genetics, Molecular Biology and Surgery. According to data from OpenAlex, Andrew D. Paterson has authored 329 papers receiving a total of 12.9k indexed citations (citations by other indexed papers that have themselves been cited), including 161 papers in Genetics, 107 papers in Molecular Biology and 46 papers in Surgery. Recurrent topics in Andrew D. Paterson's work include Genetic Associations and Epidemiology (66 papers), Diabetes and associated disorders (32 papers) and Genetics and Neurodevelopmental Disorders (30 papers). Andrew D. Paterson is often cited by papers focused on Genetic Associations and Epidemiology (66 papers), Diabetes and associated disorders (32 papers) and Genetics and Neurodevelopmental Disorders (30 papers). Andrew D. Paterson collaborates with scholars based in Canada, United States and United Kingdom. Andrew D. Paterson's co-authors include Ian Johnston, York Pei, Hubert H.M. Van Tol, Artūras Petronis, Vida Asghari, Suparna Sanyal, Vera Jovanović, Alpha S. Yap, Lei Sun and Shelley B. Bull and has published in prestigious journals such as Science, The Lancet and Journal of Biological Chemistry.

In The Last Decade

Andrew D. Paterson

320 papers receiving 12.6k citations

Hit Papers

align trajectories sort by overperformance

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Modulation of Intracellular Cyclic AMP Levels by Different Human Dopamine D4 Receptor Variants

1995 725 citations Andrew D. Paterson et al. profile →
Association of host genome with intestinal microbial composition in a large healthy cohort

2016 322 citations Osvaldo Espin‐Garcia, Andrew D. Paterson et al. profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Andrew D. Paterson Canada	59	5.2k	3.9k	1.1k	1.1k	1.0k	329	12.9k
Henry H. Heng United States	60	7.0k 1.4×	2.9k 0.7×	989 0.9×	1.2k 1.1×	1.3k 1.3×	202	11.8k
Aarno Palotie Finland	63	5.7k 1.1×	4.1k 1.0×	1.2k 1.1×	1.1k 1.0×	804 0.8×	334	14.9k
Thomas Meitinger Germany	69	11.2k 2.2×	5.5k 1.4×	779 0.7×	1.2k 1.1×	1.1k 1.1×	319	19.1k
Shrikant Mane United States	41	6.5k 1.3×	2.8k 0.7×	1.2k 1.0×	994 0.9×	419 0.4×	100	12.5k
Giuseppe Novelli Italy	61	8.1k 1.6×	2.2k 0.6×	765 0.7×	1.5k 1.4×	654 0.6×	636	15.5k
Keiichi Ozono Japan	55	4.2k 0.8×	2.3k 0.6×	1.4k 1.2×	902 0.8×	1.0k 1.0×	432	10.6k
Benjamin Tycko United States	59	9.1k 1.8×	4.0k 1.0×	1.7k 1.5×	768 0.7×	971 1.0×	171	14.7k
Michael A. Levine United States	69	6.3k 1.2×	4.9k 1.3×	2.3k 2.1×	2.3k 2.1×	824 0.8×	371	16.1k
Mariza de Andrade United States	60	4.0k 0.8×	2.9k 0.7×	2.1k 1.8×	1.3k 1.2×	236 0.2×	248	12.0k
Jeffrey C. Barrett United Kingdom	32	6.2k 1.2×	8.5k 2.2×	993 0.9×	2.0k 1.8×	612 0.6×	53	18.4k

Countries citing papers authored by Andrew D. Paterson

Since Specialization

Citations

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

Fields of papers citing papers by Andrew D. Paterson

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Andrew D. Paterson. 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 Andrew D. Paterson. The network helps show where Andrew D. Paterson may publish in the future.

Co-authorship network of co-authors of Andrew D. Paterson

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

All Works

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20 of 20 papers shown

Lu, Tianyuan, Wenmin Zhang, Cassianne Robinson‐Cohen, et al.. (2025). Characterization of gene–environment interactions for vitamin D through variance quantitative trait loci: a UK Biobank-based genetic epidemiology study. American Journal of Clinical Nutrition. 121(3). 731–740. 1 indexed citations

Cecil, Alexander, Cornelia Prehn, Dick Mul, et al.. (2024). Metabolomic associations of impaired awareness of hypoglycaemia in type 1 diabetes. Scientific Reports. 14(1). 4485–4485.

Gold, Nicholas D., Jingjing Cao, Dafna D. Gladman, et al.. (2023). Genetics of longitudinal kidney function in children and adults with systemic lupus erythematosus. Lara D. Veeken. 62(11). 3749–3756. 1 indexed citations

Brossard, Myriam, Andrew D. Paterson, Osvaldo Espin‐Garcia, Radu V. Craiu, & Shelley B. Bull. (2023). Characterization of direct and/or indirect genetic associations for multiple traits in longitudinal studies of disease progression. Genetics. 225(1). 2 indexed citations

Chen, D., et al.. (2023). Comprehensive whole-genome analyses of the UK Biobank reveal significant sex differences in both genotype missingness and allele frequency on the X chromosome. Human Molecular Genetics. 33(6). 543–551. 2 indexed citations

Paterson, Andrew D., et al.. (2023). The effect of ascertainment on penetrance estimates for rare variants: Implications for establishing pathogenicity and for genetic counselling. PLoS ONE. 18(9). e0290336–e0290336. 3 indexed citations

Shah, Mansi, Shaowei Qiu, Hui Li, et al.. (2022). Low c-Kit expression identifies primitive, therapy-resistant CML stem cells. JCI Insight. 8(1). 4 indexed citations

Sun, Lei, et al.. (2022). Major sex differences in allele frequencies for X chromosomal variants in both the 1000 Genomes Project and gnomAD. PLoS Genetics. 18(5). e1010231–e1010231. 14 indexed citations

Barua, Moumita & Andrew D. Paterson. (2021). Population-based studies reveal an additive role of type IV collagen variants in hematuria and albuminuria. Pediatric Nephrology. 37(2). 253–262. 11 indexed citations

10.

Ye, Xin, Nicole M. Roslin, Andrew D. Paterson, et al.. (2020). Linkage analysis identifies an isolated strabismus locus at 14q12 overlapping with FOXG1 syndrome region. Journal of Medical Genetics. 59(1). 46–55. 2 indexed citations

11.

Lanktree, Matthew B., Amirreza Haghighi, Elsa Guiard, et al.. (2018). Prevalence Estimates of Polycystic Kidney and Liver Disease by Population Sequencing. Journal of the American Society of Nephrology. 29(10). 2593–2600. 181 indexed citations

12.

Paterson, Andrew D.. (2017). HbA1c for type 2 diabetes diagnosis in Africans and African Americans: Personalized medicine NOW!. PLoS Medicine. 14(9). e1002384–e1002384. 10 indexed citations

13.

Eny, Karen, Trevor J. Orchard, Rachel G. Miller, et al.. (2015). Caffeine Consumption Contributes to Skin Intrinsic Fluorescence in Type 1 Diabetes. Diabetes Technology & Therapeutics. 17(10). 726–734. 16 indexed citations

14.

Hwang, Young‐Hwan, John Conklin, Winnie Chan, et al.. (2015). Refining Genotype-Phenotype Correlation in Autosomal Dominant Polycystic Kidney Disease. Journal of the American Society of Nephrology. 27(6). 1861–1868. 113 indexed citations

15.

Orchard, Trevor J., Wanjie Sun, Patricia A. Cleary, et al.. (2013). Haptoglobin Genotype and the Rate of Renal Function Decline in the Diabetes Control and Complications Trial/Epidemiology of Diabetes Interventions and Complications Study. Diabetes Care. 3 indexed citations

16.

Kenyon, D. M., V. Mulholland, J. Pickup, et al.. (2010). Development of a high-throughput method for the detection and species determination of PCN.. Aspects of applied biology. 13–16. 7 indexed citations

17.

Roslin, Nicole M., Jemila S. Hamid, Andrew D. Paterson, & Joseph Beyene. (2009). Genome-wide association analysis of cardiovascular-related quantitative traits in the Framingham Heart Study. BMC Proceedings. 3(S7). S117–S117. 11 indexed citations

18.

Bull, Shelley B., et al.. (2007). Bias reduction in genome-wide association studies with time-to-event phenotypes. Genetic Epidemiology. 31(6). 606. 4 indexed citations

19.

Stehbens, Samantha J., Andrew D. Paterson, Annette M. Shewan, et al.. (2006). Dynamic microtubules regulate the local concentration of E-cadherin at cell-cell contacts. Journal of Cell Science. 119(9). 1801–1811. 142 indexed citations

20.

Orlacchio, Antonio, Toshitaka Kawarai, Mario Polidoro, et al.. (2004). Lack of association between Alzheimer's disease and the promoter region polymorphisms of the nicastrin gene. Neuroscience Letters. 363(1). 49–53. 4 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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