Noël P. Burtt

28.3k total citations
26 papers, 2.0k citations indexed

About

Noël P. Burtt is a scholar working on Genetics, Molecular Biology and Surgery. According to data from OpenAlex, Noël P. Burtt has authored 26 papers receiving a total of 2.0k indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Genetics, 13 papers in Molecular Biology and 6 papers in Surgery. Recurrent topics in Noël P. Burtt's work include Genetic Associations and Epidemiology (15 papers), Metabolism, Diabetes, and Cancer (4 papers) and Pancreatic function and diabetes (4 papers). Noël P. Burtt is often cited by papers focused on Genetic Associations and Epidemiology (15 papers), Metabolism, Diabetes, and Cancer (4 papers) and Pancreatic function and diabetes (4 papers). Noël P. Burtt collaborates with scholars based in United States, Sweden and Canada. Noël P. Burtt's co-authors include David Altshuler, Leif Groop, Joel N. Hirschhorn, Mark J. Daly, Candace Guiducci, Daniel Gaudet, Sekar Kathiresan, Thomas J. Hudson, Olle Melander and Marju Orho‐Melander and has published in prestigious journals such as New England Journal of Medicine, Nature Communications and Nature Genetics.

In The Last Decade

Noël P. Burtt

25 papers receiving 2.0k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Noël P. Burtt United States 18 923 896 485 363 246 26 2.0k
Kimihiko Kato Japan 26 829 0.9× 406 0.5× 289 0.6× 255 0.7× 162 0.7× 83 1.9k
Ottavia Porzio Italy 30 1.1k 1.2× 424 0.5× 796 1.6× 848 2.3× 430 1.7× 97 2.6k
Emma Ahlqvist Sweden 25 658 0.7× 543 0.6× 535 1.1× 695 1.9× 259 1.1× 75 1.8k
Elisabeth Widén Finland 22 922 1.0× 543 0.6× 625 1.3× 740 2.0× 526 2.1× 29 2.5k
Marc Délepine France 21 1.5k 1.7× 1.1k 1.2× 859 1.8× 529 1.5× 505 2.1× 28 3.2k
Jun Nakura Japan 25 1.9k 2.0× 506 0.6× 208 0.4× 441 1.2× 512 2.1× 71 3.2k
Kiyoshi Yokoi Japan 23 541 0.6× 227 0.3× 269 0.6× 208 0.6× 131 0.5× 63 1.4k
Carl G. Brewer Canada 8 1.1k 1.2× 726 0.8× 378 0.8× 269 0.7× 470 1.9× 9 1.9k
Stefan-Martin Herrmann Germany 21 478 0.5× 277 0.3× 220 0.5× 398 1.1× 307 1.2× 24 1.9k
Stéphane Cauchi France 26 973 1.1× 1.2k 1.3× 516 1.1× 602 1.7× 357 1.5× 42 2.4k

Countries citing papers authored by Noël P. Burtt

Since Specialization
Citations

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

Fields of papers citing papers by Noël P. Burtt

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Noël P. Burtt. 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 Noël P. Burtt. The network helps show where Noël P. Burtt may publish in the future.

Co-authorship network of co-authors of Noël P. Burtt

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

All Works

20 of 20 papers shown
1.
Costanzo, Maria C., et al.. (2025). Realizing the promise of genome-wide association studies for effector gene prediction. Nature Genetics. 57(7). 1578–1587. 2 indexed citations
2.
Han, Seong Kyu, Michelle T. McNulty, Christopher J. Benway, et al.. (2023). Mapping genomic regulation of kidney disease and traits through high-resolution and interpretable eQTLs. Nature Communications. 14(1). 2229–2229. 11 indexed citations
3.
Mejhert, Niklas, Katlyn R. Gabriel, Scott Frendo‐Cumbo, et al.. (2022). The Lipid Droplet Knowledge Portal: A resource for systematic analyses of lipid droplet biology. Developmental Cell. 57(3). 387–397.e4. 54 indexed citations
4.
Forgetta, Vincenzo, Lai Jiang, Nicholas A. Vulpescu, et al.. (2022). An effector index to predict target genes at GWAS loci. Human Genetics. 141(8). 1431–1447. 28 indexed citations
5.
Westendorf, Jennifer J., Lynda F. Bonewald, Douglas P. Kiel, & Noël P. Burtt. (2021). The Musculoskeletal Knowledge Portal: improving access to multi-omics data. Nature Reviews Rheumatology. 18(1). 1–2. 8 indexed citations
6.
Shea, Jessica, Vineeta Agarwala, Anthony Philippakis, et al.. (2011). Comparing strategies to fine-map the association of common SNPs at chromosome 9p21 with type 2 diabetes and myocardial infarction. Nature Genetics. 43(8). 801–805. 65 indexed citations
7.
Guey, Lin T., Jasmina Kravić, Olle Melander, et al.. (2011). Power in the phenotypic extremes: a simulation study of power in discovery and replication of rare variants. Genetic Epidemiology. 35(4). 236–246. 78 indexed citations
8.
Burtt, Noël P.. (2011). Whole-Genome Amplification Using Φ29 DNA Polymerase. Cold Spring Harbor Protocols. 2011(1). pdb.prot5552–pdb.prot5552. 4 indexed citations
9.
Calvo, Sarah E., Elena J. Tucker, Alison G. Compton, et al.. (2010). High-throughput, pooled sequencing identifies mutations in NUBPL and FOXRED1 in human complex I deficiency. Nature Genetics. 42(10). 851–858. 279 indexed citations
10.
Keebler, Mary, Rahul C. Deo, Aarti Surti, et al.. (2010). Fine-Mapping in African Americans of 8 Recently Discovered Genetic Loci for Plasma Lipids. Circulation Cardiovascular Genetics. 3(4). 358–364. 22 indexed citations
11.
Cheng, Iona, Daniel O. Stram, Noël P. Burtt, et al.. (2009). IGF2R Missense Single-Nucleotide Polymorphisms and Breast Cancer Risk: The Multiethnic Cohort Study. Cancer Epidemiology Biomarkers & Prevention. 18(6). 1922–1924. 9 indexed citations
12.
Keebler, Mary, Christopher Sanders, Aarti Surti, et al.. (2009). Association of Blood Lipids With Common DNA Sequence Variants at 19 Genetic Loci in the Multiethnic United States National Health and Nutrition Examination Survey III. Circulation Cardiovascular Genetics. 2(3). 238–243. 45 indexed citations
13.
Kathiresan, Sekar, Olle Melander, Dragi Anevski, et al.. (2008). Polymorphisms Associated with Cholesterol and Risk of Cardiovascular Events. New England Journal of Medicine. 358(12). 1240–1249. 494 indexed citations
14.
Florez, José C., Magnus Sjögren, Christina M. Agapakis, et al.. (2007). Association testing of common variants in the insulin receptor substrate-1 gene (IRS1) with type 2 diabetes. Diabetologia. 50(6). 1209–1217. 8 indexed citations
15.
Lee, Sulggi A., Christopher A. Haiman, Noël P. Burtt, et al.. (2007). A comprehensive analysis of common genetic variation in prolactin (PRL) and PRL receptor (PRLR) genes in relation to plasma prolactin levels and breast cancer risk: the Multiethnic Cohort. BMC Medical Genetics. 8(1). 72–72. 38 indexed citations
16.
Saxena, Richa, Paul I.W. de Bakker, Vamsi K. Mootha, et al.. (2006). Comprehensive Association Testing of Common Mitochondrial DNA Variation in Metabolic Disease. The American Journal of Human Genetics. 79(1). 54–61. 150 indexed citations
17.
Lee, Jennifer Y., Paul I.W. de Bakker, Noël P. Burtt, et al.. (2006). Haplotype Structures and Large-Scale Association Testing of the 5′ AMP-Activated Protein Kinase Genes PRKAA2, PRKAB1, and PRKAB2 With Type 2 Diabetes. Diabetes. 55(3). 849–855. 21 indexed citations
18.
Setiawan, Veronica Wendy, Iona Cheng, Daniel O. Stram, et al.. (2006). A Systematic Assessment of Common Genetic Variation in CYP11A and Risk of Breast Cancer. Cancer Research. 66(24). 12019–12025. 16 indexed citations
19.
Engert, James C., Marie‐Claude Vohl, Scott M. Williams, et al.. (2002). 5′ Flanking Variants of Resistin Are Associated With Obesity. Diabetes. 51(5). 1629–1634. 138 indexed citations
20.
Hirschhorn, Joel N., Cecilia M. Lindgren, Mark J. Daly, et al.. (2001). Genomewide Linkage Analysis of Stature in Multiple Populations Reveals Several Regions with Evidence of Linkage to Adult Height. The American Journal of Human Genetics. 69(1). 106–116. 153 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Kimihiko Kato Breakdown of academic impact, for papers by Ottavia Porzio Breakdown of academic impact, for papers by Emma Ahlqvist Breakdown of academic impact, for papers by Elisabeth Widén Breakdown of academic impact, for papers by Marc Délepine Breakdown of academic impact, for papers by Jun Nakura Breakdown of academic impact, for papers by Kiyoshi Yokoi Breakdown of academic impact, for papers by Carl G. Brewer Breakdown of academic impact, for papers by Stefan-Martin Herrmann Breakdown of academic impact, for papers by Stéphane Cauchi
Rankless by CCL
2026