Peter S. Braund

27.0k total citations
18 papers, 834 citations indexed

About

Peter S. Braund is a scholar working on Molecular Biology, Genetics and Physiology. According to data from OpenAlex, Peter S. Braund has authored 18 papers receiving a total of 834 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 6 papers in Genetics and 5 papers in Physiology. Recurrent topics in Peter S. Braund's work include Ion Transport and Channel Regulation (4 papers), Hormonal Regulation and Hypertension (3 papers) and Cytokine Signaling Pathways and Interactions (3 papers). Peter S. Braund is often cited by papers focused on Ion Transport and Channel Regulation (4 papers), Hormonal Regulation and Hypertension (3 papers) and Cytokine Signaling Pathways and Interactions (3 papers). Peter S. Braund collaborates with scholars based in United Kingdom, United States and Australia. Peter S. Braund's co-authors include Nilesh J. Samani, Massimo Mangino, Stuart M. Raleigh, John R. Thompson, Mariuca Vasa‐Nicotera, Scott Brouilette, Martin D. Tobin, Mark J. Caulfield, Paul R. Burton and Andrea H. Mason and has published in prestigious journals such as Circulation, Journal of the American College of Cardiology and Hypertension.

In The Last Decade

Peter S. Braund

18 papers receiving 817 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Peter S. Braund United Kingdom	15	324	278	173	171	169	18	834
Petra Tollet‐Egnell Sweden	17	368 1.1×	256 0.9×	106 0.6×	349 2.0×	91 0.5×	20	876
Mako Yasuda‒Yamahara Japan	15	246 0.8×	175 0.6×	45 0.3×	225 1.3×	69 0.4×	24	694
Sarah Anissa Hannou France	13	372 1.1×	305 1.1×	56 0.3×	399 2.3×	93 0.6×	18	934
Nobuhiko Wada Japan	13	210 0.6×	204 0.7×	67 0.4×	207 1.2×	43 0.3×	26	671
Susan D. Blas United States	15	442 1.4×	209 0.8×	90 0.5×	304 1.8×	58 0.3×	37	776
Sandra Slusher United States	7	359 1.1×	133 0.5×	62 0.4×	138 0.8×	48 0.3×	8	653
Weihui Yu China	17	399 1.2×	122 0.4×	105 0.6×	272 1.6×	162 1.0×	40	961
Yusuke Sakamaki Japan	14	409 1.3×	139 0.5×	94 0.5×	95 0.6×	89 0.5×	23	972
Anton Y. Postnov Russia	19	635 2.0×	102 0.4×	114 0.7×	33 0.2×	50 0.3×	70	940
Jakob Bondo Hansen Denmark	14	333 1.0×	288 1.0×	53 0.3×	142 0.8×	135 0.8×	23	893

Countries citing papers authored by Peter S. Braund

Since Specialization

Citations

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

Fields of papers citing papers by Peter S. Braund

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Peter S. Braund. 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 Peter S. Braund. The network helps show where Peter S. Braund may publish in the future.

Co-authorship network of co-authors of Peter S. Braund

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

All Works

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18 of 18 papers shown

Calabrese, Claudia, Angela Pyle, Helen Griffin, et al.. (2022). Heteroplasmic mitochondrial DNA variants in cardiovascular diseases. PLoS Genetics. 18(4). e1010068–e1010068. 17 indexed citations

Morris, G E, Peter S. Braund, J. Moore, et al.. (2017). Coronary Artery Disease–Associated LIPA Coding Variant rs1051338 Reduces Lysosomal Acid Lipase Levels and Activity in Lysosomes. Arteriosclerosis Thrombosis and Vascular Biology. 37(6). 1050–1057. 27 indexed citations

Erridge, Clett, Jay Gracey, Peter S. Braund, & Nilesh J. Samani. (2013). The 9p21 Locus Does Not Affect Risk of Coronary Artery Disease Through Induction of Type 1 Interferons. Journal of the American College of Cardiology. 62(15). 1376–1381. 12 indexed citations

Büsst, Cara, Lisa D.S. Bloomer, Katrina J. Scurrah, et al.. (2011). The Epithelial Sodium Channel γ-Subunit Gene and Blood Pressure. Hypertension. 58(6). 1073–1078. 17 indexed citations

Dick, Katherine, Christopher P. Nelson, Peter S. Braund, Alison H. Goodall, & Nilesh J. Samani. (2011). 69 Genome wide methylation analysis in coronary artery disease. Heart. 97(Suppl 1). A42.1–A42. 4 indexed citations

Smart, Melissa, Marius R. Robciuc, Jackie A. Cooper, et al.. (2010). The Relationship Between Plasma Angiopoietin-like Protein 4 Levels, Angiopoietin-like Protein 4 Genotype, and Coronary Heart Disease Risk. Arteriosclerosis Thrombosis and Vascular Biology. 30(11). 2277–2282. 64 indexed citations

Samani, Nilesh J., Peter S. Braund, Jeanette Erdmann, et al.. (2008). The novel genetic variant predisposing to coronary artery disease in the region of the PSRC1 and CELSR2 genes on chromosome 1 associates with serum cholesterol. Journal of Molecular Medicine. 86(11). 1233–1241. 72 indexed citations

Mangino, Massimo, Scott Brouilette, Peter S. Braund, et al.. (2008). A regulatory SNP of the BICD1 gene contributes to telomere length variation in humans. Human Molecular Genetics. 17(16). 2518–2523. 47 indexed citations

Maznyczka, Annette, Peter S. Braund, Massimo Mangino, & Nilesh J. Samani. (2008). Arachidonate 5-lipoxygenase (5-LO) promoter genotype and risk of myocardial infarction: A case–control study. Atherosclerosis. 199(2). 328–332. 21 indexed citations

10.

Tobin, Martin D., Maciej Tomaszewski, Peter S. Braund, et al.. (2008). Common Variants in Genes Underlying Monogenic Hypertension and Hypotension and Blood Pressure in the General Population. Hypertension. 51(6). 1658–1664. 75 indexed citations

11.

Bown, Matthew J., et al.. (2008). Association Between the Coronary Artery Disease Risk Locus on Chromosome 9p21.3 and Abdominal Aortic Aneurysm. Circulation Cardiovascular Genetics. 1(1). 39–42. 47 indexed citations

12.

Manunta, Paolo, Chiara Lanzani, Peter S. Braund, et al.. (2008). Physiological Interaction Between α-Adducin and WNK1-NEDD4L Pathways on Sodium-Related Blood Pressure Regulation. Hypertension. 52(2). 366–372. 68 indexed citations

13.

Maznyczka, Annette, Massimo Mangino, Andrew K. Whittaker, et al.. (2007). Leukotriene B4 production in healthy subjects carrying variants of the arachidonate 5-lipoxygenase-activating protein gene associated with a risk of myocardial infarction. Clinical Science. 112(7). 411–416. 15 indexed citations

14.

Mangino, Massimo, Peter S. Braund, Ravi K. Singh, et al.. (2007). Association analysis of IL-12B and IL-23R polymorphisms in myocardial infarction. Journal of Molecular Medicine. 86(1). 99–103. 17 indexed citations

15.

Nsengimana, Jérémie, Mark M. Iles, Alistair S. Hall, et al.. (2006). Enhanced linkage of a locus on chromosome 2 to premature coronary artery disease in the absence of hypercholesterolemia. European Journal of Human Genetics. 15(3). 313–319. 13 indexed citations

16.

Mangino, Massimo, Peter S. Braund, Ravi Singh, et al.. (2006). LGALS2 functional variant rs7291467 is not associated with susceptibility to myocardial infarction in Caucasians. Atherosclerosis. 194(1). 112–115. 15 indexed citations

17.

Tobin, Martin D., Stuart M. Raleigh, Stephen Newhouse, et al.. (2005). Association of WNK1 Gene Polymorphisms and Haplotypes With Ambulatory Blood Pressure in the General Population. Circulation. 112(22). 3423–3429. 97 indexed citations

18.

Vasa‐Nicotera, Mariuca, Scott Brouilette, Massimo Mangino, et al.. (2004). Mapping of a Major Locus that Determines Telomere Length in Humans. The American Journal of Human Genetics. 76(1). 147–151. 206 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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