Ariel Brautbar

1.9k total citations
39 papers, 1.0k citations indexed

About

Ariel Brautbar is a scholar working on Surgery, Molecular Biology and Genetics. According to data from OpenAlex, Ariel Brautbar has authored 39 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Surgery, 16 papers in Molecular Biology and 13 papers in Genetics. Recurrent topics in Ariel Brautbar's work include Lipoproteins and Cardiovascular Health (15 papers), Genetic Associations and Epidemiology (10 papers) and Cancer, Lipids, and Metabolism (5 papers). Ariel Brautbar is often cited by papers focused on Lipoproteins and Cardiovascular Health (15 papers), Genetic Associations and Epidemiology (10 papers) and Cancer, Lipids, and Metabolism (5 papers). Ariel Brautbar collaborates with scholars based in United States, Israel and Canada. Ariel Brautbar's co-authors include Christie M. Ballantyne, Eric Boerwinkle, Salim S. Virani, Vijay Nambi, Aaron R. Folsom, Ron C. Hoogeveen, Thomas H. Mosley, Diane Catellier, Brian Davis and Josef Coresh and has published in prestigious journals such as Circulation, Journal of the American College of Cardiology and PLoS ONE.

In The Last Decade

Ariel Brautbar

38 papers receiving 978 citations

Peers

Ariel Brautbar
Sumeet A. Khetarpal United States
Fabienne Nigon France
Jacqueline S. Dron Canada
Mayumi Ishikawa Japan
Dong‐Feng Wu China
G. Tibolla Italy
Hélène Dehondt France
Christophe Marçais France
Glenda D. Talley United States
Junichiro Tohyama United States
Sumeet A. Khetarpal United States
Ariel Brautbar
Citations per year, relative to Ariel Brautbar Ariel Brautbar (= 1×) peers Sumeet A. Khetarpal

Countries citing papers authored by Ariel Brautbar

Since Specialization
Citations

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

Fields of papers citing papers by Ariel Brautbar

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ariel Brautbar

This figure shows the co-authorship network connecting the top 25 collaborators of Ariel Brautbar. A scholar is included among the top collaborators of Ariel Brautbar 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 Ariel Brautbar. Ariel Brautbar 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.
Cui, Hong, Joseph M. Devaney, Xinyue Liu, et al.. (2021). Interference of nuclear mitochondrial DNA segments in mitochondrial DNA testing resembles biparental transmission of mitochondrial DNA in humans. Genetics in Medicine. 23(8). 1514–1521. 9 indexed citations
2.
Brautbar, Ariel, et al.. (2015). Genetics of Familial Hypercholesterolemia. Current Atherosclerosis Reports. 17(4). 491–491. 61 indexed citations
3.
O’Brien, Sarah, Steven J. Schrodi, Zhan Ye, et al.. (2015). Differential Lipid Response to Statins Is Associated With Variants in the BUD13–APOA5 Gene Region. Journal of Cardiovascular Pharmacology. 66(2). 183–188. 5 indexed citations
4.
Ma, Li, Christie M. Ballantyne, Ariel Brautbar, & Alon Keinan. (2014). Analysis of Multiple Association Studies Provides Evidence of an Expression QTL Hub in Gene-Gene Interaction Network Affecting HDL Cholesterol Levels. PLoS ONE. 9(3). e92469–e92469. 10 indexed citations
5.
6.
Virani, Salim S., Vei‐Vei Lee, Ariel Brautbar, et al.. (2013). SINGLE NUCLEOTIDE POLYMORPHISMS IN CHOLESTERYL ESTER TRANSFER PROTEIN (CETP) GENE ARE NOT ASSOCIATED WITH RECURRENT CARDIOVASCULAR EVENTS OR MORTALITY IN PATIENTS WITH ESTABLISHED ATHEROSCLEROSIS: A MENDELIAN RANDOMIZATION EXPERIMENT. Journal of the American College of Cardiology. 61(10). E1391–E1391. 1 indexed citations
7.
Ma, Li, Ariel Brautbar, Eric Boerwinkle, et al.. (2012). Knowledge-Driven Analysis Identifies a Gene–Gene Interaction Affecting High-Density Lipoprotein Cholesterol Levels in Multi-Ethnic Populations. PLoS Genetics. 8(5). e1002714–e1002714. 58 indexed citations
8.
9.
Ma, Li, Christie M. Ballantyne, John W. Belmont, Alon Keinan, & Ariel Brautbar. (2012). Interaction between SNPs in the RXRA and near ANGPTL3 gene region inhibits apoB reduction after statin-fenofibric acid therapy in individuals with mixed dyslipidemia. Journal of Lipid Research. 53(11). 2425–2428. 13 indexed citations
10.
Negi, Smita, Ariel Brautbar, Salim S. Virani, et al.. (2012). A novel mutation in the ABCA1 gene causing an atypical phenotype of Tangier disease. Journal of clinical lipidology. 7(1). 82–87. 19 indexed citations
11.
Brautbar, Ariel, John W. Belmont, Salim S. Virani, et al.. (2011). Variants in the APOA5 gene region and the response to combination therapy with statins and fenofibric acid in a randomized clinical trial of individuals with mixed dyslipidemia. Atherosclerosis. 219(2). 737–742. 36 indexed citations
12.
Virani, Salim S., Ariel Brautbar, Vei-Vei Lee, et al.. (2011). Usefulness of Single Nucleotide Polymorphism in Chromosome 4q25 to Predict In-Hospital and Long-Term Development of Atrial Fibrillation and Survival in Patients Undergoing Coronary Artery Bypass Grafting. The American Journal of Cardiology. 107(10). 1504–1509. 21 indexed citations
13.
Nambi, Vijay, Kim Lawson, Ariel Brautbar, et al.. (2010). THE 9P21 GENETIC VARIANT IS ADDITIVE TO CAROTID INTIMA MEDIA THICKNESS AND PLAQUE IN IMPROVING CORONARY HEART DISEASE RISK PREDICTION IN WHITE PARTICIPANTS OF THE ATHEROSCLEROSIS RISK IN COMMUNITIES (ARIC) STUDY. Journal of the American College of Cardiology. 55(10). A155.E1454–A155.E1454. 1 indexed citations
14.
Brautbar, Ariel, Scott A. LeMaire, Luis M. Franco, et al.. (2010). FBN1 mutations in patients with descending thoracic aortic dissections. American Journal of Medical Genetics Part A. 152A(2). 413–416. 28 indexed citations
15.
Brautbar, Ariel, et al.. (2009). Is this the Coffin–Siris syndrome or the BOD syndrome?. American Journal of Medical Genetics Part A. 149A(3). 559–562. 5 indexed citations
16.
Brautbar, Ariel, Jing Wang, José E. Abdenur, et al.. (2008). The mitochondrial 13513G>A mutation is associated with Leigh disease phenotypes independent of complex I deficiency in muscle. Molecular Genetics and Metabolism. 94(4). 485–490. 35 indexed citations
17.
Wang, Jing, Ariel Brautbar, Fangyuan Li, et al.. (2008). Two mtDNA mutations 14487T>C (M63V, ND6) and 12297T>C (tRNA Leu) in a Leigh syndrome family. Molecular Genetics and Metabolism. 96(2). 59–65. 18 indexed citations
18.
Brautbar, Ariel, et al.. (2005). Fibromyalgia and Gaucher's disease. QJM. 99(2). 103–107. 5 indexed citations
19.
Brautbar, Ariel, Irith Hadas‐Halpern, Constantin Reinus, et al.. (2005). Menetrier??s disease presenting as an acute protein-losing gastroenteropathy in a 27-year-old man with Gaucher disease. European Journal of Gastroenterology & Hepatology. 17(6). 679–681. 5 indexed citations
20.
Brautbar, Ariel, et al.. (2003). Effect of enzyme replacement therapy on gammopathies in Gaucher disease. Blood Cells Molecules and Diseases. 32(1). 214–217. 57 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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