Brett H. Graham

11.3k total citations · 1 hit paper
91 papers, 4.6k citations indexed

About

Brett H. Graham is a scholar working on Molecular Biology, Clinical Biochemistry and Genetics. According to data from OpenAlex, Brett H. Graham has authored 91 papers receiving a total of 4.6k indexed citations (citations by other indexed papers that have themselves been cited), including 74 papers in Molecular Biology, 33 papers in Clinical Biochemistry and 20 papers in Genetics. Recurrent topics in Brett H. Graham's work include Mitochondrial Function and Pathology (47 papers), Metabolism and Genetic Disorders (33 papers) and ATP Synthase and ATPases Research (18 papers). Brett H. Graham is often cited by papers focused on Mitochondrial Function and Pathology (47 papers), Metabolism and Genetic Disorders (33 papers) and ATP Synthase and ATPases Research (18 papers). Brett H. Graham collaborates with scholars based in United States, Canada and Germany. Brett H. Graham's co-authors include Douglas C. Wallace, William J. Craigen, Hugo J. Bellen, Manish Jaiswal, Zhihong Li, Shinya Yamamoto, Taraka Donti, Héctor Sandoval, Ke Zhang and Barbara A. Cottrell and has published in prestigious journals such as Cell, Journal of Biological Chemistry and Nature Communications.

In The Last Decade

Brett H. Graham

91 papers receiving 4.5k citations

Hit Papers

Glial Lipid Droplets and ... 2015 2026 2018 2022 2015 200 400 600

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Brett H. Graham United States 36 3.3k 1.0k 835 574 525 91 4.6k
Aurora Pujol Spain 41 3.3k 1.0× 713 0.7× 1.5k 1.8× 472 0.8× 415 0.8× 114 4.6k
Carlo Viscomi Italy 40 4.4k 1.3× 1.6k 1.5× 810 1.0× 245 0.4× 713 1.4× 94 5.8k
Francisca Díaz United States 34 2.9k 0.9× 687 0.7× 699 0.8× 318 0.6× 713 1.4× 63 4.4k
Rolf Wibom Sweden 38 5.5k 1.7× 1.6k 1.5× 1.5k 1.7× 376 0.7× 535 1.0× 80 6.8k
Sonja Forss‐Petter Austria 30 2.8k 0.8× 362 0.3× 924 1.1× 300 0.5× 775 1.5× 59 4.1k
Myriam Baes Belgium 44 4.5k 1.4× 778 0.7× 1.4k 1.7× 515 0.9× 499 1.0× 148 6.8k
Araceli del Arco Spain 32 2.2k 0.7× 930 0.9× 484 0.6× 230 0.4× 685 1.3× 70 3.0k
Johannes N. Spelbrink Finland 40 6.6k 2.0× 2.6k 2.5× 968 1.2× 414 0.7× 645 1.2× 69 7.5k
Nigel T. Price United Kingdom 27 2.5k 0.8× 535 0.5× 746 0.9× 243 0.4× 421 0.8× 55 3.7k
Akos A. Gerencser United States 32 3.4k 1.0× 435 0.4× 1.4k 1.7× 183 0.3× 768 1.5× 58 5.0k

Countries citing papers authored by Brett H. Graham

Since Specialization
Citations

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

Fields of papers citing papers by Brett H. Graham

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Brett H. Graham. 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 Brett H. Graham. The network helps show where Brett H. Graham may publish in the future.

Co-authorship network of co-authors of Brett H. Graham

This figure shows the co-authorship network connecting the top 25 collaborators of Brett H. Graham. A scholar is included among the top collaborators of Brett H. Graham 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 Brett H. Graham. Brett H. Graham 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.
Lancaster, M., Paul S. Hafen, Andrew Law, et al.. (2024). Sucla2 Knock‐Out in Skeletal Muscle Yields Mouse Model of Mitochondrial Myopathy With Muscle Type–Specific Phenotypes. Journal of Cachexia Sarcopenia and Muscle. 15(6). 2729–2742. 1 indexed citations
2.
Kubal, Chandrashekhar A., et al.. (2024). Successful Sequential Liver and Isolated Intestine Transplantation for Mitochondrial Neurogastrointestinal Encephalopathy Syndrome: A Case Report. Annals of Transplantation. 29. e941881–e941881. 1 indexed citations
3.
Dickson, Alexa, Marcus J. Miller, Elaine Spector, et al.. (2023). Specifications of the ACMG/AMP guidelines for ACADVL variant interpretation. Molecular Genetics and Metabolism. 140(3). 107668–107668. 1 indexed citations
4.
Lancaster, M. & Brett H. Graham. (2023). Succinyl-CoA Synthetase Dysfunction as a Mechanism of Mitochondrial Encephalomyopathy: More than Just an Oxidative Energy Deficit. International Journal of Molecular Sciences. 24(13). 10725–10725. 15 indexed citations
5.
Pradhan, Geetali, Jong Han Lee, Chia‐Shan Wu, et al.. (2022). Mechanistic Investigation of GHS-R Mediated Glucose-Stimulated Insulin Secretion in Pancreatic Islets. Biomolecules. 12(3). 407–407. 4 indexed citations
6.
Wilcox, Jennifer, Sarah M. Skye, Brett H. Graham, et al.. (2021). Dietary Choline Supplements, but Not Eggs, Raise Fasting TMAO Levels in Participants with Normal Renal Function: A Randomized Clinical Trial. The American Journal of Medicine. 134(9). 1160–1169.e3. 22 indexed citations
7.
Emmerzaal, Tim L., Graeme Preston, Bram Geenen, et al.. (2020). Impaired mitochondrial complex I function as a candidate driver in the biological stress response and a concomitant stress-induced brain metabolic reprogramming in male mice. Translational Psychiatry. 10(1). 176–176. 35 indexed citations
8.
Burrage, Lindsay C., Bridget M. Stroup, Qin Sun, et al.. (2019). Untargeted metabolomic profiling reveals multiple pathway perturbations and new clinical biomarkers in urea cycle disorders. Genetics in Medicine. 21(9). 1977–1986. 46 indexed citations
9.
Lalani, Seema R., Brett H. Graham, Lindsay C. Burrage, et al.. (2018). TANGO2-Related Metabolic Encephalopathy and Arrhythmias. 7 indexed citations
10.
Pillai, Nishitha R., Rossana Sanchez Russo, Anne O’Donnell‐Luria, et al.. (2018). Megaloblastic Anemia Progressing to Severe Thrombotic Microangiopathy in Patients with Disordered Vitamin B12 Metabolism: Case Reports and Literature Review. The Journal of Pediatrics. 202. 315–319.e2. 5 indexed citations
11.
Bainbridge, Matthew N., Erin Cooney, Marcus J. Miller, et al.. (2017). Analyses of SLC13A5 -epilepsy patients reveal perturbations of TCA cycle. Molecular Genetics and Metabolism. 121(4). 314–319. 47 indexed citations
12.
Wangler, Michael F., Vafa Bayat, Νικόλαος Γιαγτζόγλου, et al.. (2017). Peroxisomal biogenesis is genetically and biochemically linked to carbohydrate metabolism in Drosophila and mouse. PLoS Genetics. 13(6). e1006825–e1006825. 32 indexed citations
13.
Wu, San‐Pin, Chad J. Creighton, Yang Jin, et al.. (2015). Increased COUP-TFII expression in adult hearts induces mitochondrial dysfunction resulting in heart failure. RePEc: Research Papers in Economics. 1 indexed citations
14.
Bainbridge, Matthew N., Hao Hu, Donna M. Muzny, et al.. (2013). De novo truncating mutations in ASXL3 are associated with a novel clinical phenotype with similarities to Bohring-Opitz syndrome. Genome Medicine. 5(2). 11–11. 102 indexed citations
15.
Bayat, Vafa, Isabelle Thiffault, Manish Jaiswal, et al.. (2012). Mutations in the Mitochondrial Methionyl-tRNA Synthetase Cause a Neurodegenerative Phenotype in Flies and a Recessive Ataxia (ARSAL) in Humans. PLoS Biology. 10(3). e1001288–e1001288. 121 indexed citations
16.
Sheiko, Tatiana, et al.. (2011). Voltage-dependant anion channels: Novel insights into isoform function through genetic models. Biochimica et Biophysica Acta (BBA) - Biomembranes. 1818(6). 1477–1485. 72 indexed citations
17.
Rea, Shane L., Brett H. Graham, Eiko Nakamaru‐Ogiso, Adwitiya Kar, & Marni J. Falk. (2010). Bacteria, yeast, worms, and flies: Exploiting simple model organisms to investigate human mitochondrial diseases. PubMed. 16(2). 200–218. 47 indexed citations
18.
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
19.
Sano, Motoaki, Yasukatsu Izumi, Katja Helenius, et al.. (2007). Ménage-à-Trois 1 Is Critical for the Transcriptional Function of PPARγ Coactivator 1. Cell Metabolism. 5(2). 129–142. 50 indexed citations
20.
Graham, Brett H. & Carlos A. Bacino. (2003). Male patient with non‐mosaic deleted Y‐chromosome and clinical features of Turner syndrome. American Journal of Medical Genetics Part A. 119A(2). 234–237. 6 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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