Renata C. Gallagher

2.2k total citations
26 papers, 881 citations indexed

About

Renata C. Gallagher is a scholar working on Molecular Biology, Clinical Biochemistry and Rheumatology. According to data from OpenAlex, Renata C. Gallagher has authored 26 papers receiving a total of 881 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Molecular Biology, 16 papers in Clinical Biochemistry and 7 papers in Rheumatology. Recurrent topics in Renata C. Gallagher's work include Metabolism and Genetic Disorders (16 papers), Folate and B Vitamins Research (7 papers) and Mitochondrial Function and Pathology (6 papers). Renata C. Gallagher is often cited by papers focused on Metabolism and Genetic Disorders (16 papers), Folate and B Vitamins Research (7 papers) and Mitochondrial Function and Pathology (6 papers). Renata C. Gallagher collaborates with scholars based in United States, Netherlands and Germany. Renata C. Gallagher's co-authors include Johan L.K. Van Hove, Mohammed Al Balwi, Uta Francke, Birgit Pils, Aashish N. Adhikari, Curtis R. Coughlin, Elizabeth H. Blackburn, Stephen I. Goodman, Jerry Vockley and Gunter Scharer and has published in prestigious journals such as Proceedings of the National Academy of Sciences, SHILAP Revista de lepidopterología and PLoS ONE.

In The Last Decade

Renata C. Gallagher

25 papers receiving 860 citations

Peers

Renata C. Gallagher

GENET

PPCH

RHEUM

Shlomo Almashanu Israel

Zuhair N. Al‐Hassnan Saudi Arabia

Alice Masurel‐Paulet France

Shawn E. McCandless United States

Jim McGill Australia

Libor Kozák Czechia

K. Narisawa Japan

Jean Rey France

T. Ohura Japan

Hélène Ogier France

Shlomo Almashanu Israel

Renata C. Gallagher

390 ×0.8

271 ×0.7

136 ×0.5

GENET

134 ×0.7

PPCH

67 ×0.6

RHEUM

Citations per year, relative to Renata C. Gallagher Renata C. Gallagher (= 1×) peers Shlomo Almashanu

Countries citing papers authored by Renata C. Gallagher

Since Specialization

Citations

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

Fields of papers citing papers by Renata C. Gallagher

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Renata C. Gallagher. 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 Renata C. Gallagher. The network helps show where Renata C. Gallagher may publish in the future.

Co-authorship network of co-authors of Renata C. Gallagher

This figure shows the co-authorship network connecting the top 25 collaborators of Renata C. Gallagher. A scholar is included among the top collaborators of Renata C. Gallagher 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 Renata C. Gallagher. Renata C. Gallagher 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

McInnes, Gregory, Julia E. H. Brown, Neil Thomas, et al.. (2022). Functional genomics of OCTN2 variants informs protein-specific variant effect predictor for Carnitine Transporter Deficiency. Proceedings of the National Academy of Sciences. 119(46). e2210247119–e2210247119. 12 indexed citations

Shieh, Joseph T.C., K. Wong, Michal Levy‐Sakin, et al.. (2021). Application of full-genome analysis to diagnose rare monogenic disorders. npj Genomic Medicine. 6(1). 77–77. 29 indexed citations

Gallagher, Renata C., et al.. (2021). The Use of Whole Genome and Exome Sequencing for Newborn Screening: Challenges and Opportunities for Population Health. Frontiers in Pediatrics. 9. 663752–663752. 55 indexed citations

McInnes, Gregory, Andrew G. Sharo, Julia E. H. Brown, et al.. (2021). Opportunities and challenges for the computational interpretation of rare variation in clinically important genes. The American Journal of Human Genetics. 108(4). 535–548. 38 indexed citations

Gallagher, Renata C., et al.. (2018). Laboratory analysis of organic acids, 2018 update: a technical standard of the American College of Medical Genetics and Genomics (ACMG). Genetics in Medicine. 20(7). 683–691. 31 indexed citations

Mendelsohn, Bryce A., Jacque L. Duncan, Anthony T. Moore, et al.. (2018). Cobalamin D Deficiency Identified Through Newborn Screening. JIMD Reports. 44. 73–77. 6 indexed citations

Stabler, Sally P., et al.. (2017). Potential Misdiagnosis of Hyperhomocysteinemia due to Cystathionine Beta-Synthase Deficiency During Pregnancy. JIMD Reports. 37. 55–61. 1 indexed citations

Karnebeek, Clara van, J.M.F. Niermeijer, Bwee Tien Poll‐The, et al.. (2016). Pyridoxine-Dependent Epilepsy: An Expanding Clinical Spectrum. Pediatric Neurology. 59. 6–12. 108 indexed citations

Greene, Carol L., Erin T. Strovel, Elaine Spector, et al.. (2016). The M405V allele of the glutaryl-CoA dehydrogenase gene is an important marker for glutaric aciduria type I (GA-I) low excretors. Molecular Genetics and Metabolism. 119(1-2). 50–56. 11 indexed citations

10.

Laemmle, Alexander, Renata C. Gallagher, Adrian Keogh, et al.. (2016). Frequency and Pathophysiology of Acute Liver Failure in Ornithine Transcarbamylase Deficiency (OTCD). PLoS ONE. 11(4). e0153358–e0153358. 37 indexed citations

11.

Chatfield, Kathryn C., Curtis R. Coughlin, Marisa W. Friederich, et al.. (2015). Mitochondrial energy failure in HSD10 disease is due to defective mtDNA transcript processing. Mitochondrion. 21. 1–10. 45 indexed citations

12.

Gelfand, Amy A. & Renata C. Gallagher. (2015). Cyclic vomiting syndrome versus inborn errors of metabolism: A review with clinical recommendations. Headache The Journal of Head and Face Pain. 56(1). 215–221. 20 indexed citations

13.

Quadros, Edward V., Yasumi Nakayama, Jeffrey M. Sequeira, et al.. (2010). Positive newborn screen for methylmalonic aciduria identifies the first mutation in TCblR/CD320, the gene for cellular uptake of transcobalamin-bound vitamin B12. Human Mutation. 31(8). 924–929. 49 indexed citations

14.

Scharer, Gunter, Chad Brocker, Vasilis Vasiliou, et al.. (2010). The genotypic and phenotypic spectrum of pyridoxine‐dependent epilepsy due to mutations in ALDH7A1. Journal of Inherited Metabolic Disease. 33(5). 571–581. 70 indexed citations

15.

Urban, Thomas, Renata C. Gallagher, Chaline Brown, et al.. (2006). Functional Genetic Diversity in the High-Affinity Carnitine Transporter OCTN2 (SLC22A5). Molecular Pharmacology. 70(5). 1602–1611. 42 indexed citations

16.

Adam, Margaret P, Susan Schelley, Renata C. Gallagher, et al.. (2006). Clinical features and management issues in Mowat–Wilson syndrome. American Journal of Medical Genetics Part A. 140A(24). 2730–2741. 68 indexed citations

17.

Gallagher, Renata C., Tina M. Cowan, Stephen I. Goodman, & Gregory M. Enns. (2005). Glutaryl-CoA dehydrogenase deficiency and newborn screening: Retrospective analysis of a low excretor provides further evidence that some cases may be missed. Molecular Genetics and Metabolism. 86(3). 417–420. 35 indexed citations

18.

Gallagher, Renata C., Birgit Pils, Mohammed Al Balwi, & Uta Francke. (2002). Evidence for the Role of PWCR1/HBII-85 C/D Box Small Nucleolar RNAs in Prader-Willi Syndrome. The American Journal of Human Genetics. 71(3). 669–678. 97 indexed citations

19.

Gallagher, Renata C., et al.. (1995). Replication of an rRNA Gene Origin Plasmid in the Tetrahymena thermophila Macronucleus is Prevented by Transcription through the Origin from an RNA Polymerase I Promoter. Molecular and Cellular Biology. 15(6). 3372–3381. 23 indexed citations

20.

Gallagher, Renata C., Jay Mehta, Rodney H. Adkins, Edward M. Copeland, & T. James Gallagher. (1984). THE EFFECTS OF FAT EMULSION ON HEMODYNAMICS, GAS EXCHANGE, AND EXTRAVASCULAR LUNG WATER IN ADULT RESPIRATORY DISTRESS SYNDROME. Anesthesiology. 61(3). A116–A116. 1 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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