Mitzi L. Murray

2.9k total citations
13 papers, 467 citations indexed

About

Mitzi L. Murray is a scholar working on Genetics, Molecular Biology and Rheumatology. According to data from OpenAlex, Mitzi L. Murray has authored 13 papers receiving a total of 467 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Genetics, 7 papers in Molecular Biology and 3 papers in Rheumatology. Recurrent topics in Mitzi L. Murray's work include Connective tissue disorders research (7 papers), Dermatological and Skeletal Disorders (3 papers) and Genomics and Rare Diseases (2 papers). Mitzi L. Murray is often cited by papers focused on Connective tissue disorders research (7 papers), Dermatological and Skeletal Disorders (3 papers) and Genomics and Rare Diseases (2 papers). Mitzi L. Murray collaborates with scholars based in United States, United Kingdom and Austria. Mitzi L. Murray's co-authors include Peter H. Byers, Melanie Pepin, Robin L. Bennett, Gail P. Jarvik, Suzanne E. Peterson, Ruslan I. Sadreyev, Hensin Tsao, Jamison D. Feramisco, Nick V. Grishin and Ulrike Schwarze and has published in prestigious journals such as The American Journal of Human Genetics, Journal of Investigative Dermatology and Acta Neuropathologica.

In The Last Decade

Mitzi L. Murray

13 papers receiving 455 citations

Peers

Mitzi L. Murray
Anthony Vandersteen United Kingdom
Anita Wischmeijer Italy
Silvia Majore Italy
Harikiran Nistala United States
Robin Schwartz United States
B Lee United States
Vanesa López‐González Spain
Hermine E. Veenstra‐Knol Netherlands
Valerie M. Carlberg United States
Neeti Ghali United Kingdom
Anthony Vandersteen United Kingdom
Mitzi L. Murray
Citations per year, relative to Mitzi L. Murray Mitzi L. Murray (= 1×) peers Anthony Vandersteen

Countries citing papers authored by Mitzi L. Murray

Since Specialization
Citations

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

Fields of papers citing papers by Mitzi L. Murray

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Mitzi L. Murray. 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 Mitzi L. Murray. The network helps show where Mitzi L. Murray may publish in the future.

Co-authorship network of co-authors of Mitzi L. Murray

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

All Works

13 of 13 papers shown
1.
Olson, Sydney L., Mitzi L. Murray, & Nedaa Skeik. (2019). A Novel Frameshift COL3A1 Variant in Vascular Ehlers-Danlos Syndrome. Annals of Vascular Surgery. 61. 472.e9–472.e13. 3 indexed citations
2.
Osbun, Joshua W., Philip D. Tatman, Luis F. Gonzalez‐Cuyar, et al.. (2019). Somatic PDGFRB Activating Variants in Fusiform Cerebral Aneurysms. The American Journal of Human Genetics. 104(5). 968–976. 26 indexed citations
3.
Shalhub, Sherene, Gabriel S. Aldea, Peter H. Byers, et al.. (2017). Endovascular Repair of Internal Mammary Artery Aneurysms in 2 Sisters with SMAD3 Mutation. Annals of Vascular Surgery. 41. 283.e5–283.e9. 9 indexed citations
4.
5.
Pepin, Melanie, et al.. (2015). The challenge of comprehensive and consistent sequence variant interpretation between clinical laboratories. Genetics in Medicine. 18(1). 20–24. 44 indexed citations
6.
Murray, Mitzi L., Melanie Pepin, Suzanne E. Peterson, & Peter H. Byers. (2014). Pregnancy-related deaths and complications in women with vascular Ehlers–Danlos syndrome. Genetics in Medicine. 16(12). 874–880. 101 indexed citations
7.
Murray, Mitzi L., et al.. (2014). FKBP14‐related Ehlers‐Danlos syndrome: Expansion of the phenotype to include vascular complications. American Journal of Medical Genetics Part A. 164(7). 1750–1755. 18 indexed citations
8.
Byers, Peter H. & Mitzi L. Murray. (2013). Ehlers–Danlos syndrome: A showcase of conditions that lead to understanding matrix biology. Matrix Biology. 33. 10–15. 40 indexed citations
9.
Byers, Peter H. & Mitzi L. Murray. (2012). Heritable Collagen Disorders: The Paradigm of the Ehlers—Danlos Syndrome. Journal of Investigative Dermatology. 132(E1). E6–E11. 34 indexed citations
10.
Murray, Mitzi L., et al.. (2011). Follow-up of carriers of BRCA1 and BRCA2 variants of unknown significance: Variant reclassification and surgical decisions. Genetics in Medicine. 13(12). 998–1005. 110 indexed citations
11.
Juric‐Sekhar, Gordana, Raj P. Kapur, Ian A. Glass, et al.. (2010). Neuronal migration disorders in microcephalic osteodysplastic primordial dwarfism type I/III. Acta Neuropathologica. 121(4). 545–554. 16 indexed citations
12.
Feramisco, Jamison D., Ruslan I. Sadreyev, Mitzi L. Murray, Nick V. Grishin, & Hensin Tsao. (2009). Phenotypic and Genotypic Analyses of Genetic Skin Disease through the Online Mendelian Inheritance in Man (OMIM) Database. Journal of Investigative Dermatology. 129(11). 2628–2636. 51 indexed citations
13.
Johnson, Kelly S., et al.. (2002). Temporal modulation of pyrrolizidine alkaloid intake and genetic variation in performance of Utetheisa ornatrix caterpillars.. Journal of Chemical Ecology. 28(4). 669–685. 8 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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