Natasha Shur

2.3k total citations
40 papers, 543 citations indexed

About

Natasha Shur is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Molecular Biology. According to data from OpenAlex, Natasha Shur has authored 40 papers receiving a total of 543 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Genetics, 15 papers in Pediatrics, Perinatology and Child Health and 11 papers in Molecular Biology. Recurrent topics in Natasha Shur's work include Genomic variations and chromosomal abnormalities (7 papers), Metabolism and Genetic Disorders (6 papers) and Child and Adolescent Health (6 papers). Natasha Shur is often cited by papers focused on Genomic variations and chromosomal abnormalities (7 papers), Metabolism and Genetic Disorders (6 papers) and Child and Adolescent Health (6 papers). Natasha Shur collaborates with scholars based in United States, Poland and United Kingdom. Natasha Shur's co-authors include Susan T. Iannaccone, Kyriacos Markianos, Carlos Hidalgo, Pankaj B. Agrawal, Klaus Schmitz‐Abe, William G. Fairbrother, Henk Granzier, Rachel Soemedi, Lindsay C. Swanson and Nasim Vasli and has published in prestigious journals such as Neurology, PEDIATRICS and Radiology.

In The Last Decade

Natasha Shur

37 papers receiving 530 citations

Peers

Natasha Shur

GENET

CCM

GENET

Alice Masurel‐Paulet France

Rehab Ali Qatar

Emiliano González‐Vioque Spain

F. A. Beemer Netherlands

Monica H. Wojcik United States

Elena Procopio Italy

Esmée Oussoren Netherlands

Luigina Spaccini Italy

Hanna Faghfoury Canada

Dora Janeth Fonseca Colombia

Alice Masurel‐Paulet France

Natasha Shur

344 ×1.1

386 ×2.4

GENET

39 ×0.3

CCM

164 ×1.6

49 ×0.7

GENET

Citations per year, relative to Natasha Shur Natasha Shur (= 1×) peers Alice Masurel‐Paulet

Countries citing papers authored by Natasha Shur

Since Specialization

Citations

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

Fields of papers citing papers by Natasha Shur

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Natasha Shur

This figure shows the co-authorship network connecting the top 25 collaborators of Natasha Shur. A scholar is included among the top collaborators of Natasha Shur 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 Natasha Shur. Natasha Shur 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

Leon, Eyby, Natasha Shur, Kimberly A. Chapman, et al.. (2024). Death associated with brain herniation in classical MSUD patients from underrepresented populations. Molecular Genetics and Metabolism. 141(4). 108297–108297.

Flore, Leigh Anne, April Rasala Lehman, Natasha Shur, et al.. (2023). Clinical, biochemical and molecular characterization of 12 patients with pyruvate carboxylase deficiency treated with triheptanoin. Molecular Genetics and Metabolism. 139(2). 107605–107605. 2 indexed citations

Shur, Natasha, et al.. (2023). The past, present, and future of child growth monitoring: A review and primer for clinical genetics. American Journal of Medical Genetics Part A. 191(4). 948–961. 4 indexed citations

Shur, Natasha, et al.. (2021). Genetic causes of fractures and subdural hematomas: fact versus fiction. Pediatric Radiology. 51(6). 1029–1043. 3 indexed citations

Carpenter, Austin B., et al.. (2021). A Symposium on the Clinic of the Future and Telehealth: Highlights and Future Directions. Cureus. 13(5). e15234–e15234. 6 indexed citations

Regier, Debra S., Jamie L. Fraser, Kimberly A. Chapman, et al.. (2020). Use of dexamethasone in idiopathic, acute pediatric rhabdomyolysis. American Journal of Medical Genetics Part A. 185(2). 500–507. 4 indexed citations

Regier, Debra S., et al.. (2020). Mucopolysaccharidosis type I newborn screening: Importance of second tier testing for ethnically diverse populations. American Journal of Medical Genetics Part A. 185(1). 134–140. 9 indexed citations

Shur, Natasha, et al.. (2020). Rapid deployment of a telemedicine care model for genetics and metabolism during COVID‐19. American Journal of Medical Genetics Part A. 185(1). 68–72. 32 indexed citations

Shur, Natasha. (2019). A case of broken bones and systems: The threat of irresponsible testimony. American Journal of Medical Genetics Part A. 179(3). 429–434. 3 indexed citations

10.

Shur, Natasha, et al.. (2019). Lysinuric protein intolerance: Pearls to detect this otherwise easily missed diagnosis. PubMed. 5(1-2). 81–86. 9 indexed citations

11.

Zori, Roberto T., Janet A. Thomas, Natasha Shur, et al.. (2018). Induction, titration, and maintenance dosing regimen in a phase 2 study of pegvaliase for control of blood phenylalanine in adults with phenylketonuria. Molecular Genetics and Metabolism. 125(3). 217–227. 25 indexed citations

12.

Vogel, Beth, Darius J. Adams, Kristin D׳Aco, et al.. (2015). Newborn screening for X-linked adrenoleukodystrophy in New York State: Diagnostic protocol, surveillance protocol and treatment guidelines. Molecular Genetics and Metabolism. 114(4). 599–603. 84 indexed citations

13.

Shur, Natasha, et al.. (2015). The clinical geneticist and the evaluation of failure to thrive versus failure to feed. American Journal of Medical Genetics Part C Seminars in Medical Genetics. 169(4). 337–348. 7 indexed citations

14.

Shang, Linshan, Lindsay B. Henderson, Megan T. Cho, et al.. (2015). De novo missense variants in PPP2R5D are associated with intellectual disability, macrocephaly, hypotonia, and autism. Neurogenetics. 17(1). 43–49. 52 indexed citations

15.

Shur, Natasha. (2011). The real tiger mother: From the clinical geneticist's perspective. American Journal of Medical Genetics Part A. 155(9). 2088–2090. 1 indexed citations

16.

Donahue, John E., et al.. (2011). Case 168: Rhabdoid Predisposition Syndrome—Familial Cancer Syndromes in Children. Radiology. 259(1). 298–302. 4 indexed citations

17.

Shur, Natasha, et al.. (2010). Picture of the Month—Quiz Case. Archives of Pediatrics and Adolescent Medicine. 164(1). 97–8.

18.

Shur, Natasha. (2009). The genetics of twinning: From splitting eggs to breaking paradigms. American Journal of Medical Genetics Part C Seminars in Medical Genetics. 151C(2). 105–109. 21 indexed citations

19.

Shur, Natasha & Dianne Abuelo. (2009). Genetic Syndromes: From Clinical Suspicion to Referral to Diagnosis. Pediatric Annals. 38(8). 419–425. 3 indexed citations

20.

Shur, Natasha, Janet M. Cowan, & Patricia G. Wheeler. (2003). Craniosynostosis and congenital heart anomalies associated with a maternal deletion of 15q15‐22.1. American Journal of Medical Genetics Part A. 120A(4). 542–546. 17 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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