Anita E. Beck

4.1k total citations
32 papers, 482 citations indexed

About

Anita E. Beck is a scholar working on Molecular Biology, Genetics and Genetics. According to data from OpenAlex, Anita E. Beck has authored 32 papers receiving a total of 482 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Molecular Biology, 11 papers in Genetics and 9 papers in Genetics. Recurrent topics in Anita E. Beck's work include Neurogenetic and Muscular Disorders Research (8 papers), Genetic Syndromes and Imprinting (6 papers) and Muscle Physiology and Disorders (6 papers). Anita E. Beck is often cited by papers focused on Neurogenetic and Muscular Disorders Research (8 papers), Genetic Syndromes and Imprinting (6 papers) and Muscle Physiology and Disorders (6 papers). Anita E. Beck collaborates with scholars based in United States, Canada and Australia. Anita E. Beck's co-authors include Michael J. Bamshad, Michael Regnier, Alice Ward Racca, Heidi Gildersleeve, Kathryn M. Shively, Gregory M. Enns, Margaret J. McMillin, H. Eugene Hoyme, Louanne Hudgins and Renkui Bai and has published in prestigious journals such as SHILAP Revista de lepidopterología, The Journal of Physiology and PEDIATRICS.

In The Last Decade

Anita E. Beck

28 papers receiving 465 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Anita E. Beck United States 13 277 165 121 102 59 32 482
John D. Stratigis United States 9 214 0.8× 31 0.2× 104 0.9× 21 0.2× 69 1.2× 19 365
Alexandra Calle Spain 14 318 1.1× 72 0.4× 75 0.6× 19 0.2× 136 2.3× 24 651
Y. Takehara Japan 16 142 0.5× 73 0.4× 51 0.4× 26 0.3× 279 4.7× 30 833
Bruno Diaz Paredes Brazil 12 168 0.6× 105 0.6× 16 0.1× 30 0.3× 15 0.3× 23 521
Francisco Galán Spain 12 106 0.4× 34 0.2× 139 1.1× 15 0.1× 63 1.1× 18 355
Mark G. Lathrop France 5 211 0.8× 177 1.1× 108 0.9× 15 0.1× 23 0.4× 6 362
M. Vandervorst Belgium 14 162 0.6× 103 0.6× 216 1.8× 13 0.1× 464 7.9× 17 755
Rosemarie Rupps Canada 12 153 0.6× 30 0.2× 122 1.0× 27 0.3× 60 1.0× 23 337
Yanhuan Zhao China 10 119 0.4× 56 0.3× 52 0.4× 24 0.2× 7 0.1× 25 330
Jesper Just Denmark 12 263 0.9× 7 0.0× 121 1.0× 33 0.3× 17 0.3× 29 426

Countries citing papers authored by Anita E. Beck

Since Specialization
Citations

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

Fields of papers citing papers by Anita E. Beck

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Anita E. Beck. 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 Anita E. Beck. The network helps show where Anita E. Beck may publish in the future.

Co-authorship network of co-authors of Anita E. Beck

This figure shows the co-authorship network connecting the top 25 collaborators of Anita E. Beck. A scholar is included among the top collaborators of Anita E. Beck 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 Anita E. Beck. Anita E. Beck 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.
Beck, Anita E., et al.. (2025). Concordance of Whole-Genome Long-Read Sequencing with Standard Clinical Testing for Prader-Willi and Angelman Syndromes. Journal of Molecular Diagnostics. 27(3). 166–176. 1 indexed citations
2.
Beck, Anita E., et al.. (2023). O33: Concordance of long-read genome sequencing with methylation calling with clinical testing for individuals with Prader-Willi or Angelman Syndrome*. SHILAP Revista de lepidopterología. 1(1). 100459–100459. 1 indexed citations
3.
Quintero‐Rivera, Fabiola, Kelly L. Jones, Małgorzata J.M. Nowaczyk, et al.. (2021). 5q35 duplication presents with psychiatric and undergrowth phenotypes mediated by NSD1 overexpression and mTOR signaling downregulation. Human Genetics. 140(4). 681–690. 8 indexed citations
4.
Sheppard, Sarah E., Emilie Lalonde, N. Scott Adzick, et al.. (2019). Androgenetic chimerism as an etiology for Beckwith–Wiedemann syndrome: diagnosis and management. Genetics in Medicine. 21(11). 2644–2649. 12 indexed citations
5.
Salehi, Parisa, et al.. (2017). Silent aspiration in infants with Prader–Willi syndrome identified by videofluoroscopic swallow study. Medicine. 96(50). e9256–e9256. 10 indexed citations
6.
Salehi, Parisa, et al.. (2016). Abnormal Videofluoroscopic Swallow Studies (VFSS) in Infants with Prader-Willi Syndrome Indicate a High Rate of Silent Aspiration. 86. 1 indexed citations
7.
Racca, Alice Ward, et al.. (2015). The embryonic myosin R672C mutation that underlies Freeman-Sheldon syndrome impairs cross-bridge detachment and cycling in adult skeletal muscle. Human Molecular Genetics. 24(12). 3348–3358. 37 indexed citations
8.
Racca, Alice Ward, Anita E. Beck, Michael J. Bamshad, & Michael Regnier. (2014). Differences in Activation and Relaxation Kinetics of Human Fetal Skeletal and Cardiac Myofibrils. Biophysical Journal. 106(2). 562a–562a. 1 indexed citations
9.
Tabor, Holly K., et al.. (2014). Single-nucleotide polymorphism arrays and unexpected consanguinity: considerations for clinicians when returning results to families. Genetics in Medicine. 17(5). 400–404. 2 indexed citations
10.
Beck, Anita E., Margaret J. McMillin, Heidi Gildersleeve, et al.. (2013). Spectrum of mutations that cause distal arthrogryposis types 1 and 2B. American Journal of Medical Genetics Part A. 161(3). 550–555. 53 indexed citations
11.
Racca, Alice Ward, Anita E. Beck, Vijay S. Rao, et al.. (2013). Contractility and kinetics of human fetal and human adult skeletal muscle. The Journal of Physiology. 591(12). 3049–3061. 34 indexed citations
12.
Below, Jennifer E., Anita E. Beck, Heidi Gildersleeve, et al.. (2012). Mutations in ECEL1 Cause Distal Arthrogryposis Type 5D. The American Journal of Human Genetics. 92(1). 150–156. 52 indexed citations
13.
Blanton, Susan H., Michael J. Bamshad, Anita E. Beck, et al.. (2011). Variants in genes that encode muscle contractile proteins influence risk for isolated clubfoot. American Journal of Medical Genetics Part A. 155(9). 2170–2179. 34 indexed citations
14.
15.
Enns, Gregory M., Renkui Bai, Anita E. Beck, & Lee‐Jun C. Wong. (2006). Molecular–clinical correlations in a family with variable tissue mitochondrial DNA T8993G mutant load. Molecular Genetics and Metabolism. 88(4). 364–371. 32 indexed citations
16.
Beck, Anita E., Louanne Hudgins, & H. Eugene Hoyme. (2005). Autosomal dominant microtia and ocular coloboma: New syndrome or an extension of the oculo‐auriculo‐vertebral spectrum?. American Journal of Medical Genetics Part A. 134A(4). 359–362. 20 indexed citations
17.
Adam, Margaret P, Melanie A. Manning, Anita E. Beck, et al.. (2003). Methotrexate/misoprostol embryopathy: Report of four cases resulting from failed medical abortion. American Journal of Medical Genetics Part A. 123A(1). 72–78. 33 indexed citations
18.
Klein, Michael, et al.. (1991). Das diagnostische Potential von Amniozentesen in den ersten 12 Schwangerschaftswochen. Geburtshilfe und Frauenheilkunde. 51(11). 886–889. 2 indexed citations
19.
Klein, Michael, et al.. (1991). Die Konisation in der Gravidität und deren Bedeutung für den weiteren Schwangerschaftsverlauf*. Geburtshilfe und Frauenheilkunde. 51(12). 990–992. 2 indexed citations
20.
Beck, Anita E., et al.. (1966). Case of stillbirth due to infection with Listeria monocytogenes. Journal of Clinical Pathology. 19(6). 567–569. 7 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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