T. Beck

938 total citations
12 papers, 566 citations indexed

About

T. Beck is a scholar working on Genetics, Surgery and Molecular Biology. According to data from OpenAlex, T. Beck has authored 12 papers receiving a total of 566 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Genetics, 4 papers in Surgery and 4 papers in Molecular Biology. Recurrent topics in T. Beck's work include Advances in Oncology and Radiotherapy (3 papers), Congenital Diaphragmatic Hernia Studies (3 papers) and Advanced Radiotherapy Techniques (3 papers). T. Beck is often cited by papers focused on Advances in Oncology and Radiotherapy (3 papers), Congenital Diaphragmatic Hernia Studies (3 papers) and Advanced Radiotherapy Techniques (3 papers). T. Beck collaborates with scholars based in United States, United Kingdom and Netherlands. T. Beck's co-authors include James C. Mullikin, Daryl A. Scott, Roxanne E. Jensen, Christine M. Colvis, Karlie R. Sharma, Luca Foschini, Kenneth Gersing, Kenneth D. Mandl, Noel Southall and Elaine Collier and has published in prestigious journals such as Nucleic Acids Research, PLoS ONE and Human Molecular Genetics.

In The Last Decade

T. Beck

12 papers receiving 557 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
T. Beck United States	9	221	139	87	85	85	12	566
Omri Bar United States	8	154 0.7×	172 1.2×	98 1.1×	69 0.8×	95 1.1×	16	653
Ferdinand Dhombres France	15	242 1.1×	172 1.2×	139 1.6×	50 0.6×	93 1.1×	64	787
Christine M. Cutillo United States	7	118 0.5×	202 1.5×	21 0.2×	90 1.1×	91 1.1×	7	504
John L. Burns United States	10	171 0.8×	51 0.4×	125 1.4×	40 0.5×	28 0.3×	17	510
Dominic Amara United States	11	84 0.4×	81 0.6×	166 1.9×	106 1.2×	41 0.5×	32	574
Tara Montgomery United Kingdom	9	230 1.0×	120 0.9×	43 0.5×	49 0.6×	33 0.4×	12	481
Matthias A. Fink Germany	12	110 0.5×	24 0.2×	44 0.5×	128 1.5×	89 1.0×	31	542
Nicole Fleischer United States	9	172 0.8×	213 1.5×	15 0.2×	44 0.5×	92 1.1×	18	545
David Ziyou Chen Singapore	13	168 0.8×	47 0.3×	29 0.3×	211 2.5×	96 1.1×	36	764
Geoffrey Smith United States	13	73 0.3×	27 0.2×	71 0.8×	21 0.2×	98 1.2×	45	492

Countries citing papers authored by T. Beck

Since Specialization

Citations

This map shows the geographic impact of T. 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 T. Beck with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites T. Beck more than expected).

Fields of papers citing papers by T. Beck

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of T. Beck

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

All Works

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12 of 12 papers shown

Cutillo, Christine M., Karlie R. Sharma, Luca Foschini, et al.. (2020). Machine intelligence in healthcare—perspectives on trustworthiness, explainability, usability, and transparency. npj Digital Medicine. 3(1). 47–47. 197 indexed citations

Yu, James B., T. Beck, Mitchell S. Anscher, et al.. (2019). Analysis of the 2017 American Society for Radiation Oncology (ASTRO) Research Portfolio. International Journal of Radiation Oncology*Biology*Physics. 103(2). 297–304. 4 indexed citations

Dominello, M.M., Judith C. Keen, T. Beck, et al.. (2018). Responses to the 2017 “1 Million Gray Question”: ASTRO Membership's Opinions on the Most Important Research Question Facing Radiation Oncology. International Journal of Radiation Oncology*Biology*Physics. 102(2). 249–250. 1 indexed citations

Mouw, Kent W., T. Beck, Judith C. Keen, & Adam P. Dicker. (2018). Assessing the Training and Research Environment for Genomics, Bioinformatics, and Immunology in Radiation Oncology. JCO Clinical Cancer Informatics. 2(2). 1–9. 2 indexed citations

Beck, T., et al.. (2016). Systematic Evaluation of Sanger Validation of Next-Generation Sequencing Variants. Clinical Chemistry. 62(4). 647–654. 116 indexed citations

Beck, T., Philippe M. Campeau, Shalini N. Jhangiani, et al.. (2015). FBN1 contributing to familial congenital diaphragmatic hernia. American Journal of Medical Genetics Part A. 167(4). 831–836. 23 indexed citations

Zaveri, Hitisha P., T. Beck, Andrés Hernández, et al.. (2014). Identification of Critical Regions and Candidate Genes for Cardiovascular Malformations and Cardiomyopathy Associated with Deletions of Chromosome 1p36. PLoS ONE. 9(1). e85600–e85600. 35 indexed citations

Beck, T., Oleg A. Shchelochkov, Zhiyin Yu, et al.. (2013). Novel Frem1-Related Mouse Phenotypes and Evidence of Genetic Interactions with Gata4 and Slit3. PLoS ONE. 8(3). e58830–e58830. 13 indexed citations

Wat, Margaret, T. Beck, Andrés Hernández, et al.. (2012). Mouse model reveals the role of SOX7 in the development of congenital diaphragmatic hernia associated with recurrent deletions of 8p23.1. Human Molecular Genetics. 21(18). 4115–4125. 64 indexed citations

10.

Beck, T., Danielle Veenma, Oleg A. Shchelochkov, et al.. (2012). Deficiency of FRAS1-related extracellular matrix 1 (FREM1) causes congenital diaphragmatic hernia in humans and mice. Human Molecular Genetics. 22(5). 1026–1038. 31 indexed citations

11.

Beck, T., et al.. (2009). A 1q42 deletion involving DISC1, DISC2, and TSNAX in an autism spectrum disorder. American Journal of Medical Genetics Part A. 149A(8). 1758–1762. 48 indexed citations

12.

Wu, Gang, et al.. (2006). SGDB: a database of synthetic genes re-designed for optimizing protein over-expression. Nucleic Acids Research. 35(Database). D76–D79. 32 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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