Tamara Beck

780 total citations
11 papers, 301 citations indexed

About

Tamara Beck is a scholar working on Molecular Biology, Genetics and Oncology. According to data from OpenAlex, Tamara Beck has authored 11 papers receiving a total of 301 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 7 papers in Genetics and 3 papers in Oncology. Recurrent topics in Tamara Beck's work include Epigenetics and DNA Methylation (5 papers), Genetic Syndromes and Imprinting (4 papers) and Cancer Cells and Metastasis (3 papers). Tamara Beck is often cited by papers focused on Epigenetics and DNA Methylation (5 papers), Genetic Syndromes and Imprinting (4 papers) and Cancer Cells and Metastasis (3 papers). Tamara Beck collaborates with scholars based in Australia, United States and United Kingdom. Tamara Beck's co-authors include Matthew E. Ritchie, Marnie E. Blewitt, Andrew Keniry, Quentin Gouil, Kelsey Breslin, Geoffrey J. Lindeman, Gordon K. Smyth, Jane E. Visvader, Scott Gigante and Matthew Tinning and has published in prestigious journals such as Nucleic Acids Research, Nature Communications and Nature Cell Biology.

In The Last Decade

Tamara Beck

11 papers receiving 301 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Tamara Beck Australia	8	251	101	55	45	26	11	301
И. А. Драчкова Russia	10	235 0.9×	113 1.1×	41 0.7×	33 0.7×	15 0.6×	31	351
Marika Zanotti Italy	6	454 1.8×	83 0.8×	34 0.6×	42 0.9×	11 0.4×	7	506
Sabine Stolzenburg United States	9	497 2.0×	114 1.1×	52 0.9×	57 1.3×	9 0.3×	11	549
Mónica Román-Trufero United Kingdom	9	502 2.0×	124 1.2×	33 0.6×	35 0.8×	26 1.0×	14	560
Lizhi Yi China	9	275 1.1×	54 0.5×	77 1.4×	16 0.4×	25 1.0×	16	350
Jane M. vanWert United States	11	370 1.5×	158 1.6×	40 0.7×	26 0.6×	17 0.7×	12	446
Mariko Yamane Japan	10	308 1.2×	86 0.9×	21 0.4×	20 0.4×	29 1.1×	17	388
Ino D. Karemaker Netherlands	10	562 2.2×	113 1.1×	63 1.1×	29 0.6×	10 0.4×	14	610
Andrew Perez United States	7	349 1.4×	90 0.9×	48 0.9×	21 0.5×	8 0.3×	8	394
Krishna Kanchi United States	7	171 0.7×	128 1.3×	116 2.1×	70 1.6×	11 0.4×	9	303

Countries citing papers authored by Tamara Beck

Since Specialization

Citations

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

Fields of papers citing papers by Tamara Beck

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Tamara Beck

This figure shows the co-authorship network connecting the top 25 collaborators of Tamara Beck. A scholar is included among the top collaborators of Tamara 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 Tamara Beck. Tamara 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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11 of 11 papers shown

Keniry, Andrew, Natasha Jansz, Peter F. Hickey, et al.. (2022). A method for stabilising the XX karyotype in female mESC cultures. Development. 149(22). 1 indexed citations

Gouil, Quentin, Tamara Beck, Kelsey Breslin, et al.. (2022). Maternal SMCHD1 regulates Hox gene expression and patterning in the mouse embryo. Nature Communications. 13(1). 4295–4295. 11 indexed citations

Kinkel, Sarah, Tamara Beck, Kelsey Breslin, et al.. (2022). Maternal SMCHD1 controls both imprinted Xist expression and imprinted X chromosome inactivation. Epigenetics & Chromatin. 15(1). 26–26. 5 indexed citations

Kinkel, Sarah, Joy Liu, Tamara Beck, et al.. (2022). Epigenetic modifier SMCHD1 maintains a normal pool of long-term hematopoietic stem cells. iScience. 25(7). 104684–104684. 2 indexed citations

Gouil, Quentin, Sarah Kinkel, Tamara Beck, et al.. (2020). Smchd1 is a maternal effect gene required for genomic imprinting. eLife. 9. 21 indexed citations

Gigante, Scott, Quentin Gouil, Alexis Lucattini, et al.. (2019). Using long-read sequencing to detect imprinted DNA methylation. Nucleic Acids Research. 47(8). e46–e46. 79 indexed citations

Jansz, Natasha, Andrew Keniry, Marie Trussart, et al.. (2018). Smchd1 regulates long-range chromatin interactions on the inactive X chromosome and at Hox clusters. Nature Structural & Molecular Biology. 25(9). 766–777. 70 indexed citations

Ritchie, Matthew E., et al.. (2016). High concordance between Illumina HiSeq2500 and NextSeq500 for reduced representation bisulfite sequencing (RRBS). Genomics Data. 10. 97–100. 9 indexed citations

Pal, Bhupinder, Yunshun Chen, Andrew G. Bert, et al.. (2015). Integration of microRNA signatures of distinct mammary epithelial cell types with their gene expression and epigenetic portraits. Breast Cancer Research. 17(1). 85–85. 23 indexed citations

10.

Fu, Nai Yang, Anne C. Rios, Bhupinder Pal, et al.. (2015). EGF-mediated induction of Mcl-1 at the switch to lactation is essential for alveolar cell survival. Nature Cell Biology. 17(4). 365–375. 55 indexed citations

11.

Sheridan, Julie M., Matthew E. Ritchie, Sarah A. Best, et al.. (2015). A pooled shRNA screen for regulators of primary mammary stem and progenitor cells identifies roles for Asap1 and Prox1. BMC Cancer. 15(1). 221–221. 25 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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