Sandra Burkett

2.9k total citations
66 papers, 1.8k citations indexed

About

Sandra Burkett is a scholar working on Molecular Biology, Oncology and Genetics. According to data from OpenAlex, Sandra Burkett has authored 66 papers receiving a total of 1.8k indexed citations (citations by other indexed papers that have themselves been cited), including 36 papers in Molecular Biology, 19 papers in Oncology and 19 papers in Genetics. Recurrent topics in Sandra Burkett's work include DNA Repair Mechanisms (17 papers), CRISPR and Genetic Engineering (15 papers) and Genomics and Chromatin Dynamics (10 papers). Sandra Burkett is often cited by papers focused on DNA Repair Mechanisms (17 papers), CRISPR and Genetic Engineering (15 papers) and Genomics and Chromatin Dynamics (10 papers). Sandra Burkett collaborates with scholars based in United States, Italy and Canada. Sandra Burkett's co-authors include Ira B. Lamster, Evanthia Lalla, Bin Cheng, Carol Kunzel, Shyam K. Sharan, Philipp Oberdoerffer, Yi Tang, Steven Y. Cheng, Ying E. Zhang and Michael Blank and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Clinical Investigation and Nature Medicine.

In The Last Decade

Sandra Burkett

66 papers receiving 1.7k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Sandra Burkett United States	25	1.0k	392	314	273	177	66	1.8k
William C. Hyun United States	25	753 0.7×	128 0.3×	192 0.6×	167 0.6×	148 0.8×	46	1.7k
Irina Golovleva Sweden	25	927 0.9×	284 0.7×	225 0.7×	44 0.2×	174 1.0×	78	1.9k
Nusi P. Dekker United States	19	480 0.5×	78 0.2×	282 0.9×	138 0.5×	202 1.1×	25	1.3k
Naoko Shimada Japan	20	391 0.4×	105 0.3×	379 1.2×	134 0.5×	198 1.1×	54	1.3k
Jens Berthelsen Denmark	25	1.8k 1.7×	511 1.3×	129 0.4×	26 0.1×	123 0.7×	51	2.7k
Dominique Ploton France	14	786 0.8×	141 0.4×	165 0.5×	56 0.2×	161 0.9×	19	1.3k
Edward G. Fey United States	16	803 0.8×	152 0.4×	319 1.0×	24 0.1×	103 0.6×	24	1.4k
Natini Jinawath Thailand	21	834 0.8×	175 0.4×	337 1.1×	17 0.1×	382 2.2×	59	1.5k
M. Menager France	13	794 0.8×	136 0.3×	132 0.4×	52 0.2×	145 0.8×	14	1.2k
P J Stambrook United States	28	1.6k 1.6×	363 0.9×	774 2.5×	26 0.1×	454 2.6×	60	2.3k

Countries citing papers authored by Sandra Burkett

Since Specialization

Citations

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

Fields of papers citing papers by Sandra Burkett

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sandra Burkett

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

Ma, Linyuan, Siyuan Liu, Madelynn N. Whittaker, et al.. (2024). High-fidelity PAMless base editing of hematopoietic stem cells to treat chronic granulomatous disease. Science Translational Medicine. 16(769). eadj6779–eadj6779. 7 indexed citations

Hu, Xiaoju, Kuppusamy Balamurugan, Alexander Y. Mitrophanov, et al.. (2024). Mismatch repair protein MLH1 suppresses replicative stress in BRCA2-deficient breast tumors. Journal of Clinical Investigation. 134(7). 6 indexed citations

Sahu, Sounak, Teresa Sullivan, Alexander Y. Mitrophanov, et al.. (2023). Saturation genome editing of 11 codons and exon 13 of BRCA2 coupled with chemotherapeutic drug response accurately determines pathogenicity of variants. PLoS Genetics. 19(9). e1010940–e1010940. 8 indexed citations

Hartford, Suzanne A., Sounak Sahu, Teresa Sullivan, et al.. (2023). Characterization of BRCA2 R3052Q variant in mice supports its functional impact as a low-risk variant. Cell Death and Disease. 14(11). 753–753. 1 indexed citations

Cheng, Robert Y.S., Sandra Burkett, Stefan Ambs, et al.. (2023). Chronic Exposure to Nitric Oxide Induces P53 Mutations and Malignant-like Features in Human Breast Epithelial Cells. Biomolecules. 13(2). 311–311. 3 indexed citations

Cecchi, Franco, Karen Rex, Cathy D. Vocke, et al.. (2023). Rilotumumab Resistance Acquired by Intracrine Hepatocyte Growth Factor Signaling. Cancers. 15(2). 460–460. 3 indexed citations

Hartford, Suzanne A., Sounak Sahu, Kimberly D. Klarmann, et al.. (2022). BRCA2-DSS1 interaction is dispensable for RAD51 recruitment at replication-induced and meiotic DNA double strand breaks. Nature Communications. 13(1). 1751–1751. 15 indexed citations

Vijayakurup, Vinod, Hye Seung Lee, Sandra Burkett, et al.. (2022). Thymidylate synthase accelerates Men1-mediated pancreatic tumor progression and reduces survival. JCI Insight. 7(19). 6 indexed citations

Biswas, Kajal, Martin Couillard, Luca Cavallone, et al.. (2021). A novel mouse model of PMS2 founder mutation that causes mismatch repair defect due to aberrant splicing. Cell Death and Disease. 12(9). 838–838. 8 indexed citations

10.

Xu, Xiaoping, Kai Ni, Yafeng He, et al.. (2021). The epigenetic regulator LSH maintains fork protection and genomic stability via MacroH2A deposition and RAD51 filament formation. Nature Communications. 12(1). 3520–3520. 24 indexed citations

11.

Ding, Xia, Manish Singh, Sandra Burkett, et al.. (2020). Degradation of 5hmC-marked stalled replication forks by APE1 causes genomic instability. Science Signaling. 13(645). 44 indexed citations

12.

Papapanou, Panos N., Heekuk Park, Bin Cheng, et al.. (2020). Subgingival microbiome and clinical periodontal status in an elderly cohort: The WHICAP ancillary study of oral health. Journal of Periodontology. 91(S1). S56–S67. 51 indexed citations

13.

Sweeney, Colin L., Jizhong Zou, Uimook Choi, et al.. (2017). Targeted Repair of CYBB in X-CGD iPSCs Requires Retention of Intronic Sequences for Expression and Functional Correction. Molecular Therapy. 25(2). 321–330. 37 indexed citations

14.

Aprelikova, Olga, Christine C. Tomlinson, Mark J. Hoenerhoff, et al.. (2016). Development and Preclinical Application of an Immunocompetent Transplant Model of Basal Breast Cancer with Lung, Liver and Brain Metastases. PLoS ONE. 11(5). e0155262–e0155262. 11 indexed citations

15.

Sorber, Rebecca, Yaroslav Teper, Abisola Abisoye-Ogunniyan, et al.. (2016). Whole Genome Sequencing of Newly Established Pancreatic Cancer Lines Identifies Novel Somatic Mutation (c.2587G>A) in Axon Guidance Receptor Plexin A1 as Enhancer of Proliferation and Invasion. PLoS ONE. 11(3). e0149833–e0149833. 22 indexed citations

16.

Sekula, David, Yun Lu, Andrew J. Giustini, et al.. (2015). Mice null for the deubiquitinase USP18 spontaneously develop leiomyosarcomas. BMC Cancer. 15(1). 886–886. 15 indexed citations

17.

Kalra, Neetu, Jingli Zhang, Anish Thomas, et al.. (2015). Mesothelioma patient derived tumor xenografts with defined BAP1 mutations that mimic the molecular characteristics of human malignant mesothelioma. BMC Cancer. 15(1). 376–376. 21 indexed citations

18.

Perelman, Polina L., Alexander S. Graphodatsky, Jerry W. Dragoo, et al.. (2008). Chromosome painting shows that skunks (Mephitidae, Carnivora) have highly rearranged karyotypes. Chromosome Research. 16(8). 1215–1231. 12 indexed citations

19.

Roohi, Jasmin, David Tegay, John Pomeroy, et al.. (2008). A de novo apparently balanced translocation [46,XY,t(2;9)(p13;p24)] interrupting RAB11FIP5 identifies a potential candidate gene for autism spectrum disorder. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 147B(4). 411–417. 14 indexed citations

20.

Urzúa, Ulises, et al.. (2005). Microarray Comparative Genomic Hybridization Profile of a Murine Model for Epithelial Ovarian Cancer Reveals Genomic Imbalances Resembling Human Ovarian Carcinomas. Tumor Biology. 26(5). 236–244. 20 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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