Payal P. Khincha

2.0k total citations
47 papers, 938 citations indexed

About

Payal P. Khincha is a scholar working on Molecular Biology, Oncology and Physiology. According to data from OpenAlex, Payal P. Khincha has authored 47 papers receiving a total of 938 indexed citations (citations by other indexed papers that have themselves been cited), including 26 papers in Molecular Biology, 21 papers in Oncology and 10 papers in Physiology. Recurrent topics in Payal P. Khincha's work include Cancer-related Molecular Pathways (19 papers), Epigenetics and DNA Methylation (15 papers) and Telomeres, Telomerase, and Senescence (9 papers). Payal P. Khincha is often cited by papers focused on Cancer-related Molecular Pathways (19 papers), Epigenetics and DNA Methylation (15 papers) and Telomeres, Telomerase, and Senescence (9 papers). Payal P. Khincha collaborates with scholars based in United States, Brazil and Canada. Payal P. Khincha's co-authors include Sharon A. Savage, Jennifer T. Loud, Renée C. Bremer, June A. Peters, L. Phuong, Rosamma DeCastro, Ana F. Best, Philip S. Rosenberg, Blanche P. Alter and Neelam Giri and has published in prestigious journals such as Journal of Clinical Oncology, Blood and PLoS ONE.

In The Last Decade

Payal P. Khincha

42 papers receiving 920 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Payal P. Khincha United States 15 414 328 283 188 179 47 938
Rosamma DeCastro United States 11 246 0.6× 481 1.5× 200 0.7× 426 2.3× 137 0.8× 15 1.2k
Miharu Yabe Japan 21 509 1.2× 225 0.7× 134 0.5× 130 0.7× 102 0.6× 84 1.3k
Michele G. Mehaffey United States 13 480 1.2× 205 0.6× 422 1.5× 26 0.1× 108 0.6× 18 878
Susanne Timshel Denmark 15 343 0.8× 281 0.9× 150 0.5× 36 0.2× 364 2.0× 20 1.1k
Jason D. Engel United States 18 718 1.7× 124 0.4× 130 0.5× 96 0.5× 82 0.5× 39 1.5k
Bożenna Dembowska–Bagińska Poland 17 448 1.1× 218 0.7× 104 0.4× 36 0.2× 186 1.0× 68 1.0k
Lizet E. van der Kolk Netherlands 17 308 0.7× 322 1.0× 359 1.3× 24 0.1× 146 0.8× 33 1.3k
Eva Atsidaftos United States 11 955 2.3× 197 0.6× 256 0.9× 82 0.4× 79 0.4× 25 1.3k
Susi Scappaticci Italy 18 374 0.9× 124 0.4× 262 0.9× 120 0.6× 67 0.4× 47 784
Fiona Connell United Kingdom 10 296 0.7× 503 1.5× 152 0.5× 197 1.0× 32 0.2× 15 916

Countries citing papers authored by Payal P. Khincha

Since Specialization
Citations

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

Fields of papers citing papers by Payal P. Khincha

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Payal P. Khincha. 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 Payal P. Khincha. The network helps show where Payal P. Khincha may publish in the future.

Co-authorship network of co-authors of Payal P. Khincha

This figure shows the co-authorship network connecting the top 25 collaborators of Payal P. Khincha. A scholar is included among the top collaborators of Payal P. Khincha 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 Payal P. Khincha. Payal P. Khincha 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.
Rising, Camella J., Alix G. Sleight, Patrick Boyd, et al.. (2024). Relating to the Body Under Chronic Cancer Threat: Implications for Psychosocial Health Among Adolescents and Young Adults with Cancer Predisposition Syndromes. Journal of Adolescent and Young Adult Oncology. 14(2). 151–159.
2.
Nakano, Yoshiko, Roland P. Kuiper, Kim E. Nichols, et al.. (2024). Update on Recommendations for Cancer Screening and Surveillance in Children with Genomic Instability Disorders. Clinical Cancer Research. 30(22). 5009–5020. 8 indexed citations
3.
Maese, Luke, Marcin W. Włodarski, Alison A. Bertuch, et al.. (2024). Update on Recommendations for Surveillance for Children with Predisposition to Hematopoietic Malignancy. Clinical Cancer Research. 30(19). 4286–4295. 3 indexed citations
4.
Rising, Camella J., William M. P. Klein, Alix G. Sleight, et al.. (2024). Diet and physical activity behaviors: how are they related to illness perceptions, coping, and health-related quality of life in young people with hereditary cancer syndromes?. Journal of Behavioral Medicine. 47(4). 707–720. 2 indexed citations
5.
Thompson, M.B., et al.. (2024). Characterization of sarcoma topography in Li-Fraumeni syndrome. Frontiers in Oncology. 14. 1415636–1415636. 1 indexed citations
6.
Seastedt, Kenneth P., et al.. (2024). Characterizing Lung Cancer in Li-Fraumeni Syndrome. JAMA Oncology. 10(9). 1284–1284.
7.
Andrade, Kelvin C. de, et al.. (2023). Spectrum and Excess Risk of Gastrointestinal Tumors in Li-Fraumeni Syndrome. Clinical Gastroenterology and Hepatology. 22(3). 662–665.e1. 1 indexed citations
8.
Andrade, Kelvin C. de, Natasha T. Strande, Jung Kim, et al.. (2023). Genome-first approach of the prevalence and cancer phenotypes of pathogenic or likely pathogenic germline TP53 variants. Human Genetics and Genomics Advances. 5(1). 100242–100242. 6 indexed citations
9.
Sargen, Michael R., et al.. (2022). Spectrum and Incidence of Skin Cancer among Individuals with Li-Fraumeni Syndrome. Journal of Investigative Dermatology. 142(9). 2534–2537.e1. 3 indexed citations
10.
Sleight, Alix G., et al.. (2022). “I can control what I do with my daily life”: Occupational experiences of adolescents and young adults with Li-Fraumeni Syndrome. Journal of Occupational Science. 30(4). 661–672. 6 indexed citations
11.
Werner‐Lin, Allison, et al.. (2022). Embodied risk for families with Li-Fraumeni syndrome: Like electricity through my body. Social Science & Medicine. 301. 114905–114905. 5 indexed citations
12.
Werner‐Lin, Allison, Camella J. Rising, Patrick Boyd, et al.. (2022). How do young people with a hereditary cancer predisposition syndrome understand and experience cancer survivorship? “With Li‐Fraumeni syndrome, it’s just an intermission”. Psycho-Oncology. 32(3). 375–382. 4 indexed citations
13.
Young, Jennifer L., Shana L. Merrill, Jennifer T. Loud, et al.. (2021). Family Identity and Roles in the Context of Li-Fraumeni Syndrome: “No One’s Like Us Mutants”. Health & Social Work. 46(4). 299–307. 12 indexed citations
14.
Frone, Megan N., Douglas R. Stewart, Sharon A. Savage, & Payal P. Khincha. (2021). Quantification of Discordant Variant Interpretations in a Large Family-Based Study of Li-Fraumeni Syndrome. JCO Precision Oncology. 5(5). 1727–1737. 6 indexed citations
15.
Fortuño, Cristina, Jessica L. Mester, Tina Pesaran, et al.. (2020). Suggested application of HER2+ breast tumor phenotype for germline TP53 variant classification within ACMG/AMP guidelines. Human Mutation. 41(9). 1555–1562. 14 indexed citations
16.
Werner‐Lin, Allison, et al.. (2020). Waiting and “weighted down”: the challenge of anticipatory loss for individuals and families with Li-Fraumeni Syndrome. Familial Cancer. 19(3). 259–268. 16 indexed citations
17.
Andrade, Kelvin C. de, Megan N. Frone, Talía Wegman-Ostrosky, et al.. (2018). Variable population prevalence estimates of germline TP53 variants: A gnomAD-based analysis. Human Mutation. 40(1). 97–105. 62 indexed citations
18.
Khincha, Payal P., Alison A. Bertuch, Shahinaz M. Gadalla, et al.. (2018). Similar telomere attrition rates in androgen-treated and untreated patients with dyskeratosis congenita. Blood Advances. 2(11). 1243–1249. 24 indexed citations
19.
20.
Khincha, Payal P. & Sharon A. Savage. (2015). Neonatal manifestations of inherited bone marrow failure syndromes. Seminars in Fetal and Neonatal Medicine. 21(1). 57–65. 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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