Sandeep Kumar Botla

1.8k citations
7 papers · 1.4k · 1 hit paper · h-index 7

Impact in

Papers in

    • Cancer Genomics and Diagnostics 2
    • CRISPR and Genetic Engineering 3
    • Epigenetics and DNA Methylation 3
    • Identification and Quantification in Food 1
    • RNA modifications and cancer 1
    • Cancer-related gene regulation 1
    • Retinal Development and Disorders 1

Sandeep Kumar Botla

7 papers receiving 1.3k citations

Sandeep Kumar Botla's Hit Papers

CRISPR–Cas9 genome editing induces a p53-mediated DNA damage response 2018 · 978 citations
9780+2+5Years since publication250500750

Peers

Sandeep Kumar Botla
Comparison fields: 5 of 93
  • Business and International Management 89
  • Aging 64
  • Molecular Biology 1.1k
  • Genetics 320
  • Cancer Research 112
Replace Juan Pablo Fernández with:
Juan Pablo Fernández United States
Nicholas J. Brideau United States
Wenfang Spring Tan United States
Yamila N. Torres Cleuren Norway
Maximilian Krause Norway
Håkon Tjeldnes Norway
Silvia Colleoni Italy
Xiaoyan Wang China
Jean-Baptiste Renaud France
Ni Hong China
Sandeep Kumar Botla relative to Juan Pablo Fernández United States Juan Pablo Fernández's profile →
Citations per field
00.5×1.5×1.9×
Juan Pablo Fernández · 1×
Citations per year

Countries citing papers authored by Sandeep Kumar Botla

Since Specialization
Citations

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

Fields of papers citing papers by Sandeep Kumar Botla

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Sandeep Kumar Botla. 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 Sandeep Kumar Botla. The network helps show where Sandeep Kumar Botla may publish in the future.

Co-authors

The 25 scholars most cited alongside Sandeep Kumar Botla, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Sandeep Kumar Botla Line = papers co-authored together Sandeep Kumar Botla links everyone, so they are left out of the graph.

All Works

7 of 7 papers shown
#Work
1
CRISPR–Cas9 genome editing induces a p53-mediated DNA damage response
Hit paper breakdown →
2018978
2 2010194
3 201673
4 201750
5 201528
6 201826
7 201216

About Sandeep Kumar Botla

Sandeep Kumar Botla is a scholar working on Cancer Research, Molecular Biology, Pathology and Forensic Medicine, Genetics and Epidemiology, having authored 7 papers that have together received 1.4k indexed citations. Recurring topics across this work include CRISPR and Genetic Engineering (3 papers), Epigenetics and DNA Methylation (3 papers), Cancer Genomics and Diagnostics (2 papers), Identification and Quantification in Food (1 paper), RNA modifications and cancer (1 paper), Cancer-related gene regulation (1 paper), Retinal Development and Disorders (1 paper) and Genetic Syndromes and Imprinting (1 paper). The work is most often cited by research in Business and International Management (89 citations), Aging (64 citations), Molecular Biology (1.1k citations), Genetics (320 citations) and Cancer Research (112 citations). Sandeep Kumar Botla has collaborated with scholars based in Germany, Sweden and Finland. Frequent co-authors include Bernhard Schmierer, Jussi Taipale, Jenna Persson, Emma Maria Haapaniemi, Jilin Zhang, Teemu Kivioja, Mikko M. Turunen, Evgeny A. Moskalev, Jörg D. Hoheisel and Pouria Jandaghi. Their work appears in journals such as Nature Medicine, Breast Cancer Research and Treatment, PLoS ONE, Oncotarget and Molecular Systems Biology.

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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