Srikanth Jammulapati

2.9k citations
8 papers · 1.1k indexed · 1 hit paper · h-index 6

Srikanth Jammulapati

8 papers receiving 1.1k citations

Hit Papers

Patterns of genomic loss of heterozygosity predict homolo...4942012202620162021100200300400

Peers

Srikanth Jammulapati
Comparison fields: 5 of 74
  • Cancer Research 251
  • Oncology 445
  • Reproductive Medicine 127
  • Genetics 331
  • Molecular Biology 598
Replace Erling A. Høivik with:
Erling A. Høivik Norway
Efraim H. Rosenberg Netherlands
Bettina Hanstein Germany
Diana M. Cittelly United States
Donghai Dai United States
Tianjie Shen United States
Xiaoai Zhao China
Stéphan Jalaguier France
Minghao Zhong United States
Ke Hao China
Srikanth Jammulapati relative to Erling A. Høivik Norway Erling A. Høivik's profile →
Citations per field
00.5×1.5×
Erling A. Høivik · 1×
Citations per year

Countries citing papers authored by Srikanth Jammulapati

Since Specialization
Citations

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

Fields of papers citing papers by Srikanth Jammulapati

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network

The 25 scholars most cited alongside Srikanth Jammulapati, 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 Srikanth Jammulapati Line = papers co-authored together Srikanth Jammulapati links everyone, so they are left out of the graph.

All Works

8 of 8 papers shown
#Work
1 20191
2
Patterns of genomic loss of heterozygosity predict homologous recombination repair defects in epithelial ovarian cancerbreakdown →
2012494
3 20122
4 200883
5 2006119
6 2004259
7 200142
8 1996142

About Srikanth Jammulapati

Srikanth Jammulapati is a scholar working on Genetics, Molecular Biology and Cancer Research, having authored 8 papers that have together received 1.1k indexed citations. Recurring topics across this work include Genetic Associations and Epidemiology (3 papers), BRCA gene mutations in cancer (3 papers), DNA Repair Mechanisms (2 papers), CRISPR and Genetic Engineering (2 papers), Nutrition, Genetics, and Disease (1 paper), Protein Kinase Regulation and GTPase Signaling (1 paper), Genetics and Neurodevelopmental Disorders (1 paper) and Nuclear Receptors and Signaling (1 paper). The work is most often cited by research in Cancer Research (251 citations), Oncology (445 citations) and Reproductive Medicine (127 citations). Srikanth Jammulapati has collaborated with scholars based in United States, Ireland and Germany. Frequent co-authors include Kirsten M. Timms, Mark H. Skolnick, Donna Shattuck, Alexander Gutin, Victor Abkevich, Diana Iliev, Jennifer Potter, Mark Samuels, Howard Goldfine and Paul N. Hopkins. Their work appears in journals such as Nature Genetics, Cancer Research and Human Molecular Genetics.

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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