Srinivas Malladi

3.6k total citations · 1 hit paper
28 papers, 1.9k citations indexed

About

Srinivas Malladi is a scholar working on Molecular Biology, Oncology and Immunology. According to data from OpenAlex, Srinivas Malladi has authored 28 papers receiving a total of 1.9k indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 10 papers in Oncology and 6 papers in Immunology. Recurrent topics in Srinivas Malladi's work include Cell death mechanisms and regulation (5 papers), Phagocytosis and Immune Regulation (4 papers) and Synthesis of heterocyclic compounds (3 papers). Srinivas Malladi is often cited by papers focused on Cell death mechanisms and regulation (5 papers), Phagocytosis and Immune Regulation (4 papers) and Synthesis of heterocyclic compounds (3 papers). Srinivas Malladi collaborates with scholars based in United States, India and Spain. Srinivas Malladi's co-authors include Joan Massagué, Edi Brogi, Shawn B. Bratton, Patrick G. Morris, Katia Manova‐Todorova, Nancy Hogg, Venkatraman Seshan, Larry Norton, Margaret Leversha and Swarnali Acharyya and has published in prestigious journals such as Cell, Journal of Biological Chemistry and Nature Communications.

In The Last Decade

Srinivas Malladi

25 papers receiving 1.9k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

A CXCL1 Paracrine Network Links Cancer Chemoresistance and Metastasis

2012 859 citations Swarnali Acharyya, Thórdur Óskarsson et al. Cell profile →

Peers

Srinivas Malladi

MB

ONCOL

IMMUN

CR

PRM

Xinhui Wang United States

Christian D. Young United States

Yanyan Han China

Ángel García-Díaz Spain

Ravikanth Maddipati United States

Jason R. Pitarresi United States

Anna E. Vilgelm United States

Yuhan Huang China

Annemilaï Tijeras‐Raballand France

Xinhui Wang United States

Srinivas Malladi

828 ×0.8

MB

917 ×1.0

ONCOL

536 ×0.9

IMMUN

459 ×1.2

CR

251 ×1.2

PRM

Citations per year, relative to Srinivas Malladi Srinivas Malladi (= 1×) peers Xinhui Wang

Countries citing papers authored by Srinivas Malladi

Since Specialization

Citations

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

Fields of papers citing papers by Srinivas Malladi

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Srinivas Malladi

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

1.

Valiente, Manuel, Carey K. Anders, Nuria Kotecki, et al.. (2025). The evolving landscape of brain metastasis: volume II. Trends in cancer. 12(2). 116–146.

2.

Parida, Pravat Kumar & Srinivas Malladi. (2025). Metabolic adaptations of brain metastasis. Nature reviews. Cancer. 25(9). 723–739. 1 indexed citations

3.

Herrera, L, Pravat Kumar Parida, Suvranil Ghosh, et al.. (2024). AXL/WRNIP1 Mediates Replication Stress Response and Promotes Therapy Resistance and Metachronous Metastasis in HER2+ Breast Cancer. Cancer Research. 84(5). 675–687. 7 indexed citations

4.

Kim, Dae-Seok, Cristel V. Camacho, Srinivas Malladi, et al.. (2022). Functional Characterization of lncRNA152 as an Angiogenesis-Inhibiting Tumor Suppressor in Triple-Negative Breast Cancers. Molecular Cancer Research. 20(11). 1623–1635. 8 indexed citations

5.

Huang, Huocong, Pravat Kumar Parida, Lan He, et al.. (2022). Cell Competition Shapes Metastatic Latency and Relapse. Cancer Discovery. 13(1). 85–97. 13 indexed citations

6.

Jung, Ji-Ung, Pravat Kumar Parida, Tuyen T. Dang, et al.. (2021). WNK1 Enhances Migration and Invasion in Breast Cancer Models. Molecular Cancer Therapeutics. 20(10). 1800–1808. 33 indexed citations

7.

Malladi, Srinivas, et al.. (2019). Metastatic Latency, a Veiled Threat. Frontiers in Immunology. 10. 1836–1836. 20 indexed citations

8.

Er, Ekrem Emrah, Manuel Valiente, Karuna Ganesh, et al.. (2018). Pericyte-like spreading by disseminated cancer cells activates YAP and MRTF for metastatic colonization. Nature Cell Biology. 20(8). 966–978. 194 indexed citations

9.

Nair, Vidhya R. & Srinivas Malladi. (2018). Mouse Models to Study Natural Killer Cell-Mediated Immunosurveillance and Metastatic Latency. Methods in molecular biology. 1884. 141–150. 4 indexed citations

10.

Malladi, Srinivas, et al.. (2016). Estimating the Economic Incentive to Adopt FiberMax Cotton Variety. 15. 1–6.

11.

Lee, Sun Hee, et al.. (2016). The Apaf-1 apoptosome induces formation of caspase-9 homo- and heterodimers with distinct activities. Nature Communications. 7(1). 13565–13565. 64 indexed citations

12.

Zhang, Xiang H.-F., Xin Jin, Srinivas Malladi, et al.. (2013). Selection of Bone Metastasis Seeds by Mesenchymal Signals in the Primary Tumor Stroma. Cell. 154(5). 1060–1073. 321 indexed citations

13.

Acharyya, Swarnali, Thórdur Óskarsson, Sakari Vanharanta, et al.. (2012). A CXCL1 Paracrine Network Links Cancer Chemoresistance and Metastasis. Cell. 150(1). 165–178. 859 indexed citations breakdown →

14.

Malladi, Srinivas, et al.. (2011). Deletion mutational analysis of BMRP, a pro-apoptotic protein that binds to Bcl-2. Molecular and Cellular Biochemistry. 351(1-2). 217–232. 8 indexed citations

15.

Labenski, Matthew, Srinivas Malladi, J. D. Chapman, et al.. (2011). The Frequency of 1,4-Benzoquinone-Lysine Adducts in Cytochrome c Correlate with Defects in Apoptosome Activation. Toxicological Sciences. 122(1). 64–72. 11 indexed citations

16.

Choi, Young Eun, Michael Butterworth, Srinivas Malladi, et al.. (2009). The E3 Ubiquitin Ligase cIAP1 Binds and Ubiquitinates Caspase-3 and -7 via Unique Mechanisms at Distinct Steps in Their Processing. Journal of Biological Chemistry. 284(19). 12772–12782. 131 indexed citations

17.

Malladi, Srinivas, et al.. (2009). The Apaf‐1•procaspase‐9 apoptosome complex functions as a proteolytic‐based molecular timer. The EMBO Journal. 28(13). 1916–1925. 103 indexed citations

18.

Labenski, Matthew, Srinivas Malladi, Vijay Gokhale, et al.. (2007). Quinone Electrophiles Selectively Adduct “Electrophile Binding Motifs” within Cytochrome c. Biochemistry. 46(39). 11090–11100. 50 indexed citations

19.

Malladi, Srinivas, Brett J. Pellock, Shankar Varadarajan, et al.. (2007). Drosophila Omi, a mitochondrial‐localized IAP antagonist and proapoptotic serine protease. The EMBO Journal. 26(13). 3144–3156. 43 indexed citations

20.

Chintharlapalli, Sudhakar, et al.. (2004). BMRP is a Bcl‐2 binding protein that induces apoptosis. Journal of Cellular Biochemistry. 94(3). 611–626. 38 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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