Milind Mahajan

11.4k total citations · 1 hit paper
42 papers, 2.3k citations indexed

About

Milind Mahajan is a scholar working on Molecular Biology, Cancer Research and Genetics. According to data from OpenAlex, Milind Mahajan has authored 42 papers receiving a total of 2.3k indexed citations (citations by other indexed papers that have themselves been cited), including 26 papers in Molecular Biology, 10 papers in Cancer Research and 8 papers in Genetics. Recurrent topics in Milind Mahajan's work include RNA modifications and cancer (11 papers), Epigenetics and DNA Methylation (7 papers) and Genomics and Chromatin Dynamics (6 papers). Milind Mahajan is often cited by papers focused on RNA modifications and cancer (11 papers), Epigenetics and DNA Methylation (7 papers) and Genomics and Chromatin Dynamics (6 papers). Milind Mahajan collaborates with scholars based in United States, Japan and India. Milind Mahajan's co-authors include Sherman M. Weissman, Stephan Ripke, Sven Sandin, Kathryn Roeder, Arthur P. Goldberg, Oscar Svantesson, Pamela Sklar, Ann B. Lee, Stephan Sanders and Trent Gaugler and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Communications and Nature Genetics.

In The Last Decade

Milind Mahajan

42 papers receiving 2.3k citations

Hit Papers

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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.

Most genetic risk for autism resides with common variation

2014 774 citations Milind Mahajan et al. profile →

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author						Papers	Cites
Milind Mahajan	1.1k	703	573	329	203	42	2.3k
Stacey B. Gabriel	1.7k 1.5×	1.6k 2.3×	262 0.5×	418 1.3×	121 0.6×	13	3.6k
Tibor A. Rauch	2.7k 2.4×	887 1.3×	151 0.3×	492 1.5×	166 0.8×	50	3.6k
Mary E. Winn	859 0.8×	337 0.5×	167 0.3×	357 1.1×	75 0.4×	43	1.9k
Leda Dalprà	1.5k 1.3×	1.2k 1.6×	206 0.4×	491 1.5×	76 0.4×	119	3.3k
Bernhard Korn	2.5k 2.2×	1.0k 1.4×	171 0.3×	354 1.1×	113 0.6×	54	3.6k
Thomas Vaissière	1.6k 1.4×	367 0.5×	201 0.4×	266 0.8×	86 0.4×	28	2.1k
Toshiro Nagai	2.0k 1.7×	1.8k 2.5×	99 0.2×	99 0.3×	183 0.9×	138	3.5k
Jueng Soo You	2.0k 1.8×	247 0.4×	84 0.1×	459 1.4×	172 0.8×	46	2.5k
Kathleen Freson	1.3k 1.1×	705 1.0×	92 0.2×	147 0.4×	189 0.9×	143	3.6k
Ana Cristina Victorino Krepischi	1.4k 1.2×	1.4k 2.0×	115 0.2×	438 1.3×	67 0.3×	146	2.7k

Countries citing papers authored by Milind Mahajan

Since Specialization

Citations

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

Fields of papers citing papers by Milind Mahajan

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Milind Mahajan

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

Hasselt, J. G. Coen van, Rayees Rahman, Jens Hansen, et al.. (2020). Transcriptomic profiling of human cardiac cells predicts protein kinase inhibitor-associated cardiotoxicity. Nature Communications. 11(1). 4809–4809. 28 indexed citations

Liang, Raymond, Tasleem Arif, Svetlana Kalmykova, et al.. (2020). Restraining Lysosomal Activity Preserves Hematopoietic Stem Cell Quiescence and Potency. Cell stem cell. 26(3). 359–376.e7. 164 indexed citations

Kandel-Kfir, Michal, Rolando García-Milian, Ilan Ben‐Zvi, et al.. (2019). IFNγ potentiates TNFα/TNFR1 signaling to induce FAT10 expression in macrophages. Molecular Immunology. 117. 101–109. 12 indexed citations

Koduru, Srinivas V., Ashley N. Leberfinger, Yuka Imamura Kawasawa, et al.. (2018). Non-coding RNAs in Various Stages of Liver Disease Leading to Hepatocellular Carcinoma: Differential Expression of miRNAs, piRNAs, lncRNAs, circRNAs, and sno/mt-RNAs. Scientific Reports. 8(1). 7967–7967. 32 indexed citations

Labgaa, Ismaïl, Carlos Villacorta-Martín, Delia D’Avola, et al.. (2018). A pilot study of ultra-deep targeted sequencing of plasma DNA identifies driver mutations in hepatocellular carcinoma. Oncogene. 37(27). 3740–3752. 89 indexed citations

Koduru, Srinivas V., Amit K. Tiwari, Sprague W. Hazard, Milind Mahajan, & Dino J. Ravnic. (2017). Exploration of small RNA-seq data for small non-coding RNAs in Human Colorectal Cancer. PubMed. 5. 16–31. 29 indexed citations

Torrecilla, Sara, Daniela Sia, Andrew Harrington, et al.. (2017). Trunk mutational events present minimal intra- and inter-tumoral heterogeneity in hepatocellular carcinoma. Journal of Hepatology. 67(6). 1222–1231. 118 indexed citations

Linderman, Michael D., Tracy Brandt, Lisa Edelmann, et al.. (2014). Analytical validation of whole exome and whole genome sequencing for clinical applications. BMC Medical Genomics. 7(1). 20–20. 57 indexed citations

Bandyopadhyay, Urmi, Justin Cotney, Mária Nagy, et al.. (2013). RNA-Seq Profiling of Spinal Cord Motor Neurons from a Presymptomatic SOD1 ALS Mouse. PLoS ONE. 8(1). e53575–e53575. 47 indexed citations

10.

Liu, Li, Subhradip Karmakar, Ruby Dhar, et al.. (2013). Regulation of Gγ-Globin Gene by ATF2 and Its Associated Proteins through the cAMP-Response Element. PLoS ONE. 8(11). e78253–e78253. 11 indexed citations

11.

Tanaka, Yujiro, et al.. (2011). Dual Function of Histone H3 Lysine 36 Methyltransferase ASH1 in Regulation of Hox Gene Expression. PLoS ONE. 6(11). e28171–e28171. 34 indexed citations

12.

Walker, Ruth H., Vincent Schulz, Irina R. Tikhonova, et al.. (2011). Genetic diagnosis of neuroacanthocytosis disorders using exome sequencing. Movement Disorders. 27(4). 539–543. 17 indexed citations

13.

Wontakal, Sandeep N., Xingyi Guo, Britta Will, et al.. (2011). A Large Gene Network in Immature Erythroid Cells Is Controlled by the Myeloid and B Cell Transcriptional Regulator PU.1. PLoS Genetics. 7(6). e1001392–e1001392. 38 indexed citations

14.

Karmakar, Subhradip, et al.. (2010). A multiprotein complex necessary for both transcription and DNA replication at the β‐globin locus. The EMBO Journal. 29(19). 3260–3271. 26 indexed citations

15.

Steiner, Laurie A., Yelena Maksimova, Vincent Schulz, et al.. (2009). Chromatin Architecture and Transcription Factor Binding Regulate Expression of Erythrocyte Membrane Protein Genes. Molecular and Cellular Biology. 29(20). 5399–5412. 27 indexed citations

16.

Lian, Zheng, Alexander Karpikov, Lian Jin, et al.. (2008). A genomic analysis of RNA polymerase II modification and chromatin architecture related to 3′ end RNA polyadenylation. Genome Research. 18(8). 1224–1237. 47 indexed citations

17.

Mahajan, Milind. (2006). Multi-protein complexes at the -globin locus. Briefings in Functional Genomics and Proteomics. 5(1). 62–65. 8 indexed citations

18.

Nakayama, Yasuhiro, Paul R. Stabach, Stephen E. Maher, et al.. (2006). A limited number of genes are involved in the differentiation of germinal center B cells. Journal of Cellular Biochemistry. 99(5). 1308–1325. 19 indexed citations

19.

Horak, Christine E., Milind Mahajan, Nicholas M. Luscombe, et al.. (2002). GATA-1 binding sites mapped in the β-globin locus by using mammalian chIp-chip analysis. Proceedings of the National Academy of Sciences. 99(5). 2924–2929. 136 indexed citations

20.

Mahajan, Milind, Prashant S. Phale, & C.S. Vaidyanathan. (1994). Evidence for the involvement of multiple pathways in the biodegradation of 1- and 2-methylnaphthalene by Pseudomonas putida CSV86. Archives of Microbiology. 161(5). 425–433. 94 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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