Author

Aditya Ramdas Iyer

Institute of Genomics and Integrative Biology

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Cancer Biology· 1 Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:deep learning· 1 Research Focus:drug response / drug discovery· 1 Approach:experimental assay· 1 Assay:proteomics· 1 Approach:statistical model· 1 Research Focus:variant calling· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Mehwish NafiziD· 2 shared Sivaprakash RamalingamiD· 2 shared Aashi Singh· 1 shared Amit Kumar SrivastavaiD· 1 shared Areej Akhtar· 1 shared Arvinden VRiD· 1 shared Divya· 1 shared Gaurav KharyaiD· 1 shared

Activity by Year

2023-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 33 mutual co-author links

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2 shared papersCancer Biology

Mehwish NafizORCID

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Author profile →

2 papers

Recent·Most cited

AI-Guided CAR Designs and AKT3 Degradation Synergize to Enhance Bispecific and Trispecific CAR-T Cell Persistence and Overcome Antigen Escape

Md Sufyan Ansari, Varnit Chauhan, Aashi Singh, Areej Akhtar, Nisha Chaudhary, Reegina Tyagi, Divya, Kashif Husain, Sheetal Sharma, Raquib Alam, Md Shakir, Mehak Pracha, Samreen Anjum, Mohd Nadeem, Md Imam Faizan, , Tanveer Ahmad

This study designs and evaluates AI-optimized CAR-T cells with AKT3 degradation to improve persistence and overcome antigen escape in cancer therapy.

bioRxiv · Jun 12, 2025 · PreprintCancer Biology

Scalable noninvasive amplicon-based precision sequencing (SNAPseq) for genetic diagnosis and screening of β-thalassemia and sickle cell disease using a next-generation sequencing platform

Pragya Gupta, Arvinden VR, Priya Thakur, Rahul C. Bhoyar, Vinodh Saravanakumar, Narendra Varma Gottumukkala, Sangam Giri Goswami, Mehwish Nafiz, Aditya Ramdas Iyer, Harie Vignesh, Rajat Soni, Nupur Bhargava, Padma Gunda, Suman Lata Jain, Vivek Gupta, , Sivaprakash Ramalingam

This paper introduces SNAPseq, a high-throughput NGS method for detecting β-thalassemia and sickle cell disease with 100% sensitivity and specificity using noninvasive samples.

Frontiers in Molecular Biosciences · Dec 13, 2023Peer-reviewedGenetic & Genomic Medicine