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Year Number of Results
2015 1
2017 2
2019 1
2020 2
2021 2
2022 1
2023 3
2024 9
2025 3
2026 2

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23 results

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Page 1
A metastasis map of human cancer cell lines.
Jin X, Demere Z, Nair K, Ali A, Ferraro GB, Natoli T, Deik A, Petronio L, Tang AA, Zhu C, Wang L, Rosenberg D, Mangena V, Roth J, Chung K, Jain RK, Clish CB, Vander Heiden MG, Golub TR. Jin X, et al. Among authors: nair k. Nature. 2020 Dec;588(7837):331-336. doi: 10.1038/s41586-020-2969-2. Epub 2020 Dec 9. Nature. 2020. PMID: 33299191 Free PMC article.
De novo variants underlying monogenic syndromes with intellectual disability in a neurodevelopmental cohort from India.
Pande S, Majethia P, Nair K, Rao LP, Mascarenhas S, Kaur N, do Rosario MC, Neethukrishna K, Chaurasia A, Hunakunti B, Jadhav N, Xavier S, Kumar J, Bhat V, Bhavani GS, Narayanan DL, Yatheesha BL, Patil SJ, Nampoothiri S, Kamath N, Aroor S, Bhat Y R, Lewis LE, Sharma S, Bajaj S, Sankhyan N, Siddiqui S, Nayak SS, Bielas S, Girisha KM, Shukla A. Pande S, et al. Among authors: nair k. Eur J Hum Genet. 2024 Oct;32(10):1291-1298. doi: 10.1038/s41431-023-01513-7. Epub 2023 Dec 20. Eur J Hum Genet. 2024. PMID: 38114583 Free PMC article.
Advancements in Neurosurgical Intraoperative Histology.
Mohamed AA, Sargent E, Williams C, Karve Z, Nair K, Lucke-Wold B. Mohamed AA, et al. Among authors: nair k. Tomography. 2024 May 9;10(5):693-704. doi: 10.3390/tomography10050054. Tomography. 2024. PMID: 38787014 Free PMC article. Review.
Neuroimaging to Genotype: Delineating the Spectrum of Disorders With Deficient Myelination in the Indian Population.
Kaur N, do Rosario MC, Majethia P, Mascarenhas S, Rao LP, Nair KV, Hunakunti B, Prasannakumar AP, Naik R, Narayanan DL, Nayak SS, Bhat V, Sharma S, Ramesh Bhat Y, Yatheesha BL, Kulkarni R, Patil SJ, Nampoothiri S, Siddiqui S, Girisha KM, Bielas S, Shukla A. Kaur N, et al. Among authors: nair kv. Am J Med Genet A. 2025 Mar;197(3):e63914. doi: 10.1002/ajmg.a.63914. Epub 2024 Oct 29. Am J Med Genet A. 2025. PMID: 39470296 Free PMC article.
Further delineation of defects in MRPS2 causing human OXPHOS deficiency and early developmental abnormalities in zebrafish.
Kandettu A, Yeole M, Sekar H, Garapati K, Kaur N, Anand A, Hegde P, Nair K, Medishetti R, Bhat V, Radhakrishnan P, Mundkur SC, Shrikiran HA, Pandey A, Sevilimedu A, Chakrabarty S, Shukla A. Kandettu A, et al. Among authors: nair k. Eur J Hum Genet. 2025 Nov;33(11):1451-1461. doi: 10.1038/s41431-025-01858-1. Epub 2025 May 13. Eur J Hum Genet. 2025. PMID: 40360742 Free PMC article.
Genetic and phenotypic landscape of pediatric-onset epilepsy in 142 Indian families: Counseling and therapeutic implications.
Majethia P, Kaur N, Mascarenhas S, Rao LP, Pande S, Narayanan DL, Bhat V, Nayak SS, Nair KV, Prasannakumar AP, Chaurasia A, Hunakunti B, Jadhav N, Farooqui S, Yeole M, Kothiwale V, Naik R, Bhat V, Aroor S, Lewis L, Purkayastha J, Bhat YR, Praveen BK, Yatheesha BL, Patil SJ, Nampoothiri S, Kamath N, Siddiqui S, Bielas S, Girisha KM, Sharma S, Shukla A. Majethia P, et al. Among authors: nair kv. Clin Genet. 2024 Jun;105(6):639-654. doi: 10.1111/cge.14495. Epub 2024 Feb 19. Clin Genet. 2024. PMID: 38374498 Free PMC article.
Report of a novel recurrent homozygous variant c.620A>T in three unrelated families with thiamine metabolism dysfunction syndrome 5 and review of literature.
Mascarenhas S, Yeole M, Rao LP, do Rosario MC, Majethia P, Nair KV, Sharma S, Barala PK, Puri RD, Pal S, Siddiqui S, Shukla A. Mascarenhas S, et al. Among authors: nair kv. Clin Dysmorphol. 2024 Oct 1;33(4):160-166. doi: 10.1097/MCD.0000000000000490. Epub 2024 Jul 16. Clin Dysmorphol. 2024. PMID: 39140381 Free PMC article. Review.
Clinical and genetic spectrum of 104 Indian families with central nervous system white matter abnormalities.
Kaur P, do Rosario MC, Hebbar M, Sharma S, Kausthubham N, Nair K, A S, Bhat Y R, Lewis LES, Nampoothiri S, Patil SJ, Suresh N, Bijarnia Mahay S, Dua Puri R, Pai S, Kaur A, Kc R, Kamath N, Bajaj S, Kumble A, Shetty R, Shenoy R, Kamate M, Shah H, Muranjan MN, Bl Y, Avabratha KS, Subramaniam G, Kadavigere R, Bielas S, Girisha KM, Shukla A. Kaur P, et al. Among authors: nair k. Clin Genet. 2021 Nov;100(5):542-550. doi: 10.1111/cge.14037. Epub 2021 Jul 30. Clin Genet. 2021. PMID: 34302356 Free PMC article.
23 results