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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1980 1
1985 1
1986 1
1988 1
2002 2
2003 1
2005 2
2006 1
2007 4
2008 4
2009 1
2011 2
2012 3
2013 1
2014 6
2015 6
2016 6
2017 7
2018 6
2019 6
2020 11
2021 10
2022 15
2023 10
2024 4

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100 results

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Page 1
Actionable Activating Oncogenic ERBB2/HER2 Transmembrane and Juxtamembrane Domain Mutations.
Pahuja KB, Nguyen TT, Jaiswal BS, Prabhash K, Thaker TM, Senger K, Chaudhuri S, Kljavin NM, Antony A, Phalke S, Kumar P, Mravic M, Stawiski EW, Vargas D, Durinck S, Gupta R, Khanna-Gupta A, Trabucco SE, Sokol ES, Hartmaier RJ, Singh A, Chougule A, Trivedi V, Dutt A, Patil V, Joshi A, Noronha V, Ziai J, Banavali SD, Ramprasad V, DeGrado WF, Bueno R, Jura N, Seshagiri S. Pahuja KB, et al. Among authors: ramprasad v. Cancer Cell. 2018 Nov 12;34(5):792-806.e5. doi: 10.1016/j.ccell.2018.09.010. Epub 2018 Oct 25. Cancer Cell. 2018. PMID: 30449325 Free PMC article.
South Asian medical cohorts reveal strong founder effects and high rates of homozygosity.
Wall JD, Sathirapongsasuti JF, Gupta R, Rasheed A, Venkatesan R, Belsare S, Menon R, Phalke S, Mittal A, Fang J, Tanneeru D, Deshmukh M, Bassi A, Robinson J, Chaudhary R, Murugan S, Ul-Asar Z, Saleem I, Ishtiaq U, Fatima A, Sheikh SS, Hameed S, Ishaq M, Rasheed SZ, Memon FU, Jalal A, Abbas S, Frossard P, Fuchsberger C, Forer L, Schoenherr S, Bei Q, Bhangale T, Tom J, Gadde SGK, B V P, Naik NK, Wang M, Kwok PY, Khera AV, Lakshmi BR, Butterworth AS, Chowdhury R, Danesh J, di Angelantonio E, Naheed A, Goyal V, Kandadai RM, Kumar H, Borgohain R, Mukherjee A, Wadia PM, Yadav R, Desai S, Kumar N, Biswas A, Pal PK, Muthane UB, Das SK, Ramprasad VL, Kukkle PL, Seshagiri S, Kathiresan S, Ghosh A, Mohan V, Saleheen D, Stawiski EW, Peterson AS. Wall JD, et al. Among authors: ramprasad vl. Nat Commun. 2023 Jun 8;14(1):3377. doi: 10.1038/s41467-023-38766-1. Nat Commun. 2023. PMID: 37291107 Free PMC article.
KBG Syndrome in 16 Indian Individuals.
Bajaj S, Nampoothiri S, Chugh R, Sheth J, Sheth F, Sheth H, Narayan V, Deshpande A, Hegde A, Dwivedi A, Yeshodharan D, Khosla I, Mittal M, Kore M, Ramprasad V, C AK, Girisha KM. Bajaj S, et al. Among authors: ramprasad v. Am J Med Genet A. 2024 Oct 15:e63907. doi: 10.1002/ajmg.a.63907. Online ahead of print. Am J Med Genet A. 2024. PMID: 39404460
The Genetic Drivers of Juvenile, Young, and Early-Onset Parkinson's Disease in India.
Andrews SV, Kukkle PL, Menon R, Geetha TS, Goyal V, Kandadai RM, Kumar H, Borgohain R, Mukherjee A, Wadia PM, Yadav R, Desai S, Kumar N, Joshi D, Murugan S, Biswas A, Pal PK, Oliver M, Nair S, Kayalvizhi A, Samson PL, Deshmukh M, Bassi A, Sandeep C, Mandloi N, Davis OB, Roberts MA, Leto DE, Henry AG, Di Paolo G, Muthane U, Das SK, Peterson AS, Sandmann T, Gupta R, Ramprasad VL; Parkinson Research Alliance of India (PRAI). Andrews SV, et al. Among authors: ramprasad vl. Mov Disord. 2024 Feb;39(2):339-349. doi: 10.1002/mds.29676. Epub 2023 Nov 28. Mov Disord. 2024. PMID: 38014556
Retinoblastoma genetics screening and clinical management.
Gupta H, Malaichamy S, Mallipatna A, Murugan S, Jeyabalan N, Suresh Babu V, Ghosh A, Ghosh A, Santhosh S, Seshagiri S, Ramprasad VL, Kumaramanickavel G. Gupta H, et al. Among authors: ramprasad vl. BMC Med Genomics. 2021 Jul 22;14(1):188. doi: 10.1186/s12920-021-01034-6. BMC Med Genomics. 2021. PMID: 34294096 Free PMC article.
Oculogyric Crisis Phenotype of Levodopa-Induced Ocular Dyskinesia.
Olszewska DA, Shetty R, Geetha TS, Ramprasad VL, Lang AE, Kukkle PL. Olszewska DA, et al. Among authors: ramprasad vl. Mov Disord Clin Pract. 2022 Feb 10;9(3):390-393. doi: 10.1002/mdc3.13416. eCollection 2022 Apr. Mov Disord Clin Pract. 2022. PMID: 36989007 Free PMC article. No abstract available.
Comprehensive laboratory diagnosis of Fanconi anaemia: comparison of cellular and molecular analysis.
Joshi G, Arthur NBJ, Geetha TS, Datari PVR, Modak K, Roy D, Chaudhury AD, Sundaraganesan P, Priyanka S, Na F, Ramprasad V, Abraham A, Srivastava VM, Srivastava A, Kulkarni UP, George B, Velayudhan SR. Joshi G, et al. Among authors: ramprasad v. J Med Genet. 2023 Aug;60(8):801-809. doi: 10.1136/jmg-2022-108714. Epub 2023 Mar 9. J Med Genet. 2023. PMID: 36894310 Free PMC article.
Scapular free flap reconstruction of pharyngoesophageal defects.
Sridharan SS, Ramprasad VH, Keller RG, Day TA, Lentsch EJ, Skoner JM. Sridharan SS, et al. Among authors: ramprasad vh. Clin Otolaryngol. 2021 Sep;46(5):1110-1113. doi: 10.1111/coa.13777. Epub 2021 Apr 21. Clin Otolaryngol. 2021. PMID: 33797863 No abstract available.
100 results