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

Year Number of Results
2011 2
2012 1
2014 1
2015 1
2016 1
2018 2
2019 1
2020 1
2021 4
2022 2
2023 3
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19 results
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Page 1
Widespread polycistronic gene expression in green algae.
Gallaher SD, Craig RJ, Ganesan I, Purvine SO, McCorkle SR, Grimwood J, Strenkert D, Davidi L, Roth MS, Jeffers TL, Lipton MS, Niyogi KK, Schmutz J, Theg SM, Blaby-Haas CE, Merchant SS. Gallaher SD, et al. Among authors: ganesan i. Proc Natl Acad Sci U S A. 2021 Feb 16;118(7):e2017714118. doi: 10.1073/pnas.2017714118. Proc Natl Acad Sci U S A. 2021. PMID: 33579822 Free PMC article.
Anaesthesia for a patient with Friedreich's ataxia.
Ganesan I. Ganesan I. Indian J Anaesth. 2011 Jul;55(4):418-20. doi: 10.4103/0019-5049.84847. Indian J Anaesth. 2011. PMID: 22013268 Free PMC article. No abstract available.
Multicenter study on the genetics of glomerular diseases among southeast and south Asians: Deciphering Diversities - Renal Asian Genetics Network (DRAGoN).
Lu L, Yap YC, Nguyen DQ, Chan YH, Ng JL, Zhang YC, Chan CY, Than M, Liu ID, Asim S, Moorani K, Naeem B, Ijaz I, Nguyen TMT, Lee ML, Eng C, Huque SS, Ng YH, Ganesan I, Chao SM, Chong SL, Tan PH, Loh A, Davila S, Kumar V, Ling JZ, Moorakonda RB, Tan KM, Ng AY, Poon KS, Schaefer F, Lipska-Zietkiewicz B, Yap HK, Ng KH; Deciphering Diversities: Renal Asian Genetics Network (DRAGoN). Lu L, et al. Among authors: ganesan i. Clin Genet. 2022 May;101(5-6):541-551. doi: 10.1111/cge.14116. Epub 2022 Feb 1. Clin Genet. 2022. PMID: 35064937
A multipoint guidance mechanism for β-barrel folding on the SAM complex.
Takeda H, Busto JV, Lindau C, Tsutsumi A, Tomii K, Imai K, Yamamori Y, Hirokawa T, Motono C, Ganesan I, Wenz LS, Becker T, Kikkawa M, Pfanner N, Wiedemann N, Endo T. Takeda H, et al. Among authors: ganesan i. Nat Struct Mol Biol. 2023 Feb;30(2):176-187. doi: 10.1038/s41594-022-00897-2. Epub 2023 Jan 5. Nat Struct Mol Biol. 2023. PMID: 36604501
A recurrent, homozygous EMC10 frameshift variant is associated with a syndrome of developmental delay with variable seizures and dysmorphic features.
Shao DD, Straussberg R, Ahmed H, Khan A, Tian S, Hill RS, Smith RS, Majmundar AJ, Ameziane N, Neil JE, Yang E, Al Tenaiji A, Jamuar SS, Schlaeger TM, Al-Saffar M, Hovel I, Al-Shamsi A, Basel-Salmon L, Amir AZ, Rento LM, Lim JY, Ganesan I, Shril S, Evrony G, Barkovich AJ, Bauer P, Hildebrandt F, Dong M, Borck G, Beetz C, Al-Gazali L, Eyaid W, Walsh CA. Shao DD, et al. Among authors: ganesan i. Genet Med. 2021 Jun;23(6):1158-1162. doi: 10.1038/s41436-021-01097-x. Epub 2021 Feb 2. Genet Med. 2021. PMID: 33531666 Free PMC article.
19 results