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

Year Number of Results
2002 2
2003 2
2004 1
2005 1
2006 4
2008 6
2009 1
2010 2
2011 2
2012 2
2013 3
2014 9
2015 8
2016 12
2017 4
2018 8
2019 6
2020 14
2021 13
2022 10
2023 5
2024 2

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96 results

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Page 1
PD-1 Blockade in Mismatch Repair-Deficient, Locally Advanced Rectal Cancer.
Cercek A, Lumish M, Sinopoli J, Weiss J, Shia J, Lamendola-Essel M, El Dika IH, Segal N, Shcherba M, Sugarman R, Stadler Z, Yaeger R, Smith JJ, Rousseau B, Argiles G, Patel M, Desai A, Saltz LB, Widmar M, Iyer K, Zhang J, Gianino N, Crane C, Romesser PB, Pappou EP, Paty P, Garcia-Aguilar J, Gonen M, Gollub M, Weiser MR, Schalper KA, Diaz LA Jr. Cercek A, et al. Among authors: iyer k. N Engl J Med. 2022 Jun 23;386(25):2363-2376. doi: 10.1056/NEJMoa2201445. Epub 2022 Jun 5. N Engl J Med. 2022. PMID: 35660797 Free PMC article. Clinical Trial.
Invited commentary.
Iyer KS. Iyer KS. Asian Cardiovasc Thorac Ann. 2015 Jul;23(6):757. doi: 10.1177/0218492314540670. Epub 2014 Jun 25. Asian Cardiovasc Thorac Ann. 2015. PMID: 24965088 No abstract available.
Editorial: Change of guard.
Iyer KS. Iyer KS. Ann Pediatr Cardiol. 2020 Oct-Dec;13(4):279-280. doi: 10.4103/apc.apc_216_20. Epub 2020 Oct 5. Ann Pediatr Cardiol. 2020. PMID: 33311914 Free PMC article. No abstract available.
Modulators of platelet function in aging.
Iyer KS, Dayal S. Iyer KS, et al. Platelets. 2020 May 18;31(4):474-482. doi: 10.1080/09537104.2019.1665641. Epub 2019 Sep 16. Platelets. 2020. PMID: 31524038 Free PMC article. Review.
Management of late presentation congenital heart disease.
Iyer PU, Moreno GE, Fernando Caneo L, Faiz T, Shekerdemian LS, Iyer KS. Iyer PU, et al. Among authors: iyer ks. Cardiol Young. 2017 Dec;27(S6):S31-S39. doi: 10.1017/S1047951117002591. Cardiol Young. 2017. PMID: 29198260 Review.
Platelet antioxidants: A conundrum in aging.
Iyer KS, Dayal S. Iyer KS, et al. EBioMedicine. 2019 Sep;47:29-30. doi: 10.1016/j.ebiom.2019.08.046. Epub 2019 Aug 27. EBioMedicine. 2019. PMID: 31471268 Free PMC article. No abstract available.
Biallelic CRELD1 variants cause a multisystem syndrome, including neurodevelopmental phenotypes, cardiac dysrhythmias, and frequent infections.
Jeffries L, Mis EK, McWalter K, Donkervoort S, Brodsky NN, Carpier JM, Ji W, Ionita C, Roy B, Morrow JS, Darbinyan A, Iyer K, Aul RB, Banka S, Chao KR, Cobbold L, Cohen S, Custodio HM, Drummond-Borg M, Elmslie F, Finanger E, Hainline BE, Helbig I, Hewson S, Hu Y, Jackson A, Josifova D, Konstantino M, Leach ME, Mak B, McCormick D, McGee E, Nelson S, Nguyen J, Nugent K, Ortega L, Goodkin HP, Roeder E, Roy S, Sapp K, Saade D, Sisodiya SM, Stals K, Towner S, Wilson W; Deciphering Developmental Disorders; Genomics England Research Consortium; Undiagnosed Disease Network; Khokha MK, Bönnemann CG, Lucas CL, Lakhani SA. Jeffries L, et al. Among authors: iyer k. Genet Med. 2024 Feb;26(2):101023. doi: 10.1016/j.gim.2023.101023. Epub 2023 Nov 7. Genet Med. 2024. PMID: 37947183
96 results