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

Year Number of Results
1982 1
1983 1
1984 1
1986 1
1987 1
2002 1
2003 1
2006 2
2007 1
2012 1
2013 1
2014 1
2015 1
2016 1
2017 1
2018 7
2019 10
2020 6
2021 4
2022 0
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Search Results

35 results
Results by year
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Page 1
Apoptotic caspases prevent the induction of type I interferons by mitochondrial DNA.
Rongvaux A, Jackson R, Harman CC, Li T, West AP, de Zoete MR, Wu Y, Yordy B, Lakhani SA, Kuan CY, Taniguchi T, Shadel GS, Chen ZJ, Iwasaki A, Flavell RA. Rongvaux A, et al. Among authors: lakhani sa. Cell. 2014 Dec 18;159(7):1563-77. doi: 10.1016/j.cell.2014.11.037. Cell. 2014. PMID: 25525875 Free PMC article.
Acid-Base Disorders.
Hsu BS, Lakhani SA, Wilhelm M. Hsu BS, et al. Among authors: lakhani sa. Pediatr Rev. 2016 Sep;37(9):361-9. doi: 10.1542/pir.2015-0093. Pediatr Rev. 2016. PMID: 27587638 Review. No abstract available.
Data Science for Child Health.
Bennett TD, Callahan TJ, Feinstein JA, Ghosh D, Lakhani SA, Spaeder MC, Szefler SJ, Kahn MG. Bennett TD, et al. Among authors: lakhani sa. J Pediatr. 2019 May;208:12-22. doi: 10.1016/j.jpeds.2018.12.041. Epub 2019 Jan 25. J Pediatr. 2019. PMID: 30686480 Free PMC article. Review. No abstract available.
Toll-like receptor signaling in sepsis.
Lakhani SA, Bogue CW. Lakhani SA, et al. Curr Opin Pediatr. 2003 Jun;15(3):278-82. doi: 10.1097/00008480-200306000-00009. Curr Opin Pediatr. 2003. PMID: 12806257 Review.
Pediatric Traumatic Brain Injury.
Schaller AL, Lakhani SA, Hsu BS. Schaller AL, et al. Among authors: lakhani sa. S D Med. 2015 Oct;68(10):457-61, 463. S D Med. 2015. PMID: 26630835
DLG5 variants are associated with multiple congenital anomalies including ciliopathy phenotypes.
Marquez J, Mann N, Arana K, Deniz E, Ji W, Konstantino M, Mis EK, Deshpande C, Jeffries L, McGlynn J, Hugo H, Widmeier E, Konrad M, Tasic V, Morotti R, Baptista J, Ellard S, Lakhani SA, Hildebrandt F, Khokha MK. Marquez J, et al. Among authors: lakhani sa. J Med Genet. 2021 Jul;58(7):453-464. doi: 10.1136/jmedgenet-2019-106805. Epub 2020 Jul 6. J Med Genet. 2021. PMID: 32631816 Free PMC article.
Expansion of NEUROD2 phenotypes to include developmental delay without seizures.
Mis EK, Sega AG, Signer RH, Cartwright T, Ji W, Martinez-Agosto JA, Nelson SF, Palmer CGS, Lee H, Mitzelfelt T, Konstantino M; Undiagnosed Diseases Network, Jeffries L, Khokha MK, Marco E, Martin MG, Lakhani SA. Mis EK, et al. Among authors: lakhani sa. Am J Med Genet A. 2021 Apr;185(4):1076-1080. doi: 10.1002/ajmg.a.62064. Epub 2021 Jan 13. Am J Med Genet A. 2021. PMID: 33438828
Novel truncating mutations in CTNND1 cause a dominant craniofacial and cardiac syndrome.
Alharatani R, Ververi A, Beleza-Meireles A, Ji W, Mis E, Patterson QT, Griffin JN, Bhujel N, Chang CA, Dixit A, Konstantino M, Healy C, Hannan S, Neo N, Cash A, Li D, Bhoj E, Zackai EH, Cleaver R, Baralle D, McEntagart M, Newbury-Ecob R, Scott R, Hurst JA, Au PYB, Hosey MT, Khokha M, Marciano DK, Lakhani SA, Liu KJ. Alharatani R, et al. Among authors: lakhani sa. Hum Mol Genet. 2020 Jul 21;29(11):1900-1921. doi: 10.1093/hmg/ddaa050. Hum Mol Genet. 2020. PMID: 32196547 Free PMC article.
35 results