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

Year Number of Results
1933 1
1960 1
1977 1
1981 1
1982 1
1983 2
1984 3
1985 3
1986 2
1987 4
1988 3
1989 4
1990 3
1991 2
1992 1
1993 2
1994 1
1995 4
1996 1
1997 5
1998 3
1999 7
2000 3
2001 4
2002 4
2003 1
2004 2
2005 2
2006 2
2007 2
2008 2
2009 5
2010 9
2011 13
2012 17
2013 14
2014 11
2015 11
2016 20
2017 22
2018 17
2019 11
2020 22
2021 21
2022 27
2023 32
2024 10

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297 results

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Page 1
Bi-allelic variants in INTS11 are associated with a complex neurological disorder.
Tepe B, Macke EL, Niceta M, Weisz Hubshman M, Kanca O, Schultz-Rogers L, Zarate YA, Schaefer GB, Granadillo De Luque JL, Wegner DJ, Cogne B, Gilbert-Dussardier B, Le Guillou X, Wagner EJ, Pais LS, Neil JE, Mochida GH, Walsh CA, Magal N, Drasinover V, Shohat M, Schwab T, Schmitz C, Clark K, Fine A, Lanpher B, Gavrilova R, Blanc P, Burglen L, Afenjar A, Steel D, Kurian MA, Prabhakar P, Gößwein S, Di Donato N, Bertini ES; Undiagnosed Diseases Network; Wangler MF, Yamamoto S, Tartaglia M, Klee EW, Bellen HJ. Tepe B, et al. Among authors: prabhakar p. Am J Hum Genet. 2023 May 4;110(5):774-789. doi: 10.1016/j.ajhg.2023.03.012. Epub 2023 Apr 12. Am J Hum Genet. 2023. PMID: 37054711 Free PMC article.
Mutations in ADAR1 cause Aicardi-Goutières syndrome associated with a type I interferon signature.
Rice GI, Kasher PR, Forte GM, Mannion NM, Greenwood SM, Szynkiewicz M, Dickerson JE, Bhaskar SS, Zampini M, Briggs TA, Jenkinson EM, Bacino CA, Battini R, Bertini E, Brogan PA, Brueton LA, Carpanelli M, De Laet C, de Lonlay P, del Toro M, Desguerre I, Fazzi E, Garcia-Cazorla A, Heiberg A, Kawaguchi M, Kumar R, Lin JP, Lourenco CM, Male AM, Marques W Jr, Mignot C, Olivieri I, Orcesi S, Prabhakar P, Rasmussen M, Robinson RA, Rozenberg F, Schmidt JL, Steindl K, Tan TY, van der Merwe WG, Vanderver A, Vassallo G, Wakeling EL, Wassmer E, Whittaker E, Livingston JH, Lebon P, Suzuki T, McLaughlin PJ, Keegan LP, O'Connell MA, Lovell SC, Crow YJ. Rice GI, et al. Among authors: prabhakar p. Nat Genet. 2012 Nov;44(11):1243-8. doi: 10.1038/ng.2414. Epub 2012 Sep 23. Nat Genet. 2012. PMID: 23001123 Free PMC article.
The circadian rhythm: an influential soundtrack in the diabetes story.
Hariri A, Mirian M, Zarrabi A, Kohandel M, Amini-Pozveh M, Aref AR, Tabatabaee A, Prabhakar PK, Sivakumar PM. Hariri A, et al. Among authors: prabhakar pk. Front Endocrinol (Lausanne). 2023 Jun 27;14:1156757. doi: 10.3389/fendo.2023.1156757. eCollection 2023. Front Endocrinol (Lausanne). 2023. PMID: 37441501 Free PMC article. Review.
State of newborn health in India.
Sankar MJ, Neogi SB, Sharma J, Chauhan M, Srivastava R, Prabhakar PK, Khera A, Kumar R, Zodpey S, Paul VK. Sankar MJ, et al. Among authors: prabhakar pk. J Perinatol. 2016 Dec;36(s3):S3-S8. doi: 10.1038/jp.2016.183. J Perinatol. 2016. PMID: 27924104 Free PMC article. Review.
Care of newborn in the community and at home.
Neogi SB, Sharma J, Chauhan M, Khanna R, Chokshi M, Srivastava R, Prabhakar PK, Khera A, Kumar R, Zodpey S, Paul VK. Neogi SB, et al. Among authors: prabhakar pk. J Perinatol. 2016 Dec;36(s3):S13-S17. doi: 10.1038/jp.2016.185. J Perinatol. 2016. PMID: 27924109 Free PMC article. Review.
Genetic insights into cardiac tumors: a comprehensive review.
Sankarasubramanian S, Prabhakar P, Narasimhan MK. Sankarasubramanian S, et al. Among authors: prabhakar p. Med Oncol. 2022 Aug 16;39(11):164. doi: 10.1007/s12032-022-01761-5. Med Oncol. 2022. PMID: 35972566 Review.
297 results