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

Year Number of Results
1959 1
1962 2
1965 1
1966 1
1967 1
1968 1
1969 2
1970 1
1971 1
1972 3
1973 3
1974 1
1975 1
1976 3
1977 1
1978 3
1979 4
1980 5
1981 4
1982 8
1984 7
1985 8
1986 4
1987 8
1988 9
1989 15
1990 13
1991 9
1992 17
1993 12
1994 13
1995 20
1996 24
1997 15
1998 20
1999 23
2000 25
2001 25
2002 27
2003 26
2004 34
2005 22
2006 42
2007 53
2008 36
2009 46
2010 71
2011 87
2012 79
2013 75
2014 88
2015 83
2016 105
2017 140
2018 135
2019 147
2020 182
2021 189
2022 196
2023 173
2024 214
2025 142

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2,413 results

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Page 1
Heterozygous ANKRD17 loss-of-function variants cause a syndrome with intellectual disability, speech delay, and dysmorphism.
Chopra M, McEntagart M, Clayton-Smith J, Platzer K, Shukla A, Girisha KM, Kaur A, Kaur P, Pfundt R, Veenstra-Knol H, Mancini GMS, Cappuccio G, Brunetti-Pierri N, Kortüm F, Hempel M, Denecke J, Lehman A; CAUSES Study; Kleefstra T, Stuurman KE, Wilke M, Thompson ML, Bebin EM, Bijlsma EK, Hoffer MJV, Peeters-Scholte C, Slavotinek A, Weiss WA, Yip T, Hodoglugil U, Whittle A, diMonda J, Neira J, Yang S, Kirby A, Pinz H, Lechner R, Sleutels F, Helbig I, McKeown S, Helbig K, Willaert R, Juusola J, Semotok J, Hadonou M, Short J; Genomics England Research Consortium; Yachelevich N, Lala S, Fernández-Jaen A, Pelayo JP, Klöckner C, Kamphausen SB, Abou Jamra R, Arelin M, Innes AM, Niskakoski A, Amin S, Williams M, Evans J, Smithson S, Smedley D, de Burca A, Kini U, Delatycki MB, Gallacher L, Yeung A, Pais L, Field M, Martin E, Charles P, Courtin T, Keren B, Iascone M, Cereda A, Poke G, Abadie V, Chalouhi C, Parthasarathy P, Halliday BJ, Robertson SP, Lyonnet S, Amiel J, Gordon CT. Chopra M, et al. Among authors: amin s. Am J Hum Genet. 2021 Jun 3;108(6):1138-1150. doi: 10.1016/j.ajhg.2021.04.007. Epub 2021 Apr 27. Am J Hum Genet. 2021. PMID: 33909992 Free PMC article.
Primary intraocular lymphoma.
Sagoo MS, Mehta H, Swampillai AJ, Cohen VM, Amin SZ, Plowman PN, Lightman S. Sagoo MS, et al. Among authors: amin sz. Surv Ophthalmol. 2014 Sep-Oct;59(5):503-16. doi: 10.1016/j.survophthal.2013.12.001. Epub 2013 Dec 31. Surv Ophthalmol. 2014. PMID: 24560125 Free article. Review.
Bone graft substitutes.
Laurencin C, Khan Y, El-Amin SF. Laurencin C, et al. Among authors: el amin sf. Expert Rev Med Devices. 2006 Jan;3(1):49-57. doi: 10.1586/17434440.3.1.49. Expert Rev Med Devices. 2006. PMID: 16359252 Review.
Osteoporosis in men.
Khosla S, Amin S, Orwoll E. Khosla S, et al. Among authors: amin s. Endocr Rev. 2008 Jun;29(4):441-64. doi: 10.1210/er.2008-0002. Epub 2008 May 1. Endocr Rev. 2008. PMID: 18451258 Free PMC article. Review.
Allergens in Common Brands of Clobetasol.
Ramani L, Haidari W, Hall S, Amin S, Chisolm S, Feldman S. Ramani L, et al. Among authors: amin s. J Drugs Dermatol. 2023 May 1;22(5):491-495. doi: 10.36849/JDD.4651. J Drugs Dermatol. 2023. PMID: 37133477
Severity Assessment in CDKL5 Deficiency Disorder.
Demarest S, Pestana-Knight EM, Olson HE, Downs J, Marsh ED, Kaufmann WE, Partridge CA, Leonard H, Gwadry-Sridhar F, Frame KE, Cross JH, Chin RFM, Parikh S, Panzer A, Weisenberg J, Utley K, Jaksha A, Amin S, Khwaja O, Devinsky O, Neul JL, Percy AK, Benke TA. Demarest S, et al. Among authors: amin s. Pediatr Neurol. 2019 Aug;97:38-42. doi: 10.1016/j.pediatrneurol.2019.03.017. Epub 2019 Mar 27. Pediatr Neurol. 2019. PMID: 31147226 Free PMC article. Review.
2,413 results