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Results by year

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

Year Number of Results
1967 1
1968 2
1970 1
1973 1
1975 1
1977 1
1978 3
1980 3
1981 5
1982 8
1983 36
1984 21
1985 19
1986 6
1987 10
1988 8
1989 7
1990 2
1991 3
1992 2
1993 1
1995 1
1996 4
1997 2
1998 3
1999 4
2000 1
2002 5
2005 1
2006 1
2007 2
2008 2
2009 1
2010 1
2011 1
2012 1
2013 5
2014 6
2015 8
2016 7
2017 6
2018 6
2019 5
2020 2
2021 1
2024 0

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Search Results

212 results

Results by year

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Page 1
Synaptic, transcriptional and chromatin genes disrupted in autism.
De Rubeis S, He X, Goldberg AP, Poultney CS, Samocha K, Cicek AE, Kou Y, Liu L, Fromer M, Walker S, Singh T, Klei L, Kosmicki J, Shih-Chen F, Aleksic B, Biscaldi M, Bolton PF, Brownfeld JM, Cai J, Campbell NG, Carracedo A, Chahrour MH, Chiocchetti AG, Coon H, Crawford EL, Curran SR, Dawson G, Duketis E, Fernandez BA, Gallagher L, Geller E, Guter SJ, Hill RS, Ionita-Laza J, Jimenz Gonzalez P, Kilpinen H, Klauck SM, Kolevzon A, Lee I, Lei I, Lei J, Lehtimäki T, Lin CF, Ma'ayan A, Marshall CR, McInnes AL, Neale B, Owen MJ, Ozaki N, Parellada M, Parr JR, Purcell S, Puura K, Rajagopalan D, Rehnström K, Reichenberg A, Sabo A, Sachse M, Sanders SJ, Schafer C, Schulte-Rüther M, Skuse D, Stevens C, Szatmari P, Tammimies K, Valladares O, Voran A, Li-San W, Weiss LA, Willsey AJ, Yu TW, Yuen RK; DDD Study; Homozygosity Mapping Collaborative for Autism; UK10K Consortium; Cook EH, Freitag CM, Gill M, Hultman CM, Lehner T, Palotie A, Schellenberg GD, Sklar P, State MW, Sutcliffe JS, Walsh CA, Scherer SW, Zwick ME, Barett JC, Cutler DJ, Roeder K, Devlin B, Daly MJ, Buxbaum JD. De Rubeis S, et al. Nature. 2014 Nov 13;515(7526):209-15. doi: 10.1038/nature13772. Epub 2014 Oct 29. Nature. 2014. PMID: 25363760 Free PMC article.
Vulvar dermatofibrosarcoma protuberans.
Barnhill DR, Boling R, Nobles W, Crooks L, Burke T. Barnhill DR, et al. Among authors: crooks l. Gynecol Oncol. 1988 May;30(1):149-52. doi: 10.1016/0090-8258(88)90059-5. Gynecol Oncol. 1988. PMID: 3366391
Bi-allelic Loss-of-Function CACNA1B Mutations in Progressive Epilepsy-Dyskinesia.
Gorman KM, Meyer E, Grozeva D, Spinelli E, McTague A, Sanchis-Juan A, Carss KJ, Bryant E, Reich A, Schneider AL, Pressler RM, Simpson MA, Debelle GD, Wassmer E, Morton J, Sieciechowicz D, Jan-Kamsteeg E, Paciorkowski AR, King MD, Cross JH, Poduri A, Mefford HC, Scheffer IE, Haack TB, McCullagh G; Deciphering Developmental Disorders Study; UK10K Consortium; NIHR BioResource; Millichap JJ, Carvill GL, Clayton-Smith J, Maher ER, Raymond FL, Kurian MA. Gorman KM, et al. Am J Hum Genet. 2019 May 2;104(5):948-956. doi: 10.1016/j.ajhg.2019.03.005. Epub 2019 Apr 11. Am J Hum Genet. 2019. PMID: 30982612 Free PMC article.
Nuclear magnetic resonance imaging.
Crooks L, Herfkens R, Kaufman L, Hoenninger J, Arakawa M, McRee R, Watts J. Crooks L, et al. Prog Nucl Med. 1981;7:149-63. Prog Nucl Med. 1981. PMID: 7323305
Magnetic resonance imaging of the cardiovascular system.
Higgins CB, Kaufman L, Crooks LE. Higgins CB, et al. Among authors: crooks le. Am Heart J. 1985 Jan;109(1):136-52. doi: 10.1016/0002-8703(85)90426-0. Am Heart J. 1985. PMID: 3880990 Review. No abstract available.
212 results