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

Year Number of Results
1981 2
1983 4
1984 2
1985 5
1986 10
1987 10
1988 7
1989 7
1990 8
1991 2
1992 2
1993 5
1994 3
1995 1
1996 4
1997 8
1998 6
1999 7
2001 1
2002 1
2003 3
2004 2
2005 3
2006 3
2008 4
2009 1
2010 2
2011 2
2013 3
2014 4
2016 2
2019 1
2021 1
2022 1
2024 1

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126 results

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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.
Kenny-Caffey syndrome: an Arab variant?
Sabry MA, Farag TI, Shaltout AA, Zaki M, Al-Mazidi Z, Abulhassan SJ, Al-Torki N, Quishawi A, Al Awadi SA. Sabry MA, et al. Among authors: al awadi sa. Clin Genet. 1999 Jan;55(1):44-9. doi: 10.1034/j.1399-0004.1999.550108.x. Clin Genet. 1999. PMID: 10066031 Review.
Apparently nonmosaic trisomy 22: clinical report and review.
Sundareshan TS, Naguib KK, al-Awadi SA, Redha MA, Hamoud MS. Sundareshan TS, et al. Among authors: al awadi sa. Am J Med Genet. 1990 May;36(1):7-10. doi: 10.1002/ajmg.1320360103. Am J Med Genet. 1990. PMID: 2185636 Review.
Disease profile of 400 institutionalized mentally retarded patients in Kuwait.
Farag TI, al-Awadi SA, el-Badramary MH, Aref MA, Kasrawi B, Krishna Murthy DS, el-Khalifa MY, Yadav G, Marafie MJ, Bastaki L, et al. Farag TI, et al. Among authors: al awadi sa. Clin Genet. 1993 Dec;44(6):329-34. doi: 10.1111/j.1399-0004.1993.tb03910.x. Clin Genet. 1993. PMID: 8131306 Review.
Mosaic Turner syndrome: cytogenetics versus FISH.
Abulhasan SJ, Tayel SM, al-Awadi SA. Abulhasan SJ, et al. Among authors: al awadi sa. Ann Hum Genet. 1999 May;63(Pt 3):199-206. doi: 10.1046/j.1469-1809.1999.6330199.x. Ann Hum Genet. 1999. PMID: 10738532
Anencephaly: disappearing in Kuwait?
Al-Awadi SA, Farag TI, Teebi AS, Naguib KK, El-Khalifa MY. Al-Awadi SA, et al. Lancet. 1984 Sep 22;2(8404):701-2. doi: 10.1016/s0140-6736(84)91264-9. Lancet. 1984. PMID: 6147729 No abstract available.
Down syndrome in Kuwait.
al-Awadi SA, Farag TI, Teebi AS, Naguib KK, Sundareshan TS, Murthy DS. al-Awadi SA, et al. Am J Med Genet Suppl. 1990;7:87-8. doi: 10.1002/ajmg.1320370717. Am J Med Genet Suppl. 1990. PMID: 2149982
126 results