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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 2
2025 0

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127 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.
Fibrodysplasia ossificans progressiva.
Al-Awadi SA, Farag TI, el-Khalifa MY, Al-Ansari AG. Al-Awadi SA, et al. J R Soc Med. 1985 Oct;78(10):881-2. J R Soc Med. 1985. PMID: 4045897 Free PMC article. No abstract available.
Consanguinity among the Kuwaiti population.
Al-Awadi SA, Moussa MA, Naguib KK, Farag TI, Teebi AS, el-Khalifa M, el-Dossary L. Al-Awadi SA, et al. Clin Genet. 1985 May;27(5):483-6. doi: 10.1111/j.1399-0004.1985.tb00236.x. Clin Genet. 1985. PMID: 4006273
Phenylketonuria in Kuwait and Arab countries.
Teebi AS, Al-Awadi SA, Farag TI, Naguib KK, el-Khalifa MY. Teebi AS, et al. Among authors: al awadi sa. Eur J Pediatr. 1987 Jan;146(1):59-60. doi: 10.1007/BF00647286. Eur J Pediatr. 1987. PMID: 3582406
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
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
Penile enlargement in 3q23-q25 deletion syndrome.
Naguib KK, al-Awadi SA, Farag TI, Mohammed FM. Naguib KK, et al. Among authors: al awadi sa. Am J Med Genet. 1990 Jul;36(3):361-2. doi: 10.1002/ajmg.1320360325. Am J Med Genet. 1990. PMID: 2363439 No abstract available.
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.
127 results