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

Year Number of Results
1970 1
1981 7
1982 2
1983 2
1984 8
1985 2
1986 6
1987 4
1988 4
1989 5
1990 4
1991 7
1992 4
1993 6
1994 5
1995 6
1996 4
1997 6
1998 7
1999 6
2000 3
2001 2
2002 10
2003 2
2004 3
2005 6
2006 5
2007 4
2008 4
2009 5
2010 9
2011 8
2012 3
2013 4
2014 6
2015 7
2016 4
2017 2
2018 2
2019 8
2020 2
2023 2
2024 1

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186 results

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Page 1
X-exome sequencing of 405 unresolved families identifies seven novel intellectual disability genes.
Hu H, Haas SA, Chelly J, Van Esch H, Raynaud M, de Brouwer AP, Weinert S, Froyen G, Frints SG, Laumonnier F, Zemojtel T, Love MI, Richard H, Emde AK, Bienek M, Jensen C, Hambrock M, Fischer U, Langnick C, Feldkamp M, Wissink-Lindhout W, Lebrun N, Castelnau L, Rucci J, Montjean R, Dorseuil O, Billuart P, Stuhlmann T, Shaw M, Corbett MA, Gardner A, Willis-Owen S, Tan C, Friend KL, Belet S, van Roozendaal KE, Jimenez-Pocquet M, Moizard MP, Ronce N, Sun R, O'Keeffe S, Chenna R, van Bömmel A, Göke J, Hackett A, Field M, Christie L, Boyle J, Haan E, Nelson J, Turner G, Baynam G, Gillessen-Kaesbach G, Müller U, Steinberger D, Budny B, Badura-Stronka M, Latos-Bieleńska A, Ousager LB, Wieacker P, Rodríguez Criado G, Bondeson ML, Annerén G, Dufke A, Cohen M, Van Maldergem L, Vincent-Delorme C, Echenne B, Simon-Bouy B, Kleefstra T, Willemsen M, Fryns JP, Devriendt K, Ullmann R, Vingron M, Wrogemann K, Wienker TF, Tzschach A, van Bokhoven H, Gecz J, Jentsch TJ, Chen W, Ropers HH, Kalscheuer VM. Hu H, et al. Among authors: anneren g. Mol Psychiatry. 2016 Jan;21(1):133-48. doi: 10.1038/mp.2014.193. Epub 2015 Feb 3. Mol Psychiatry. 2016. PMID: 25644381 Free PMC article.
Genotype-phenotype analysis of 18q12.1-q12.2 copy number variation in autism.
Wang P, Carrion P, Qiao Y, Tyson C, Hrynchak M, Calli K, Lopez-Rangel E, Andrieux J, Delobel B, Duban-Bedu B, Thuresson AC, Annerén G, Liu X, Rajcan-Separovic E, Suzanne Lewis ME. Wang P, et al. Among authors: anneren g. Eur J Med Genet. 2013 Aug;56(8):420-5. doi: 10.1016/j.ejmg.2013.05.006. Epub 2013 May 29. Eur J Med Genet. 2013. PMID: 23727450 Review.
Autism needs to be considered in children with Down Syndrome.
Wester Oxelgren U, Åberg M, Myrelid Å, Annerén G, Westerlund J, Gustafsson J, Fernell E. Wester Oxelgren U, et al. Among authors: anneren g. Acta Paediatr. 2019 Nov;108(11):2019-2026. doi: 10.1111/apa.14850. Epub 2019 Jun 9. Acta Paediatr. 2019. PMID: 31090964
Cardio-facio-cutaneous syndrome: does genotype predict phenotype?
Allanson JE, Annerén G, Aoki Y, Armour CM, Bondeson ML, Cave H, Gripp KW, Kerr B, Nystrom AM, Sol-Church K, Verloes A, Zenker M. Allanson JE, et al. Among authors: anneren g. Am J Med Genet C Semin Med Genet. 2011 May 15;157C(2):129-35. doi: 10.1002/ajmg.c.30295. Epub 2011 Apr 14. Am J Med Genet C Semin Med Genet. 2011. PMID: 21495173 Free PMC article.
Chromosomal anomalies in first-trimester miscarriages.
Ljunger E, Cnattingius S, Lundin C, Annerén G. Ljunger E, et al. Among authors: anneren g. Acta Obstet Gynecol Scand. 2005 Nov;84(11):1103-7. doi: 10.1111/j.0001-6349.2005.00882.x. Acta Obstet Gynecol Scand. 2005. PMID: 16232180 Free article.
186 results