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Results: 1 to 20 of 66

1.

Variants in SNAP25 are targets of natural selection and influence verbal performances in women.

Cagliani R, Riva S, Marino C, Fumagalli M, D'Angelo MG, Riva V, Comi GP, Pozzoli U, Forni D, Cáceres M, Bresolin N, Clerici M, Sironi M.

Cell Mol Life Sci. 2012 May;69(10):1705-15. doi: 10.1007/s00018-011-0896-y. Epub 2011 Dec 23.

PMID:
22193912
[PubMed - indexed for MEDLINE]
2.

Common variants underlying cognitive ability: further evidence for association between the SNAP-25 gene and cognition using a family-based study in two independent Dutch cohorts.

Gosso MF, de Geus EJ, Polderman TJ, Boomsma DI, Heutink P, Posthuma D.

Genes Brain Behav. 2008 Apr;7(3):355-64. Epub 2007 Oct 1.

PMID:
17908175
[PubMed - indexed for MEDLINE]
3.

Supporting the generalist genes hypothesis for intellectual ability/disability: the case of SNAP25.

Rizzi TS, Beunders G, Rizzu P, Sistermans E, Twisk JW, van Mechelen W, Deijen JB, Meijers-Heijboer H, Verhage M, Heutink P, Posthuma D.

Genes Brain Behav. 2012 Oct;11(7):767-71. doi: 10.1111/j.1601-183X.2012.00819.x. Epub 2012 Jul 28.

PMID:
22762387
[PubMed - indexed for MEDLINE]
4.

Allelic variants of SNAP25 in a family-based sample of ADHD.

Renner TJ, Walitza S, Dempfle A, Eckert L, Romanos M, Gerlach M, Schäfer H, Warnke A, Lesch KP, Jacob C.

J Neural Transm. 2008;115(2):317-21. doi: 10.1007/s00702-007-0840-3. Epub 2008 Feb 4.

PMID:
18250960
[PubMed - indexed for MEDLINE]
5.

Gender differences in cognitive ability associated with genetic variants of NLGN4.

Zhang K, Gao X, Qi H, Li J, Zheng Z, Zhang F.

Neuropsychobiology. 2010;62(4):221-8. doi: 10.1159/000319948. Epub 2010 Aug 14.

PMID:
20714171
[PubMed - indexed for MEDLINE]
6.

A SNAP25 promoter variant is associated with early-onset bipolar disorder and a high expression level in brain.

Etain B, Dumaine A, Mathieu F, Chevalier F, Henry C, Kahn JP, Deshommes J, Bellivier F, Leboyer M, Jamain S.

Mol Psychiatry. 2010 Jul;15(7):748-55. doi: 10.1038/mp.2008.148. Epub 2009 Jan 6.

PMID:
19125158
[PubMed - indexed for MEDLINE]
Free PMC Article
7.

Candidate genes involved in neural plasticity and the risk for attention-deficit hyperactivity disorder: a meta-analysis of 8 common variants.

Forero DA, Arboleda GH, Vasquez R, Arboleda H.

J Psychiatry Neurosci. 2009 Sep;34(5):361-6.

PMID:
19721846
[PubMed - indexed for MEDLINE]
Free PMC Article
8.

Long-term balancing selection maintains trans-specific polymorphisms in the human TRIM5 gene.

Cagliani R, Fumagalli M, Biasin M, Piacentini L, Riva S, Pozzoli U, Bonaglia MC, Bresolin N, Clerici M, Sironi M.

Hum Genet. 2010 Dec;128(6):577-88. doi: 10.1007/s00439-010-0884-6. Epub 2010 Sep 2.

PMID:
20811909
[PubMed - indexed for MEDLINE]
9.

KLOTHO genotype and cognitive ability in childhood and old age in the same individuals.

Deary IJ, Harris SE, Fox HC, Hayward C, Wright AF, Starr JM, Whalley LJ.

Neurosci Lett. 2005 Apr 11;378(1):22-7. Epub 2005 Jan 22.

PMID:
15763166
[PubMed - indexed for MEDLINE]
10.

Interrogating 11 fast-evolving genes for signatures of recent positive selection in worldwide human populations.

Moreno-Estrada A, Tang K, Sikora M, Marquès-Bonet T, Casals F, Navarro A, Calafell F, Bertranpetit J, Stoneking M, Bosch E.

Mol Biol Evol. 2009 Oct;26(10):2285-97. doi: 10.1093/molbev/msp134. Epub 2009 Jul 3.

PMID:
19578157
[PubMed - indexed for MEDLINE]
Free Article
11.

A Functional polymorphism under positive evolutionary selection in ADRB2 is associated with human intelligence with opposite effects in the young and the elderly.

Bochdanovits Z, Gosso FM, van den Berg L, Rizzu P, Polderman TJ, Pardo LM, Houlihan LM, Luciano M, Starr JM, Harris SE, Deary IJ, de Geus EJ, Boomsma DI, Heutink P, Posthuma D.

Behav Genet. 2009 Jan;39(1):15-23. doi: 10.1007/s10519-008-9233-0. Epub 2008 Oct 15.

PMID:
18855131
[PubMed - indexed for MEDLINE]
12.

An evolutionary history of the selectin gene cluster in humans.

Fumagalli M, Fracassetti M, Cagliani R, Forni D, Pozzoli U, Comi GP, Marini F, Bresolin N, Clerici M, Sironi M.

Heredity (Edinb). 2012 Aug;109(2):117-26. doi: 10.1038/hdy.2012.20. Epub 2012 May 2.

PMID:
22549518
[PubMed - indexed for MEDLINE]
Free PMC Article
13.

Multiple rare variants as a cause of a common phenotype: several different lactase persistence associated alleles in a single ethnic group.

Ingram CJ, Raga TO, Tarekegn A, Browning SL, Elamin MF, Bekele E, Thomas MG, Weale ME, Bradman N, Swallow DM.

J Mol Evol. 2009 Dec;69(6):579-88. doi: 10.1007/s00239-009-9301-y. Epub 2009 Nov 24.

PMID:
19937006
[PubMed - indexed for MEDLINE]
14.

Sequence variation in human succinate dehydrogenase genes: evidence for long-term balancing selection on SDHA.

Baysal BE, Lawrence EC, Ferrell RE.

BMC Biol. 2007 Mar 21;5:12.

PMID:
17376234
[PubMed - indexed for MEDLINE]
Free PMC Article
15.

Replication study of candidate genes for cognitive abilities: the Lothian Birth Cohort 1936.

Houlihan LM, Harris SE, Luciano M, Gow AJ, Starr JM, Visscher PM, Deary IJ.

Genes Brain Behav. 2009 Mar;8(2):238-47. doi: 10.1111/j.1601-183X.2008.00470.x. Epub 2008 Dec 10.

PMID:
19077115
[PubMed - indexed for MEDLINE]
16.

The SNAP25 gene as a susceptibility gene contributing to attention-deficit hyperactivity disorder.

Feng Y, Crosbie J, Wigg K, Pathare T, Ickowicz A, Schachar R, Tannock R, Roberts W, Malone M, Swanson J, Kennedy JL, Barr CL.

Mol Psychiatry. 2005 Nov;10(11):998-1005, 973.

PMID:
16088329
[PubMed - indexed for MEDLINE]
17.

Genetic variability in the ACE gene region surrounding the Alu I/D polymorphism is maintained by balancing selection in human populations.

Cagliani R, Fumagalli M, Riva S, Pozzoli U, Comi GP, Bresolin N, Sironi M.

Pharmacogenet Genomics. 2010 Feb;20(2):131-4. doi: 10.1097/FPC.0b013e3283333532.

PMID:
20038859
[PubMed - indexed for MEDLINE]
18.

Population genetics of IFIH1: ancient population structure, local selection, and implications for susceptibility to type 1 diabetes.

Fumagalli M, Cagliani R, Riva S, Pozzoli U, Biasin M, Piacentini L, Comi GP, Bresolin N, Clerici M, Sironi M.

Mol Biol Evol. 2010 Nov;27(11):2555-66. doi: 10.1093/molbev/msq141. Epub 2010 Jun 10.

PMID:
20538742
[PubMed - indexed for MEDLINE]
Free Article
19.

Association of interleukin-1β genetic polymorphisms with cognitive performance in elderly females without dementia.

Sasayama D, Hori H, Teraishi T, Hattori K, Ota M, Matsuo J, Kawamoto Y, Kinoshita Y, Higuchi T, Amano N, Kunugi H.

J Hum Genet. 2011 Aug;56(8):613-6. doi: 10.1038/jhg.2011.56. Epub 2011 May 26.

PMID:
21614008
[PubMed - indexed for MEDLINE]
20.

Identification of a new susceptibility variant for multiple sclerosis in OAS1 by population genetics analysis.

Cagliani R, Fumagalli M, Guerini FR, Riva S, Galimberti D, Comi GP, Agliardi C, Scarpini E, Pozzoli U, Forni D, Caputo D, Asselta R, Biasin M, Paraboschi EM, Bresolin N, Clerici M, Sironi M.

Hum Genet. 2012 Jan;131(1):87-97. doi: 10.1007/s00439-011-1053-2. Epub 2011 Jul 7.

PMID:
21735172
[PubMed - indexed for MEDLINE]

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