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Items: 1 to 20 of 48

1.

Eye color and the prediction of complex phenotypes from genotypes.

Liu F, van Duijn K, Vingerling JR, Hofman A, Uitterlinden AG, Janssens AC, Kayser M.

Curr Biol. 2009 Mar 10;19(5):R192-3. doi: 10.1016/j.cub.2009.01.027. No abstract available.

2.

Prediction of eye color in the Slovenian population using the IrisPlex SNPs.

Kastelic V, Pośpiech E, Draus-Barini J, Branicki W, Drobnič K.

Croat Med J. 2013 Aug;54(4):381-6.

3.

Genotyping of five single nucleotide polymorphisms in the OCA2 and HERC2 genes associated with blue-brown eye color in the Japanese population.

Iida R, Ueki M, Takeshita H, Fujihara J, Nakajima T, Kominato Y, Nagao M, Yasuda T.

Cell Biochem Funct. 2009 Jul;27(5):323-7. doi: 10.1002/cbf.1572.

PMID:
19472299
4.

Model-based prediction of human hair color using DNA variants.

Branicki W, Liu F, van Duijn K, Draus-Barini J, Pośpiech E, Walsh S, Kupiec T, Wojas-Pelc A, Kayser M.

Hum Genet. 2011 Apr;129(4):443-54. doi: 10.1007/s00439-010-0939-8.

5.

DNA-based eye colour prediction across Europe with the IrisPlex system.

Walsh S, Wollstein A, Liu F, Chakravarthy U, Rahu M, Seland JH, Soubrane G, Tomazzoli L, Topouzis F, Vingerling JR, Vioque J, Fletcher AE, Ballantyne KN, Kayser M.

Forensic Sci Int Genet. 2012 May;6(3):330-40. doi: 10.1016/j.fsigen.2011.07.009.

PMID:
21813346
6.

Genotype-phenotype associations and human eye color.

White D, Rabago-Smith M.

J Hum Genet. 2011 Jan;56(1):5-7. doi: 10.1038/jhg.2010.126. Review.

PMID:
20944644
7.

Accuracy of genome-wide imputation of untyped markers and impacts on statistical power for association studies.

Hao K, Chudin E, McElwee J, Schadt EE.

BMC Genet. 2009 Jun 16;10:27. doi: 10.1186/1471-2156-10-27.

8.

Evaluation of the IrisPlex DNA-based eye color prediction assay in a United States population.

Dembinski GM, Picard CJ.

Forensic Sci Int Genet. 2014 Mar;9:111-7. doi: 10.1016/j.fsigen.2013.12.003.

PMID:
24528589
9.

The STAT4 gene influences the genetic predisposition to systemic sclerosis phenotype.

Rueda B, Broen J, Simeon C, Hesselstrand R, Diaz B, Suárez H, Ortego-Centeno N, Riemekasten G, Fonollosa V, Vonk MC, van den Hoogen FH, Sanchez-Román J, Aguirre-Zamorano MA, García-Portales R, Pros A, Camps MT, Gonzalez-Gay MA, Coenen MJ, Airo P, Beretta L, Scorza R, van Laar J, Gonzalez-Escribano MF, Nelson JL, Radstake TR, Martin J.

Hum Mol Genet. 2009 Jun 1;18(11):2071-7. doi: 10.1093/hmg/ddp119.

10.

Pigment phenotype and biogeographical ancestry from ancient skeletal remains: inferences from multiplexed autosomal SNP analysis.

Bouakaze C, Keyser C, Crubézy E, Montagnon D, Ludes B.

Int J Legal Med. 2009 Jul;123(4):315-25. doi: 10.1007/s00414-009-0348-5.

PMID:
19415315
11.

Blue eyes in lemurs and humans: same phenotype, different genetic mechanism.

Bradley BJ, Pedersen A, Mundy NI.

Am J Phys Anthropol. 2009 Jun;139(2):269-73. doi: 10.1002/ajpa.21010.

PMID:
19278018
13.

Further analyses support the association between light eye color and alcohol dependence.

Sulovari A, Kranzler HR, Farrer LA, Gelernter J, Li D.

Am J Med Genet B Neuropsychiatr Genet. 2015 Dec;168(8):757-60. doi: 10.1002/ajmg.b.32357. No abstract available.

PMID:
26290254
14.

Association between the NBS1 E185Q polymorphism and cancer risk: a meta-analysis.

Lu M, Lu J, Yang X, Yang M, Tan H, Yun B, Shi L.

BMC Cancer. 2009 Apr 24;9:124. doi: 10.1186/1471-2407-9-124.

15.

[Association between nicotine dependence and the -521 promoter polymorfism of the dopamine D4 receptor in patients with major depression].

Kótyuk E, Kovács-Nagy R, Faludi G, Urbán R, Rónai Z, Sasvári-Székely M, Székely A.

Neuropsychopharmacol Hung. 2009 Jun;11(2):59-67. Hungarian.

16.

Phenotype-genotype interactions on renal function in type 2 diabetes: an analysis using structural equation modelling.

Song XY, Lee SY, Ma RC, So WY, Cai JH, Tam C, Lam V, Ying W, Ng MC, Chan JC.

Diabetologia. 2009 Aug;52(8):1543-53. doi: 10.1007/s00125-009-1400-1.

PMID:
19479237
17.

Further evidence for an association between mandibular height and the growth hormone receptor gene in a Japanese population.

Tomoyasu Y, Yamaguchi T, Tajima A, Nakajima T, Inoue I, Maki K.

Am J Orthod Dentofacial Orthop. 2009 Oct;136(4):536-41. doi: 10.1016/j.ajodo.2007.10.054.

PMID:
19815155
18.

Association between variants in the genes for leptin, leptin receptor, and proopiomelanocortin with chronic heart failure in the Czech population.

Bienertová-Vasků JA, Spinarová L, Bienert P, Vasků A.

Heart Vessels. 2009 Mar;24(2):131-7. doi: 10.1007/s00380-008-1090-5.

PMID:
19337797
19.

Association of nicotinic acetylcholine receptor subunit alpha 4 polymorphisms with nicotine dependence in 5500 Germans.

Breitling LP, Dahmen N, Mittelstrass K, Rujescu D, Gallinat J, Fehr C, Giegling I, Lamina C, Illig T, Müller H, Raum E, Rothenbacher D, Wichmann HE, Brenner H, Winterer G.

Pharmacogenomics J. 2009 Aug;9(4):219-24. doi: 10.1038/tpj.2009.6.

PMID:
19290018
20.

TNF block haplotypes associated with conserved MHC haplotypes in European, Asian and Australian Aboriginal donors.

Valente FP, Tan C, Phipps M, Witt CS, Kaur G, Gut I, Allcock R, Price P.

Tissue Antigens. 2009 Jul;74(1):57-61. doi: 10.1111/j.1399-0039.2009.01258.x.

PMID:
19392789
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