Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 133


Additive genetic variation in schizophrenia risk is shared by populations of African and European descent.

de Candia TR, Lee SH, Yang J, Browning BL, Gejman PV, Levinson DF, Mowry BJ, Hewitt JK, Goddard ME, O'Donovan MC, Purcell SM, Posthuma D; International Schizophrenia Consortium; Molecular Genetics of Schizophrenia Collaboration, Visscher PM, Wray NR, Keller MC.

Am J Hum Genet. 2013 Sep 5;93(3):463-70. doi: 10.1016/j.ajhg.2013.07.007. Epub 2013 Aug 15.


Type 2 diabetes risk alleles demonstrate extreme directional differentiation among human populations, compared to other diseases.

Chen R, Corona E, Sikora M, Dudley JT, Morgan AA, Moreno-Estrada A, Nilsen GB, Ruau D, Lincoln SE, Bustamante CD, Butte AJ.

PLoS Genet. 2012;8(4):e1002621. doi: 10.1371/journal.pgen.1002621. Epub 2012 Apr 12.


Genome-wide association study of multiplex schizophrenia pedigrees.

Levinson DF, Shi J, Wang K, Oh S, Riley B, Pulver AE, Wildenauer DB, Laurent C, Mowry BJ, Gejman PV, Owen MJ, Kendler KS, Nestadt G, Schwab SG, Mallet J, Nertney D, Sanders AR, Williams NM, Wormley B, Lasseter VK, Albus M, Godard-Bauché S, Alexander M, Duan J, O'Donovan MC, Walsh D, O'Neill A, Papadimitriou GN, Dikeos D, Maier W, Lerer B, Campion D, Cohen D, Jay M, Fanous A, Eichhammer P, Silverman JM, Norton N, Zhang N, Hakonarson H, Gao C, Citri A, Hansen M, Ripke S; Schizophrenia Psychiatric GWAS Consortium, Dudbridge F, Holmans PA.

Am J Psychiatry. 2012 Sep;169(9):963-73.


LPA and PLG sequence variation and kringle IV-2 copy number in two populations.

Crawford DC, Peng Z, Cheng JF, Boffelli D, Ahearn M, Nguyen D, Shaffer T, Yi Q, Livingston RJ, Rieder MJ, Nickerson DA.

Hum Hered. 2008;66(4):199-209. doi: 10.1159/000143403. Epub 2008 Jul 9.


Variability of 128 schizophrenia-associated gene variants across distinct ethnic populations.

Ohi K, Shimada T, Yasuyama T, Uehara T, Kawasaki Y.

Transl Psychiatry. 2017 Jan 3;7(1):e988. doi: 10.1038/tp.2016.260.


Recent Positive Selection Drives the Expansion of a Schizophrenia Risk Nonsynonymous Variant at SLC39A8 in Europeans.

Li M, Wu DD, Yao YG, Huo YX, Liu JW, Su B, Chasman DI, Chu AY, Huang T, Qi L, Zheng Y; CHARGE Nutrition Working Group; DietGen Consortium, Luo XJ.

Schizophr Bull. 2016 Jan;42(1):178-90. doi: 10.1093/schbul/sbv070. Epub 2015 May 25.


Allelic differences between Han Chinese and Europeans for functional variants in ZNF804A and their association with schizophrenia.

Li M, Luo XJ, Xiao X, Shi L, Liu XY, Yin LD, Diao HB, Su B.

Am J Psychiatry. 2011 Dec;168(12):1318-25. doi: 10.1176/appi.ajp.2011.11030381. Epub 2011 Sep 2.


Replication of genetic loci for ages at menarche and menopause in the multi-ethnic Population Architecture using Genomics and Epidemiology (PAGE) study.

Carty CL, Spencer KL, Setiawan VW, Fernandez-Rhodes L, Malinowski J, Buyske S, Young A, Jorgensen NW, Cheng I, Carlson CS, Brown-Gentry K, Goodloe R, Park A, Parikh NI, Henderson B, Le Marchand L, Wactawski-Wende J, Fornage M, Matise TC, Hindorff LA, Arnold AM, Haiman CA, Franceschini N, Peters U, Crawford DC.

Hum Reprod. 2013 Jun;28(6):1695-706. doi: 10.1093/humrep/det071. Epub 2013 Mar 18.


Whole-genome patterns of common DNA variation in three human populations.

Hinds DA, Stuve LL, Nilsen GB, Halperin E, Eskin E, Ballinger DG, Frazer KA, Cox DR.

Science. 2005 Feb 18;307(5712):1072-9.


Association between a disrupted-in-schizophrenia 1 (DISC1) single nucleotide polymorphism and schizophrenia in a combined Scandinavian case-control sample.

Saetre P, Agartz I, De Franciscis A, Lundmark P, Djurovic S, Kähler A, Andreassen OA, Jakobsen KD, Rasmussen HB, Werge T, Hall H, Terenius L, Jönsson EG.

Schizophr Res. 2008 Dec;106(2-3):237-41. doi: 10.1016/j.schres.2008.08.024. Epub 2008 Sep 24.


Investigation of Caucasian rheumatoid arthritis susceptibility loci in African patients with the same disease.

Viatte S, Flynn E, Lunt M, Barnes J, Singwe-Ngandeu M, Bas S, Barton A, Gabay C.

Arthritis Res Ther. 2012 Nov 3;14(6):R239. doi: 10.1186/ar4082.


Genomic ancestry of North Africans supports back-to-Africa migrations.

Henn BM, Botigué LR, Gravel S, Wang W, Brisbin A, Byrnes JK, Fadhlaoui-Zid K, Zalloua PA, Moreno-Estrada A, Bertranpetit J, Bustamante CD, Comas D.

PLoS Genet. 2012 Jan;8(1):e1002397. doi: 10.1371/journal.pgen.1002397. Epub 2012 Jan 12.


Racial/ethnic variation in the association of lipid-related genetic variants with blood lipids in the US adult population.

Chang MH, Ned RM, Hong Y, Yesupriya A, Yang Q, Liu T, Janssens AC, Dowling NF.

Circ Cardiovasc Genet. 2011 Oct;4(5):523-33. doi: 10.1161/CIRCGENETICS.111.959577. Epub 2011 Aug 10.


Mapping of disease-associated variants in admixed populations.

Shriner D, Adeyemo A, Ramos E, Chen G, Rotimi CN.

Genome Biol. 2011;12(5):223. doi: 10.1186/gb-2011-12-5-223. Epub 2011 May 30. Review.


Potential Signals of Natural Selection in the Top Risk Loci for Coronary Artery Disease: 9p21 and 10q11.

Zanetti D, Carreras-Torres R, Esteban E, Via M, Moral P.

PLoS One. 2015 Aug 7;10(8):e0134840. doi: 10.1371/journal.pone.0134840. eCollection 2015.


ATRIUM: testing untyped SNPs in case-control association studies with related individuals.

Wang Z, McPeek MS.

Am J Hum Genet. 2009 Nov;85(5):667-78. doi: 10.1016/j.ajhg.2009.10.006.


HLA polymorphism and evaluation of European, African, and Amerindian contribution to the white and mulatto populations from Paraná, Brazil.

Probst CM, Bompeixe EP, Pereira NF, de O Dalalio MM, Visentainer JE, Tsuneto LT, Petzl-Erler ML.

Hum Biol. 2000 Aug;72(4):597-617.


Current limitations of SNP data from the public domain for studies of complex disorders: a test for ten candidate genes for obesity and osteoporosis.

Dvornyk V, Long JR, Xiong DH, Liu PY, Zhao LJ, Shen H, Zhang YY, Liu YJ, Rocha-Sanchez S, Xiao P, Recker RR, Deng HW.

BMC Genet. 2004 Feb 25;5:4.


Association of polymorphisms at the ADIPOR1 regulatory region with type 2 diabetes and body mass index in a Brazilian population with European or African ancestry.

Yeh E, Kimura L, Errera FI, Angeli CB, Mingroni-Netto RC, Silva ME, Canani LH, Passos-Bueno MR.

Braz J Med Biol Res. 2008 Jun;41(6):468-72.

Supplemental Content

Support Center