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Items: 1 to 20 of 186


Pharmacogenetic Analysis of Functional Glutamate System Gene Variants and Clinical Response to Clozapine.

Taylor DL, Tiwari AK, Lieberman JA, Potkin SG, Meltzer HY, Knight J, Remington G, Müller DJ, Kennedy JL.

Mol Neuropsychiatry. 2017 Feb;2(4):185-197. doi: 10.1159/000449224.


A Case-Control Study of the Association between Polymorphisms in the Fibrinogen Alpha Chain Gene and Schizophrenia.

Rao W, Zhou N, Zhang H, Liu R, Zhang S, Su Y, Yang G, Ma Y, Shi J, Yu Y, Yu Q.

Dis Markers. 2017;2017:3104180. doi: 10.1155/2017/3104180.


SLC12A3 variants modulate LDL cholesterol levels in the Mongolian population.

An C, Zhang K, Su X.

Lipids Health Dis. 2017 Feb 6;16(1):29. doi: 10.1186/s12944-017-0413-x.


Association of nsv823469 copy number loss with decreased risk of chronic obstructive pulmonary disease and pulmonary function in Chinese.

Chen X, Lu X, Chen J, Wu D, Qiu F, Xiong H, Pan Z, Yang L, Yang B, Xie C, Zhou Y, Huang D, Zhou Y, Lu J.

Sci Rep. 2017 Jan 12;7:40060. doi: 10.1038/srep40060.


Association between the KRAS Gene Polymorphisms and Papillary Thyroid Carcinoma in a Chinese Han Population.

Ning L, Rao W, Yu Y, Liu X, Pan Y, Ma Y, Liu R, Zhang S, Sun H, Yu Q.

J Cancer. 2016 Dec 9;7(15):2420-2426.


A cross-ethnic survey of CFB and SLC44A4, Indian ulcerative colitis GWAS hits, underscores their potential role in disease susceptibility.

Gupta A, Juyal G, Sood A, Midha V, Yamazaki K, Vich Vila A, Esaki M, Matsui T, Takahashi A, Kubo M, Weersma RK, Thelma BK.

Eur J Hum Genet. 2016 Jan;25(1):111-122. doi: 10.1038/ejhg.2016.131.


Transcriptional regulation of PNPLA3 and its impact on susceptibility to nonalcoholic fatty liver Disease (NAFLD) in humans.

Liu W, Anstee QM, Wang X, Gawrieh S, Gamazon ER, Athinarayanan S, Liu YL, Darlay R, Cordell HJ, Daly AK, Day CP, Chalasani N.

Aging (Albany NY). 2016 Oct 13;9(1):26-40. doi: 10.18632/aging.101067.


Monoamine oxidase B gene variants associated with attention deficit hyperactivity disorder in the Indo-Caucasoid population from West Bengal.

Karmakar A, Maitra S, Chakraborti B, Verma D, Sinha S, Mohanakumar KP, Rajamma U, Mukhopadhyay K.

BMC Genet. 2016 Jun 24;17(1):92. doi: 10.1186/s12863-016-0401-6.


LILRA6 copy number variation correlates with susceptibility to atopic dermatitis.

López-Álvarez MR, Jiang W, Jones DC, Jayaraman J, Johnson C, Cookson WO, Moffatt MF, Trowsdale J, Traherne JA.

Immunogenetics. 2016 Oct;68(9):743-7. doi: 10.1007/s00251-016-0924-z. Epub 2016 Jun 22.


Testing for the mediating role of endophenotypes using molecular genetic data in a twin study of ADHD traits.

Pinto R, Asherson P, Ilott N, Cheung CH, Kuntsi J.

Am J Med Genet B Neuropsychiatr Genet. 2016 Oct;171(7):982-92. doi: 10.1002/ajmg.b.32463.


Risk Alleles in/near ADCY5, ADRA2A, CDKAL1, CDKN2A/B, GRB10, and TCF7L2 Elevate Plasma Glucose Levels at Birth and in Early Childhood: Results from the FAMILY Study.

Sohani ZN, Anand SS, Robiou-du-Pont S, Morrison KM, McDonald SD, Atkinson SA, Teo KK, Meyre D.

PLoS One. 2016 Apr 6;11(4):e0152107. doi: 10.1371/journal.pone.0152107.


Dissecting the Genetic Susceptibility to Graves' Disease in a Cohort of Patients of Italian Origin.

Lombardi A, Menconi F, Greenberg D, Concepcion E, Leo M, Rocchi R, Marinó M, Keddache M, Tomer Y.

Front Endocrinol (Lausanne). 2016 Mar 8;7:21. doi: 10.3389/fendo.2016.00021.


Loss of Nicastrin from Oligodendrocytes Results in Hypomyelination and Schizophrenia with Compulsive Behavior.

Dries DR, Zhu Y, Brooks MM, Forero DA, Adachi M, Cenik B, West JM, Han YH, Yu C, Arbella J, Nordin A, Adolfsson R, Del-Favero J, Lu QR, Callaerts P, Birnbaum SG, Yu G.

J Biol Chem. 2016 May 27;291(22):11647-56. doi: 10.1074/jbc.M116.715078.


A Locus at 5q33.3 Confers Resistance to Tuberculosis in Highly Susceptible Individuals.

Sobota RS, Stein CM, Kodaman N, Scheinfeldt LB, Maro I, Wieland-Alter W, Igo RP Jr, Magohe A, Malone LL, Chervenak K, Hall NB, Modongo C, Zetola N, Matee M, Joloba M, Froment A, Nyambo TB, Moore JH, Scott WK, Lahey T, Boom WH, von Reyn CF, Tishkoff SA, Sirugo G, Williams SM.

Am J Hum Genet. 2016 Mar 3;98(3):514-24. doi: 10.1016/j.ajhg.2016.01.015.


Family-Based Multi-SNP X Chromosome Analysis Using Parent Information.

Wise AS, Shi M, Weinberg CR.

Front Genet. 2016 Feb 22;7:20. doi: 10.3389/fgene.2016.00020.


Fine Mapping Implicates a Deletion of CFHR1 and CFHR3 in Protection from IgA Nephropathy in Han Chinese.

Xie J, Kiryluk K, Li Y, Mladkova N, Zhu L, Hou P, Ren H, Wang W, Zhang H, Chen N, Gharavi AG.

J Am Soc Nephrol. 2016 Oct;27(10):3187-3194.


Systematic Evaluation of Genes and Genetic Variants Associated with Type 1 Diabetes Susceptibility.

Ram R, Mehta M, Nguyen QT, Larma I, Boehm BO, Pociot F, Concannon P, Morahan G.

J Immunol. 2016 Apr 1;196(7):3043-53. doi: 10.4049/jimmunol.1502056.


No Evidence for Enrichment in Schizophrenia for Common Allelic Associations at Imprinted Loci.

Escott-Price V, Kirov G, Rees E, Isles AR, Owen MJ, O'Donovan MC.

PLoS One. 2015 Dec 3;10(12):e0144172. doi: 10.1371/journal.pone.0144172.


Targeted Deep Sequencing in Multiple-Affected Sibships of European Ancestry Identifies Rare Deleterious Variants in PTPN22 That Confer Risk for Type 1 Diabetes.

Ge Y, Onengut-Gumuscu S, Quinlan AR, Mackey AJ, Wright JA, Buckner JH, Habib T, Rich SS, Concannon P.

Diabetes. 2016 Mar;65(3):794-802. doi: 10.2337/db15-0322.


GABRB2 Haplotype Association with Heroin Dependence in Chinese Population.

Kim YS, Yang M, Mat WK, Tsang SY, Su Z, Jiang X, Ng SK, Liu S, Hu T, Pun F, Liao Y, Tang J, Chen X, Hao W, Xue H.

PLoS One. 2015 Nov 12;10(11):e0142049. doi: 10.1371/journal.pone.0142049.

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