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Cited In for PubMed (Select 11525833)


New insights from monogenic diabetes for "common" type 2 diabetes.

Tallapragada DS, Bhaskar S, Chandak GR.

Front Genet. 2015 Aug 7;6:251. doi: 10.3389/fgene.2015.00251. eCollection 2015. Review.


Allelic Spectra of Risk SNPs Are Different for Environment/Lifestyle Dependent versus Independent Diseases.

Gorlov IP, Gorlova OY, Amos CI.

PLoS Genet. 2015 Jul 22;11(7):e1005371. doi: 10.1371/journal.pgen.1005371. eCollection 2015 Jul.


Targeted massively parallel sequencing of autism spectrum disorder-associated genes in a case control cohort reveals rare loss-of-function risk variants.

Griswold AJ, Dueker ND, Van Booven D, Rantus JA, Jaworski JM, Slifer SH, Schmidt MA, Hulme W, Konidari I, Whitehead PL, Cuccaro ML, Martin ER, Haines JL, Gilbert JR, Hussman JP, Pericak-Vance MA.

Mol Autism. 2015 Jul 7;6:43. doi: 10.1186/s13229-015-0034-z. eCollection 2015.


Alcohol Dependence Genetics: Lessons Learned From Genome-Wide Association Studies (GWAS) and Post-GWAS Analyses.

Hart AB, Kranzler HR.

Alcohol Clin Exp Res. 2015 Aug;39(8):1312-27. doi: 10.1111/acer.12792. Epub 2015 Jun 25.


Common Polymorphisms in the Age of Research Domain Criteria (RDoC): Integration and Translation.

Glatt CE, Lee FS.

Biol Psychiatry. 2015 Jan 8. pii: S0006-3223(15)00004-9. doi: 10.1016/j.biopsych.2014.12.020. [Epub ahead of print] Review.


The emergence of human-evolutionary medical genomics.

Crespi BJ.

Evol Appl. 2011 Mar;4(2):292-314. doi: 10.1111/j.1752-4571.2010.00156.x. Epub 2010 Oct 12.


Genetics of allergic diseases.

Ortiz RA, Barnes KC.

Immunol Allergy Clin North Am. 2015 Feb;35(1):19-44. doi: 10.1016/j.iac.2014.09.014. Epub 2014 Nov 21. Review.


Gene-based rare allele analysis identified a risk gene of Alzheimer's disease.

Kim JH, Song P, Lim H, Lee JH, Lee JH, Park SA; Alzheimer’s Disease Neuroimaging Initiative.

PLoS One. 2014 Oct 20;9(10):e107983. doi: 10.1371/journal.pone.0107983. eCollection 2014.


Early-onset colorectal cancer: a sporadic or inherited disease?

Stigliano V, Sanchez-Mete L, Martayan A, Anti M.

World J Gastroenterol. 2014 Sep 21;20(35):12420-30. doi: 10.3748/wjg.v20.i35.12420. Review.


Fine mapping of type 2 diabetes susceptibility loci.

Morris AP.

Curr Diab Rep. 2014;14(11):549. doi: 10.1007/s11892-014-0549-2. Review. Erratum in: Curr Diab Rep. 2015 Jan;15(1):575.


Genetic variation in iron metabolism is associated with neuropathic pain and pain severity in HIV-infected patients on antiretroviral therapy.

Kallianpur AR, Jia P, Ellis RJ, Zhao Z, Bloss C, Wen W, Marra CM, Hulgan T, Simpson DM, Morgello S, McArthur JC, Clifford DB, Collier AC, Gelman BB, McCutchan JA, Franklin D, Samuels DC, Rosario D, Holzinger E, Murdock DG, Letendre S, Grant I; CHARTER Study Group.

PLoS One. 2014 Aug 21;9(8):e103123. doi: 10.1371/journal.pone.0103123. eCollection 2014.


The genetic basis of music ability.

Tan YT, McPherson GE, Peretz I, Berkovic SF, Wilson SJ.

Front Psychol. 2014 Jun 27;5:658. doi: 10.3389/fpsyg.2014.00658. eCollection 2014. Review.


Elevated blood pressure: Our family's fault? The genetics of essential hypertension.

Natekar A, Olds RL, Lau MW, Min K, Imoto K, Slavin TP.

World J Cardiol. 2014 May 26;6(5):327-37. doi: 10.4330/wjc.v6.i5.327.


Resequencing the susceptibility gene, ITGAM, identifies two functionally deleterious rare variants in systemic lupus erythematosus cases.

Roberts AL, Thomas ER, Bhosle S, Game L, Obraztsova O, Aitman TJ, Vyse TJ, Rhodes B.

Arthritis Res Ther. 2014 May 21;16(3):R114. doi: 10.1186/ar4566.


A genetic variant in the LDLR promoter is responsible for part of the LDL-cholesterol variability in primary hypercholesterolemia.

De Castro-Orós I, Pérez-López J, Mateo-Gallego R, Rebollar S, Ledesma M, León M, Cofán M, Casasnovas JA, Ros E, Rodríguez-Rey JC, Civeira F, Pocoví M.

BMC Med Genomics. 2014 Apr 7;7:17. doi: 10.1186/1755-8794-7-17.


Architecture of inherited susceptibility to colorectal cancer: a voyage of discovery.

Whiffin N, Houlston RS.

Genes (Basel). 2014 Mar 27;5(2):270-84. doi: 10.3390/genes5020270.


Genetic profiling for risk reduction in human cardiovascular disease.

Puckelwartz MJ, McNally EM.

Genes (Basel). 2014 Mar 12;5(1):214-34. doi: 10.3390/genes5010214.


Searching for missing heritability: designing rare variant association studies.

Zuk O, Schaffner SF, Samocha K, Do R, Hechter E, Kathiresan S, Daly MJ, Neale BM, Sunyaev SR, Lander ES.

Proc Natl Acad Sci U S A. 2014 Jan 28;111(4):E455-64. doi: 10.1073/pnas.1322563111. Epub 2014 Jan 17.

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