Deletion of TOP3?, a component of FMRP-containing mRNPs, contributes to neurodevelopmental disorders.
Nat Neurosci. 2013;16(9):1228-37 - PMID: 23912948 - PMCID: PMC3986889
Evaluation of intraoperative cone beam computed tomography and optical drill tracking in temporal bone surgery.
Laryngoscope. 2013;123(11):2823-8 - PMID: 23918182
Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs.
Nat Genet. 2013;45(9):984-94 - PMID: 23933821 - PMCID: PMC3800159
Integrated model of de novo and inherited genetic variants yields greater power to identify risk genes.
PLoS Genet. 2013;9(8):e1003671 - PMID: 23966865 - PMCID: PMC3744441
De novo mutation in the dopamine transporter gene associates dopamine dysfunction with autism spectrum disorder.
Mol Psychiatry. 2013;18(12):1315-23 - PMID: 23979605 - PMCID: PMC4046646
Genome-wide association study implicates a novel RNA gene, the lincRNA AC068718.1, as a risk factor for post-traumatic stress disorder in women.
Psychoneuroendocrinology. 2013;38(12):3029-38 - PMID: 24080187 - PMCID: PMC3844079
Multilocus genetic risk scores for coronary heart disease prediction.
Arterioscler Thromb Vasc Biol. 2013;33(9):2267-72 - PMID: 23685553
Utilizing twins as controls for non-twin case-materials in genome wide association studies.
PLoS One. 2013;8(12):e83101 - PMID: 24340086 - PMCID: PMC3858365
Probing the brain of comorbidity.
Sci Transl Med. 2013;5(183):183fs15, 1-3 - PMID: 23636091
Genome-wide Association Study for Radiographic Vertebral Fractures: A Potential Role for the 16q24 BMD Locus versus Lessons Learned from Challenging Phenotype Definition.
Bone. 2013;:ePub - PMID: 24513584
Sequence variants in SLC16A11 are a common risk factor for type 2 diabetes in Mexico.
Nature. 2013;506(7486):97-101 - PMID: 24390345
Transcriptome and genome sequencing uncovers functional variation in humans.
Nature. 2013;501(7468):506-11 - PMID: 24037378 - PMCID: PMC3918453
Common Variants on Xq28 Conferring Risk of Schizophrenia in Han Chinese.
Schizophr Bull. 2013;:ePub - PMID: 24043878
Deep resequencing of GWAS loci identifies rare variants in CARD9, IL23R and RNF186 that are associated with ulcerative colitis.
PLoS Genet. 2013;9(9):e1003723 - PMID: 24068945 - PMCID: PMC3772057
Rare variants in CFI, C3 and C9 are associated with high risk of advanced age-related macular degeneration.
Nat Genet. 2013;45(11):1366-70 - PMID: 24036952 - PMCID: PMC3902040
Integrative annotation of variants from 1092 humans: application to cancer genomics.
Science. 2013;342(6154):1235587 - PMID: 24092746 - PMCID: PMC3947637
Identification of small exonic CNV from whole-exome sequence data and application to autism spectrum disorder.
Am J Hum Genet. 2013;93(4):607-19 - PMID: 24094742 - PMCID: PMC3791269
Common variants associated with plasma triglycerides and risk for coronary artery disease.
Nat Genet. 2013;45(11):1345-52 - PMID: 24097064 - PMCID: PMC3904346
A genome wide survey supports the involvement of large copy number variants in schizophrenia with and without intellectual disability.
Am J Med Genet B Neuropsychiatr Genet. 2013;162(8):847-54 - PMID: 24115684
Selective modulation of autophagy, innate immunity, and adaptive immunity by small molecules.
ACS Chem Biol. 2013;8(12):2724-33 - PMID: 24168452 - PMCID: PMC3951132
Partitioning the heritability of Tourette syndrome and obsessive compulsive disorder reveals differences in genetic architecture.
PLoS Genet. 2013;9(10):e1003864 - PMID: 24204291 - PMCID: PMC3812053
Mismatch repair genes Mlh1 and Mlh3 modify CAG instability in Huntington's disease mice: genome-wide and candidate approaches.
PLoS Genet. 2013;9(10):e1003930 - PMID: 24204323 - PMCID: PMC3814320
Responses of Mn2+ speciation in Deinococcus radiodurans and Escherichia coli to ?-radiation by advanced paramagnetic resonance methods.
Proc Natl Acad Sci U S A. 2013;110(15):5945-50 - PMID: 23536297 - PMCID: PMC3625348
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