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Lyons, Michael

One or more keywords matched the following items that are connected to Lyons, Michael

Item Type	Name
Academic Article	Stability, consistency, and heritability of electrodermal response lability in middle-aged male twins.
Academic Article	Is there heterogeneity among syndromes of substance use disorder for illicit drugs?
Academic Article	Clinical and molecular phenotype of Aicardi-Goutieres syndrome.
Academic Article	Factor structure of planning and problem-solving: a behavioral genetic analysis of the Tower of London task in middle-aged twins.
Academic Article	FG syndrome, an X-linked multiple congenital anomaly syndrome: the clinical phenotype and an algorithm for diagnostic testing.
Academic Article	Salivary cortisol and prefrontal cortical thickness in middle-aged men: A twin study.
Academic Article	Genetic architecture of context processing in late middle age: more than one underlying mechanism.
Academic Article	Hierarchical genetic organization of human cortical surface area.
Academic Article	Shared and distinct genetic influences among different measures of pulmonary function.
Academic Article	Genetic and environmental contributions to the development of alcohol dependence in male twins.
Academic Article	Specificity of familial vulnerability for alcoholism versus major depression in men.
Academic Article	Pretrauma cognitive ability and risk for posttraumatic stress disorder: a twin study.
Academic Article	Is the Wisconsin Card Sorting Test a useful neurocognitive endophenotype?
Academic Article	Common genetic liability to major depression and posttraumatic stress disorder in men.
Academic Article	Early onset alpha-mannosidosis with slow progression in three Hispanic males.
Academic Article	Cortical thickness is influenced by regionally specific genetic factors.
Academic Article	Genetic vulnerability and phenotypic expression of depression and risk for ischemic heart disease in the Vietnam era twin study of aging.
Academic Article	Chromosome 22q11.2 deletion syndrome in African-American patients: a diagnostic challenge.
Academic Article	LIS1 duplication: expanding the phenotype.
Academic Article	Genetic architecture of the Delis-Kaplan Executive Function System Trail Making Test: evidence for distinct genetic influences on executive function.
Academic Article	Genetic and environmental influences of white and gray matter signal contrast: a new phenotype for imaging genetics?
Academic Article	Genetic and environmental influences of daily and intra-individual variation in testosterone levels in middle-aged men.
Concept	Phenotype
Academic Article	Conceptual and data-based investigation of genetic influences and brain asymmetry: a twin study of multiple structural phenotypes.
Academic Article	Imputing observed blood pressure for antihypertensive treatment: impact on population and genetic analyses.
Academic Article	Neurodevelopmental delays and macrocephaly in 17p13.1 microduplication syndrome.
Academic Article	Does degree of gyrification underlie the phenotypic and genetic associations between cortical surface area and cognitive ability?
Academic Article	Genetic and environmental contributions to the relationships between brain structure and average lifetime cigarette use.
Academic Article	Comparison of Twin and Extended Pedigree Designs for Obtaining Heritability Estimates.
Academic Article	Genetic and environmental architecture of changes in episodic memory from middle to late middle age.
Academic Article	The CODATwins Project: The Cohort Description of Collaborative Project of Development of Anthropometrical Measures in Twins to Study Macro-Environmental Variation in Genetic and Environmental Effects on Anthropometric Traits.
Academic Article	A novel familial autosomal dominant mutation in ARID1B causing neurodevelopmental delays, short stature, and dysmorphic features.
Academic Article	Genetic and environmental influences on mean diffusivity and volume in subcortical brain regions.
Academic Article	Brain structure mediates the association between height and cognitive ability.
Academic Article	Genetic and Environmental Influences on Verbal Fluency in Middle Age: A Longitudinal Twin Study.
Academic Article	Variants in exons 5 and 6 of ACTB cause syndromic thrombocytopenia.
Academic Article	Genetic architecture of hippocampal subfields on standard resolution MRI: How the parts relate to the whole.
Academic Article	Phenotype and mutation expansion of the PTPN23 associated disorder characterized by neurodevelopmental delay and structural brain abnormalities.
Academic Article	Clinical spectrum of individuals with pathogenic NF1 missense variants affecting p.Met1149, p.Arg1276, and p.Lys1423: genotype-phenotype study in neurofibromatosis type 1.
Academic Article	Mutations in FAM50A suggest that Armfield XLID syndrome is a spliceosomopathy.
Academic Article	Genetic correlations and genome-wide associations of cortical structure in general population samples of 22,824 adults.
Academic Article	Lysosomal cholesterol accumulation contributes to the movement phenotypes associated with NUS1 haploinsufficiency.
Academic Article	CSNK2B: A broad spectrum of neurodevelopmental disability and epilepsy severity.
Academic Article	Rare variant association study of veteran twin whole-genomes links severe depression with a nonsynonymous change in the neuronal gene BHLHE22.
Academic Article	Enhancing Discovery of Genetic Variants for Posttraumatic Stress Disorder Through Integration of Quantitative Phenotypes and Trauma Exposure Information.
Academic Article	Loeys-Dietz syndrome caused by 1q41 deletion including TGFB2 is associated with a neurodevelopmental phenotype.
Academic Article	Further clinical and molecular characterization of an XLID syndrome associated with BRWD3 variants, a gene implicated in the leukemia-related JAK-STAT pathway.
Academic Article	Deleterious, protein-altering variants in the transcriptional coregulator ZMYM3 in 27 individuals with a neurodevelopmental delay phenotype.
Academic Article	SRSF1 haploinsufficiency is responsible for a syndromic developmental disorder associated with intellectual disability.
Academic Article	Jansen-de Vries syndrome: Expansion of the PPM1D clinical and phenotypic spectrum in 34 families.
Academic Article	Characterization of the prenatal renal phenotype associated with 17q12, HNF1B, microdeletions.
Academic Article	Variant-specific pathophysiological mechanisms of AFF3 differently influence transcriptome profiles.
Academic Article	A twin analysis to estimate genetic and environmental factors contributing to variation in weighted gene co-expression network module eigengenes.

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