Cognitive genomics: Searching for the genetic roots of neuropsychological functioning.
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[1] D. Geschwind,et al. Enhancing the Informativeness and Replicability of Imaging Genomics Studies , 2017, Biological Psychiatry.
[2] Robert Plomin,et al. Genome-wide association meta-analysis of 78,308 individuals identifies new loci and genes influencing human intelligence , 2017, Nature Genetics.
[3] D. Serie,et al. African American exome sequencing identifies potential risk variants at Alzheimer disease loci , 2017, Neurology: Genetics.
[4] D. Glahn,et al. Using Polygenic Risk Scores to Establish Endophenotypes: Considerations and Current Constraints. , 2017, Biological psychiatry. Cognitive neuroscience and neuroimaging.
[5] L. Tan,et al. A Genome-Wide Association Study Identifies Genetic Variants Associated with Mathematics Ability , 2017, Scientific Reports.
[6] Tyrone D. Cannon,et al. GWAS meta-analysis reveals novel loci and genetic correlates for general cognitive function: a report from the COGENT consortium , 2017, Molecular Psychiatry.
[7] Alcino J. Silva,et al. Randomized placebo-controlled study of lovastatin in children with neurofibromatosis type 1 , 2016, Neurology.
[8] David M. Evans,et al. A Genome-Wide Association Meta-Analysis of Attention-Deficit/Hyperactivity Disorder Symptoms in Population-Based Pediatric Cohorts. , 2016, Journal of the American Academy of Child and Adolescent Psychiatry.
[9] Tom R. Gaunt,et al. LD Hub: a centralized database and web interface to perform LD score regression that maximizes the potential of summary level GWAS data for SNP heritability and genetic correlation analysis , 2016, bioRxiv.
[10] Stuart J. Ritchie,et al. Genome-wide association study of cognitive functions and educational attainment in UK Biobank (N=112 151) , 2016, Molecular Psychiatry.
[11] Jonathan P. Beauchamp,et al. Genome-wide association study identifies 74 loci associated with educational attainment , 2016, Nature.
[12] Catherine A. Sugar,et al. A randomized placebo‐controlled lovastatin trial for neurobehavioral function in neurofibromatosis I , 2016, Annals of clinical and translational neurology.
[13] R. Marioni,et al. Assessing the genetic overlap between BMI and cognitive function , 2016, Molecular Psychiatry.
[14] T. Toulopoulou,et al. Cognitive intermediate phenotype and genetic risk for psychosis , 2016, Current Opinion in Neurobiology.
[15] D. Rujescu,et al. Impact of KIBRA Polymorphism on Memory Function and the Hippocampus in Older Adults , 2016, Neuropsychopharmacology.
[16] Robert Plomin,et al. Top 10 Replicated Findings From Behavioral Genetics , 2016, Perspectives on psychological science : a journal of the Association for Psychological Science.
[17] R. Plomin,et al. Discontinuity in the genetic and environmental causes of the intellectual disability spectrum , 2015, Proceedings of the National Academy of Sciences.
[18] M. Owen,et al. Evidence of Common Genetic Overlap Between Schizophrenia and Cognition , 2015, Schizophrenia bulletin.
[19] Stuart J. Ritchie,et al. Shared genetic aetiology between cognitive functions and physical and mental health in UK Biobank (N=112 151) and 24 GWAS consortia , 2015, Molecular Psychiatry.
[20] A. Dale,et al. The Genetic Association Between Neocortical Volume and General Cognitive Ability Is Driven by Global Surface Area Rather Than Thickness. , 2015, Cerebral cortex.
[21] Laura E. Engelhardt,et al. Genes Unite Executive Functions in Childhood , 2015, Psychological science.
[22] I. Deary,et al. Independent evidence for an association between general cognitive ability and a genetic locus for educational attainment , 2015, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.
[23] J. Bressler,et al. Genome-wide Studies of Verbal Declarative Memory in Nondemented Older People: The Cohorts for Heart and Aging Research in Genomic Epidemiology Consortium , 2015, Biological Psychiatry.
[24] M. Daly,et al. An Atlas of Genetic Correlations across Human Diseases and Traits , 2015, Nature Genetics.
[25] K. Kendler,et al. Family environment and the malleability of cognitive ability: A Swedish national home-reared and adopted-away cosibling control study , 2015, Proceedings of the National Academy of Sciences.
[26] M J Wright,et al. Common polygenic risk for autism spectrum disorder (ASD) is associated with cognitive ability in the general population , 2015, Molecular Psychiatry.
[27] C. Reynolds,et al. A Meta-analysis of Heritability of Cognitive Aging: Minding the “Missing Heritability” Gap , 2015, Neuropsychology Review.
[28] C. Reynolds,et al. A Meta-analysis of Heritability of Cognitive Aging: Minding the “Missing Heritability” Gap , 2015, Neuropsychology Review.
[29] A Hofman,et al. Genetic contributions to variation in general cognitive function: a meta-analysis of genome-wide association studies in the CHARGE consortium (N=53 949) , 2015, Molecular Psychiatry.
[30] Thomas E. Nichols,et al. Common genetic variants influence human subcortical brain structures , 2015, Nature.
[31] P. Fox,et al. Discovering Schizophrenia Endophenotypes in Randomly Ascertained Pedigrees , 2015, Biological Psychiatry.
[32] Nicholas Timpson,et al. Assessing the utility of intermediate phenotypes for genetic mapping of psychiatric disease , 2014, Trends in Neurosciences.
[33] N. Wray,et al. Research review: Polygenic methods and their application to psychiatric traits. , 2014, Journal of child psychology and psychiatry, and allied disciplines.
[34] Ross M. Fraser,et al. Defining the role of common variation in the genomic and biological architecture of adult human height , 2014, Nature Genetics.
[35] Common genetic variants associated with cognitive performance identified using the proxy-phenotype method , 2014, Proceedings of the National Academy of Sciences.
[36] C. Spencer,et al. Biological Insights From 108 Schizophrenia-Associated Genetic Loci , 2014, Nature.
[37] Matti Pirinen,et al. The correlation between reading and mathematics ability at age twelve has a substantial genetic component , 2014, Nature Communications.
[38] Kosha Ruparel,et al. The genetic architecture of pediatric cognitive abilities in the Philadelphia Neurodevelopmental Cohort , 2014, Molecular Psychiatry.
[39] B. Pierce,et al. Genetic susceptibility to accelerated cognitive decline in the US Health and Retirement Study , 2014, Neurobiology of Aging.
[40] C. Sabatti,et al. Multisystem component phenotypes of bipolar disorder for genetic investigations of extended pedigrees. , 2014, JAMA psychiatry.
[41] N. Cox,et al. Obesity-associated variants within FTO form long-range functional connections with IRX3 , 2014, Nature.
[42] E. Thorland,et al. Novel de novo SPOCK1 mutation in a proband with developmental delay, microcephaly and agenesis of corpus callosum. , 2014, European journal of medical genetics.
[43] John Blangero,et al. Arguments for the sake of endophenotypes: Examining common misconceptions about the use of endophenotypes in psychiatric genetics , 2014, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.
[44] M. Daly,et al. LD Score regression distinguishes confounding from polygenicity in genome-wide association studies , 2014, Nature Genetics.
[45] P. Visscher,et al. Childhood intelligence is heritable, highly polygenic and associated with FNBP1L , 2014, Molecular Psychiatry.
[46] P. Fox,et al. Genome‐wide significant localization for working and spatial memory: Identifying genes for psychosis using models of cognition , 2014, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.
[47] Adam J. Schwarz,et al. CNVs conferring risk of autism or schizophrenia affect cognition in controls , 2013, Nature.
[48] I. Deary,et al. Molecular Genetic Evidence for Genetic Overlap between General Cognitive Ability and Risk for Schizophrenia: A Report from the Cognitive Genomics Consortium (COGENT) , 2013, Molecular Psychiatry.
[49] Jonathan P. Beauchamp,et al. GWAS of 126,559 Individuals Identifies Genetic Variants Associated with Educational Attainment , 2013, Science.
[50] P. Visscher,et al. Pitfalls of predicting complex traits from SNPs , 2013, Nature Reviews Genetics.
[51] T. Insel,et al. Toward the future of psychiatric diagnosis: the seven pillars of RDoC , 2013, BMC Medicine.
[52] P. Visscher,et al. DNA Evidence for Strong Genome-Wide Pleiotropy of Cognitive and Learning Abilities , 2013, Behavior genetics.
[53] F. Dudbridge. Power and Predictive Accuracy of Polygenic Risk Scores , 2013, PLoS genetics.
[54] M. Lenzenweger. ENDOPHENOTYPE, INTERMEDIATE PHENOTYPE, BIOMARKER: DEFINITIONS, CONCEPT COMPARISONS, CLARIFICATIONS , 2013, Depression and anxiety.
[55] Jonathan Flint,et al. Candidate and non-candidate genes in behavior genetics , 2013, Current Opinion in Neurobiology.
[56] Lisa G Shaffer,et al. Genetic basis of intellectual disability. , 2013, Annual review of medicine.
[57] Hans-Jochen Heinze,et al. Association of KIBRA with episodic and working memory: A meta‐analysis , 2012, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.
[58] B. V. van Bon,et al. Diagnostic exome sequencing in persons with severe intellectual disability. , 2012, The New England journal of medicine.
[59] K. Christensen,et al. Growing Old but Not Growing Apart: Twin Similarity in the Latter Half of the Lifespan , 2012, Behavior Genetics.
[60] J. Veltman,et al. De novo mutations in human genetic disease , 2012, Nature Reviews Genetics.
[61] Jonathan P. Beauchamp,et al. The Promises and Pitfalls of Genoeconomics* , 2012, Annual review of economics.
[62] P. Visscher,et al. Multivariate Genetic Analyses of Cognition and Academic Achievement from Two Population Samples of 174,000 and 166,000 School Children , 2012, Behavior Genetics.
[63] Jason J. Corneveaux,et al. A genome-wide scan for common variants affecting the rate of age-related cognitive decline , 2012, Neurobiology of Aging.
[64] E. Mercuri,et al. Mutations in KANSL1 cause the 17q21.31 microdeletion syndrome phenotype , 2012, Nature Genetics.
[65] Marisa O. Hollinshead,et al. Identification of common variants associated with human hippocampal and intracranial volumes , 2012, Nature Genetics.
[66] E. Lander,et al. The mystery of missing heritability: Genetic interactions create phantom heritability , 2012, Proceedings of the National Academy of Sciences.
[67] J. Flynn,et al. Intelligence: new findings and theoretical developments. , 2012, The American psychologist.
[68] P. Fox,et al. High Dimensional Endophenotype Ranking in the Search for Major Depression Risk Genes , 2012, Biological Psychiatry.
[69] D. Glahn,et al. Why endophenotype development requires families , 2011 .
[70] W. Kremen,et al. Genetic architecture of learning and delayed recall: a twin study of episodic memory. , 2011, Neuropsychology.
[71] Lorna M. Lopez,et al. Genome-wide association studies establish that human intelligence is highly heritable and polygenic , 2011, Molecular Psychiatry.
[72] Ian J Deary,et al. Stability and change in intelligence from age 11 to ages 70, 79, and 87: the Lothian Birth Cohorts of 1921 and 1936. , 2011, Psychology and aging.
[73] G. Yeo,et al. From GWAS to biology: lessons from FTO , 2011, Annals of the New York Academy of Sciences.
[74] K. Hawkins,et al. The effects of apolipoprotein E on non-impaired cognitive functioning: A meta-analysis , 2011, Neurobiology of Aging.
[75] P. Visscher,et al. GCTA: a tool for genome-wide complex trait analysis. , 2011, American journal of human genetics.
[76] D. Posthuma,et al. Phenotypic Complexity, Measurement Bias, and Poor Phenotypic Resolution Contribute to the Missing Heritability Problem in Genetic Association Studies , 2010, PloS one.
[77] D. Lubinski,et al. The heritability of general cognitive ability increases linearly from childhood to young adulthood , 2010, Molecular Psychiatry.
[78] P. Visscher,et al. A versatile gene-based test for genome-wide association studies. , 2010, American journal of human genetics.
[79] Teri A Manolio,et al. Genomewide association studies and assessment of the risk of disease. , 2010, The New England journal of medicine.
[80] P. Visscher,et al. Common SNPs explain a large proportion of the heritability for human height , 2010, Nature Genetics.
[81] Jason J. Corneveaux,et al. Evidence for an association between KIBRA and late-onset Alzheimer's disease , 2010, Neurobiology of Aging.
[82] Jason H. Moore,et al. Missing heritability and strategies for finding the underlying causes of complex disease , 2010, Nature Reviews Genetics.
[83] Thomas D. Dyer,et al. Quantitative Trait Nucleotide Analysis Using Bayesian Model Selection , 2010, Human biology.
[84] M. Hall. A New Role for Endophenotypes in the GWAS Era: Functional Characterization of Risk Variants , 2010, Harvard review of psychiatry.
[85] Thomas R. Insel,et al. Endophenotypes: Bridging Genomic Complexity and Disorder Heterogeneity , 2009, Biological Psychiatry.
[86] P. Visscher,et al. Common polygenic variation contributes to risk of schizophrenia and bipolar disorder , 2009, Nature.
[87] Roger D. Cox,et al. A Mouse Model for the Metabolic Effects of the Human Fat Mass and Obesity Associated FTO Gene , 2009, PLoS genetics.
[88] R. Plomin,et al. Learning abilities and disabilities: Generalist genes in early adolescence , 2009, Cognitive neuropsychiatry.
[89] N. Pedersen,et al. Genetic variance in processing speed drives variation in aging of spatial and memory abilities. , 2009, Developmental psychology.
[90] I. Deary,et al. Genetic foundations of human intelligence , 2009, Human Genetics.
[91] R. Kahn,et al. A genetic analysis of brain volumes and IQ in children , 2009 .
[92] Jiannis Ragoussis,et al. Association of the KIAA0319 dyslexia susceptibility gene with reading skills in the general population. , 2008, The American journal of psychiatry.
[93] Hans-Jürgen Möller,et al. Failure to replicate effect of kibra on human memory in two large cohorts of European origin , 2008, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.
[94] F. Jessen,et al. KIBRA gene variants are associated with episodic memory in healthy elderly , 2008, Neurobiology of Aging.
[95] S. Kapitanović,et al. Neurofibromatosis type 1 , 2008, Nature Reviews Disease Primers.
[96] Ulrich Ettinger,et al. Substantial genetic overlap between neurocognition and schizophrenia: genetic modeling in twin samples , 2008, Archives of general psychiatry.
[97] Shuhong Zhao,et al. Candidate Gene Identification Approach: Progress and Challenges , 2007, International journal of biological sciences.
[98] Beverley Balkau,et al. Variation in FTO contributes to childhood obesity and severe adult obesity , 2007, Nature Genetics.
[99] Kenny Q. Ye,et al. Strong Association of De Novo Copy Number Mutations with Autism , 2007, Science.
[100] H. Nicolini,et al. Adjudicating neurocognitive endophenotypes for schizophrenia , 2007, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.
[101] Jason J. Corneveaux,et al. Common Kibra Alleles Are Associated with Human Memory Performance , 2006, Science.
[102] K. McDermott,et al. Genetic influences on free and cued recall in long-term memory tasks. , 2006, Twin research and human genetics : the official journal of the International Society for Twin Studies.
[103] N. Freimer,et al. Endophenotypes for psychiatric disorders: ready for primetime? , 2006, Trends in genetics : TIG.
[104] Richard Wade-Martins,et al. The chromosome 6p22 haplotype associated with dyslexia reduces the expression of KIAA0319, a novel gene involved in neuronal migration. , 2006, Human molecular genetics.
[105] Robert Plomin,et al. Generalist genes: implications for the cognitive sciences , 2006, Trends in Cognitive Sciences.
[106] I. Gottesman,et al. Psychiatric endophenotypes and the development of valid animal models , 2006, Genes, brain, and behavior.
[107] Alcino J. Silva,et al. The HMG-CoA Reductase Inhibitor Lovastatin Reverses the Learning and Attention Deficits in a Mouse Model of Neurofibromatosis Type 1 , 2005, Current Biology.
[108] A. Danek,et al. The pattern of cognitive performance in CADASIL: a monogenic condition leading to subcortical ischemic vascular dementia. , 2005, The American journal of psychiatry.
[109] R. Plomin,et al. Generalist genes and learning disabilities. , 2005, Psychological bulletin.
[110] Michael A. McDaniel. Big-brained people are smarter: A meta-analysis of the relationship between in vivo brain volume and intelligence , 2005 .
[111] G. Geffen,et al. The Genetic Basis of Academic Achievement on the Queensland Core Skills Test and its Shared Genetic Variance with IQ , 2005, Behavior genetics.
[112] Lars Bäckman,et al. Apolipoprotein E and cognitive performance: a meta-analysis. , 2004, Psychology and aging.
[113] S. Gygi,et al. Toca-1 Mediates Cdc42-Dependent Actin Nucleation by Activating the N-WASP-WIP Complex , 2004, Cell.
[114] Mark F Bear,et al. The mGluR theory of fragile X mental retardation , 2004, Trends in Neurosciences.
[115] J. Blangero. Localization and identification of human quantitative trait loci: king harvest has surely come. , 2004, Current opinion in genetics & development.
[116] I. Gottesman,et al. PSYCHOLOGICAL SCIENCE Research Article SOCIOECONOMIC STATUS MODIFIES HERITABILITY OF IQ , 2022 .
[117] I. Gottesman,et al. The endophenotype concept in psychiatry: etymology and strategic intentions. , 2003, The American journal of psychiatry.
[118] L. Almasy. Quantitative risk factors as indices of alcoholism susceptibility , 2003, Annals of medicine.
[119] Shaun Purcell,et al. Variance components models for gene-environment interaction in twin analysis. , 2002, Twin research : the official journal of the International Society for Twin Studies.
[120] L. Peltonen,et al. Classical twin studies and beyond , 2002, Nature Reviews Genetics.
[121] Oili Salonen,et al. Contributions of genetic risk and fetal hypoxia to hippocampal volume in patients with schizophrenia or schizoaffective disorder, their unaffected siblings, and healthy unrelated volunteers. , 2002, The American journal of psychiatry.
[122] Caroline Hayward,et al. Ageing: Cognitive change and the APOE ɛ4 allele , 2002, Nature.
[123] Ger J. A. Ramakers,et al. Rho proteins, mental retardation and the cellular basis of cognition , 2002, Trends in Neurosciences.
[124] D. Carmelli,et al. Evidence for genetic mediation of executive control: a study of aging male twins. , 2002, The journals of gerontology. Series B, Psychological sciences and social sciences.
[125] Alcino J. Silva,et al. Mechanism for the learning deficits in a mouse model of neurofibromatosis type 1 , 2002, Nature.
[126] S. Kosslyn,et al. Genes, brain and cognition , 2001, Nature Neuroscience.
[127] D. Posthuma,et al. Perceptual Speed and IQ Are Associated Through Common Genetic Factors , 2001, Behavior genetics.
[128] G. Geffen,et al. Genetic Covariance Among Measures of Information Processing Speed, Working Memory, and IQ , 2001, Behavior genetics.
[129] M. Posner,et al. Assessing the heritability of attentional networks , 2001, BMC Neuroscience.
[130] P. Vernon,et al. Heritability Estimates of Intelligence in Twins: Effect of Chorion Type , 2001, Behavior genetics.
[131] L. Almasy,et al. Endophenotypes as quantitative risk factors for psychiatric disease: rationale and study design. , 2001, American journal of medical genetics.
[132] A. Neubauer,et al. Genetic and Environmental Influences on Two Measures of Speed of Information Processing and Their Relation to Psychometric Intelligence: Evidence from the German Observational Study of Adult Twins. , 2000 .
[133] Eric Turkheimer,et al. Three Laws of Behavior Genetics and What They Mean , 2000 .
[134] Mark S. Cohen,et al. Patterns of brain activation in people at risk for Alzheimer's disease. , 2000, The New England journal of medicine.
[135] Tyrone D. Cannon,et al. The inheritance of neuropsychological dysfunction in twins discordant for schizophrenia. , 2000, American journal of human genetics.
[136] Howard Wainer,et al. Computerized Adaptive Testing: A Primer , 2000 .
[137] Alcino J. Silva,et al. Molecular and cellular mechanisms of cognitive function: implications for psychiatric disorders , 2000, Biological Psychiatry.
[138] Robert Plomin,et al. Genetics and general cognitive ability , 1999, Nature.
[139] W. Ewens. Genetics and analysis of quantitative traits , 1999 .
[140] P. Wolf,et al. Differential genetic influence for components of memory in aging adult twins. , 1999, Archives of neurology.
[141] I. Craig,et al. DNA pooling identifies QTLs on chromosome 4 for general cognitive ability in children. , 1999, Human molecular genetics.
[142] J. Kogan,et al. A mouse model for learning and memory defects associated with neurofibromatosis type I. , 1998, Pathologie-biologie.
[143] R. Plomin,et al. Multivariate Path Analysis of Specific Cognitive Abilities Data at 12 Years of Age in the Colorado Adoption Project , 1998, Behavior genetics.
[144] S. Petrill. Molarity Versus Modularity of Cognitive Functioning? , 1997 .
[145] N Risch,et al. The Future of Genetic Studies of Complex Human Diseases , 1996, Science.
[146] Michael F. Green,et al. What are the functional consequences of neurocognitive deficits in schizophrenia? , 1996, The American journal of psychiatry.
[147] E. Lander,et al. Genetic dissection of complex traits: guidelines for interpreting and reporting linkage results , 1995, Nature Genetics.
[148] N. Pedersen,et al. Heritability of cognitive abilities in adult twins: Comparison of Minnesota and Swedish data , 1995, Behavior genetics.
[149] M. Owen,et al. The genetic basis of complex human behaviors. , 1994, Science.
[150] Jurg Ott,et al. Handbook of Human Genetic Linkage , 1994 .
[151] M. McGue,et al. The origins of individual differences in memory among the elderly: a behavior genetic analysis. , 1993, Psychology and aging.
[152] J. Flynn. Skodak and skeels: The inflated mother-child IQ gap , 1993 .
[153] J. Haines,et al. Gene dose of apolipoprotein E type 4 allele and the risk of Alzheimer's disease in late onset families. , 1993, Science.
[154] M. Pericak-Vance,et al. Apolipoprotein E: high-avidity binding to beta-amyloid and increased frequency of type 4 allele in late-onset familial Alzheimer disease. , 1993, Proceedings of the National Academy of Sciences of the United States of America.
[155] S. Fortmann,et al. Socioeconomic status and health: how education, income, and occupation contribute to risk factors for cardiovascular disease. , 1992, American journal of public health.
[156] N. Tommerup,et al. Direct diagnosis by DNA analysis of the fragile X syndrome of mental retardation. , 1991, The New England journal of medicine.
[157] M. Pericak-Vance,et al. Linkage studies in familial Alzheimer disease: evidence for chromosome 19 linkage. , 1991, American journal of human genetics.
[158] R. Nicoll,et al. A persistent postsynaptic modification mediates long-term potentiation in the hippocampus , 1988, Neuron.
[159] R. Nicoll,et al. NMDA application potentiates synaptic transmission in the hippocampus , 1988, Nature.
[160] K. White. The relation between socioeconomic status and academic achievement. , 1982 .
[161] T. Bouchard,et al. Familial studies of intelligence: a review. , 1981, Science.
[162] Arthur Falek,et al. Schizophrenia and genetics: A twin study vantage point. , 1976 .
[163] A. Jensen,et al. Heritability of IQ. , 1976, Science.
[164] Marie Skodak,et al. A Final Follow-Up Study of One Hundred Adopted Children , 1949 .
[165] M. Skodak,et al. A final follow-up study of 100 adopted children. , 1949, The Journal of genetic psychology.
[166] J. Haldane,et al. A Clinical and Genetic Study of 1,280 Cases of Mental Defect , 1938, Mental Welfare.
[167] A. Wallace. Hereditary Genius, an Inquiry into its Laws and Consequences , 1870, Nature.
[168] M. O’Donovan,et al. Schizophrenia risk alleles and neurodevelopmental outcomes in childhood: a population-based cohort study. , 2017, The lancet. Psychiatry.
[169] Kai-Uwe Eckardt,et al. Novel genetic loci associated with hippocampal , 2017 .
[170] P. Visscher,et al. Meta-analysis of the heritability of human traits based on fifty years of twin studies. , 2015, Nature genetics.
[171] E. Tucker-Drob,et al. Continuity of genetic and environmental influences on cognition across the life span: a meta-analysis of longitudinal twin and adoption studies. , 2014, Psychological bulletin.
[172] Lorna M. Lopez,et al. A genome-wide association study implicates the APOE locus in nonpathological cognitive ageing , 2014, Molecular Psychiatry.
[173] Irving I. Gottesman,et al. Beyond Heritability: Twin Studies in Behavioral Research. , 2010, Current directions in psychological science.
[174] R. Malenka. The role of postsynaptic calcium in the induction of long-term potentiation , 2008, Molecular Neurobiology.
[175] Ian J Deary,et al. The impact of childhood intelligence on later life: following up the Scottish mental surveys of 1932 and 1947. , 2004, Journal of personality and social psychology.
[176] Robert Plomin,et al. Intelligence: genetics, genes, and genomics. , 2004, Journal of personality and social psychology.
[177] Y. Ono,et al. Genetic Structure of Spatial and Verbal Working Memory , 2001, Behavior genetics.
[178] K. Christensen,et al. The heritability of cognitive functioning in very old adults: evidence from Danish twins aged 75 years and older. , 2001, Psychology and aging.
[179] International Human Genome Sequencing Consortium. Initial sequencing and analysis of the human genome , 2001, Nature.
[180] J. Lamb,et al. A quantitative-trait locus on chromosome 6p influences different aspects of developmental dyslexia. , 1999, American journal of human genetics.
[181] L. Gottfredson. Why g matters: The complexity of everyday life , 1997 .
[182] S. Covey,et al. Substantial Genetic Influence on Cognitive Abilities in Twins 80 or More Years Old , 1997 .
[183] N. Pedersen,et al. Genetic influences on memory performance in adulthood: comparison of Minnesota and Swedish twin data. , 1995, Psychology and aging.
[184] D. Lykken,et al. Genetic and environmental influences on special mental abilities in a sample of twins reared apart. , 1990, Acta geneticae medicae et gemellologiae.
[185] H. Birx,et al. The Mismeasure of Man , 1981 .
[186] F. Galton. Hereditary Genius: An Inquiry into its Laws and Consequences , 1914, Nature.
[187] Armin Schneider,et al. Frontiers in Aging Neuroscience Aging Neuroscience Review Article the Kibra Gene and Protein , 2022 .
[188] R Plomin,et al. © 2009 The Authors Journal compilation © 2009 Blackwell Publishing Ltd/International Behavioural and Neural Genetics Society , 2022 .