Aspects of the inheritance of intellectual abilities

Heredity, Environment, and the Structure of the California Psychological Inventory.

Multivariate behavioral research·2016

Food-entrained rhythmic expression of PER2 and BMAL1 in murine megakaryocytes does not correlate with circadian rhythms in megakaryopoiesis.

Journal of thrombosis and haemostasis : JTH·2008

Genes, evolution, and personality.

Behavior genetics·2001

Discrimination between bacterial spore types using time-of-flight mass spectrometry and matrix-free infrared laser desorption and ionization.

Analytical chemistry·2001

Expression of alpha- and beta-globin genes occurs within different nuclear domains in haemopoietic cells.

Nature cell biology·2001

Presence of a phospholipase D (PLD) distinct from PLD1 or PLD2 in human neutrophils: immunobiochemical characterization and initial purification.

Biochimica et biophysica acta·2001

Uncovering the Role of Biological Sex in the Divergent Genetic Profiles of Early and Late-Diagnosed.

Behavior genetics·2026

Genetic and Environmental Associations Between Depressive Symptomatology and Loneliness in Adulthood.

Behavior genetics·2026

Selective Breeding for Voluntary Wheel-Running Behavior in Mice is not Associated with Reduced Lifetime Reproductive Success or Lifespan Under Long-Term Paired Breeding Conditions.

Behavior genetics·2026

TALE and Hox Transcription Factors Modulate Adult Behaviors in Zebrafish.

Behavior genetics·2026

ADHD and Student Grades in Children from the ABCD Study®: A Twin and Siblings Study.

Behavior genetics·2026

Growing Up with Parents Who Smoke: Genetic and Environmental Effects on Offspring Substance Use and Externalizing Psychopathology From a 20-Year Minnesota Study of Adoptive Families.

Behavior genetics·2026

Generation and characterization of an isogenic gene-corrected iPSC line CARIMi009-A-1 from a Hutchinson-Gilford Progeria Syndrome (HGPS) patient with a heterozygous G608G mutation in the LMNA gene.

Stem cell research·2026

A Rare De Novo Missense Mutation in IFT122 Confers a Genetic Susceptibility Factor of Idiopathic Pediatric Uveitis Via Trio-based Whole-Exome Sequencing.

Advanced science (Weinheim, Baden-Wurttemberg, Germany)·2026

Integrated Genomic and Proteomic Analysis Reveals T-B Lymphocyte Signatures in the MYCN Driven "Immune Desert" of Specific Neuroblastoma Subtypes.

CNS neuroscience & therapeutics·2026

Genetic Modifiers of Cardiac Remodeling Severity in IVS4+919G>A-Associated Fabry Cardiomyopathy.

International journal of molecular sciences·2026

Dissecting Missing Heritability in Rare Inherited Macular Dystrophies.

Genes·2026

Site-Resolved Plasma-Protein Architecture of Infection Susceptibility: A Cis-pQTL Mendelian Randomization and Colocalization Study.

Genes·2026

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Aspects of the inheritance of intellectual abilities

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Heredity, Environment, and the Structure of the California Psychological Inventory.

Food-entrained rhythmic expression of PER2 and BMAL1 in murine megakaryocytes does not correlate with circadian rhythms in megakaryopoiesis.

Genes, evolution, and personality.

Discrimination between bacterial spore types using time-of-flight mass spectrometry and matrix-free infrared laser desorption and ionization.

Expression of alpha- and beta-globin genes occurs within different nuclear domains in haemopoietic cells.

Presence of a phospholipase D (PLD) distinct from PLD1 or PLD2 in human neutrophils: immunobiochemical characterization and initial purification.

Uncovering the Role of Biological Sex in the Divergent Genetic Profiles of Early and Late-Diagnosed.

Genetic and Environmental Associations Between Depressive Symptomatology and Loneliness in Adulthood.

Selective Breeding for Voluntary Wheel-Running Behavior in Mice is not Associated with Reduced Lifetime Reproductive Success or Lifespan Under Long-Term Paired Breeding Conditions.

TALE and Hox Transcription Factors Modulate Adult Behaviors in Zebrafish.

ADHD and Student Grades in Children from the ABCD Study®: A Twin and Siblings Study.

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Generation and characterization of an isogenic gene-corrected iPSC line CARIMi009-A-1 from a Hutchinson-Gilford Progeria Syndrome (HGPS) patient with a heterozygous G608G mutation in the LMNA gene.

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Aspects of the inheritance of intellectual abilities

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