Related Experiment Videos
Presidential address: the genetics of human behavior--lessons for two societies
1Department of Medical Genetics, City of Hope Medical Center, Duarte, CA 91010.
American Journal of Human Genetics
|April 1, 1989
Abstract
No abstract available in PubMed .
Related Concept Videos
Articles linked to this work by shared authors, journal, and citation graph.
Association between the estrogen receptor TA polymorphism and Harm avoidance.
Neuroscience letters·2009
A "line item" approach to the identification of genes involved in polygenic behavioral disorders: the adrenergic alpha2A (ADRA2A) gene.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics·2003
The additive effect of neurotransmitter genes in pathological gambling.
Clinical genetics·2001
Cholecystokinin (CCK) gene as a possible risk factor for smoking: a replication in two independent samples.
Molecular genetics and metabolism·2001
Clinical and molecular genetics of ADHD and Tourette syndrome. Two related polygenic disorders.
Annals of the New York Academy of Sciences·2001
The LEP gene and age of menarche: maternal age as a potential cause of hidden stratification in association studies.
Molecular genetics and metabolism·2001
Monoallelic loss-of-function variants in ZNF536 are associated with a neurodevelopmental disorder with prominent behavioral features.
American journal of human genetics·2026
Beyond exons: Linking noncoding heritability and polygenicity across complex human traits and disorders.
American journal of human genetics·2026
Phenome- and laboratory-wide meta-analyses of sickle cell trait reveal multi-system disease associations.
American journal of human genetics·2026
Mutation rate heterogeneity biases variant effect prediction and reveals genuine mutational robustness.
American journal of human genetics·2026
A phenotypic paradigm for cerebral palsy genetics.
American journal of human genetics·2026
Androgens mediate sexual dimorphism in Pilarowski-Bjornsson syndrome.
American journal of human genetics·2026
Beyond in silico prediction: multi-omics to identify a pathogenic deep intronic HNRNPK variant in Au-Kline syndrome.
Journal of human genetics·2026
Phenotypes of Hereditary Diseases Associated With Rauch-Steindl Syndrome.
Human mutation·2026
Multi-omics Mendelian Randomization Prioritizes Neutrophil Extracellular Trap-related Genes Associated with Atrial Fibrillation Risk.
Endocrine, metabolic & immune disorders drug targets·2026
Developmental and cellular vulnerabilities underlie genetic architecture of schizophrenia.
Molecular psychiatry·2026
Exploring the genetic spectrum of parkinsonism in Brazil.
Parkinsonism & related disorders·2026