Articles tagged with Behavior Genetics
A large-scale genome-wide study found that genetic signals and genetic correlations differ by social context, age, and reporter. The study identified six genome regions associated with social behavior, with distinct patterns emerging across different social domains and informants.
Researchers at UMass Chan Medical School and the Marine Biological Laboratory identified four core clock genes controlling circadian rhythms in a crustacean, which also regulate circatidal behavior. The genetic system is highly malleable, allowing the tiny shrimp to maintain both a 24-hour and a 12.4-hour clock.
A new research tool, PGS-TRI, analyzes family data to understand how genetics and environment contribute to autism risk. The tool provides a more precise look at how 'nature' and 'nurture' interact within families, allowing researchers to better understand the complex factors that shape a child's health.
Researchers found that only back stroking calmed infant movements, while in mouse pups, it slowed heart rate and blunted stress hormone surge. In mice raised without mothers, the response didn't develop, suggesting a need for contact with the mother to build this calming effect.
Research reveals bacteria rely on circadian clocks to organize colonies, controlling gene expression and pattern formation. The discovery has important implications for understanding bacterial ecology and improving plant growth.
A team studied 173 multiplex families from the Azores and Madeira islands, finding a single broken gene that travels through three generations and causes different illnesses. The CHD2 mutation is rare and affects schizophrenia, mood disorder, and autism in different family members.
The University of Bath has recruited leading psychiatric geneticist Professor Laura Huckins to lead mental health research, focusing on eating disorders and PTSD. She aims to provide answers and treatments for vulnerable populations, combining genetic data and human brain studies to predict individual responses to their environment.
Mount Sinai researchers have uncovered a substantial genetic component to postpartum psychosis, a rare psychiatric illness that occurs after childbirth. The study found rare damaging mutations in the HMGCR gene and significant genetic overlap with bipolar disorder, schizophrenia, and autoimmune diseases.
A University of Connecticut study used genomic data to predict which guide dogs are likely to succeed, revealing a better predictor than traditional evaluations for at least 11 traits. This breakthrough could inform breeding values and lead to improvements in the population over time.
Researchers have identified a long non-coding RNA gene, PTCHD1-AS, as a contributor to increased likelihood of Autism Spectrum Disorder (ASD) in males. The study found that deletions within this gene influence social interaction and repetitive behaviors without affecting cognition.
A massive Swedish study of over 2 million individuals reveals that genetic risk for mental illness is far less disorder-specific than clinicians have assumed. Schizophrenia shows the highest genetic specificity, while drug use disorder has a much lower specificity, scattering its genetic risk across multiple conditions.
A new study explores how artificial lighting at night shapes ecological and genetic patterns of two closely related isopod species, Ligia laticarpa and L. furcata, in Tokyo Bay. The research reveals a clear ecological boundary between the two species, consistent with patterns of urban illumination.
A study by Max Planck Institute for Psycholinguistics found that genetic variations account for approximately 30% of the variation in experiencing aesthetic chills. The research also identified shared genetic influences across music, poetry, and visual art, linked to broader personality traits like openness to experience.
Chronic alcohol consumption alters endocannabinoid gene expression in reward- and decision-related brain regions, offering insights into addiction biology. This study reveals changes in CB1 and CB2 receptor genes, as well as GPR55 and FAAH enzymes, potentially leading to targeted therapeutic strategies.
A comprehensive genetic investigation by Dr. Feng Liu and collaborators identifies shared genetic loci between schizophrenia and osteoporosis, suggesting overlapping biological pathways. The study found that psychiatric patients face elevated fracture risks due to these molecular connections.
Professor Dan Stein was a visionary who bridged neuroscience, clinical care, and philosophy to transform psychiatric research in Africa. His integrative approach produced scholarship of extraordinary range, with over 1,600 peer-reviewed publications and a Google Scholar h-index exceeding 220.
Researchers identified a gene that actively causes a decline in food-seeking behavior after reproduction, potentially benefiting the population by reducing competition for resources. This discovery challenges traditional views on aging and offers new insights into programmed mechanisms driving age-related decline.
A large-scale study found that individuals with ADHD are at higher risk of being convicted of crimes compared to those without ADHD. Relatives of individuals with ADHD also show increased risk, even if they themselves do not have ADHD. Early identification and treatment of ADHD in high-risk families may help mitigate these risks.
A recent study has identified five categories of psychiatric disorders that share similar genetic factors, including compulsive features, internalizing conditions, substance use disorders, neurodevelopmental conditions, and a category combining bipolar disorder and schizophrenia. The research suggests that these shared genetic factors ...
Researchers developed a new suite of statistical methods to pinpoint DNA changes responsible for important traits in livestock. The work addresses challenges in fine-mapping, especially in populations with closely related animals, and introduces tools that incorporate 'relatedness-adjusted' genomic correlations.
Researchers prove that solutions with low-energy initial values decay exponentially, while those exceeding the energy threshold blow up in finite time. The study employs concentration-compactness principle to establish regularity for global solutions.
Researchers identified 12 genes linked to canine behaviour also associated with human traits like anxiety, depression, and intelligence. The study provides insights into understanding dog emotional worlds and tailoring training or care to suit their needs.
Researchers found consistent parental monitoring can offset genetic risk for developing behavior problems during adolescence. High levels of parental monitoring appeared to buffer the influence of genetic risk, making a measurable difference even for children who are more vulnerable biologically.
Researchers identified a genetic inflammatory signature that defines specific depression subtypes and influences antidepressant outcomes. Higher CRP polygenic scores were associated with reduced weight and appetite loss, earlier age of onset, and lower employment status after treatment.
Researchers studied 18 individuals with non-degron SETBP1 variants, revealing a distinct disorder with wide range of cognitive, speech and motor impairments. Functional experiments showed that many variants disrupt DNA-binding, transcription and neuronal differentiation capacity.
Research in African populations aims to understand the link between depression and hypertension, two conditions affecting millions worldwide. The study will focus on identifying shared genetic mechanisms, which could lead to more effective treatment strategies for complex diseases.
A large observational study found a U-shaped association between alcohol consumption and dementia risk, with non-drinkers and heavy drinkers at higher risk. Genetic analyses also showed that increased genetic risk for all three exposure levels was associated with an increased risk of dementia.
Researchers at Kobe University have discovered a specific set of neurons that direct mice's attention to peers in need and those who are friends. These 'PV interneurons' play a crucial role in modulating social behavior, including empathy and preference for social targets.
Researchers successfully transferred a gift-giving courtship behavior from Drosophila subobscura to Drosophila melanogaster by manipulating a single gene in insulin-producing neurons. This study represents the first example of transferring behavior between species through genetic manipulation.
Early primates transitioned to grass-based diets without typical adaptations, with changes in dental morphology lagging behavioral shifts by 700,000 years. This supports the concept of behavioral drive in primate evolution, suggesting that behavior can precede and initiate morphological specialization.
A new genetic study has identified genes involved in neuronal signalling and sensory pathways as key drivers of chronic cough. The findings advance our understanding of cough reflex hypersensitivity as a nervous system-mediated process, opening up opportunities for targeted treatments.
A study published in Nature Communications reveals that genetic diversity within groups of fruit flies improves their ability to evade predators and forage more efficiently. The research team identified a key gene, Ptp99A, that regulates group behavior and promotes survival performance.
Researchers have discovered two signaling molecules that can reprogram ant duties, mirroring gene-expression patterns found in eusocial naked mole-rats. These findings suggest a convergent molecular mechanism dating back hundreds of millions of years, hinting at the evolutionary depth of social behavior.
Professor Benedetti's research explores the intersection of genetics, environmental factors, and treatment response in mood disorders. His work has led to breakthroughs in chronotherapeutics and immuno-psychiatry, revealing crucial insights into immune-inflammatory mechanisms and gene variants influencing brain function.
ADHD researcher Barbara Franke's work transforms understanding of neurodevelopmental disorders through innovative molecular approaches. Her research combines cutting-edge bioinformatics with experimental models to identify genes and pathways underlying behavioral differences.
Researchers created first complete genetic activity map of a branching worm, revealing how it controls reproduction across its multiple body branches. The study highlights the unique genetic toolkit and challenges understanding of animal bodies' organization.
A comprehensive dataset captures individual and group behaviors across genetically diverse strains of fruit flies, shedding light on how genes shape animal behavior. The study's findings have potential implications for mental health conditions with known or suspected genetic components.
Researchers have found that puberty triggers significant changes in brain connectivity patterns in individuals with a rare genetic disorder tied to autism. The study suggests that synaptic dysfunction during development may contribute to the condition's behavioral challenges.
A new study found that genetic predisposition to sedentary behavior is associated with a higher risk of developing the most common cardiovascular diseases. Individuals with the highest genetic predisposition accumulated more daily sedentary time and had a 20% higher risk of cardiovascular diseases.
A new study has revealed that Beagle dogs carrying mutations in the Shank3 gene exhibit face processing abnormalities, similar to those observed in human ASD patients. The research provides direct experimental evidence that mutations in Shank3 lead to ASD-like deficits in face processing, contributing to social impairments.
A novel AI-based method called scNET combines gene expression data with networks of possible gene interactions to identify biological patterns in response to drug treatments. The system reveals complex mechanisms underlying cellular behavior, providing insights for new therapeutic approaches.
Research by the Max Planck Institute reveals how nematodes can shift to 100% predatory behaviour over 101 generations in response to dietary changes. The study highlights the role of multi-generational genetic memory and microRNA involvement in shaping evolutionary adaptations.
A UK study found that children of obese mothers are more likely to become obese adults, suggesting that societal and early-life factors play a significant role in obesity. The study analyzed data from over 17,000 people born in the same week in 1958 and found that these early life factors persisted through adulthood.
A study published in Biological Psychiatry identified the Shisa7 gene as a key driver of heroin addiction. The research team used machine learning to analyze brain tissue from human opioid users and found that modulating this gene's expression influenced heroin-seeking behavior and cognitive flexibility.
Dr. Consuelo Walss-Bass shares her groundbreaking research on schizophrenia, emphasizing the importance of considering both genetic predisposition and environmental factors. She also discusses her work with induced pluripotent stem cells to develop personalized psychiatry and reduce stigma around mental health.
Dr. Guy Rouleau, a renowned geneticist and neurologist, has founded the world's first academic institution committed to open science principles. The Neuro institute aims to transform how brain disease research is conducted worldwide by promoting data sharing and collaboration.
A new study discovered that violence can alter human genes for generations, even in grandchildren who never experienced violence themselves. Researchers found epigenetic changes in the genomes of Syrian families affected by the Hama massacre and subsequent civil war.
Researchers discovered a genetic mutation that increases glycine decarboxylase enzyme, linked to schizophrenia behaviors in mice. The study provides a direct genetic link to psychosis and sheds light on the biochemical pathways involved.
Scientists studied painted lady butterflies' migration patterns and found that environmental conditions shape their travel behavior, with some crossing the Sahara Desert. Contrary to previous belief, genetic analysis revealed no difference in DNA sequences between short- and long-trip butterflies.
Researchers link neuropilin2 gene to autism and seizure development, highlighting its role in regulating neural circuits. The study suggests targeting specific phases of neuronal development could lead to therapeutic interventions for individuals with autism.
Dr. Cathy Barr's groundbreaking research sheds light on the genetic foundations of conditions including depression, ADHD, reading disabilities, and Tourette syndrome. Her work has the potential to lead to more targeted treatments and reduce stigma around psychiatric disorders.
Scientists investigated the role of ancient VR type-1 (ancV1R) receptor in pheromone detection using knockout mice. The study found that ancV1R-deficient female mice had impaired pheromone detection and exhibited abnormal sexual behavior.
Researchers at MUSC discover an RNA:DNA 'sandwich' plays a key role in how the brain interprets emotional experiences and brings about behavioral adaptations. The discovery could lead to better RNA therapies for treating brain disorders.
A free webinar will explore the genetic and biological mechanisms that predispose to early-onset psychotic illnesses. Dr. Catherine Astrid Brownstein will discuss her research on using real-world data for genetic discovery in partnership with Inspire.com.
Three Texas A&M biologists have received NIH Maximizing Investigators’ Research Awards to support their research on type IV pili, darter fish social behaviors and bacteriophages. Drs Koch, Moran and Ramsey will explore bacterial behavior, genetic mechanisms and neural basis of paternal care in fish.
Researchers have identified structural grey matter differences in the brains of women with a history of peripartum depression compared to those without. The study found that hormone fluctuations during pregnancy and childbirth may be key to understanding this condition.
A UT Health San Antonio study found that brain volume changes correlate with social behavior differences in psychiatric conditions such as autism spectrum disorder and schizophrenia. Tbx1 deficiency was associated with decreased brain volume in the amygdala and surrounding cortical regions, affecting desire for social interaction.
A recent study published in Nature Human Behaviour reveals that the Linear Pottery Culture (LBK) people showed no signs of population stratification, with homogeneous cultural traces across thousands of kilometers. The lack of genetic diversity among families also suggests social equality.
Researchers found overlapping genetic underpinnings between rhythm-related skills and language-related traits, including dyslexia. The study identified 16 regions of the genome that overlapped between rhythm and language, suggesting a complex genetic architecture shared by these fundamental human traits.
Knowing family health history is crucial for reducing heart attack and stroke risk. Experts recommend following Life's Essential 8 - five health behaviors and three health factors to lower genetic risks.