Population-specific putative causal variants shape quantitative traits - Nature.com

Largest-ever genetic study of epilepsy finds possible therapeutic targets - Medical Xpress

The mountains where Neanderthals forever changed human genetics - Big Think

Gene Activity in Depression Linked to Immune System and Inflammation - Neuroscience News

As 23andMe Struggles, Concerns Surface About Its Genetic Data - The New York Times

Plants have a backup plan - EurekAlert

Ancient DNA Uncovers The Genetic Background Of Japanese People: Study - NDTV

Genetic database shows some fungal crops became completely reliant on ants 27 million years ago - Phys.org

NHS England to screen 100,000 babies for more than 200 genetic conditions - The Guardian

Researchers Create New System to Decode Genetic Risk for Psychiatric Disorders - UNC Health and UNC School of Medicine

People Are Not Peas—Why Genetics Education Needs an Overhaul - SAPIENS

Curriculum in Genetics and Molecular Biology - The University of North Carolina at Chapel Hill

MHC Hammer reveals genetic and non-genetic HLA disruption in cancer evolution - Nature.com

Multivariate genomic analysis of 5 million people elucidates the genetic architecture of shared components of the metabolic syndrome - Nature.com

Gene discovery and biological insights into anxiety disorders from a large-scale multi-ancestry genome-wide association study - Nature.com

Integrative multi-omics analysis reveals genetic and heterotic contributions to male fertility and yield in potato - Nature.com

Genetic and non-genetic HLA disruption is widespread in lung and breast tumors - Nature.com

Heterogeneous genetic architectures of prostate cancer susceptibility in sub-Saharan Africa - Nature.com

Aneuploidy as a driver of human cancer - Nature.com

Valid inference for machine learning-assisted genome-wide association studies - Nature.com

Context transcription factors establish cooperative environments and mediate enhancer communication - Nature.com

Five latent factors underlie response to immunotherapy - Nature.com

Integration of variant annotations using deep set networks boosts rare variant association testing - Nature.com

Multiomic profiling identifies predictors of survival in African American patients with acute myeloid leukemia - Nature.com

Federated analysis of autosomal recessive coding variants in 29,745 developmental disorder patients from diverse populations - Nature.com

Exome sequencing of 20,979 individuals with epilepsy reveals shared and distinct ultra-rare genetic risk across disorder subtypes - Nature.com

NSD2 is a requisite subunit of the AR/FOXA1 neo-enhanceosome in promoting prostate tumorigenesis - Nature.com

Standardizing variant naming in literature with VariantValidator to increase diagnostic rates - Nature.com

Research reveals considerable genetic origin for unselected cerebral palsy - Illumina

Homozygosity for a stop-gain variant in CCDC201 causes primary ovarian insufficiency - Nature.com

China’s winemakers turn to genetics, AI to futureproof against climate change - Hong Kong Free Press

Identifying genetic variants that influence the abundance of cell states in single-cell data - Nature.com

Angus Genetics Inc. gathers breeders, industry, academia in forum - Beef Magazine

Biallelic and monoallelic variants in EFEMP1 can cause a severe and distinct subtype of heritable connective tissue disorder - Nature.com

Cracking the Genetic Code on Facial Features - DISCOVER Magazine

Lars Steinmetz is new chair of Stanford Medicine Department of Genetics - Stanford Medical Center Report

Genetic and Immune-Mediated Biomarkers in Aging - Frontiers

Genome-wide association analyses identify 95 risk loci and provide insights into the neurobiology of post-traumatic stress disorder - Nature.com

Next-generation phenotyping integrated in a national framework for patients with ultrarare disorders improves genetic diagnostics and yields new molecular findings - Nature.com

Comprehensive molecular profiling of multiple myeloma identifies refined copy number and expression subtypes - Nature.com

Deciphering the genetics and mechanisms of predisposition to multiple myeloma - Nature.com

Genome-wide meta-analyses of restless legs syndrome yield insights into genetic architecture, disease biology and risk prediction - Nature.com

Understanding the genetic complexity of puberty timing across the allele frequency spectrum - Nature.com

Systematic decoding of cis gene regulation defines context-dependent control of the multi-gene costimulatory receptor locus in human T cells - Nature.com

The genome and population genomics of allopolyploid Coffea arabica reveal the diversification history of modern coffee cultivars - Nature.com

Genetic and clinical correlates of two neuroanatomical AI dimensions in the Alzheimer’s disease continuum - Nature.com

Competition shapes the landscape of X-chromosome-linked genetic diversity - Nature.com

Genetics of child aggression, a systematic review - Translational Psychiatry - Nature.com

Unlocking plant genetics with telomere-to-telomere genome assemblies - Nature.com

Genomic analyses reveal the stepwise domestication and genetic mechanism of curd biogenesis in cauliflower - Nature.com

Can Genetics Help Explain Rare ALS Reversals? - ALS Association

Saturation genome editing of BAP1 functionally classifies somatic and germline variants - Nature.com

This Shark Lives 400 Years. Its DNA May Explain Why. - The New York Times

Largest-Ever Genetic Study on Epilepsy Uncovers Potential Therapeutic Paths - Technology Networks

Establishing African genomics and bioinformatics programs through annual regional workshops - Nature.com

Genome-wide analysis in over 1 million individuals of European ancestry yields improved polygenic risk scores for blood pressure traits - Nature.com

Isolated communities are more at risk of rare genetic diseases - The Economist

Metabolic gene function discovery platform GeneMAP identifies SLC25A48 as necessary for mitochondrial choline import - Nature.com

Genetic drivers of heterogeneity in type 2 diabetes pathophysiology - Nature.com

NIH Recognizes Yale’s Expertise in the Genetics of Rare Diseases - Yale School of Medicine

Researchers Highlight the Genetic Complexity of Schizophrenia - UNC Health and UNC School of Medicine

The Medical Minute: Genetics play big role in ovarian cancer - Penn State Health News

Yale Scientists Uncover Genetic Predisposition to Anxiety - Yale School of Medicine

Genomes of multicellular algal sisters to land plants illuminate signaling network evolution - Nature.com

Children's Mercy offers in-house genetics testing to guide treatment - The Business Journals

ADHD and DNA: Bedside-to-bench, International Study Sheds Light on Genetics - Yale School of Medicine

Functional variants in a TTTG microsatellite on 15q26.1 cause familial nonautoimmune thyroid abnormalities - Nature.com

Fussy eating in children largely down to genetics, research shows - The Guardian

Exome sequence analysis identifies rare coding variants associated with a machine learning-based marker for coronary artery disease - Nature.com

Genetic mapping across autoimmune diseases reveals shared associations and mechanisms - Nature.com

Research explores genetic treatment for rare arrhythmias - Medical Xpress

Penn State researchers receive USDA-NIFA grant to study male cattle genetics - Penn State University

The Mercedes-AMG C63 is bold, but beholden to its genetics - Newsweek

A GGC-repeat expansion in ZFHX3 encoding polyglycine causes spinocerebellar ataxia type 4 and impairs autophagy - Nature.com

Genetic modifiers of rare variants in monogenic developmental disorder loci - Nature.com

Systematic rare variant analyses identify RAB32 as a susceptibility gene for familial Parkinson’s disease - Nature.com

FMD - Research heralds new era for genetics - QMUL

Ancestry vs. 23andMe: How to Pick the Best DNA Testing Kit for You - CNET

Analysis of somatic mutations in whole blood from 200,618 individuals identifies pervasive positive selection and novel drivers of clonal hematopoiesis - Nature.com

ASU’s first genetic counseling master's students complete their work - ASU News Now

Genetic Testing - Roswell Park Comprehensive Cancer Center

Comparative cofactor screens show the influence of transactivation domains and core promoters on the mechanisms of transcription - Nature.com

Body mass index stratification optimizes polygenic prediction of type 2 diabetes in cross-biobank analyses - Nature.com

Unveiling genetic insights: how PAI-1 polymorphisms influence COVID-19 outcomes - EurekAlert

Schizophrenia genomics: genetic complexity and functional insights - Nature.com

Integrating population genetics, stem cell biology and cellular genomics to study complex human diseases - Nature.com

Genome-wide association analyses of breast cancer in women of African ancestry identify new susceptibility loci and improve risk prediction - Nature.com

The sociopolitical in human genetics education - Science

Pathway level subtyping identifies a slow-cycling biological phenotype associated with poor clinical outcomes in colorectal cancer - Nature.com

Human genetic structure in Northwest France provides new insights into West European historical demography - Nature.com

Navigating Genetic Data Privacy and Law Enforcement Access - The Regulatory Review

The Austin Chronic: Texas A&M’s Hemp Breeding Program Adds Drought-Resistant Genetics to the National Collection - Austin Chronicle

Genetics and AI Help Patients with Early Detection of Breast Cancer Risk - Adventist Review

Remembering genetics pioneer, professor Charis Eng - The Daily | Case Western Reserve University

The genetics behind age at menarche - Nature.com

Shared Genetics Found in Bipolar Disorder and Epilepsy - Neuroscience News

Elevated genetic risk for multiple sclerosis emerged in steppe pastoralist populations - Nature.com

MYC activity at enhancers drives prognostic transcriptional programs through an epigenetic switch - Nature.com

Genetic variations in remote UK regions linked to higher disease risk - Medical Xpress