MeSH tree: N06.850.520.445.392
The largest genetic analysis of stuttering has demonstrated a clear genetic basis for the speech disorder, highlighting neurological pathways of risk. The study, published July 28 in the journal Nature Genetics, used data ...
Jul 28, 2025
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Emeli Chatterjee, Ph.D., of the Cardiovascular Research Center at Massachusetts General Hospital, is the lead author and Saumya Das, MD, Ph.D., of the Division of Cardiology at Massachusetts General Hospital, is the senior ...
Jul 15, 2025
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Genetic changes can signal evidence of disease, but pinpointing which genes and what's changed can be difficult.
Jul 15, 2025
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An EHU study analyzing different genetic markers associated with facial features of the European population has shown a strong link between 10 of these markers and the facial morphology of people from the Iberian Peninsula. ...
Jul 3, 2025
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A new update, led by researchers at the UNC School of Medicine and the Gillings School of Global Public Health, describes major findings from the past half decade in the realm of psychiatric genomics and next steps for researchers.
Jun 27, 2025
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The newly launched South African Blood Regulatory (SABR) dataset reveals how genetic variation influences blood traits and gene activity in African populations, providing crucial insights into diseases like diabetes and heart ...
Jun 24, 2025
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A new international study coordinated by the European Alzheimer's and Dementia Biobank (EADB) consortium sheds light on how genetic risk factors for Alzheimer's disease (AD) vary—and remain consistent—across global populations. ...
Jun 18, 2025
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A research team has identified genetic factors that influence the shape of subcortical brain regions—far beyond volume measurements. The results could open up new approaches for the early detection of neurological and mental ...
Jun 16, 2025
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Northwestern University biophysicists have developed a new computational tool for identifying the gene combinations underlying complex illnesses like diabetes, cancer and asthma.
Jun 9, 2025
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In a first-of-its-kind genome-wide association study (GWAS) researchers have discovered two genes, RNF144B and ENPP1, that cause calcium pyrophosphate deposition (CPPD) disease in Americans of European and African descent. ...
May 28, 2025
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