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Genetics news
Genetics
Largest genetic study to date identifies 13 new DNA regions linked to dyslexia
Dyslexia is a neurodevelopmental condition estimated to affect between 5–10% of people living in most countries, irrespective of their educational and cultural background. Dyslexic individuals experience persistent difficulties ...
19 hours ago
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Genetics
One-time gene therapy could end lifelong transfusions for rare blood disease
Thanks to in-utero blood transfusion technology, what was once a fatal diagnosis in the womb can now result in live births. However, this medical advancement created a new challenge: a growing population of children born ...
Sep 18, 2025
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Telomere protection failure: How genetic mutations cause pulmonary fibrosis
A research group from the National Cancer Research Center (CNIO) has found that an alteration in the POT1 gene prevents lung tissue from regenerating, which over time makes breathing difficult. The mutation prevents telomeres, ...
Sep 18, 2025
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Genetic test predicts response to weight-loss drugs
Mayo Clinic researchers have developed a genetic test that can help predict how people will respond to weight loss medications such as GLP-1s.
Sep 18, 2025
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Study identifies genetic loci that link brain structure and various psychiatric disorders
The development of many psychiatric disorders, including depression, schizophrenia and bipolar disorder, is known to be in great part influenced by genetics. Past research has identified various genes that appear to be associated ...
Late-life virginity: Mapping genetic, psychological and social factors in adults who have never had sex
Researchers from Karolinska Institutet, the Max Planck Institute for Empirical Aesthetics (Germany), Amsterdam UMC (Netherlands), in collaboration with other international partners, have conducted the most extensive study ...
Sep 17, 2025
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CRISPR approach offers hope for severe childhood brain disorder
When brain development gets off to a bad start, the consequences are lifelong. One example is a condition called SCN2A haploinsufficiency, in which children are born with just one functioning copy of the SCN2A gene—instead ...
Sep 17, 2025
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Gene editing may represent a new way to treat inherited kidney disease
Researchers in Berlin have used base editing to repair mutations that cause the kidney disorder ADPKD in cells from both mice and humans. In mice, a team led by Michael Kaminski was able to ease a key symptom of the difficult-to-treat ...
Sep 17, 2025
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Reprogramming the epigenetic code affects growth and survival of tumor cells in multiple myeloma
In the cancer type multiple myeloma, the malignant cells differ significantly from normal cells regarding the layer of chemical "tags" on DNA and proteins that control whether genes are turned on or off. These "tags" affect ...
Sep 17, 2025
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AI-powered CRISPR could lead to faster gene therapies
Stanford Medicine researchers have developed an artificial intelligence tool to help scientists better plan gene-editing experiments. The technology, CRISPR-GPT, acts as a gene-editing "copilot" supported by AI to help researchers—even ...
Sep 16, 2025
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Uncovering drivers of—and possible treatment for—Noonan syndrome heart defects
Noonan syndrome with multiple lentigines (NSML) is a rare genetic disorder that causes short stature, distinctive facial features, and clusters of dark skin spots called lentigines. But its most serious impact is a dangerous ...
Sep 16, 2025
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How HIV enters the genome—study decodes previously unknown mechanism
Researchers at the German Center for Infection Research (DZIF) at Heidelberg University Hospital have decoded a previously unknown mechanism by which HIV-1 selects its integration targets in the human genome. A research team ...
Sep 15, 2025
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Genetic variants may explain why obesity affects people differently
An international team of researchers led by Icahn School of Medicine at Mount Sinai and the University of Copenhagen in Denmark has pinpointed some of the reasons why obesity does not affect everyone in the same way. Their ...
Sep 15, 2025
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Research links DNA replication failure to cancer therapy
A new study from Karolinska Institutet, published in Nature Communications, reveals that cyclin-dependent kinases (CDK) promote DNA replication licensing in human cells by relieving inhibitory signals from RB tumor suppressor ...
Sep 15, 2025
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Finding patterns in genetic uncertainty: Clues for inborn errors of immunity
Behind every unexplained medical condition is a patient hoping for clarity and understanding. For people with suspected inborn errors of immunity (IEIs), genetic testing can facilitate individually tailored and effective ...
Sep 15, 2025
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Gene therapy safeguards hearing, balance in preclinical test
Scientists from the Gray Faculty of Medical & Health Sciences at Tel Aviv University introduced an innovative gene therapy method to treat impairments in hearing and balance caused by inner ear dysfunction. According to the ...
Sep 15, 2025
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Researchers work to make blood cancer a manageable illness with mutation identification
As blood cancers are constantly evolving and developing mutations that grow resistance to current treatments, researchers in the University of Cincinnati Cancer Center's Leukemia and Drug Development Lab (LDDL) are constantly ...
Sep 15, 2025
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Genetic deletion in cerebellum impedes hemisphere formation, study finds
The cerebellum, a brain region located at the back of the head that has long been known to support the coordination of muscle movements, has recently also been implicated in more sophisticated mental functions. Purkinje cells ...
The 'aldehyde storm': How a gene mutation found in East Asian people increases liver disease risk
Researchers have identified the mechanism by which a common genetic mutation increases liver disease risk. Their findings suggest that healthy choices, such as increasing antioxidants and limiting exposure to smoke, may reduce ...
Sep 12, 2025
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Cannabis use may harm reproductive health and reduce healthy embryos in IVF
CReATe Fertility Center in Toronto reports that tetrahydrocannabinol (THC) reaches the ovarian follicle, aligns with higher oocyte maturation, and associates with lower embryo euploid rates in IVF, with in vitro exposure ...
Customized gene-editing technology shows potential to treat lethal pediatric disease
Multisystemic smooth muscle dysfunction syndrome (MSMDS) is a rare condition associated with stroke, aortic dissection (tearing) and death in childhood. Currently, there is no effective treatment or cure for MSMDS.
Sep 11, 2025
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Cell defect in exosomes linked to development of Alzheimer's
They're tiny particles—with potentially huge human consequences. Researchers from Aarhus University have identified a defect in the production of so-called exosomes in cells, associated with a mutation seen in dementia ...
Sep 11, 2025
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Genetic peptides that shape gut bacteria may protect against obesity and diabetes
New research from the University of Sydney's Charles Perkins Center has found that genes play an active role in shaping the bacteria found in our gut, questioning the idea that gut health is influenced only by diet.
Sep 11, 2025
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Surprising new roles discovered for known blood cancer gene DNMT3A
A gene called DNMT3A is important for guiding blood stem cells into forming all the cell types present in blood, including red blood cells, white blood cells and platelets. When this gene accumulates mutations—which might ...
Sep 11, 2025
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Multi-disciplinary approach sheds light on the role of mitochondrial DNA mutations in cancer
Mitochondria act as energy factories in cells and have their own, separate DNA. Mutations to mitochondrial DNA (mtDNA) have been observed in cancer, but it has been unclear how these changes might affect cancer growth.
Sep 11, 2025
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