Genetic medicine can leave people with rare mutations behind. But there's new hope

Updated on: May 04,2025 0

Genetic medicine can leave people with rare mutations behind. But there's new hope

Updated on:May 04,2025 0

Genetic overlaps in 72 long-term health conditions identified

by Louise Vennells,University of ExeterCredit: Pixabay/CC0 Public DomainThe largest study to date to analyze millions of both genetic and patient records on the long-term health conditions of la

Updated on: February 18,2025 0

Genetic overlaps in 72 long-term health conditions identified

by Louise Vennells,University of ExeterCredit: Pixabay/CC0 Public DomainThe largest study to date to analyze millions of both genetic and patient records on the long-term health conditions of la

Updated on:February 18,2025 0

Epistasis: Unlocking the secrets of complex diseases

by Naomi Stekelenburg and Laura Harrison,CSIROCredit: Unsplash/CC0 Public DomainImagine your doctor calls you to discuss the results of your genetic testing. They tell you your results indicate

Updated on: February 19,2025 0

Epistasis: Unlocking the secrets of complex diseases

by Naomi Stekelenburg and Laura Harrison,CSIROCredit: Unsplash/CC0 Public DomainImagine your doctor calls you to discuss the results of your genetic testing. They tell you your results indicate

Updated on:February 19,2025 0

How a former navy mechanic defied the genetic odds of inherited Alzheimer's disease

by Justin Jackson , Medical XpressSchematic representation of the pedigree for the DIAN family carriers of the pathogenic mutation PSEN2 p.Asn141Ile. Credit:Nature Medicine(2025). DOI: 10.

Updated on: February 19,2025 0

How a former navy mechanic defied the genetic odds of inherited Alzheimer's disease

by Justin Jackson , Medical XpressSchematic representation of the pedigree for the DIAN family carriers of the pathogenic mutation PSEN2 p.Asn141Ile. Credit:Nature Medicine(2025). DOI: 10.

Updated on:February 19,2025 0

Unexpected X chromosome findings challenge assumptions about sex differences in human disease

by Karin Söderlund Leifler,Linköping UniversitySome of the group members in the Nestor lab at Linköping University. Credit: Johan Sjöholm/Linköping UniversityResearchers at Linköping University

Updated on: February 19,2025 0

Unexpected X chromosome findings challenge assumptions about sex differences in human disease

by Karin Söderlund Leifler,Linköping UniversitySome of the group members in the Nestor lab at Linköping University. Credit: Johan Sjöholm/Linköping UniversityResearchers at Linköping University

Updated on:February 19,2025 0

More barriers to genetic testing found for Black children than white children

byAmerican Academy of NeurologyCredit: nappy from PexelsFor children with signs of neurological conditions such as autism, epilepsy and global developmental delay, genetic testing can help make

Updated on: February 19,2025 0

More barriers to genetic testing found for Black children than white children

byAmerican Academy of NeurologyCredit: nappy from PexelsFor children with signs of neurological conditions such as autism, epilepsy and global developmental delay, genetic testing can help make

Updated on:February 19,2025 0

Previously unknown genetic links provide insights into autism's prevalence among males

byThe Hospital for Sick ChildrenCredit: Pixabay/CC0 Public DomainResearch published inThe American Journal of Human Geneticshas identified a previously unknown genetic link to autism

Updated on: January 08,2025 0

Previously unknown genetic links provide insights into autism's prevalence among males

byThe Hospital for Sick ChildrenCredit: Pixabay/CC0 Public DomainResearch published inThe American Journal of Human Geneticshas identified a previously unknown genetic link to autism

Updated on:January 08,2025 0

Boosting autophagy in eggs may reduce DNA damage and reproductive complications

by Brian Consiglio,University of MissouriSchematic model summarizing the impact of DNA double-strand breaks on oocyte meiosis I and the role of autophagy in DNA damage repair. Credit:Natur

Updated on: February 19,2025 0

Boosting autophagy in eggs may reduce DNA damage and reproductive complications

by Brian Consiglio,University of MissouriSchematic model summarizing the impact of DNA double-strand breaks on oocyte meiosis I and the role of autophagy in DNA damage repair. Credit:Natur

Updated on:February 19,2025 0

Ancient viral DNA in the human genome linked to multiple sclerosis and amyotrophic lateral sclerosis

byKing's College LondonRetrotranscriptome-wide association studies of neurodegenerative diseases. Credit:Brain, Behavior, and Immunity(2024). DOI: 10.1016/j.bbi.2024.10.020New re

Updated on: October 31,2024 0

Ancient viral DNA in the human genome linked to multiple sclerosis and amyotrophic lateral sclerosis

byKing's College LondonRetrotranscriptome-wide association studies of neurodegenerative diseases. Credit:Brain, Behavior, and Immunity(2024). DOI: 10.1016/j.bbi.2024.10.020New re

Updated on:October 31,2024 0

Consortium creates a robust, open-access platform to define the clinical relevance of genes and variants

by Molly Chiu,Baylor College of MedicineCredit:Genetics in Medicine(2024). DOI: 10.1016/j.gim.2024.101228The Clinical Genome Resource (ClinGen), a resource that works to define the c

Updated on: October 31,2024 0

Consortium creates a robust, open-access platform to define the clinical relevance of genes and variants

by Molly Chiu,Baylor College of MedicineCredit:Genetics in Medicine(2024). DOI: 10.1016/j.gim.2024.101228The Clinical Genome Resource (ClinGen), a resource that works to define the c

Updated on:October 31,2024 0

Genetic mechanisms underlying Duchenne muscular dystrophy point to potential treatments

byMax Planck SocietyTranscriptional adaptation drivesUTRNupregulation uponDMDRNA decay. Credit:Nature(2025). DOI: 10.1038/s41586-024-08539-xDuchenne muscular

Updated on: February 19,2025 0

Genetic mechanisms underlying Duchenne muscular dystrophy point to potential treatments

byMax Planck SocietyTranscriptional adaptation drivesUTRNupregulation uponDMDRNA decay. Credit:Nature(2025). DOI: 10.1038/s41586-024-08539-xDuchenne muscular

Updated on:February 19,2025 0

Researchers develop new tool to predict the impact of genetic variants

byBrigham and Women’s HospitalCredit: Pixabay/CC0 Public DomainA studypublishedin the journalCell Genomicsintroduces a new tool called FUSE (Functional Substitution Estim

Updated on: October 31,2024 0

Researchers develop new tool to predict the impact of genetic variants

byBrigham and Women’s HospitalCredit: Pixabay/CC0 Public DomainA studypublishedin the journalCell Genomicsintroduces a new tool called FUSE (Functional Substitution Estim

Updated on:October 31,2024 0