RareInsight simplifies the communication of genetic results for rare disease patients
RareInsight is an interactive dashboard designed to support the dissemination and interpretation of genetic test results for clinicians,…
Returning of individual genetic findings to biobank participants: a mixed methods study results in Lithuania | BMC Medical Ethics
Attitudes of the Lithuanian public and experts towards the return of IGF The results of the quantitative study…
Bengal gets its 3rd genomic lab to help detect foetal anomalies, cancer | Kolkata News
Kolkata: A state-of-the-art genomics lab that will not just deal with onco-genetics (for cancer detection) but will also…
Experts issue warning after tiny creatures breed to form hybrid species — here’s why it could become a serious problem
Researchers in Australia have sounded the alarm after discovering that a threatened frog species has been interbreeding with…
Research, support and early diagnosis crucial for rare chromosome disorders | News
Rare Chromosome Awareness Day, celebrated in June, is an opportunity to increase public knowledge about rare chromosome and…
Docs Urged to Use Genome Tests to Diagnose Kids Early
Clinicians should prioritize genetic testing for young children who show signs of intellectual disability (ID) or developmental delays,…
Emplify Health joins statewide effort to expand genetic testing for newborns | News
LA CROSSE, Wis. (WXOW) – Starting next month, Emplify Health by Gundersen in La Crosse is joining a statewide…
Familial and Genetic Risk in Ovarian Cancer
Maurie Markman, MD Malignant ovarian neoplasms are a significant cause of cancer mortality in women.[1] Important risk factors…
First Awareness, Then Action: The Life-Saving Power Of Cancer Genetic Screening | Marketplace
Photo Caption: Dr. Shoshana Ungerleider, MD—San Francisco internist and jscreen.org board member—shares how hereditary testing saves lives during…
Using large-scale population-based data to improve disease risk assessment of clinical variants
Turro, E. et al. Whole-genome sequencing of patients with rare diseases in a national health system. Nature 583,…