Bionano Genomics, Inc. (Nasdaq: BNGO) today announced that studies featuring optical genome mapping (OGM) at the 2026 European Society of Human Genetics (ESHG) ...

Bionano Genomics, Inc. (Nasdaq: BNGO) today announced that studies featuring optical genome mapping (OGM) at the 2026 European Society of Human Genetics (ESHG) conference grew substantially compared ...

Definition: A microarray is a small, flat substrate carrying an ordered grid of microscopic probe features, each containing a known biological molecule, that is used to measure many molecular targets ...

Congenital heart disease (CHD) is the most common birth defect and a leading cause of infant mortality. CHD often has a genetic cause, and recent studies demonstrate the utility of genetic testing. In ...

Intellectual disability affects a person's ability to reason, practice good judgment, problem-solve, and communicate. Children with intellectual disabilities may have trouble with communication, ...

‌Although genetics are hereditary, a phenomenon in genetic alterations occurs when male babies receive an extra Y chromosome in each of their cells, resulting in an XYY combination. The syndrome is ...

Abstract: Intellectual disability disorder (IDD) is a kind of neurodevelopmental disorder that adversely affects an individual's quality of life. Discriminating normal brain patterns from abnormal ...

To assess the possibility that a foetus may be born with a genetic disorder or a pregnancy-related complication, prenatal screening is made available to all pregnant women. As a result, it assists in ...

aSergievsky Center, Taub Institute, Department of Neurology, Vagelos College of Physicians and Surgeons, Columbia University, New York, NY, USA bDepartment of Epidemiology, Mailman School of Public ...

Objective: Genetic variants cause a significant portion of developmental disorders and intellectual disabilities (DD/ID), but clinical and genetic heterogeneity makes identification challenging.

Phelan-McDermid syndrome is a rare genetic condition impacting speech, mobility, and cognitive development. It typically occurs due to an alteration in chromosome 22 and is present from birth. It can ...