EXPLORE OUR TOPICS
LATEST ARTICLES
All about autism spectrum disorder: Understanding the causes, symptoms, and treatment
Autism spectrum disorder (ASD) is a neurological developmental disorder that affects brain development and function. This affects how people learn, behave, communicate and interact with others, leadi..
Revolutionizing newborn care: Machine learning and whole-genome sequencing for early diagnosis of sick newborns
Researchers have developed a method called “Mendelian Phenotype Search Engine” (MPSE) to identify which sick infants in the neonatal intensive care unit (NICU) would benefit most from newborn whole-g..
Wisdom teeth and genetics: Why some people do not have wisdom teeth
Did you know that wisdom teeth are actually an evolutionary leftover from our ancient ancestors that no longer serve their original purpose? These molars were once necessary to grind up tough, uncook..
Understanding azoospermia, one of the most common causes of male infertility
Azoospermia is a medical condition characterized by the absence of sperm in the ejaculate and is a major cause of male infertility. It affects 1 in 10 infertile men and overall 1 in 100 men worldwide..
Women in genetics – a celebration of discoveries and contributions made by female scientists
Science has traditionally been a male dominated subject; however, women have also been hard at work in this field for decades. We put together this infographic for International Women’s Day to celebr..
Whole-genome sequencing could help lower infant mortality rates
What is the percentage of infant deaths caused by genetic diseases? According to a study published in JAMA Network: 41% of infant deaths were caused by single-gene diseases. For 30% of th..
Folic acid and pregnancy – preventing neural tube defects with supplements
Each year, 300,000 babies are born with Neural Tube Defects (NTDs) worldwide [1]. NTDs are developmental defects of the brain and spinal cord occurring during early fetal development. Most of these c..
INFOGRAPHICS
Spinal muscular atrophy explained: Key facts at a glance
Spinal muscular atrophy is a rare genetic condition that weakens muscles by affecting the motor nerve cells in the spinal cord. It is a leading genetic cause of infant death, but advances in research..
Hereditary diseases
Understanding Down Syndrome
Down syndrome is a genetic condition caused by the presence of an extra copy of chromosome 21. It affects physical growth, facial features, and cognitive development. While each person with Down synd..
All about genetics
10 facts about DNA
Every year on April 25th, DNA Day celebrates the discovery of DNA’s double helix and the advances we’ve made in understanding genetics. DNA, or deoxyribonucleic acid, is the genetic bluep..
All about genetics
Spinal muscular atrophy explained: Key facts at a glance
Spinal muscular atrophy is a rare genetic condition that weakens muscles by affecting the motor nerve cells in the spinal cord. It is a leading genetic cause of infant death, but advances in research..
Hereditary diseases
Understanding Down Syndrome
Down syndrome is a genetic condition caused by the presence of an extra copy of chromosome 21. It affects physical growth, facial features, and cognitive development. While each person with Down synd..
All about genetics
10 facts about DNA
Every year on April 25th, DNA Day celebrates the discovery of DNA’s double helix and the advances we’ve made in understanding genetics. DNA, or deoxyribonucleic acid, is the genetic bluep..
All about genetics
See blog articles by subject
EDITORIAL TEAM
Our editors are a diverse group of scientists and physicians specialized in different areas of genetics and genetic testing technologies. Owing to our various backgrounds, our editors represent a broad range of expertise and are responsible for the content shared on our website. Only evidence-based, peer-reviewed, and up-to-date content is shared, and all text is continuously edited to maximize its correctness.
