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New collaboration to study early detection of developmental differences in children


New collaboration to study early detection of developmental differences in children
The University of Washington s School of Medicine Brotman Baty Institute for Precision Medicine is collaborating with Illumina, Inc. and GeneDx, Inc., a wholly owned subsidiary of BioReference Laboratories, Inc., an OPKO Health company, to study early detection of developmental differences in children.
The project, SeqFirst, will provide early access to whole-genome sequencing (WGS) to 100 children suspected of having developmental differences at the point of diagnosis.
Scientists anticipate this will lead to earlier, more rapid diagnoses, as well as lowering health care costs and improving subsequent treatment for these children. Illumina will support the study by providing advanced sequencing reagents and GeneDx will perform state-of-the-art diagnostic WGS. ....

Michael Bamshad , Jeremy Preston , Kyle Retterer , Emily Henderson , University Of Washington , Genedx Inc , Illumina Inc , Bioreference Laboratories Inc , Medicine Brotman Baty Institute , Precision Medicine , Bioreference Laboratories , Project Principal , Senior Vice President , Chief Technology Officer , Seattle Children , ஜெர்மி ப்ரெஸ்டந் , எமிலி ஹென்டர்சன் , பல்கலைக்கழகம் ஆஃப் வாஷிங்டன் , இல்லுமின இன்க் , ப்ரிஸிஶந் மருந்து , ப்ராஜெக்ட் ப்ரிந்ஸிபல் , மூத்தவர் துணை ப்ரெஸிடெஂட் , தலைமை தொழில்நுட்பம் அதிகாரி , சீட்டில் குழந்தைகள் ,

Genetic changes linked to neurodevelopmental disabilities, cerebral palsy


Genetic changes linked to neurodevelopmental disabilities, cerebral palsy
Researchers have discovered a strong link between genetic changes known to cause neurodevelopmental disabilities and cerebral palsy.
Cerebral palsy affects movement and posture and often co-occurs with other neurodevelopmental disorders, including intellectual disability, epilepsy and autism spectrum disorder. Individual cases of cerebral palsy are often attributed to birth asphyxia, although recent studies indicate that asphyxia accounts for less than 10% of cases. A growing body of research indicates that cerebral palsy may be caused by genetic changes, as is the case in other neurodevelopmental disorders.
The research team, which included investigators from Geisinger and GeneDx Inc., a wholly owned subsidiary of BioReference Laboratories Inc., an OPKO Health company and global leader in genetic diagnostics, studied the DNA sequence of 1,526 children and adults with cerebral palsy. ....

United States , Christa Martin , Kyle Retterer , Francisca Millan , Emily Henderson , Geisinger Health System , Genedx Inc , Autism Developmental Medicine Institute , Senior Study Co , Bioreference Laboratories Inc , Journal Of The American Medical Association , Senior Study Co Author , Developmental Medicine Institute , Geisinger Health , American Medical Association , Andres Moreno De Luca , ஒன்றுபட்டது மாநிலங்களில் , கிறிஸ்டா மார்டின் , பிரான்சிஸ்கா மில்லன் , எமிலி ஹென்டர்சன் , கேய்சிங்கேர் ஆரோக்கியம் அமைப்பு , மன இறுக்கம் வளர்ச்சி மருந்து நிறுவனம் , மூத்தவர் படிப்பு இணை , இதழ் ஆஃப் தி அமெரிக்கன் மருத்துவ சங்கம் , மூத்தவர் படிப்பு இணை நூலாசிரியர் , வளர்ச்சி மருந்து நிறுவனம் ,

Geisinger-GeneDx research identifies frequent genetic causes of cerebral palsy


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DANVILLE, Pa. and GAITHERSBURG, Md. - Researchers have discovered a strong link between genetic changes known to cause neurodevelopmental disabilities and cerebral palsy.
Cerebral palsy affects movement and posture and often co-occurs with other neurodevelopmental disorders, including intellectual disability, epilepsy and autism spectrum disorder. Individual cases of cerebral palsy are often attributed to birth asphyxia, although recent studies indicate that asphyxia accounts for less than 10% of cases. A growing body of research indicates that cerebral palsy may be caused by genetic changes, as is the case in other neurodevelopmental disorders.
The research team, which included investigators from Geisinger and GeneDx Inc., a wholly owned subsidiary of BioReference Laboratories Inc., an OPKO Health company and global leader in genetic diagnostics, studied the DNA sequence of 1,526 children and adults with cerebral palsy. The team found disease-causing change ....

United States , Christa Martin , Kyle Retterer , Francisca Millan , Abigail Geisinger , Journal Of The American Medical Association , National Institute Of Mental Health , Geisinger Autism Developmental Medicine Institute , Genedx Inc , Geisinger Commonwealth School Of Medicine , Bioreference Laboratories Inc , Developmental Medicine , American Medical Association , Andres Moreno De Luca , National Institute , Geisinger Commonwealth School , ஒன்றுபட்டது மாநிலங்களில் , கிறிஸ்டா மார்டின் , பிரான்சிஸ்கா மில்லன் , பாங்கி கேய்சிங்கேர் , இதழ் ஆஃப் தி அமெரிக்கன் மருத்துவ சங்கம் , தேசிய நிறுவனம் ஆஃப் மன ஆரோக்கியம் , கேய்சிங்கேர் மன இறுக்கம் வளர்ச்சி மருந்து நிறுவனம் , கேய்சிங்கேர் காமன்வெல்த் பள்ளி ஆஃப் மருந்து , வளர்ச்சி மருந்து , அமெரிக்கன் மருத்துவ சங்கம் ,