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newborn screening

Luminex's recent decision to reduce its workforce by 5 percent, close an office in Australia, and seek a buyer for its newborn screening business, was in part influenced by its attempt to obtain US regulatory clearance for its NeoPlex4 test, according to the firm's CEO.

NEW YORK (GenomeWeb News) – Luminex said after the close of the market Wednesday that it will undertake a restructuring that will result in an undisclosed number of employees being laid off and its Brisbane, Australia office being closed.

NEW YORK (GenomeWeb News) – A bipartisan pair of lawmakers in the US House of Representatives have introduced the Newborn Screening Saves Lives Reauthorization Act, which has several provisions to help guide and support disease-risk screening programs across the US.

NEW YORK (GenomeWeb News) – The American College of Medical Genetics and Genomics and the American Academy of Pediatrics have released a joint policy statement detailing their latest recommendations for how genetic tests and newborn screening should be used in the care of children.

NEW YORK (GenomeWeb News) – The committee that advises the US Department of Health and Human Services on matters related to newborn screening for genetic diseases, and sets the newborn screening standards followed by many states, is set to expire in April and advocates are pressing to get it reau

NEW YORK (GenomeWeb News) – Blood samples that are left over from newborn screening tests offer a treasure trove of research materials for scientists seeking to uncover the role of genes in diseases and health, and the science community should be pushing for policies that promote their use in res

NEW YORK (GenomeWeb News) – The National Human Genome Research Institute and the Eunice Kennedy Shriver National Institute of Child Health and Human Development are preparing a new grant program that will provide $25 million to fund studies that look at how genome sequencing may be used in newbor

Asuragen has been awarded a one-year, $346,000 grant from the National Institute of Child Health and Human Development to develop a high-throughput version of its PCR-based fragile X syndrome test for use in newborn population screening, according to a recently published grant ab

Blood spots may be a benefit to public health research, but the mandatory collection process may be stoking public concerns about government and privacy, one pediatrician argues.

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A new analysis founds that nearly half the late-stage clinical trials sponsored by a US National Cancer Institute program influence patient care.

Technology Review reports that sickle cell patients are optimistic about gene editing to treat their disease, but are worried about how available it will be.

The owner of the GEDmatch website tells CBS12 he is considering charging law enforcement a fee to use the site.

In Nature this week: babies born by caesarean section are more likely to have altered gut microbiota profiles, and more.