Ciara Curtin is a freelance science writer based in Atlanta. Her work focuses mostly on genetics and medicine. Ciara has an M.A. in molecular, cellular and developmental biology from the University of California, Santa Barbara, and one in journalism from New York University’s science writing program.
Ciara Curtin
From this contributor
Brain scans reveal subtypes of fragile X syndrome in boys
Differences in brain structure may distinguish boys with relatively mild features of fragile X syndrome from those with a severe form of the condition.
Brain scans reveal subtypes of fragile X syndrome in boys
Data do-over backs dominance of genetics in autism risk
A reanalysis of data from more than 2 million children in Sweden suggests inherited genetic factors account for 83 percent of autism risk.
Data do-over backs dominance of genetics in autism risk
Rat study ties Rett syndrome gene to pain processing
Mutations in MECP2, the gene mutated in Rett syndrome, may alter the proportions and activity of sensory neurons in rats.
Rat study ties Rett syndrome gene to pain processing
Autism drugs may alter brain connectivity
Children with autism who take certain medications have different patterns of brain connectivity than do unmedicated children with the condition.
Twin tots reveal autism traits arise mostly from genes
Genes are bigger contributors to autism features than are environmental factors, according to a study of nearly 39,000 twins.
Twin tots reveal autism traits arise mostly from genes
Explore more from The Transmitter
Cracking the code of the extracellular matrix
Despite evidence for a role in plasticity and other crucial functions, many neuroscientists still view these proteins as “brain goop.” The field needs technical advances and a shift in scientific thinking to move beyond this outdated perspective.
Cracking the code of the extracellular matrix
Despite evidence for a role in plasticity and other crucial functions, many neuroscientists still view these proteins as “brain goop.” The field needs technical advances and a shift in scientific thinking to move beyond this outdated perspective.
Huntington’s disease gene variants past a certain size poison select cells
The findings—providing “the next step in the whole pathway”—help explain the disease’s late onset and offer hope that it has an extended therapeutic window.
Huntington’s disease gene variants past a certain size poison select cells
The findings—providing “the next step in the whole pathway”—help explain the disease’s late onset and offer hope that it has an extended therapeutic window.
X marks the spot in search for autism variants
Genetic variants on the X chromosome, including those in the gene DDX53, contribute to autism’s gender imbalance, two new studies suggest.
X marks the spot in search for autism variants
Genetic variants on the X chromosome, including those in the gene DDX53, contribute to autism’s gender imbalance, two new studies suggest.