The father of a boy with a rare genetic mutation has accused a scientist of exploiting his child by proclaiming the defect a “genetic syndrome” and naming it after herself.
At an impasse with scientists investigating, publicizing, and interpreting his son’s condition, the father seems willing to use any leverage he can muster to remove the “syndrome” entry in an online genetic disease database. Based solely on an email he obtained from the database director, the father became convinced that if the paper underpinning the entry were retracted, the syndrome would go down with it. So earlier this year, he withdrew his consent and asked the journal that published the paper for a retraction, based on improper patient consent. He has also threatened to lob accusations of research misconduct at the paper’s last author. Continue reading Fearing “stigmatization,” patient’s father seeks retraction of paper on rare genetic mutation

A once-prominent researcher in the field of infectious disease — who was found 

The week at Retraction Watch featured the 

August 3rd is a big day around here — it’s our birthday. Today, we celebrate seven years since two science journalists decided, not exactly on whim but close to it, to launch a blog about retractions. Little did they know. (To hear our co-founder Ivan Oransky talk more about this milestone, check out his
Post-publication peer review isn’t just for scientists. Newspaper reporters can help correct the scientific record, too.