RettSearch

iconAbout RettSearch

RettSearch is an international, multi-center collaborative network of clinically-oriented researchers. Its mission is to promote the development of new therapeutic approaches for Rett syndrome (RTT) by collecting information and pursuing research in areas of relevance to clinical trials in RTT. Under the leadership of the Executive Committee - Sarojini Budden, M.D., FRCPC; John Christodoulou, , F.R.A.C.P., Ph.D., A.R.C.P.A..; Daniel Glaze, M.D.; Helen Leonard, M.B.Ch.B., M.P.H.;Jeff Neul, M.D.; Carolyn Schanen, M.D.; Francesca Mari, M.D., Ph.D; and Walter Kaufmann, M.D. (Chair) - members are grouped into committees or "working groups," each with a specific theme and task. Clinical researchers interested in applying for membership should send a current CV to the RettSearch Coordinator. Learn more about our History/Mission and Expected Outcomes.


iconInterRett

InterRettInterRett: The Value
of International Data
Learn more...

iconRettBase

The IRSF MECP2 Variation Database

RettBASE aims to provide a list of all published MECP2 gene variations (including polymorphisms), whereby unpublished data can be submitted and made available to all researchers. Learn more...


iconLinks to NIH Funding Resources



iconAre you a RettSearch member looking for funding?

Consider applying for a RettSearch microgrant!


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