Publications and scholarly work
Fung WL, Butcher NJ, Costain G, Andrade DM, Boot E, Chow EW, Chung B, Cytrynbaum C, Faghfoury H, Fishman L, García-Miñaúr S, George S, Lang AE, Repetto G, Shugar A, Silversides C, Swillen A, van Amelsvoort T, McDonald-McGinn DM, Bassett AS.
Practical guidelines for managing adults with 22q11.2 deletion syndrome
Genet Med, 2015
Day GS, Prüss H, Benseler SM, Paton TA, Paterson AD, Andrade DM.
GRIN1 polymorphisms do not affect susceptibility or phenotype in NMDA receptor encephalitis
Neurol Neuroimmunol Neuroinflamm, 2015
Merico D, Zarrei M, Costain G, Ogura L, Alipanahi B, Gazzellone MJ, Butcher NJ, Thiruvahindrapuram B, Nalpathamkalam T, Chow EW, Andrade DM, Frey BJ, Marshall CR, Scherer SW, Bassett AS.
Whole-Genome Sequencing Suggests Schizophrenia Risk Mechanisms in Humans with 22q11.2 Deletion Syndrome
G3 (Bethesda), 2015
Boot E, Butcher NJ, van Amelsvoort TA, Lang AE, Marras C, Pondal M, Andrade DM, Fung WL, Bassett AS.
Movement disorders and other motor abnormalities in adults with 22q11.2 deletion syndrome
Am J Med Genet A, 2015
Vincent JB, Jamil T, Rafiq MA, Anwar Z, Ayaz M, Hameed A, Nasr T, Naeem F, Khattak NA, Carter M, Ahmed I, John P, Wiame E, Andrade DM, Schaftingen EV, Mir A, Ayub M.
Phosphoserine phosphatase (PSPH) gene mutation in an intellectual disability family from Pakistan
Clin Genet, 2015