Publications and scholarly work
Law R, Dixon-Salazar T, Jerber J, Cai N, Abbasi AA, Zaki MS, Mittal K, Gabriel SB, Rafiq MA, Khan V, Nguyen M, Ali G, Copeland B, Scott E, Vasli N, Mikhailov A, Khan MN, Andrade DM, Ayaz M, Ansar M, Ayub M, Vincent JB, Gleeson JG.
Biallelic truncating mutations in FMN2, encoding the actin-regulatory protein Formin 2, cause nonsyndromic autosomal-recessive intellectual disability
Am J Hum Genet, 2014
Steriade C, Andrade DM, Faghfoury H, Tarnopolsky MA, Tai P.
Reply from the authors
Pediatr Neurol, 2014
Cheung EN, George SR, Andrade DM, Chow EW, Silversides CK, Bassett AS.
Neonatal hypocalcemia, neonatal seizures, and intellectual disability in 22q11.2 deletion syndrome
Genet Med, 2014
Cheung EN, George SR, Costain GA, Andrade DM, Chow EW, Silversides CK, Bassett AS.
Prevalence of hypocalcaemia and its associated features in 22q11·2 deletion syndrome
Clin Endocrinol (Oxf), 2014
Steriade C, Andrade DM, Faghfoury H, Tarnopolsky MA, Tai P.
Mitochondrial encephalopathy with lactic acidosis and stroke-like episodes (MELAS) may respond to adjunctive ketogenic diet
Pediatr Neurol, 2014