Anath C. Lionel

1. Genome-Wide Analysis of Copy Number Variants in Attention Deficit Hyperactivity Disorder: The Role of Rare Variants and Duplications at 15q13.3
   2011/12/30 by Nigel Williams, Nigel M. Williams, Barbara Franke +63 · 30 citations
   Biochemistry, Genetics and Molecular Biology · Medicine · Neuroscience · Psychology · #Attention Deficit Hyperactivity Disorder #Attention deficit hyperactivity disorder #Autism Spectrum Disorder Research #Biology #Copy-number variation #Gene #Genetics #Genome #Genome-wide association study #Genomic variations and chromosomal abnormalities #Genotype #Psychiatry #Psychology #Single-nucleotide polymorphism
2. CHD2 haploinsufficiency is associated with developmental delay, intellectual disability, epilepsy and neurobehavioural problems
   2014/04/22 by Sébastien Chénier, Grace Yoon, Bob Argiropoulos +15 · 1 citation
   Biochemistry, Genetics and Molecular Biology · Medicine · #Genomics and Rare Diseases #PARP inhibition in cancer therapy #BRCA gene mutations in cancer
3. Deletions in 16q24.2 are associated with autism spectrum disorder, intellectual disability and congenital renal malformation
   2013/01/18 by Gregory R. Handrigan, David Chitayat, Anath C. Lionel +17 · 1 citation
   Biochemistry, Genetics and Molecular Biology · #Congenital heart defects research #Genomic variations and chromosomal abnormalities #Genomics and Rare Diseases