Exome sequencing in multiplex autism families suggests a major role for heterozygous truncating mutations
Claudio Toma(Universitat de Barcelona), Bru Cormand(Instituto de Salud Carlos III), Marta Morgade Salgado(Universidad Autónoma de Madrid), C. Arenas(Universitat de Barcelona), Vanesa Padillo(Hospital Sant Joan de Déu Barcelona), Bàrbara Torrico(Universitat de Barcelona), Rafael Valdés‐Mas(Weizmann Institute of Science), Amaia Hervás(Mútua Terrassa), Xosé S. Puente(Universidad de Oviedo), Mónica Bayés(Centro Nacional de Análisis Genómico), Marta Maristany(Hospital Sant Joan de Déu Barcelona), Alba Tristán‐Noguero(Universitat de Barcelona)
Cited by 124
Related Papers
Signatures of mutational processes in human cancer
|Nature|2013|10.1k
Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder
|Nature Genetics|2018|2.3k
Whole-genome sequencing identifies recurrent mutations in chronic lymphocytic leukaemia
|Nature|2011|1.5k
Non-coding recurrent mutations in chronic lymphocytic leukaemia
|Nature|2015|851
The genome of a songbird
|Nature|2010|837