Aarno Palotie, Ph.D., M.D.
This page shows the publications co-authored by Aarno Palotie and Tarjinder Singh.
The contribution of rare variants to risk of schizophrenia in individuals with and without intellectual disability. Nat Genet. 2017 Aug; 49(8):1167-1173.
Rare loss-of-function variants in SETD1A are associated with schizophrenia and developmental disorders. Nat Neurosci. 2016 Apr; 19(4):571-7.
De novo variants in neurodevelopmental disorders with epilepsy. Nat Genet. 2018 07; 50(7):1048-1053.
The connection strength for co-authors is the sum of the scores for each of their shared publications.
Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.