1.
Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis
by Smoller, J.W
The Lancet (British edition), 2013, Vol.381 (9875), p.1371-1379
2.
Estimating Missing Heritability for Disease from Genome-wide Association Studies
by Lee, Sang Hong
American journal of human genetics, 2011, Vol.88 (3), p.294-305
3.
The implications of the shared genetics of psychiatric disorders
by O'Donovan, Michael C
Nature medicine, 2016-11, Vol.22 (11), p.1214-1219
4.
Brief Report: A Gene Enrichment Approach Applied to Sleep and Autism
by Abel, Emily A
Journal of autism and developmental disorders, 2019-02-21, Vol.50 (5), p.1834-1840
5.
Developmental timing and critical windows for the treatment of psychiatric disorders
by Marin, Oscar
Nature medicine, 2016-11, Vol.22 (11), p.1229-1238
6.
Autism Spectrum Disorder, Developmental and Psychiatric Features in 16p11.2 Duplication
by Green Snyder, LeeAnne
Journal of autism and developmental disorders, 2016-05-21, Vol.46 (8), p.2734-2748
7.
Joint Analysis of Psychiatric Disorders Increases Accuracy of Risk Prediction for Schizophrenia, Bipolar Disorder, and Major Depressive Disorder
by Moser, Gerhard
American journal of human genetics, 2015-02-05, Vol.96 (2), p.283-294
8.
Association of GTF2i in the Williams-Beuren Syndrome Critical Region with Autism Spectrum Disorders
by Malenfant, Patrick
Journal of autism and developmental disorders, 2011-11-03, Vol.42 (7), p.1459-1469
9.
Zebrafish Ciliopathy Screen Plus Human Mutational Analysis Identifies C21orf59 and CCDC65 Defects as Causing Primary Ciliary Dyskinesia
by Austin-Tse, Christina
American journal of human genetics, 2013-10-03, Vol.93 (4), p.672-686
10.
Childhood Antecedents and Risk for Adult Mental Disorders
by Pine, Daniel S
Annual review of psychology, 2015-01-03, Vol.66 (1), p.459-485
11.
Mutations in DNAJB13, Encoding an HSP40 Family Member, Cause Primary Ciliary Dyskinesia and Male Infertility
by El Khouri, Elma
American journal of human genetics, 2016-08-04, Vol.99 (2), p.489-500
12.
BCL11A Haploinsufficiency Causes an Intellectual Disability Syndrome and Dysregulates Transcription
by Dias, Cristina
American journal of human genetics, 2016-08-04, Vol.99 (2), p.253-274
13.
The promises and challenges of human brain organoids as models of neuropsychiatric disease
by Quadrato, Giorgia
Nature medicine, 2016-11, Vol.22 (11), p.1220-1228
14.
Mutations in PIH1D3 Cause X-Linked Primary Ciliary Dyskinesia with Outer and Inner Dynein Arm Defects
by Paff, Tamara
American journal of human genetics, 2017-01-05, Vol.100 (1), p.160-168
15.
De Novo Mutations in MLL Cause Wiedemann-Steiner Syndrome
by Jones, Wendy D
American journal of human genetics, 2012-08-10, Vol.91 (2), p.358-364
16.
RAD21 Mutations Cause a Human Cohesinopathy
by Deardorff, Matthew A
American journal of human genetics, 2012-06-08, Vol.90 (6), p.1014-1027
17.
OTUD7A Regulates Neurodevelopmental Phenotypes in the 15q13.3 Microdeletion Syndrome
by Uddin, Mohammed
American journal of human genetics, 2018-02-01, Vol.102 (2), p.278-295
18.
Whole-Exome Capture and Sequencing Identifies HEATR2 Mutation as a Cause of Primary Ciliary Dyskinesia
by HORANI, Amjad
American journal of human genetics, 2012, Vol.91 (4), p.685-693
19.
Mutations in SRCAP, Encoding SNF2-Related CREBBP Activator Protein, Cause Floating-Harbor Syndrome
by Hood, Rebecca L
American journal of human genetics, 2012-02-10, Vol.90 (2), p.308-313
20.
Structural Variation of Chromosomes in Autism Spectrum Disorder
by Marshall, Christian R
American journal of human genetics, 2008, Vol.82 (2), p.477-488
