Detalhe da pesquisa
1.
Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism.
Cell
; 180(3): 568-584.e23, 2020 02 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-31981491
2.
Coexpression networks implicate human midfetal deep cortical projection neurons in the pathogenesis of autism.
Cell
; 155(5): 997-1007, 2013 Nov 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-24267886
3.
Direct additive genetics and maternal effect contribute to the risk of Tourette disorder.
J Neurol Neurosurg Psychiatry
; 94(8): 638-642, 2023 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-37100590
4.
Genome-wide association identifies the first risk loci for psychosis in Alzheimer disease.
Mol Psychiatry
; 26(10): 5797-5811, 2021 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-34112972
5.
Semisoft clustering of single-cell data.
Proc Natl Acad Sci U S A
; 116(2): 466-471, 2019 01 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-30587579
6.
Functional connectome fingerprinting accuracy in youths and adults is similar when examined on the same day and 1.5-years apart.
Hum Brain Mapp
; 41(15): 4187-4199, 2020 10 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-32652852
7.
Synaptic, transcriptional and chromatin genes disrupted in autism.
Nature
; 515(7526): 209-15, 2014 Nov 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-25363760
8.
Cohort profile: Epidemiology and Genetics of Obsessive-compulsive disorder and chronic tic disorders in Sweden (EGOS).
Soc Psychiatry Psychiatr Epidemiol
; 55(10): 1383-1393, 2020 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-31907560
9.
Transcriptional consequences of 16p11.2 deletion and duplication in mouse cortex and multiplex autism families.
Am J Hum Genet
; 94(6): 870-83, 2014 Jun 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-24906019
10.
Convergence of genes and cellular pathways dysregulated in autism spectrum disorders.
Am J Hum Genet
; 94(5): 677-94, 2014 May 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-24768552
11.
A Pleiotropic Missense Variant in SLC39A8 Is Associated With Crohn's Disease and Human Gut Microbiome Composition.
Gastroenterology
; 151(4): 724-32, 2016 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-27492617
12.
Functional impact of global rare copy number variation in autism spectrum disorders.
Nature
; 466(7304): 368-72, 2010 Jul 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-20531469
13.
Genome-wide transcriptome profiling reveals the functional impact of rare de novo and recurrent CNVs in autism spectrum disorders.
Am J Hum Genet
; 91(1): 38-55, 2012 Jul 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-22726847
14.
Autism genome-wide copy number variation reveals ubiquitin and neuronal genes.
Nature
; 459(7246): 569-73, 2009 May 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-19404257
15.
Individual common variants exert weak effects on the risk for autism spectrum disorders.
Hum Mol Genet
; 21(21): 4781-92, 2012 Nov 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-22843504
16.
Characterizing runs of homozygosity and their impact on risk for psychosis in a population isolate.
Am J Med Genet B Neuropsychiatr Genet
; 165B(6): 521-30, 2014 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-24980794
17.
Heritable Composite Phenotypes Defined by Combinations of Conduct Problem, Depression, and Temperament Features: Contributions to risk for Alcohol Problems.
Res Child Adolesc Psychopathol
; 52(4): 535-550, 2024 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-37773317
18.
Evaluating and improving health equity and fairness of polygenic scores.
HGG Adv
; 5(2): 100280, 2024 Apr 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-38402414
19.
Vitamin D insufficiency and severe asthma exacerbations in Puerto Rican children.
Am J Respir Crit Care Med
; 186(2): 140-6, 2012 Jul 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-22652028
20.
African ancestry and lung function in Puerto Rican children.
J Allergy Clin Immunol
; 129(6): 1484-90.e6, 2012 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-22560959