Detalhe da pesquisa
1.
Impact on Quality of Life After Parathyroidectomy for Asymptomatic Primary Hyperparathyroidism.
J Surg Res
; 261: 139-145, 2021 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-33429222
2.
DNA Methylation Profiling of Uniparental Disomy Subjects Provides a Map of Parental Epigenetic Bias in the Human Genome.
Am J Hum Genet
; 99(3): 555-566, 2016 09 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-27569549
3.
Mapping autism risk loci using genetic linkage and chromosomal rearrangements.
Nat Genet
; 39(3): 319-28, 2007 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-17322880
4.
Common genetic variants on 5p14.1 associate with autism spectrum disorders.
Nature
; 459(7246): 528-33, 2009 May 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-19404256
5.
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
6.
A genome-wide CNV analysis of schizophrenia reveals a potential role for a multiple-hit model.
Am J Med Genet B Neuropsychiatr Genet
; 165B(8): 619-26, 2014 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-25228354
7.
Copy number variations on chromosome 12q14 in patients with normal tension glaucoma.
Hum Mol Genet
; 20(12): 2482-94, 2011 Jun 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-21447600
8.
Multifaceted genomic risk for brain function in schizophrenia.
Neuroimage
; 61(4): 866-75, 2012 Jul 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-22440650
9.
Genome-wide analyses of exonic copy number variants in a family-based study point to novel autism susceptibility genes.
PLoS Genet
; 5(6): e1000536, 2009 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-19557195
10.
Generation of a human induced pluripotent stem cell line from a patient diagnosed with schizophrenia carrying a 16p11.2 deletion.
Stem Cell Res
; 59: 102636, 2022 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-34953327
11.
Modeling Human Cerebellar Development In Vitro in 2D Structure.
J Vis Exp
; (187)2022 09 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-36190246
12.
DISC1 is associated with cortical thickness and neural efficiency.
Neuroimage
; 57(4): 1591-600, 2011 Aug 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-21642004
13.
Genome-wide analysis of copy number variants in age-related macular degeneration.
Hum Genet
; 129(1): 91-100, 2011 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-20981449
14.
MTHFR 677C --> T genotype disrupts prefrontal function in schizophrenia through an interaction with COMT 158Val --> Met.
Proc Natl Acad Sci U S A
; 105(45): 17573-8, 2008 Nov 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-18988738
15.
G72 influences longitudinal change in frontal lobe volume in schizophrenia.
Am J Med Genet B Neuropsychiatr Genet
; 153B(2): 640-647, 2010 Mar 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-19760675
16.
Unexpected changes in clinical diagnosis: early abdomino-pelvic computed tomography compared with clinical evaluation.
Abdom Imaging
; 34(6): 783-7, 2009 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-17901913
17.
Basic helix-loop-helix transcription factor NEUROG1 and schizophrenia: effects on illness susceptibility, MRI brain morphometry and cognitive abilities.
Schizophr Res
; 106(2-3): 192-9, 2008 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-18799289
18.
Cerebral cortical gray matter overgrowth and functional variation of the serotonin transporter gene in autism.
Arch Gen Psychiatry
; 64(6): 709-17, 2007 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-17548752
19.
Cortical enlargement in autism is associated with a functional VNTR in the monoamine oxidase A gene.
Am J Med Genet B Neuropsychiatr Genet
; 147B(7): 1145-51, 2008 Oct 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-18361446
20.
Association between brain-derived neurotrophic factor Val66Met gene polymorphism and progressive brain volume changes in schizophrenia.
Am J Psychiatry
; 164(12): 1890-9, 2007 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-18056245