Detalhe da pesquisa
1.
Rapid and pervasive changes in genome-wide enhancer usage during mammalian development.
Cell;
155(7): 1521-31, 2013 Dec 19.
Artigo
em Inglês
| MEDLINE
| ID: mdl-24360275
2.
A high-resolution enhancer atlas of the developing telencephalon.
Cell;
152(4): 895-908, 2013 Feb 14.
Artigo
em Inglês
| MEDLINE
| ID: mdl-23375746
3.
Association of neurotransmitter pathway polygenic risk with specific symptom profiles in psychosis.
Mol Psychiatry;
2024 Mar 15.
Artigo
em Inglês
| MEDLINE
| ID: mdl-38491343
4.
Noncoding deletions reveal a gene that is critical for intestinal function.
Nature;
571(7763): 107-111, 2019 07.
Artigo
em Inglês
| MEDLINE
| ID: mdl-31217582
5.
Single cell enhancer activity distinguishes GABAergic and cholinergic lineages in embryonic mouse basal ganglia.
Proc Natl Acad Sci U S A;
119(15): e2108760119, 2022 04 12.
Artigo
em Inglês
| MEDLINE
| ID: mdl-35377797
6.
Transcriptional network orchestrating regional patterning of cortical progenitors.
Proc Natl Acad Sci U S A;
118(51)2021 12 21.
Artigo
em Inglês
| MEDLINE
| ID: mdl-34921112
7.
Dlx1 and Dlx2 Promote Interneuron GABA Synthesis, Synaptogenesis, and Dendritogenesis.
Cereb Cortex;
28(11): 3797-3815, 2018 11 01.
Artigo
em Inglês
| MEDLINE
| ID: mdl-29028947
8.
Tissue-specific SMARCA4 binding at active and repressed regulatory elements during embryogenesis.
Genome Res;
24(6): 920-9, 2014 Jun.
Artigo
em Inglês
| MEDLINE
| ID: mdl-24752179
9.
Function-based identification of mammalian enhancers using site-specific integration.
Nat Methods;
11(5): 566-71, 2014 May.
Artigo
em Inglês
| MEDLINE
| ID: mdl-24658141
10.
Tissue-specific RNA expression marks distant-acting developmental enhancers.
PLoS Genet;
10(9): e1004610, 2014 Sep.
Artigo
em Inglês
| MEDLINE
| ID: mdl-25188404
11.
Genomic Views of Transcriptional Enhancers: Essential Determinants of Cellular Identity and Activity-Dependent Responses in the CNS.
J Neurosci;
35(41): 13819-26, 2015 Oct 14.
Artigo
em Inglês
| MEDLINE
| ID: mdl-26468181
12.
Spectrum of DNA variants for non-syndromic deafness in a large cohort from multiple continents.
Hum Genet;
135(8): 953-61, 2016 08.
Artigo
em Inglês
| MEDLINE
| ID: mdl-27344577
13.
Formation of chimeric genes by copy-number variation as a mutational mechanism in schizophrenia.
Am J Hum Genet;
93(4): 697-710, 2013 Oct 03.
Artigo
em Inglês
| MEDLINE
| ID: mdl-24094746
14.
Learning about mammalian gene regulation from functional enhancer assays in the mouse.
Genomics;
106(3): 178-184, 2015 Sep.
Artigo
em Inglês
| MEDLINE
| ID: mdl-26079655
15.
Mutations in 12 genes for inherited ovarian, fallopian tube, and peritoneal carcinoma identified by massively parallel sequencing.
Proc Natl Acad Sci U S A;
108(44): 18032-7, 2011 Nov 01.
Artigo
em Inglês
| MEDLINE
| ID: mdl-22006311
16.
Congenital heart defects in patients with deletions upstream of SOX9.
Hum Mutat;
34(12): 1628-31, 2013 Dec.
Artigo
em Inglês
| MEDLINE
| ID: mdl-24115316
17.
Genomic duplication and overexpression of TJP2/ZO-2 leads to altered expression of apoptosis genes in progressive nonsyndromic hearing loss DFNA51.
Am J Hum Genet;
87(1): 101-9, 2010 Jul 09.
Artigo
em Inglês
| MEDLINE
| ID: mdl-20602916
18.
Targeted capture and sequencing for detection of mutations causing early onset epileptic encephalopathy.
Epilepsia;
54(7): 1262-9, 2013 Jul.
Artigo
em Inglês
| MEDLINE
| ID: mdl-23662938
19.
Detection of inherited mutations for breast and ovarian cancer using genomic capture and massively parallel sequencing.
Proc Natl Acad Sci U S A;
107(28): 12629-33, 2010 Jul 13.
Artigo
em Inglês
| MEDLINE
| ID: mdl-20616022
20.
Association of neurotransmitter pathway polygenic risk with specific symptom profiles in psychosis.
medRxiv;
2023 Nov 15.
Artigo
em Inglês
| MEDLINE
| ID: mdl-37292649