Detalhe da pesquisa
1.
Population Variation and Genetic Control of Modular Chromatin Architecture in Humans.
Cell
; 162(5): 1039-50, 2015 Aug 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-26300124
2.
Genomic basis for RNA alterations in cancer.
Nature
; 578(7793): 129-136, 2020 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-32025019
3.
Highly accurate quantification of allelic gene expression for population and disease genetics.
Genome Res
; 2022 Jul 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-35794008
4.
Author Correction: Genomic basis for RNA alterations in cancer.
Nature
; 614(7948): E37, 2023 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-36697831
5.
Corrigendum: Common genetic variation drives molecular heterogeneity in human iPSCs.
Nature
; 546(7660): 686, 2017 06 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-28614302
6.
Common genetic variation drives molecular heterogeneity in human iPSCs.
Nature
; 546(7658): 370-375, 2017 06 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-28489815
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.
Transcriptome and genome sequencing uncovers functional variation in humans.
Nature
; 501(7468): 506-11, 2013 Sep 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-24037378
9.
How next-generation sequencing is transforming complex disease genetics.
Trends Genet
; 29(1): 23-30, 2013 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-23103023
10.
Identification and removal of low-complexity sites in allele-specific analysis of ChIP-seq data.
Bioinformatics
; 30(2): 165-71, 2014 Jan 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-24255646
11.
Genetic and epigenetic contribution to complex traits.
Hum Mol Genet
; 21(R1): R24-8, 2012 Oct 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-22976472
12.
Histone lysine methyltransferase-related neurodevelopmental disorders: current knowledge and saRNA future therapies.
Front Cell Dev Biol
; 11: 1090046, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-36923252
13.
Somatic mutations alter the differentiation outcomes of iPSC-derived neurons.
Cell Genom
; 3(4): 100280, 2023 Apr 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-37082143
14.
CRISPR activation enables high-fidelity reprogramming into human pluripotent stem cells.
Stem Cell Reports
; 17(2): 413-426, 2022 02 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-35063129
15.
Differentiation of human induced pluripotent stem cells into cortical neural stem cells.
Front Cell Dev Biol
; 10: 1023340, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-36684426
16.
Linkage and linkage disequilibrium scan for autism loci in an extended pedigree from Finland.
Hum Mol Genet
; 18(15): 2912-21, 2009 Aug 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-19454485
17.
Identification of rare and common regulatory variants in pluripotent cells using population-scale transcriptomics.
Nat Genet
; 53(3): 313-321, 2021 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-33664507
18.
Population-scale proteome variation in human induced pluripotent stem cells.
Elife
; 92020 08 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-32773033
19.
Publisher Correction: Molecular and functional variation in iPSC-derived sensory neurons.
Nat Genet
; 51(7): 1190, 2019 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-31160811
20.
Molecular and functional variation in iPSC-derived sensory neurons.
Nat Genet
; 50(1): 54-61, 2018 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-29229984