Detalhe da pesquisa
1.
CNVs: harbingers of a rare variant revolution in psychiatric genetics.
Cell
; 148(6): 1223-41, 2012 Mar 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-22424231
2.
Whole-genome sequencing in autism identifies hot spots for de novo germline mutation.
Cell
; 151(7): 1431-42, 2012 Dec 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-23260136
3.
Altered human oligodendrocyte heterogeneity in multiple sclerosis.
Nature
; 566(7745): 543-547, 2019 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-30747918
4.
Frequency and Complexity of De Novo Structural Mutation in Autism.
Am J Hum Genet
; 98(4): 667-79, 2016 Apr 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-27018473
5.
Marker chromosome genomic structure and temporal origin implicate a chromoanasynthesis event in a family with pleiotropic psychiatric phenotypes.
Hum Mutat
; 39(7): 939-946, 2018 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-29696747
6.
Duplications of the neuropeptide receptor gene VIPR2 confer significant risk for schizophrenia.
Nature
; 471(7339): 499-503, 2011 Mar 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-21346763
7.
Single-nucleus and spatial transcriptomic profiling of human temporal cortex and white matter reveals novel associations with AD pathology.
bioRxiv
; 2024 Apr 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-38712204
8.
Genetics: Fish heads and human disease.
Nature
; 485(7398): 318-9, 2012 May 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-22596152
9.
A structured evaluation of cryopreservation in generating single-cell transcriptomes from cerebrospinal fluid.
Cell Rep Methods
; 3(7): 100533, 2023 07 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-37533636
10.
Disease-specific selective vulnerability and neuroimmune pathways in dementia revealed by single cell genomics.
bioRxiv
; 2023 Sep 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-37808727
11.
Schizophrenia risk conferred by rare protein-truncating variants is conserved across diverse human populations.
Nat Genet
; 55(3): 369-376, 2023 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-36914870
12.
Reduced NMDAR1 expression in the Sp4 hypomorphic mouse may contribute to endophenotypes of human psychiatric disorders.
Hum Mol Genet
; 19(19): 3797-805, 2010 Oct 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-20634195
13.
Association of variants in BAT1-LTA-TNF-BTNL2 genes within 6p21.3 region show graded risk to leprosy in unrelated cohorts of Indian population.
Hum Genet
; 131(5): 703-16, 2012 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-22071774
14.
Leprosy and the adaptation of human toll-like receptor 1.
PLoS Pathog
; 6: e1000979, 2010 Jul 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-20617178
15.
Genetic variations and interactions in anti-inflammatory cytokine pathway genes in the outcome of leprosy: a study conducted on a MassARRAY platform.
J Infect Dis
; 204(8): 1264-73, 2011 Oct 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-21917900
16.
Cell-type-specific cis-eQTLs in eight human brain cell types identify novel risk genes for psychiatric and neurological disorders.
Nat Neurosci
; 25(8): 1104-1112, 2022 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-35915177
17.
Epigenomic priming of immune genes implicates oligodendroglia in multiple sclerosis susceptibility.
Neuron
; 110(7): 1193-1210.e13, 2022 04 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-35093191
18.
CellMixS: quantifying and visualizing batch effects in single-cell RNA-seq data.
Life Sci Alliance
; 4(6)2021 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-33758076
19.
muscat detects subpopulation-specific state transitions from multi-sample multi-condition single-cell transcriptomics data.
Nat Commun
; 11(1): 6077, 2020 11 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-33257685
20.
Tau Pathology Drives Dementia Risk-Associated Gene Networks toward Chronic Inflammatory States and Immunosuppression.
Cell Rep
; 33(7): 108398, 2020 11 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-33207193