Detalhe da pesquisa
1.
Identification and prioritization of myeloid malignancy germline variants in a large cohort of adult patients with AML.
Blood
; 139(8): 1208-1221, 2022 02 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-34482403
2.
Functional genomic landscape of acute myeloid leukaemia.
Nature
; 562(7728): 526-531, 2018 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-30333627
3.
Secondary fusion proteins as a mechanism of BCR::ABL1 kinase-independent resistance in chronic myeloid leukaemia.
Br J Haematol
; 200(3): 323-328, 2023 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-36264026
4.
Genomic landscape of neutrophilic leukemias of ambiguous diagnosis.
Blood
; 134(11): 867-879, 2019 09 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-31366621
5.
Smaller total brain volume but not subcortical structure volume related to common genetic risk for ADHD.
Psychol Med
; 51(8): 1279-1288, 2021 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-31973781
6.
Whole-genome sequencing identifies EN1 as a determinant of bone density and fracture.
Nature
; 526(7571): 112-7, 2015 Oct 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-26367794
7.
Evaluating chronic emotional dysregulation and irritability in relation to ADHD and depression genetic risk in children with ADHD.
J Child Psychol Psychiatry
; 61(2): 205-214, 2020 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-31605387
8.
Polymorphisms in oxidative stress pathway genes and prostate cancer risk.
Cancer Causes Control
; 30(12): 1365-1375, 2019 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-31667711
9.
Gender-Specific Effects of Selection for Drinking in the Dark on the Network Roles of Coding and Noncoding RNAs.
Alcohol Clin Exp Res
; 42(8): 1454-1465, 2018 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-29786871
10.
NFAT5 and SLC4A10 Loci Associate with Plasma Osmolality.
J Am Soc Nephrol
; 28(8): 2311-2321, 2017 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-28360221
11.
Functional and genomic context in pathway analysis of GWAS data.
Trends Genet
; 30(9): 390-400, 2014 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-25154796
12.
HitWalker2: visual analytics for precision medicine and beyond.
Bioinformatics
; 32(8): 1253-5, 2016 04 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-26708334
13.
Sequencing of sporadic Attention-Deficit Hyperactivity Disorder (ADHD) identifies novel and potentially pathogenic de novo variants and excludes overlap with genes associated with autism spectrum disorder.
Am J Med Genet B Neuropsychiatr Genet
; 174(4): 381-389, 2017 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-28332277
14.
Oncogenic CSF3R mutations in chronic neutrophilic leukemia and atypical CML.
N Engl J Med
; 368(19): 1781-90, 2013 May 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-23656643
15.
Aurora A kinase as a target for therapy in TCF3-HLF rearranged acute lymphoblastic leukemia.
Haematologica
; 106(11): 2990-2994, 2021 11 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-34233449
16.
Methylomic analysis of salivary DNA in childhood ADHD identifies altered DNA methylation in VIPR2.
J Child Psychol Psychiatry
; 57(2): 152-60, 2016 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-26304033
17.
Pathway analysis in attention deficit hyperactivity disorder: An ensemble approach.
Am J Med Genet B Neuropsychiatr Genet
; 171(6): 815-26, 2016 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-27004716
18.
plethy: management of whole body plethysmography data in R.
BMC Bioinformatics
; 16: 134, 2015 Apr 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-25924931
19.
Splicing landscape of the eight collaborative cross founder strains.
BMC Genomics
; 16: 52, 2015 Feb 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-25652416
20.
PLA2G6, encoding a phospholipase A2, is mutated in neurodegenerative disorders with high brain iron.
Nat Genet
; 38(7): 752-4, 2006 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-16783378