Detalhe da pesquisa
1.
Developmental dyslexia susceptibility genes DNAAF4, DCDC2, and NRSN1 are associated with brain function in fluently reading adolescents and young adults.
Cereb Cortex
; 34(4)2024 Apr 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-38610086
2.
Effects of exercise on whole-blood transcriptome profile in children with overweight/obesity.
Am J Hum Biol
; 36(2): e23983, 2024 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-37715654
3.
Viral infection-related gene upregulation in monocytes in children with signs of ß-cell autoimmunity.
Pediatr Diabetes
; 23(6): 703-713, 2022 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-35419920
4.
Otitis media susceptibility and shifts in the head and neck microbiome due to SPINK5 variants.
J Med Genet
; 58(7): 442-452, 2021 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-32709676
5.
FUT2 Variants Confer Susceptibility to Familial Otitis Media.
Am J Hum Genet
; 103(5): 679-690, 2018 11 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-30401457
6.
Distinct whole-blood transcriptome profile of children with metabolic healthy overweight/obesity compared to metabolic unhealthy overweight/obesity.
Pediatr Res
; 89(7): 1687-1694, 2021 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-33230195
7.
Genome-wide meta-analysis and replication studies in multiple ethnicities identify novel adolescent idiopathic scoliosis susceptibility loci.
Hum Mol Genet
; 27(22): 3986-3998, 2018 11 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-30395268
8.
Acute wheeze-specific gene module shows correlation with vitamin D and asthma medication.
Eur Respir J
; 55(1)2020 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31619476
9.
Rare variants in dynein heavy chain genes in two individuals with situs inversus and developmental dyslexia: a case report.
BMC Med Genet
; 21(1): 87, 2020 05 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-32357925
10.
Estrogen receptor ß, a regulator of androgen receptor signaling in the mouse ventral prostate.
Proc Natl Acad Sci U S A
; 114(19): E3816-E3822, 2017 05 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-28439009
11.
Gain-of-function CEBPE mutation causes noncanonical autoinflammatory inflammasomopathy.
J Allergy Clin Immunol
; 144(5): 1364-1376, 2019 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-31201888
12.
Guide for library design and bias correction for large-scale transcriptome studies using highly multiplexed RNAseq methods.
BMC Bioinformatics
; 20(1): 418, 2019 Aug 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-31409293
13.
A2ML1 and otitis media: novel variants, differential expression, and relevant pathways.
Hum Mutat
; 40(8): 1156-1171, 2019 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-31009165
14.
A multiethnic meta-analysis defined the association of rs12946942 with severe adolescent idiopathic scoliosis.
J Hum Genet
; 64(5): 493-498, 2019 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-30787423
15.
MANF protects human pancreatic beta cells against stress-induced cell death.
Diabetologia
; 61(10): 2202-2214, 2018 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-30032427
16.
Mlh1 deficiency in normal mouse colon mucosa associates with chromosomally unstable colon cancer.
Carcinogenesis
; 39(6): 788-797, 2018 05 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-29701748
17.
Moritella viscosa in lumpfish (Cyclopterus lumpus) and Atlantic salmon (Salmo salar).
J Fish Dis
; 41(11): 1751-1758, 2018 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-30132897
18.
Damaging heterozygous mutations in NFKB1 lead to diverse immunologic phenotypes.
J Allergy Clin Immunol
; 140(3): 782-796, 2017 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-28115215
19.
Optimizing bone morphogenic protein 4-mediated human embryonic stem cell differentiation into trophoblast-like cells using fibroblast growth factor 2 and transforming growth factor-ß/activin/nodal signalling inhibition.
Reprod Biomed Online
; 35(3): 253-263, 2017 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-28647356
20.
Targeted high-throughput sequencing of candidate genes for chronic obstructive pulmonary disease.
BMC Pulm Med
; 16(1): 146, 2016 11 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-27835950