Detalhe da pesquisa
1.
Core planar cell polarity genes VANGL1 and VANGL2 in predisposition to congenital vertebral malformations.
Proc Natl Acad Sci U S A
; 121(18): e2310283121, 2024 Apr 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-38669183
2.
Biological insights into systemic lupus erythematosus through an immune cell-specific transcriptome-wide association study.
Ann Rheum Dis
; 2022 May 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-35609976
3.
Genome-wide association study of colorectal polyps identified highly overlapping polygenic architecture with colorectal cancer.
J Hum Genet
; 67(3): 149-156, 2022 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-34671089
4.
Eight novel susceptibility loci and putative causal variants in atopic dermatitis.
J Allergy Clin Immunol
; 148(5): 1293-1306, 2021 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-34116867
5.
Computed Tomography-Based Navigation System in Current Spine Surgery: A Narrative Review.
Medicina (Kaunas)
; 58(2)2022 Feb 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-35208565
6.
Meta-analysis of 208370 East Asians identifies 113 susceptibility loci for systemic lupus erythematosus.
Ann Rheum Dis
; 80(5): 632-640, 2021 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-33272962
7.
Genome-wide association study of epilepsy in a Japanese population identified an associated region at chromosome 12q24.
Epilepsia
; 62(6): 1391-1400, 2021 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-33913524
8.
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
9.
Bi-allelic loss of function variants of TBX6 causes a spectrum of malformation of spine and rib including congenital scoliosis and spondylocostal dysostosis.
J Med Genet
; 56(9): 622-628, 2019 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-31015262
10.
Relationship between Plantar Pressure and Sensory Disturbance in Patients with Hansen's Disease-Preliminary Research and Review of the Literature.
Sensors (Basel)
; 20(23)2020 Dec 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-33291332
11.
Identification of novel LFNG mutations in spondylocostal dysostosis.
J Hum Genet
; 64(3): 261-264, 2019 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-30531807
12.
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
13.
A genome-wide association study identifies a locus associated with knee extension strength in older Japanese individuals.
Commun Biol
; 7(1): 513, 2024 May 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-38769351
14.
Association of genetic variation in COL11A1 with adolescent idiopathic scoliosis.
Elife
; 122024 Jan 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-38277211
15.
GWAS for systemic sclerosis identifies six novel susceptibility loci including one in the Fcγ receptor region.
Nat Commun
; 15(1): 319, 2024 Jan 31.
Artigo
em Inglês
| MEDLINE | ID: mdl-38296975
16.
Clinical Results after Release of Sternocleidomastoid Muscle Surgery for Neglected Congenital Muscular Torticollis-Unipolar vs. Bipolar Release Surgery.
J Clin Med
; 13(1)2023 Dec 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-38202137
17.
Interrogating Causal Effects of Body Composition and Puberty-Related Risk Factors on Adolescent Idiopathic Scoliosis: A Two-Sample Mendelian Randomization Study.
JBMR Plus
; 7(12): e10830, 2023 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-38130750
18.
Upper End Vertebra of Proximal Thoracic Curve At T1 is a Novel Risk Factor of Postoperative Shoulder Imbalance in Lenke Type 2 Adolescent Idiopathic Scoliosis.
Global Spine J
; 13(5): 1223-1229, 2023 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-34121483
19.
Androgen receptor binding sites enabling genetic prediction of mortality due to prostate cancer in cancer-free subjects.
Nat Commun
; 14(1): 4863, 2023 08 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-37612283
20.
Association of genetic variation in COL11A1 with adolescent idiopathic scoliosis.
bioRxiv
; 2023 Nov 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-37292598