Detalhe da pesquisa
1.
PhenoApt leverages clinical expertise to prioritize candidate genes via machine learning.
Am J Hum Genet
; 109(2): 270-281, 2022 02 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-35063063
2.
Perturbations of genes essential for Müllerian duct and Wölffian duct development in Mayer-Rokitansky-Küster-Hauser syndrome.
Am J Hum Genet
; 108(2): 337-345, 2021 02 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-33434492
3.
Novel Modic grading scoring system and its clinical validation: a preliminary investigation.
Eur Spine J
; 33(1): 84-92, 2024 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-37955751
4.
Pentraxin 3 deficiency ameliorates the severity of osteoarthritis and alleviates inflammation.
Biochem Biophys Res Commun
; 677: 20-25, 2023 Oct 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-37542771
5.
Sacroiliac joint degeneration in degenerative lumbar spondylolisthesis and related risk factors: a retrospective study.
Eur Spine J
; 32(4): 1375-1382, 2023 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-36826600
6.
Safety and accuracy of cannulated pedicle screw placement in scoliosis surgery: a comparison of robotic-navigation, O-arm-based navigation, and freehand techniques.
Eur Spine J
; 32(9): 3094-3104, 2023 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-37273031
7.
Anterior cervical tunnectomy and fusion (ACTF): a novel technique for cervical canal decompression.
Eur Spine J
; 32(6): 2110-2119, 2023 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-37067599
8.
Co-exposure to nanoplastics and acetaminophen causes skeletal dysplasia and behavioral abnormalities in zebrafish.
Ecotoxicol Environ Saf
; 253: 114640, 2023 Mar 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-36796208
9.
The utility of hierarchical genetic testing in paediatric liver disease.
Liver Int
; 42(5): 1097-1108, 2022 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-35257483
10.
Diagnostic yield and clinical impact of exome sequencing in early-onset scoliosis (EOS).
J Med Genet
; 58(1): 41-47, 2021 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-32381727
11.
Increased TBX6 gene dosages induce congenital cervical vertebral malformations in humans and mice.
J Med Genet
; 57(6): 371-379, 2020 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-31888956
12.
Factors and predictive model associated with perioperative complications after long fusion in the treatment of adult non-degenerative scoliosis.
BMC Musculoskelet Disord
; 22(1): 483, 2021 May 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-34034738
13.
TBX6 missense variants expand the mutational spectrum in a non-Mendelian inheritance disease.
Hum Mutat
; 41(1): 182-195, 2020 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31471994
14.
A novel COMP mutation in a Chinese family with multiple epiphyseal dysplasia.
BMC Med Genet
; 21(1): 115, 2020 05 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-32460719
15.
Identification of novel FBN1 variations implicated in congenital scoliosis.
J Hum Genet
; 65(3): 221-230, 2020 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-31827250
16.
Estrogen Receptors (ESRs) Mutations in Adolescent Idiopathic Scoliosis: A Cross-Sectional Study.
Med Sci Monit
; 26: e921611, 2020 Mar 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-32218412
17.
The mutational burden and oligogenic inheritance in Klippel-Feil syndrome.
BMC Musculoskelet Disord
; 21(1): 220, 2020 Apr 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-32278351
18.
Cervical sagittal alignment in adolescent idiopathic scoliosis patients (Lenke type 1-6).
J Orthop Sci
; 22(2): 254-259, 2017 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-28025024
19.
Impact of bilateral facet joint violation on radiographic degeneration of superior adjacent segments and clinical outcomes.
J Neurosurg Spine
; : 1-8, 2024 Apr 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-38579351
20.
Risk Factors for Surgical Treatment of Lumbar Degenerative Disc Disease in Middle-aged and Older Women: A Prospective Case-Control Study of 2370 Subjects.
Orthop Surg
; 2024 Apr 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-38637331