McCallum-Loudeac J, Moody E, Williams J, Johnstone G, Sircombe K, Clarkson A
Hum Mol Genet. 2024; 33(9):787-801.
PMID: 38280229
PMC: 11031364.
DOI: 10.1093/hmg/ddae011.
Raimondi L, De Luca A, Gallo A, Perna F, Cuscino N, Cordaro A
Int J Mol Sci. 2024; 25(1).
PMID: 38203740
PMC: 10779108.
DOI: 10.3390/ijms25010570.
Pjanic S, Jevtic N, Grivas T
J Clin Med. 2024; 13(1).
PMID: 38202139
PMC: 10779587.
DOI: 10.3390/jcm13010132.
Torres P, Castilho A, Lopes K, Pellizzoni L, Righesso O, Falavigna A
Rev Bras Ortop (Sao Paulo). 2023; 58(4):e625-e631.
PMID: 37663184
PMC: 10468233.
DOI: 10.1055/s-0042-1749462.
Meng N, Wong K, Zhao M, Cheung J, Zhang T
EClinicalMedicine. 2023; 61:102050.
PMID: 37425371
PMC: 10329130.
DOI: 10.1016/j.eclinm.2023.102050.
A New Clinical Tool for Scoliosis Risk Analysis: Scoliosis Tele-Screening Test.
Yilmaz H, Buyukaslan A, Kusvuran A, Turan Z, Tuna F, Tunc H
Asian Spine J. 2023; 17(4):656-665.
PMID: 37226382
PMC: 10460665.
DOI: 10.31616/asj.2022.0299.
Whole-Exome Sequencing Identifies Genetic Variants for Severe Adolescent Idiopathic Scoliosis in a Taiwanese Population.
Lin M, Chou P, Huang K, Ting J, Liu C, Chou W
J Pers Med. 2023; 13(1).
PMID: 36675693
PMC: 9865588.
DOI: 10.3390/jpm13010032.
Polymorphisms in paired box 1 gene were associated with susceptibility of adolescent idiopathic scoliosis: A case-control study.
Pedrosa A, de Azevedo G, Cardoso J, Matheus Guimaraes J, Defino H, Perini J
J Craniovertebr Junction Spine. 2022; 13(3):318-324.
PMID: 36263348
PMC: 9574104.
DOI: 10.4103/jcvjs.jcvjs_54_22.
Is There a Relationship between Idiopathic Scoliosis and Body Mass? A Scoping Review.
Scaturro D, Balbo A, Vitagliani F, Stramazzo L, Camarda L, Letizia Mauro G
Nutrients. 2022; 14(19).
PMID: 36235665
PMC: 9572444.
DOI: 10.3390/nu14194011.
Association of LBX1 Gene Methylation Level with Disease Severity in Patients with Idiopathic Scoliosis: Study on Deep Paravertebral Muscles.
Janusz P, Toklowicz M, Andrusiewicz M, Kotwicka M, Kotwicki T
Genes (Basel). 2022; 13(9).
PMID: 36140724
PMC: 9498322.
DOI: 10.3390/genes13091556.
Resolving primary pathomechanisms driving idiopathic-like spinal curvature using a new scoliosis model.
Meyer-Miner A, Van Gennip J, Henke K, Harris M, Ciruna B
iScience. 2022; 25(9):105028.
PMID: 36105588
PMC: 9464966.
DOI: 10.1016/j.isci.2022.105028.
Epidemiological and diagnostic characteristics of scoliosis in children in a single tertiary centre in Abidjan.
Yaokreh J, Yapo Kouame G, Ali C, Odehouri-Koudou T, Ouattara O
Afr J Paediatr Surg. 2022; 19(3):171-175.
PMID: 35775520
PMC: 9290356.
DOI: 10.4103/ajps.AJPS_62_21.
Genetic variants associated with the occurrence and progression of adolescent idiopathic scoliosis: a systematic review protocol.
Terhune E, Heyn P, Piper C, Hadley-Miller N
Syst Rev. 2022; 11(1):118.
PMID: 35681176
PMC: 9178937.
DOI: 10.1186/s13643-022-01991-8.
Association of FBN1 polymorphism with susceptibility of adolescent idiopathic scoliosis: a case-control study.
de Azevedo G, Perini J, Araujo Junior A, Moliterno L, Andrande R, Matheus Guimaraes J
BMC Musculoskelet Disord. 2022; 23(1):430.
PMID: 35526034
PMC: 9077855.
DOI: 10.1186/s12891-022-05370-1.
Genetic animal modeling for idiopathic scoliosis research: history and considerations.
Terhune E, Monley A, Cuevas M, Wethey C, Gray R, Hadley-Miller N
Spine Deform. 2022; 10(5):1003-1016.
PMID: 35430722
DOI: 10.1007/s43390-022-00488-7.
Asymmetrical activation and asymmetrical weakness as two different mechanisms of adolescent idiopathic scoliosis.
Park Y, Ko J, Jang J, Lee S, Beom J, Ryu J
Sci Rep. 2021; 11(1):17582.
PMID: 34475442
PMC: 8413345.
DOI: 10.1038/s41598-021-96882-8.
Whole Exome Sequencing of 23 Multigeneration Idiopathic Scoliosis Families Reveals Enrichments in Cytoskeletal Variants, Suggests Highly Polygenic Disease.
Terhune E, Wethey C, Cuevas M, Monley A, Baschal E, Bland M
Genes (Basel). 2021; 12(6).
PMID: 34208743
PMC: 8235452.
DOI: 10.3390/genes12060922.
Saturation mutagenesis defines novel mouse models of severe spine deformity.
Rios J, Denton K, Yu H, Manickam K, Garner S, Russell J
Dis Model Mech. 2021; 14(6).
PMID: 34142127
PMC: 8246263.
DOI: 10.1242/dmm.048901.
Methylation of Estrogen Receptor 1 Gene in the Paraspinal Muscles of Girls with Idiopathic Scoliosis and Its Association with Disease Severity.
Janusz P, Chmielewska M, Andrusiewicz M, Kotwicka M, Kotwicki T
Genes (Basel). 2021; 12(6).
PMID: 34064195
PMC: 8224318.
DOI: 10.3390/genes12060790.
A Survey of Compound Heterozygous Variants in Pediatric Cancers and Structural Birth Defects.
Miller D, Piccolo S
Front Genet. 2021; 12:640242.
PMID: 33828584
PMC: 8019969.
DOI: 10.3389/fgene.2021.640242.