Terhune EA - Search Results

1

Definitions, terminology, and related concepts of "racial health equity": a scoping review protocol.

Heyn PC, Terhune EA, Dagne MB, Piper C, Welch VA, Francis D, Pizarro AB, Rizvi A, Sathe N, Dewidar O, Ovelman C, Duque T, Baker TA, Turner RW 2nd, Viswanathan M, Riddle D. Heyn PC, et al. Among authors: terhune ea. Syst Rev. 2023 Sep 30;12(1):185. doi: 10.1186/s13643-023-02357-4. Syst Rev. 2023. PMID: 37777803 Free PMC article.

2

Genetic variants associated with the occurrence and progression of adolescent idiopathic scoliosis: a systematic review protocol.

Terhune EA, Heyn PC, Piper CR, Hadley-Miller N. Terhune EA, et al. Syst Rev. 2022 Jun 9;11(1):118. doi: 10.1186/s13643-022-01991-8. Syst Rev. 2022. PMID: 35681176 Free PMC article.

3

Association between genetic polymorphisms and risk of adolescent idiopathic scoliosis in case-control studies: a systematic review.

Terhune E, Heyn P, Piper C, Wethey C, Monley A, Cuevas M, Hadley Miller N. Terhune E, et al. J Med Genet. 2024 Jan 19;61(2):196-206. doi: 10.1136/jmg-2022-108993. J Med Genet. 2024. PMID: 37696603

4

Cytoskeletal Keratins Are Overexpressed in a Zebrafish Model of Idiopathic Scoliosis.

Cuevas M, Terhune E, Wethey C, James M, Netsanet R, Grofova D, Monley A, Hadley Miller N. Cuevas M, et al. Genes (Basel). 2023 May 9;14(5):1058. doi: 10.3390/genes14051058. Genes (Basel). 2023. PMID: 37239418 Free PMC article.

5

Genetic animal modeling for idiopathic scoliosis research: history and considerations.

Terhune EA, Monley AM, Cuevas MT, Wethey CI, Gray RS, Hadley-Miller N. Terhune EA, et al. Spine Deform. 2022 Sep;10(5):1003-1016. doi: 10.1007/s43390-022-00488-7. Epub 2022 Apr 16. Spine Deform. 2022. PMID: 35430722 Review.

6

Severity of Idiopathic Scoliosis Is Associated with Differential Methylation: An Epigenome-Wide Association Study of Monozygotic Twins with Idiopathic Scoliosis.

Carry PM, Terhune EA, Trahan GD, Vanderlinden LA, Wethey CI, Ebrahimi P, McGuigan F, Åkesson K, Hadley-Miller N. Carry PM, et al. Among authors: terhune ea. Genes (Basel). 2021 Jul 30;12(8):1191. doi: 10.3390/genes12081191. Genes (Basel). 2021. PMID: 34440365 Free PMC article.

7

Whole Exome Sequencing of 23 Multigeneration Idiopathic Scoliosis Families Reveals Enrichments in Cytoskeletal Variants, Suggests Highly Polygenic Disease.

Terhune EA, Wethey CI, Cuevas MT, Monley AM, Baschal EE, Bland MR, Baschal R, Trahan GD, Taylor MRG, Jones KL, Hadley Miller N. Terhune EA, et al. Genes (Basel). 2021 Jun 16;12(6):922. doi: 10.3390/genes12060922. Genes (Basel). 2021. PMID: 34208743 Free PMC article.

8

Mutations in KIF7 implicated in idiopathic scoliosis in humans and axial curvatures in zebrafish.

Terhune EA, Cuevas MT, Monley AM, Wethey CI, Chen X, Cattell MV, Bayrak MN, Bland MR, Sutphin B, Trahan GD, Taylor MRG, Niswander LA, Jones KL, Baschal EE, Antunes L, Dobbs M, Gurnett C, Appel B, Gray R, Hadley Miller N. Terhune EA, et al. Hum Mutat. 2021 Apr;42(4):392-407. doi: 10.1002/humu.24162. Epub 2021 Feb 7. Hum Mutat. 2021. PMID: 33382518 Free PMC article.

9

Idiopathic Scoliosis Families Highlight Actin-Based and Microtubule-Based Cellular Projections and Extracellular Matrix in Disease Etiology.

Baschal EE, Terhune EA, Wethey CI, Baschal RM, Robinson KD, Cuevas MT, Pradhan S, Sutphin BS, Taylor MRG, Gowan K, Pearson CG, Niswander LA, Jones KL, Miller NH. Baschal EE, et al. Among authors: terhune ea. G3 (Bethesda). 2018 Jul 31;8(8):2663-2672. doi: 10.1534/g3.118.200290. G3 (Bethesda). 2018. PMID: 29930198 Free PMC article.

10

Rare Coding Variants in Patients with Non-Syndromic Vestibular Dysfunction.

Sumalde AAM, Scholes MA, Kalmanson OA, Terhune EA, Frejo L, Wethey CI, Roman-Naranjo P, Carry PM, Gubbels SP, Lopez-Escamez JA, Hadley-Miller N, Santos-Cortez RLP. Sumalde AAM, et al. Among authors: terhune ea. Genes (Basel). 2023 Mar 30;14(4):831. doi: 10.3390/genes14040831. Genes (Basel). 2023. PMID: 37107589 Free PMC article.

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