NCBI Bibliography

Select publications:

  1. Haller G, McCall K, Jenkitkasemwong S, Sadler B, Antunes L, Nikolov M, Whittle J, Upshaw Z, Shin J, Baschal E, Cruchaga C, Harms M, Raggio C, Morcuende JA, Giampietro P, Miller NH, Wise C, Gray RS, Solnica-Krezel L, Knutson M, Dobbs MB, Gurnett CA. A missense variant in SLC39A8 is associated with severe idiopathic scoliosis. Nat Commun. 2018 Oct 9;9(1):4171. doi: 10.1038/s41467-018-06705-0. PubMed PMID: 30301978; PubMed Central PMCID: PMC6177404.
  2. 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. Idiopathic Scoliosis Families Highlight Actin-Based and Microtubule-Based Cellular Projections and Extracellular Matrix in Disease Etiology. G3 (Bethesda). 2018 Jul 31;8(8):2663-2672. doi: 10.1534/g3.118.200290. PubMed PMID: 29930198; PubMed Central PMCID: PMC6071588.
  3. Justice CM, Bishop K, Carrington B, Mullikin JC, Swindle K, Marosy B, Sood R, Miller NH, Wilson AF. Evaluation of IRX Genes and Conserved Noncoding Elements in a Region on 5p13.3 Linked to Families with Familial Idiopathic Scoliosis and Kyphosis. G3 (Bethesda). 2016 Jun 1;6(6):1707-12. doi: 10.1534/g3.116.029975. PubMed PMID: 27172222; PubMed Central PMCID: PMC4889666.
  4. Haller G, Alvarado D, Mccall K, Yang P, Cruchaga C, Harms M, Goate A, Willing M, Morcuende JA, Baschal E, Miller NH, Wise C, Dobbs MB, Gurnett CA. A polygenic burden of rare variants across extracellular matrix genes among individuals with adolescent idiopathic scoliosis. Hum Mol Genet. 2016 Jan 1;25(1):202-9. doi: 10.1093/hmg/ddv463. Epub 2015 Nov 12. PubMed PMID: 26566670; PubMed Central PMCID: PMC4690498.
  5. Miller NH, Carry PM, Mark BJ, Engelman GH, Georgopoulos G, Graham S, Dobbs MB. Does Strict Adherence to the Ponseti Method Improve Isolated Clubfoot Treatment Outcomes? A Two-institution Review. Clin Orthop Relat Res. 2016 Jan;474(1):237-43. doi: 10.1007/s11999-015-4559-4. Epub 2015 Sep 22. PubMed PMID: 26394639; PubMed Central PMCID: PMC4686485.
  6. Baschal EE, Swindle K, Justice CM, Baschal RM, Perera A, Wethey CI, Poole A, Pourquié O, Tassy O, Miller NH. Sequencing of the TBX6 Gene in Families with Familial Idiopathic Scoliosis. Spine Deform. 2015 Jul;3(4):288-296. doi: 10.1016/j.jspd.2015.01.005. PubMed PMID: 26120555; PubMed Central PMCID: PMC4480874.
  7. Buchan JG, Alvarado DM, Haller G, Aferol H, Miller NH, Dobbs MB, Gurnett CA. Are copy number variants associated with adolescent idiopathic scoliosis?. Clin Orthop Relat Res. 2014 Oct;472(10):3216-25. doi: 10.1007/s11999-014-3766-8. Epub 2014 Jul 9. PubMed PMID: 25005481; PubMed Central PMCID: PMC4160470.
  8. Buchan JG, Alvarado DM, Haller GE, Cruchaga C, Harms MB, Zhang T, Willing MC, Grange DK, Braverman AC, Miller NH, Morcuende JA, Tang NL, Lam TP, Ng BK, Cheng JC, Dobbs MB, Gurnett CA. Rare variants in FBN1 and FBN2 are associated with severe adolescent idiopathic scoliosis. Hum Mol Genet. 2014 Oct 1;23(19):5271-82. doi: 10.1093/hmg/ddu224. Epub 2014 May 15. PubMed PMID: 24833718; PubMed Central PMCID: PMC4159151.
  9. Thompson ME, Kohring JM, McFann K, McNair B, Hansen JK, Miller NH. Predicting excessive hemorrhage in adolescent idiopathic scoliosis patients undergoing posterior spinal instrumentation and fusion. Spine J. 2014 Aug 1;14(8):1392-8. doi: 10.1016/j.spinee.2013.08.022. Epub 2013 Oct 18. PubMed PMID: 24139751.