Department of  Neurosurgery
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Publications

  1. Gause, M. et al. Functional links between Drosophila Nipped-B and cohesin in somatic and meiotic cells. Chromosoma 117, 51-66, doi:10.1007/s00412-007-0125-5 (2008).
  2. Haller, G., Torgerson, D. G., Ober, C. & Thompson, E. E. Sequencing the IL4 locus in African Americans implicates rare noncoding variants in asthma susceptibility. J Allergy Clin Immunol 124, 1204-1209 e1209, doi:10.1016/j.jaci.2009.09.013 (2009).
  3. Thompson, E. E. et al. Sequence variations at the human leukocyte antigen-linked olfactory receptor cluster do not influence female preferences for male odors. Hum Immunol 71, 100-103, doi:10.1016/j.humimm.2009.10.004 (2010).
  4. Cruchaga, C. et al. Rare variants in APP, PSEN1 and PSEN2 increase risk for AD in late-onset Alzheimer's disease families. PLoS One 7, e31039, doi:10.1371/journal.pone.0031039 (2012).
  5. Haller, G. et al. Rare missense variants in CHRNB4 are associated with reduced risk of nicotine dependence. Hum Mol Genet 21, 647-655, doi:10.1093/hmg/ddr498 (2012).
  6. Baschal, E. E. et al. Exome sequencing identifies a rare HSPG2 variant associated with familial idiopathic scoliosis. G3 (Bethesda) 5, 167-174, doi:10.1534/g3.114.015669 (2014).
  7. Buchan, J. G. et al. Are copy number variants associated with adolescent idiopathic scoliosis? Clin Orthop Relat Res 472, 3216-3225, doi:10.1007/s11999-014-3766-8 (2014).
  8. Buchan, J. G. et al. Rare variants in FBN1 and FBN2 are associated with severe adolescent idiopathic scoliosis. Hum Mol Genet 23, 5271-5282, doi:10.1093/hmg/ddu224 (2014).
  9. Haller, G. et al. Rare missense variants in CHRNB3 and CHRNA3 are associated with risk of alcohol and cocaine dependence. Hum Mol Genet 23, 810-819, doi:10.1093/hmg/ddt463 (2014).
  10. Haller, G. et al. Functional characterization improves associations between rare non-synonymous variants in CHRNB4 and smoking behavior. PLoS One 9, e96753, doi:10.1371/journal.pone.0096753 (2014).
  11. Sadler, B. et al. Variants near CHRNB3-CHRNA6 are associated with DSM-5 cocaine use disorder: evidence for pleiotropy. Sci Rep 4, 4497, doi:10.1038/srep04497 (2014).
  12. Zhang, T. X. et al. Genome-wide association study identifies new disease loci for isolated clubfoot. J Med Genet 51, 334-339, doi:10.1136/jmedgenet-2014-102303 (2014).
  13. Haller, G. et al. Genetic Risk for Aortic Aneurysm in Adolescent Idiopathic Scoliosis. J Bone Joint Surg Am 97, 1411-1417, doi:10.2106/JBJS.O.00290 (2015).
  14. Sadler, B. et al. Positive Selection on Loci Associated with Drug and Alcohol Dependence. PLoS One 10, e0134393, doi:10.1371/journal.pone.0134393 (2015).
  15. Haller, G. et al. Massively parallel single-nucleotide mutagenesis using reversibly terminated inosine. Nat Methods 13, 923-924, doi:10.1038/nmeth.4015 (2016).
  16. Haller, G. et al. A polygenic burden of rare variants across extracellular matrix genes among individuals with adolescent idiopathic scoliosis. Hum Mol Genet 25, 202-209, doi:10.1093/hmg/ddv463 (2016).
  17. Haller, G. et al. A missense variant in SLC39A8 is associated with severe idiopathic scoliosis. Nat Commun 9, 4171, doi:10.1038/s41467-018-06705-0 (2018).
  18. Haller, G. et al. Lack of joint hypermobility increases the risk of surgery in adolescent idiopathic scoliosis. J Pediatr Orthop B 27, 152-158, doi:10.1097/BPB.0000000000000489 (2018).
  19. Sadler, B. et al. Distal chromosome 16p11.2 duplications containing SH2B1 in patients with scoliosis. J Med Genet 56, 427-433, doi:10.1136/jmedgenet-2018-105877 (2019).
  20. Sadler, B. et al. Prevalence and Impact of Underlying Diagnosis and Comorbidities on Chiari 1 Malformation. Pediatr Neurol, doi:10.1016/j.pediatrneurol.2019.12.005 (2020).
  21. Haller, G. et al. Obex position is associated with syringomyelia and use of posterior fossa decompression among patients with Chiari I malformation. J Neurosurg Pediat doi: 10.3171/2020.2.PEDS19486