Haller G, McCall K, et al. A missense variant in SLC39A8 is associated with severe idiopathic scoliosis. Nature Communications (2018). (PDF)
Haller, G., H. Zabriskie, S. Spehar, T. Kuensting, X. Bledsoe, A. Syed, C. A. Gurnett and M. B. Dobbs (2017). Lack of joint hypermobility increases the risk of surgery in adolescent idiopathic scoliosis. J Pediatr Orthop B. 27, 152-158 (2017). (PDF)
largecoverHaller, G., Alvarado, D., McCall, K., Mitra, R., Dobbs, M., Gurnett, C. (2016) Massively parallel single nucleotide mutagenesis using reversibly-terminated inosine. Nature Methods doi:10.1038/nmeth.4015. (PDF)

 

front-matter_Page_1Haller, G., Alvarado, D., McCall, K., Yang, P., Cruchaga, C., Harms, M., Goate, A., Willing, M., Morcuende, J.A., Baschal, E. et al. (2016) A polygenic burden of rare variants across extracellular matrix genes among individuals with adolescent idiopathic scoliosis. Human molecular genetics, 25, 202-209. (PDF)
 journal.pone.0134393_Page_01Sadler, B., Haller, G., Edenberg, H., Tischfield, J., Brooks, A., Kramer, J., Schuckit, M., Nurnberger, J. and Goate, A. (2015) Positive Selection on Loci Associated with Drug and Alcohol Dependence. PloS one, 10, e0134393. (PDF)

 

1411.full (1)_Page_1Haller, G., Alvarado, D.M., Willing, M.C., Braverman, A.C., Bridwell, K.H., Kelly, M., Lenke, L.G., Luhmann, S.J., Gurnett, C.A. and Dobbs, M.B. (2015) Genetic Risk for Aortic Aneurysm in Adolescent Idiopathic Scoliosis. The Journal of bone and joint surgery. American volume, 97, 1411-1417. (PDF)
Baschal, E.Screen Shot 2015-07-26 at 11.20.05 AM E.; Wethey, C. I.; Swindle, K.; Baschal, R. M.; Gowan, K.; Tang, N. L.; Alvarado, D. M.; Haller, G.; Dobbs, M. B.; Taylor, M. R.; Gurnett, C. A.; Jones, K. L.; Miller, N. H., Exome sequencing identifies a rare HSPG2 variant associated with familial idiopathic scoliosis. G3 2015, 5 (2), 167-74 (PDF)
Screen Shot 2015-07-26 at 11.25.28 AMBuchan, J. G.; Alvarado, D. M.; Haller, G.; Aferol, H.; Miller, N. H.; Dobbs, M. B.; Gurnett, C. A., Are copy number variants associated with adolescent idiopathic scoliosis? Clin Orthop Relat Res 2014, 472 (10), 3216-25 (PDF)
Screen Shot 2015-07-26 at 10.54.34 AMBuchan, J. G.; Alvarado, D. M.; Haller, G.; Cruchaga, C.; Harms, M. B.; Zhang, T.; Willing, M. C.; Grange, D. K.; Braverman, A. C.; Miller, N. H.; Morcuende, J. A.; Tang, N. L.; Lam, T. P.; Ng, B. K.; Cheng, J. C.; Dobbs, M. B.; Gurnett, C. A., Rare variants in FBN1 and FBN2 are associated with severe adolescent idiopathic scoliosis. Human molecular genetics 2014, 23 (19), 5271-82 (PDF)
Screen Shot 2015-07-26 at 11.26.01 AMHaller, G.; Li, P.; Esch, C.; Hsu, S.; Goate, A. M.; Steinbach, J. H., Functional characterization improves associations between rare non-synonymous variants in CHRNB4 and smoking behavior. PloS one 2014, 9 (5), e96753 (PDF)
Screen Shot 2015-07-26 at 11.26.54 AMSadler, B.; Haller, G.; Agrawal, A.; Culverhouse, R.; Bucholz, K.; Brooks, A.; Tischfield, J.; Johnson, E. O.; Edenberg, H.; Schuckit, M.; Saccone, N.; Bierut, L.; Goate, A., Variants near CHRNB3CHRNA6 are associated with DSM-5 cocaine use disorder: evidence for pleiotropy. Sci Rep 2014, 4, 4497 (PDF)
F1.mediumZhang, T. X.; Haller, G.; Lin, P.; Alvarado, D. M.; Hecht, J. T.; Blanton, S. H.; Stephens Richards, B.; Rice, J. P.; Dobbs, M. B.; Gurnett, C. A., Genome-wide association study identifies new disease loci for isolated clubfoot. J Med Genet 2014, 51 (5), 334-9. (PDF)
Screen Shot 2015-07-26 at 10.55.06 AMHaller, G.; Kapoor, M.; Budde, J.; Xuei, X.; Edenberg, H.; Nurnberger, J.; Kramer, J.; Brooks, A.; Tischfield, J.; Almasy, L.; Agrawal, A.; Bucholz, K.; Rice, J.; Saccone, N.; Bierut, L.; Goate, A., Rare missense variants in CHRNB3 and CHRNA3 are associated with risk of alcohol and cocaine dependence. Human molecular genetics 2014, 23 (3), 810-9 (PDF)
Haller, GScreen Shot 2015-07-26 at 10.55.18 AM.; Druley, T.; Vallania, F. L.; Mitra, R. D.; Li, P.; Akk, G.; Steinbach, J. H.; Breslau, N.; Johnson, E.; Hatsukami, D.; Stitzel, J.; Bierut, L. J.; Goate, A. M., Rare missense variants in CHRNB4 are associated with reduced risk of nicotine dependence. Human molecular genetics 2012, 21 (3), 647-55 (PDF)
Screen Shot 2015-07-26 at 11.33.12 AMCruchaga, C.; Haller, G.; Chakraverty, S.; Mayo, K.; Vallania, F. L.; Mitra, R. D.; Faber, K.; Williamson, J.; Bird, T.; Diaz-Arrastia, R.; Foroud, T. M.; Boeve, B. F.; Graff-Radford, N. R.; St Jean, P.; Lawson, M.; Ehm, M. G.; Mayeux, R.; Goate, A. M.; Consortium, N.-L. N. F. S., Rare variants in APP, PSEN1 and PSEN2 increase risk for AD in late-onset Alzheimer’s disease families. PloS one 2012, 7 (2), e31039 (PDF)
1-s2.0-S0198885915X00061-cov150hThompson, E. E.; Haller, G.; Pinto, J. M.; Sun, Y.; Zelano, B.; Jacob, S.; McClintock, M. K.; Nicolae, D. L.; Ober, C., Sequence variations at the human leukocyte antigen-linked olfactory receptor cluster do not influence female preferences for male odors. Human immunology 2010, 71 (1), 100-3 (PDF)
 Screen Shot 2015-07-26 at 11.34.25 AMHaller, G.; Torgerson, D. G.; Ober, C.; Thompson, E. E., Sequencing the IL4 locus in African Americans implicates rare noncoding variants in asthma susceptibility. The Journal of allergy and clinical immunology 2009, 124 (6), 1204-9 e9 (PDF)
00412Gause, M.; Webber, H. A.; Misulovin, Z.; Haller, G.; Rollins, R. A.; Eissenberg, J. C.; Bickel, S. E.; Dorsett, D., Functional links between Drosophila Nipped-B and cohesin in somatic and meiotic cells. Chromosoma 2008, 117 (1), 51-66 (PDF)
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