| Rare Variants in APP, PSEN1 and PSEN2 Increase Risk for AD in Late-Onset Alzheimer's Disease Families C Cruchaga, S Chakraverty, K Mayo, FLM Vallania, RD Mitra, K Faber, ... PloS one 7 (2), e31039, 2012 | 393 | 2012 |
| Rare variants in FBN1 and FBN2 are associated with severe adolescent idiopathic scoliosis JG Buchan, DM Alvarado, GE Haller, C Cruchaga, MB Harms, T Zhang, ... Human molecular genetics 23 (19), 5271-5282, 2014 | 132 | 2014 |
| Functional links between Drosophila Nipped-B and cohesin in somatic and meiotic cells M Gause, HA Webber, Z Misulovin, G Haller, RA Rollins, JC Eissenberg, ... Chromosoma 117, 51-66, 2008 | 80 | 2008 |
| A polygenic burden of rare variants across extracellular matrix genes among individuals with adolescent idiopathic scoliosis G Haller, D Alvarado, K Mccall, P Yang, C Cruchaga, M Harms, A Goate, ... Human molecular genetics 25 (1), 202-209, 2016 | 79 | 2016 |
| Rare missense variants in CHRNB4 are associated with reduced risk of nicotine dependence G Haller, T Druley, FL Vallania, RD Mitra, P Li, G Akk, JH Steinbach, ... Human molecular genetics 21 (3), 647-655, 2012 | 77 | 2012 |
| A missense variant in SLC39A8 is associated with severe idiopathic scoliosis G Haller, K McCall, S Jenkitkasemwong, B Sadler, L Antunes, M Nikolov, ... Nature communications 9 (1), 4171, 2018 | 73 | 2018 |
| Exome Sequencing Identifies a Rare HSPG2 Variant Associated with Familial Idiopathic Scoliosis EE Baschal, CI Wethey, K Swindle, RM Baschal, K Gowan, NLS Tang, ... G3: Genes, Genomes, Genetics 5 (2), 167-174, 2015 | 64 | 2015 |
| Sequencing the IL4 locus in African Americans implicates rare noncoding variants in asthma susceptibility G Haller, DG Torgerson, C Ober, EE Thompson Journal of allergy and clinical immunology 124 (6), 1204-1209. e9, 2009 | 61 | 2009 |
| Rare missense variants in CHRNB3 and CHRNA3 are associated with risk of alcohol and cocaine dependence G Haller, M Kapoor, J Budde, X Xuei, H Edenberg, J Nurnberger, ... Human molecular genetics 23 (3), 810-819, 2014 | 55 | 2014 |
| Prevalence and impact of underlying diagnosis and comorbidities on Chiari 1 malformation B Sadler, T Kuensting, J Strahle, TS Park, M Smyth, DD Limbrick, ... Pediatric neurology 106, 32-37, 2020 | 49 | 2020 |
| Rare and de novo coding variants in chromodomain genes in Chiari I malformation B Sadler, J Wilborn, L Antunes, T Kuensting, AT Hale, SR Gannon, ... The American Journal of Human Genetics 108 (1), 100-114, 2021 | 36 | 2021 |
| Genome-wide association study identifies new disease loci for isolated clubfoot TX Zhang, G Haller, P Lin, DM Alvarado, JT Hecht, SH Blanton, ... Journal of medical genetics 51 (5), 334-339, 2014 | 29 | 2014 |
| Lack of joint hypermobility increases the risk of surgery in adolescent idiopathic scoliosis G Haller, H Zabriskie, S Spehar, T Kuensting, X Bledsoe, A Syed, ... Journal of Pediatric Orthopaedics B 27 (2), 152-158, 2018 | 28 | 2018 |
| Are copy number variants associated with adolescent idiopathic scoliosis? JG Buchan, DM Alvarado, G Haller, H Aferol, NH Miller, MB Dobbs, ... Clinical Orthopaedics and Related Research® 472 (10), 3216-3225, 2014 | 24 | 2014 |
| Occipital-cervical fusion and ventral decompression in the surgical management of Chiari-1 malformation and syringomyelia: analysis of data from the Park-Reeves Syringomyelia … TS CreveCoeur, AT Yahanda, CO Maher, GW Johnson, LL Ackerman, ... Neurosurgery 88 (2), 332-341, 2021 | 23 | 2021 |
| ATRAID regulates the action of nitrogen-containing bisphosphonates on bone LE Surface, DT Burrow, J Li, J Park, S Kumar, C Lyu, N Song, Z Yu, ... Science translational medicine 12 (544), eaav9166, 2020 | 20 | 2020 |
| Massively parallel single-nucleotide mutagenesis using reversibly terminated inosine G Haller, D Alvarado, K McCall, RD Mitra, MB Dobbs, CA Gurnett Nature methods 13 (11), 923-924, 2016 | 19 | 2016 |
| Functional characterization improves associations between rare non-synonymous variants in CHRNB4 and smoking behavior G Haller, P Li, C Esch, S Hsu, AM Goate, JH Steinbach PLoS One 9 (5), e96753, 2014 | 19 | 2014 |
| Distal chromosome 16p11. 2 duplications containing SH2B1 in patients with scoliosis B Sadler, G Haller, L Antunes, X Bledsoe, J Morcuende, P Giampietro, ... Journal of medical genetics 56 (7), 427-433, 2019 | 16 | 2019 |
| Obex position is associated with syringomyelia and use of posterior fossa decompression among patients with Chiari I malformation G Haller, B Sadler, T Kuensting, N Lakshman, JK Greenberg, JM Strahle, ... Journal of Neurosurgery: Pediatrics 26 (1), 45-52, 2020 | 15 | 2020 |
