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Neurosurgery Clinics of North America|November 24, 2022
Elucidating the Genetic Basis of Chiari I MalformationGabe Haller, Brooke SadlerGenes|February 25, 2022
Current and Future Approaches to Classify VUSs in LGMD-Related GenesChengcheng Li, Gabe Haller, Conrad C WeihlThe Journal of Allergy and Clinical Immunology|November 14, 2009
Sequencing the IL4 locus in African Americans implicates rare noncoding variants in asthma susceptibilityGabe Haller, Dara G Torgerson, Carole Ober, et al.Blood|February 8, 2021
von Willebrand factor antigen levels are associated with burden of rare nonsynonymous variants in the VWF geneBrooke Sadler, Pamela A Christopherson, Gabe Haller, et al.Plos One|May 9, 2014
Functional characterization improves associations between rare non-synonymous variants in CHRNB4 and smoking behaviorGabe Haller, Ping Li, Caroline Esch, et al.Nature Methods|October 4, 2016
Massively parallel single-nucleotide mutagenesis using reversibly terminated inosineGabe Haller, David Alvarado, Kevin McCall, et al.Proceedings of the National Academy of Sciences of the United States of America|February 1, 2024
Streamlined identification of clinically and functionally relevant genetic regulators of lower-tract urogenital developmentMeade Haller, Yan Yin, Gabe Haller, et al.Journal of Medical Genetics|June 11, 2020
Rare and de novo duplications containing SHOX in clubfootBrooke Sadler, Gabe Haller, Lilian Antunes, et al.Plos One|August 14, 2015
Positive Selection on Loci Associated with Drug and Alcohol DependenceBrooke Sadler, Gabe Haller, Howard Edenberg, et al.Journal of Pediatric Orthopedics. Part B|August 5, 2017
Lack of joint hypermobility increases the risk of surgery in adolescent idiopathic scoliosisGabe Haller, Hannah Zabriskie, Shelby Spehar, et al.Pageof 4