Gabe Haller

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Exome Sequencing Identifies a Rare HSPG2 Variant Associated with Familial Idiopathic Scoliosis

Kenneth L. Jones, Matthew R. G. Taylor, M. Dobbs, 2014, G3: Genes, Genomes, Genetics.

Variants near CHRNB3-CHRNA6 are associated with DSM-5 cocaine use disorder: evidence for pleiotropy

L. Bierut, K. Bucholz, M. Schuckit, 2014, Scientific Reports.

Distal chromosome 16p11.2 duplications containing SH2B1 in patients with scoliosis

Nephi A. Walton, Yared H. Kidane, T. Druley, 2019, Journal of Medical Genetics.

Sequence variations at the HLA-linked olfactory receptor cluster do not influence female preferences for male odors

Ying Sun, D. Nicolae, M. McClintock, 2013 .

Occipital-Cervical Fusion and Ventral Decompression in the Surgical Management of Chiari-1 Malformation and Syringomyelia: Analysis of Data From the Park-Reeves Syringomyelia Research Consortium.

W. J. Oakes, Daniel J. Guillaume, Jodi L. Smith, 2020, Neurosurgery.

Current and Future Approaches to Classify VUSs in LGMD-Related Genes

C. Weihl, Gabe Haller, Chengcheng Li, 2022, Genes.

Sequencing the IL4 locus in African Americans implicates rare noncoding variants in asthma susceptibility.

Dara G Torgerson, Carole Ober, C. Ober, 2009, The Journal of allergy and clinical immunology.

Rare and de novo coding variants in chromodomain genes in Chiari I malformation.

D. Conrad, A. Reymond, A. Hale, 2020, American journal of human genetics.

A polygenic burden of rare variants across extracellular matrix genes among individuals with adolescent idiopathic scoliosis.

A. Goate, Carlos Cruchaga, Ping Yang, 2016, Human molecular genetics.

Rare missense variants in CHRNB3 and CHRNA3 are associated with risk of alcohol and cocaine dependence.

L. Bierut, J. Rice, J. Nurnberger, 2014, Human molecular genetics.

Identification and Characterization of Rare Variants in Cholinergic Nicotinic Receptor Genes and their Contribution to Substance Dependence

Gabe Haller, 2013 .

Rare missense variants in CHRNB4 are associated with reduced risk of nicotine dependence.

L. Bierut, Francesco Vallania, T. Druley, 2012, Human molecular genetics.

Are Copy Number Variants Associated With Adolescent Idiopathic Scoliosis?

J. Buchan, M. Dobbs, N. Miller, 2014, Clinical orthopaedics and related research.

Rare variants in FBN1 and FBN2 are associated with severe adolescent idiopathic scoliosis.

Carlos Cruchaga, J. Buchan, J. Morcuende, 2014, Human molecular genetics.

Rare variants in FBN 1 and FBN 2 are associated with severe adolescent idiopathic scoliosis

Carlos Cruchaga, J. Buchan, J. Morcuende, 2014 .

A missense variant in SLC39A8 is associated with severe idiopathic scoliosis

C. Cruchaga, Carlos Cruchaga, P. Giampietro, 2018, Nature Communications.

ATRAID regulates the action of nitrogen-containing bisphosphonates on bone

Jonathan C. Baker, M. Gardner, D. Sabatini, 2020, Science Translational Medicine.

Positive Selection on Loci Associated with Drug and Alcohol Dependence

J. Nurnberger, M. Schuckit, A. Goate, 2015, PloS one.

Functional Characterization Improves Associations between Rare Non-Synonymous Variants in CHRNB4 and Smoking Behavior

A. Goate, J. Steinbach, S. Hsu, 2014, PloS one.

Genome-wide association study identifies new disease loci for isolated clubfoot

J. Rice, S. Blanton, J. Hecht, 2014, Journal of Medical Genetics.

Global cerebrospinal fluid circulation mapping using gold nanoparticle enhanced X-ray microtomography reveals region-specific brain and spinal cord CSF pathways

S. Achilefu, J. Quirk, J. Fitzpatrick, 2021, bioRxiv.

Obex position is associated with syringomyelia and use of posterior fossa decompression among patients with Chiari I malformation.

Jacob K. Greenberg, D. Limbrick, M. Dobbs, 2020, Journal of neurosurgery. Pediatrics.

Genetic Risk for Aortic Aneurysm in Adolescent Idiopathic Scoliosis.

L. Lenke, K. Bridwell, S. Luhmann, 2015, The Journal of bone and joint surgery. American volume.

Sequence variations at the human leukocyte antigen-linked olfactory receptor cluster do not influence female preferences for male odors.

Ying Sun, D. Nicolae, C. Ober, 2010, Human immunology.

Functional links between Drosophila Nipped-B and cohesin in somatic and meiotic cells

D. Dorsett, S. Bickel, J. C. Eissenberg, 2008, Chromosoma.

Elucidating the Genetic Basis of Chiari I Malformation.

B. Sadler, Gabe Haller, 2023, Neurosurgery clinics of North America.

Rare and de novo duplications containing SHOX in clubfoot

B. Coe, M. Dobbs, B. Sadler, 2020, Journal of Medical Genetics.

Extradural decompression versus duraplasty in Chiari malformation type I with syrinx: outcomes on scoliosis from the Park-Reeves Syringomyelia Research Consortium.

Daniel J. Guillaume, Jodi L. Smith, M. Smyth, 2021, Journal of neurosurgery. Pediatrics.

Whole-exome analysis of adolescents with low VWF and heavy menstrual bleeding identifies novel genetic associations

S. O’Brien, J. Di Paola, C. Minard, 2021, Blood advances.

von Willebrand factor antigen levels are associated with burden of rare nonsynonymous variants in the VWF gene

R. Montgomery, P. Christopherson, J. Di Paola, 2021, Blood.

Quantitative determination of SLC2A1 variant functional effects in GLUT1 deficiency syndrome

P. Hruz, K. Engelstad, D. D. De Vivo, 2023, Annals of clinical and translational neurology.

ATRAID, a genetic factor that regulates the clinical action of nitrogen-containing bisphosphonates on bone

Jonathan C. Baker, M. Gardner, D. Sabatini, 2018, bioRxiv.

A missense variant in SLC39A8 is associated with severe idiopathic scoliosis

Carlos Cruchaga, P. Giampietro, J. Morcuende, 2018, Nature Communications.

Prevalence and Impact of Underlying Diagnosis and Comorbidities on Chiari 1 Malformation.

M. Smyth, D. Limbrick, M. Dobbs, 2020, Pediatric neurology.

Comprehensive functional characterization of SGCB coding variants predicts pathogenicity in limb-girdle muscular dystrophy type R4/2E

C. Weihl, J. Díaz-Manera, Jackson Wilborn, 2023, The Journal of clinical investigation.

Lack of joint hypermobility increases the risk of surgery in adolescent idiopathic scoliosis

M. Dobbs, C. Gurnett, Gabe Haller, 2017, Journal of pediatric orthopedics. Part B.

Massively parallel single-nucleotide mutagenesis using reversibly terminated inosine

R. Mitra, M. Dobbs, C. Gurnett, 2016, Nature Methods.

Rare and de novo coding variants in chromodomain genes in Chiari I malformation.

D. Conrad, A. Reymond, A. Hale, 2021, American journal of human genetics.