Gabe Haller

Also affiliated with Missouri Institute of Mental Health, Neurological Surgery

MedicineBiochemistry, Genetics and Molecular Biology

Pilot corpus only

This score is computed over theSindex pilot corpus and does not cover the full scientific literature. Scores are relative to papers we have ingested — papers, authors, and institutions outside the pilot are not represented. Methodology.

Top 100%percentile

0Author DataRank

Indexed papers

0in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Papers

Driven by 10 papers. Top paper: “Rare missense variants in FNDC1 are associated with severe adolescent idiopathic scoliosis”.

Rare missense variants in FNDC1 are associated with severe adolescent idiopathic scoliosis

Journal of Medical Genetics(2025)10.1136/jmg-2024-110586

N/A

0.104DataRank · unranked

1 citations

Gabe Haller, Julia Whittle, Momchil Nikolov, Addison Avery, José A. Morcuende +12 more

Rare and de novo duplications containing SHOX in clubfoot

Journal of Medical Genetics(2020)10.1136/jmedgenet-2020-106842

N/A

0DataRank · unranked

16 citations

Gabe Haller, Lilian Antunes, Momchil Nikolov, Ina Amarillo, Bradley P. Coe +3 more

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

Neurosurgery(2020)10.1093/neuros/nyaa460

N/A

0DataRank · unranked

28 citations

Alexander T. Yahanda, Cormac O. Maher, Gabrielle W. Johnson, Laurie L. Ackerman, P. David Adelson +63 more

ATRAID regulates the action of nitrogen-containing bisphosphonates on bone

Science Translational Medicine(2020)10.1126/scitranslmed.aav9166

N/A

0DataRank · unranked

25 citations

Damon T. Burrow, Jinmei Li, Jiwoong Park, Sandeep Kumar, Cheng Lyu +33 more

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

Blood(2021)10.1182/blood.2020009999

N/A

0DataRank · unranked

22 citations

Pamela A. Christopherson, Gabe Haller, Robert R. Montgomery, Jorge Di Paola, Brooke Sadler

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

Pediatric Neurology(2020)10.1016/j.pediatrneurol.2019.12.005

N/A

0DataRank · unranked

70 citations

Timothy Kuensting, Jennifer M. Strahle, Tae Sung Park, Matthew D. Smyth, David D. Limbrick +4 more

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

Journal of Clinical Investigation(2023)10.1172/jci168156

N/A

0DataRank · unranked

19 citations

Jackson Wilborn, Sara K. Pittman, Jil Daw, Jorge Alonso‐Pérez, Jordi Díaz‐Manera +3 more

Quantitative determination of SLC2A1 variant functional effects in GLUT1 deficiency syndrome

Annals of Clinical and Translational Neurology(2023)10.1002/acn3.51767

N/A

0DataRank · unranked

8 citations

Brian X. León-Ricardo, Kevin McCall, Elvisa Mehinovic, Kristin Engelstad, Vincent Huynh +10 more

Characterization of copy-number variants in a large cohort of patients with von Willebrand disease reveals a relationship between disrupted regions and disease type

Research and Practice in Thrombosis and Haemostasis(2023)10.1016/j.rpth.2023.102232

N/A

0DataRank · unranked

2 citations

Pamela A. Christopherson, Crystal L. Perry, Daniel B. Bellissimo, Sandra L. Haberichter, Gabe Haller +5 more

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

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.12.18.473250

N/A

0DataRank · unranked

0 citations

Dakota DeFreitas, Sruthi Ramagiri, Peter O. Bayguinov, Carl D. Hacker, Abraham Z. Snyder +13 more