Matthew B. Dobbs

MedicineEngineeringBiochemistry, 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 9 papers. Top paper: “Comprehensive In Vivo Interrogation Reveals Phenotypic Impact of Human Enhancer Variants”.

Comprehensive In Vivo Interrogation Reveals Phenotypic Impact of Human Enhancer Variants

Cell(2020)10.1016/j.cell.2020.02.031

N/A

0DataRank · unranked

194 citations

Yiwen Zhu, Guy Kelman, Catherine S. Novak, Ingrid Plajzer-Frick, Momoe Kato +22 more

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

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

Genetic association and characterization ofFSTL5in isolated clubfoot

Human Molecular Genetics(2020)10.1093/hmg/ddaa236

N/A

0DataRank · unranked

10 citations

Yared H. Kidane, Julia Kozlitina, Reuel Cornelia, Alexandra Rafipay, Vanessa D. de Mello +13 more

Whole Exome Sequencing in Individuals with Idiopathic Clubfoot Reveals a Recurrent Filamin B (FLNB) Deletion

Clinical Orthopaedics and Related Research(2021)10.1097/corr.0000000000001957

N/A

0DataRank · unranked

8 citations

Wu‐Lin Charng, Lilian Antunes, Momchil Nikolov, Xavier Bledsoe, Jacqueline T. Hecht +3 more

An in vivo approach to characterize novel variants associated with musculoskeletal disorders

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.05.27.445925

N/A

0DataRank · unranked

0 citations

Shuo Yang, Tiffany Ou, Gary Huang, Matthew B. Dobbs, Christina A. Gurnett +2 more

A pathogenic mechanism associated with myopathies and structural birth defects involves TPM2-directed myogenesis

JCI Insight(2022)10.1172/jci.insight.152466

N/A

0DataRank · unranked

14 citations

Shuo Yang, Tiffany Ou, Gary Huang, Matthew B. Dobbs, Christina A. Gurnett +3 more

Diagnostic yield of exome sequencing in congenital vertical talus

European Journal of Medical Genetics(2022)10.1016/j.ejmg.2022.104514

N/A

0DataRank · unranked

6 citations

Wu‐Lin Charng, Patricia Dickson, Matthew B. Dobbs, Christina A. Gurnett, Naeimeh Tayebi

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

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

N/A

0DataRank · unranked

1 citations

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