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Anxhela Gjyshi Gustafson

Observed names: Anxhela G. Gustafson, Anxhela Gustafson
ORCID: 0009-0002-3165-9564
Observed ORCID: 0009-0002-3165-9564
OpenAlex ID: A5072720406
The Clinical and Genotypic Spectrum of Scoliosis in Multiple Pterygium Syndrome: A Case Series on 12 Children
2021 · Noémi Dahan-Oliel, Klaus Dieterich, et al. · Genes · 13
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A Genomic Approach to Delineating the Occurrence of Scoliosis in Arthrogryposis Multiplex Congenita
2021 · Xenia Latypova, Stefan Giovanni Creadore, et al. · Genes · 12
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De novoTRPM3missense variant associated with neurodevelopmental delay and manifestations of cerebral palsy
2023 · Jagadish Chandrabose Sundaramurthi, Anita M. Bagley, et al. · Molecular Case Studies · 11
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Whole genome sequencing in adolescent idiopathic scoliosis cohort implicates multiple biological pathways
2025 · Islam Oguz Tuncay, Eun Kyoung Lee, et al. · npj Genomic Medicine · 10
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Improved genomic characterization of a clinically heterogeneous pediatric cohort with WGS vs. WES
2025 · Awtum M. Brashear, Anxhela G. Gustafson, et al. · Scientific Reports · 3
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MYC Distant Enhancers Underlie Ovarian Cancer Susceptibility at the 8q24.21 Locus
2018 · Anxhela Gjyshi Gustafson · Digital Commons - University of South Florida (University of South Florida) · 1
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Runs of Homozygosity Analysis Reveals 1,900-Year-Old ECEL1 Arthrogryposis Mexican Founder Variant
2026 · Paul McKay, Daniel Ramírez-García, et al. · Research Square
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A phenotypic paradigm for cerebral palsy genetics
2026 · Adam S. Arterbery, Michael A. Gargano, et al. · The American Journal of Human Genetics
Arthrogryposis With CNS Involvement in AFF3 ‐Related KINSSHIP Syndrome: A Detailed Phenotypic Characterization From a Mexican Patient and Review of the Literature
2026 · Thania Ordaz‐Robles, Daniel Ramírez‐García, et al. · American Journal of Medical Genetics Part A
Works count: 9
Citation count: 50
H-index: 4
I10-index: 4
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