Goli Compoginis

WRN mutations in Werner syndrome patients: genomic rearrangements, unusual intronic mutations and ethnic-specific alterations

Katrin Friedrich, Lin Lee, Dru F. Leistritz et al. · Human Genetics · 2010 · 101 citations · Full text

Unusual Intronic Mutations, Somatic Variant, Mendelian Disorder +10

Remission of alopecia universalis in a patient with atopic dermatitis treated with dupilumab

Jan Smogorzewski, Tiffany J. Sierro, Goli Compoginis et al. · JAAD Case Reports · 2019 · 37 citations · Full text

Neutrophilic panniculitis developing after treatment of metastatic melanoma with vemurafenib

Gene Kim, Alan L. Levy, Goli Compoginis · Journal of Cutaneous Pathology · 2013 · 34 citations

Inflammation, Neutrophilic Panniculitis, V600e Braf Mutation +12

SMAD4 mutations and cross-talk between TGF-β/IFNγ signaling accelerate rates of DNA damage and cellular senescence, resulting in a segmental progeroid syndrome—the Myhre syndrome

Renuka Kandhaya‐Pillai, Deyin Hou, Jiaming Zhang et al. · GeroScience · 2021 · 16 citations · Full text

Dna Damage, Autoimmune Disease, Disease Mechanism +10