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Frontiers in Cell and Developmental Biology|April 25, 2022
Modeling Patient-Specific Muscular Dystrophy Phenotypes and Therapeutic Responses in Reprogrammed Myotubes Engineered on Micromolded Gelatin HydrogelsFlorian Barthélémy, Jeffrey W Santoso, Laura Rabichow, et al.Plos One|March 3, 2011
Phenotype sequencing: identifying the genes that cause a phenotype directly from pooled sequencing of independent mutantsMarc A Harper, Zugen Chen, Traci Toy, et al.Journal of Medical Genetics|March 29, 2014
Expanding the phenotype of mutations in DICER1: mosaic missense mutations in the RNase IIIb domain of DICER1 cause GLOW syndromeSteven Klein, Hane Lee, Shahnaz Ghahremani, et al.Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|December 8, 2010
Gene expression profile correlates with T-cell infiltration and relative survival in glioblastoma patients vaccinated with dendritic cell immunotherapyRobert M Prins, Horacio Soto, Vera Konkankit, et al.Journal of Managed Care & Specialty Pharmacy|February 6, 2025
Real-world treatment and health care utilization among patients with Duchenne muscular dystrophy by race and ethnicity in a Medicaid populationNathaniel Posner, Janna Manjelievskaia, Anna K Talaga, et al.Oncogene|August 2, 2003
Gene expression profiling identifies molecular subtypes of gliomasRuty Shai, Tao Shi, Thomas J Kremen, et al.Bioinformatics (Oxford, England)|August 11, 2011
Exome sequencing-based copy-number variation and loss of heterozygosity detection: ExomeCNVJarupon Fah Sathirapongsasuti, Hane Lee, Basil A J Horst, et al.American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|June 17, 2010
Accuracy of phenotyping of autistic children based on Internet implemented parent reportHane Lee, Alison R Marvin, Tamara Watson, et al.Muscle & Nerve|August 22, 2020
A well-tolerated core needle muscle biopsy process suitable for children and adultsFlorian Barthelemy, Jeremy D Woods, Shirley Nieves-Rodriguez, et al.Plos One|February 6, 2013
Functional consequences of a novel variant of PCSK1Lindsay A Pickett, Michael Yourshaw, Valeria Albornoz, et al.Pageof 26