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International Journal of Radiation Oncology, Biology, Physics|January 1, 1995
The Electronic View Box: a software tool for radiation therapy treatment verificationW R Bosch, D A Low, R L Gerber, et al.
Annals of Neurology|February 16, 2012
Exome sequencing reveals DNAJB6 mutations in dominantly-inherited myopathyMatthew B Harms, R Brian Sommerville, Peggy Allred, et al.
BMC Genomics|January 26, 2024
LUSTR: a new customizable tool for calling genome-wide germline and somatic short tandem repeat variantsJinfeng Lu, Camilo Toro, David R Adams, et al.
Neuromuscular Disorders : NMD|January 25, 2015
Targeted sequencing and identification of genetic variants in sporadic inclusion body myositisConrad C Weihl, Robert H Baloh, Youjin Lee, et al.
Neurology|July 26, 2015
SQSTM1 splice site mutation in distal myopathy with rimmed vacuolesRobert C Bucelli, Khalid Arhzaouy, Alan Pestronk, et al.
Cell Death & Disease|August 6, 2021
Precision genetic cellular models identify therapies protective against ER stressIrina V Lebedeva, Michelle V Wagner, Sunil Sahdeo, et al.
International Journal of Radiation Oncology, Biology, Physics|May 15, 1991
Interinstitutional experience in verification of external photon dose calculationsM E Masterson, G Barest, C S Chui, et al.
Seminars in Radiation Oncology|March 28, 2002
Trade-off to low-grade toxicity with conformal radiation therapy for prostate cancer on Radiation Therapy Oncology Group 9406Jeff M Michalski, Kathryn Winter, James A Purdy, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 14, 2021
High-impact rare genetic variants in severe schizophreniaAnthony W Zoghbi, Ryan S Dhindsa, Terry E Goldberg, et al.
Neurobiology of Aging|April 20, 2013
Lack of C9ORF72 coding mutations supports a gain of function for repeat expansions in amyotrophic lateral sclerosisMatthew B Harms, Janet Cady, Craig Zaidman, et al.
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