Co-Regulation of p16(INK4a) and Migratory Genes in Culture Conditions that Lead to Premature Senescence in Human Keratinocytes

le Darbro, Benjamin W., Schneider, Galen B., Klingelhutz, Aloysius J.
Foilsithe 2005

Lactobacillus delbrueckii as the Cause of Urinary Tract Infection

le Darbro, Benjamin W., Petroelje, Brian K., Doern, Gary V.
Foilsithe 2009

Development of Secondary Acute Myeloid Leukemia in a Pediatric Patient Concurrently Receiving Primary Therapy for Ewing Sarcoma

le McNew, Brandon R., Darbro, Benjamin W., Ma, Deqin, Gordon, David J.
Foilsithe in J Pediatr Hematol Oncol (2017)

Interstitial duplication of 8q22.1‐q23.1‐ A case report and review of the literature

le Leary, Steven, Porterfield, Harry S., Kotlarek, Jaclyn R., Darbro, Benjamin W., Sidhu, Alpa
Foilsithe in Clin Case Rep (2019)

Progressive optic disc cupping over 20 years in a patient with TBK1-associated glaucoma

le Sears, Nathan C., Darbro, Benjamin W., Alward, Wallace L.M., Fingert, John H.
Foilsithe in Ophthalmol Glaucoma (2019)

Autism Linked to Increased Oncogene Mutations but Decreased Cancer Rate

le Darbro, Benjamin W., Singh, Rohini, Zimmerman, M. Bridget, Mahajan, Vinit B., Bassuk, Alexander G.
Foilsithe in PLoS One (2016)

Amplification of the chromosome 20q region is associated with expression of HPV-16 E7 in human airway and anogenital epithelial cells

le Klingelhutz, Aloysius J., Qian, Qining, Phillips, Stacia L., Gourronc, Francoise A., Darbro, Benjamin W., Patil, Shivanand R.
Foilsithe 2005

CNV-ROC: A cost effective, computer-aided analytical performance evaluator of chromosomal microarrays

le Goodman, Corey W., Major, Heather J., Walls, William D., Sheffield, Val C., Casavant, Thomas L., Darbro, Benjamin W.
Foilsithe in J Biomed Inform (2015)

Candidate modifier genes for immune function in 22q11.2 deletion syndrome

le Pinnaro, Catherina T., Henry, Travis, Major, Heather J., Parida, Mrutyunjaya, DesJardin, Lucy E., Manak, John R., Darbro, Benjamin W.
Foilsithe in Mol Genet Genomic Med (2019)

Genome-wide copy number variation analysis of a Branchio-Oto-Renal syndrome cohort identifies a recombination hotspot and implicates new candidate genes

le Brophy, Patrick D., Alasti, Fatemeh, Darbro, Benjamin W., Clarke, Jason, Nishimura, Carla, Cobb, Bryan, Smith, Richard J., Manak, J. Robert
Foilsithe 2013

Combination therapies for MPNSTs targeting RABL6A-RB1 signaling

le Kohlmeyer, Jordan L., Gordon, David J., Tanas, Munir R., Dodd, Rebecca D., Monga, Varun, Darbro, Benjamin W., Quelle, Dawn E.
Foilsithe in Oncotarget (2021)

In trans variant calling reveals enrichment for compound heterozygous variants in genes involved in neuronal development and growth.

le Cox, Allison J., Grady, Fillan, Velez, Gabriel, Mahajan, Vinit B., Ferguson, Polly J., Kitchen, Andrew, Darbro, Benjamin W., Bassuk, Alexander G.
Foilsithe in Genet Res (Camb) (2019)

Evaluating Familial Essential Tremor with Novel Genetic Approaches: Is it a Genotyping or Phenotyping Issue?

le Gonzalez-Alegre, Pedro, Di Paola, Jorge, Wang, Kai, Fabbro, Shay, Yu, Hung-Chun, Shaikh, Tamim H., Darbro, Benjamin W., Bassuk, Alexander G.
Foilsithe in Tremor Other Hyperkinet Mov (N Y) (2014)

Esophageal cancer in a family with hamartomatous tumors and germline PTEN frameshift and SMAD7 missense mutations

le Sherman, Scott K., Maxwell, Jessica E., Qian, Qining, Bellizzi, Andrew M., Braun, Terry A., Iannettoni, Mark D., Darbro, Benjamin W., Howe, James R.
Foilsithe in Cancer Genet (2014)

The Eating-Disorder Associated HDAC4(A778T) Mutation Alters Feeding Behaviors in Female Mice

le Lutter, Michael, Khan, Michael Z., Satio, Kenji, Davis, Kevin C., Kidder, Ian J., McDaniel, Latisha, Darbro, Benjamin W., Pieper, Andrew A., Cui, Huxing
Foilsithe in Biol Psychiatry (2016)

Uniparental disomy unveils a novel recessive mutation in POMT2

le Brun, Brianna N, Willer, Tobias, Darbro, Benjamin W, Gonorazky, Hernan D, Naumenko, Sergey, Dowling, James J, Campbell, Kevin P, Moore, Steven A, Mathews, Katherine D
Foilsithe in Neuromuscul Disord (2018)

TBK1 and Flanking Genes in Human Retina

le Fingert, John H., Darbro, Benjamin W., Qian, Qining, Van Rheeden, Richard, Miller, Kathy, Riker, Megan, Solivan-Timpe, Frances, Roos, Ben R., Robin, Alan L., Mullins, Robert F.
Foilsithe 2013

Promoting improved utilization of laboratory testing through changes in an electronic medical record: experience at an academic medical center

le Krasowski, Matthew D, Chudzik, Deborah, Dolezal, Anna, Steussy, Bryan, Gailey, Michael P, Koch, Benjamin, Kilborn, Sara B, Darbro, Benjamin W, Rysgaard, Carolyn D, Klesney-Tait, Julia A
Foilsithe in BMC Med Inform Decis Mak (2015)

Recessive coding and regulatory mutations in FBLIM1 underlie the pathogenesis of chronic recurrent multifocal osteomyelitis (CRMO)

le Cox, Allison J., Darbro, Benjamin W., Laxer, Ronald M., Velez, Gabriel, Bing, Xinyu, Finer, Alexis L., Erives, Albert, Mahajan, Vinit B., Bassuk, Alexander G., Ferguson, Polly J.
Foilsithe in PLoS One (2017)

Correction: Recessive coding and regulatory mutations in FBLIM1 underlie the pathogenesis of chronic recurrent multifocal osteomyelitis (CRMO)

le Cox, Allison J., Darbro, Benjamin W., Laxer, Ronald M., Velez, Gabriel, Bing, Xinyu, Finer, Alexis L., Erives, Albert, Mahajan, Vinit B., Bassuk, Alexander G., Ferguson, Polly J.
Foilsithe in PLoS One (2017)