Allen E. Bale
Affiliations: | Yale University, New Haven, CT |
Area:
Genetics, Pharmacology, Molecular BiologyGoogle:
"Allen Bale"Children
Sign in to add trainee| Kanya Suphapeetiporn | grad student | 2002 | Yale |
| Valeria Busygina | grad student | 2005 | Yale |
| Lorri R. Marek | grad student | 2007 | Yale |
| Molly C. Kottemann | grad student | 2009 | Yale |
BETA: Related publications
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Publications
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| Cruz-Aviles LM, Bale A, Carpenter TO. (2020) SAT-065 A Novel De Novo GATA3 Gene Mutation in an Adolescent with HDR Syndrome Journal of the Endocrine Society. 4 |
| Phatak A, Athar M, Crowell JA, et al. (2019) Global gene expression of histologically normal primary skin cells from BCNS subjects reveals "single-hit" effects that are influenced by rapamycin. Oncotarget. 10: 1360-1387 |
| Jaime Villalonga A, Bale A, Smith M, et al. (2019) SAT-082 Severe Hypertriglyceridemia Associated with a PRKAA1 Gene Mutation Coding for the Alpha1-Subunit of AMPK Journal of the Endocrine Society. 3 |
| Penque BA, Su L, Wang J, et al. (2018) A homozygous variant in RRM2B is associated with severe metabolic acidosis and early neonatal death. European Journal of Medical Genetics |
| Jeffries L, Olivieri JE, Ji W, et al. (2018) Two siblings with a novel nonsense variant provide further delineation of the spectrum of recessive KLHL7 diseases. European Journal of Medical Genetics |
| Gulati A, Bale AE, Dykas DJ, et al. (2018) TREX1 Mutation Causing Autosomal Dominant Thrombotic Microangiopathy and CKD-A Novel Presentation. American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation |
| Shevell LM, Lee E, Dhodapkar R, et al. (2018) Whole Exome Sequencing and Extended Thrombophilia Testing in Patients with Venous Thromboembolism Blood. 132: 2506-2506 |
| Lee EJ, Dykas DJ, Leavitt AD, et al. (2017) Whole-exome sequencing in evaluation of patients with venous thromboembolism. Blood Advances. 1: 1224-1237 |
| Couto PP, Bastos-Rodrigues L, Schayek H, et al. (2017) Spectrum of germline mutations in smokers and non-smokers in Brazilian non-small lung cancer (NSCLC) patients. Carcinogenesis |
| Melo FM, Couto PP, Bale AE, et al. (2016) Whole-exome identifies RXRG and TH germline variants in familial isolated prolactinoma. Cancer Genetics |