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Genome Biology|January 9, 2020
Chromatin interactome mapping at 139 independent breast cancer risk signalsJonathan Beesley, Haran Sivakumaran, Mahdi Moradi Marjaneh, et al.American Journal of Human Genetics|June 4, 2016
A Common Variant at the 14q32 Endometrial Cancer Risk Locus Activates AKT1 through YY1 BindingJodie N Painter, Susanne Kaufmann, Tracy A O'Mara, et al.Human Mutation|July 4, 2012
Identification of fifteen novel germline variants in the BRCA1 3'UTR reveals a variant in a breast cancer case that introduces a functional miR-103 target siteBrooke L Brewster, Francesca Rossiello, Juliet D French, et al.Genome Biology|January 9, 2020
Non-coding RNAs underlie genetic predisposition to breast cancerMahdi Moradi Marjaneh, Jonathan Beesley, Tracy A O'Mara, et al.Nature Communications|February 5, 2025
Suppressing recurrence in Sonic Hedgehog subgroup medulloblastoma using the OLIG2 inhibitor CT-179Yuchen Li, Chaemin Lim, Taylor Dismuke, et al.Research Square|June 19, 2023
Preventing recurrence in Sonic Hedgehog Subgroup Medulloblastoma using the OLIG2 inhibitor CT-179Yuchen Li, Chaemin Lim, Taylor Dismuke, et al.American Journal of Human Genetics|August 5, 2017
Long Noncoding RNAs CUPID1 and CUPID2 Mediate Breast Cancer Risk at 11q13 by Modulating the Response to DNA DamageJoshua A Betts, Mahdi Moradi Marjaneh, Fares Al-Ejeh, et al.American Journal of Human Genetics|January 8, 2019
De Novo Variants in MAPK8IP3 Cause Intellectual Disability with Variable Brain AnomaliesKonrad Platzer, Heinrich Sticht, Stacey L Edwards, et al.Human Mutation|September 12, 2018
BRCA1 and BRCA2 5' noncoding region variants identified in breast cancer patients alter promoter activity and protein bindingLeslie J Burke, Jan Sevcik, Gaetana Gambino, et al.Oncotarget|February 4, 2016
Germline polymorphisms in an enhancer of PSIP1 are associated with progression-free survival in epithelial ovarian cancerJuliet D French, Sharon E Johnatty, Yi Lu, et al.Pageof 7