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Nature|April 13, 2012
The clonal and mutational evolution spectrum of primary triple-negative breast cancersSohrab P Shah, Andrew Roth, Rodrigo Goya, et al.The New England Journal of Medicine|June 9, 2016
Exome Sequencing and the Management of Neurometabolic DisordersMaja Tarailo-Graovac, Casper Shyr, Colin J Ross, et al.Brain : a Journal of Neurology|January 23, 2019
PLPHP deficiency: clinical, genetic, biochemical, and mechanistic insightsDevon L Johnstone, Hilal H Al-Shekaili, Maja Tarailo-Graovac, et al.Proceedings of the National Academy of Sciences of the United States of America|September 3, 2010
A regulatory toolbox of MiniPromoters to drive selective expression in the brainElodie Portales-Casamar, Douglas J Swanson, Li Liu, et al.Nature Biotechnology|August 23, 2017
An integrated expression atlas of miRNAs and their promoters in human and mouseDerek de Rie, Imad Abugessaisa, Tanvir Alam, et al.The Journal of Experimental Medicine|March 8, 2023
Human germline heterozygous gain-of-function STAT6 variants cause severe allergic diseaseMehul Sharma, Daniel Leung, Mana Momenilandi, et al.Science Immunology|January 20, 2023
A multimorphic mutation in IRF4 causes human autosomal dominant combined immunodeficiency, Oriol Fornes, Alicia Jia, et al.Science (New York, N.Y.)|February 14, 2015
Transcribed enhancers lead waves of coordinated transcription in transitioning mammalian cellsErik Arner, Carsten O Daub, Kristoffer Vitting-Seerup, et al.Genome Biology|March 31, 2012
The transcription factor encyclopediaDimas Yusuf, Stefanie L Butland, Magdalena I Swanson, et al.Genome Research|July 29, 2020
Functional annotation of human long noncoding RNAs via molecular phenotypingJordan A Ramilowski, Chi Wai Yip, Saumya Agrawal, et al.Pageof 29