Select Publications
Preprints
, 2017, Universal alternative splicing of noncoding exons, http://dx.doi.org/10.1101/136275
, 2016, Machine-learning annotation of human splicing branchpoints, http://dx.doi.org/10.1101/094003
, 2016, RNA-seq reveals more consistent reference genes for gene expression studies in human non-melanoma skin cancers, http://dx.doi.org/10.7287/peerj.preprints.2331
, 2016, RNA-seq reveals more consistent reference genes for gene expression studies in human non-melanoma skin cancers, http://dx.doi.org/10.7287/peerj.preprints.2331v1
, 2016, High temporal resolution of gene expression dynamics in developing mouse embryonic stem cells, http://dx.doi.org/10.1101/084442
Other
, 2023, Data from Lipid Uptake Is an Androgen-Enhanced Lipid Supply Pathway Associated with Prostate Cancer Disease Progression and Bone Metastasis, http://dx.doi.org/10.1158/1541-7786.c.6540525.v1
, 2023, Data from Lipid Uptake Is an Androgen-Enhanced Lipid Supply Pathway Associated with Prostate Cancer Disease Progression and Bone Metastasis, http://dx.doi.org/10.1158/1541-7786.c.6540525
, 2023, Supplemental Files from Lipid Uptake Is an Androgen-Enhanced Lipid Supply Pathway Associated with Prostate Cancer Disease Progression and Bone Metastasis, http://dx.doi.org/10.1158/1541-7786.22513437.v1
, 2023, Supplemental Files from Lipid Uptake Is an Androgen-Enhanced Lipid Supply Pathway Associated with Prostate Cancer Disease Progression and Bone Metastasis, http://dx.doi.org/10.1158/1541-7786.22513437
, 2023, Supplementary Data from Lipid Uptake Is an Androgen-Enhanced Lipid Supply Pathway Associated with Prostate Cancer Disease Progression and Bone Metastasis, http://dx.doi.org/10.1158/1541-7786.22513434
, 2023, Supplementary Data from Lipid Uptake Is an Androgen-Enhanced Lipid Supply Pathway Associated with Prostate Cancer Disease Progression and Bone Metastasis, http://dx.doi.org/10.1158/1541-7786.22513434.v1
, 2019, Erratum: De Novo Variants Disrupting the HX Repeat Motif of ATN1 Cause a Recognizable Non-progressive Neurocognitive Syndrome (The American Journal of Human Genetics (2019) 104(3) (542–552), (S0002929719300138), (10.1016/j.ajhg.2019.01.013)), Elsevier, http://dx.doi.org/10.1016/j.ajhg.2019.03.016