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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 Research|July 29, 2020
Functional annotation of human long noncoding RNAs via molecular phenotypingJordan A Ramilowski, Chi Wai Yip, Saumya Agrawal, et al.
American Journal of Medical Genetics. Part A|January 22, 2015
Characterization of human disease phenotypes associated with mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, ADAR, and IFIH1Yanick J Crow, Diana S Chase, Johanna Lowenstein Schmidt, et al.
Nature Genetics|April 21, 2009
The transcriptional network that controls growth arrest and differentiation in a human myeloid leukemia cell line, Harukazu Suzuki, Alistair R R Forrest, et al.
JAMA Neurology|December 23, 2014
Rarity of the Alzheimer disease-protective APP A673T variant in the United StatesLi-San Wang, Adam C Naj, Robert R Graham, et al.
JAMA Neurology|September 10, 2014
Effects of multiple genetic loci on age at onset in late-onset Alzheimer disease: a genome-wide association studyAdam C Naj, Gyungah Jun, Christiane Reitz, et al.
Nature|March 28, 2014
A promoter-level mammalian expression atlas, Alistair R R Forrest, Hideya Kawaji, et al.
Scientific Data|July 11, 2020
The FLUXNET2015 dataset and the ONEFlux processing pipeline for eddy covariance dataGilberto Pastorello, Carlo Trotta, Eleonora Canfora, et al.
Medrxiv : the Preprint Server for Health Sciences|July 18, 2023
Multi-ancestry genome-wide meta-analysis of 56,241 individuals identifies LRRC4C, LHX5-AS1 and nominates ancestry-specific loci PTPRK , GRB14 , and KIAA0825 as novel risk loci for Alzheimer's disease: the Alzheimer's Disease Genetics ConsortiumFarid Rajabli, Penelope Benchek, Giuseppe Tosto, et al.
Nature|June 16, 2007
Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project, Ewan Birney, John A Stamatoyannopoulos, et al.
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