Corpus 1,273 assessed · 1,174 scored · 643 reproduced ≥75 · 169 flagged ·∅ 74.1/100

Publications 58 Datasets 392.5k Experiments 4.7k

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58 matching publication(s)

Publication	Journal	Year	Score	Verdict
Viewing RNA-seq data on the entire human genome. PMID 28979763	F1000Res	2017	50	L1 50/100
The cold-induced lipokine 12,13-diHOME promotes fatty acid transport into brown adipose tissue PMID 28346411	Nature Medicine	2017	78	L1 78/100
Thermogenic adipocytes promote HDL turnover and reverse cholesterol transport PMID 28422089	Nature Communications	2017	—	L1 No computation
Spatial organization shapes the turnover of a bacterial transcriptome. PMID 27198188	Elife	2016	71	L1 71/100
Cell Specific eQTL Analysis without Sorting Cells. PMID 25955312	PLoS Genet	2015	90	L1 90/100
Brown fat activation reduces hypercholesterolaemia and protects from atherosclerosis development PMID 25754609	—	2015	—	L1 No computation
WDR11, a WD protein that interacts with transcription factor EMX1, is mutated in idiopathic hypogonadotropic hypogonadism and Kallmann syndrome. PMID 20887964	—	2010	—	L1 No computation
Mutations in CHD7, encoding a chromatin-remodeling protein, cause idiopathic hypogonadotropic hypogonadism and Kallmann syndrome. PMID 18834967	—	2008	70	L1 70/100

Viewing RNA-seq data on the entire human genome.

PMID 28979763 · F1000Res · 2017

L1 50/100

The cold-induced lipokine 12,13-diHOME promotes fatty acid transport into brown adipose tissue

PMID 28346411 · Nature Medicine · 2017

L1 78/100

Thermogenic adipocytes promote HDL turnover and reverse cholesterol transport

PMID 28422089 · Nature Communications · 2017

L1 No computation

Spatial organization shapes the turnover of a bacterial transcriptome.

PMID 27198188 · Elife · 2016

L1 71/100

Cell Specific eQTL Analysis without Sorting Cells.

PMID 25955312 · PLoS Genet · 2015

L1 90/100

Brown fat activation reduces hypercholesterolaemia and protects from atherosclerosis development

PMID 25754609 · · 2015

L1 No computation

WDR11, a WD protein that interacts with transcription factor EMX1, is mutated in idiopathic hypogonadotropic hypogonadism and Kallmann syndrome.

PMID 20887964 · · 2010

L1 No computation

Mutations in CHD7, encoding a chromatin-remodeling protein, cause idiopathic hypogonadotropic hypogonadism and Kallmann syndrome.

PMID 18834967 · · 2008

L1 70/100