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
Large-Scale Phylogenomics of the Lactobacillus casei Group Highlights Taxonomic Inconsistencies and Reveals Novel Clade-Associated Features. PMID 28845461	mSystems	2017	94	L1 94/100
Roar: detecting alternative polyadenylation with standard mRNA sequencing libraries. PMID 27756200	BMC Bioinformatics	2016	75	75/100
The role of the multidisciplinary health care team in the management of patients with Marfan syndrome. PMID 27843325	—	2016	—	L1 No computation
Distinct lncRNA transcriptional fingerprints characterize progressive stages of multiple myeloma. ⚑ PMID 26895470	Oncotarget	2016	36	L1 36/100 ⚑
Cell Specific eQTL Analysis without Sorting Cells. PMID 25955312	PLoS Genet	2015	90	L1 90/100
Mutations of the mitochondrial holocytochrome c-type synthase in X-linked dominant microphthalmia with linear skin defects syndrome. PMID 17033964	—	2006	75	L1 75/100
Mutations in CHD7, encoding a chromatin-remodeling protein, cause idiopathic hypogonadotropic hypogonadism and Kallmann syndrome. PMID 18834967	—	2008	70	L1 70/100
Duplication of Glu37 in the switch I region of HRAS impairs effector/GAP binding and underlies Costello syndrome by promoting enhanced growth factor-dependent MAPK and AKT activation. PMID 19995790	—	2010	—	L1 No computation

Large-Scale Phylogenomics of the Lactobacillus casei Group Highlights Taxonomic Inconsistencies and Reveals Novel Clade-Associated Features.

PMID 28845461 · mSystems · 2017

L1 94/100

Roar: detecting alternative polyadenylation with standard mRNA sequencing libraries.

PMID 27756200 · BMC Bioinformatics · 2016

75/100

The role of the multidisciplinary health care team in the management of patients with Marfan syndrome.

PMID 27843325 · · 2016

L1 No computation

Distinct lncRNA transcriptional fingerprints characterize progressive stages of multiple myeloma.⚑

PMID 26895470 · Oncotarget · 2016

L1 36/100 ⚑

Cell Specific eQTL Analysis without Sorting Cells.

PMID 25955312 · PLoS Genet · 2015

L1 90/100

Mutations of the mitochondrial holocytochrome c-type synthase in X-linked dominant microphthalmia with linear skin defects syndrome.

PMID 17033964 · · 2006

L1 75/100

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

PMID 18834967 · · 2008

L1 70/100

Duplication of Glu37 in the switch I region of HRAS impairs effector/GAP binding and underlies Costello syndrome by promoting enhanced growth factor-dependent MAPK and AKT activation.

PMID 19995790 · · 2010

L1 No computation