Corpus 1,280 assessed · 1,181 scored · 646 reproduced ≥75 · 170 flagged ·∅ 74/100

Publications 6 Datasets 392.5k Experiments 5.2k

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6 matching publication(s)

Publication	Journal	Year	Score	Verdict
The genome and development-dependent transcriptomes of Pyronema confluens: a window into fungal evolution. PMID 24068976	PLoS Genet	2013	76	L1 76/100
Mutually exclusive teams-like patterns of gene regulation characterize phenotypic heterogeneity along the noradrenergic-mesenchymal axis in neuroblastoma. PMID 38230570	Cancer Biol Ther	2024	87	L1 87/100
MirDIP 5.2: tissue context annotation and novel microRNA curation. PMID 36453996	Nucleic Acids Res	2023	89	L1 89/100
BaRTv2: a highly resolved barley reference transcriptome for accurate transcript-specific RNA-seq quantification. PMID 35704392	Plant J	2022	94	L1 94/100
Prospects of telomere-to-telomere assembly in barley: Analysis of sequence gaps in the MorexV3 reference genome. PMID 35338551	Plant Biotechnol J	2022	71	71/100
A novel missense variant in the SDR domain of the WWOX gene leads to complete loss of WWOX protein with early-onset epileptic encephalopathy and severe developmental delay. PMID 29808465	—	2018	76	L1 76/100

The genome and development-dependent transcriptomes of Pyronema confluens: a window into fungal evolution.

PMID 24068976 · PLoS Genet · 2013

L1 76/100

Mutually exclusive teams-like patterns of gene regulation characterize phenotypic heterogeneity along the noradrenergic-mesenchymal axis in neuroblastoma.

PMID 38230570 · Cancer Biol Ther · 2024

L1 87/100

MirDIP 5.2: tissue context annotation and novel microRNA curation.

PMID 36453996 · Nucleic Acids Res · 2023

L1 89/100

BaRTv2: a highly resolved barley reference transcriptome for accurate transcript-specific RNA-seq quantification.

PMID 35704392 · Plant J · 2022

L1 94/100

Prospects of telomere-to-telomere assembly in barley: Analysis of sequence gaps in the MorexV3 reference genome.

PMID 35338551 · Plant Biotechnol J · 2022

71/100

A novel missense variant in the SDR domain of the WWOX gene leads to complete loss of WWOX protein with early-onset epileptic encephalopathy and severe developmental delay.

PMID 29808465 · · 2018

L1 76/100