Citation Impact
Citing Papers
Characterizing and explaining the impact of disease-associated mutations in proteins without known structures or structural homologs
2022 StandoutNobel
Human-specific gene ARHGAP11B promotes basal progenitor amplification and neocortex expansion
2015 StandoutScienceNobel
Predictive Effects of Circulating miR-221, miR-130a and miR-155 for Coronary Heart Disease: A Multi-Ethnic Study in China.
2017 Standout
The miR-17/92 cluster: a comprehensive update on its genomics, genetics, functions and increasingly important and numerous roles in health and disease
2013
Critical contribution of 3′ non-seed base pairing to the in vivo function of the evolutionarily conserved let-7a microRNA
2022 StandoutNobel
The biological functions of miRNAs: lessons from in vivo studies
2014
Regulation of microRNA function in animals
2018 Standout
Constitutional aneuploidy and cancer predisposition
2009
Transfection of microRNA Mimics Should Be Used with Caution
2015
Review The Cancer Genome Atlas (TCGA): an immeasurable source of knowledge
2015 Standout
ALFY-Controlled DVL3 Autophagy Regulates Wnt Signaling, Determining Human Brain Size
2016
The emerging role of lncRNAs in cancer
2015 Standout
The Decapping Scavenger Enzyme DCS-1 Controls MicroRNA Levels in Caenorhabditis elegans
2013 StandoutNobel
The Role of MicroRNAs in Human Diseases
2013
Long Noncoding RNAs in Cancer Pathways
2016 Standout
Growth and folding of the mammalian cerebral cortex: from molecules to malformations
2014
22q11.21 Deletion Syndromes: A Review of Proximal, Central, and Distal Deletions and Their Associated Features
2015 Standout
Neurobehavioral Alterations in a Genetic Murine Model of Feingold Syndrome 2
2015
Global mapping of miRNA-target interactions in cattle (Bos taurus)
2017 StandoutNobel
Antiviral resistance of stem cells
2018 StandoutNobel
Biological Functions of Autophagy Genes: A Disease Perspective
2019 Standout
Signature MicroRNA expression patterns identified in humans with 22q11.2 deletion/DiGeorge syndrome
2013
MicroRNAs and other non-coding RNAs as targets for anticancer drug development
2013
Metazoan MicroRNAs
2018 Standout
Overview of MicroRNA Biogenesis, Mechanisms of Actions, and Circulation
2018 Standout
An allelic series of miR-17∼92–mutant mice uncovers functional specialization and cooperation among members of a microRNA polycistron
2015
An efficient and sensitive method for preparing cDNA libraries from scarce biological samples
2014 StandoutNobel
MicroRNA biogenesis pathways in cancer
2015 Standout
U1 snRNP regulates cancer cell migration and invasion in vitro
2020 Standout
MicroRNA therapeutics: towards a new era for the management of cancer and other diseases
2017 Standout
MicroRNAs in Human Cancer
2012
The Noncoding RNA Revolution—Trashing Old Rules to Forge New Ones
2014 Standout
MicroRNAs in Stress Signaling and Human Disease
2012
Mutations in the noncoding genome
2015
Hypoxia-inducible factor 1 and breast cancer metastasis
2015 StandoutNobel
Phenotypic variability of distal 22q11.2 copy number abnormalities
2011
MicroRNA
2017 Standout
The Role of miRNAs in Regulating Gene Expression Networks
2013
Modeling neurodevelopmental disorder-associated humanAGO1mutations inCaenorhabditis elegansArgonautealg-1
2024 StandoutNobel
Long Noncoding RNA and Cancer: A New Paradigm
2017 Standout
Loss of microRNA-7a2 induces hypogonadotropic hypogonadism and infertility
2017
Epithelial Mesenchymal Transition in Tumor Metastasis
2018 Standout
Longer metaphase and fewer chromosome segregation errors in modern human than Neanderthal brain development
2022 StandoutNobel
A Biogenesis Step Upstream of Microprocessor Controls miR-17∼92 Expression
2015
The Versatile Role of microRNA-30a in Human Cancer
2017 Standout
A single splice site mutation in human-specific ARHGAP11B causes basal progenitor amplification
2016 StandoutNobel
Phenotypic Characterization of miR-92a−/− Mice Reveals an Important Function of miR-92a in Skeletal Development
2014
Works of Patrick Callier being referenced
Microcephaly is not mandatory for the diagnosis of mosaic variegated aneuploidy syndrome
2005
Dissection of the MYCN locus in Feingold syndrome and isolated oesophageal atresia
2011
Germline deletion of the miR-17∼92 cluster causes skeletal and growth defects in humans
2011
Polymicrogyria in a child with inv dup del(9p) and 22q11.2 microduplication
2009
The DYRK1A gene is a cause of syndromic intellectual disability with severe microcephaly and epilepsy
2012
Congenital Heart Defects in Patients with Deletions Upstream ofSOX9
2013