Citation Impact
Citing Papers
Neurexin and Neuroligin Mediate Retrograde Synaptic Inhibition in C. elegans
2012 Science
Chromosome Abnormalities and Genetic Counseling
2011
Bone Morphogenetic Protein (BMP) signaling in development and human diseases
2014 Standout
Bone grafts and biomaterials substitutes for bone defect repair: A review
2017 Standout
Multiple Autism-Linked Genes Mediate Synapse Elimination via Proteasomal Degradation of a Synaptic Scaffold PSD-95
2012
Dnmt3 and G9a Cooperate for Tissue-specific Development in Zebrafish
2009
Latrophilins Function as Heterophilic Cell-adhesion Molecules by Binding to Teneurins
2013 StandoutNobel
Age at onset of mental disorders worldwide: large-scale meta-analysis of 192 epidemiological studies
2021 Standout
Fracture healing: mechanisms and interventions
2014 Standout
Phosphorylation of ETS1 by Src Family Kinases Prevents Its Recognition by the COP1 Tumor Suppressor
2014 StandoutNobel
RINGs of good and evil: RING finger ubiquitin ligases at the crossroads of tumour suppression and oncogenesis
2011
A locus for an auditory processing deficit and language impairment in an extended pedigree maps to 12p13.31‐q14.3
2010 StandoutNobel
To read or not to read: A meta-analysis of print exposure from infancy to early adulthood.
2011 Standout
Foxp2 controls synaptic wiring of corticostriatal circuits and vocal communication by opposing Mef2c
2016 StandoutNobel
Presynaptic Neurexin-3 Alternative Splicing trans-Synaptically Controls Postsynaptic AMPA Receptor Trafficking
2013 StandoutNobel
Accurate detection of complex structural variations using single-molecule sequencing
2018
The Axon Guidance Receptor Gene ROBO1 Is a Candidate Gene for Developmental Dyslexia
2005
Mutation screening of BMP4 and Id2 genes in Chinese patients with congenital ureteropelvic junction obstruction
2011
Gene × Environment interactions in speech sound disorder predict language and preliteracy outcomes
2007
FGFR3 targeting strategies for achondroplasia
2012
cGMP-Dependent Protein Kinases and cGMP Phosphodiesterases in Nitric Oxide and cGMP Action
2010 Standout
Role of FGFs/FGFRs in skeletal development and bone regeneration
2012
Evaluation of the Therapeutic Potential of a CNP Analog in a Fgfr3 Mouse Model Recapitulating Achondroplasia
2012
High Affinity Neurexin Binding to Cell Adhesion G-protein-coupled Receptor CIRL1/Latrophilin-1 Produces an Intercellular Adhesion Complex
2012 StandoutNobel
Neurodevelopmental theory of depression
2017
Applications of CRISPR technologies in research and beyond
2016 StandoutNobel
Postnatal Loss of Mef2c Results in Dissociation of Effects on Synapse Number and Learning and Memory
2015
Clonal evolution in cancer
2012 StandoutNature
CRISPR-Based Technologies for the Manipulation of Eukaryotic Genomes
2016 Standout
Health Supervision for Children With Down Syndrome
2011 Standout
Natriuretic Peptides: Their Structures, Receptors, Physiologic Functions and Therapeutic Applications
2008
Minimap2: pairwise alignment for nucleotide sequences
2018 Standout
The Fibroblast Growth Factor signaling pathway
2015 Standout
Epigenetic regulation in pluripotent stem cells: a key to breaking the epigenetic barrier
2012 StandoutNobel
Latrophilin 1 and its endogenous ligand Lasso/teneurin-2 form a high-affinity transsynaptic receptor pair with signaling capabilities
2011
Xenografts of highly resistant leukemia recapitulate the clonal composition of the leukemogenic compartment
2011
CRISPR/Cas9-mediated heterozygous knockout of the autism gene CHD8 and characterization of its transcriptional networks in neurodevelopment
2015
Works of Silvana Beri being referenced
Low-copy repeats at the human VIPR2 gene predispose to recurrent and nonrecurrent rearrangements
2012
Genotype–phenotype relationship in three cases with overlapping 19p13.12 microdeletions
2010
DNA methylation regulates tissue‐specific expression of Shank3
2007
A 46,X,inv(Y) young woman with gonadal dysgenesis and gonadoblastoma: Cytogenetics, molecular, and methylation studies
2005
Mutations in SOX17 are associated with congenital anomalies of the kidney and the urinary tract
2010
The tumor suppressor gene TRC8/RNF139 is disrupted by a constitutional balanced translocation t(8;22)(q24.13;q11.21) in a young girl with dysgerminoma
2009
Overexpression of the C-type natriuretic peptide (CNP) is associated with overgrowth and bone anomalies in an individual with balanced t(2;7) translocation
2007
A family-based association study does not support DYX1C1 on 15q21.3 as a candidate gene in developmental dyslexia
2005
Different molecular mechanisms causing 9p21 deletions in acute lymphoblastic leukemia of childhood
2009
Molecular and cytogenetic analysis of the spreading of X inactivation in a girl with microcephaly, mild dysmorphic features and t(X;5)(q22.1;q31.1)
2008
SLC6A4 methylation as an epigenetic marker of life adversity exposures in humans: A systematic review of literature
2016
Refining the phenotype associated with MEF2C haploinsufficiency
2010