Citation Impact
Citing Papers
MicroRNA-mediated gene regulation and the resilience of multicellular animals
2024 StandoutNobel
Chromosome Abnormalities and Genetic Counseling
2011
RIM1α and Interacting Proteins Involved in Presynaptic Plasticity Mediate Prepulse Inhibition and Additional Behaviors Linked to Schizophrenia
2010 StandoutNobel
Understanding Synapses: Past, Present, and Future
2008 StandoutNobel
Transcriptional Regulation and Its Misregulation in Disease
2013
Structure of a Voltage-Dependent K+ Channel β Subunit
1999 StandoutNobel
DNA-Methylation Patterns in Trisomy 21 Using Cells from Monozygotic Twins
2015
LRRTM2 Functions as a Neurexin Ligand in Promoting Excitatory Synapse Formation
2009 StandoutNobel
The Common Feature of Leukemia-Associated IDH1 and IDH2 Mutations Is a Neomorphic Enzyme Activity Converting α-Ketoglutarate to 2-Hydroxyglutarate
2010 Standout
Foxp2 controls synaptic wiring of corticostriatal circuits and vocal communication by opposing Mef2c
2016 StandoutNobel
Neurexins Physically and Functionally Interact with GABAA Receptors
2010 StandoutNobel
Neuroligin-2 Deletion Selectively Decreases Inhibitory Synaptic Transmission Originating from Fast-Spiking but Not from Somatostatin-Positive Interneurons
2009 StandoutNobel
Two Exon-Skipping Mutations as the Molecular Basis of Succinic Semialdehyde Dehydrogenase Deficiency (4-Hydroxybutyric Aciduria)
1998
Reprogramming human fibroblasts to neurons by recapitulating an essential microRNA-chromatin switch
2013
Presynaptic Neurexin-3 Alternative Splicing trans-Synaptically Controls Postsynaptic AMPA Receptor Trafficking
2013 StandoutNobel
SynCAM 1 Adhesion Dynamically Regulates Synapse Number and Impacts Plasticity and Learning
2010 StandoutNobel
β-Neurexin Is a Ligand for the Staphylococcus aureus MSCRAMM SdrC
2010 StandoutNobel
Neurotransmitter Release: The Last Millisecond in the Life of a Synaptic Vesicle
2013 StandoutNobel
Synaptic Dysfunction in Neurodevelopmental Disorders Associated with Autism and Intellectual Disabilities
2012
The Human Transcription Factors
2018 Standout
Predicting the sequence specificities of DNA- and RNA-binding proteins by deep learning
2015 Standout
Cancer-associated IDH1 mutations produce 2-hydroxyglutarate
2009 StandoutNature
The emerging role of synaptic cell-adhesion pathways in the pathogenesis of autism spectrum disorders
2009
What a difference a hydroxyl makes: mutant IDH, (R)-2-hydroxyglutarate, and cancer
2013 StandoutNobel
Super-Enhancers in the Control of Cell Identity and Disease
2013 Standout
Genome Scan, Fine-Mapping, and Candidate Gene Analysis of Non-Syndromic Cleft Lip with or without Cleft Palate Reveals Phenotype-Specific Differences in Linkage and Association Results
2009
Cleft lip and palate: understanding genetic and environmental influences
2011 Standout
Metazoan MicroRNAs
2018 Standout
Autism-Associated Neuroligin-3 Mutations Commonly Disrupt Tonic Endocannabinoid Signaling
2013 StandoutNobel
Neocortical excitation/inhibition balance in information processing and social dysfunction
2011 StandoutNature
An autism‐associated point mutation in the neuroligin cytoplasmic tail selectively impairs AMPA receptor‐mediated synaptic transmission in hippocampus
2011 StandoutNobel
Mir-132/212 is required for maturation of binocular matching of orientation preference and depth perception
2017
Psychiatric genetics: progress amid controversy
2008
High Affinity Neurexin Binding to Cell Adhesion G-protein-coupled Receptor CIRL1/Latrophilin-1 Produces an Intercellular Adhesion Complex
2012 StandoutNobel
Beyond diathesis stress: Differential susceptibility to environmental influences.
2009 Standout
Neuroligin-1 Deletion Results in Impaired Spatial Memory and Increased Repetitive Behavior
2010 StandoutNobel
Leucine-Rich Repeat Transmembrane Proteins Are Essential for Maintenance of Long-Term Potentiation
2013 StandoutNobel
THE γ-HYDROXYBUTYRATE SIGNALLING SYSTEM IN BRAIN: ORGANIZATION AND FUNCTIONAL IMPLICATIONS
1997
Neuroligins and neurexins link synaptic function to cognitive disease
2008 StandoutNatureNobel
D‐2‐hydroxyglutaric acid induces oxidative stress in cerebral cortex of young rats
2003
Postnatal Loss of Mef2c Results in Dissociation of Effects on Synapse Number and Learning and Memory
2015
Health Supervision for Children With Down Syndrome
2011 Standout
Down syndrome
2020 Standout
A Neuroligin-4 Missense Mutation Associated with Autism Impairs Neuroligin-4 Folding and Endoplasmic Reticulum Export
2009 StandoutNobel
Neuroligin‐1 performs neurexin‐dependent and neurexin‐independent functions in synapse validation
2009 StandoutNobel
GABA in plants: just a metabolite?
2004 Standout
Complementary Chimeric Isoforms Reveal Dscam1 Binding Specificity In Vivo
2012 StandoutNobel
MDGAs interact selectively with neuroligin-2 but not other neuroligins to regulate inhibitory synapse development
2012 StandoutNobel
The neurexin ligands, neuroligins and leucine-rich repeat transmembrane proteins, perform convergent and divergent synaptic functions in vivo
2011 StandoutNobel
Molecular cloning, expression and catalytic activity of a human AKR7 member of the aldo–keto reductase superfamily: evidence that the major 2-carboxybenzaldehyde reductase from human liver is a homologue of rat aflatoxin B1-aldehyde reductase
1998
Autism-linked neuroligin-3 R451C mutation differentially alters hippocampal and cortical synaptic function
2011 StandoutNobel
Neuroligins/LRRTMs prevent activity- and Ca2+/calmodulin-dependent synapse elimination in cultured neurons
2011 StandoutNobel
Candidate autism gene screen identifies critical role for cell-adhesion molecule CASPR2 in dendritic arborization and spine development
2012 StandoutNobel
Neurons generated by direct conversion of fibroblasts reproduce synaptic phenotype caused by autism-associated neuroligin-3 mutation
2013 StandoutNobel
Mouse neurexin-1α deletion causes correlated electrophysiological and behavioral changes consistent with cognitive impairments
2009 StandoutNobel
Works of Eva Rossier being referenced
Molecular cytogenetic analysis of a familial interstitial deletion Xp22.2‐22.3 with a highly variable phenotype in female carriers
2006
Haploinsufficiency of ARID1B, a Member of the SWI/SNF-A Chromatin-Remodeling Complex, Is a Frequent Cause of Intellectual Disability
2012
Chromosome 11p15 duplication in Silver‐Russell syndrome due to a maternally inherited translocation t(11;15)
2010
Enzymatic and Immunologic Identification of Succinic Semialdehyde Dehydrogenase in Rat and Human Neural and Nonneural Tissues
1995
De novo MECP2 duplication in two females with random X-inactivation and moderate mental retardation
2011
Molecular cytogenetic analysis of a constitutional de novo interstitial deletion of chromosome 12p in a boy with developmental delay and congenital anomalies
2002
Mutations in MEF2C from the 5q14.3q15 microdeletion syndrome region are a frequent cause of severe mental retardation and diminish MECP2 and CDKL5 expression
2010
Characterization of a t(5;8)(q31;q21) translocation in a patient with mental retardation and congenital heart disease: implications for involvement of RUNX1T1 in human brain and heart development
2009
Pre‐ and postnatal diagnosis of succinic semialdehyde dehydrogenase deficiency using enzyme and metabolite assays
1994
Vigabatrin therapy in six patients with succinic semialdehyde dehydrogenase deficiency
1995
New case of mosaic tetrasomy 9p with additional neurometabolic findings
1998