Citation Impact
Citing Papers
2014 ESC Guidelines on diagnosis and management of hypertrophic cardiomyopathy
2014 Standout
Persistent epigenetic differences associated with prenatal exposure to famine in humans
2008 Standout
Induction of human neuronal cells by defined transcription factors
2011 StandoutNatureNobel
Adults with genetic syndromes and cardiovascular abnormalities: clinical history and management
2008
RIM1α and Interacting Proteins Involved in Presynaptic Plasticity Mediate Prepulse Inhibition and Additional Behaviors Linked to Schizophrenia
2010 StandoutNobel
Maternal Famine, De Novo Mutations, and Schizophrenia
2006
Understanding Synapses: Past, Present, and Future
2008 StandoutNobel
The impact of chromosomal microarray on clinical management: a retrospective analysis
2014
Epigenetic regulation of the glucocorticoid receptor in human brain associates with childhood abuse
2009 Standout
LRRTM2 Functions as a Neurexin Ligand in Promoting Excitatory Synapse Formation
2009 StandoutNobel
A Model for Neural Development and Treatment of Rett Syndrome Using Human Induced Pluripotent Stem Cells
2010
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
Modeling familial Alzheimer's disease with induced pluripotent stem cells
2011 StandoutNobel
Presynaptic Neurexin-3 Alternative Splicing trans-Synaptically Controls Postsynaptic AMPA Receptor Trafficking
2013 StandoutNobel
Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology
2015 Standout
SynCAM 1 Adhesion Dynamically Regulates Synapse Number and Impacts Plasticity and Learning
2010 StandoutNobel
Current Developments in the Genetics of Autism: From Phenome to Genome
2008
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
Autism spectrum disorder in fragile X syndrome: A longitudinal evaluation
2009
Temperature-Responsive Competitive Inhibition of CRISPR-Cas9
2018 StandoutNobel
Maternal and child undernutrition: consequences for adult health and human capital
2008 Standout
TRIBE: Hijacking an RNA-Editing Enzyme to Identify Cell-Specific Targets of RNA-Binding Proteins
2016 StandoutNobel
Functional dependence of neuroligin on a new non-PDZ intracellular domain
2011
The Role of Ionotropic Glutamate Receptors in Childhood Neurodevelopmental Disorders: Autism Spectrum Disorders and Fragile X Syndrome
2014
The emerging role of synaptic cell-adhesion pathways in the pathogenesis of autism spectrum disorders
2009
Increased Dentate Gyrus Excitability in Neuroligin-2-Deficient Mice in Vivo
2010
FMRP Stalls Ribosomal Translocation on mRNAs Linked to Synaptic Function and Autism
2011 Standout
Autism-Associated Neuroligin-3 Mutations Commonly Disrupt Tonic Endocannabinoid Signaling
2013 StandoutNobel
Clinical Application of Microarray-Based Molecular Cytogenetics: An Emerging New Era of Genomic Medicine
2009
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
Rescue of Fragile X Syndrome Neurons by DNA Methylation Editing of the FMR1 Gene
2018
The essence of senescence: Figure 1.
2010 Standout
Behavioural phenotyping assays for mouse models of autism
2010
Autism genetic database (AGD): a comprehensive database including autism susceptibility gene-CNVs integrated with known noncoding RNAs and fragile sites
2009
Genetic Basis for Congenital Heart Defects: Current Knowledge
2007
High Affinity Neurexin Binding to Cell Adhesion G-protein-coupled Receptor CIRL1/Latrophilin-1 Produces an Intercellular Adhesion Complex
2012 StandoutNobel
Neuroligin-1 Deletion Results in Impaired Spatial Memory and Increased Repetitive Behavior
2010 StandoutNobel
Minimal aberrant behavioral phenotypes of neuroligin‐3 R451C knockin mice
2008
Leucine-Rich Repeat Transmembrane Proteins Are Essential for Maintenance of Long-Term Potentiation
2013 StandoutNobel
Autism
2013 Standout
Neuroligins and neurexins link synaptic function to cognitive disease
2008 StandoutNatureNobel
Altered Neuronal and Circuit Excitability in Fragile X Syndrome
2015
Coming of age: ten years of next-generation sequencing technologies
2016 Standout
Microbiota Modulate Behavioral and Physiological Abnormalities Associated with Neurodevelopmental Disorders
2013 Standout
Hypomethylation of MB-COMT promoter is a major risk factor for schizophrenia and bipolar disorder
2006
Why Are Autism Spectrum Conditions More Prevalent in Males?
2011
Research Domain Criteria (RDoC): Toward a New Classification Framework for Research on Mental Disorders
2010 Standout
Overexpression of the cell adhesion protein neuroligin‐1 induces learning deficits and impairs synaptic plasticity by altering the ratio of excitation to inhibition in the hippocampus
2009
Structural Bases of Desensitization in AMPA Receptor-Auxiliary Subunit Complexes
2017 StandoutNobel
A Neuroligin-4 Missense Mutation Associated with Autism Impairs Neuroligin-4 Folding and Endoplasmic Reticulum Export
2009 StandoutNobel
Induced Neuronal Cells: How to Make and Define a Neuron
2011 StandoutNobel
Neuroligin‐1 performs neurexin‐dependent and neurexin‐independent functions in synapse validation
2009 StandoutNobel
Complementary Chimeric Isoforms Reveal Dscam1 Binding Specificity In Vivo
2012 StandoutNobel
Neuroligin Trafficking Deficiencies Arising from Mutations in the α/β-Hydrolase Fold Protein Family
2010 Nobel
MDGAs interact selectively with neuroligin-2 but not other neuroligins to regulate inhibitory synapse development
2012 StandoutNobel
Derivation Conditions Impact X-Inactivation Status in Female Human Induced Pluripotent Stem Cells
2012 StandoutNobel
Elucidation of AMPA receptor–stargazin complexes by cryo–electron microscopy
2016 StandoutScienceNobel
The neurexin ligands, neuroligins and leucine-rich repeat transmembrane proteins, perform convergent and divergent synaptic functions in vivo
2011 StandoutNobel
Whole Genome Sequencing as a Diagnostic Test: Challenges and Opportunities
2013
Endogenous expression of Hras G12V induces developmental defects and neoplasms with copy number imbalances of the oncogene
2009
Input-specific synaptic plasticity in the amygdala is regulated by neuroligin-1 via postsynaptic NMDA receptors
2010 Nobel
ACC/AHA 2008 Guidelines for the Management of Adults With Congenital Heart Disease: Executive Summary
2008 Standout
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
CRISPR-Cas guides the future of genetic engineering
2018 StandoutScienceNobel
Neurodevelopmental Outcomes in Children With Congenital Heart Disease: Evaluation and Management
2012 Standout
Mouse neurexin-1α deletion causes correlated electrophysiological and behavioral changes consistent with cognitive impairments
2009 StandoutNobel
Works of Jonathan Picker being referenced
Chromosomal microarray testing influences medical management
2011
An altered neonatal behavioral phenotype in Mecp2 mutant mice
2006
Clinical Diagnosis by Whole-Genome Sequencing of a Prenatal Sample
2012
Familial deletion within NLGN4 associated with autism and Tourette syndrome
2008
Do Maternal Folate and Homocysteine Levels Play a Role in Neurodevelopmental Processes That Increase Risk for Schizophrenia?
2005
Further delineation of cardiac abnormalities in Costello syndrome
2002
EEG abnormalities and seizures in genetically diagnosed Fragile X syndrome
2014
Microduplications of 22q11.2 are frequently inherited and are associated with variable phenotypes
2008
Advances in the Treatment of Fragile X Syndrome
2008