Citation Impact
Citing Papers
A Neuroligin-3 Mutation Implicated in Autism Increases Inhibitory Synaptic Transmission in Mice
2007 StandoutScienceNobel
Hypogonadotropic hypogonadism due to loss of function of the KiSS1-derived peptide receptor GPR54
2003 Standout
X-Linked Mental Retardation and Autism Are Associated with a Mutation in the NLGN4 Gene, a Member of the Neuroligin Family
2004
How Malaria Has Affected the Human Genome and What Human Genetics Can Teach Us about Malaria
2005
Regional Specificity of Brain Atrophy in Huntington's Disease
1998
Phenotypic determinants of uncontrolled asthma
2009
Selective Capability of SynCAM and Neuroligin for Functional Synapse Assembly
2005 StandoutNobel
A gene related to Caenorhabditis elegans spermatogenesis factor fer-1 is mutated in limb-girdle muscular dystrophy type 2B
1998
Increased Basal Activity Is a Key Determinant in the Severity of Human Skeletal Dysplasia Caused by TRPV4 Mutations
2011
Linkage and associated studies of schizophrenia
2000
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
Omission of exon 12 in cystic fibrosis transmembrane conductance regulator (CFTR) gene transcripts
1992
A Systematic Review of the Prevalence of Schizophrenia
2005
Inclusion body formation reduces levels of mutant huntingtin and the risk of neuronal death
2004 StandoutNature
Prevalence of Hemochromatosis among 11,065 Presumably Healthy Blood Donors
1988 Standout
The GPR54 Gene as a Regulator of Puberty
2003 Standout
Synaptic transmission: A bidirectional and self-modifiable form of cell-cell communication
1993 StandoutNobel
cDNAs with long CAG trinucleotide repeats from human brain
1997
Structures of Neuroligin-1 and the Neuroligin-1/Neurexin-1β Complex Reveal Specific Protein-Protein and Protein-Ca2+ Interactions
2007 StandoutNobel
FMRP Stalls Ribosomal Translocation on mRNAs Linked to Synaptic Function and Autism
2011 Standout
Dissecting muscle and neuronal disorders in a Drosophila model of muscular dystrophy
2007 StandoutNobel
Super-Enhancers in the Control of Cell Identity and Disease
2013 Standout
Global burden of disease attributable to mental and substance use disorders: findings from the Global Burden of Disease Study 2010
2013 Standout
Dissection of Synapse Induction by Neuroligins
2005 StandoutNobel
Neuroligins Determine Synapse Maturation and Function
2006 StandoutNobel
Molecular Genetics of Huntington’s Disease
1998
Parkinson's disease
2015 Standout
A role for microRNAs in the Drosophila circadian clock
2009 StandoutNobel
Maternal and child undernutrition: global and regional exposures and health consequences
2008 Standout
Disorder-associated mutations lead to functional inactivation of neuroligins
2004
Toward a developmental neurobiology of autism
2004
Genomic DNA sequence of the cystic fibrosis transmembrane conductance regulator (CFTR) gene
1991
Rethinking schizophrenia
2010 StandoutNature
The CEPH Consortium Linkage Map of Human Chromosome 13
1993
RNA Cargoes Associating with FMRP Reveal Deficits in Cellular Functioning in Fmr1 Null Mice
2003
Structure of the TRPV1 ion channel determined by electron cryo-microscopy
2013 StandoutNatureNobel
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
MicroRNA (miRNA) Transcriptome of Mouse Retina and Identification of a Sensory Organ-specific miRNA Cluster
2007
A Novel Multiple PDZ Domain-containing Molecule Interacting withN-Methyl-d-aspartateReceptors and Neuronal Cell Adhesion Proteins
1998 StandoutNobel
Neuroligins and neurexins link synaptic function to cognitive disease
2008 StandoutNatureNobel
Whole Brain Segmentation
2002 Standout
Airway Mucus Function and Dysfunction
2010 Standout
Synaptotagmins: Why So Many?
2002 StandoutNobel
The role of SOX10 during enteric nervous system development
2013
FOXP2 Is Not a Major Susceptibility Gene for Autism or Specific Language Impairment
2002
Molecular basis of muscular dystrophies
2000
Genomic and epigenetic evidence for oxytocin receptor deficiency in autism
2009
Activity-Dependent Validation of Excitatory versus Inhibitory Synapses by Neuroligin-1 versus Neuroligin-2
2007 StandoutNobel
Polymorphisms in leucine-rich repeat genes are associated with autism spectrum disorder susceptibility in populations of European ancestry
2010
Mutations in the Cystic Fibrosis Gene in Patients with Congenital Absence of the Vas Deferens
1995 Standout
Molecular evolution of FOXP2, a gene involved in speech and language
2002 StandoutNatureNobel
A Neuroligin-4 Missense Mutation Associated with Autism Impairs Neuroligin-4 Folding and Endoplasmic Reticulum Export
2009 StandoutNobel
A Calcineurin-Dependent Transcriptional Pathway for Cardiac Hypertrophy
1998 Standout
The Human Condition—A Molecular Approach
2014 StandoutNobel
Neuroligin‐1 performs neurexin‐dependent and neurexin‐independent functions in synapse validation
2009 StandoutNobel
Control of Cachectin (Tumor Necrosis Factor) Synthesis: Mechanisms of Endotoxin Resistance
1986 StandoutScienceNobel
The mouse and human genes encoding the recognition component of the N-end rule pathway
1998 StandoutNobel
Variation of the CGG repeat at the fragile X site results in genetic instability: Resolution of the Sherman paradox
1991 Standout
Chromosome-breaking agent of low molecular weight in human systemic Lypus Erythematosus
1980
Polymorphic DNA haplotypes at the phenylalanine hydroxylase (PAH) locus in Asian families with phenylketonuria (PKU).
1989
Interactive effect of Gm allotypes and HLA-B locus antigens on the human antibody response to a bacterial antigen.
1980
What Genetics Tells us About the Causes and Mechanisms of Parkinson's Disease
2011
The candidate gene for the X-linked Kallmann syndrome encodes a protein related to adhesion molecules
1991
Measuring the thickness of the human cerebral cortex from magnetic resonance images
2000 Standout
An Alternative Pathway for Meiotic Chromosome Segregation in Yeast
1986 StandoutScienceNobel
Autism-linked neuroligin-3 R451C mutation differentially alters hippocampal and cortical synaptic function
2011 StandoutNobel
Genealogical analysis of cystic fibrosis families and chromosome 7q RFLP haplotypes in the Hutterite Brethren.
1989
Identification of the Cystic Fibrosis Gene: Genetic Analysis
1989 StandoutScience
Familial Hypertrophic Cardiomyopathy
1998
THE IMPORTANCE OF THE PERIOD OF MALARIAL INFECTION DURING PREGNANCY ON BIRTH WEIGHT IN TROPICAL AFRICA
2007
Dietary Carcinogens and Anticarcinogens
1983 StandoutScience
Neuroligins/LRRTMs prevent activity- and Ca2+/calmodulin-dependent synapse elimination in cultured neurons
2011 StandoutNobel
Multiple DNA fragment polymorphisms associated with immunoglobulin mu chain switch-like regions in man.
1983 StandoutNobel
Genetic instability in human ovarian cancer cell lines.
1994
Mapping the locus for hereditary hemochromatosis: localization between HLA-B and HLA-A.
1986
TRISOMY IN MAN
1984
Genetic control of lipopolysaccharide induced generation of serum colony stimulating factor and proliferation of splenic granulocyte/macrophage precursor cells
1976
Candidate autism gene screen identifies critical role for cell-adhesion molecule CASPR2 in dendritic arborization and spine development
2012 StandoutNobel
Effect of COMT Val 108/158 Met genotype on frontal lobe function and risk for schizophrenia
2001 Standout
Restoration of mismatch repair to nuclear extracts of H6 colorectal tumor cells by a heterodimer of human MutL homologs.
1995 StandoutNobel
Links between genetics and pathophysiology in the autism spectrum disorders
2011
Unusually rapid evolution of Neuroligin-4 in mice
2008 StandoutNobel
Neuropsychological functioning among the nonpsychotic relatives of schizophrenic patients: A diagnostic efficiency analysis.
1995
The Molecular Biology of Axon Guidance
1996 StandoutScience
Mutations in the proteolytic enzyme calpain 3 cause limb-girdle muscular dystrophy type 2A
1995
Works of J Feingold being referenced
Evidence for a Pseudoautosomal Locus for Schizophrenia
1992
Risk Factors of Malaria Infection during Pregnancy in Burkina Faso: Suggestion of a Genetic Influence
1993
Further epidemiological evidence for anticipation in schizophrenia
1997
A one year prevalence study of schizophrenia on Reunion Island
1997
Epistatic interactions with a common hypomorphicRET allele in syndromic Hirschsprung disease
2007
Evidence for a Pseudoautosomal Locus for Schizophrenia
1992
Genetic control of blood infection levels in human malaria: evidence for a complex genetic model.
1998
Frequency of the cystic fibrosis ΔF508 mutation in a large sample of the French population
1990
Diagnosis of “sporadic” Huntington's disease
1995
Genome-Wide Scan for Autism Susceptibility Genes
1999
Revisiting metatropic dysplasia: Presentation of a series of 19 novel patients and review of the literature
2008
Mode of Inheritance in Familial Cases of Primary Gonadotropic Deficiency
1988
Are cognitive changes the first symptoms of Huntington's disease? A study of gene carriers
1998
Juvenile limb-girdle muscular dystrophy
1996
LOW DISEASE RISK IN RELATIVES OF NORTH AFRICAN LRRK2 PARKINSON DISEASE PATIENTS
2010
Anticipation in schizophrenia: new light on a controversial problem [published erratum appears in Am J Psychiatry 1997 Apr;154(4):590]
1996
[Idiopathic hemochromatosis linkage with the HLA system (author's transl)].
1978
Gender and age at onset in schizophrenia: impact of family history
1995
Penetrance of familial hypertrophic cardiomyopathy.
1997
Polygenic regulation of antibody synthesis to sheep erythrocytes in the mouse: a genetic analysis
1976
A gene for limb-girdle muscular dystrophy maps to chromosome 15 by linkage.
1991
EGEA (Epidemiological study on the Genetics and Environment of Asthma, bronchial hyperresponsiveness and atopy)-- descriptive characteristics.
1999
Clinical and molecular heterogeneity of phenylalanine hydroxylase deficiencies in France.
1988
[Chromosome studies of collagen diseases].
1974
Segregation analysis detects a major gene controlling blood infection levels in human malaria.
1992
Cluster of cystic fibrosis cases in a limited area of Brittany (France)
1978
Genetic control of macrophage functions. I. Polygenic regulation of phagocytosis stimulation produced by Glyceryl Trioleate.
1975
Reexamination of paternal age effect in Down's syndrome
1983