Citation Impact
Citing Papers
Regulation of nuclear-cytoplasmic partitioning by the lin-28 - lin-46 pathway reinforces microRNA repression of HBL-1 to confer robust cell-fate progression in C. elegans
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Widespread Parallel Evolution in Sticklebacks by Repeated Fixation of Ectodysplasin Alleles
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Serotonin Transporter Genetic Variation and the Response of the Human Amygdala
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Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis
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Serotonin transporter gene polymorphisms, alcoholism, and suicidal behavior
2000
Deciphering the structural framework of glycine receptor anchoring by gephyrin
2006
A Gja8 (Cx50) point mutation causes an alteration of alpha3 connexin (Cx46) in semi-dominant cataracts of Lop10 mice
2002
CRYBA3/A1 Gene Mutation Associated with Suture-Sparing Autosomal Dominant Congenital Nuclear Cataract: A Novel Phenotype
2004
Are different events involved in the development of sporadic versus hereditary tumours? The possible importance of the microenvironment in hereditary cancer
1990
Looping versus linking: toward a model for long-distance gene activation
1999
Patterns of Positive Selection in Six Mammalian Genomes
2008
Frequency of long allele in serotonin transporter gene is increased in depressed suicide victims
1999
Neuroligin 2 Drives Postsynaptic Assembly at Perisomatic Inhibitory Synapses through Gephyrin and Collybistin
2009
Huntington's disease
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Neural Synchrony in Brain Disorders: Relevance for Cognitive Dysfunctions and Pathophysiology
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Mammalian phosphoinositide kinases and phosphatases
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Imipramine Treatment and Resiliency Exhibit Similar Chromatin Regulation in the Mouse Nucleus Accumbens in Depression Models
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The Neurovascular Unit Coming of Age: A Journey through Neurovascular Coupling in Health and Disease
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Neuroticism and polymorphisms in the serotonin transporter gene
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A family-based association study of schizophrenia with polymorphisms at three candidate genes
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1998
Deductive Genomics
2002
Chapter 32 The Role of Musculoskeletal Mechanics in Motor Coordination
1999
Tumor suppressor genes
1991 Standout
Genetic analysis of synaptotagmin 2 in spontaneous and Ca2+‐triggered neurotransmitter release
2006 StandoutNobel
A deletion mutation in the ?A1/A3 crystallin gene (CRYBA1/A3) is associated with autosomal dominant congenital nuclear cataract in a Chinese family
2004
Genome-wide scan for schizophrenia in the Finnish population: evidence for a locus on chromosome 7q22
2000
The Cellular Phase of Alzheimer’s Disease
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Alzheimer Disease: An Update on Pathobiology and Treatment Strategies
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Genetic epilepsy model derived from common inbred mouse strains.
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Gap junctions and the connexin protein family
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1998
Autism-Associated Neuroligin-3 Mutations Commonly Disrupt Tonic Endocannabinoid Signaling
2013 StandoutNobel
Ataxia, arrhythmia and ion-channel gene defects
1998
Risk factors for suicidal thoughts and behaviors: A meta-analysis of 50 years of research.
2016 Standout
Periventricular Heterotopia: An X-Linked Dominant Epilepsy Locus Causing Aberrant Cerebral Cortical Development
1996
An autism‐associated point mutation in the neuroligin cytoplasmic tail selectively impairs AMPA receptor‐mediated synaptic transmission in hippocampus
2011 StandoutNobel
European Resuscitation Council Guidelines for Resuscitation 2010 Section 4. Adult advanced life support
2010 Standout
Splice-specific Functions of Gephyrin in Molybdenum Cofactor Biosynthesis
2008
Beyond diathesis stress: Differential susceptibility to environmental influences.
2009 Standout
Regulation of β-globin gene expression: straightening out the locus
1996
Neural Science: A Century of Progress and the Mysteries that Remain
2000 StandoutNobel
Courtship and Other Behaviors Affected by a Heat-Sensitive, Molecularly Novel Mutation in the cacophony Calcium-Channel Gene of Drosophila
2002 StandoutNobel
Serotonin transporter gene polymorphisms are associated with anxiety‐related personality traits in women
2001
Major Depressive Disorder
2008 Standout
Crystallin γB-I4F Mutant Protein Binds to α-Crystallin and Affects Lens Transparency
2005 StandoutNobel
The PtdIns(3,4)P2 phosphatase INPP4A is a suppressor of excitotoxic neuronal death
2010 StandoutNatureNobel
Meta-analyses of genetic studies on major depressive disorder
2007
Gephyrin: where do we stand, where do we go?
2008
Meta-analysis of serotonin transporter polymorphisms and affective disorders
2004
The Endophenotype Concept in Psychiatry: Etymology and Strategic Intentions
2003 Standout
Glycine receptor antibodies in PERM and related syndromes: characteristics, clinical features and outcomes
2014
The glial growth factors deficiency and synaptic destabilization hypothesis of schizophrenia
2002
Cell death triggered by a novel mutation in the alphaA-crystallin gene underlies autosomal dominant cataract linked to chromosome 21q
2003
Socio-economic status covaries with central nervous system serotonergic responsivity as a function of allelic variation in the serotonin transporter gene-linked polymorphic region
2003
The molecular neurobiology of depression
2008 StandoutNature
Molecular Neurobiology and Genetics: Investigation of Neural Function and Dysfunction
1998
The Human Condition—A Molecular Approach
2014 StandoutNobel
Distinct and predictive chromatin signatures of transcriptional promoters and enhancers in the human genome
2007 Standout
Single-cell transcriptomic analysis of Alzheimer’s disease
2019 StandoutNature
The Neuropathology of Huntington’s Disease
2014
Decreased apoptosis in the brain and premature lethality in CPP32-deficient mice
1996 StandoutNature
Beta and Gamma Range EEG Power‐Spectrum Correlation with Spiking Discharges in DBA/2J Mice Absence Model: Role of GABAB Receptors
2006
Pharmacogenetics and the serotonin system: initial studies and future directions
2000
Monoamine Oxidase in Neuropsychiatry and Behavior
1999
MDGAs interact selectively with neuroligin-2 but not other neuroligins to regulate inhibitory synapse development
2012 StandoutNobel
Ligand-Gated Ion Channels: New Insights into Neurological Disorders and Ligand Recognition
2012
Synthesis of Serotonin by a Second Tryptophan Hydroxylase Isoform
2003 StandoutScience
Antibody-Mediated Encephalitis
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Inactivation of a Serotonin-Gated Ion Channel by a Polypeptide Toxin from Marine Snails
1998 StandoutScienceNobel
Multiple Sclerosis
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Disruption ofGja8(α8 connexin) in mice leads to microphthalmia associated with retardation of lens growth and lens fiber maturation
2002
The Human Genome Project and Its Impact on Psychiatry
2002
Metal insertion into the molybdenum cofactor: product–substrate channelling demonstrates the functional origin of domain fusion in gephyrin
2012
Neural Science
2000 StandoutNobel
Human TKTL1 implies greater neurogenesis in frontal neocortex of modern humans than Neanderthals
2022 StandoutScienceNobel
CONNEXINS AND CELL SIGNALING IN DEVELOPMENT AND DISEASE
2004
Influence of Life Stress on Depression: Moderation by a Polymorphism in the 5-HTT Gene
2003 StandoutScience
A novel mutation in GJA3 (connexin46) for autosomal dominant congenital nuclear pulverulent cataract.
2003
Location of a Major Susceptibility Locus for Familial Schizophrenia on Chromosome 1q21-q22
2000 Science
Vertebrate-specific sequences in the gephyrin E-domain regulate cytosolic aggregation and postsynaptic clustering
2007
Neuroligins/LRRTMs prevent activity- and Ca2+/calmodulin-dependent synapse elimination in cultured neurons
2011 StandoutNobel
Genetic Dissection of Complex Traits
1994 StandoutScience
Imaging neurochemical endophenotypes: promises and pitfalls
2001
A novel missense mutation in the gene for gap-junction protein alpha3 (GJA3) associated with autosomal dominant "nuclear punctate" cataracts linked to chromosome 13q.
2004
A novel connexin46 (GJA3) mutation in autosomal dominant congenital nuclear pulverulent cataract.
2004
2015
The Mononuclear Molybdenum Enzymes
2014 Standout
CpG island clones from a deletion encompassing the gene for adenomatous polyposis coli.
1989
Effect of COMT Val 108/158 Met genotype on frontal lobe function and risk for schizophrenia
2001 Standout
Emerging Targets in Photopharmacology
2016 StandoutNobel
Current Understanding of Pathogenesis and Treatment of TMJ Osteoarthritis
2015 Standout
Histone H3K27ac separates active from poised enhancers and predicts developmental state
2010 Standout
How Animals Move: An Integrative View
2000 StandoutScience
The β Subunit of Voltage-Gated Ca2+Channels
2010
Vascular Degeneration in P arkinson's Disease
2012
Conservation of sequence and structure flanking the mouse and human β-globin loci: The β-globin genes are embedded within an array of odorant receptor genes
1999 StandoutNobel
Physiology of Microglia
2011 Standout
Diverse gap junctions modulate distinct mechanisms for fiber cell formation during lens development and cataractogenesis
2006 StandoutNobel
LINKAGE ANALYSIS IN PSYCHIATRIC DISORDERS : The Emerging Picture
2002
Works of Mark I. Rees being referenced
Dynamic changes in myelin aberrations and oligodendrocyte generation in chronic amyloidosis in mice and men
2012
Hyperekplexia associated with compound heterozygote mutations in the beta-subunit of the human inhibitory glycine receptor (GLRB)
2002
The genetics of hyperekplexia: more than startle!
2008
GABAA receptor subunit and gephyrin protein changes differ in the globus pallidus in Huntington's diseased brain
2003
TUBA1A mutations cause wide spectrum lissencephaly (smooth brain) and suggest that multiple neuronal migration pathways converge on alpha tubulins
2010
Compound heterozygosity and nonsense mutations in the α1-subunit of the inhibitory glycine receptor in hyperekplexia
2001
Immunohistochemical staining of post-mortem adult human brain sections
2006
A Two-Stage Genome Scan for Schizophrenia Susceptibility Genes in 196 Affected Sibling Pairs
1999
The GDP-GTP Exchange Factor Collybistin: An Essential Determinant of Neuronal Gephyrin Clustering
2004
Autosome search for schizophrenia susceptibility genes in multiply affected families
1999
No evidence for allelic association between bipolar disorder and monoamine oxidase a gene polymorphisms
1995
Isoform Heterogeneity of the Human Gephyrin Gene (GPHN), Binding Domains to the Glycine Receptor, and Mutation Analysis in Hyperekplexia
2003
Red cell dimorphism in a young man with a constitutional chromosomal translocation t(11;22)(p15.5;q11.21)
1994
A genomewide linkage study of age at onset in schizophrenia*
2001
Further evidence of autosomal dominant congenital zonular pulverulent cataracts linked to 13q11 (CZP3) and a novel mutation in connexin 46 (GJA 3 )
2000
Linkage analysis in an autosomal dominant ‘zonular nuclear pulverulent’ congenital cataract, mapped to chromosome 13q11-13
2000
Misdiagnosis of Long QT Syndrome as Epilepsy at First Presentation
2009
Bipolar disorder and the serotonin transporter gene: a family-based association study
1999
Evidence for recessive as well as dominant forms of startle disease (hyperekplexia) caused by mutations in the α1 subunit of the inhibitory glycine receptor
1994
Mutations in the gene encoding GlyT2 (SLC6A5) define a presynaptic component of human startle disease
2006
Chromosome 5 allele loss in familial and sporadic colorectal adenomas
1989
Osteoarthritis in temporomandibular joint of Col2a1 mutant mice
2013
Association studies of bipolar disorder at the human serotonin transporter gene (hSERT; 5HTT)
1997
Differential localization of γ‐aminobutyric acid type a and glycine receptor subunits and gephyrin in the human pons, medulla oblongata and uppermost cervical segment of the spinal cord: An immunohistochemical study
2009
Linkage analysis of idiopathic generalized epilepsy (IGE) and marker loci on chromosome 6p in families of patients with juvenile myoclonic epilepsy: no evidence for an epilepsy locus in the HLA region.
1993
Linkage analysis between idiopathic generalized epilepsies and the GABAA receptor α5, β3 and γ3 subunit gene cluster on chromosome 15
2009
Studies of the lethargic (lh/lh) mouse model of absence seizures: regulatory mechanisms and identification of the lh gene.
1999