Citation Impact
Citing Papers
A functional genetic variation of adenosine deaminase affects the duration and intensity of deep sleep in humans
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Persistent epigenetic differences associated with prenatal exposure to famine in humans
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Complement Factor H Polymorphism and Age-Related Macular Degeneration
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Normal gut microbiota modulates brain development and behavior
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The 2.6 Angstrom Crystal Structure of a Human A 2A Adenosine Receptor Bound to an Antagonist
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Complement Factor H Polymorphism in Age-Related Macular Degeneration
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Pregnancy, Delivery, and Neonatal Complications in a Population Cohort of Women With Schizophrenia and Major Affective Disorders
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The relationship between stressful life events, the serotonin transporter (5-HTTLPR) genotype and major depression
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No health without mental health
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RIM1α and Interacting Proteins Involved in Presynaptic Plasticity Mediate Prepulse Inhibition and Additional Behaviors Linked to Schizophrenia
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Mutation analysis of the human dystrobrevin-binding protein 1 gene in schizophrenic patients
2004
Base-excision repair of oxidative DNA damage
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Vitamin D and type 1 diabetes mellitus: state of the art
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Effect of Antidepressant Drugs in Mice Lacking the Norepinephrine Transporter
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Role of glutamate in schizophrenia: integrating excitatory avenues of research
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Psoriasis
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Two stage genome–wide search in inflammatory bowel disease provides evidence for susceptibility loci on chromosomes 3, 7 and 12
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High Prevalence of Vitamin D Inadequacy and Implications for Health
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Linkage and associated studies of schizophrenia
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Schizophrenia, vitamin D, and brain development
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Dynamic control of neuroexocytosis by phosphoinositides in health and disease
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Age-related changes in the expression of schizophrenia susceptibility genes in the human prefrontal cortex
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Mammalian phosphoinositide kinases and phosphatases
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Identification and characterization of a spinal muscular atrophy-determining gene
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Cis-acting variation in the expression of a high proportion of genes in human brain
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Pathogenesis and therapy of psoriasis
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Pharmacodynamics of Intravenous and Oral Midazolam in Preterm Infants
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A Two-Stage Genome Scan for Schizophrenia Susceptibility Genes in 196 Affected Sibling Pairs
1999
Synaptic defects in ataxia mice result from a mutation in Usp14, encoding a ubiquitin-specific protease
2002
Vitamin D Deficiency
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Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's disease
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The DTNBP1 (Dysbindin) Gene Contributes to Schizophrenia, Depending on Family History of the Disease
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Maternal and child undernutrition and overweight in low-income and middle-income countries
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A Genomic and Functional Inventory of Deubiquitinating Enzymes
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Lessons from Hereditary Colorectal Cancer
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International Union of Basic and Clinical Pharmacology. LXXXI. Nomenclature and Classification of Adenosine Receptors—An Update
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Human Dysbindin (DTNBP1) Gene Expression inNormal Brain and in Schizophrenic Prefrontal Cortex and Midbrain
2004
PLINK: A Tool Set for Whole-Genome Association and Population-Based Linkage Analyses
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Linkage of the Gene for an Autosomal Dominant Form of Juvenile Amyotrophic Lateral Sclerosis to Chromosome 9q34
1998
Head-up tilt induced syncope and adenosine A2A receptor gene polymorphism
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Principal components analysis corrects for stratification in genome-wide association studies
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The Molecular Genetics of Schizophrenia
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A Test for Linkage and Association in General Pedigrees: The Pedigree Disequilibrium Test
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Evidence of novel neuronal functions of dysbindin, a susceptibility gene for schizophrenia
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Psoriasis
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Membrane protein sequestering by ionic protein–lipid interactions
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A Genetic Variation in the Adenosine A2A Receptor Gene (ADORA2A) Contributes to Individual Sensitivity to Caffeine Effects on Sleep
2007
Investigation of the G protein subunit Gαolf gene (GNAL) in attention deficit/hyperactivity disorder
2006
Meta-analysis of association between the T102C polymorphism of the 5HT2a receptor gene and schizophrenia
2003
A T1083C polymorphism in the human adenosine A2a receptor gene is not associated with essential hypertension
1998
Inflammatory Bowel Disease
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Crystal structure of a bacterial homologue of Na+/Cl--dependent neurotransmitter transporters
2005 StandoutNature
Neocortical excitation/inhibition balance in information processing and social dysfunction
2011 StandoutNature
Neurocognitive correlates of the COMT Val158Met polymorphism in chronic schizophrenia
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Genes for schizophrenia? Recent findings and their pathophysiological implications
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The ABC of APC
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Adenosine A2A receptor gene: Evidence for association of risk variants with panic disorder and anxious personality
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Rethinking schizophrenia
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Association Between A2a Receptor Gene Polymorphisms and Caffeine-Induced Anxiety
2003
Sequence and Haplotype Analysis Supports HLA-C as the Psoriasis Susceptibility 1 Gene
2006
Identification in 2 Independent Samples of a Novel Schizophrenia RiskHaplotype of the Dystrobrevin Binding Protein Gene (DTNBP1)
2004
Genomewide Scan of Multiple Sclerosis in Finnish Multiplex Families
1997
Chromosome 1 loci in Finnish schizophrenia families
2001
Schizophrenia genes, gene expression, and neuropathology: on the matter of their convergence
2004 Standout
Strong evidence for association between the dystrobrevin binding protein 1 gene (DTNBP1) and schizophrenia in 488 parent-offspring trios from Bulgaria
2004
Support for RGS4 as a susceptibility gene for schizophrenia
2004
A schizophrenia-linked mutation in PIP5K2A fails to activate neuronal M channels
2008
Evidence for Genetic Linkage Between a Polymorphism in the Adenosine 2A Receptor and Panic Disorder
2003
The adenomatous polyposis coli (APC) tumor suppressor
1997
Major Depressive Disorder
2008 Standout
The molecular genetics of schizophrenia: new findings promise new insights
2003
Distribution, biochemistry and function of striatal adenosine A2A receptors
1999
Polymorphisms in Adenosine Receptor Genes are Associated with Infarct Size in Patients with Ischemic Cardiomyopathy
2007
Dysbindin-1 is reduced in intrinsic, glutamatergic terminals of the hippocampal formation in schizophrenia
2004
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
Airway Mucus Function and Dysfunction
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BTLA is a lymphocyte inhibitory receptor with similarities to CTLA-4 and PD-1
2003 StandoutNobel
Multiple Sclerosis
2000 Standout
Association between ADORA2A and DRD2 Polymorphisms and Caffeine-Induced Anxiety
2008
Vitamin D and autoimmune diabetes
2003
Monoamine transporter gene structure and polymorphisms in relation to psychiatric and other complex disorders
2002
The molecular classification of the clinical manifestations of Crohn's disease
2002
Current knowledge of Japanese type 1 diabetic syndrome
2002
Circumventing multiple testing: A multilocus Monte Carlo approach to testing for association
2000
Environmental and Heritable Factors in the Causation of Cancer — Analyses of Cohorts of Twins from Sweden, Denmark, and Finland
2000 Standout
Polymorphisms in the 3′-untranslated region of human and monkey dopamine transporter genes affect reporter gene expression
2002
Examination of G72 and D-amino-acid oxidase as genetic risk factors for schizophrenia and bipolar affective disorder
2004
The glial growth factors deficiency and synaptic destabilization hypothesis of schizophrenia
2002
Common Genetic Vulnerability to Depressive Symptoms and Coronary Artery Disease: A Review and Development of Candidate Genes Related to Inflammation and Serotonin
2006
Linkage of schizophrenia with chromosome 1q loci in Taiwanese families
2003
The molecular neurobiology of depression
2008 StandoutNature
Hermansky-Pudlak syndrome type 7 (HPS-7) results from mutant dysbindin, a member of the biogenesis of lysosome-related organelles complex 1 (BLOC-1)
2003
Neuregulin 1 and schizophrenia
2004
Amyotrophic Lateral Sclerosis
2001 Standout
Association Between a Functional Catechol O-Methyltransferase Gene Polymorphism and Schizophrenia: Meta-Analysis of Case-Control and Family-Based Studies
2003
Uropathic Observations in Mice Expressing a Constitutively Active Point Mutation in the 5-HT3AReceptor Subunit
2004 StandoutNobel
Pharmacogenetics and the serotonin system: initial studies and future directions
2000
Developmental Pharmacology — Drug Disposition, Action, and Therapy in Infants and Children
2003 Standout
Interleukin-1β Causes Pulmonary Inflammation, Emphysema, and Airway Remodeling in the Adult Murine Lung
2005
Attenuated familial adenomatous polyposis due to a mutation in the 3′ part of the APC gene. A clue for understanding the function of the APC protein
1996
Slc15a4, AP-3, and Hermansky-Pudlak syndrome proteins are required for Toll-like receptor signaling in plasmacytoid dendritic cells
2010 StandoutNobel
Synthesis of Serotonin by a Second Tryptophan Hydroxylase Isoform
2003 StandoutScience
GABAAReceptors Mediate Trophic Effects of GABA on Embryonic Brainstem Monoamine NeuronsIn Vitro
1997
Gain of Function Mutants: Ion Channels and G Protein-Coupled Receptors
2000
Severe Gardner syndrome in families with mutations restricted to a specific region of the APC gene.
1995
GABAA receptors mediate trophic effects of GABA on embryonic brainstem monoamine neurons in vitro.
1997
Haplotype analysis in population genetics and association studies
2003
Nod2-Dependent Regulation of Innate and Adaptive Immunity in the Intestinal Tract
2005 StandoutScience
β-Arrestin1 modulates lymphoid enhancer factor transcriptional activity through interaction with phosphorylated dishevelled proteins
2001 StandoutNobel
Association between Ag1-CA alleles and severity of autosomal recessive proximal spinal muscular atrophy.
1994
The Future of Genetic Studies of Complex Human Diseases
1996 StandoutScience
Genetic Dissection of Complex Traits
1994 StandoutScience
Activation of β-Catenin-Tcf Signaling in Colon Cancer by Mutations in β-Catenin or APC
1997 StandoutScience
The cyclin D1 gene is a target of the β-catenin/LEF-1 pathway
1999 Standout
Effect of COMT Val 108/158 Met genotype on frontal lobe function and risk for schizophrenia
2001 Standout
International Union of Pharmacology. XXV. Nomenclature and Classification of Adenosine Receptors
2001 Standout
Association of Anxiety-Related Traits with a Polymorphism in the Serotonin Transporter Gene Regulatory Region
1996 StandoutScience
Genetics of psychosis; insights from views across the genome
2009
Dysbindin-1 is reduced in intrinsic, glutamatergic terminals of the hippocampal formation in schizophrenia
2004
Quantitative high-throughput analysis of DNA methylation patterns by base-specific cleavage and mass spectrometry
2005
Cleft palate in mice with a targeted mutation in the γ-aminobutyric acid-producing enzyme glutamic acid decarboxylase 67
1997 StandoutNobel
Works of Michael Knapp being referenced
Linkage Analysis in Nuclear Families
1994
Adenosine A1 receptor and bipolar affective disorder: systematic screening of the gene and association studies
1998
Familial adenomatous polyposis: mutation at codon 1309 and early onset of colon cancer
1994
Support for Association of Schizophrenia with Genetic Variation in the 6p22.3 Gene, Dysbindin, in Sib-Pair Families with Linkage and in an Additional Sample of Triad Families
2003
Systematic mutation screening and association study of the A1 and A2a adenosine receptor genes in panic disorder suggest a contribution of the A2a gene to the development of disease
1998
Association between hSKCa3 and schizophrenia not confirmed by transmission disequilibrium test in 193 offspring/parents trios
1999
Human adenosine A2a receptor (A2aAR) gene: systematic mutation screening in patients with schizophrenia
1996
Maximum‐likelihood estimation of haplotype frequencies in nuclear families
2004
The human dopamine transporter gene: the 5′-flanking region reveals five diallelic polymorphic sites in a Caucasian population sample
2001
Association analysis of the functional monoamine oxidase a gene promoter polymorphism in psychiatric disorders
2001
Serotonin transporter gene and schizophrenia: evidence for association/linkage disequilibrium in families with affected siblings
2000
Systematic screening for DNA sequence variation in the coding region of the human dopamine transporter gene (DAT1)
2000
Association study of the low-activity allele of catechol-O-methyltransferase and alcoholism using a family-based approach
2000
Large Linkage Analysis in 100 Families with Autosomal Recessive Spinal Muscular Atrophy (SMA) and 11 CEPH Families Using 15 Polymorphic Loci in the Region 5q11.2-q13.3
1994
Early ontogeny of the central benzodiazepine receptor in human embryos and fetuses
1988
Short CAG repeats within the hSKCa3 gene associated with schizophrenia
1998
Ontogeny of the Benzodiazepine Receptor in Human Brain: Fluorographic, Immunochemical, and Reversible Binding Studies
1991
Systematic search for variation in the human norepinephrine transporter gene: Identification of five naturally occurring missense mutations and study of association with major psychiatric disorders
1996
Support for a Chromosome 18p Locus Conferring Susceptibility to Functional Psychoses in Families with Schizophrenia, by Association and Linkage Analysis
1998
The Transmission/Disequilibrium Test and Parental-Genotype Reconstruction: The Reconstruction-Combined Transmission/ Disequilibrium Test
1999
Further evidence for the involvement ofMYH9in the etiology of non‐syndromic cleft lip with or without cleft palate
2009
Efficiency of Haplotype Frequency Estimation when Nuclear Familiy Information Is Included
2002
Systematic screening for mutations in the human serotonin-2A (5-HT2A) receptor gene: Identification of two naturally occurring receptor variants and association analysis in schizophrenia
1996
Gene and Haplotype Frequencies of HLA Antigens in 269 Patients with Crohn's Disease
1990
Association of tumor necrosis factor alpha gene -G308A polymorphism with schizophrenia
2003
High-resolution snp scan of chromosome 6p21 in pooled samples from patients with complex diseases
2003
High ethanol tolerance in young adults is associated with the low-activity variant of the promoter of the human serotonin transporter gene
1998
Linkage Analysis in Nuclear Families
1994
Association of the Interleukin-1 Receptor Antagonist Gene with Asthma
2004
The haplotype-relative-risk (HRR) method for analysis of association in nuclear families.
1993
Evidence for association of DNA sequence variants in the phosphatidylinositol-4-phosphate 5-kinase IIα gene (PIP5K2A) with schizophrenia
2006
Vitamin D receptor allele combinations influence genetic susceptibility to type 1 diabetes in Germans.
2000