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Genome-wide association study identifies new HLA class II haplotypes strongly protective against narcolepsy

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

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Molecular Genetics of Sleep Disorders
inferredcites →https://doi.org/10.1016/j.gde.2007.04.007openalex-snapshot
Narcolepsy and familial advanced sleep-phase syndrome: molecular genetics of sleep disorders
inferredcites →https://doi.org/10.1016/j.smrv.2007.04.001openalex-snapshot
Diagnosis of narcolepsy and idiopathic hypersomnia. An update based on the International Classification of Sleep Disorders, 2nd edition
inferredcites →https://doi.org/10.1016/s0140-6736(99)05582-8openalex-snapshot
Hypocretin (orexin) deficiency in human narcolepsy
inferredcites →https://doi.org/10.1016/s0166-4328(01)00297-2openalex-snapshot
Controlling the false discovery rate in behavior genetics research
inferredcites →https://doi.org/10.1016/s0896-6273(00)00058-1openalex-snapshot
Reduced Number of Hypocretin Neurons in Human Narcolepsy
inferredcites →https://doi.org/10.1038/79690openalex-snapshot
A mutation in a case of early onset narcolepsy and a generalized absence of hypocretin peptides in human narcoleptic brains
inferredcites →https://doi.org/10.1038/nature05329openalex-snapshot
Global variation in copy number in the human genome
inferredcites →https://doi.org/10.1038/nature06884openalex-snapshot
The complete genome of an individual by massively parallel DNA sequencing
inferredcites →https://doi.org/10.1038/nature07331openalex-snapshot
Genes mirror geography within Europe
inferredcites →https://doi.org/10.1038/nature08979openalex-snapshot
Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls
inferredcites →https://doi.org/10.1038/ng.231openalex-snapshot
Variant between CPT1B and CHKB associated with susceptibility to narcolepsy
inferredcites →https://doi.org/10.1038/ng.238openalex-snapshot
Integrated detection and population-genetic analysis of SNPs and copy number variation
inferredcites →https://doi.org/10.1038/ng.372openalex-snapshot
Narcolepsy is strongly associated with the T-cell receptor alpha locus
inferredcites →https://doi.org/10.1038/nrg1960openalex-snapshot
Genetic relatedness analysis: modern data and new challenges
inferredcites →https://doi.org/10.1056/nejm200009073431006openalex-snapshot
The HLA System
inferredcites →https://doi.org/10.1056/nejm200009143431106openalex-snapshot
The HLA System
inferredcites →https://doi.org/10.1073/pnas.0703834104openalex-snapshot
Systematic prediction and validation of breakpoints associated with copy-number variants in the human genome
inferredcites →https://doi.org/10.1086/318799openalex-snapshot
Complex HLA-DR and -DQ Interactions Confer Risk of Narcolepsy-Cataplexy in Three Ethnic Groups
inferredcites →https://doi.org/10.1086/510560openalex-snapshot
A Comprehensive Analysis of Common Copy-Number Variations in the Human Genome
inferredcites →https://doi.org/10.1093/hmg/ddn246openalex-snapshot
Autoimmune diseases: insights from genome-wide association studies
inferredcites →https://doi.org/10.1093/sleep/17.suppl_8.s60openalex-snapshot
DQB1*0602 and DQA1*0102 (DQ1) Are Better Markers Than DR2 for Narcolepsy in Caucasian and Black Americans
inferredcites →https://doi.org/10.1101/gr.082016.108openalex-snapshot
Copy number variation and evolution in humans and chimpanzees
inferredcites →https://doi.org/10.1111/j.1399-0039.1997.tb02761.xopenalex-snapshot
Extensive HLA class II studies in 58 non‐DRB1*15 (DR2) narcoleptic patients with cataplexy
inferredcites →https://doi.org/10.1146/annurev.genom.9.081307.164242openalex-snapshot
Genotype Imputation
inferredcites →https://doi.org/10.1172/jci41366openalex-snapshot
Elevated Tribbles homolog 2–specific antibody levels in narcolepsy patients
inferredcites →https://doi.org/10.1186/1471-2261-8-6openalex-snapshot
The CoLaus study: a population-based study to investigate the epidemiology and genetic determinants of cardiovascular risk factors and metabolic syndrome

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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Molecular Genetics of Sleep Disorders
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Anti‐LGI1 encephalitis is associated with unique HLA subtypes
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Narcolepsy in Children: Sleep disorders in children, A rapidly evolving field seeking consensus
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Depression in Narcolepsy
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Genetics of Sleep and Sleep Disorders
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Genetics of Central Disorders of Hypersomnolence
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Sonstige neurologische Erkrankungen
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Better Understanding of Severe Immunological Reactions: Autoimmune Diseases
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Genetic Factors in Sleep Disorders: What Are the Roles of Genetic Factors in the Pathogenesis of Sleep Disorders?
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Distribution of HLA-DQB1 in Czech Patients with Central Hypersomnias
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Narkolepsie
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HLA dosage effect in narcolepsy with cataplexy
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Coexisting narcolepsy (with and without cataplexy) and multiple sclerosis
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Higher basophil count decreases narcolepsy risk: a Mendelian randomization study
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Narkolepsie – mit Beachtung der Kataplexie als Differenzialdiagnose epileptischer Anfälle
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Kleine–Levin syndrome
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Genetische Aspekte der REM-Schlaf-Verhaltensstörung
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Genetische Diagnostik von Schlafstörungen
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Narcolepsy in the Pediatric Population
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Narcolepsy Type 1 as an Autoimmune Disorder: Evidence, and Implications for Pharmacological Treatment
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Familial and Genetic Factors
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Immunologic Disorders
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Immunologic and Genetic Aspects of Type 1 Narcolepsy
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Immunologic Disorders: Autoimmunity: Genetics and Immunologic Mechanisms
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Physiopathology of Narcolepsy and Other Central Hypersomnias
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Sleep disorders and the hypothalamus
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Narcolepsy Type I as an autoimmune disorder
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Familial and genetic factors
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Genetics and Genomic Basis of Sleep Disorders in Humans
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Narcolepsy
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Genetics of Sleep and Sleep Disorders in Humans
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Narcolepsy
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Génétique du sommeil normal et des rythmes circadiens
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Narcolepsie
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Narcolepsies
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A Missense Mutation in Myelin Oligodendrocyte Glycoprotein as a Cause of Familial Narcolepsy with Cataplexy
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Abundant Pleiotropy in Human Complex Diseases and Traits
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A Multi-SNP Locus-Association Method Reveals a Substantial Fraction of the Missing Heritability
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Sleep disorders, obesity, and aging: The role of orexin
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Predicting and analyzing early wake-up associated gene expressions by integrating GWAS and eQTL studies
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Cerebrospinal fluid and serum cytokine profiles in narcolepsy with cataplexy: A case-control study
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Immune dysregulation in depression: Evidence from genome-wide association
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Orexin receptors: Multi-functional therapeutic targets for sleeping disorders, eating disorders, drug addiction, cancers and other physiological disorders
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Narcolepsy with hypocretin/orexin deficiency, infections and autoimmunity of the brain
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DQB1*06:02 allele-specific expression varies by allelic dosage, not narcolepsy status
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The MHC, disease and selection
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Genetic association, seasonal infections and autoimmune basis of narcolepsy
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Narcolepsy, 2009 A(H1N1) pandemic influenza, and pandemic influenza vaccinations: What is known and unknown about the neurological disorder, the role for autoimmunity, and vaccine adjuvants
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Impact of cytokine in type 1 narcolepsy: Role of pandemic H1N1 vaccination ?
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Selected human leukocyte antigen class II polymorphisms and risk of adult glioma
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H1N1 hemagglutinin-specific HLA-DQ6-restricted CD4+ T cells can be readily detected in narcolepsy type 1 patients and healthy controls
inferred← citeshttps://doi.org/10.1016/j.jns.2014.09.047openalex-snapshot
miRNA profiles in cerebrospinal fluid from patients with central hypersomnias
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Genetics of Narcolepsy
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Narcolepsy
inferred← citeshttps://doi.org/10.1016/j.neulab.2016.10.001openalex-snapshot
Narkolepsie
inferred← citeshttps://doi.org/10.1016/j.neurol.2011.04.003openalex-snapshot
Narcolepsie avec cataplexie après vaccination anti-H1N1
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Narcolepsie avec cataplexie : maladie modèle de somnolence diurne
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Epidemiology and Pathophysiology of Childhood Narcolepsy
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Genetics of Sleep Disorders
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TCRA, P2RY11, and CPT1B/CHKB associations in Chinese narcolepsy
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Health, social, and economic consequences of narcolepsy: A controlled national study evaluating the societal effect on patients and their partners
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A patient with narcolepsy with cataplexy and multiple sclerosis: two different diseases that may share pathophysiologic mechanisms?
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Correlation between HLA-DQB1*06:02 and narcolepsy with and without cataplexy: approving a safe and sensitive genetic test in four major ethnic groups. A systematic meta-analysis
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Connecting the dots: An updated review of the role of autoimmunity in narcolepsy and emerging immunotherapeutic approaches
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Unraveling the pathophysiology of narcolepsy type 1 through hypothesis-driven and hypothesis-generating approaches
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Catechol-O-methyltransferase, dopamine, and sleep-wake regulation
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The clinical spectrum of childhood narcolepsy
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Neurobiological and immunogenetic aspects of narcolepsy: Implications for pharmacotherapy
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Diagnosis of central disorders of hypersomnolence: A reappraisal by European experts
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Narcolepsy as an adverse event following immunization: Case definition and guidelines for data collection, analysis and presentation
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Narcolepsie : Lien avec l’infection et la vaccination antigrippale H1N1 ?
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Quel apport des centres de référence maladies rares dans la prise en charge des hypersomnies rares ?
inferred← citeshttps://doi.org/10.1016/s1474-4422(14)70075-4openalex-snapshot
Narcolepsy as an autoimmune disease: the role of H1N1 infection and vaccination
inferred← citeshttps://doi.org/10.1016/s1474-4422(14)70218-2openalex-snapshot
Hypocretin (orexin) biology and the pathophysiology of narcolepsy with cataplexy
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Pleiotropic genetic effects influencing sleep and neurological disorders
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Generalprinciples of genetics and genomics
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Genome-wide association study (GWAS) approaches to sleep phenotypes
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Geneticsof sleep and circadian rhythms
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Narcolepsyand hypersomnias
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Genome-wideassociation studies in narcolepsy
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The immunogenetics of narcolepsy associated with A(H1N1)pdm09 vaccination (Pandemrix) supports a potent gene–environment interaction
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An association analysis of HLA-DQB1 with narcolepsy without cataplexy and idiopathic hypersomnia with/without long sleep time in a Japanese population
inferred← citeshttps://doi.org/10.1038/ng.734openalex-snapshot
Common variants in P2RY11 are associated with narcolepsy
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Erratum: Corrigendum: Genome-wide association study identifies new HLA class II haplotypes strongly protective against narcolepsy
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Tissue-specific regulatory circuits reveal variable modular perturbations across complex diseases
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Narcolepsy
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Cataplexy—clinical aspects, pathophysiology and management strategy
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A decade in psychiatric GWAS research
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Genetics of narcolepsy
inferred← citeshttps://doi.org/10.1038/s41467-019-11456-7openalex-snapshot
Genome-wide association analysis of self-reported daytime sleepiness identifies 42 loci that suggest biological subtypes
inferred← citeshttps://doi.org/10.1038/s41467-023-36120-zopenalex-snapshot
Narcolepsy risk loci outline role of T cell autoimmunity and infectious triggers in narcolepsy
inferred← citeshttps://doi.org/10.1038/s41576-022-00519-zopenalex-snapshot
Genetics of circadian rhythms and sleep in human health and disease
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The immunopathogenesis of narcolepsy type 1
inferred← citeshttps://doi.org/10.1038/s41582-019-0226-9openalex-snapshot
Narcolepsy — clinical spectrum, aetiopathophysiology, diagnosis and treatment
inferred← citeshttps://doi.org/10.1038/s41582-023-00776-4openalex-snapshot
Origins and immunopathogenesis of autoimmune central nervous system disorders
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The neurobiological basis of narcolepsy
inferred← citeshttps://doi.org/10.1038/s41598-021-82195-3openalex-snapshot
HLA-DRB1 allelic epitopes that associate with autoimmune disease risk or protection activate reciprocal macrophage polarization
inferred← citeshttps://doi.org/10.1038/s41598-023-37511-4openalex-snapshot
Narcolepsy type I-associated DNA methylation and gene expression changes in the human leukocyte antigen region
inferred← citeshttps://doi.org/10.1038/srep25230openalex-snapshot
Absence of NMDA receptor antibodies in the rare association between Type 1 Narcolepsy and Psychosis
inferred← citeshttps://doi.org/10.1051/jbio/2019026openalex-snapshot
Narcolepsie : une maladie auto-immune affectant un peptide de l’éveil liée à un mimétisme moléculaire avec des épitopes du virus de la grippe
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Diagnosis and Management of Narcolepsy
inferred← citeshttps://doi.org/10.1073/pnas.1818150116openalex-snapshot
Autoimmunity to hypocretin and molecular mimicry to flu in type 1 narcolepsy
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Characterization of T cell receptors reactive to HCRT NH2 , pHA 273-287 , and NP 17-31 in control and narcolepsy patients
inferred← citeshttps://doi.org/10.1080/00207454.2020.1835903openalex-snapshot
The impact of the HLA DQB1 gene and amino acids on the development of narcolepsy
inferred← citeshttps://doi.org/10.1093/brain/awr244openalex-snapshot
Complex movement disorders at disease onset in childhood narcolepsy with cataplexy
inferred← citeshttps://doi.org/10.1093/brain/awt187openalex-snapshot
Increased risk of narcolepsy in children and adults after pandemic H1N1 vaccination in France
inferred← citeshttps://doi.org/10.1093/brain/awt277openalex-snapshot
Clinical and polysomnographic course of childhood narcolepsy with cataplexy
inferred← citeshttps://doi.org/10.1093/hmg/ddu480openalex-snapshot
New susceptibility variants to narcolepsy identified in HLA class II region
inferred← citeshttps://doi.org/10.1093/intimm/dxab079openalex-snapshot
The major histocompatibility complex: new insights from old molecules into the pathogenesis of autoimmunity
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Narcolepsy type 1: what have we learned from genetics?
inferred← citeshttps://doi.org/10.1093/sleep/zsw036openalex-snapshot
Anti-Tribbles Pseudokinase 2 (TRIB2)-Immunization Modulates Hypocretin/Orexin Neuronal Functions
inferred← citeshttps://doi.org/10.1093/sleep/zsw053openalex-snapshot
Familial Aggregation of Insomnia
inferred← citeshttps://doi.org/10.1093/sleep/zsy145openalex-snapshot
Widespread white matter changes in post-H1N1 patients with narcolepsy type 1 and first-degree relatives
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Mechanisms of REM sleep in health and disease
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Autoimmunity in narcolepsy
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Constructing gene network for type 1 narcolepsy based on genome-wide association study and differential gene expression analysis (STROBE)
inferred← citeshttps://doi.org/10.1101/373555openalex-snapshot
Narcolepsy risk loci are enriched in immune cells and suggest autoimmune modulation of the T cell receptor repertoire
inferred← citeshttps://doi.org/10.1101/378109openalex-snapshot
Autoimmunity to hypocretin and molecular mimicry to flu antigens in Type 1 narcolepsy
inferred← citeshttps://doi.org/10.1101/gr.116681.110openalex-snapshot
Pervasive haplotypic variation in the spliceo-transcriptome of the human major histocompatibility complex
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Different fates of excessive daytime sleepiness: survival analysis for remission
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A remarkable effect of alemtuzumab in a patient suffering from narcolepsy with cataplexy
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HLA ‐ DQ association and allele competition in Chinese narcolepsy
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Sleepiness that cannot be overcome: Narcolepsy and cataplexy
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The startle syndromes: Physiology and treatment
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Clinical, polysomnographic and genome‐wide association analyses of narcolepsy with cataplexy: a European Narcolepsy Network study
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Narcolepsy with cataplexy and comorbid immunopathological diseases
inferred← citeshttps://doi.org/10.1111/jsr.70083openalex-snapshot
Orexin Restoration in Narcolepsy: Breakthroughs in Cellular Therapy
inferred← citeshttps://doi.org/10.1111/liv.12492openalex-snapshot
Small duct primary sclerosing cholangitis without inflammatory bowel disease is genetically different from large duct disease
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Influencing circadian and sleep–wake regulation for prevention and intervention in mood and anxiety disorders: what makes a good homeostat?
inferred← citeshttps://doi.org/10.1152/physrev.00032.2011openalex-snapshot
Control of Sleep and Wakefulness
inferred← citeshttps://doi.org/10.1177/10738584211052263openalex-snapshot
Brain Circuits Underlying Narcolepsy
inferred← citeshttps://doi.org/10.1210/endrev/bnad033openalex-snapshot
Appetite- and Weight-Regulating Neuroendocrine Circuitry in Hypothalamic Obesity
inferred← citeshttps://doi.org/10.1371/journal.pcbi.1004711openalex-snapshot
Erosion of Conserved Binding Sites in Personal Genomes Points to Medical Histories
inferred← citeshttps://doi.org/10.1371/journal.pgen.1003225openalex-snapshot
Loci Associated with N-Glycosylation of Human Immunoglobulin G Show Pleiotropy with Autoimmune Diseases and Haematological Cancers
inferred← citeshttps://doi.org/10.1371/journal.pgen.1003270openalex-snapshot
ImmunoChip Study Implicates Antigen Presentation to T Cells in Narcolepsy
inferred← citeshttps://doi.org/10.1371/journal.pgen.1003880openalex-snapshot
Genome Wide Analysis of Narcolepsy in China Implicates Novel Immune Loci and Reveals Changes in Association Prior to Versus After the 2009 H1N1 Influenza Pandemic
inferred← citeshttps://doi.org/10.1371/journal.pone.0020433openalex-snapshot
Low Vitamin D in Narcolepsy with Cataplexy
inferred← citeshttps://doi.org/10.1371/journal.pone.0033536openalex-snapshot
AS03 Adjuvanted AH1N1 Vaccine Associated with an Abrupt Increase in the Incidence of Childhood Narcolepsy in Finland
inferred← citeshttps://doi.org/10.1371/journal.pone.0033723openalex-snapshot
Increased Incidence and Clinical Picture of Childhood Narcolepsy following the 2009 H1N1 Pandemic Vaccination Campaign in Finland
inferred← citeshttps://doi.org/10.1371/journal.pone.0114361openalex-snapshot
Antigenic Differences between AS03 Adjuvanted Influenza A (H1N1) Pandemic Vaccines: Implications for Pandemrix-Associated Narcolepsy Risk
inferred← citeshttps://doi.org/10.1371/journal.pone.0154296openalex-snapshot
No Evidence for Disease History as a Risk Factor for Narcolepsy after A(H1N1)pdm09 Vaccination
inferred← citeshttps://doi.org/10.1371/journal.pone.0222882openalex-snapshot
HLA high-resolution typing by next-generation sequencing in Pandemrix-induced narcolepsy
inferred← citeshttps://doi.org/10.1378/chest.10-1313openalex-snapshot
Genome-Wide Association Studies of Sleep Disorders
inferred← citeshttps://doi.org/10.1517/17460441.2012.651454openalex-snapshot
Models for narcolepsy with cataplexy drug discovery
inferred← citeshttps://doi.org/10.1517/21678707.2013.854701openalex-snapshot
Treatment options in narcolepsy
inferred← citeshttps://doi.org/10.1586/14760584.2015.1038249openalex-snapshot
Adversomics: a new paradigm for vaccine safety and design
inferred← citeshttps://doi.org/10.1586/eci.13.9openalex-snapshot
Systems level immune response analysis and personalized medicine
inferred← citeshttps://doi.org/10.1586/ern.12.165openalex-snapshot
Next-generation sequencing in understanding complex neurological disease
inferred← citeshttps://doi.org/10.17241/smr.2011.2.2.39openalex-snapshot
Immunological and Genetic Aspects of Narcolepsy
inferred← citeshttps://doi.org/10.18632/oncotarget.3001openalex-snapshot
Multilevel-analysis identify a cis-expression quantitative trait locus associated with risk of renal cell carcinoma
inferred← citeshttps://doi.org/10.19271/irons-000125-2020-33openalex-snapshot
NARCOLEPSY
inferred← citeshttps://doi.org/10.21037/atm.2019.12.95openalex-snapshot
Association between genetic risk scores and risk of narcolepsy: a case-control study
inferred← citeshttps://doi.org/10.2147/agg.s57139openalex-snapshot
On the genetics of sleep disorders: genome-wide association studies and beyond
inferred← citeshttps://doi.org/10.2147/ndt.s23624openalex-snapshot
Narcolepsy: a review
inferred← citeshttps://doi.org/10.2147/nss.s195650openalex-snapshot
Immune-mediated comorbidities in Saudi patients with narcolepsy
inferred← citeshttps://doi.org/10.2147/nss.s56077openalex-snapshot
Unmet needs of patients with narcolepsy: perspectives on emerging treatment options
inferred← citeshttps://doi.org/10.2533/chimia.2022.1052openalex-snapshot
PhenoExplorer: An Interactive Web-based Platform for Exploring (Epi)Genome-Wide Associations Using a Swiss Population-based Study
inferred← citeshttps://doi.org/10.3109/00365548.2011.580777openalex-snapshot
Explorations of clinical trials and pharmacovigilance databases of MF59®-adjuvanted influenza vaccines for associated cases of narcolepsy
inferred← citeshttps://doi.org/10.3109/01677063.2011.628426openalex-snapshot
Pharmacological Validation of Candidate Causal Sleep Genes Identified in an N2 Cross
inferred← citeshttps://doi.org/10.33588/rn.5802.2013361openalex-snapshot
Utilidad de la caracterización genética de la narcolepsia y la hipersomnia en la definición del fenotipo: estudio en pacientes portugueses
inferred← citeshttps://doi.org/10.3384/diss.diva-153629openalex-snapshot
Brain Networks and Dynamics in Narcolepsy
inferred← citeshttps://doi.org/10.3389/fgene.2024.1404516openalex-snapshot
More evidence for widespread antagonistic pleiotropy in polymorphic disease alleles
inferred← citeshttps://doi.org/10.3389/fimmu.2022.814967openalex-snapshot
HLA-G and the MHC Cusp Theory
inferred← citeshttps://doi.org/10.3389/fneur.2015.00123openalex-snapshot
REM Sleep at its Core – Circuits, Neurotransmitters, and Pathophysiology
inferred← citeshttps://doi.org/10.3390/neurosci4040022openalex-snapshot
Exploring the Literature on Narcolepsy: Insights into the Sleep Disorder That Strikes during the Day
inferred← citeshttps://doi.org/10.34626/h6vb-jt96openalex-snapshot
Identificação de Factores Genéticos de Risco em Indivíduos com Patologias do Sono
inferred← citeshttps://doi.org/10.4103/1673-5374.280322openalex-snapshot
Differences in clinical and genetic characteristics between early- and late-onset narcolepsy in a Han Chinese cohort
inferred← citeshttps://doi.org/10.4161/hv.27412openalex-snapshot
Narcolepsy and A(H1N1)pdm09 vaccination
inferred← citeshttps://doi.org/10.4274/jtsm.02.001openalex-snapshot
Narcolepsy, Along with an Update
inferred← citeshttps://doi.org/10.4414/smf.2011.07512openalex-snapshot
Neurologie: Jahresrückblick 2010. Teil 1
inferred← citeshttps://doi.org/10.4414/smf.2011.07517openalex-snapshot
Neurologie: Jahresrückblick 2010. Teil 2
inferred← citeshttps://doi.org/10.4414/smf.2012.07734openalex-snapshot
Neurologie: Narkolepsie, eine Folge der H1N1-Grippeimpfung?
inferred← citeshttps://doi.org/10.5255/ukda-sn-855743openalex-snapshot
Drugs and (Dis)order Spatial Borderland Biography Myanmar, 2017-2021
inferred← citeshttps://doi.org/10.5664/jcsm.10748openalex-snapshot
A series of 7 cases of patients with narcolepsy with hypocretin deficiency without the HLA DQB1*06:02 allele
inferred← citeshttps://doi.org/10.5664/jcsm.11300openalex-snapshot
Association between human leukocyte antigen class II-DR-DQ and narcolepsy: a case control study
inferred← citeshttps://doi.org/10.5664/jcsm.11368openalex-snapshot
Increased neutrophil-to-lymphocyte ratio as a possible marker to detect neuroinflammation in patients with narcolepsy type 1
inferred← citeshttps://doi.org/10.5665/sleep.1366openalex-snapshot
Genetic Underpinnings of Obstructive Sleep Apnea: Are We Making Progress?
inferred← citeshttps://doi.org/10.5665/sleep.2706openalex-snapshot
Comorbidity and Mortality of Narcolepsy: A Controlled Retro- and Prospective National Study
inferred← citeshttps://doi.org/10.5665/sleep.2880openalex-snapshot
Sleep Transitions in Hypocretin-Deficient Narcolepsy
inferred← citeshttps://doi.org/10.5665/sleep.3300openalex-snapshot
DQB1 Locus Alone Explains Most of the Risk and Protection in Narcolepsy with Cataplexy in Europe
inferred← citeshttps://doi.org/10.5665/sleep.5532openalex-snapshot
Narcolepsy-Associated HLA Class I Alleles Implicate Cell-Mediated Cytotoxicity
inferred← citeshttps://doi.org/10.70675/a0cc808czdf74z4a99z91f8zd5b53280d506openalex-snapshot
Séléction de CD8 non conventionnel au cours de la thymopoïèse humaine
inferred← citeshttps://doi.org/10.70675/e85baa14za470z42efz9c22z80d16e6155bfopenalex-snapshot
Étude génétique de la voie sérotonine-N-acétylsérotonine-mélatonine et de ses anomalies dans la vulnérabilité aux Troubles du Spectre Autistique (TSA) et dans la prématurité
inferred← citeshttps://doi.org/10.7150/ijms.41812openalex-snapshot
Analyzing Functional Pathways and constructing gene-gene network for Narcolepsy based on candidate genes
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