| review article | Q7318358 |
| scholarly article | Q13442814 |
| P356 | DOI | 10.1097/J.PAIN.0000000000001099 |
| P8608 | Fatcat ID | release_pqfubr6embcehkkrvjsmsciuq4 |
| P932 | PMC publication ID | 5828382 |
| P698 | PubMed publication ID | 29240606 |
| P50 | author | Marc Parisien | Q42754877 |
| Katerina Zorina-Lichtenwalter | Q116455839 | ||
| P2093 | author name string | Luda Diatchenko | |
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| The Domain II S4-S5 Linker in Nav1.9: A Missense Mutation Enhances Activation, Impairs Fast Inactivation, and Produces Human Painful Neuropathy. | Q41190621 | ||
| Interactions of sympathetic and primary afferent neurons following nerve injury and tissue trauma | Q41330826 | ||
| TNF Block Gene Variants Associate With Pain Intensity in Black Southern Africans With HIV-associated Sensory Neuropathy | Q41440466 | ||
| Association of functional variations in COMT and GCH1 genes with postherniotomy pain and related impairment | Q41564087 | ||
| Identification of a novel nonsense mutation of the neurotrophic tyrosine kinase receptor type 1 gene in two siblings with congenital insensitivity to pain with anhidrosis | Q41775115 | ||
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| The COMT rs4680 Met allele contributes to long-lasting low back pain, sciatica and disability after lumbar disc herniation. | Q44293079 | ||
| KCNS1, but not GCH1, is associated with pain intensity in a black southern African population with HIV-associated sensory neuropathy: a genetic association study | Q44297950 | ||
| Pain intensity the first year after lumbar disc herniation is associated with the A118G polymorphism in the opioid receptor mu 1 gene: evidence of a sex and genotype interaction. | Q44335213 | ||
| The interleukin-1α gene C>T polymorphism rs1800587 is associated with increased pain intensity and decreased pressure pain thresholds in patients with lumbar radicular pain | Q44346774 | ||
| Hereditary sensory and autonomic neuropathy type IID caused by an SCN9A mutation | Q45221134 | ||
| Chronic non-paroxysmal neuropathic pain - Novel phenotype of mutation in the sodium channel SCN9A gene | Q45343737 | ||
| Gain-of-function mutations in sodium channel Na(v)1.9 in painful neuropathy | Q45771999 | ||
| A novel mutation in SCN9A in a child with congenital insensitivity to pain | Q45803976 | ||
| NaV1.7 gain-of-function mutations as a continuum: A1632E displays physiological changes associated with erythromelalgia and paroxysmal extreme pain disorder mutations and produces symptoms of both disorders. | Q46301976 | ||
| Small-fiber neuropathy Nav1.8 mutation shifts activation to hyperpolarized potentials and increases excitability of dorsal root ganglion neurons. | Q46987387 | ||
| Early- and late-onset inherited erythromelalgia: genotype-phenotype correlation | Q48001757 | ||
| Novel mutation in the replication focus targeting sequence domain of DNMT1 causes hereditary sensory and autonomic neuropathy IE. | Q48114368 | ||
| Pathological C-fibres in patients with a chronic painful condition | Q48395852 | ||
| Functional profiles of SCN9A variants in dorsal root ganglion neurons and superior cervical ganglion neurons correlate with autonomic symptoms in small fibre neuropathy. | Q48430447 | ||
| Variation in the dopamine D2 receptor gene plays a key role in human pain and its modulation by transcranial magnetic stimulation | Q48569654 | ||
| Analysis of a previously identified "pain-protective" haplotype and individual polymorphisms in the GCH1 gene in Africans with HIV-associated sensory neuropathy: a genetic association study | Q48682392 | ||
| High association of IL-4 gene intron 3 VNTR polymorphism with diabetic peripheral neuropathy. | Q50903298 | ||
| Identification of a novel gene (HSN2) causing hereditary sensory and autonomic neuropathy type II through the Study of Canadian Genetic Isolates | Q24323217 | ||
| Mutations in FAM134B, encoding a newly identified Golgi protein, cause severe sensory and autonomic neuropathy | Q24336807 | ||
| Transcriptional regulator PRDM12 is essential for human pain perception | Q24337786 | ||
| Tissue-specific expression of a splicing mutation in the IKBKAP gene causes familial dysautonomia | Q24536194 | ||
| Familial dysautonomia is caused by mutations of the IKAP gene | Q24536229 | ||
| Mutations in DNMT1 cause hereditary sensory neuropathy with dementia and hearing loss | Q24630545 | ||
| Mutations in the nervous system--specific HSN2 exon of WNK1 cause hereditary sensory neuropathy type II | Q24648539 | ||
| Mutations in SCN9A, encoding a sodium channel alpha subunit, in patients with primary erythermalgia | Q24675844 | ||
| Trigeminal neuralgia: New classification and diagnostic grading for practice and research | Q26745858 | ||
| Genetic predictors of human chronic pain conditions | Q26753046 | ||
| Neuropathic pain phenotyping by international consensus (NeuroPPIC) for genetic studies: a NeuPSIG systematic review, Delphi survey, and expert panel recommendations | Q26782743 | ||
| SCN9A mutations in paroxysmal extreme pain disorder: allelic variants underlie distinct channel defects and phenotypes | Q28118877 | ||
| Heritability of nociception I: responses of 11 inbred mouse strains on 12 measures of nociception | Q28141653 | ||
| SPTLC1 is mutated in hereditary sensory neuropathy, type 1 | Q28204237 | ||
| Mutations in SPTLC1, encoding serine palmitoyltransferase, long chain base subunit-1, cause hereditary sensory neuropathy type I | Q28204289 | ||
| Identification of a novel common genetic risk factor for lumbar disk disease | Q28213177 | ||
| An SCN9A channelopathy causes congenital inability to experience pain | Q28278844 | ||
| A de novo gain-of-function mutation in SCN11A causes loss of pain perception | Q28298515 | ||
| Oral and craniofacial manifestations and two novel missense mutations of the NTRK1 gene identified in the patient with congenital insensitivity to pain with anhidrosis | Q28533935 | ||
| GTP cyclohydrolase and tetrahydrobiopterin regulate pain sensitivity and persistence | Q28567229 | ||
| UK biobank: an open access resource for identifying the causes of a wide range of complex diseases of middle and old age | Q28650740 | ||
| Transient receptor potential channel polymorphisms are associated with the somatosensory function in neuropathic pain patients | Q28741571 | ||
| Taking pain out of NGF: a "painless" NGF mutant, linked to hereditary sensory autonomic neuropathy type V, with full neurotrophic activity | Q28742340 | ||
| A new multipoint method for genome-wide association studies by imputation of genotypes | Q29547209 | ||
| Gain of function NaV1.7 mutations in idiopathic small fiber neuropathy | Q30048469 | ||
| Variations in potassium channel genes are associated with breast pain in women prior to breast cancer surgery. | Q33670792 | ||
| Pain perception is altered by a nucleotide polymorphism in SCN9A | Q33739909 | ||
| Gain and loss of function of P2X7 receptors: mechanisms, pharmacology and relevance to diabetic neuropathic pain. | Q33812164 | ||
| The serotonin transporter gene polymorphism is associated with the susceptibility and the pain severity in idiopathic trigeminal neuralgia patients | Q33841625 | ||
| Congenital insensitivity to pain with anhidrosis (CIPA) in Israeli-Bedouins: genetic heterogeneity, novel mutations in the TRKA/NGF receptor gene, clinical findings, and results of nerve conduction studies | Q33906447 | ||
| Glial activation: a driving force for pathological pain | Q33953790 | ||
| Osteoarthritis pain: nociceptive or neuropathic? | Q51098399 | ||
| Novel NTRK1 Frameshift Mutation in Congenital Insensitivity to Pain With Anhidrosis. | Q51107047 | ||
| Recurrent and novel mutations in the NTRK1 gene lead to rare congenital insensitivity to pain with anhidrosis in two Chinese patients. | Q51140126 | ||
| Economic burden of back and neck pain: effect of a neuropathic component. | Q51243122 | ||
| Novel NTRK1 mutations cause hereditary sensory and autonomic neuropathy type IV: demonstration of a founder mutation in the Turkish population. | Q51574823 | ||
| Prevalence of diabetic peripheral neuropathy and its relation to glycaemic control and potential risk factors: the EURODIAB IDDM Complications Study. | Q51578736 | ||
| Association of the functional A118G polymorphism of OPRM1 in diabetic patients with foot ulcer pain. | Q51756681 | ||
| Mutation and polymorphism analysis of the TRKA (NTRK1) gene encoding a high-affinity receptor for nerve growth factor in congenital insensitivity to pain with anhidrosis (CIPA) families. | Q51974122 | ||
| A neuropathic pain component is common in acute whiplash and associated with a more complex clinical presentation. | Q52851853 | ||
| Exome sequencing identifies novel NTRK1 mutations in patients with HSAN-IV phenotype. | Q53640716 | ||
| [A novel mutation of NTRK1 gene in a family with congenital insensitivity to pain with anhidrosis]. | Q54316744 | ||
| Primary erythermalgia as a sodium channelopathy: screening for SCN9A mutations: exclusion of a causal role of SCN10A and SCN11A. | Q54541742 | ||
| Characterization of a familial case with primary erythromelalgia from Taiwan. | Q55043177 | ||
| A novel NTRK1 mutation in a patient with congenital insensitivity to pain with anhidrosis. | Q55069212 | ||
| Painful micturition in a small child: an unusual clinical picture of paroxysmal extreme pain disorder | Q57715626 | ||
| A Novel Mutation in Motor Domain of KIF5A Associated With an HSP/Axonal Neuropathy Phenotype | Q57898426 | ||
| A new definition of neuropathic pain | Q57987223 | ||
| Is the interleukin-6 haplotype a prognostic factor for sciatica? | Q59154797 | ||
| The MMP1 rs1799750 2G Allele is Associated With Increased Low Back Pain, Sciatica, and Disability After Lumbar Disk Herniation | Q63442826 | ||
| Heritability of symptoms in an experimental model of neuropathic pain | Q68594599 | ||
| HLA-A33 and -B44 and susceptibility to postherpetic neuralgia (PHN) | Q77323891 | ||
| Association of HLA-A*3303-B*4403-DRB1*1302 haplotype, but not of TNFA promoter and NKp30 polymorphism, with postherpetic neuralgia (PHN) in the Japanese population | Q78675668 | ||
| Mutation hotspots of SCN9A in primary erythermalgia | Q79690531 | ||
| Trigeminal neuralgia | Q81424129 | ||
| Genetic variations in IL6 associate with intervertebral disc disease characterized by sciatica | Q81446218 | ||
| Association between Caspase-9 promoter region polymorphisms and discogenic low back pain | Q82522458 | ||
| HLA alleles are associated with postherpetic neuralgia but not with herpes zoster | Q83406254 | ||
| Association of single nucleotide polymorphisms of ABCB1, OPRM1 and COMT with pain perception in cancer patients | Q86531926 | ||
| Painful small fiber neuropathy with gastroparesis: A new phenotype with a novel mutation in the SCN10A gene | Q86986194 | ||
| Two novel mutant alleles of the gene encoding neurotrophic tyrosine kinase receptor type 1 (NTRK1) in a patient with congenital insensitivity to pain with anhidrosis: a splice junction mutation in intron 5 and cluster of four mutations in exon 15 | Q93945611 | ||
| Susceptibility to chronic pain following nerve injury is genetically affected by CACNG2. | Q34085118 | ||
| Multiple chronic pain states are associated with a common amino acid-changing allele in KCNS1 | Q34088667 | ||
| Role of IL1A rs1800587, IL1B rs1143627 and IL1RN rs2234677 genotype regarding development of chronic lumbar radicular pain; a prospective one-year study | Q34160342 | ||
| Prevalence and aetiology of neuropathic pain in cancer patients: a systematic review | Q34235831 | ||
| Congenital insensitivity to pain: novel SCN9A missense and in-frame deletion mutations | Q34254861 | ||
| A nonsense mutation in the SCN9A gene in congenital insensitivity to pain | Q34263684 | ||
| A mutation in the nerve growth factor beta gene (NGFB) causes loss of pain perception | Q34300023 | ||
| Gain-of-function Nav1.8 mutations in painful neuropathy. | Q34309236 | ||
| Electrophysiological properties of mutant Nav1.7 sodium channels in a painful inherited neuropathy. | Q34350866 | ||
| SCN9A mutations define primary erythermalgia as a neuropathic disorder of voltage gated sodium channels | Q34426317 | ||
| Gain-of-function mutation in Nav1.7 in familial erythromelalgia induces bursting of sensory neurons | Q34426737 | ||
| Role of the immune system in chronic pain. | Q34431134 | ||
| Congenital insensitivity to pain: a case report and review of the literature. | Q34443172 | ||
| Autosomal dominant erythermalgia associated with a novel mutation in the voltage-gated sodium channel alpha subunit Nav1.7. | Q34458611 | ||
| Molecular basis of congenital insensitivity to pain with anhidrosis (CIPA): mutations and polymorphisms in TRKA (NTRK1) gene encoding the receptor tyrosine kinase for nerve growth factor | Q34465802 | ||
| Clinical, pathological and genetic characterization of hereditary sensory and autonomic neuropathy type 1 (HSAN I). | Q34477997 | ||
| Sporadic onset of erythermalgia: a gain-of-function mutation in Nav1.7. | Q34481638 | ||
| Neuropathic pain: an updated grading system for research and clinical practice | Q34523633 | ||
| An infant with primary tooth loss and palmar hyperkeratosis: a novel mutation in the NTRK1 gene causing congenital insensitivity to pain with anhidrosis | Q34536668 | ||
| Neuropathic pain: redefinition and a grading system for clinical and research purposes | Q34713765 | ||
| SNPs in PTGS2 and LTA predict pain and quality of life in long term lung cancer survivors | Q35038872 | ||
| Role of TNF block genetic variants in HIV-associated sensory neuropathy in black Southern Africans | Q35079928 | ||
| Associations between cytokine gene variations and severe persistent breast pain in women following breast cancer surgery | Q35091181 | ||
| KIF1A, an axonal transporter of synaptic vesicles, is mutated in hereditary sensory and autonomic neuropathy type 2. | Q35161567 | ||
| No Fabry Disease in Patients Presenting with Isolated Small Fiber Neuropathy | Q35920645 | ||
| MAPK1/ERK2 as novel target genes for pain in head and neck cancer patients | Q35922750 | ||
| Genetically determined P2X7 receptor pore formation regulates variability in chronic pain sensitivity | Q35953669 | ||
| Discogenic pain | Q35961458 | ||
| Adult-onset painful axonal polyneuropathy caused by a dominant NAGLU mutation | Q35974498 | ||
| Existence of a neuropathic pain component in patients with osteoarthritis of the knee | Q36053417 | ||
| Novel and novel de novo mutations in NTRK1 associated with congenital insensitivity to pain with anhidrosis: a case report | Q36151639 | ||
| Mutations in the Heme Exporter FLVCR1 Cause Sensory Neurodegeneration with Loss of Pain Perception | Q36214268 | ||
| A Genome-wide Association Study Provides Evidence of Sex-specific Involvement of Chr1p35.1 (ZSCAN20-TLR12P) and Chr8p23.1 (HMGB1P46) With Diabetic Neuropathic Pain | Q36251379 | ||
| Immune and inflammatory mechanisms in neuropathic pain | Q36358514 | ||
| P275 | copyright license | Creative Commons Attribution-NonCommercial-NoDerivatives | Q6937225 |
| P433 | issue | 3 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | genetic variation | Q349856 |
| neuralgia | Q1136940 | ||
| neuropathic pain | Q2798704 | ||
| genetic predisposition to disease | Q64843122 | ||
| biomedical investigative technique | Q66648976 | ||
| P304 | page(s) | 583-594 | |
| P577 | publication date | 2018-03-01 | |
| P1433 | published in | Pain | Q2317902 |
| P1476 | title | Genetic studies of human neuropathic pain conditions: a review. | |
| P478 | volume | 159 |
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