Genetic predictors of human chronic pain conditions (Q26753046)

Katerina Zorina-Lichtenwalter

Europe PubMed Central

title

Genetic predictors of human chronic pain conditions (English)

0 references

main subject

chronic pain

0 references

author

1

object named as

Katerina Zorina-Lichtenwalter

0 references

author name string

C B Meloto

2

0 references

S Khoury

3

0 references

L Diatchenko

Primary erythermalgia as a sodium channelopathy: screening for SCN9A mutations: exclusion of a causal role of SCN10A and SCN11A.

4

0 references

language of work or name

English

0 references

publication date

30 April 2016

0 references

published in

Neuroscience

0 references

cites work

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Autosomal dominant erythermalgia associated with a novel mutation in the voltage-gated sodium channel alpha subunit Nav1.7.

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Executive subprocesses in working memory: relationship to catechol-O-methyltransferase Val158Met genotype and schizophrenia

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

The homozygous C677T mutation in the methylenetetrahydrofolate reductase gene is a genetic risk factor for migraine

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Genetic influences on cervical and lumbar disc degeneration: a magnetic resonance imaging study in twins

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Possible association of fibromyalgia with a polymorphism in the serotonin transporter gene regulatory region

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Three major haplotypes of the beta2 adrenergic receptor define psychological profile, blood pressure, and the risk for development of a common musculoskeletal pain disorder

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Genetic association studies of the chromosome 15 GABA-A receptor cluster in migraine with aura

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

No association of migraine to the GABA-A receptor complex on chromosome 15

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

SNP variants within the vanilloid TRPV1 and TRPV3 receptor genes are associated with migraine in the Spanish population.

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Deciphering migraine mechanisms: clues from familial hemiplegic migraine genotypes

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Migraine and MTHFR C677T genotype in a population-based sample.

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Sporadic onset of erythermalgia: a gain-of-function mutation in Nav1.7.

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

MTHFR C677T polymorphism and migraine with aura

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

A dopamine D4 receptor exon 3 VNTR allele protecting against migraine without aura.

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

A sodium channel gene SCN9A polymorphism that increases nociceptor excitability

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Gain of function NaV1.7 mutations in idiopathic small fiber neuropathy

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Expression of estrogen receptor alpha (ER alpha) in the rat temporomandibular joint

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Association of adrenergic receptor gene polymorphisms with different fibromyalgia syndrome domains.

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Genetic variation in the SMAD3 gene is associated with hip and knee osteoarthritis

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Large candidate gene association study reveals genetic risk factors and therapeutic targets for fibromyalgia.

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Behavioral testing in rodent models of orofacial neuropathic and inflammatory pain.

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Advances in the epidemiology, pathogenesis and management of diabetic peripheral neuropathy

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Congenital insensitivity to pain with anhidrosis (CIPA): novel mutations of the TRKA (NTRK1) gene, a putative uniparental disomy, and a linkage of the mutant TRKA and PKLR genes in a family with CIPA and pyruvate kinase deficiency

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Signal peptide variants that impair secretion of pancreatic secretory trypsin inhibitor (SPINK1) cause autosomal dominant hereditary pancreatitis

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Congenital insensitivity to pain: novel SCN9A missense and in-frame deletion mutations

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Two novel severe mutations in the pancreatic secretory trypsin inhibitor gene (SPINK1) cause familial and/or hereditary pancreatitis

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Heritability of chronic pain in 2195 extended families

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

The COMT rs4680 Met allele contributes to long-lasting low back pain, sciatica and disability after lumbar disc herniation.

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Genetic variation in the beta-2 adrenergic receptor is associated with chronic musculoskeletal complaints in adolescents

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Pain sensitivity in fibromyalgia is associated with catechol-O-methyltransferase (COMT) gene

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Pain distribution and predictors of widespread pain in the immediate aftermath of motor vehicle collision

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

The effects of psychological stress on humans: increased production of pro-inflammatory cytokines and a Th1-like response in stress-induced anxiety.

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Single-nucleotide polymorphism alleles in the insulin receptor gene are associated with typical migraine.

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

The T102C polymorphism of the 5-HT2A-receptor gene in fibromyalgia

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Prevalence of diabetic peripheral neuropathy and its relation to glycaemic control and potential risk factors: the EURODIAB IDDM Complications Study.

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Which genotype of MAO gene that the patients have are likely to be most susceptible to the symptoms of fibromyalgia?

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Association of T102C polymorphism of the 5-HT2A receptor gene with psychiatric status in fibromyalgia syndrome.

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Influence of catechol-O-methyltransferase (COMT) gene polymorphisms in pain sensibility of Brazilian fibromialgia patients

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Candidate gene studies of fibromyalgia: a systematic review and meta-analysis

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

A SMAD3 gene polymorphism is related with osteoarthritis in a Northeast Chinese population

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Etiology of chronic prostatitis/chronic pelvic pain syndrome: psychoimmunoneurendocrine dysfunction (PINE syndrome) or just a really bad infection?

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

The G-308A promoter variant of the tumor necrosis factor-alpha gene is associated with migraine without aura.

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Characterization of a familial case with primary erythromelalgia from Taiwan.

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Migraine and tumour necrosis factor gene polymorphism. An association study in a Sardinian sample

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Investigation of TNFA 308G > A and TNFB 252G > A polymorphisms in genetic susceptibility to migraine.

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

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.

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Molecular genetics of migraine

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Symptom clusters of pain, depressed mood, and fatigue in lung cancer: assessing the role of cytokine genes

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Association between the -1306C/T polymorphism of matrix metalloproteinase-2 gene and lumbar disc disease in Chinese young adults

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Catechol-O-methyltransferase (COMT) gene polymorphisms are associated with baseline disability but not long-term treatment outcome in patients with chronic low back pain

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Influence of variation in the catechol-O-methyltransferase gene on the clinical outcome after lumbar spine surgery for one-level symptomatic disc disease: a report on 176 cases

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Investigation of the functional brain-derived neurotrophic factor gene variant Val66MET in migraine

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

The estrogen receptor 1 G594A polymorphism is associated with migraine susceptibility in two independent case/control groups.

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Investigation of hormone receptor genes in migraine.

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Association between migraine and a functional polymorphism at the dopamine beta-hydroxylase locus

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

A genome-wide analysis of 'Bounty' descendants implicates several novel variants in migraine susceptibility

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Migraine genetics: current findings and future lines of research

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Dopaminergic symptoms in migraine

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Lack of association between GRIA1 polymorphisms and haplotypes with migraine without aura or response to triptans

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

A genetic association study of migraine with dopamine receptor 4, dopamine transporter and dopamine-beta-hydroxylase genes

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Screening for genetic and acquiredthrombophilia in a cohort of young migrainous patients.

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Association between migraine and HLA-DRB1 gene polymorphisms.

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Evidence for an association between migraine and the hypocretin receptor 1 gene

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Variants in the human potassium channel gene (KCNN3) are associated with migraine in a high risk genetic isolate

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Genetics of migraine in the age of genome-wide association studies

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Future possibilities in migraine genetics

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Recent advances in the understanding of genetic susceptibility to chronic pain and somatic symptoms

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Identification of a novel ANKK1 and other dopaminergic (DRD2 and DBH) gene variants in migraine susceptibility

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Complex multilocus effects of catechol-O-methyltransferase haplotypes predict pain and pain interference 6 weeks after motor vehicle collision

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

The Domain II S4-S5 Linker in Nav1.9: A Missense Mutation Enhances Activation, Impairs Fast Inactivation, and Produces Human Painful Neuropathy.

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Migraine: Role of the TRESK two-pore potassium channel

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Catechol-o-methyltransferase, cognition, and psychosis: Val158Met and beyond

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Congenital insensitivity to pain: Fracturing without apparent skeletal pathobiology caused by an autosomal dominant, second mutation in SCN11A encoding voltage-gated sodium channel 1.9.

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Clustering of symptoms associated with fibromyalgia in a Finnish Twin Cohort

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Association study of the calcitonin gene-related polypeptide-alpha (CALCA) and the receptor activity modifying 1 (RAMP1) genes with migraine.

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Cox-2 gene variants in migraine

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Association between estrogen receptor polymorphism and pain susceptibility in female temporomandibular joint osteoarthritis patients.

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Cytokines sing the blues: inflammation and the pathogenesis of depression

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Association of the functional A118G polymorphism of OPRM1 in diabetic patients with foot ulcer pain.

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Investigation of the low-density lipoprotein receptor gene and cholesterol as a risk factor for migraine.

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Association between a 19 bp deletion polymorphism at the dopamine beta-hydroxylase (DBH) locus and migraine with aura.

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Role of the ACE ID and MTHFR C677T polymorphisms in genetic susceptibility of migraine in a north Indian population

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Chronic non-paroxysmal neuropathic pain - Novel phenotype of mutation in the sodium channel SCN9A gene

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Association analysis of TNFRSF1B polymorphism with susceptibility for migraine in the Chinese Han population.

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Painful small fiber neuropathy with gastroparesis: A new phenotype with a novel mutation in the SCN10A gene

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

The effects of estrogen receptor α polymorphism on the prevalence of symptomatic temporomandibular disorders

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Estrogen receptor-alpha polymorphisms and predisposition to TMJ disorder

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

A candidate gene association study of 77 polymorphisms in migraine

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Catechol O-methyltransferase haplotype predicts immediate musculoskeletal neck pain and psychological symptoms after motor vehicle collision

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Associations between pro- and anti-inflammatory cytokine genes and breast pain in women prior to breast cancer surgery

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

The OPPERA study: Act One

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Potential genetic risk factors for chronic TMD: genetic associations from the OPPERA case control study

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Catechol-O-methyltransferase Val158Met polymorphism influences anxiety, depression, and disability, but not pressure pain sensitivity, in women with fibromyalgia syndrome

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

μ-Opioid receptor gene A118G polymorphism predicts pain recovery after sexual assault

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Anxiety and depression are associated with migraine and pain in general: an investigation of the interrelationships.

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

An opposite-direction modulation of the COMT Val158Met polymorphism on the clinical response to intrathecal morphine and triptans.

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Psychological factors associated with development of TMD: the OPPERA prospective cohort study.

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Associations between cytokine gene variations and severe persistent breast pain in women following breast cancer surgery

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

μ-Opioid Receptor Gene A118 G Variants and Persistent Pain Symptoms Among Men and Women Experiencing Motor Vehicle Collision

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Genetic variants of angiotensin converting enzyme and methylenetetrahydrofolate reductase may act in combination to increase migraine susceptibility.

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Thymidylate synthase promoter tandem repeat and MTHFD1 R653Q polymorphisms modulate the risk for migraine conferred by the MTHFR T677 allele

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Evidence for orexinergic mechanisms in migraine

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Recent findings on how proinflammatory cytokines cause pain: peripheral mechanisms in inflammatory and neuropathic hyperalgesia.

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Association of the insertion/deletion polymorphism of the angiotensin I-converting enzyme gene in patients of migraine with aura.

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Association of MTHFR C677T polymorphism with susceptibility to migraine in the Chinese population.

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

SCN9A mutations in paroxysmal extreme pain disorder: allelic variants underlie distinct channel defects and phenotypes

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Novel missense, insertion and deletion mutations in the neurotrophic tyrosine kinase receptor type 1 gene (NTRK1) associated with congenital insensitivity to pain with anhidrosis

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Possible association of interleukin 1 gene locus polymorphisms with low back pain.

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Changes in cerebrospinal fluid levels of pro-inflammatory cytokines in CRPS

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Catechol-O-methyltransferase inhibition increases pain sensitivity through activation of both beta2- and beta3-adrenergic receptors

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Heritability of low back pain and the role of disc degeneration

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

The evidence for pharmacological treatment of neuropathic pain

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

COMT moderates the relation of daily maladaptive coping and pain in fibromyalgia

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Cytokine biomarkers and chronic pain: association of genes, transcription, and circulating proteins with temporomandibular disorders and widespread palpation tenderness

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Polymorphisms in the glucocorticoid receptor co-chaperone FKBP5 predict persistent musculoskeletal pain after traumatic stress exposure

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Facial pain with localized and widespread manifestations: separate pathways of vulnerability.

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Genome-wide analysis of single nucleotide polymorphisms and copy number variants in fibromyalgia suggest a role for the central nervous system.

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

A novel mutation in SCN9A in a child with congenital insensitivity to pain

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

A novel nonsense mutation in SCN9A in a Moroccan child with congenital insensitivity to pain

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Apolipoprotein e4 genotype increases the risk of being diagnosed with posttraumatic fibromyalgia

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

High anxiety and migraine are associated with the s allele of the 5HTTLPR gene polymorphism

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Phenotype variations affect genetic association studies of degenerative disc disease: conclusions of analysis of genetic association of 58 single nucleotide polymorphisms with highly specific phenotypes for disc degeneration in 332 subjects

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Pain genetics: past, present and future

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Polymorphism in the SCN9A voltage-gated sodium channel gene associated with interstitial cystitis/bladder pain syndrome.

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Significance of serotonin transporter gene polymorphism in migraine.

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Investigation of an LDLR gene polymorphism (19p13.2) in susceptibility to migraine without aura

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Familial hemiplegic migraine and episodic ataxia type-2 are caused by mutations in the Ca2+ channel gene CACNL1A4

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Mutation in the neuronal voltage-gated sodium channel SCN1A in familial hemiplegic migraine

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Identification of new susceptibility loci for osteoarthritis (arcOGEN): a genome-wide association study

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

1 reference

7 January 2021

Association of the C677T and A1298C polymorphisms in the 5,10 methylenetetrahydrofolate reductase gene in patients with migraine risk

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Animal and cellular models of chronic pain

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Estrogen and progesterone receptors in temporomandibular joint discs of symptomatic and asymptomatic persons: a preliminary study.

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Synovial fluid cytokines and proteinases as markers of temporomandibular joint disease

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Sensitivity of patients with painful temporomandibular disorders to experimentally evoked pain: evidence for altered temporal summation of pain.

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Transgenic studies of pain

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

A Cacna1a knockin migraine mouse model with increased susceptibility to cortical spreading depression

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

X Chromosomal short tandem repeat polymorphisms near the phosphoglycerate kinase gene in men with chronic prostatitis

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Sodium channel genes in pain-related disorders: phenotype-genotype associations and recommendations for clinical use.

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

A functional polymorphism in the 5' UTR of GDF5 is associated with susceptibility to osteoarthritis

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Interleukin-1 beta as a potent hyperalgesic agent antagonized by a tripeptide analogue

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Mutations in the gene encoding the serine protease inhibitor, Kazal type 1 are associated with chronic pancreatitis

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Meta-analysis of genome-wide association for migraine in six population-based European cohorts

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

An SCN9A channelopathy causes congenital inability to experience pain

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Mutations in the TRKA/NGF receptor gene in patients with congenital insensitivity to pain with anhidrosis

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Hereditary pancreatitis is caused by a mutation in the cationic trypsinogen gene

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Hereditary pancreatitis caused by triplication of the trypsinogen locus

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Genome-wide association analysis identifies susceptibility loci for migraine without aura

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Genome-wide meta-analysis identifies new susceptibility loci for migraine

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

A de novo gain-of-function mutation in SCN11A causes loss of pain perception

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Genome-wide association study of migraine implicates a common susceptibility variant on 8q22.1.

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Genome-wide association study reveals three susceptibility loci for common migraine in the general population

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

GTP cyclohydrolase and tetrahydrobiopterin regulate pain sensitivity and persistence

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

A dominant-negative mutation in the TRESK potassium channel is linked to familial migraine with aura

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Genetically determined P2X7 receptor pore formation regulates variability in chronic pain sensitivity

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Coding of facial expressions of pain in the laboratory mouse

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Animal models of pain: progress and challenges

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Diencephalic and brainstem mechanisms in migraine

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

The phenotypic and genetic signatures of common musculoskeletal pain conditions.

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Erratum: An association between fibromyalgia and the dopamine D4 receptor exon III repeat polymorphism and relationship to novelty seeking personality traits

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Manganese superoxide dismutase polymorphism in chronic pelvic pain syndrome patients

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Tumor necrosis factor gene polymorphism in migraine

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

A polymorphism in the serotonin transporter gene regulatory region and frequency of migraine attacks

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Mutations in the cationic trypsinogen gene are associated with recurrent acute and chronic pancreatitis

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Cystic fibrosis gene mutations and pancreatitis risk: relation to epithelial ion transport and trypsin inhibitor gene mutations

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Mutations of the cystic fibrosis gene in patients with chronic pancreatitis

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Possible association of temporomandibular joint pain and dysfunction with a polymorphism in the serotonin transporter gene

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Depression and somatization in patients with temporomandibular disorders

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Gain-of-function Nav1.8 mutations in painful neuropathy.

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Hereditary pancreatitis caused by a novel PRSS1 mutation (Arg-122 --> Cys) that alters autoactivation and autodegradation of cationic trypsinogen

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

A new susceptibility locus for migraine with aura in the 15q11-q13 genomic region containing three GABA-A receptor genes

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

The incidence and lifetime prevalence of neurological disorders in a prospective community-based study in the UK.

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Gain-of-function mutation in Nav1.7 in familial erythromelalgia induces bursting of sensory neurons

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Multiple chronic pain states are associated with a common amino acid-changing allele in KCNS1

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Functional profiles of SCN9A variants in dorsal root ganglion neurons and superior cervical ganglion neurons correlate with autonomic symptoms in small fibre neuropathy.

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Gain-of-function mutations in sodium channel Na(v)1.9 in painful neuropathy

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Genetic basis for individual variations in pain perception and the development of a chronic pain condition

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

A meta-analysis of European and Asian cohorts reveals a global role of a functional SNP in the 5' UTR of GDF5 with osteoarthritis susceptibility

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Cytokines play an aetiopathogenetic role in fibromyalgia: a hypothesis and pilot study

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

The role of psychosocial factors in predicting the onset of chronic widespread pain: results from a prospective population-based study.

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Clinical Effectiveness and Cost-Effectiveness of Treatments for Patients With Chronic Pain

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Notch signaling in vascular morphogenesis

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Association of migraine and ESR1 G325C polymorphism

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Efficacy of opioids for chronic pain: a review of the evidence

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

The MMP1 rs1799750 2G Allele is Associated With Increased Low Back Pain, Sciatica, and Disability After Lumbar Disk Herniation

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Association Between the Aggrecan Gene Variable Number of Tandem Repeats Polymorphism and Intervertebral Disc Degeneration

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Polymorphic variation of the guanosine triphosphate cyclohydrolase 1 gene predicts outcome in patients undergoing surgical treatment for lumbar degenerative disc disease

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Association between estrogen receptor gene polymorphism and back pain intensity in female patients with degenerative lumbar spondylolisthesis.

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

COMT gene locus: new functional variants

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

CRHBP polymorphisms predict chronic pain development following motor vehicle collision

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Novel and novel de novo mutations in NTRK1 associated with congenital insensitivity to pain with anhidrosis: a case report

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

KCNS1, but not GCH1, is associated with pain intensity in a black southern African population with HIV-associated sensory neuropathy: a genetic association study

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Calcitonin gene-related peptide and migraine

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Prevalence of migraine in persons with the 3243A>G mutation in mitochondrial DNA.

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Association of a GRIA3 gene polymorphism with migraine in an Australian case-control cohort.

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

PRDM16 rs2651899 variant is a risk factor for Chinese common migraine patients

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Genome-wide-associated variants in migraine susceptibility: a replication study from North India

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Replication of migraine GWAS susceptibility loci in Chinese Han population

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Investigation of Brain-Derived Neurotrophic Factor (BDNF) Gene Variants in Migraine

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Diamine oxidase rs10156191 and rs2052129 variants are associated with the risk for migraine.

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Association of RAMP1 rs7590387 with the risk of migraine transformation into medication overuse headache.

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

SCN9A mutations define primary erythermalgia as a neuropathic disorder of voltage gated sodium channels

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

1 reference

7 January 2021

Lack of association of hormone receptor polymorphisms with migraine

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Metabolic and genetic risk factors for migraine in children.

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Testing of Variants of the MTHFR and ESR1 Genes in 1798 Finnish Individuals Fails to Confirm the Association with Migraine with Aura

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Combined effects of ACE and MMP-3 polymorphisms on migraine development

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Serotonin and migraine: biology and clinical implications

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Association of von Willebrand factor activity with ACE I/D and MTHFR C677T polymorphisms in migraine.

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Genetic association study of endothelin-1 and its receptors EDNRA and EDNRB in migraine with aura

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Migraine as a systemic vasculopathy

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Familial PRRT2 mutation with heterogeneous paroxysmal disorders including paroxysmal torticollis and hemiplegic migraine

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

The emerging role of trace amine-associated receptor 1 in the functional regulation of monoamine transporters and dopaminergic activity

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Migraine and concomitant symptoms among 8167 adult twin pairs.

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

The medical costs of migraine and comorbid anxiety and depression.

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Platelet levels of dopamine are increased in migraine and cluster headache

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Endothelial nitric oxide synthase (Glu298Asp) polymorphism is an independent risk factor for migraine with aura

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Multilocus analyses reveal involvement of the ESR1, ESR2, and FSHR genes in migraine.

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Identification of novel genes involved in migraine.

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Cytokine polymorphism in patients with migraine: some suggestive clues of migraine and inflammation

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Genetic variations in tumor necrosis factor alpha, interleukin-10 genes, and migraine susceptibility.

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Cytokines in temporomandibular joint arthritis

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

T102C polymorphism of the 5-HT2A receptor gene may be associated with temporomandibular dysfunction.

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

TMD pain is partly heritable. A systematic review of family studies and genetic association studies

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Association of GDF5, SMAD3 and RUNX2 polymorphisms with temporomandibular joint osteoarthritis in female Han Chinese.

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

COMT val158met genotype affects mu-opioid neurotransmitter responses to a pain stressor

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Genome-wide association study meta-analysis of chronic widespread pain: evidence for involvement of the 5p15.2 region

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Genetic variation in the hypothalamic-pituitary-adrenal stress axis influences susceptibility to musculoskeletal pain: results from the EPIFUND study

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Mutations in SCN9A, encoding a sodium channel alpha subunit, in patients with primary erythermalgia

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Neuropathic pain: a maladaptive response of the nervous system to damage

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Cd14, Gbp1, and Pla2g2a: three major candidate genes for experimental IBD identified by combining QTL and microarray analyses

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

The C677T polymorphism in MTHFR is not associated with migraine in Portugal.

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Canadian Orofacial Pain Team workshop report on the global year against orofacial pain

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Cytokine genes and pain severity in lung cancer: exploring the influence of TNF-alpha-308 G/A IL6-174G/C and IL8-251T/A.

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Role of inflammation gene polymorphisms on pain severity in lung cancer patients

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Angiotensin-converting enzyme gene deletion polymorphism determines an increase in frequency of migraine attacks in patients suffering from migraine without aura

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Epidemiology and Clinical Features of Idiopathic Trigeminal Neuralgia and Glossopharyngeal Neuralgia: Similarities and Differences, Rochester, Minnesota, 1945-1984

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

A nonsense mutation in the SCN9A gene in congenital insensitivity to pain

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Notch signaling in vascular development

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Migraine mediates the influence of C677T MTHFR genotypes on ischemic stroke risk with a stroke-subtype effect.

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

The endophenotype concept in psychiatry: etymology and strategic intentions

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

BDNF and CGRP interaction: implications in migraine susceptibility.

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Association of oestrogen-receptor gene (ESR1) polymorphisms with migraine in the large Norfolk Island pedigree.

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Influence of psychological factors on risk of temporomandibular disorders.

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Estrogen receptor-alpha polymorphism in patients with and without degenerative disease of the temporomandibular joint.

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

The prevalence of chronic pain with an analysis of countries with a Human Development Index less than 0.9: a systematic review without meta-analysis

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Genetic variants in the NOTCH4 gene influence the clinical features of migraine

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Abstracts of the European Headache and Migraine Trust International Congress, September 20-23, 2012, London, United Kingdom

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Effect of genetic deletion and pharmacological antagonism of P2X7 receptors in a mouse animal model of migraine

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

The serotonin transporter gene polymorphism is associated with the susceptibility and the pain severity in idiopathic trigeminal neuralgia patients

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Genetic polymorphisms in folate pathway enzymes, DRD4 and GSTM1 are related to temporomandibular disorder.

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Association between promoter -1607 polymorphism of MMP1 and lumbar disc disease in Southern Chinese

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Effects of MTHFR gene polymorphism on the clinical and electrophysiological characteristics of migraine

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Angiotensin-converting enzyme gene insertion/deletion polymorphism in migraine patients

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

A SCN9A gene-encoded dorsal root ganglia sodium channel polymorphism associated with severe fibromyalgia

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Genetic contribution of catechol-O-methyltransferase variants in treatment outcome of low back pain: a prospective genetic association study

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Treatment outcome of chronic low back pain and radiographic lumbar disc degeneration are associated with inflammatory and matrix degrading gene variants: a prospective genetic association study

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Subjective health complaints in patients with lumbar radicular pain and disc herniation are associated with a sex - OPRM1 A118G polymorphism interaction: a prospective 1-year observational study

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

The methylenetetrahydrofolate reductase gene variant C677T influences susceptibility to migraine with aura

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Gain and loss of function of P2X7 receptors: mechanisms, pharmacology and relevance to diabetic neuropathic pain.

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Compound heterozygosity in sodium channel Nav1.7 in a family with hereditary erythermalgia

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Chronic pain after lower abdominal surgery: do catechol-O-methyl transferase/opioid receptor μ-1 polymorphisms contribute?

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Analysis of the MTHFR C677T variant with migraine phenotypes.

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Catechol-O-methyltransferase gene haplotypes in Mexican and Spanish patients with fibromyalgia

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Association of genetic loci for migraine susceptibility in the she people of China

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Variation of the serotonin transporter gene SLC6A4 in the susceptibility to migraine with aura.

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Interrelationships among the MTHFR 677C>T polymorphism, migraine, and cardiovascular disease

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

ACE D/I polymorphism, migraine, and cardiovascular disease in women

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Genetic analysis for a shared biological basis between migraine and coronary artery disease

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

PRRT2 mutations cause hemiplegic migraine

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Association between dopamine receptor genes and migraine without aura in a Sardinian sample

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

The prevalence and characteristics of migraine in a population-based cohort: the GEM study

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Association between migraine and endothelin type A receptor (ETA -231 A/G) gene polymorphism.

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

The association of degeneration of the intervertebral disc with 5a/6a polymorphism in the promoter of the human matrix metalloproteinase-3 gene

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Potential role of aromatase over estrogen receptor gene polymorphisms in migraine susceptibility: a case control study from North India

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Oral and craniofacial manifestations and two novel missense mutations of the NTRK1 gene identified in the patient with congenital insensitivity to pain with anhidrosis

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Opioids for chronic noncancer pain: a meta-analysis of effectiveness and side effects.

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

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.

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Electrophysiological properties of mutant Nav1.7 sodium channels in a painful inherited neuropathy.

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Small-fiber neuropathy Nav1.8 mutation shifts activation to hyperpolarized potentials and increases excitability of dorsal root ganglion neurons.

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

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.

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

An infant with primary tooth loss and palmar hyperkeratosis: a novel mutation in the NTRK1 gene causing congenital insensitivity to pain with anhidrosis

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Association between Caspase-9 promoter region polymorphisms and discogenic low back pain

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Analysis of association between IL-1β, CASP-9, and GDF5 variants and low-back pain in Chinese male soldier: clinical article.

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

The TNF-α-308G/A polymorphism is associated with migraine risk: A meta-analysis

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Association of guanosine triphosphate cyclohydrolase 1 gene polymorphisms with fibromyalgia syndrome in a Korean population.

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Association between the G252A Tumor Necrosis Factor-β Gene Polymorphism and Medication-Overuse Headache

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Novel nonsense and frameshift NTRK1 gene mutations in Chinese patients with congenital insensitivity to pain with anhidrosis

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

Association of temporomandibular dysfunction with the 102T-C polymorphism in the serotonin receptor gene in Brazilian patients

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021

The effectiveness and risks of long-term opioid therapy for chronic pain: a systematic review for a National Institutes of Health Pathways to Prevention Workshop

1 reference

https://api.crossref.org/works/10.1016%2FJ.NEUROSCIENCE.2016.04.041

7 January 2021