Associated Papers
Cross-ancestry comparison of aptamer and antibody protein measures.
Nicholas JC et al.
Nature Communications, 2026
Molecular Determinants of the Human Retinal Pigment Epithelium Cell Fate and Potential Pharmacogenomic Targets for Precision Medicine.
Zibetti C
International Journal of Molecular Sciences, 2025
Investigation of UCHL3 and HNMT Gene Polymorphisms in Greek Patients with Type 2 Diabetes Mellitus and Diabetic Retinopathy.
Flindris K et al.
Biomedicines, 2025
A systematic review and functional in-silico analysis of genes and variants associated with amyotrophic lateral sclerosis.
Arreola-Aldape CA et al.
Frontiers in Neuroscience, 2025
APF2: an improved ensemble method for pharmacogenomic variant effect prediction.
Zhou Y et al.
The Pharmacogenomics Journal, 2024
Targeting the non-coding genome and temozolomide signature enables CRISPR-mediated glioma oncolysis.
Tan IL et al.
Cell Reports, 2023
Prevalence of Genetic Diamine Oxidase (DAO) Deficiency in Female Patients with Fibromyalgia in Spain.
Okutan G et al.
Biomedicines, 2023
The Thr105Ile Variant (rs11558538) of the Histamine N-methyltransferase Gene may be associated with Reduced Risk of Parkinson Disease: A Meta-analysis.
Lu Y et al.
Genetic Testing and Molecular Biomarkers, 2022
Individualized Proteogenomics Reveals the Mutational Landscape of Melanoma Patients in Response to Immunotherapy.
Schmitt M et al.
Cancers, 2021
Genomic Markers for Essential Tremor.
Jiménez-Jiménez FJ et al.
Pharmaceuticals (basel, Switzerland), 2021
Serum vitamin D, vitamin D receptor and binding protein genes polymorphisms in restless legs syndrome.
Jiménez-Jiménez FJ et al.
Journal of Neurology, 2021
Common Endothelial Nitric Oxide Synthase Single Nucleotide Polymorphisms are not Related With the Risk for Restless Legs Syndrome.
Jiménez-Jiménez FJ et al.
Frontiers in Pharmacology, 2021
Exome-Wide Search for Genes Associated With Central Nervous System Inflammatory Demyelinating Diseases Following CHIKV Infection: The Tip of the Iceberg.
Alves-Leon SV et al.
Frontiers in Genetics, 2021
Association Analyses of SNAP25, HNMT, FCHSD1, and DBH Single-Nucleotide Polymorphisms with Parkinson's Disease in a Northern Chinese Population.
Dai C et al.
Neuropsychiatric Disease and Treatment, 2021
Adult male patient with severe intellectual disability caused by a homozygous mutation in the HNMT gene.
Verhoeven WMA et al.
Bmj Case Reports, 2020
An optimized prediction framework to assess the functional impact of pharmacogenetic variants.
Zhou Y et al.
The Pharmacogenomics Journal, 2019
Unique characteristics of the genetics epidemiology of amyotrophic lateral sclerosis in China.
Wei Q et al.
Science China. Life Sciences, 2019
Assessment of coding region variants in Kuwaiti population: implications for medical genetics and population genomics.
John SE et al.
Scientific Reports, 2018
Gamma-aminobutyric acid (GABA) receptors genes polymorphisms and risk for restless legs syndrome.
Jiménez-Jiménez FJ et al.
The Pharmacogenomics Journal, 2018
Determining the Effect of the HNMT, STK39, and NMD3 Polymorphisms on the Incidence of Parkinson's Disease, Amyotrophic Lateral Sclerosis, and Multiple System Atrophy in Chinese Populations.
Chen Y et al.
Journal of Molecular Neuroscience : Mn, 2018
Association of diamine oxidase and histamine N-methyltransferase polymorphisms with presence of migraine in a group of Mexican mothers of children with allergies.
Meza-Velázquez R et al.
Neurologia (barcelona, Spain), 2017
Histaminergic gene polymorphisms associated with sedation in clozapine-treated patients.
Solismaa A et al.
European Neuropsychopharmacology : the Journal of the European College of Neuropsychopharmacology, 2017
Thr105Ile (rs11558538) polymorphism in the histamine-1-methyl-transferase (HNMT) gene and risk for restless legs syndrome.
Jiménez-Jiménez FJ et al.
Journal of Neural Transmission (vienna, Austria : 1996), 2017
Leucine 208 in human histamine N-methyltransferase emerges as a hotspot for protein stability rationalizing the role of the L208P variant in intellectual disability.
Tongsook C et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease, 2017
Impact of genetic variation on three dimensional structure and function of proteins.
Bhattacharya R et al.
Plos One, 2017
Thr105Ile (rs11558538) polymorphism in the histamine N-methyltransferase (HNMT) gene and risk for Parkinson disease: A PRISMA-compliant systematic review and meta-analysis.
Jiménez-Jiménez FJ et al.
Medicine, 2016
Genetic Variation in the Histamine Production, Response, and Degradation Pathway Is Associated with Histamine Pharmacodynamic Response in Children with Asthma.
Jones BL et al.
Frontiers in Pharmacology, 2016
Genetic Variation along the Histamine Pathway in Children with Allergic versus Nonallergic Asthma.
Anvari S et al.
American Journal of Respiratory Cell and Molecular Biology, 2015
Genetic variation within the histamine pathway among patients with asthma--a pilot study.
Raje N et al.
The Journal of Asthma : Official Journal of the Association for the Care of Asthma, 2015
Diamine oxidase rs10156191 and rs2052129 variants are associated with the risk for migraine.
García-Martín E et al.
Headache, 2015
Association of histamine N-methyltransferase Thr105Ile polymorphism with Parkinson's disease and schizophrenia in Han Chinese: a case-control study.
Yang X et al.
Plos One, 2015
The eSNV-detect: a computational system to identify expressed single nucleotide variants from transcriptome sequencing data.
Tang X et al.
Nucleic Acids Research, 2014
Association of myasthenia gravis with polymorphisms in the gene of histamine N-methyltransferase.
Kellermayer B et al.
Human Immunology, 2013
Polymorphisms and genetic linkage of histamine receptors.
Micallef S et al.
Life Sciences, 2013
Integrating precision medicine in the study and clinical treatment of a severely mentally ill person.
O'Rawe JA et al.
Peerj, 2013
Histamine N-methyltransferase Thr105Ile polymorphism is associated with Parkinson's disease.
Palada V et al.
Neurobiology of Aging, 2012
Involvement of human histamine N-methyltransferase gene polymorphisms in susceptibility to atopic dermatitis in korean children.
Lee HS et al.
Allergy, Asthma & Immunology Research, 2012
H1-MAPT and the risk for familial essential tremor.
García-Martín E et al.
Plos One, 2012
The diamine oxidase gene is associated with hypersensitivity response to non-steroidal anti-inflammatory drugs.
Agúndez JA et al.
Plos One, 2012
Identification of functional genetic variation in exome sequence analysis.
Jaffe A et al.
Bmc Proceedings, 2011
Association of single nucleotide polymorphisms in the diamine oxidase gene with diamine oxidase serum activities.
Maintz L et al.
Allergy, 2011
No association between histamine N-methyltransferase functional polymorphism Thr105Ile and Alzheimer's disease.
Marasović-Šušnjara I et al.
Neuroscience Letters, 2011
Polymorphisms of two histamine-metabolizing enzymes genes and childhood allergic asthma: a case control study.
Szczepankiewicz A et al.
Clinical and Molecular Allergy : Cma, 2010
Polymorphisms and disease: hotspots of inactivation in methyltransferases.
Rutherford K et al.
Trends in Biochemical Sciences, 2010
Histamine-N-methyl transferase polymorphism and risk for multiple sclerosis.
García-Martín E et al.
European Journal of Neurology, 2010
Histamine N-methyltransferase Thr105Ile is not associated with Parkinson's disease or essential tremor.
Keeling BH et al.
Parkinsonism & Related Disorders, 2010
Histamine N-methyltransferase 939A>G polymorphism affects mRNA stability in patients with acetylsalicylic acid-intolerant chronic urticaria.
Kim SH et al.
Allergy, 2009