Associated Papers
Systems-Level Integration of Multi-Omics Identifies Genetic Modifiers of TANGO2 Deficiency Disorder.
Airoldi M et al.
Biomolecules, 2025
Association of genetic variation in COL11A1 with adolescent idiopathic scoliosis.
Yu H et al.
Elife, 2024
Association of genetic variation in COL11A1 with adolescent idiopathic scoliosis.
Yu H et al.
Biorxiv : the Preprint Server for Biology, 2023
Rare variants with large effects provide functional insights into the pathology of migraine subtypes, with and without aura.
Bjornsdottir G et al.
Nature Genetics, 2023
Association of the p75NTR Ser205Leu Polymorphism with Asymptomatic HTLV-1 Infection.
Queiroz MAF et al.
Viruses, 2022
Case report: Whole-exome sequencing identifies a novel DES mutation (p. E434K) in a Chinese family with cardiomyopathy and sudden cardiac death.
Liu YX et al.
Frontiers in Cardiovascular Medicine, 2022
Charcot-Marie-Tooth Type 2B: A New Phenotype Associated with a Novel RAB7A Mutation and Inhibited EGFR Degradation.
Saveri P et al.
Cells, 2020
BDNF and NGF gene polymorphisms and urine BDNF-NGF levels in children with primary monosymptomatic nocturnal enuresis.
Ece A et al.
Journal of Pediatric Urology, 2019
X-linked ADGRG2 mutation and obstructive azoospermia in a large Pakistani family.
Khan MJ et al.
Scientific Reports, 2018
Involvement of polymorphisms of the nerve growth factor and its receptor encoding genes in the etiopathogenesis of ischemic stroke.
Stepanyan A et al.
Bmc Medical Genetics, 2018
Association of brain-derived neurotrophic factor and nerve growth factor gene polymorphisms with susceptibility to migraine.
Coskun S et al.
Neuropsychiatric Disease and Treatment, 2016
Rare variants in the neurotrophin signaling pathway implicated in schizophrenia risk.
Kranz TM et al.
Schizophrenia Research, 2015
Evaluation of Hybridization Capture Versus Amplicon-Based Methods for Whole-Exome Sequencing.
Samorodnitsky E et al.
Human Mutation, 2015
Whole genome sequencing of an ethnic Pathan (Pakhtun) from the north-west of Pakistan.
Ilyas M et al.
Bmc Genomics, 2015
Sex-specific association between nerve growth factor polymorphism and cardiac vagal modulation.
Chang CC et al.
Psychosomatic Medicine, 2014
Nerve growth factor and its receptor in schizophrenia.
Zakharyan R et al.
Bba Clinical, 2014
Early-onset severe hereditary sensory and autonomic neuropathy type 1 with S331F SPTLC1 mutation.
Suh BC et al.
Molecular Medicine Reports, 2014
Neurotrophin serum concentrations and polymorphisms of neurotrophins and their receptors in children with asthma.
Szczepankiewicz A et al.
Respiratory Medicine, 2013
The regulated secretory pathway and human disease: insights from gene variants and single nucleotide polymorphisms.
Lin WJ et al.
Frontiers in Endocrinology, 2013
Nerve growth factor β polypeptide (NGFB) genetic variability: association with the methadone dose required for effective maintenance treatment.
Levran O et al.
The Pharmacogenomics Journal, 2012
Neurotrophic gene polymorphisms and response to psychological therapy.
Lester KJ et al.
Translational Psychiatry, 2012
Multilocus analysis of candidate genes involved in neurogenic inflammation in pediatric asthma and related phenotypes: a case-control study.
Szczepankiewicz A et al.
The Journal of Asthma : Official Journal of the Association for the Care of Asthma, 2012
Association between nerve growth factor gene polymorphism and executive dysfunction in Japanese patients with early-stage Alzheimer's disease and amnestic mild cognitive impairment.
Nagata T et al.
Dementia and Geriatric Cognitive Disorders, 2011
Variation in the BDNF and NGFB genes in German atopic dermatitis patients.
Hoffjan S et al.
Molecular and Cellular Probes, 2009
Functional nonsynonymous single nucleotide polymorphisms from the TGF-beta protein interaction network.
Savas S et al.
Physiological Genomics, 2007
Establishment and Characterization of 10 Human Pancreatic Cancer Cell Lines Including a HER2 Overexpressed Cell Line.
Kim SC et al.
Pancreas, 0