Search Results - "Haiying Meng"
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DCDC2 Is Associated with Reading Disability and Modulates Neuronal Development in the Brain
Published in Proceedings of the National Academy of Sciences - PNAS (22-11-2005)“…DYX2 on 6p22 is the most replicated reading disability (RD) locus. By saturating a previously identified peak of association with single nucleotide…”
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2
DCDC2 genetic variants and susceptibility to developmental dyslexia
Published in Psychiatric genetics (01-02-2012)“…Developmental dyslexia is a heritable condition, with genetic factors accounting for 44-75% of the variance in performance tests of reading component…”
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3
Analysis of the Relationship between Transformational Leadership and Educational Management in Higher Education Based on Deep Learning
Published in Computational intelligence and neuroscience (15-06-2022)“…Leadership behavior has been emphasized as one of the most important influencing factors in the innovation process. Leaders can encourage subordinates to…”
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4
TDT-association analysis of EKN1 and dyslexia in a Colorado twin cohort
Published in Human genetics (01-11-2005)“…A candidate gene, EKN1, was recently described in a cohort from Finland for the dyslexia locus on chromosome 15q, DYX1. This report described a (2;15) (q11;21)…”
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5
Actual causes of death in Chaoyang District of Beijing, China, 2007
Published in Postgraduate medical journal (01-01-2011)“…ObjectivesTo identify and quantify major external (non-genetic) factors that contribute to death in Chaoyang District of Beijing, China in 2007.MethodsThe…”
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6
Dielectric analysis of different spherical polyelectrolyte brushes: Influence of pH and mass fraction on movement of counterions and electrical properties for different SPBs
Published in Colloids and surfaces. A, Physicochemical and engineering aspects (05-11-2016)“…[Display omitted] Two remarkable relaxations are observed for the SPBs (composed of PS core and PAA and PAEMH chains) suspension, and the mechanisms of the…”
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7
Sensorless Starting Control of the Brushless Synchronous Starter/Generator by Using the Main Exciter as a Quasi-Resolver at Low Speed
Published in IEEE transactions on power electronics (01-04-2023)“…The main generator (MG) and the main exciter (ME) are mounted on the same shaft in the brushless synchronous starter/generator (BSSG). Besides, the internal…”
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8
Detection of Turner Syndrome Using High-Throughput Quantitative Genotyping
Published in The journal of clinical endocrinology and metabolism (01-06-2005)“…Context: Turner syndrome (TS) is the most common genetic problem affecting women and occurs when an X chromosome is completely deleted, portions of an X…”
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A transcription map of the 6p22.3 reading disability locus identifying candidate genes
Published in BMC genomics (30-06-2003)“…Reading disability (RD) is a common syndrome with a large genetic component. Chromosome 6 has been identified in several linkage studies as playing a…”
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10
Dysgerminoma in a Patient With 45,X: A Challenge to Endocrinologists and Geneticists
Published in American journal of clinical pathology (01-10-2015)“…Since she lacked features of virilization and a Y chromosome counterpart, a screening for dysgerminoma or a prophylactic oophorectomy was not performed. FISH…”
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Ambient air quality and the effects of air pollutants on otolaryngology in Beijing
Published in Environmental monitoring and assessment (01-08-2015)“…To investigate temporal patterns, pollution concentrations and the health effects of air pollutants in Beijing we carried out time-series analyses on daily…”
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12
A low phase noise local oscillator module for instrumentation application
Published in 2013 IEEE International Wireless Symposium (IWS) (01-04-2013)“…In this paper we have developed a novel Local Oscillator Module for down conversion application in Signal Source Analyzer with low phase noise, which covers…”
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Conference Proceeding -
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Variants in the DYX2 locus are associated with altered brain activation in reading-related brain regions in subjects with reading disability
Published in NeuroImage (Orlando, Fla.) (15-10-2012)“…Reading disability (RD) is a complex genetic disorder with unknown etiology. Genes on chromosome 6p22, including DCDC2, KIAA0319, and TTRAP, have been…”
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14
Clinical Impact and Cost-Effectiveness of Whole Exome Sequencing as a Diagnostic Tool: A Pediatric Center's Experience
Published in Frontiers in pediatrics (03-08-2015)“…There are limited reports of the use of whole exome sequencing (WES) as a clinical diagnostic tool. Moreover, there are no reports addressing the cost burden…”
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THE EFFECTS OF A COMPREHENSIVE HEALTH EDUCATION PROGRAMME IN CHINESE PATIENTS AFTER PERCUTANEOUS CORONARY INTERVENTION: PP.32.100
Published in Journal of hypertension (01-06-2011)Get full text
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16
A Dyslexia-Associated Variant in DCDC2 Changes Gene Expression
Published in Behavior genetics (01-01-2011)“…Reading disability (RD) or dyslexia is a common neurogenetic disorder. Two genes, KIAA0319 and DCDC2 , have been identified by association studies of the DYX2…”
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Polymorphism of DCDC2 Reveals Differences in Cortical Morphology of Healthy Individuals—A Preliminary Voxel Based Morphometry Study
Published in Brain imaging and behavior (01-03-2008)“…Objective The purpose of this investigation was to determine whether there is an association between the putative reading disability (RD) susceptibility gene…”
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Journal Article -
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From the cover: DCDC2 is associated with reading disability and modulates neuronal development in the brain
Published in Proceedings of the National Academy of Sciences - PNAS (22-11-2005)“…DYX2 on 6p22 is the most replicated reading disability (RD) locus. By saturating a previously identified peak of association with single nucleotide…”
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Journal Article -
19
Investigation of the DCDC2 intron 2 deletion/compound short tandem repeat polymorphism in a large German dyslexia sample
Published in Psychiatric genetics (01-12-2008)“…Dyslexia is a complex disorder manifested by difficulties in learning to read and spell despite conventional instruction, adequate intelligence and…”
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Genetic approaches to complications of prematurity
Published in Frontiers in bioscience (01-01-2007)“…Over the last 15 years neonatal morbidity and mortality have changed little for very low birth weight (VLBW) babies despite significant technological and…”
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