H. Meng

发表

Clinical Impact and Cost-Effectiveness of Whole Exome Sequencing as a Diagnostic Tool: A Pediatric Center’s Experience

F. Zou, J. Harley, R. Hopkin, 2015, Front. Pediatr..

TDT-association analysis of EKN1 and dyslexia in a Colorado twin cohort

B. Pennington, G. Page, R. Olson, 2005, Human Genetics.

DCDC2 is associated with reading disability and modulates neuronal development in the brain.

P. Skudlarski, B. Pennington, B. Shaywitz, 2005, Proceedings of the National Academy of Sciences of the United States of America.

Oncology—Acquired

H. Meng, 2019, Self-Assessment Questions for Clinical Molecular Genetics.

A transcription map of the 6p22.3 reading disability locus identifying candidate genes

E. Londin, J. Gruen, H. Meng, 2003, BMC Genomics.

Detection of Turner syndrome using high-throughput quantitative genotyping.

S. Rivkees, J. Gruen, H. Meng, 2005, Journal of Clinical Endocrinology and Metabolism.

Investigation of the DCDC2 intron 2 deletion/compound short tandem repeat polymorphism in a large German dyslexia sample

M. Nöthen, J. Kere, I. König, 2008, Psychiatric genetics.

Analysis of the Relationship between Transformational Leadership and Educational Management in Higher Education Based on Deep Learning

H. Meng, 2022, Computational intelligence and neuroscience.

Neuromuscular Disorders

H. Meng, 2019, Self-Assessment Questions for Clinical Molecular Genetics.

Other Common Genetic Syndromes

H. Meng, 2019, Self-Assessment Questions for Clinical Molecular Genetics.

Genetic Counseling—Introduction

H. Meng, 2019, Self-Assessment Questions for Clinical Molecular Genetics.

A Dyslexia-Associated Variant in DCDC2 Changes Gene Expression

Grier P Page, Ling Tang, Haiying Meng, 2011, Behavior genetics.

Oncology—Constitutional

H. Meng, 2019, Self-Assessment Questions for Clinical Molecular Genetics.

General Molecular Genetic Knowledge

H. Meng, 2019, Self-Assessment Questions for Clinical Molecular Genetics.

Polymorphism of DCDC2 Reveals Differences in Cortical Morphology of Healthy Individuals—A Preliminary Voxel Based Morphometry Study

Vince D. Calhoun, Godfrey D. Pearlson, Shashwath A. Meda, 2008, Brain Imaging and Behavior.

Variants in the DYX2 locus are associated with altered brain activation in reading-related brain regions in subjects with reading disability

R. Todd Constable, Grier P. Page, Robert K. Fulbright, 2012, NeuroImage.

DCDC2 genetic variants and susceptibility to developmental dyslexia

Haiying Meng, Roberto Giorda, Massimo Molteni, 2012, Psychiatric genetics.

Cystic Fibrosis

H. Meng, 2019, Self-Assessment Questions for Clinical Molecular Genetics.

Clinical Molecular Genetic Laboratory Practice, Where We Stand in 2018

H. Meng, W. Xu, 2018 .

Prenatal, Newborn Screen, and Metabolic Disorders

H. Meng, 2019, Self-Assessment Questions for Clinical Molecular Genetics.

Lysosomal Storage Disorders

H. Meng, 2019, Self-Assessment Questions for Clinical Molecular Genetics.

Molecular Genetic Nomenclature

H. Meng, 2019, Self-Assessment Questions for Clinical Molecular Genetics.

Genetic approaches to complications of prematurity.

J. Gruen, H. Meng, 2007, Frontiers in bioscience : a journal and virtual library.

Disorders of Unstable Repeat Sequences

H. Meng, 2019, Self-Assessment Questions for Clinical Molecular Genetics.

Nonneoplastic Hematological Disorders

H. Meng, 2019, Self-Assessment Questions for Clinical Molecular Genetics.

Clinical Impact and Cost-Effectiveness of Whole Exome Sequencing as a Diagnostic Tool: A Pediatric Center’s Experience

F. Zou, J. Harley, R. Hopkin, 2015, Front. Pediatr..