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Haiying Meng
Observed name:
Meng H
Observed institutions:
Cincinnati Children's Hospital Medical Center,
University of Denver,
Baystate Medical Center,
University of Colorado Boulder,
Sichuan University,
Yale University,
University of Nebraska Medical Center,
University of Cincinnati
show all 8
OpenAlex ID:
A5043625370
DCDC2 is associated with reading disability and modulates neuronal development in the brain
2005
·
Haiying Meng
, Shelley D. Smith
, et al.
·
Proceedings of the National Academy of Sciences
·
382
Clinical Impact and Cost-Effectiveness of Whole Exome Sequencing as a Diagnostic Tool: A Pediatric Center’s Experience
2015
·
C. Alexander Valencia
, Ammar Husami
, et al.
·
Frontiers in Pediatrics
·
185
PDF
DCDC2 genetic variants and susceptibility to developmental dyslexia
2011
·
Cecilia Marino
, Haiying Meng
, et al.
·
Psychiatric Genetics
·
81
TDT-association analysis of EKN1 and dyslexia in a Colorado twin cohort
2005
·
Haiying Meng
, Karl Hager
, et al.
·
Human Genetics
·
76
Polymorphism of DCDC2 Reveals Differences in Cortical Morphology of Healthy Individuals—A Preliminary Voxel Based Morphometry Study
2007
·
Shashwath A. Meda
, Joel Gelernter
, et al.
·
Brain Imaging and Behavior
·
64
Variants in the DYX2 locus are associated with altered brain activation in reading-related brain regions in subjects with reading disability
2012
·
Natalie Cope
, John D. Eicher
, et al.
·
NeuroImage
·
61
A Dyslexia-Associated Variant in DCDC2 Changes Gene Expression
2010
·
Haiying Meng
, Natalie R. Powers
, et al.
·
Behavior Genetics
·
59
Investigation of the DCDC2 intron 2 deletion/compound short tandem repeat polymorphism in a large German dyslexia sample
2008
·
Kerstin U. Ludwig
, Johannes Schumacher
, et al.
·
Psychiatric Genetics
·
51
A transcription map of the 6p22.3 reading disability locus identifying candidate genes
2003
·
Eric R Londin
, Haiying Meng
, et al.
·
BMC Genomics
·
28
PDF
Detection of Turner Syndrome Using High-Throughput Quantitative Genotyping
2005
·
Haiying Meng
, Karl Hager
, et al.
·
The Journal of Clinical Endocrinology & Metabolism
·
18
Genetic approaches to complications of prematurity
2006
·
Haiying Meng
·
Frontiers in bioscience
·
4
PDF
Clinical Molecular Genetic Laboratory Practice, Where We Stand in 2018
2018
·
Meng H
, Xu W
·
Journal of Molecular and Genetic Medicine
·
2
Prenatal, Newborn Screen, and Metabolic Disorders
2019
·
Haiying Meng
·
Elsevier eBooks
·
1
Gender Identification Differences Observed For DNA Quantification versus STR Genotyping of Mummified Human Remains-How it Relates to Human Identifications in Forensic Science.
2009
·
Kate M. Reidy
, Amanda Gareis
, et al.
·
1
Nonneoplastic Hematological Disorders
2019
·
Haiying Meng
·
Elsevier eBooks
Molecular Genetic Nomenclature
2019
·
Haiying Meng
·
Elsevier eBooks
Genetic Counseling—Introduction
2019
·
Haiying Meng
·
Elsevier eBooks
General Molecular Genetic Knowledge
2019
·
Haiying Meng
·
Elsevier eBooks
Other Common Genetic Syndromes
2019
·
Haiying Meng
·
Elsevier eBooks
Dysgerminoma in a Patient With 45,X: A Challenge to Endocrinologists and Geneticists
2015
·
Susmitha Edappallath
, Rahul Jawale
, et al.
·
American Journal of Clinical Pathology
[Relationship between HFE gene and hereditary hemochromatosis].
2002
·
Haiying Meng
, Yiping Hou
·
PubMed
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Works count:
22
Citation count:
1,013
H-index:
10
I10-index:
10
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