<i>DCDC2</i> is associated with reading disability and modulates neuronal development in the brain

Haiying Meng, Shelley D. Smith, Karl Hager, +17

Proceedings of the National Academy of Sciences

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

C. Alexander Valencia, Ammar Husami, Jennifer Holle, +22

Frontiers in Pediatrics

DCDC2 genetic variants and susceptibility to developmental dyslexia

Cecilia Marino, Haiying Meng, Sara Mascheretti, +5

Psychiatric Genetics

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

Haiying Meng, Karl Hager, Matthew A. Held, +6

Human Genetics

Colorado Twin CohortLanguage DisorderTdt-association AnalysisRehabilitationNeurology +4

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

Shashwath A. Meda, Joel Gelernter, Jeffrey R. Gruen, +4

Brain Imaging and Behavior

Dcdc2 Reveals DifferencesMorphometry StudyBrain DevelopmentNeuroanatomyCortical Remodeling +7

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

Natalie Cope, John D. Eicher, Haiying Meng, +7

NeuroImage

Neurological DisorderReading DifficultiesDyx2 LocusReading-related Brain RegionsEducation +7

A Dyslexia-Associated Variant in DCDC2 Changes Gene Expression

Haiying Meng, Natalie R. Powers, Ling Tang, +6

Behavior Genetics

Dyslexia-associated VariantNeuroscienceDegenerative DiseaseCorticobasal Degeneration

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

Kerstin U. Ludwig, Johannes Schumacher, Gerd Schulte‐Körne, +13

Psychiatric Genetics

Neurodevelopmental DisordersMendelian DisorderGenetic DisorderMedicineNeurolinguistics +13

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

Eric Londin, Haiying Meng, Jeffrey R. Gruen

BMC Genomics

Detection of Turner Syndrome Using High-Throughput Quantitative Genotyping

Haiying Meng, Karl Hager, Scott A. Rivkees, +1

The Journal of Clinical Endocrinology & Metabolism