H. Qiu

发表

Age group and sex differences in performance on a computerized neurocognitive battery in children age 8-21.

Raquel E Gur, Ruben C Gur, James Loughead, 2012, Neuropsychology.

Electronic Health Record Based Algorithm to Identify Patients with Autism Spectrum Disorder

Finale Doshi-Velez, Pei Chen, Joseph Bochenek, 2016, PloS one.

The Philadelphia Neurodevelopmental Cohort: constructing a deep phenotyping collaborative.

Kosha Ruparel, Theodore D Satterthwaite, David R Roalf, 2015, Journal of child psychology and psychiatry, and allied disciplines.

GWAS of blood cell traits identifies novel associated loci and epistatic interactions in Caucasian and African-American children.

Yiran Guo, Joseph T. Glessner, Hakon Hakonarson, 2013, Human molecular genetics.

Identification of Novel Loci Shared by Juvenile Idiopathic Arthritis Subtypes Through Integrative Genetic Analysis

J. Glessner, H. Hakonarson, B. Lie, 2022, Arthritis & rheumatology.

Integrative Genetics Analysis of Juvenile Idiopathic Arthritis Identifies Novel Loci

John J. Connolly, Joseph T. Glessner, Debra K. Shivers, 2020, medRxiv.

Meta-analysis of shared genetic architecture across ten pediatric autoimmune diseases

Constantin Polychronakos, Yiran Guo, Dong Li, 2016 .

Common variants in MMP20 at 11q22.2 predispose to 11q deletion and neuroblastoma risk

Joseph T. Glessner, J. Glessner, H. Hakonarson, 2017, Nature Communications.

The impact of the metabotropic glutamate receptor and other gene family interaction networks on autism

Thomas Bourgeron, Ellen M. Wijsman, Gillian Baird, 2014, Nature Communications.

Identification of risk variants related to malignant tumors in children with birth defects by whole genome sequencing

Joseph T. Glessner, J. Glessner, H. Hakonarson, 2022, Biomarker Research.

A Genome-Wide Meta-Analysis of Six Type 1 Diabetes Cohorts Identifies Multiple Associated Loci

Constantin Polychronakos, Struan F. A. Grant, Joseph T. Glessner, 2011, PLoS genetics.

Rare Recurrent Variants in Noncoding Regions Impact Attention-Deficit Hyperactivity Disorder (ADHD) Gene Networks in Children of both African American and European American Ancestry

Joseph T. Glessner, J. Glessner, H. Hakonarson, 2021, Genes.

Examination of genetic variants influencing lipid traits in pediatric populations

Joseph T. Glessner, Alexa J Moy, J. Glessner, 2012, Journal of Pediatric Genetics.

Non-coding structural variation differentially impacts attention-deficit hyperactivity disorder (ADHD) gene networks in African American vs Caucasian children

J. Glessner, H. Hakonarson, H. Qu, 2020, Scientific Reports.

Erratum: A genome-wide association study of anorexia nervosa suggests a risk locus implicated in dysregulated leptin signaling

H. Hakonarson, Cecilia Kim, Yiran Guo, 2017, Scientific Reports.

A genome-wide association study of anorexia nervosa suggests a risk locus implicated in dysregulated leptin signaling

John J. Connolly, I. Ntalla, E. Zeggini, 2017, Scientific Reports.

The Philadelphia Neurodevelopmental Cohort: A publicly available resource for the study of normal and abnormal brain development in youth

Mark A. Elliott, David R. Roalf, Kosha Ruparel, 2016, NeuroImage.

The psychosis spectrum in a young U.S. community sample: findings from the Philadelphia Neurodevelopmental Cohort

Kosha Ruparel, Theodore D Satterthwaite, Tyler M Moore, 2014, World psychiatry : official journal of the World Psychiatric Association.

Duplication of the SLIT3 Locus on 5q35.1 Predisposes to Major Depressive Disorder

Struan F. A. Grant, Joseph T. Glessner, Hakon Hakonarson, 2010, PloS one.

Variants in CXCR4 associate with juvenile idiopathic arthritis susceptibility

Joseph T. Glessner, Debra K. Shivers, J. Glessner, 2016, BMC Medical Genetics.

Rare copy number variants in over 100,000 European ancestry subjects reveal multiple disease associations

Joseph T. Glessner, Bradley P. Coe, B. Coe, 2020, Nature Communications.

Rare copy number variants in over 100,000 European ancestry subjects reveal multiple disease associations

B. Coe, E. Eichler, J. Glessner, 2020, Nature Communications.

Expanding the SPECC1L mutation phenotypic spectrum to include Teebi hypertelorism syndrome

E. Zackai, H. Hakonarson, Cecilia Kim, 2015, American journal of medical genetics. Part A.

Common variants in MMP20 at 11q22.2 predispose to 11q deletion and neuroblastoma risk

Joseph T. Glessner, J. Glessner, H. Hakonarson, 2017, Nature Communications.

Genome-Wide Association Study of Serum Minerals Levels in Children of Different Ethnic Background

H. Hakonarson, Cecilia Kim, Yiran Guo, 2015, PloS one.

Genome-wide association study reveals two loci for serum magnesium concentrations in European-American children

Joseph T. Glessner, J. Glessner, H. Hakonarson, 2015, Scientific Reports.

A Naïve Bayes classifier for differential diagnosis of Long QT Syndrome in children

Peter S. White, Geoffrey L. Bird, Long Qu, 2010, 2010 IEEE International Conference on Bioinformatics and Biomedicine (BIBM).

Genomic information of children with malignant brain tumors for the prediction of length of hospitalization.

J. Glessner, H. Hakonarson, H. Qu, 2023, Cancer Communications.

Meta-analysis of shared genetic architecture across ten pediatric autoimmune diseases

John J. Connolly, J. Glessner, H. Hakonarson, 2015, Nature Medicine.

Genome-Wide Association Study of Serum Minerals Levels in Children of Different Ethnic Background

H. Hakonarson, Cecilia Kim, Yiran Guo, 2015, PloS one.

Age group and sex differences in performance on a computerized neurocognitive battery in children age 8-21.

John J. Connolly, H. Hakonarson, R. Gur, 2012, Neuropsychology.

Meta-analysis of shared genetic architecture across ten pediatric autoimmune diseases

J. Glessner, H. Hakonarson, Cecilia Kim, 2015, Nature Medicine.

Meta-analysis of shared genetic architecture across ten pediatric autoimmune diseases

John J. Connolly, J. Glessner, H. Hakonarson, 2015, Nature Medicine.

High Comorbidity of Pediatric Cancers in Patients with Birth Defects: Insights from Whole Genome Sequencing Analysis of Copy Number Variations.

J. Glessner, H. Hakonarson, H. Qu, 2023, Translational research : the journal of laboratory and clinical medicine.

A genome-wide association study of anorexia nervosa suggests a risk locus implicated in dysregulated leptin signaling

John J. Connolly, I. Ntalla, E. Zeggini, 2017, Scientific Reports.