Author details

Full Name

Joseph T Glessner

Affiliation

ORCID

Career Start Year

2007

Papers

178

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
37865391	A Protective Role of Low Polygenic Risk Score in Healthy Individuals Carrying Attention-Deficit/Hyperactivity Disorder-Associated Copy Number Variations.	Biol Psychiatry	2024
35902206	Identification of novel loci in obstructive sleep apnea in European American and African American children.	Sleep	2024
37989391	High Comorbidity of Pediatric Cancers in Patients with Birth Defects: Insights from Whole Genome Sequencing Analysis of Copy Number Variations.	Transl Res	2024
37543594	Genomic variants exclusively identified in children with birth defects and concurrent malignant tumors predispose to cancer development.	Mol Cancer	2023
36302597	Genomic Disorders in CKD across the Lifespan.	J Am Soc Nephrol	2023
36089080	Genetic architecture of asthma in African American patients.	J Allergy Clin Immunol	2023
36316489	ParseCNV2: efficient sequencing tool for copy number variation genome-wide association studies.	Eur J Hum Genet	2023
37572794	Biliary atresia is associated with polygenic susceptibility in ciliogenesis and planar polarity effector genes.	J Hepatol	2023
37559342	Genomic information of children with malignant brain tumors for the prediction of length of hospitalization.	Cancer Commun (Lond)	2023
38072244	Mitochondrial DNA Haplogroup K Is Protective Against Autism Spectrum Disorder Risk in Populations of European Ancestry.	J Am Acad Child Adolesc Psychiatry	2023
37700208	The Circassians and the Chechens in Jordan: results of a decade of epidemiological and genetic studies.	J Community Genet	2023
37963017	The molecular genetic landscape of human brain size variation.	Cell Rep	2023
37450379	Trans-ethnic genomic informed risk assessment for Alzheimer's disease: An International Hundred K+ Cohorts Consortium study.	Alzheimers Dement	2023
37120522	Rare recurrent copy number variations in metabotropic glutamate receptor interacting genes in children with neurodevelopmental disorders.	J Neurodev Disord	2023
37425875	High density SNP array and reanalysis of genome sequencing uncovers CNVs associated with neurodevelopmental disorders in KOLF2.1J iPSCs.	bioRxiv	2023
36672883	Single Cell Transcriptome Analysis of Peripheral Blood Mononuclear Cells in Freshly Isolated versus Stored Blood Samples.	Genes (Basel)	2023
37227088	TOPORS as a novel causal gene for Joubert syndrome.	Am J Med Genet A	2023
34930020	Arrhythmia Variant Associations and Reclassifications in the eMERGE-III Sequencing Study.	Circulation	2022
35594287	Mendelian randomization analysis of plasma levels of CD209 and MICB proteins and the risk of varicose veins of lower extremities.	PLoS One	2022
35524249	Burden of rare coding variants reveals genetic heterogeneity between obese and non-obese asthma patients in the African American population.	Respir Res	2022
35386517	Expansion of Schizophrenia Gene Network Knowledge Using Machine Learning Selected Signals From Dorsolateral Prefrontal Cortex and Amygdala RNA-seq Data.	Front Psychiatry	2022
35642741	Mutation burden analysis of six common mental disorders in African Americans by whole genome sequencing.	Hum Mol Genet	2022
35811841	Metabolomic profiling of samples from pediatric patients with asthma unveils deficient nutrients in African Americans.	iScience	2022
35690720	An electronic health record (EHR) phenotype algorithm to identify patients with attention deficit hyperactivity disorders (ADHD) and psychiatric comorbidities.	J Neurodev Disord	2022
35544191	Copy Number Variant Risk Scores Associated With Cognition, Psychopathology, and Brain Structure in Youths in the Philadelphia Neurodevelopmental Cohort.	JAMA Psychiatry	2022
36384586	Identification of risk variants related to malignant tumors in children with birth defects by whole genome sequencing.	Biomark Res	2022
36051697	COVID-19 in pediatrics: Genetic susceptibility.	Front Genet	2022
36459297	Metabolomic profiling for dyslipidemia in pediatric patients with sickle cell disease, on behalf of the IHCC consortium.	Metabolomics	2022
34506852	A genome-wide association meta-analysis identifies new eosinophilic esophagitis loci.	J Allergy Clin Immunol	2022
35203474	Circulating LIGHT (TNFSF14) and Interleukin-18 Levels in Sepsis-Induced Multi-Organ Injuries.	Biomedicines	2022
35171267	Genetic analysis for type 1 diabetes genes in juvenile dermatomyositis unveils genetic disease overlap.	Rheumatology (Oxford)	2022
35134187	Identification of Mitochondrial DNA Variants Associated With Risk of Neuroblastoma.	J Natl Cancer Inst	2022
34997821	Improved genetic risk scoring algorithm for type 1 diabetes prediction.	Pediatr Diabetes	2022
34997195	Application of deep learning algorithm on whole genome sequencing data uncovers structural variants associated with multiple mental disorders in African American patients.	Mol Psychiatry	2022
35347896	Identification of Novel Loci Shared by Juvenile Idiopathic Arthritis Subtypes Through Integrative Genetic Analysis.	Arthritis Rheumatol	2022
35101533	Mendelian randomization study of obesity and type 2 diabetes in hospitalized COVID-19 patients.	Metabolism	2022
34362956	Insights into non-autoimmune type 1 diabetes with 13 novel loci in low polygenic risk score patients.	Sci Rep	2021
34180972	Association Between a Common, Benign Genotype and Unnecessary Bone Marrow Biopsies Among African American Patients.	JAMA Intern Med	2021
33805976	Machine Learning Reduced Gene/Non-Coding RNA Features That Classify Schizophrenia Patients Accurately and Highlight Insightful Gene Clusters.	Int J Mol Sci	2021
34233526	Deep learning prediction of attention-deficit hyperactivity disorder in African Americans by copy number variation.	Exp Biol Med (Maywood)	2021
33479212	Integrative analysis of genome-wide association studies identifies novel loci associated with neuropsychiatric disorders.	Transl Psychiatry	2021
33627065	MONTAGE: a new tool for high-throughput detection of mosaic copy number variation.	BMC Genomics	2021
33950547	Combined application of genetic and polygenic risk scores for type 1 diabetes risk prediction.	Diabetes Obes Metab	2021
33671795	Rare Recurrent Variants in Noncoding Regions Impact Attention-Deficit Hyperactivity Disorder (ADHD) Gene Networks in Children of both African American and European American Ancestry.	Genes (Basel)	2021
33942034	Genetic correlations between COVID-19 and a variety of traits and diseases.	Innovation (Camb)	2021
34093663	Genome-Wide Detection of Copy Number Variations and Their Association With Distinct Phenotypes in the World's Sheep.	Frontiers in Genetics	2021
34302048	Genetic architecture of type 1 diabetes with low genetic risk score informed by 41 unreported loci.	Commun Biol	2021
33369054	Ciliopathies: Coloring outside of the lines.	Am J Med Genet A	2021
33429424	DeepCNV: a deep learning approach for authenticating copy number variations.	Brief Bioinform	2021
33408077	Association of novel rare coding variants with juvenile idiopathic arthritis.	Ann Rheum Dis	2021