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Author Details

Frank D Mentch
Center for Applied Genomics (CAG), Children's Hospital of Philadelphia
1987
101
33
PMIDPaper TitleJournal TitlePublished Year
35902206Identification of novel loci in obstructive sleep apnea in European American and African American children.Sleep2024
35902206Identification of novel loci in obstructive sleep apnea in European American and African American children.Sleep2024
37989391High Comorbidity of Pediatric Cancers in Patients with Birth Defects: Insights from Whole Genome Sequencing Analysis of Copy Number Variations.Transl Res2024
37989391High Comorbidity of Pediatric Cancers in Patients with Birth Defects: Insights from Whole Genome Sequencing Analysis of Copy Number Variations.Transl Res2024
36089080Genetic architecture of asthma in African American patients.J Allergy Clin Immunol2023
36089080Genetic architecture of asthma in African American patients.J Allergy Clin Immunol2023
37559342Genomic information of children with malignant brain tumors for the prediction of length of hospitalization.Cancer Commun (Lond)2023
36653407Molecular diagnosis and novel genes and phenotypes in a pediatric thoracic insufficiency cohort.Sci Rep2023
36712066Trans-ethnic Polygenic Risk Scores for Body Mass Index: An International Hundred K+ Cohorts Consortium Study.medRxiv2023
37450379Trans-ethnic genomic informed risk assessment for Alzheimer's disease: An International Hundred K+ Cohorts Consortium study.Alzheimers Dement2023
37120522Rare recurrent copy number variations in metabotropic glutamate receptor interacting genes in children with neurodevelopmental disorders.J Neurodev Disord2023
36621880Returning integrated genomic risk and clinical recommendations: The eMERGE study.Genet Med2023
37369742Ambient air pollution sensitivity and severity of pediatric asthma.J Expo Sci Environ Epidemiol2023
36737471Evaluation of the portability of computable phenotypes with natural language processing in the eMERGE network.Sci Rep2023
36688686Elevated Levels of the Cytokine LIGHT in Pediatric Crohn's Disease.J Immunol2023
37543594Genomic variants exclusively identified in children with birth defects and concurrent malignant tumors predispose to cancer development.Mol Cancer2023
37559342Genomic information of children with malignant brain tumors for the prediction of length of hospitalization.Cancer Commun (Lond)2023
37543594Genomic variants exclusively identified in children with birth defects and concurrent malignant tumors predispose to cancer development.Mol Cancer2023
37120522Rare recurrent copy number variations in metabotropic glutamate receptor interacting genes in children with neurodevelopmental disorders.J Neurodev Disord2023
37450379Trans-ethnic genomic informed risk assessment for Alzheimer's disease: An International Hundred K+ Cohorts Consortium study.Alzheimers Dement2023
37369742Ambient air pollution sensitivity and severity of pediatric asthma.J Expo Sci Environ Epidemiol2023
36653407Molecular diagnosis and novel genes and phenotypes in a pediatric thoracic insufficiency cohort.Sci Rep2023
36621880Returning integrated genomic risk and clinical recommendations: The eMERGE study.Genet Med2023
36688686Elevated Levels of the Cytokine LIGHT in Pediatric Crohn's Disease.J Immunol2023
36712066Trans-ethnic Polygenic Risk Scores for Body Mass Index: An International Hundred K+ Cohorts Consortium Study.medRxiv2023
36737471Evaluation of the portability of computable phenotypes with natural language processing in the eMERGE network.Sci Rep2023
34506852A genome-wide association meta-analysis identifies new eosinophilic esophagitis loci.J Allergy Clin Immunol2022
36372681Quantifying the phenome-wide disease burden of obesity using electronic health records and genomics.Obesity (Silver Spring)2022
35595084Multiancestral polygenic risk score for pediatric asthma.J Allergy Clin Immunol2022
35524249Burden of rare coding variants reveals genetic heterogeneity between obese and non-obese asthma patients in the African American population.Respir Res2022
35642741Mutation burden analysis of six common mental disorders in African Americans by whole genome sequencing.Hum Mol Genet2022
35577121Contribution of Mendelian Disorders in a Population-Based Pediatric Neurodegeneration Cohort.J Pediatr2022
35811841Metabolomic profiling of samples from pediatric patients with asthma unveils deficient nutrients in African Americans.iScience2022
35690720An electronic health record (EHR) phenotype algorithm to identify patients with attention deficit hyperactivity disorders (ADHD) and psychiatric comorbidities.J Neurodev Disord2022
36384586Identification of risk variants related to malignant tumors in children with birth defects by whole genome sequencing.Biomark Res2022
36051697COVID-19 in pediatrics: Genetic susceptibility.Front Genet2022
36459297Metabolomic profiling for dyslipidemia in pediatric patients with sickle cell disease, on behalf of the IHCC consortium.Metabolomics2022
34506852A genome-wide association meta-analysis identifies new eosinophilic esophagitis loci.J Allergy Clin Immunol2022
35171267Genetic analysis for type 1 diabetes genes in juvenile dermatomyositis unveils genetic disease overlap.Rheumatology (Oxford)2022
34380996Genetic association of primary nonresponse to anti-TNFα therapy in patients with inflammatory bowel disease.Pharmacogenet Genomics2022
35090449Under-specification as the source of ambiguity and vagueness in narrative phenotype algorithm definitions.BMC Med Inform Decis Mak2022
34997821Improved genetic risk scoring algorithm for type 1 diabetes prediction.Pediatr Diabetes2022
34997195Application of deep learning algorithm on whole genome sequencing data uncovers structural variants associated with multiple mental disorders in African American patients.Mol Psychiatry2022
35347896Identification of Novel Loci Shared by Juvenile Idiopathic Arthritis Subtypes Through Integrative Genetic Analysis.Arthritis Rheumatol2022
35347896Identification of Novel Loci Shared by Juvenile Idiopathic Arthritis Subtypes Through Integrative Genetic Analysis.Arthritis Rheumatol2022
35642741Mutation burden analysis of six common mental disorders in African Americans by whole genome sequencing.Hum Mol Genet2022
35577121Contribution of Mendelian Disorders in a Population-Based Pediatric Neurodegeneration Cohort.J Pediatr2022
35690720An electronic health record (EHR) phenotype algorithm to identify patients with attention deficit hyperactivity disorders (ADHD) and psychiatric comorbidities.J Neurodev Disord2022
35595084Multiancestral polygenic risk score for pediatric asthma.J Allergy Clin Immunol2022
35524249Burden of rare coding variants reveals genetic heterogeneity between obese and non-obese asthma patients in the African American population.Respir Res2022
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Collaborators

Hakon Hakonarson
The Center for Applied Genomics, Children's Hospital of Philadelphia
Co-authored papers 92
Patrick M A Sleiman
The Center for Applied Genomics, Children's Hospital of Philadelphia
Co-authored papers 58
Joseph T Glessner
Co-authored papers 43
John J Connolly
Center for Applied Genomics, Children's Hospital of Philadelphia
Co-authored papers 30
Cecilia E Kim
Co-authored papers 29
Jonathan P Bradfield
Co-authored papers 26
Rosetta M Chiavacci
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Struan F A Grant
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Co-authored papers 22
Jin Li
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Zhi Wei
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Michael E March
Co-authored papers 16
Kelly Thomas
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Gail P Jarvik
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Joshua C Denny
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Haitao Zhang
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Yiran Guo
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Bahram Namjou
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Kai Wang
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Edward C Frackelton
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Fengxiang Wang
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Dong Li
Co-authored papers 9
Jennifer A Pacheco
University of Pennsylvania
Co-authored papers 8
David R Crosslin
University of Washington Medical Center
Co-authored papers 8
David S Carrell
Kaiser Permanente Washington Health Research Institute
Co-authored papers 8
Eric B Larson
University of Washington
Co-authored papers 7
Andr?? G Uitterlinden
Erasmus University Medical Center
Co-authored papers 7
Fernando Rivadeneira
University Medical Center Rotterdam
Co-authored papers 7
Nicholas J Timpson
Co-authored papers 7
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