Skip to Main Content

Author Details

Patrick M A Sleiman
The Center for Applied Genomics, Children's Hospital of Philadelphia
1999
224
62
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
36316489ParseCNV2: efficient sequencing tool for copy number variation genome-wide association studies.Eur J Hum Genet2023
36089080Genetic architecture of asthma in African American patients.J Allergy Clin Immunol2023
36403896Differences in Self-Reported Food Allergy and Food-Associated Anaphylaxis by Race and Ethnicity Among SAPPHIRE Cohort Participants.J Allergy Clin Immunol Pract2023
36316489ParseCNV2: efficient sequencing tool for copy number variation genome-wide association studies.Eur J Hum Genet2023
37572794Biliary atresia is associated with polygenic susceptibility in ciliogenesis and planar polarity effector genes.J Hepatol2023
37794016European and multi-ancestry genome-wide association meta-analysis of atopic dermatitis highlights importance of systemic immune regulation.Nat Commun2023
37790445Genetic Sex Validation for Sample Tracking in Clinical Testing.Res Sq2023
36653407Molecular diagnosis and novel genes and phenotypes in a pediatric thoracic insufficiency cohort.Sci Rep2023
37028392Evidence of epistasis in regions of long-range linkage disequilibrium across five complex diseases in the UK Biobank and eMERGE datasets.Am J Hum Genet2023
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
36864747Functional characterization of all missense variants in <i>LEPR, PCSK1</i>, and <i>POMC</i> genes arising from single-nucleotide variants.Expert Rev Endocrinol Metab2023
36688686Elevated Levels of the Cytokine LIGHT in Pediatric Crohn's Disease.J Immunol2023
37794016European and multi-ancestry genome-wide association meta-analysis of atopic dermatitis highlights importance of systemic immune regulation.Nat Commun2023
37790445Genetic Sex Validation for Sample Tracking in Clinical Testing.Res Sq2023
37572794Biliary atresia is associated with polygenic susceptibility in ciliogenesis and planar polarity effector genes.J Hepatol2023
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
37028392Evidence of epistasis in regions of long-range linkage disequilibrium across five complex diseases in the UK Biobank and eMERGE datasets.Am J Hum Genet2023
36653407Molecular diagnosis and novel genes and phenotypes in a pediatric thoracic insufficiency cohort.Sci Rep2023
36403896Differences in Self-Reported Food Allergy and Food-Associated Anaphylaxis by Race and Ethnicity Among SAPPHIRE Cohort Participants.J Allergy Clin Immunol Pract2023
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
36864747Functional characterization of all missense variants in <i>LEPR, PCSK1</i>, and <i>POMC</i> genes arising from single-nucleotide variants.Expert Rev Endocrinol Metab2023
36089080Genetic architecture of asthma in African American patients.J Allergy Clin Immunol2023
34506852A genome-wide association meta-analysis identifies new eosinophilic esophagitis loci.J Allergy Clin Immunol2022
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
35446370Association of Pathogenic Variants in Hereditary Cancer Genes With Multiple Diseases.JAMA Oncol2022
35386517Expansion of Schizophrenia Gene Network Knowledge Using Machine Learning Selected Signals From Dorsolateral Prefrontal Cortex and Amygdala RNA-seq Data.Front Psychiatry2022
35642741Mutation burden analysis of six common mental disorders in African Americans by whole genome sequencing.Hum Mol Genet2022
36016708Frataxin controls ketone body metabolism through regulation of OXCT1.PNAS Nexus2022
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
35869121Genome-wide association study in minority children with asthma implicates DNAH5 in bronchodilator responsiveness.Sci Rep2022
35543309Saudi Arabian CML patient with a novel four-way translocation at t(9;22;5;2)(q34;q11.2;p13;q44).Mol Genet Genomic Med2022
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
35203474Circulating LIGHT (TNFSF14) and Interleukin-18 Levels in Sepsis-Induced Multi-Organ Injuries.Biomedicines2022
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
35134187Identification of Mitochondrial DNA Variants Associated With Risk of Neuroblastoma.J Natl Cancer Inst2022
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
34930020Arrhythmia Variant Associations and Reclassifications in the eMERGE-III Sequencing Study.Circulation2022
  • 1 - 50 of 448

Recommended Authors

John D Overton
Regeneron Pharmaceuticals
Career Start Year 2008
Number of shared co-authors 37
Hana Lango Allen
Institute of Metabolic Science, University of Cambridge
Career Start Year 2007
Number of shared co-authors 44
Elizabeth T Cirulli
Duke University
Career Start Year 2007
Number of shared co-authors 21
Per Hoffmann
Institute of Human Genetics, University of Bonn and University Hospital Bonn
Career Start Year 2005
Number of shared co-authors 120
Ali Torkamani
Scripps Science Institute
Career Start Year 2005
Number of shared co-authors 33
Beth Wilmot
Knight Cancer Institute, Oregon Health & Science University
Career Start Year 2004
Number of shared co-authors 59
Anna C Need
Imperial College London
Career Start Year 2003
Number of shared co-authors 17
Michael A Simpson
King's College London
Career Start Year 2002
Number of shared co-authors 18
Stefan Herms
Institute of Human Genetics, University of Bonn
Career Start Year 2001
Number of shared co-authors 94
Stacey Gabriel
Broad Institute of MIT and Harvard
Career Start Year 2001
Number of shared co-authors 137
Nathan Pankratz
University of Minnesota
Career Start Year 2001
Number of shared co-authors 89
Johannes Schumacher
Philipps University of Marburg
Career Start Year 2000
Number of shared co-authors 53
Ilja M Nolte
University of Groningen, University Medical Center Groningen
Career Start Year 2000
Number of shared co-authors 103
Jo Knight
Data Science Institute and Lancaster University Medical School
Career Start Year 2000
Number of shared co-authors 54
Nicole Soranzo
Wellcome Sanger Institute
Career Start Year 1998
Number of shared co-authors 118
Joshua D Smith
University of Washington
Career Start Year 1998
Number of shared co-authors 85
Yi-Ju Li
Duke University School of Medicine
Career Start Year 1998
Number of shared co-authors 11
Michael M Barmada
Graduate School of Public Health, University of Pittsburgh
Career Start Year 1996
Number of shared co-authors 49
Szabolcs Szelinger
College of American Pathologists
Career Start Year 1996
Number of shared co-authors 33
David J Cutler
Emory University School of Medicine
Career Start Year 1994
Number of shared co-authors 45
Dimitrios Avramopoulos
Johns Hopkins School of Medicine
Career Start Year 1992
Number of shared co-authors 20
Rafa?? P??oski
Medical University of Warsaw
Career Start Year 1992
Number of shared co-authors 16
David Altshuler
Broad Institute of Harvard and Massachusetts Institute of Technology (MIT)
Career Start Year 1992
Number of shared co-authors 116
William C L Stewart
Middle Tennessee State University
Career Start Year 1992
Number of shared co-authors 3
Andrew D Paterson
The Hospital for Sick Children
Career Start Year 1991
Number of shared co-authors 73
Andrew A Hicks
Institute for Biomedicine, Affiliated institute of the University of Lubeck
Career Start Year 1990
Number of shared co-authors 101
Juha Kere
Folkhalsan Research Center, University of Helsinki
Career Start Year 1987
Number of shared co-authors 43
Thomas Meitinger
Technical University of Munich, Institute of Human Genetics
Career Start Year 1982
Number of shared co-authors 135
Guy A Rouleau
McGill University, Canada Montreal Neurological Institute and Hospital
Career Start Year 1981
Number of shared co-authors 79
Kari Stefansson
University of Iceland
Career Start Year 1980
Number of shared co-authors 194

Collaborators

Hakon Hakonarson
The Center for Applied Genomics, Children's Hospital of Philadelphia
Co-authored papers 167
Joseph T Glessner
Co-authored papers 73
Frank D Mentch
Center for Applied Genomics (CAG), Children's Hospital of Philadelphia
Co-authored papers 58
Cecilia E Kim
Co-authored papers 38
Jonathan P Bradfield
Co-authored papers 36
Michael E March
Co-authored papers 35
Nicholas W Wood
UCL Queen Square Institute of Neurology
Co-authored papers 35
Rosetta M Chiavacci
Co-authored papers 33
John J Connolly
Center for Applied Genomics, Children's Hospital of Philadelphia
Co-authored papers 31
Struan F A Grant
Center for Spatial and Functional Genomics, The Children's Hospital of Philadelphia
Co-authored papers 29
Jin Li
Co-authored papers 28
Kelly Thomas
Co-authored papers 21
Edward C Frackelton
Co-authored papers 20
Haitao Zhang
Co-authored papers 18
Zhi Wei
Co-authored papers 17
Gail P Jarvik
University of Washington Medical Center
Co-authored papers 16
Kai Wang
University of Pennsylvania
Co-authored papers 15
Raquel E Gur
University of Pennsylvania Perelman School of Medicine
Co-authored papers 14
Frederick G Otieno
Co-authored papers 14
Dong Li
Co-authored papers 14
Renata Pellegrino
Co-authored papers 12
Yiran Guo
Center for Data-Driven Discovery in Biomedicine, Children's Hospital of Philadelphia
Co-authored papers 12
Marcin Imielinski
Co-authored papers 12
Iftikhar J Kullo
Mayo Clinic
Co-authored papers 10
Esteban G Burchard
University of California San Francisco (UCSF)
Co-authored papers 10
Fengxiang Wang
Co-authored papers 10
Brendan J Keating
Perelman School of Medicine, University of Pennsylvania
Co-authored papers 9
Scott T Weiss
Brigham and Women's Hospital, Harvard Medical School
Co-authored papers 9
David R Crosslin
University of Washington Medical Center
Co-authored papers 9
Berta Almoguera
Center for Biomedical Research in Rare Diseases Network
Co-authored papers 9
Release 1.2