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Author Details

Michael E Zwick
Rutgers University-New Brunswick, Rutgers University
1989
74
27
PMIDPaper TitleJournal TitlePublished Year
37165454High level of complexity and global diversity of the 3q29 locus revealed by optical mapping and long-read sequencing.Genome Med2023
37165454High level of complexity and global diversity of the 3q29 locus revealed by optical mapping and long-read sequencing.Genome Med2023
35177588Metabolic effects of the schizophrenia-associated 3q29 deletion.Transl Psychiatry2022
35911904Novel Missense <i>CNTNAP2</i> Variant Identified in Two Consanguineous Pakistani Families With Developmental Delay, Epilepsy, Intellectual Disability, and Aggressive Behavior.Front Neurol2022
35617426Identification of <i>PSMB5</i> as a genetic modifier of fragile X-associated tremor/ataxia syndrome.Proc Natl Acad Sci U S A2022
35931052Loss of function of OTUD7A in the schizophrenia- associated 15q13.3 deletion impairs synapse development and function in human neurons.Am J Hum Genet2022
35177588Metabolic effects of the schizophrenia-associated 3q29 deletion.Transl Psychiatry2022
35617426Identification of <i>PSMB5</i> as a genetic modifier of fragile X-associated tremor/ataxia syndrome.Proc Natl Acad Sci U S A2022
35911904Novel Missense <i>CNTNAP2</i> Variant Identified in Two Consanguineous Pakistani Families With Developmental Delay, Epilepsy, Intellectual Disability, and Aggressive Behavior.Front Neurol2022
35931052Loss of function of OTUD7A in the schizophrenia- associated 15q13.3 deletion impairs synapse development and function in human neurons.Am J Hum Genet2022
32015465Genetic contributors to risk of schizophrenia in the presence of a 22q11.2 deletion.Mol Psychiatry2021
32015465Genetic contributors to risk of schizophrenia in the presence of a 22q11.2 deletion.Mol Psychiatry2021
34016428Identifying susceptibility genes for primary ovarian insufficiency on the high-risk genetic background of a fragile X premutation.Fertil Steril2021
34121934Staff Scientist Perspectives on Onboarding and Professional Development: A Case Study.J Biomol Tech2021
34285246Author Correction: Identifying genetic factors that contribute to the increased risk of congenital heart defects in infants with Down syndrome.Sci Rep2021
34002220Site- and Taxa-Specific Disease-Associated Oral Microbial Structures Distinguish Inflammatory Bowel Diseases.Inflamm Bowel Dis2021
33875724Induced pluripotent stem cells from subjects with Lesch-Nyhan disease.Sci Rep2021
33600772Whole-genome sequencing of African Americans implicates differential genetic architecture in inflammatory bowel disease.Am J Hum Genet2021
34025222Organizing core facilities as force multipliers: strategies for research universities.J Biomol Tech2021
33600772Whole-genome sequencing of African Americans implicates differential genetic architecture in inflammatory bowel disease.Am J Hum Genet2021
33875724Induced pluripotent stem cells from subjects with Lesch-Nyhan disease.Sci Rep2021
34016428Identifying susceptibility genes for primary ovarian insufficiency on the high-risk genetic background of a fragile X premutation.Fertil Steril2021
34121934Staff Scientist Perspectives on Onboarding and Professional Development: A Case Study.J Biomol Tech2021
34285246Author Correction: Identifying genetic factors that contribute to the increased risk of congenital heart defects in infants with Down syndrome.Sci Rep2021
34002220Site- and Taxa-Specific Disease-Associated Oral Microbial Structures Distinguish Inflammatory Bowel Diseases.Inflamm Bowel Dis2021
34025222Organizing core facilities as force multipliers: strategies for research universities.J Biomol Tech2021
32154651New phenotypes associated with 3q29 duplication syndrome: Results from the 3q29 registry.Am J Med Genet A2020
32154651New phenotypes associated with 3q29 duplication syndrome: Results from the 3q29 registry.Am J Med Genet A2020
32986729Signatures of somatic mutations and gene expression from p16INK4A positive head and neck squamous cell carcinomas (HNSCC).PLoS One2020
32639515Bayesian Pathway Analysis for Complex Interactions.Am J Epidemiol2020
32986729Signatures of somatic mutations and gene expression from p16INK4A positive head and neck squamous cell carcinomas (HNSCC).PLoS One2020
32639515Bayesian Pathway Analysis for Complex Interactions.Am J Epidemiol2020
29593342Genetic variants and pathways implicated in a pediatric inflammatory bowel disease cohort.Genes Immun2019
30124884Genetic and Transcriptomic Variation Linked to Neutrophil Granulocyte-Macrophage Colony-Stimulating Factor Signaling in Pediatric Crohn's Disease.Inflamm Bowel Dis2019
29593342Genetic variants and pathways implicated in a pediatric inflammatory bowel disease cohort.Genes Immun2019
31235766Neutrophil GM-CSF signaling in inflammatory bowel disease patients is influenced by non-coding genetic variants.Sci Rep2019
31350265Inherited genetic susceptibility to acute lymphoblastic leukemia in Down syndrome.Blood2019
31346402Neuropsychiatric phenotypes and a distinct constellation of ASD features in 3q29 deletion syndrome: results from the 3q29 registry.Mol Autism2019
30124884Genetic and Transcriptomic Variation Linked to Neutrophil Granulocyte-Macrophage Colony-Stimulating Factor Signaling in Pediatric Crohn's Disease.Inflamm Bowel Dis2019
31350265Inherited genetic susceptibility to acute lymphoblastic leukemia in Down syndrome.Blood2019
31235766Neutrophil GM-CSF signaling in inflammatory bowel disease patients is influenced by non-coding genetic variants.Sci Rep2019
31346402Neuropsychiatric phenotypes and a distinct constellation of ASD features in 3q29 deletion syndrome: results from the 3q29 registry.Mol Autism2019
29141989Analysis of Copy Number Variants on Chromosome 21 in Down Syndrome-Associated Congenital Heart Defects.G3 (Bethesda)2018
29141989Analysis of Copy Number Variants on Chromosome 21 in Down Syndrome-Associated Congenital Heart Defects.G3 (Bethesda)2018
29562276Enhanced Contribution of HLA in Pediatric Onset Ulcerative Colitis.Inflamm Bowel Dis2018
29409527Bystro: rapid online variant annotation and natural-language filtering at whole-genome scale.Genome Biol2018
29454792Clinical and Genomic Correlates of Neutrophil Reactive Oxygen Species Production in Pediatric Patients With Crohn's Disease.Gastroenterology2018
29409527Bystro: rapid online variant annotation and natural-language filtering at whole-genome scale.Genome Biol2018
29562276Enhanced Contribution of HLA in Pediatric Onset Ulcerative Colitis.Inflamm Bowel Dis2018
29454792Clinical and Genomic Correlates of Neutrophil Reactive Oxygen Species Production in Pediatric Patients With Crohn's Disease.Gastroenterology2018
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Collaborators

David J Cutler
Emory University School of Medicine
Co-authored papers 43
Christine Stevens
Co-authored papers 5
Mark J Daly
Massachusetts General Hospital
Co-authored papers 4
Kelly A Shaw
Centers for Disease Control and Prevention
Co-authored papers 4
Peter E Chen
McGill University
Co-authored papers 4
Aravinda Chakravarti
New York University Grossman School of Medicine
Co-authored papers 4
Bruce J Aronow
Cincinnati Children's Hospital Medical Center
Co-authored papers 4
Marla C Dubinsky
Co-authored papers 4
Steven R Brant
Co-authored papers 3
John D Rioux
Co-authored papers 3
Adam E Locke
Co-authored papers 3
Dermot P B McGovern
F. Widjaja Inflammatory Bowel Disease Institute
Co-authored papers 3
Zhaohui S Qin
Emory University
Co-authored papers 3
Richard H Duerr
Co-authored papers 3
Mark S Silverberg
Co-authored papers 3
Talin Haritunians
Co-authored papers 3
Judy H Cho
Co-authored papers 3
Ramnik J Xavier
Broad Institute of MIT and Harvard
Co-authored papers 3
Christian R Marshall
Co-authored papers 2
Peng Jin
Co-authored papers 2
Michael J Owen
Co-authored papers 2
Ashok R Dinasarapu
Co-authored papers 2
Yan Kou
Co-authored papers 1
Maria Cristina Digilio
Co-authored papers 1
Alan R Sanders
Center for Psychiatric Genetics, NorthShore University HealthSystem
Co-authored papers 1
Gerard D Schellenberg
Co-authored papers 1
Shin Lin
University of Washington School of Medicine
Co-authored papers 1
Stephen R Hooper
University of North Carolina-Chapel Hill
Co-authored papers 1
Stephan J Sanders
Co-authored papers 1
Xiaoqian Jiang
Carnegie Mellon University, The University of Texas Health Science Center at Houston, University of California San Diego
Co-authored papers 1
Release 1.2