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Author Details

David J Cutler
Emory University School of Medicine
1994
134
49
PMIDPaper TitleJournal TitlePublished Year
36869704Characterization of Intestinal Mesenchymal Stromal Cells From Patients With Inflammatory Bowel Disease for Autologous Cell Therapy.Stem Cells Transl Med2023
37653343Sex differences in brain protein expression and disease.Nat Med2023
37693179The Quantitative Genetics of Human Disease: 1 Foundations.ArXiv2023
36964596Longitudinal DNA methylation profiling of the rectal mucosa identifies cell-specific signatures of disease status, severity and clinical outcomes in ulcerative colitis cell-specific DNA methylation signatures of UC.Clin Epigenetics2023
37330696Rare variants found in clinical gene panels illuminate the genetic and allelic architecture of orofacial clefting.Genet Med2023
37067493POIROT: a powerful test for parent-of-origin effects in unrelated samples leveraging multiple phenotypes.Bioinformatics2023
37066311Trio-based GWAS identifies novel associations and subtype-specific risk factors for cleft palate.medRxiv2023
36869704Characterization of Intestinal Mesenchymal Stromal Cells From Patients With Inflammatory Bowel Disease for Autologous Cell Therapy.Stem Cells Transl Med2023
36688175Evaluation of AQP4 functional variants and its association with fragile X-associated tremor/ataxia syndrome.Front Aging Neurosci2023
36848716Racial and ethnic diversity of classic and clinical variant galactosemia in the United States.Mol Genet Metab2023
37653343Sex differences in brain protein expression and disease.Nat Med2023
37693179The Quantitative Genetics of Human Disease: 1 Foundations.ArXiv2023
37330696Rare variants found in clinical gene panels illuminate the genetic and allelic architecture of orofacial clefting.Genet Med2023
37067493POIROT: a powerful test for parent-of-origin effects in unrelated samples leveraging multiple phenotypes.Bioinformatics2023
37066311Trio-based GWAS identifies novel associations and subtype-specific risk factors for cleft palate.medRxiv2023
36964596Longitudinal DNA methylation profiling of the rectal mucosa identifies cell-specific signatures of disease status, severity and clinical outcomes in ulcerative colitis cell-specific DNA methylation signatures of UC.Clin Epigenetics2023
36848716Racial and ethnic diversity of classic and clinical variant galactosemia in the United States.Mol Genet Metab2023
36688175Evaluation of AQP4 functional variants and its association with fragile X-associated tremor/ataxia syndrome.Front Aging Neurosci2023
35259271Eicosatetraynoic Acid and Butyrate Regulate Human Intestinal Organoid Mitochondrial and Extracellular Matrix Pathways Implicated in Crohn's Disease Strictures.Inflamm Bowel Dis2022
35911904Novel Missense <i>CNTNAP2</i> Variant Identified in Two Consanguineous Pakistani Families With Developmental Delay, Epilepsy, Intellectual Disability, and Aggressive Behavior.Front Neurol2022
35772923LDL cholesterol is associated with higher AD neuropathology burden independent of APOE.J Neurol Neurosurg Psychiatry2022
36038634Large-scale sequencing identifies multiple genes and rare variants associated with Crohn's disease susceptibility.Nat Genet2022
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
35982160Rare coding variation provides insight into the genetic architecture and phenotypic context of autism.Nat Genet2022
35259271Eicosatetraynoic Acid and Butyrate Regulate Human Intestinal Organoid Mitochondrial and Extracellular Matrix Pathways Implicated in Crohn's Disease Strictures.Inflamm Bowel Dis2022
35172000Methylation quantitative trait loci are largely consistent across disease states in Crohn's disease.G3 (Bethesda)2022
35617426Identification of <i>PSMB5</i> as a genetic modifier of fragile X-associated tremor/ataxia syndrome.Proc Natl Acad Sci U S A2022
35772923LDL cholesterol is associated with higher AD neuropathology burden independent of APOE.J Neurol Neurosurg Psychiatry2022
35911904Novel Missense <i>CNTNAP2</i> Variant Identified in Two Consanguineous Pakistani Families With Developmental Delay, Epilepsy, Intellectual Disability, and Aggressive Behavior.Front Neurol2022
36038634Large-scale sequencing identifies multiple genes and rare variants associated with Crohn's disease susceptibility.Nat Genet2022
35931052Loss of function of OTUD7A in the schizophrenia- associated 15q13.3 deletion impairs synapse development and function in human neurons.Am J Hum Genet2022
35982160Rare coding variation provides insight into the genetic architecture and phenotypic context of autism.Nat Genet2022
35172000Methylation quantitative trait loci are largely consistent across disease states in Crohn's disease.G3 (Bethesda)2022
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
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
34271224Ileal Derived Organoids From Crohn's Disease Patients Show Unique Transcriptomic and Secretomic Signatures.Cell Mol Gastroenterol Hepatol2021
33600772Whole-genome sequencing of African Americans implicates differential genetic architecture in inflammatory bowel disease.Am J Hum Genet2021
34325702Profiling non-coding RNA levels with clinical classifiers in pediatric Crohn's disease.BMC Med Genomics2021
33817668The PAX1 locus at 20p11 is a potential genetic modifier for bilateral cleft lip.HGG Adv2021
33600772Whole-genome sequencing of African Americans implicates differential genetic architecture in inflammatory bowel disease.Am J Hum Genet2021
33817668The PAX1 locus at 20p11 is a potential genetic modifier for bilateral cleft lip.HGG Adv2021
34016428Identifying susceptibility genes for primary ovarian insufficiency on the high-risk genetic background of a fragile X premutation.Fertil Steril2021
34325702Profiling non-coding RNA levels with clinical classifiers in pediatric Crohn's disease.BMC Med Genomics2021
34271224Ileal Derived Organoids From Crohn's Disease Patients Show Unique Transcriptomic and Secretomic Signatures.Cell Mol Gastroenterol Hepatol2021
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
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Collaborators

Michael E Zwick
Rutgers University-New Brunswick, Rutgers University
Co-authored papers 43
Aravinda Chakravarti
New York University Grossman School of Medicine
Co-authored papers 18
Mark J Daly
Massachusetts General Hospital
Co-authored papers 11
Shin Lin
University of Washington School of Medicine
Co-authored papers 9
Christine Stevens
Co-authored papers 7
Allan I Levey
Emory University School of Medicine
Co-authored papers 6
Joseph D Buxbaum
Icahn School of Medicine at Mount Sinai
Co-authored papers 5
Carl S Kashuk
Co-authored papers 5
Garry R Cutting
Johns Hopkins University School of Medicine
Co-authored papers 5
Judy H Cho
Co-authored papers 5
Marla C Dubinsky
Co-authored papers 5
Steven R Brant
Co-authored papers 4
John D Rioux
Co-authored papers 4
Dermot P B McGovern
F. Widjaja Inflammatory Bowel Disease Institute
Co-authored papers 4
Richard H Duerr
Co-authored papers 4
Zhaohui S Qin
Emory University
Co-authored papers 4
Mark S Silverberg
Co-authored papers 4
Bruce J Aronow
Cincinnati Children's Hospital Medical Center
Co-authored papers 4
Talin Haritunians
Co-authored papers 4
Gon??alo R Abecasis
Regeneron Pharmaceuticals Inc.
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Dan E Arking
Co-authored papers 4
Mary L Marazita
Center for Craniofacial and Dental Genetics, University of Pittsburgh
Co-authored papers 4
Kathryn Roeder
Co-authored papers 4
Stacey Gabriel
Broad Institute of MIT and Harvard
Co-authored papers 4
Stephan J Sanders
Co-authored papers 4
James J Lah
Goizueta Alzheimer's Disease Research Center, Emory University School of Medicine
Co-authored papers 4
Bernie Devlin
Co-authored papers 4
Heather M Munro
Vanderbilt University Medical Center
Co-authored papers 3
Stephen T Sherry
National Center for Biotechnology Information, National Institutes of Health
Co-authored papers 3
Edwin H Cook
Co-authored papers 3
Release 1.2