David J Cutler

Affiliations: 
Emory University Medical School, Atlanta, GA, United States 
Area:
Population Genetics/Quantitative Genetics/Human Genetics
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"David Cutler"

Parents

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John H. Gillespie grad student 1993-1999 UC Davis
Aravinda Chakravarti post-doc 1999-2003 Johns Hopkins Medical School (Evolution Tree)

Collaborators

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David T. Okou collaborator 2006- Emory University School of Medicine (Evolution Tree)
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Publications

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Astore C, Sharma S, Nagpal S, et al. (2023) The role of admixture in the rare variant contribution to inflammatory bowel disease. Genome Medicine. 15: 97
Curtis SW, Carlson JC, Beaty TH, et al. (2023) Rare variant modifier analysis identifies variants in SEC24D associated with orofacial cleft subtypes. Human Genetics
Curtis SW, Carlson JC, Beaty TH, et al. (2023) Rare genetic variants in modify orofacial cleft phenotypes. Medrxiv : the Preprint Server For Health Sciences
Sazonovs A, Stevens CR, Venkataraman GR, et al. (2022) Large-scale sequencing identifies multiple genes and rare variants associated with Crohn's disease susceptibility. Nature Genetics
Kozlova A, Zhang S, Kotlar AV, et al. (2022) Loss of function of OTUD7A in the schizophrenia- associated 15q13.3 deletion impairs synapse development and function in human neurons. American Journal of Human Genetics. 109: 1500-1519
Badshah N, Mattison KA, Ahmad S, et al. (2022) Novel Missense Variant Identified in Two Consanguineous Pakistani Families With Developmental Delay, Epilepsy, Intellectual Disability, and Aggressive Behavior. Frontiers in Neurology. 13: 918022
Kong HE, Lim J, Linsalata A, et al. (2022) Identification of as a genetic modifier of fragile X-associated tremor/ataxia syndrome. Proceedings of the National Academy of Sciences of the United States of America. 119: e2118124119
Jurickova I, Bonkowski E, Angerman E, et al. (2022) Eicosatetraynoic Acid and Butyrate Regulate Human Intestinal Organoid Mitochondrial and Extracellular Matrix Pathways Implicated in Crohn's Disease Strictures. Inflammatory Bowel Diseases
Venkateswaran S, Somineni HK, Kilaru V, et al. (2022) Methylation Quantitative Trait Loci are Largely Consistent across Disease States in Crohn's disease. G3 (Bethesda, Md.)
Trevino CE, Holleman AM, Corbitt H, et al. (2021) Author Correction: Identifying genetic factors that contribute to the increased risk of congenital heart defects in infants with Down syndrome. Scientific Reports. 11: 15164
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