David J Cutler

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


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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)


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David T. Okou collaborator 2006- Emory University School of Medicine (Evolution Tree)
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Somineni HK, Nagpal S, Venkateswaran S, et al. (2021) Whole-genome sequencing of African Americans implicates differential genetic architecture in inflammatory bowel disease. American Journal of Human Genetics
Robins C, Liu Y, Fan W, et al. (2021) Genetic control of the human brain proteome. American Journal of Human Genetics
Trevino CE, Holleman AM, Corbitt H, et al. (2020) Identifying genetic factors that contribute to the increased risk of congenital heart defects in infants with Down syndrome. Scientific Reports. 10: 18051
Cleynen I, Engchuan W, Hestand MS, et al. (2020) Genetic contributors to risk of schizophrenia in the presence of a 22q11.2 deletion. Molecular Psychiatry
Satterstrom FK, Kosmicki JA, Wang J, et al. (2020) Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism. Cell
Venkateswaran S, Denson LA, Jurickova I, et al. (2019) Neutrophil GM-CSF signaling in inflammatory bowel disease patients is influenced by non-coding genetic variants. Scientific Reports. 9: 9168
Wingo TS, Cutler DJ, Wingo AP, et al. (2019) Association of Early-Onset Alzheimer Disease With Elevated Low-density Lipoprotein Cholesterol Levels and Rare Genetic Coding Variants of APOB. Jama Neurology
Somineni HK, Venkateswaran S, Kilaru V, et al. (2019) Blood-derived DNA Methylation Signatures of Crohn's Disease and Severity of Intestinal Inflammation. Gastroenterology
Berauer JP, Mezina AI, Okou DT, et al. (2019) Identification of PKD1L1 Gene Variants in Children with the Biliary Atresia Splenic Malformation Syndrome. Hepatology (Baltimore, Md.)
Denson LA, Jurickova I, Karns R, et al. (2018) Genetic and Transcriptomic Variation Linked to Neutrophil Granulocyte-Macrophage Colony-Stimulating Factor Signaling in Pediatric Crohn's Disease. Inflammatory Bowel Diseases
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