David J Cutler
Affiliations: | Emory University Medical School, Atlanta, GA, United States |
Area:
Population Genetics/Quantitative Genetics/Human GeneticsGoogle:
"David Cutler"Parents
Sign in to add mentor| John H. Gillespie | grad student | 1993-1999 | UC Davis |
| Aravinda Chakravarti | post-doc | 1999-2003 | Johns Hopkins Medical School (Evolution Tree) |
Collaborators
Sign in to add collaborator| David T. Okou | collaborator | 2006- | Emory University School of Medicine (Evolution Tree) |
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Publications
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| Robinson KR, Curtis SW, Paschall JE, et al. (2025) Distinguishing syndromic and nonsyndromic cleft palate through analysis of protein-altering de novo variants in 816 trios. Medrxiv : the Preprint Server For Health Sciences |
| 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.) |