Michael E. Zwick, Ph.D.
Affiliations: | Human Genetics | Emory University School of Medicine, Atlanta, GA, United States |
Area:
Human GeneticsWebsite:
http://genetics.emory.edu/labs/index.php?lab=44Google:
"Michael Zwick"Cross-listing: Computational Biology Tree
Parents
Sign in to add mentor| Charles (Chuck) H. Langley | grad student | 1993-1998 | UC Davis |
| Aravinda Chakravarti | grad student | 1999-2000 | Case Western Medical School |
| Aravinda Chakravarti | post-doc | 2000-2002 | Johns Hopkins Medical School |
Children
Sign in to add trainee| Karyn M. Meltz-Steinberg | grad student | 2006-2009 | Emory |
| David T. Okou | post-doc | 2005-2008 | Emory University School of Medicine |
BETA: Related publications
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Publications
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| 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 |
| 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 |
| Mosley TJ, Johnston HR, Cutler DJ, et al. (2021) Sex-specific recombination patterns predict parent of origin for recurrent genomic disorders. Bmc Medical Genomics. 14: 154 |
| Somineni HK, Weitzner JH, Venkateswaran S, et al. (2021) Site- and Taxa-Specific Disease-Associated Oral Microbial Structures Distinguish Inflammatory Bowel Diseases. Inflammatory Bowel Diseases |
| 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 |
| 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 |