Noah Zaitlen, Ph.D.
Affiliations: | 2009 | Bioinformatics | University of California, San Diego, La Jolla, CA |
Area:
Bioinformatics Biology, Genetics, Computer ScienceGoogle:
"Noah Zaitlen"Bio:
Parents
Sign in to add mentor| Eleazar Eskin | grad student | 2009 | UCSD (Computer Science Tree) | |
| (Methods for the Analysis of Human Genetic Variation in the Search for the Genetic Basis of Human Disease.) | ||||
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Publications
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| Shemirani R, Belbin GM, Cullina S, et al. (2025) SPC: a SPectral Component approach to address recent population structure in genomic analysis. Medrxiv : the Preprint Server For Health Sciences |
| Dybdahl Krebs M, Georgii Hellberg KL, Lundberg M, et al. (2024) Genetic liability estimated from large-scale family data improves genetic prediction, risk score profiling, and gene mapping for major depression. American Journal of Human Genetics |
| Pazokitoroudi A, Liu Z, Dahl A, et al. (2024) A scalable and robust variance components method reveals insights into the architecture of gene-environment interactions underlying complex traits. American Journal of Human Genetics |
| Pazokitoroudi A, Dahl A, Zaitlen N, et al. (2023) A scalable and robust variance components method reveals insights into the architecture of gene-environment interactions underlying complex traits. Biorxiv : the Preprint Server For Biology |
| An U, Pazokitoroudi A, Alvarez M, et al. (2023) Deep learning-based phenotype imputation on population-scale biobank data increases genetic discoveries. Nature Genetics |
| Fu B, Pazokitoroudi A, Xue A, et al. (2023) A biobank-scale test of marginal epistasis reveals genome-wide signals of polygenic epistasis. Biorxiv : the Preprint Server For Biology |
| Kachuri L, Mak ACY, Hu D, et al. (2023) Gene expression in African Americans, Puerto Ricans and Mexican Americans reveals ancestry-specific patterns of genetic architecture. Nature Genetics |
| Johnson R, Ding Y, Venkateswaran V, et al. (2022) Author Correction: Leveraging genomic diversity for discovery in an electronic health record linked biobank: the UCLA ATLAS Community Health Initiative. Genome Medicine. 14: 128 |
| Taraszka K, Zaitlen N, Eskin E. (2022) Leveraging pleiotropy for joint analysis of genome-wide association studies with per trait interpretations. Plos Genetics. 18: e1010447 |
| Thompson M, Gordon MG, Lu A, et al. (2022) Multi-context genetic modeling of transcriptional regulation resolves novel disease loci. Nature Communications. 13: 5704 |