Maja Bucan
Affiliations: | University of Pennsylvania, Philadelphia, PA, United States |
Area:
Genetics, Bioinformatics Biology, Neurobiology BiologyGoogle:
"Maja Bucan"Mean distance: 35622
Children
Sign in to add traineeAlireza S. Alavizadeh | grad student | 2001 | Penn |
David J. Kapfhamer | grad student | 2002 | Penn |
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Publications
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Ferraro NM, Strober BJ, Einson J, et al. (2020) Transcriptomic signatures across human tissues identify functional rare genetic variation. Science (New York, N.Y.). 369 |
Cacheiro P, Muñoz-Fuentes V, Murray SA, et al. (2020) Human and mouse essentiality screens as a resource for disease gene discovery. Nature Communications. 11: 655 |
Myers L, Blyth M, Moradkhani K, et al. (2019) Variable neurodevelopmental and morphological phenotypes of carriers with 12q12 duplications. Molecular Genetics & Genomic Medicine. e1013 |
Gehrman PR, Ghorai A, Goodman M, et al. (2019) Twin-based Heritability of Actimetry Traits. Genes, Brain, and Behavior. e12569 |
Kember R, Ji X, Zhang J, et al. (2019) Spectrum Of Common And Rare Mutations Contributing To Autism Risk In Families European Neuropsychopharmacology. 29 |
Kember RL, Hou L, Ji X, et al. (2018) Genetic pleiotropy between mood disorders, metabolic, and endocrine traits in a multigenerational pedigree. Translational Psychiatry. 8: 218 |
Pizzo L, Jensen M, Polyak A, et al. (2018) Rare variants in the genetic background modulate cognitive and developmental phenotypes in individuals carrying disease-associated variants. Genetics in Medicine : Official Journal of the American College of Medical Genetics |
Glahn DC, Nimgaonkar VL, Raventós H, et al. (2018) Rediscovering the value of families for psychiatric genetics research. Molecular Psychiatry |
Nakanishi M, Nomura J, Ji X, et al. (2017) Functional significance of rare neuroligin 1 variants found in autism. Plos Genetics. 13: e1006940 |
Hou L, Kember RL, Roach JC, et al. (2017) A population-specific reference panel empowers genetic studies of Anabaptist populations. Scientific Reports. 7: 6079 |