Papers: 10.1186/s40246-021-00342-3

https://doi.org/10.1186/s40246-021-00342-3

Coding and noncoding variants in EBF3 are involved in HADDS and simplex autism

Cited by: 11
Author(s): Evin M. Padhi, Tristan J. Hayeck, Cheng Zhang, Satadal Chatterjee, Brandon J. Mannion, Marta Byrska-Bishop, Marjolaine Willems, Lucile Pinson, Sylvia Redon, Caroline Bénech, Kévin Uguen, Séverine Audebert‐Bellanger, Cédric Le Marechal, Claude Férec, Stéphanie Efthymiou, Fatima Rahman, Shazia Maqbool, Reza Maroofian, Henry Houlden, Rajeeva Musunuri, Giuseppe Narzisi, Avinash Abhyankar, Riana D Hunter, Jennifer A. Akiyama, Lauren Fries, Jeffrey Ng, Elvisa Mehinovic, Nicholas Stong, Andrew S. Allen, Diane E. Dickel, Raphael Bernier, David U. Gorkin, L Pennacchio, Michael C. Zody, Tychele N. Turner
Published: over 5 years ago

Software Mentions 2

cran: denovolyzeR
Statistical Analyses of De Novo Genetic Variants
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pypi: browser
A package to prevent Dependency Confusion attacks against Yandex.
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