Most genetic risk for autism resides with common variation

Most genetic risk for autism resides with common variation

A key component of genetic architecture is the allelic spectrum influencing trait variability. For autism spectrum disorder (henceforth autism) the nature of its allelic spectrum is uncertain. Individual risk genes have been identified from rare variation, especially de novo mutations1–8. From this...

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Bibliographic Details
Main Authors: Gaugler, Trent, Klei, Lambertus, Sanders, Stephan J., Bodea, Corneliu A., Goldberg, Arthur P., Lee, Ann B., Mahajan, Milind, Manaa, Dina, Pawitan, Yudi, Reichert, Jennifer, Ripke, Stephan, Sandin, Sven, Sklar, Pamela, Svantesson, Oscar, Reichenberg, Abraham, Hultman, Christina M., Devlin, Bernie, Roeder, Kathryn, Buxbaum, Joseph D.
Format: Online
Language:English
Published: 2014
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4137411/

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https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4137411/

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