Pervasive genetic interactions modulate neurodevelopmental defects of the autism-associated 16p11.2 deletion in Drosophila melanogaster
The 16p11.2 deletion leads to a range of neurodevelopmental phenotypes, but to date, sequencing studies have not been able to pinpoint individual genes that are causative for the disease on their own. Here, using Drosophila homologs of 14 16p11.2 genes, the authors take a combinatorial approach to s...
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oai:doaj.org-article:d7ac17fe1f8f4fac96fe435cdcaaa18c2021-12-02T15:34:08ZPervasive genetic interactions modulate neurodevelopmental defects of the autism-associated 16p11.2 deletion in Drosophila melanogaster10.1038/s41467-018-04882-62041-1723https://doaj.org/article/d7ac17fe1f8f4fac96fe435cdcaaa18c2018-06-01T00:00:00Zhttps://doi.org/10.1038/s41467-018-04882-6https://doaj.org/toc/2041-1723The 16p11.2 deletion leads to a range of neurodevelopmental phenotypes, but to date, sequencing studies have not been able to pinpoint individual genes that are causative for the disease on their own. Here, using Drosophila homologs of 14 16p11.2 genes, the authors take a combinatorial approach to show that gene interactions contribute to a neurological phenotype.Janani IyerMayanglambam Dhruba SinghMatthew JensenPayal PatelLucilla PizzoEmily HuberHaley KoerselmanAlexis T. WeinerPaola LepantoKomal VadodariaAlexis KubinaQingyu WangAbigail TalbertSneha YennawarJose BadanoJ. Robert ManakMelissa M. RollsArjun KrishnanSanthosh GirirajanNature PortfolioarticleScienceQENNature Communications, Vol 9, Iss 1, Pp 1-19 (2018) |
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Science Q Janani Iyer Mayanglambam Dhruba Singh Matthew Jensen Payal Patel Lucilla Pizzo Emily Huber Haley Koerselman Alexis T. Weiner Paola Lepanto Komal Vadodaria Alexis Kubina Qingyu Wang Abigail Talbert Sneha Yennawar Jose Badano J. Robert Manak Melissa M. Rolls Arjun Krishnan Santhosh Girirajan Pervasive genetic interactions modulate neurodevelopmental defects of the autism-associated 16p11.2 deletion in Drosophila melanogaster |
description |
The 16p11.2 deletion leads to a range of neurodevelopmental phenotypes, but to date, sequencing studies have not been able to pinpoint individual genes that are causative for the disease on their own. Here, using Drosophila homologs of 14 16p11.2 genes, the authors take a combinatorial approach to show that gene interactions contribute to a neurological phenotype. |
format |
article |
author |
Janani Iyer Mayanglambam Dhruba Singh Matthew Jensen Payal Patel Lucilla Pizzo Emily Huber Haley Koerselman Alexis T. Weiner Paola Lepanto Komal Vadodaria Alexis Kubina Qingyu Wang Abigail Talbert Sneha Yennawar Jose Badano J. Robert Manak Melissa M. Rolls Arjun Krishnan Santhosh Girirajan |
author_facet |
Janani Iyer Mayanglambam Dhruba Singh Matthew Jensen Payal Patel Lucilla Pizzo Emily Huber Haley Koerselman Alexis T. Weiner Paola Lepanto Komal Vadodaria Alexis Kubina Qingyu Wang Abigail Talbert Sneha Yennawar Jose Badano J. Robert Manak Melissa M. Rolls Arjun Krishnan Santhosh Girirajan |
author_sort |
Janani Iyer |
title |
Pervasive genetic interactions modulate neurodevelopmental defects of the autism-associated 16p11.2 deletion in Drosophila melanogaster |
title_short |
Pervasive genetic interactions modulate neurodevelopmental defects of the autism-associated 16p11.2 deletion in Drosophila melanogaster |
title_full |
Pervasive genetic interactions modulate neurodevelopmental defects of the autism-associated 16p11.2 deletion in Drosophila melanogaster |
title_fullStr |
Pervasive genetic interactions modulate neurodevelopmental defects of the autism-associated 16p11.2 deletion in Drosophila melanogaster |
title_full_unstemmed |
Pervasive genetic interactions modulate neurodevelopmental defects of the autism-associated 16p11.2 deletion in Drosophila melanogaster |
title_sort |
pervasive genetic interactions modulate neurodevelopmental defects of the autism-associated 16p11.2 deletion in drosophila melanogaster |
publisher |
Nature Portfolio |
publishDate |
2018 |
url |
https://doaj.org/article/d7ac17fe1f8f4fac96fe435cdcaaa18c |
work_keys_str_mv |
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