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

Evin M. Padhi, Tristan J. Hayeck, Zhang Cheng, Sumantra Chatterjee, Brandon J. Mannion, Marta Byrska-Bishop, Marjolaine Willems, Lucile Pinson, Sylvia Redon, Caroline Benech, Kevin Uguen, Séverine Audebert-Bellanger, Cédric Le Marechal, Claude Férec, Stephanie Efthymiou, Fatima Rahman, Shazia Maqbool, Reza Maroofian, Henry Houlden, Rajeeva Musunuri, Giuseppe Narzisi, Avinash Abhyankar, Riana D. Hunter, Jennifer Akiyama, Lauren E. Fries, Jeffrey K. Ng, Elvisa Mehinovic, Nick Stong, Andrew S. Allen, Diane E. Dickel, Raphael A. Bernier, David U. Gorkin, Len A. Pennacchio, Michael C. Zody, Tychele N. Turner

Open source

DOI: 10.1186/s40246-021-00342-3
Published: 2021-07-13
Container: Human Genomics
Publisher: Springer Science and Business Media LLC
Open access: unknown

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Cite this work

BibTeX

@article{allodium:10.1186/s40246-021-00342-3,
  title = {Coding and noncoding variants in EBF3 are involved in HADDS and simplex autism},
  author = {Evin M. Padhi and Tristan J. Hayeck and Zhang Cheng and Sumantra Chatterjee and Brandon J. Mannion and Marta Byrska-Bishop and Marjolaine Willems and Lucile Pinson and Sylvia Redon and Caroline Benech and Kevin Uguen and Séverine Audebert-Bellanger and Cédric Le Marechal and Claude Férec and Stephanie Efthymiou and Fatima Rahman and Shazia Maqbool and Reza Maroofian and Henry Houlden and Rajeeva Musunuri and Giuseppe Narzisi and Avinash Abhyankar and Riana D. Hunter and Jennifer Akiyama and Lauren E. Fries and Jeffrey K. Ng and Elvisa Mehinovic and Nick Stong and Andrew S. Allen and Diane E. Dickel and Raphael A. Bernier and David U. Gorkin and Len A. Pennacchio and Michael C. Zody and Tychele N. Turner},
  year = {2021},
  journal = {Human Genomics},
  doi = {10.1186/s40246-021-00342-3},
  url = {https://doi.org/10.1186/s40246-021-00342-3}
}

RIS

TY  - JOUR
TI  - Coding and noncoding variants in EBF3 are involved in HADDS and simplex autism
AU  - Evin M. Padhi
AU  - Tristan J. Hayeck
AU  - Zhang Cheng
AU  - Sumantra Chatterjee
AU  - Brandon J. Mannion
AU  - Marta Byrska-Bishop
AU  - Marjolaine Willems
AU  - Lucile Pinson
AU  - Sylvia Redon
AU  - Caroline Benech
AU  - Kevin Uguen
AU  - Séverine Audebert-Bellanger
AU  - Cédric Le Marechal
AU  - Claude Férec
AU  - Stephanie Efthymiou
AU  - Fatima Rahman
AU  - Shazia Maqbool
AU  - Reza Maroofian
AU  - Henry Houlden
AU  - Rajeeva Musunuri
AU  - Giuseppe Narzisi
AU  - Avinash Abhyankar
AU  - Riana D. Hunter
AU  - Jennifer Akiyama
AU  - Lauren E. Fries
AU  - Jeffrey K. Ng
AU  - Elvisa Mehinovic
AU  - Nick Stong
AU  - Andrew S. Allen
AU  - Diane E. Dickel
AU  - Raphael A. Bernier
AU  - David U. Gorkin
AU  - Len A. Pennacchio
AU  - Michael C. Zody
AU  - Tychele N. Turner
PY  - 2021
JO  - Human Genomics
DO  - 10.1186/s40246-021-00342-3
UR  - https://doi.org/10.1186/s40246-021-00342-3
ER  -

APA

Padhi, E. M., Hayeck, T. J., Cheng, Z., Chatterjee, S., Mannion, B. J., Byrska-Bishop, M., Willems, M., Pinson, L., Redon, S., Benech, C., Uguen, K., Audebert-Bellanger, S., Marechal, C. L., Férec, C., Efthymiou, S., Rahman, F., Maqbool, S., Maroofian, R., Houlden, H., Musunuri, R., Narzisi, G., Abhyankar, A., Hunter, R. D., Akiyama, J., Fries, L. E., Ng, J. K., Mehinovic, E., Stong, N., Allen, A. S., Dickel, D. E., Bernier, R. A., Gorkin, D. U., Pennacchio, L. A., Zody, M. C., & Turner, T. N. (2021). Coding and noncoding variants in EBF3 are involved in HADDS and simplex autism. Human Genomics. https://doi.org/10.1186/s40246-021-00342-3

Source records

crossref · retrieved 2026-09-26T08:45:01.250Z