Genotype-first analysis of the 16p11.2 deletion defines a new type of “autism”

由 Duyzend, Michael H., Eichler, Evan E.
發表在 Biol Psychiatry (2015)

Non-DNA-binding cofactors enhance DNA-binding specificity of a transcriptional regulatory complex

由 Siggers, Trevor, Duyzend, Michael H, Reddy, Jessica, Khan, Sidra, Bulyk, Martha L
出版 2011

Maternal Modifiers and Parent-of-Origin Bias of the Autism-Associated 16p11.2 CNV

由 Duyzend, Michael H., Nuttle, Xander, Coe, Bradley P., Baker, Carl, Nickerson, Deborah A., Bernier, Raphael, Eichler, Evan E.
發表在 Am J Hum Genet (2016)

A Higher Mutational Burden in Females Supports a “Female Protective Model” in Neurodevelopmental Disorders

由 Jacquemont, Sébastien, Coe, Bradley P., Hersch, Micha, Duyzend, Michael H., Krumm, Niklas, Bergmann, Sven, Beckmann, Jacques S., Rosenfeld, Jill A., Eichler, Evan E.
出版 2014

Longitudinal report of child with de novo 16p11.2 triplication

由 Wallace, Arianne S., Hudac, Caitlin M., Steinman, Kyle J., Peterson, Jessica L., DesChamps, Trent D., Duyzend, Michael H., Nuttle, Xander, Eichler, Evan E., Bernier, Raphael A.
發表在 Clin Case Rep (2017)

The birth of a human-specific neural gene by incomplete duplication and gene fusion

由 Dougherty, Max L., Nuttle, Xander, Penn, Osnat, Nelson, Bradley J., Huddleston, John, Baker, Carl, Harshman, Lana, Duyzend, Michael H., Ventura, Mario, Antonacci, Francesca, Sandstrom, Richard, Dennis, Megan Y., Eichler, Evan E.
發表在 Genome Biol (2017)

Genome sequencing identifies multiple deleterious variants in autism patients with more severe phenotypes

由 Guo, Hui, Duyzend, Michael H., Coe, Bradley P., Baker, Carl, Hoekzema, Kendra, Gerdts, Jennifer, Turner, Tychele N., Zody, Michael C., Beighley, Jennifer S., Murali, Shwetha C., Nelson, Bradley J., Bamshad, Michael J., Nickerson, Deborah A., Bernier, Raphael A., Eichler, Evan E.
發表在 Genet Med (2018)

Genome Sequencing of Autism-Affected Families Reveals Disruption of Putative Noncoding Regulatory DNA

由 Turner, Tychele N., Hormozdiari, Fereydoun, Duyzend, Michael H., McClymont, Sarah A., Hook, Paul W., Iossifov, Ivan, Raja, Archana, Baker, Carl, Hoekzema, Kendra, Stessman, Holly A., Zody, Michael C., Nelson, Bradley J., Huddleston, John, Sandstrom, Richard, Smith, Joshua D., Hanna, David, Swanson, James M., Faustman, Elaine M., Bamshad, Michael J., Stamatoyannopoulos, John, Nickerson, Deborah A., McCallion, Andrew S., Darnell, Robert, Eichler, Evan E.
發表在 Am J Hum Genet (2016)

Emergence of a Homo sapiens-specific gene family and chromosome 16p11.2 CNV susceptibility

由 Nuttle, Xander, Giannuzzi, Giuliana, Duyzend, Michael H., Schraiber, Joshua G., Narvaiza, Iñigo, Sudmant, Peter H., Penn, Osnat, Chiatante, Giorgia, Malig, Maika, Huddleston, John, Benner, Chris, Camponeschi, Francesca, Ciofi-Baffoni, Simone, Stessman, Holly A.F., Marchetto, Maria C. N., Denman, Laura, Harshman, Lana, Baker, Carl, Raja, Archana, Penewit, Kelsi, Janke, Nicolette, Tang, W. Joyce, Ventura, Mario, Banci, Lucia, Antonacci, Francesca, Akey, Joshua M., Amemiya, Chris T., Gage, Fred H., Reymond, Alexandre, Eichler, Evan E.
發表在 Nature (2016)