Zebrafish: A Translational Model System for Studying Neuropsychiatric Disorders

od Ijaz, Sundas, Hoffman, Ellen J.
Wydane w J Am Acad Child Adolesc Psychiatry (2016)

Zebrafish Models of Neurodevelopmental Disorders: Past, Present, and Future

od Sakai, Catalina, Ijaz, Sundas, Hoffman, Ellen J.
Wydane w Front Mol Neurosci (2018)

A large-scale screen for coding variants in SERT/SLC6A4 in autism spectrum disorders

od Sakurai, Takeshi, Reichert, Jennifer, Hoffman, Ellen J., Cai, Guiqing, Jones, Hywel B., Faham, Malek, Buxbaum, Joseph D.
Wydane 2008

Effects of Ethanol on Axon Outgrowth and Branching in Developing Rat Cortical Neurons

od Hoffman, Ellen J., Mintz, C. David, Wang, Sophia, McNickle, Daniel G., Salton, Stephen R.J., Benson, Deanna L.
Wydane 2008

Multiplex ligation-dependent probe amplification for genetic screening in autism spectrum disorders: Efficient identification of known microduplications and identification of a nov...

od Cai, Guiqing, Edelmann, Lisa, Goldsmith, Juliet E, Cohen, Ninette, Nakamine, Alisa, Reichert, Jennifer G, Hoffman, Ellen J, Zurawiecki, Danielle M, Silverman, Jeremy M, Hollander, Eric, Soorya, Latha, Anagnostou, Evdokia, Betancur, Catalina, Buxbaum, Joseph D
Wydane 2008

A simple and effective F0 knockout method for rapid screening of behaviour and other complex phenotypes

od Kroll, François, Powell, Gareth T, Ghosh, Marcus, Gestri, Gaia, Antinucci, Paride, Hearn, Timothy J, Tunbak, Hande, Lim, Sumi, Dennis, Harvey W, Fernandez, Joseph M, Whitmore, David, Dreosti, Elena, Wilson, Stephen W, Hoffman, Ellen J, Rihel, Jason
Wydane w eLife (2021)

Estrogens Suppress a Behavioral Phenotype in Zebrafish Mutants of the Autism Risk Gene, CNTNAP2

od Hoffman, Ellen J., Turner, Katherine J., Fernandez, Joseph M., Cifuentes, Daniel, Ghosh, Marcus, Ijaz, Sundas, Jain, Roshan A., Kubo, Fumi, Bill, Brent R., Baier, Herwig, Granato, Michael, Barresi, Michael J. F., Wilson, Stephen W., Rihel, Jason, State, Matthew W., Giraldez, Antonio J.
Wydane w Neuron (2016)

De novo damaging DNA coding mutations are associated with obsessive-compulsive disorder and overlap with Tourette’s disorder and autism

od Cappi, Carolina, Oliphant, Melody E., Péter, Zsanett, Zai, Gwyneth, do Rosário, Maria Conceição, Sullivan, Catherine A. W., Gupta, Abha R., Hoffman, Ellen J., Virdee, Manmeet, Olfson, Emily, Abdallah, Sarah B., Willsey, A. Jeremy, Shavitt, Roseli G., Miguel, Euripedes C., Kennedy, James L., Richter, Margaret A., Fernandez, Thomas V.
Wydane w Biol Psychiatry (2019)

Exome sequencing implicates genetic disruption of prenatal neuro-gliogenesis in sporadic congenital hydrocephalus

od Jin, Sheng Chih, Dong, Weilai, Kundishora, Adam J., Panchagnula, Shreyas, Moreno-De-Luca, Andres, Furey, Charuta G., Allocco, August A., Walker, Rebecca L., Nelson-Williams, Carol, Smith, Hannah, Dunbar, Ashley, Conine, Sierra, Lu, Qiongshi, Zeng, Xue, Sierant, Michael C., Knight, James R., Sullivan, William, Duy, Phan Q., DeSpenza, Tyrone, Reeves, Benjamin C., Karimy, Jason K., Marlier, Arnaud, Castaldi, Christopher, Tikhonova, Irina R., Li, Boyang, Peña, Helena Perez, Broach, James R., Kabachelor, Edith M., Ssenyonga, Peter, Hehnly, Christine, Ge, Li, Keren, Boris, Timberlake, Andrew T., Goto, June, Mangano, Francesco T., Johnston, James M., Butler, William E., Warf, Benjamin C., Smith, Edward R., Schiff, Steven J., Limbrick, David D., Heuer, Gregory, Jackson, Eric M., Iskandar, Bermans J., Mane, Shrikant, Haider, Shozeb, Guclu, Bulent, Bayri, Yasar, Sahin, Yener, Duncan, Charles C., Apuzzo, Michael L. J., DiLuna, Michael L., Hoffman, Ellen J., Sestan, Nenad, Ment, Laura R., Alper, Seth L., Bilguvar, Kaya, Geschwind, Daniel H., Günel, Murat, Lifton, Richard P., Kahle, Kristopher T.
Wydane w Nat Med (2020)