A Wild Rotation

Por Evrony, Gilad D.
Publicado no JAMA (2016)

Somatic Mutation, Genomic Variation, and Neurological Disease

Por Poduri, Annapurna, Evrony, Gilad D., Cai, Xuyu, Walsh, Christopher A.
Publicado em 2013

Resolving rates of mutation in the brain using single-neuron genomics

Por Evrony, Gilad D, Lee, Eunjung, Park, Peter J, Walsh, Christopher A
Publicado no eLife (2016)

Tetanus toxin C fragment conjugated nanoparticles for targeted drug delivery to neurons

Por Townsend, Seth A., Evrony, Gilad D., Gu, Frank X., Schulze, Martin P., Brown, Robert H., Langer, Robert S.
Publicado em 2007

Single-Cell, Genome-wide Sequencing Identifies Clonal Somatic Copy-Number Variation in the Human Brain

Por Cai, Xuyu, Evrony, Gilad D., Lehmann, Hillel S., Elhosary, Princess C., Mehta, Bhaven K., Poduri, Annapurna, Walsh, Christopher A.
Publicado no Cell Rep (2014)

Cell lineage analysis in human brain using endogenous retroelements

Por Evrony, Gilad D., Lee, Eunjung, Mehta, Bhaven K., Benjamini, Yuval, Johnson, Robert M., Cai, Xuyu, Yang, Lixing, Haseley, Psalm, Lehmann, Hillel S., Park, Peter J., Walsh, Christopher A.
Publicado no Neuron (2015)

Single-Neuron Sequencing Analysis of L1 Retrotransposition and Somatic Mutation in the Human Brain

Por Evrony, Gilad D., Cai, Xuyu, Lee, Eunjung, Hills, L. Benjamin, Elhosary, P. Christina, Lehmann, Hillel S., Parker, J.J., Atabay, Kutay D., Gilmore, Edward C., Poduri, Annapurna, Park, Peter J., Walsh, Christopher A.
Publicado em 2012

Somatic mutation in single human neurons tracks developmental and transcriptional history

Por Lodato, Michael A., Woodworth, Mollie B., Lee, Semin, Evrony, Gilad D., Mehta, Bhaven K., Karger, Amir, Lee, Soohyun, Chittenden, Thomas W., D’Gama, Alissa M., Cai, Xuyu, Luquette, Lovelace J., Lee, Eunjung, Park, Peter J., Walsh, Christopher A.
Publicado no Science (2015)

Somatic Activation of AKT3 Causes Hemispheric Developmental Brain Malformations

Por Poduri, Annapurna, Evrony, Gilad D., Cai, Xuyu, Elhosary, Princess Christina, Beroukhim, Rameen, Lehtinen, Maria K., Hills, L. Benjamin, Heinzen, Erin L., Hill, Anthony, Hill, R. Sean, Barry, Brenda J., Bourgeois, Blaise F.D., Riviello, James J., Barkovich, A. James, Black, Peter M., Ligon, Keith L., Walsh, Christopher A.
Publicado em 2012

Microcephaly gene links Trithorax and REST/NRSF to control neural stem cell proliferation and differentiation

Por Yang, Yawei J., Baltus, Andrew E., Mathew, Rebecca S., Murphy, Elisabeth A., Evrony, Gilad D., Gonzalez, Dilenny M., Wang, Estee P., Marshall-Walker, Christine A., Barry, Brenda J., Murn, Jernej, Tatarakis, Antonis, Mahajan, Muktar A., Samuels, Herbert H., Shi, Yang, Golden, Jeffrey A., Mahajnah, Muhammad, Shenhav, Ruthie, Walsh, Christopher A.
Publicado em 2012

Evolutionarily Dynamic Alternative Splicing of GPR56 Regulates Regional Cerebral Cortical Patterning

Por Bae, Byoung-Il, Tietjen, Ian, Atabay, Kutay D., Evrony, Gilad D., Johnson, Matthew B., Asare, Ebenezer, Wang, Peter P., Murayama, Ayako Y., Im, Kiho, Lisgo, Steven N., Overman, Lynne, Šestan, Nenad, Chang, Bernard S., Barkovich, A. James, Grant, P. Ellen, Topçu, Meral, Politsky, Jeffrey, Okano, Hideyuki, Piao, Xianhua, Walsh, Christopher A.
Publicado no Science (2014)

Loss of PCLO function underlies pontocerebellar hypoplasia type III

Por Ahmed, Mustafa Y., Chioza, Barry A., Rajab, Anna, Schmitz-Abe, Klaus, Al-Khayat, Aisha, Al-Turki, Saeed, Baple, Emma L., Patton, Michael A., Al-Memar, Ali Y., Hurles, Matthew E., Partlow, Jennifer N., Hill, R. Sean, Evrony, Gilad D., Servattalab, Sarah, Markianos, Kyriacos, Walsh, Christopher A., Crosby, Andrew H., Mochida, Ganeshwaran H.
Publicado no Neurology (2015)

METTL23, a transcriptional partner of GABPA, is essential for human cognition

Por Reiff, Rachel E., Ali, Bassam R., Baron, Byron, Yu, Timothy W., Ben-Salem, Salma, Coulter, Michael E., Schubert, Christian R., Hill, R. Sean, Akawi, Nadia A., Al-Younes, Banan, Kaya, Namik, Evrony, Gilad D., Al-Saffar, Muna, Felie, Jillian M., Partlow, Jennifer N., Sunu, Christine M., Schembri-Wismayer, Pierre, Alkuraya, Fowzan S., Meyer, Brian F., Walsh, Christopher A., Al-Gazali, Lihadh, Mochida, Ganeshwaran H.
Publicado em 2014

Integrated genome and transcriptome sequencing identifies a noncoding mutation in the genome replication factor DONSON as the cause of microcephaly-micromelia syndrome

Por Evrony, Gilad D., Cordero, Dwight R., Shen, Jun, Partlow, Jennifer N., Yu, Timothy W., Rodin, Rachel E., Hill, R. Sean, Coulter, Michael E., Lam, Anh-Thu N., Jayaraman, Divya, Gerrelli, Dianne, Diaz, Diana G., Santos, Chloe, Morrison, Victoria, Galli, Antonella, Tschulena, Ulrich, Wiemann, Stefan, Martel, M. Jocelyne, Spooner, Betty, Ryu, Steven C., Elhosary, Princess C., Richardson, Jillian M., Tierney, Danielle, Robinson, Christopher A., Chibbar, Rajni, Diudea, Dana, Folkerth, Rebecca, Wiebe, Sheldon, Barkovich, A. James, Mochida, Ganeshwaran H., Irvine, James, Lemire, Edmond G., Blakley, Patricia, Walsh, Christopher A.
Publicado no Genome Res (2017)