Drosophila LIM-Only Is a Positive Regulator of Transcription During Thoracic Bristle Development

gan Zenvirt, Shamir, Nevo-Caspi, Yael, Rencus-Lazar, Sigal, Segal, Daniel
Cyhoeddwyd 2008

Exome sequencing and disease-network analysis of a single family implicate a mutation in KIF1A in hereditary spastic paraparesis

gan Erlich, Yaniv, Edvardson, Simon, Hodges, Emily, Zenvirt, Shamir, Thekkat, Pramod, Shaag, Avraham, Dor, Talya, Hannon, Gregory J., Elpeleg, Orly
Cyhoeddwyd 2011

Deleterious mutation in SYCE1 is associated with non-obstructive azoospermia

gan Maor-Sagie, Esther, Cinnamon, Yuval, Yaacov, Barak, Shaag, Avraham, Goldsmidt, Hannoch, Zenvirt, Shamir, Laufer, Neri, Richler, Carmelit, Frumkin, Ayala
Cyhoeddwyd yn J Assist Reprod Genet (2015)

Joubert Syndrome 2 (JBTS2) in Ashkenazi Jews Is Associated with a TMEM216 Mutation

gan Edvardson, Simon, Shaag, Avraham, Zenvirt, Shamir, Erlich, Yaniv, Hannon, Gregory J., Shanske, Alan L., Gomori, John Moshe, Ekstein, Joseph, Elpeleg, Orly
Cyhoeddwyd 2010

Joubert Syndrome 2 (JBTS2) in Ashkenazi Jews Is Associated with a TMEM216 Mutation

gan Edvardson, Simon, Shaag, Avraham, Zenvirt, Shamir, Erlich, Yaniv, Hannon, Gregory J., Shanske, Alan L., Gomori, John Moshe, Ekstein, Joseph, Elpeleg, Orly
Cyhoeddwyd 2010

Infantile Cerebellar-Retinal Degeneration Associated with a Mutation in Mitochondrial Aconitase, ACO2

gan Spiegel, Ronen, Pines, Ophry, Ta-Shma, Asaf, Burak, Efrat, Shaag, Avraham, Halvardson, Jonatan, Edvardson, Shimon, Mahajna, Muhammad, Zenvirt, Shamir, Saada, Ann, Shalev, Stavit, Feuk, Lars, Elpeleg, Orly
Cyhoeddwyd 2012

A Deleterious Mutation in DNAJC6 Encoding the Neuronal-Specific Clathrin-Uncoating Co-Chaperone Auxilin, Is Associated with Juvenile Parkinsonism

gan Edvardson, Simon, Cinnamon, Yuval, Ta-Shma, Asaf, Shaag, Avraham, Yim, Yang-In, Zenvirt, Shamir, Jalas, Chaim, Lesage, Suzanne, Brice, Alexis, Taraboulos, Albert, Kaestner, Klaus H., Greene, Lois E., Elpeleg, Orly
Cyhoeddwyd 2012

Infantile Cerebral and Cerebellar Atrophy Is Associated with a Mutation in the MED17 Subunit of the Transcription Preinitiation Mediator Complex

gan Kaufmann, Rami, Straussberg, Rachel, Mandel, Hanna, Fattal-Valevski, Aviva, Ben-Zeev, Bruria, Naamati, Adi, Shaag, Avraham, Zenvirt, Shamir, Konen, Osnat, Mimouni-Bloch, Aviva, Dobyns, William B., Edvardson, Simon, Pines, Ophry, Elpeleg, Orly
Cyhoeddwyd 2010