Glutamine synthetase protects against neuronal degeneration in injured retinal tissue

Por Gorovits, Rena, Avidan, Nili, Avisar, Noa, Shaked, Iftach, Vardimon, Lily
Publicado em 1997

Trick or treat: The effect of placebo on the power of pharmacogenetic association studies

Por Singer, Clara, Grossman, Iris, Avidan, Nili, Beckmann, Jacques S, Pe'er, Itsik
Publicado em 2005

Gene Expression Profiling of the Response to Interferon Beta in Epstein-Barr-Transformed and Primary B Cells of Patients with Multiple Sclerosis

Por Khsheibun, Rana, Paperna, Tamar, Volkowich, Anat, Lejbkowicz, Izabella, Avidan, Nili, Miller, Ariel
Publicado em 2014

Integrative analysis of methylome and transcriptome in human blood identifies extensive sex- and immune cell-specific differentially methylated regions

Por Mamrut, Shimrat, Avidan, Nili, Staun-Ram, Elsebeth, Ginzburg, Elizabeta, Truffault, Frederique, Berrih-Aknin, Sonia, Miller, Ariel
Publicado no Epigenetics (2015)

Interferon-Beta Induces Distinct Gene Expression Response Patterns in Human Monocytes versus T cells

Por Henig, Noa, Avidan, Nili, Mandel, Ilana, Staun-Ram, Elsebeth, Ginzburg, Elizabeta, Paperna, Tamar, Pinter, Ron Y., Miller, Ariel
Publicado em 2013

The genetics of colored sequence synesthesia: Suggestive evidence of linkage to 16q and genetic heterogeneity for the condition

Por Tomson, Steffie N., Avidan, Nili, Lee, Kwanghyuk, Sarma, Anand K., Tushe, Rejnal, Milewicz, Dianna M., Bray, Molly, Leal, Suzanne M., Eagleman, David M.
Publicado em 2011

A Missense Mutation in a Highly Conserved Region of CASQ2 Is Associated with Autosomal Recessive Catecholamine-Induced Polymorphic Ventricular Tachycardia in Bedouin Families from...

Por Lahat, Hadas, Pras, Elon, Olender, Tsviya, Avidan, Nili, Ben-Asher, Edna, Man, Orna, Levy-Nissenbaum, Etgar, Khoury, Asad, Lorber, Avraham, Goldman, Boleslaw, Lancet, Doron, Eldar, Michael
Publicado em 2001

Exome Sequencing Identifies SMAD3 Mutations as a Cause of Familial Thoracic Aortic Aneurysm and Dissection with Intracranial and Other Arterial Aneurysms

Por Regalado, Ellen S., Guo, Dong-chuan, Villamizar, Carlos, Avidan, Nili, Gilchrist, Dawna, McGillivray, Barbara, Clarke, Lorne, Bernier, Francois, Santos-Cortez, Regie L., Leal, Suzanne M., Bertoli-Avella, Aida M., Shendure, Jay, Rieder, Mark J., Nickerson, Deborah A, Milewicz, Dianna M.
Publicado em 2011

Identification of C7orf11 (TTDN1) Gene Mutations and Genetic Heterogeneity in Nonphotosensitive Trichothiodystrophy

Por Nakabayashi, Kazuhiko, Amann, Daniela, Ren, Yan, Saarialho-Kere, Ulpu, Avidan, Nili, Gentles, Simone, MacDonald, Jeffrey R., Puffenberger, Erik G., Christiano, Angela M., Martinez-Mir, Amalia, Salas-Alanis, Julio C., Rizzo, Renata, Vamos, Esther, Raams, Anja, Les, Clifford, Seboun, Eric, Jaspers, Nicolaas G. J., Beckmann, Jacques S., Jackson, Charles E., Scherer, Stephen W.
Publicado em 2005

Congenital Dyserythropoietic Anemia Type I Is Caused by Mutations in Codanin-1

Por Dgany, Orly, Avidan, Nili, Delaunay, Jean, Krasnov, Tatyana, Shalmon, Lea, Shalev, Hanna, Eidelitz-Markus, Tal, Kapelushnik, Joseph, Cattan, Daniel, Pariente, Alexandre, Tulliez, Michel, Crétien, Aurore, Schischmanoff, Pierre-Olivier, Iolascon, Achille, Fibach, Eithan, Koren, Ariel, Rössler, Jochen, Le Merrer, Martine, Yaniv, Isaac, Zaizov, Rina, Ben-Asher, Edna, Olender, Tsvyia, Lancet, Doron, Beckmann, Jacques S., Tamary, Hannah
Publicado em 2002

VAV1 and BAFF, via NFκB pathway, are genetic risk factors for myasthenia gravis

Por Avidan, Nili, Le Panse, Rozen, Harbo, Hanne F, Bernasconi, Pia, Poulas, Konstantinos, Ginzburg, Elizabeta, Cavalcante, Paola, Colleoni, Lara, Baggi, Fulvio, Antozzi, Carlo, Truffault, Frédérique, Horn-Saban, Shirley, Pöschel, Simone, Zagoriti, Zoi, Maniaol, Angelina, Lie, Benedicte A, Bernard, Isabelle, Saoudi, Abdelhadi, Illes, Zsolt, Casasnovas Pons, Carlos, Melms, Arthur, Tzartos, Socrates, Willcox, Nicholas, Kostera-Pruszczyk, Anna, Tallaksen, Chantal, Mantegazza, Renato, Berrih-Aknin, Sonia, Miller, Ariel
Publicado em 2014

Mutations in Smooth Muscle Alpha-Actin (ACTA2) Cause Coronary Artery Disease, Stroke, and Moyamoya Disease, Along with Thoracic Aortic Disease

Por Guo, Dong-Chuan, Papke, Christina L., Tran-Fadulu, Van, Regalado, Ellen S., Avidan, Nili, Johnson, Ralph Jay, Kim, Dong H., Pannu, Hariyadarshi, Willing, Marcia C., Sparks, Elizabeth, Pyeritz, Reed E., Singh, Michael N., Dalman, Ronald L., Grotta, James C., Marian, Ali J., Boerwinkle, Eric A., Frazier, Lorraine Q., LeMaire, Scott A., Coselli, Joseph S., Estrera, Anthony L., Safi, Hazim J., Veeraraghavan, Sudha, Muzny, Donna M., Wheeler, David A., Willerson, James T., Yu, Robert K., Shete, Sanjay S., Scherer, Steven E., Raman, C.S., Buja, L. Maximilian, Milewicz, Dianna M.
Publicado em 2009