Association of the Type 2 Diabetes Mellitus Susceptibility Gene, TCF7L2, with Schizophrenia in an Arab-Israeli Family Sample

von Alkelai, Anna, Greenbaum, Lior, Lupoli, Sara, Kohn, Yoav, Sarner-Kanyas, Kyra, Ben-Asher, Edna, Lancet, Doron, Macciardi, Fabio, Lerer, Bernard
Veröffentlicht 2012

TCF7L2 polymorphisms are associated with amygdalar volume in elderly individuals with Type 2 Diabetes

von Ganmore, Ithamar, Livny, Abigail, Ravona-Springer, Ramit, Cooper, Itzik, Alkelai, Anna, Shelly, Shahar, Tsarfaty, Galia, Heymann, Anthony, Schnaider Beeri, Michal, Greenbaum, Lior
Veröffentlicht in Sci Rep (2019)

Publisher Correction: TCF7L2 polymorphisms are associated with amygdalar volume in elderly individuals with Type 2 Diabetes

von Ganmore, Ithamar, Livny, Abigail, Ravona-Springer, Ramit, Cooper, Itzik, Alkelai, Anna, Shelly, Shahar, Tsarfaty, Galia, Heymann, Anthony, Schnaider Beeri, Michal, Greenbaum, Lior
Veröffentlicht in Sci Rep (2020)

The human olfactory transcriptome

von Olender, Tsviya, Keydar, Ifat, Pinto, Jayant M., Tatarskyy, Pavlo, Alkelai, Anna, Chien, Ming-Shan, Fishilevich, Simon, Restrepo, Diego, Matsunami, Hiroaki, Gilad, Yoav, Lancet, Doron
Veröffentlicht in BMC Genomics (2016)

Next-generation sequencing of patients with congenital anosmia

von Alkelai, Anna, Olender, Tsviya, Dode, Catherine, Shushan, Sagit, Tatarskyy, Pavel, Furman-Haran, Edna, Boyko, Valery, Gross-Isseroff, Ruth, Halvorsen, Matthew, Greenbaum, Lior, Milgrom, Roni, Yamada, Kazuya, Haneishi, Ayumi, Blau, Ilan, Lancet, Doron
Veröffentlicht in Eur J Hum Genet (2017)

Identification of a Functional Risk Variant for Pemphigus Vulgaris in the ST18 Gene

von Vodo, Dan, Sarig, Ofer, Geller, Shamir, Ben-Asher, Edna, Olender, Tsviya, Bochner, Ron, Goldberg, Ilan, Nosgorodsky, Judith, Alkelai, Anna, Tatarskyy, Pavel, Peled, Alon, Baum, Sharon, Barzilai, Aviv, Ibrahim, Saleh M., Zillikens, Detlef, Lancet, Doron, Sprecher, Eli
Veröffentlicht in PLoS Genet (2016)

Mutation in TECPR2 Reveals a Role for Autophagy in Hereditary Spastic Paraparesis

von Oz-Levi, Danit, Ben-Zeev, Bruria, Ruzzo, Elizabeth K., Hitomi, Yuki, Gelman, Amir, Pelak, Kimberly, Anikster, Yair, Reznik-Wolf, Haike, Bar-Joseph, Ifat, Olender, Tsviya, Alkelai, Anna, Weiss, Meira, Ben-Asher, Edna, Ge, Dongliang, Shianna, Kevin V., Elazar, Zvulun, Goldstein, David B., Pras, Elon, Lancet, Doron
Veröffentlicht 2012

VarElect: the phenotype-based variation prioritizer of the GeneCards Suite

von Stelzer, Gil, Plaschkes, Inbar, Oz-Levi, Danit, Alkelai, Anna, Olender, Tsviya, Zimmerman, Shahar, Twik, Michal, Belinky, Frida, Fishilevich, Simon, Nudel, Ron, Guan-Golan, Yaron, Warshawsky, David, Dahary, Dvir, Kohn, Asher, Mazor, Yaron, Kaplan, Sergey, Iny Stein, Tsippi, Baris, Hagit N., Rappaport, Noa, Safran, Marilyn, Lancet, Doron
Veröffentlicht in BMC Genomics (2016)

Commonalities across computational workflows for uncovering explanatory variants in undiagnosed cases

von Kobren, Shilpa Nadimpalli, Baldridge, Dustin, Velinder, Matt, Krier, Joel B., LeBlanc, Kimberly, Esteves, Cecilia, Pusey, Barbara N., Züchner, Stephan, Blue, Elizabeth, Lee, Hane, Huang, Alden, Bastarache, Lisa, Bican, Anna, Cogan, Joy, Marwaha, Shruti, Alkelai, Anna, Murdock, David R., Liu, Pengfei, Wegner, Daniel J., Paul, Alexander J., Sunyaev, Shamil R., Kohane, Isaac S.
Veröffentlicht in Genet Med (2021)

Variants in SCAF4 Cause a Neurodevelopmental Disorder and Are Associated with Impaired mRNA Processing

von Fliedner, Anna, Kirchner, Philipp, Wiesener, Antje, van de Beek, Irma, Waisfisz, Quinten, van Haelst, Mieke, Scott, Daryl A., Lalani, Seema R., Rosenfeld, Jill A., Azamian, Mahshid S., Xia, Fan, Dutra-Clarke, Marina, Martinez-Agosto, Julian A., Lee, Hane, Noh, Grace J., Lippa, Natalie, Alkelai, Anna, Aggarwal, Vimla, Agre, Katherine E., Gavrilova, Ralitza, Mirzaa, Ghayda M., Straussberg, Rachel, Cohen, Rony, Horist, Brooke, Krishnamurthy, Vidya, McWalter, Kirsty, Juusola, Jane, Davis-Keppen, Laura, Ohden, Lisa, van Slegtenhorst, Marjon, de Man, Stella A., Ekici, Arif B., Gregor, Anne, van de Laar, Ingrid, Zweier, Christiane
Veröffentlicht in Am J Hum Genet (2020)

Noncoding Deletions Expose a Novel Gene Critical for Intestinal Function

von Oz-Levi, Danit, Olender, Tsviya, Bar-Joseph, Ifat, Zhu, Yiwen, Marek-Yagel, Dina, Barozzi, Iros, Osterwalder, Marco, Alkelai, Anna, Ruzzo, Elizabeth K., Han, Yujun, Vos, Erica S. M., Reznik-Wolf, Haike, Hartman, Corina, Shamir, Raanan, Weiss, Batia, Shapiro, Rivka, Pode-Shakked, Ben, Tatarskyy, Pavlo, Milgrom, Roni, Schvimer, Michael, Barshack, Iris, Imai, Denise M., Coleman-Derr, Devin, Dickel, Diane E., Nord, Alex S., Afzal, Veena, van Bueren, Kelly Lammerts, Barnes, Ralston M., Black, Brian L., Mayhew, Christopher N., Kuhar, Matthew F., Pitstick, Amy, Tekman, Mehmet, Stanescu, Horia C., Wells, James M., Kleta, Robert, de Laat, Wouter, Goldstein, David B., Pras, Elon, Visel, Axel, Lancet, Doron, Anikster, Yair, Pennacchio, Len A.
Veröffentlicht in Nature (2019)