The UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase gene is mutated in recessive hereditary inclusion body myopathy von Mitrani-Rosenbaum, Stella, Eisenberg, Iris, Avidan, Nili, Potikha, Tamara, Hochner, Hagit, Chen, Miriam, Olender, Tsviya, Barash, Mark, Shemesh, Moshe, Sadeh, Menachem, Grabov-Nardini, Gil, Shmilevich, Inna, Friedmann, Adam, Karpati, George, Bradley, Walter G, Baumbach, Lisa, Lancet, Doron, Asher, Edna Ben, Beckmann, Jacques S, Argov, Zohar

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Identification of new schizophrenia susceptibility loci in an ethnically homogeneous, family‐based, Arab‐Israeli sample von Alkelai, Anna, Lupoli, Sara, Greenbaum, Lior, Giegling, Ina, Kohn, Yoav, Sarner‐Kanyas, Kyra, Ben‐Asher, Edna, Lancet, Doron, Rujescu, Dan, Macciardi, Fabio, Lerer, Bernard

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Haplotype structure and selection of the MDM2 oncogene in humans von Atwal, Gurinder Singh, Bond, Gareth L, Metsuyanim, Sally, Papa, Moshe, Friedman, Eitan, Distelman-Menachem, Tal, Ben Asher, Edna, Lancet, Doron, Ross, David A, Sninsky, John, White, Tomas J, Levine, Arnold J, Yarden, Ronit

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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

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Single-nucleotide polymorphisms in the p53 pathway genes modify cancer risk in BRCA1 and BRCA2 carriers of Jewish-Ashkenazi descent von Yarden, Ronit I., Friedman, Eitan, Metsuyanim, Sally, Olender, Tzvia, Ben-Asher, Edna, Papa, Moshe Z.

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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

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Personal receptor repertoires: olfaction as a model von Olender, Tsviya, Waszak, Sebastian M, Viavant, Maya, Khen, Miriam, Ben-Asher, Edna, Reyes, Alejandro, Nativ, Noam, Wysocki, Charles J, Ge, Dongliang, Lancet, Doron

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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

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General Olfactory Sensitivity Database (GOSdb): Candidate Genes and their Genomic Variations von Keydar, Ifat, Ben-Asher, Edna, Feldmesser, Ester, Nativ, Noam, Oshimoto, Arisa, Restrepo, Diego, Matsunami, Hiroaki, Chien, Ming-Shan, Pinto, Jayant M., Gilad, Yoav, Olender, Tsviya, Lancet, Doron

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Genome-wide linkage scan, fine mapping, and haplotype analysis in a large, inbred, Arab Israeli pedigree suggest a schizophrenia susceptibility locus on chromosome 20p13 von Teltsh, Omri, Kanyas, Kyra, Karni, Osnat, Levi, Adi, Korner, Mira, Ben-Asher, Edna, Lancet, Doron, Hamdan, Adnan, Lerer, Bernard, Kohn, Yoav

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DOCK4 and CEACAM21 as novel schizophrenia candidate genes in the Jewish population von Alkelai, Anna, Lupoli, Sara, Greenbaum, Lior, Kohn, Yoav, Kanyas-Sarner, Kyra, Ben-Asher, Edna, Lancet, Doron, Macciardi, Fabio, Lerer, Bernard

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Identification of the gene causing mucolipidosis type IV von Bach, Gideon, Bargal, Ruth, Avidan, Nili, Ben-Asher, Edna, Olender, Zvia, Zeigler, Marcia, Frumkin, Ayala, Raas-Rothschild, Annick, Glusman, Gustavo, Lancet, Doron

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Fine mapping of AHI1 as a schizophrenia susceptibility gene: from association to evolutionary evidence von Torri, Federica, Akelai, Anna, Lupoli, Sara, Sironi, Manuela, Amann-Zalcenstein, Daniela, Fumagalli, Matteo, Fiume, Chiara Dal, Ben-Asher, Edna, Kanyas, Kyra, Cagliani, Rachele, Cozzi, Paolo, Trombetti, Gabriele, Lievers, Luisa Strik, Salvi, Erika, Orro, Alessandro, Beckmann, Jacques S, Lancet, Doron, Kohn, Yoav, Milanesi, Luciano, Ebstein, Richard B, Lerer, Bernard, Macciardi, Fabio

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Lymphoblast and brain expression of AHI1 and the novel primate-specific gene, C6orf217 , in schizophrenia and bipolar disorder von Slonimsky, Alexandra, Levy, Itzchak, Kohn, Yoav, Rigbi, Amihai, Ben-Asher, Edna, Lancet, Doron, Agam, Galila, Lerer, Bernard

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CATSPER2, a human autosomal nonsyndromic male infertility gene von Avidan, Nili, Tamary, Hannah, Dgany, Orly, Cattan, Daniel, Pariente, Alexandre, Thulliez, Michel, Borot, Nicolas, Moati, Lucien, Barthelme, Alain, Shalmon, Lea, Krasnov, Tatyana, Ben-Asher, Edna, Olender, Tsvyia, Khen, Miriam, Yaniv, Issac, Zaizov, Rina, Shalev, Hanna, Delaunay, Jean, Fellous, Marc, Lancet, Doron, Beckmann, Jacques S

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

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Genotype phenotype correlations in Israeli colorectal cancer patients von Starinsky, Sigal, Figer, Arie, Ben‐Asher, Edna, Geva, Ravit, Flex, Dov, Fidder, Herma H., Zidan, Jamal, Lancet, Doron, Friedman, Eitan

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Architecture and anatomy of the genomic locus encoding the human leukemia-associated transcription factor RUNX1/AML1 von Levanon, D, Glusman, G, Bangsow, T, Ben-Asher, E, Male, D A, Avidan, N, Bangsow, C, Hattori, M, Taylor, T D, Taudien, S, Blechschmidt, K, Shimizu, N, Rosenthal, A, Sakaki, Y, Lancet, D, Groner, Y

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Mucolipidosis type IV: Novel MCOLN1 mutations in Jewish and non-Jewish patients and the frequency of the disease in the Ashkenazi Jewish population von Bargal, Ruth, Avidan, Nili, Olender, Tzvia, Ben Asher, Edna, Zeigler, Marcia, Raas-Rothschild, Annick, Frumkin, Ayala, Ben-Yoseph, Omer, Friedlender, Yechiel, Lancet, Doron, Bach, Gideon

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

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