Application of machine learning approaches in predicting clinical outcomes in older adults – a systematic review and meta-analysis von Olender, Robert T, Roy, Sandipan, Nishtala, Prasad S

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A role for TENM1 mutations in congenital general anosmia von Alkelai, A., Olender, T., Haffner‐Krausz, R., Tsoory, M.M., Boyko, V., Tatarskyy, P., Gross‐Isseroff, R., Milgrom, R., Shushan, S., Blau, I., Cohn, E., Beeri, R., Levy-Lahad, E., Pras, E., Lancet, D.

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Drug Burden Index Is a Modifiable Predictor of 30-Day Hospitalization in Community-Dwelling Older Adults With Complex Care Needs: Machine Learning Analysis of InterRAI Data von Olender, Robert T, Roy, Sandipan, Jamieson, Hamish A, Hilmer, Sarah N, Nishtala, Prasad S

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Exome sequencing as a differential diagnosis tool: resolving mild trichohepatoenteric syndrome von Oz-Levi, D., Weiss, B., Lahad, A., Greenberger, S., Pode-Shakked, B., Somech, R., Olender, T., Tatarsky, P., Marek-Yagel, D., Pras, E., Anikster, Y., Lancet, D.

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The CC2D1A, a member of a new gene family with C2 domains, is involved in autosomal recessive non-syndromic mental retardation von Basel-Vanagaite, L, Attia, R, Yahav, M, Ferland, R J, Anteki, L, Walsh, C A, Olender, T, Straussberg, R, Magal, N, Taub, E, Drasinover, V, Alkelai, A, Bercovich, D, Rechavi, G, Simon, A J, Shohat, M

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Why do young women smoke? I. Direct and interactive effects of environment, psychological characteristics and nicotinic cholinergic receptor genes von GREENBAUM, L, KANYAS, K, KARNI, O, MERBL, Y, OLENDER, T, HOROWITZ, A, YAKIR, A, LANCET, D, BEN-ASHER, E, LERER, B

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Evidence for an interaction of schizophrenia susceptibility loci on chromosome 6q23.3 and 10q24.33-q26.13 in Arab Israeli families von Alkelai, A., Kohn, Y., Olender, T., Sarner-Kanyas, K., Rigbi, A., Hamdan, A., Ben-Asher, E., Lancet, D., Lerer, B.

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Human olfaction: from genomic variation to phenotypic diversity von Hasin-Brumshtein, Yehudit, Lancet, Doron, Olender, Tsviya

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Genomic organisation of the UDP-N-acetylglucosamine-1-phosphotransferase gamma subunit (GNPTAG) and its mutations in mucolipidosis III von Raas-Rothschild, A, Bargal, R, Goldman, O, Ben-Asher, E, Groener, J E M, Toutain, A, Stemmer, E, Ben-Neriah, Z, Flusser, H, Beemer, F A, Penttinen, M, Olender, T, Rein, A J J T, Bach, G, Zeigler, M

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GeneCards Version 3: the human gene integrator von Safran, Marilyn, Dalah, Irina, Alexander, Justin, Rosen, Naomi, Iny Stein, Tsippi, Shmoish, Michael, Nativ, Noam, Bahir, Iris, Doniger, Tirza, Krug, Hagit, Sirota-Madi, Alexandra, Olender, Tsviya, Golan, Yaron, Stelzer, Gil, Harel, Arye, Lancet, Doron

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P.1.01 An association of the glial cell line-derived neurotrophic factor family receptor alpha-1 gene with schizophrenia von Alkelai, A, Kohn, Y, Lupoli, S, Olender, T, Sarner-Kanyas, K, Ben-Asher, E, Lancet, D, Macciardi, F, Lerer, B

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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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Localization of SNPs in the CHRNB2 gene von Greenbaum, L, Kanyas, K, Karni, O, Merbl, Y, Olender, T, Horowitz, A, Yakir, A, Lancet, D, Ben-Asher, E, Lerer, B

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Evolutionary Grass Roots for Odor Recognition von OLENDER, Tsviya, LANCET, Doron

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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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Genome sequence of the pattern forming Paenibacillus vortex bacterium reveals potential for thriving in complex environments von Sirota-Madi, A, Olender, T, Helman, Y, Ingham, C, Brainis, I, Roth, D, Hagi, E, Brodsky, L, Leshkowitz, D, Galatenko, V, Nikolaev, V, Mugasimangalam, R.C, Bransburg-Zabary, S, Gutnick, D.L, Lancet, D, Ben-Jacob, E

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Noncoding deletions reveal a gene that is critical for intestinal function von Oz-Levi, D, Olender, T, Bar-Joseph, I, Zhu, Y, Marek-Yagel, D, Barozzi, I, Osterwalder, M, Alkelai, A, Ruzzo, EK, Han, Y, Vos, ESM, Reznik-Wolf, H, Hartman, C, Shamir, R, Weiss, B, Shapiro, R, Pode-Shakked, B, Tatarskyy, P, Milgrom, R, Schvimer, M, Barshack, I, Imai, DM, Coleman-Derr, D, Dickel, DE, Nord, AS, Afzal, V, Van Bueren, KL, Barnes, RM, Black, BL, Mayhew, CN, Kuhar, MF, Pitstick, A, Tekman, M, Stanescu, HC, Wells, JM, Kleta, R, De Laat, W, Goldstein, DB, Pras, E, Visel, A, Lancet, D, Anikster, Y, Pennacchio, LA

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GeneCards™ 2002: towards a complete, object-oriented, human gene compendium von Safran, Marilyn, Solomon, Irina, Shmueli, Orit, Lapidot, Michal, Shen-Orr, Shai, Adato, Avital, Ben-Dor, Uri, Esterman, Nir, Rosen, Naomi, Peter, Inga, Olender, Tsviya, Chalifa-Caspi, Vered, Lancet, Doron

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GeneDecks: Paralog Hunting and Gene-Set Distillation with GeneCards Annotation von Stelzer, Gil, Inger, Aron, Olender, Tsviya, Iny-Stein, Tsippi, Dalah, Irina, Harel, Arye, Safran, Marilyn, Lancet, Doron

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Human Gene-Centric Databases at the Weizmann Institute of Science: GeneCards, UDB, CroW 21 and HORDE von Safran, Marilyn, Chalifa-Caspi, Vered, Shmueli, Orit, Olender, Tsviya, Lapidot, Michal, Rosen, Naomi, Shmoish, Michael, Peter, Yakov, Glusman, Gustavo, Feldmesser, Ester, Adato, Avital, Peter, Inga, Khen, Miriam, Atarot, Tal, Groner, Yoram, Lancet, Doron

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