Multilocus Genotypes of the Wheat Leaf Rust Fungus Puccinia triticina in Worldwide Regions Indicate Past and Current Long-Distance Migration von Kolmer, J A, Ordoñez, M E, German, S, Morgounov, A, Pretorius, Z, Visser, B, Goyeau, H, Anikster, Y, Acevedo, M

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Endemic and panglobal genetic groups, and divergence of host-associated forms in worldwide collections of the wheat leaf rust fungus Puccinia triticina as determined by genotyping... von Kolmer, J. A., Herman, A., Ordonez, M. E., German, S., Morgounov, A., Pretorius, Z., Visser, B., Anikster, Y., Acevedo, M.

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SLC1A4 mutations cause a novel disorder of intellectual disability, progressive microcephaly, spasticity and thin corpus callosum von Heimer, G., Marek-Yagel, D., Eyal, E., Barel, O., Oz Levi, D., Hoffmann, C., Ruzzo, E.K., Ganelin-Cohen, E., Lancet, D., Pras, E., Rechavi, G., Nissenkorn, A., Anikster, Y., Goldstein, D.B., Ben Zeev, B.

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Mutations in AIFM1 cause an X-linked childhood cerebellar ataxia partially responsive to riboflavin von Heimer, G., Eyal, E., Zhu, X., Ruzzo, E.K., Marek-Yagel, D., Sagiv, Doron, Anikster, Y., Reznik-Wolf, H., Pras, E., Oz Levi, D., Lancet, D., Ben-Zeev, B., Nissenkorn, A.

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Mitochondrial epileptic encephalopathy, 3‐methylglutaconic aciduria and variable complex V deficiency associated with TIMM50 mutations von Shahrour, M.A., Staretz‐Chacham, O., Dayan, D., Stephen, J., Weech, A., Damseh, N., Pri Chen, H., Edvardson, S., Mazaheri, S., Saada, A., Hershkovitz, E., Shaag, A., Huizing, M., Abu‐Libdeh, B., Gahl, W.A, Azem, A., Anikster, Y., Vilboux, T., Elpeleg, O., Malicdan, M.C.

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A New Rust Disease on Wild Coffee (Psychotria nervosa) Caused by Puccinia mysuruensis sp. nov von Mahadevakumar, S, Szabo, Les J, Eilam, T, Anikster, Y, Janardhana, G R

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Nuclear DNA amount and genome downsizing in natural and synthetic allopolyploids of the genera Aegilops and Triticum von Eilam, T, Anikster, Y, Millet, E, Manisterski, J, Feldman, M

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Microcephaly, intractable seizures and developmental delay caused by biallelic variants in TBCD: further delineation of a new chaperone‐mediated tubulinopathy von Pode‐Shakked, B., Barash, H., Ziv, L., Gripp, K.W., Flex, E., Barel, O., Carvalho, K.S., Scavina, M., Chillemi, G., Niceta, M., Eyal, E., Kol, N., Ben‐Zeev, B., Bar‐Yosef, O., Marek‐Yagel, D., Bertini, E., Duker, A.L., Anikster, Y., Tartaglia, M., Raas‐Rothschild, A.

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Genome size and genome evolution in diploid Triticeae species von Eilam, T, Anikster, Y, Millet, E, Manisterski, J, Sagi-Assif, O, Feldman, M

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Infusion of platelets transiently reduces nucleoside overload in MNGIE von LARA, M. C, WEISS, B, ILLA, I, MADOZ, P, MASSUET, L, ANDREU, A. L, VALENTINO, M. L, ANIKSTER, Y, HIRANO, M, MARTI, R

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Genetic Differentiation of Puccinia triticina Populations in the Middle East and Genetic Similarity with Populations in Central Asia von Kolmer, J.A, Ordoñez, M.E, Manisterski, J, Anikster, Y

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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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Creatine transporter deficiency: Novel mutations and functional studies von Ardon, O., Procter, M., Mao, R., Longo, N., Landau, Y.E., Shilon-Hadass, A., Gabis, L.V., Hoffmann, C., Tzadok, M., Heimer, G., Sada, S., Ben-Zeev, B., Anikster, Y.

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Peak bone mass in patients with phenylketonuria von Modan‐Moses, D., Vered, I., Schwartz, G., Anikster, Y., Abraham, S., Segev, R., Efrati, Ori

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The Neuropsychological profile of patients with 3-Methylglutaconic aciduria type III, Costeff syndrome von Sofer, S., Schweiger, A., Blumkin, L., Yahalom, G., Anikster, Y., Lev, D., Ben-Zeev, B., Lerman-Sagie, T., Hassin-Baer, S.

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Hermansky-Pudlak Syndrome and Chediak-Higashi Syndrome: Disorders of Vesicle Formation and Trafficking von Huizing, Marjan, Anikster, Yair, Gahl, William A.

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Overwintering and epidemiology of Puccinia dracunculina, the causal agent of rust in open tarragon fields von Cohen, R., Anikster, Y., Vintal, H., Manisterski, J., Shtienberg, D.

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Mutations in AIFM1 cause a potentially treatable X-linked childhood cerebellar ataxia von Nissenkorn, A, Eyal, E, Zhou, X, Ruzzo, E.K, Goldstein, D.B, Anikster, Y, Pras, E, Oz-Levi, D, Lancet, D, Ben-Zeev, B, Heimer, G

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Spatio-temporal genetic variation in populations of wild emmer wheat, Triticum turgidum ssp. dicoccoides, as revealed by AFLP analysis von Ozbek, O, Millet, E, Anikster, Y, Arslan, O, Feldman, M

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Morphology, life cycle biology, and DNA sequence analysis of rust fungi on garlic and chives from California von ANIKSTER, Y, SZABO, L. J, EILAM, T, MANISTERSKI, J, KOIKE, S. T, BUSHNELL, W. R

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