Multilocus Genotypes of the Wheat Leaf Rust Fungus Puccinia triticina in Worldwide Regions Indicate Past and Current Long-Distance Migration
Kolmer, J A, Ordoñez, M E, German, S, Morgounov, A, Pretorius, Z, Visser, B, Goyeau, H, Anikster, Y, Acevedo, M
Published in Phytopathology (01.08.2019)
Published in Phytopathology (01.08.2019)
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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 by sequencing
Kolmer, J A, Herman, A, Ordoñez, M E, German, S, Morgounov, A, Pretorius, Z, Visser, B, Anikster, Y, Acevedo, M
Published in Heredity (01.03.2020)
Published in Heredity (01.03.2020)
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SLC1A4 mutations cause a novel disorder of intellectual disability, progressive microcephaly, spasticity and thin corpus callosum
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.
Published in Clinical genetics (01.10.2015)
Published in Clinical genetics (01.10.2015)
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Mutations in AIFM1 cause an X-linked childhood cerebellar ataxia partially responsive to riboflavin
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.
Published in European journal of paediatric neurology (01.01.2018)
Published in European journal of paediatric neurology (01.01.2018)
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Mitochondrial epileptic encephalopathy, 3‐methylglutaconic aciduria and variable complex V deficiency associated with TIMM50 mutations
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.
Published in Clinical genetics (01.05.2017)
Published in Clinical genetics (01.05.2017)
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A New Rust Disease on Wild Coffee (Psychotria nervosa) Caused by Puccinia mysuruensis sp. nov
Mahadevakumar, S, Szabo, Les J, Eilam, T, Anikster, Y, Janardhana, G R
Published in Plant disease (01.07.2016)
Published in Plant disease (01.07.2016)
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Microcephaly, intractable seizures and developmental delay caused by biallelic variants in TBCD: further delineation of a new chaperone‐mediated tubulinopathy
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.
Published in Clinical genetics (01.05.2017)
Published in Clinical genetics (01.05.2017)
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Infusion of platelets transiently reduces nucleoside overload in MNGIE
Lara, M C, Weiss, B, Illa, I, Madoz, P, Massuet, L, Andreu, A L, Valentino, M L, Anikster, Y, Hirano, M, Martí, R
Published in Neurology (24.10.2006)
Published in Neurology (24.10.2006)
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Exome sequencing as a differential diagnosis tool: resolving mild trichohepatoenteric syndrome
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.
Published in Clinical genetics (01.06.2015)
Published in Clinical genetics (01.06.2015)
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Genome size and genome evolution in diploid Triticeae species
Eilam, T, Anikster, Y, Millet, E, Manisterski, J, Sagi-Assif, O, Feldman, M
Published in Genome (01.11.2007)
Published in Genome (01.11.2007)
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Creatine transporter deficiency: Novel mutations and functional studies
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.
Published in Molecular genetics and metabolism reports (01.09.2016)
Published in Molecular genetics and metabolism reports (01.09.2016)
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Peak bone mass in patients with phenylketonuria
Modan‐Moses, D., Vered, I., Schwartz, G., Anikster, Y., Abraham, S., Segev, R., Efrati, Ori
Published in Journal of inherited metabolic disease (01.04.2007)
Published in Journal of inherited metabolic disease (01.04.2007)
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The Neuropsychological profile of patients with 3-Methylglutaconic aciduria type III, Costeff syndrome
Sofer, S., Schweiger, A., Blumkin, L., Yahalom, G., Anikster, Y., Lev, D., Ben-Zeev, B., Lerman-Sagie, T., Hassin-Baer, S.
Published in American journal of medical genetics. Part B, Neuropsychiatric genetics (01.04.2015)
Published in American journal of medical genetics. Part B, Neuropsychiatric genetics (01.04.2015)
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Overwintering and epidemiology of Puccinia dracunculina, the causal agent of rust in open tarragon fields
Cohen, R., Anikster, Y., Vintal, H., Manisterski, J., Shtienberg, D.
Published in Plant pathology (01.02.2013)
Published in Plant pathology (01.02.2013)
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Mutations in AIFM1 cause a potentially treatable X-linked childhood cerebellar ataxia
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
Published in European journal of paediatric neurology (01.06.2017)
Published in European journal of paediatric neurology (01.06.2017)
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