Research output per year
Research output per year
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Dive into the research topics where Yair Anikster is active. These topic labels come from the works of this person. Together they form a unique fingerprint.
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Collaborations and top research areas from the last five years
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Addition of galactose-1-phosphate measurement enhances newborn screening for classical galactosemia
Daas, S., Abu Salah, N., Anikster, Y., Barel, O., Damseh, N. S., Dumin, E., Fattal-Valevski, A., Falik-Zaccai, T. C., Habib, C., Josefsberg, S., Korman, S. H., Kneller, K., Landau, Y., Lerman-Sagie, T., Mandel, H., Manor, Y., Moady Abdalla, T., Rock, R., Rostami, N., Saada, A., & 9 others, Mar 2023, In: Journal of Inherited Metabolic Disease. 46, 2, p. 232-242 11 p.Research output: Contribution to journal › Article › peer-review
Open Access -
Clinical impact of exome sequencing in the setting of a general pediatric ward for hospitalized children with suspected genetic disorders
Kagan, M., Semo-Oz, R., Ben Moshe, Y., Atias-Varon, D., Tirosh, I., Stern-Zimmer, M., Eliyahu, A., Raas-Rothschild, A., Bivas, M., Shlomovitz, O., Chorin, O., Rock, R., Tzadok, M., Ben-Zeev, B., Heimer, G., Bolkier, Y., Gruber, N., Dagan, A., Bar Aluma, B. E., Pessach, I. M., & 5 others, 9 Jan 2023, In: Frontiers in Genetics. 13, 1018062.Research output: Contribution to journal › Article › peer-review
Open Access -
Corrigendum to: Prevalence of DDC genotypes in patients with aromatic L-amino acid decarboxylase (AADC) deficiency and in silico prediction of structural protein changes (Molecular Genetics and Metabolism (2023) 139(3), (S1096719223002548), (10.1016/j.ymgme.2023.107624))
Himmelreich, N., Bertoldi, M., Alfadhel, M., Alghamdi, M. A., Anikster, Y., Bao, X., Bashiri, F. A., Zeev, B. B., Bisello, G., Ceylan, A. C., Chien, Y. H., Choy, Y. S., Elsea, S. H., Flint, L., García-Cazorla, À., Gijavanekar, C., Gümüş, E. Y., Hamad, M. H., Hişmi, B., Honzik, T., & 30 others, Aug 2023, In: Molecular Genetics and Metabolism. 139, 4, 107647.Research output: Contribution to journal › Comment/debate
Open Access -
Hereditary orotic aciduria identified by newborn screening
Staretz-Chacham, O., Damseh, N. S., Daas, S., Abu Salah, N., Anikster, Y., Barel, O., Dumin, E., Fattal-Valevski, A., Falik-Zaccai, T. C., Hershkovitz, E., Josefsberg, S., Landau, Y., Lerman-Sagie, T., Mandel, H., Rock, R., Rostami, N., Saraf-Levy, T., Shaul Lotan, N., Spiegel, R., Tal, G., & 4 others, 2023, In: Frontiers in Genetics. 14, 1135267.Research output: Contribution to journal › Article › peer-review
Open Access -
Nonsense mutation in the novel PERCC1 gene as a genetic cause of congenital diarrhea and enteropathy
Marek-Yagel, D., Stenke, E., Pode-Shakked, B., Dunne, C., Crushell, E., Bryce-Smith, A., McDermott, M., O’Sullivan, M. J., Veber, A., Krishnamurthy, M., Wells, J. M., Anikster, Y. & Bourke, B., May 2023, In: Human Genetics. 142, 5, p. 691-696 6 p.Research output: Contribution to journal › Article › peer-review
Open Access