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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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Bioenergetic Signatures of DLD Deficiency: Dissecting PDHc- and α-KGDHc-Linked Defects
Haham Zarbib, Y., Huri Ohev-Shalom, S., Lyskov, S. K., Mazor, Y., Anekstein-Spigel, M., Shalva, N., Spiegel, R., Staretz-Chacham, O., Manor, J., Saada, A., Rock, R., Anikster, Y. & Yardeni, T., Jan 2026, In: Antioxidants. 15, 1, 19.Research output: Contribution to journal › Article › peer-review
Open Access -
Biallelic MED29 variants cause pontocerebellar hypoplasia with cataracts
Arkush, L., van Woerden, G. M., Ziv, L., Marek-Yagel, D., Fonseca, R., Brevé, E., Barel, O., Shalva, N., Veber, A., Anikster, Y., Ben-Ami Raichman, D., Musallam, B., Marcu, S., Nissenkorn, A., Mandel, H., Kushner, S. A., Ben Zeev, B. & Heimer, G., Oct 2025, In: European Journal of Human Genetics. 33, 10, p. 1271-1280 10 p.Research output: Contribution to journal › Article › peer-review
Open Access1 Scopus citations -
Biallelic PIGM Coding Variant Causes Intractable Epilepsy and Intellectual Disability Without Thrombotic Events
Heimer, G., Pode-Shakked, B., Marek-Yagel, D., Vernitsky, H., Tzadok, M., Barel, O., Eyal, E., Ben-Zeev, B., Atzmon, G. & Anikster, Y., Feb 2025, In: Clinical Genetics. 107, 2, p. 179-187 9 p.Research output: Contribution to journal › Article › peer-review
Open Access1 Scopus citations -
Endocrine Abnormalities and Growth Pattern in Single Large-Scale Mitochondrial DNA Deletion Syndromes
Daka, A., Lahav, E., Yosef, O. B., Bolkier, Y., Levy-Shraga, Y., Anikster, Y., Jacoby, E. & Gruber, N., Aug 2025, In: Acta Paediatrica, International Journal of Paediatrics. 114, 8, p. 1857-1867 11 p.Research output: Contribution to journal › Article › peer-review
Open Access1 Scopus citations -
In depth profiling of dihydrolipoamide dehydrogenase deficiency in primary patients fibroblasts reveals metabolic reprogramming secondary to mitochondrial dysfunction
Sprecher, U., Dsouza, J., Marisat, M., Barasch, D., Mishra, K., Kakhlon, O., Manor, J., Anikster, Y. & Weil, M., Mar 2025, In: Molecular Genetics and Metabolism Reports. 42, 101172.Research output: Contribution to journal › Article › peer-review
Open Access1 Scopus citations