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Dive into the research topics where Dorit Lev 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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Parental counselling and autopsy results: A retrospective diagnostic cohort study at a multidisciplinary fetal neurology clinic
Shariv, A., Gafner, M., Leibovitz, Z., Schreiber, L., Kidron, D., Arad, A., Hadi, E., Libzon, S., Ben Sira, L., Goldschmidt Manor, M., Lev, D., Lerman-Sagie, T. & Gindes, L., Mar 2026, In: Developmental Medicine and Child Neurology. 68, 3, p. 441-452 12 p.Research output: Contribution to journal › Article › peer-review
Open Access3 Scopus citations -
The Clinical, Histological, and Genetic Spectrum of RYR1 Variants—A Multi-Center Israeli Cohort Study
Ginsberg, M., Michelson, M., Aharoni, S., Sagie, L., Michaeli, Y., Rotenberg, D., Finkelshtein, V., Yosovich, K., Argov, Z., Nissenkorn, A., Lev, D., Sadeh, M. & Dabby, R., Feb 2026, In: Journal of Clinical Medicine. 15, 4, 1388.Research output: Contribution to journal › Article › peer-review
Open Access -
Clinical profiling and medical management of Israeli individuals with Phelan McDermid syndrome
Chorin, O., Greenbaum, L., Lev-Hochberg, S., Feinstein-Goren, N., Eliyahu, A., Shani, H., Pras, E., Weissbach, T., Bolkier, Y., Heimer, G., Lev, D., Michelson, M., Regev, M., Josefsberg, S., Batzir, N. A., Shalata, A., Spiegel, R., Segel, R., Lobel, O. & Abu-Libdeh, B. & 5 others, , Dec 2025, In: Orphanet Journal of Rare Diseases. 20, 1, 132.Research output: Contribution to journal › Article › peer-review
Open Access -
EEFSEC deficiency: A selenopathy with early-onset neurodegeneration
Laugwitz, L., Buchert, R., Olguín, P., Estiar, M. A., Atanasova, M., Jr., W. M., Enssle, J., Marsden, B., Avilés, J., González-Gutiérrez, A., Candia, N., Fabiano, M., Morlot, S., Peralta, S., Groh, A., Schillinger, C., Kuehn, C., Sofan, L., Sturm, M. & Bender, B. & 30 others, , 2 Jan 2025, In: American Journal of Human Genetics. 112, 1, p. 168-180 13 p.Research output: Contribution to journal › Article › peer-review
Open Access4 Scopus citations -
Genome sequencing provides high diagnostic yield and new etiological insights for intellectual disability and developmental delay
Hamanaka, K., Fujita, A., Miyatake, S., Misawa, K., Koshimizu, E., Uchiyama, Y., Tsuchida, N., Seyama, R., Sakamoto, M., Iwama, K., Nishimura, N., Utsuno, Y., Fu, L., Takizawa, M., Liang, Q., Itai, T., Saida, K., Ohori, S., Kameyama, S. & Fukuda, H. & 47 others, , Dec 2025, In: npj Genomic Medicine. 10, 1, 60.Research output: Contribution to journal › Article › peer-review
Open Access2 Scopus citations