A role for TENM1 mutations in congenital general anosmia von Alkelai, A., Olender, T., Haffner‐Krausz, R., Tsoory, M.M., Boyko, V., Tatarskyy, P., Gross‐Isseroff, R., Milgrom, R., Shushan, S., Blau, I., Cohn, E., Beeri, R., Levy-Lahad, E., Pras, E., Lancet, D.

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P.2.017 Differential effect of chronic stress on cognition and affect in young and old mice von Tatarskyy, P, Lotan, A, Lifschytz, T, Mernick, B, Wolf, G, Ben-Ari, H, Lerer, B

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Allelic polymorphism of F2, F5 and MTHFR genes in population of Ukraine von Tatarskyy, P, Kucherenko, A, Livshits, L

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Study of possible role of CYP1A1, GSTT1, GSTM1, GSTP1, NAT2 and ADRB2 genes polymorphisms in bronchial asthma development in children von Tatarskyy, P. F., Chumachenko, N. G., Kucherenko, A. M., Gulkovskyi, R. V., Arabskaya, L. P., Smirnova, O. A., Tolkach, S. I., Antipkin, Yu. G., Livshits, L. A.

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Human genome mutation and rearrangement studies – the way to investigate monogenic and complex disease pathogenesis von Livshits, L. A., Kravchenko, S. A., Nechyporenko, M. V., Pampukha, V. M., Hryshchenko, N. V., Livshyts, G. B., Soloviov, O. O., Tatarskyy, P. F., Fesai, O. A., Chernushyn, S. Yu, Kucherenko, A. M., Gulkovskyy, R. V.

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Comparative analysis of associations between polymorphic variants of the F2, F5, GP1BA, and ACE genes and the risk of developing stroke in Russian and Ukrainian populations von Tupitsyna, T. V., Bondarenko, E. A., Kravchenko, S. A., Tatarskyy, P. F., Shetova, I. M., Shamalov, N. A., Kuznetsova, S. M., Shul’zhenko, D. V., Skvortsova, V. I., Slominsky, P. A., Livshits, L. A., Limborska, S. A.

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Study of the possible role of polymorphisms of the detoxication and coagulation system genes in pathogenesis of pregnancy loss von Tatarskyy, P. F., Kucherenko, A. M., Khazhilenko, K. G., Zinchenko, V. M., Ilyin, I. E., Livshits, L. A.

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Noncoding deletions reveal a gene that is critical for intestinal function von Oz-Levi, D, Olender, T, Bar-Joseph, I, Zhu, Y, Marek-Yagel, D, Barozzi, I, Osterwalder, M, Alkelai, A, Ruzzo, EK, Han, Y, Vos, ESM, Reznik-Wolf, H, Hartman, C, Shamir, R, Weiss, B, Shapiro, R, Pode-Shakked, B, Tatarskyy, P, Milgrom, R, Schvimer, M, Barshack, I, Imai, DM, Coleman-Derr, D, Dickel, DE, Nord, AS, Afzal, V, Van Bueren, KL, Barnes, RM, Black, BL, Mayhew, CN, Kuhar, MF, Pitstick, A, Tekman, M, Stanescu, HC, Wells, JM, Kleta, R, De Laat, W, Goldstein, DB, Pras, E, Visel, A, Lancet, D, Anikster, Y, Pennacchio, LA

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A role for TENM1 mutations in congenital general anosmia: A role for TENM1 mutations in CGA von Alkelai, A., Olender, T., Haffner-Krausz, R., Tsoory, M.M., Boyko, V., Tatarskyy, P., Gross-Isseroff, R., Milgrom, R., Shushan, S., Blau, I., Cohn, E., Beeri, R., Levy-Lahad, E., Pras, E., Lancet, D.

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Ischemic stroke in Ukrainian population: possible involvement of the F2 G20210A, F5 G1691A and MTHFR C677T gene variants von Tatarskyy, P. F., Kucherenko, A. M., Kravchenko, S. A., Shulzenko, D. V., Kuznetsova, S. M., Livshits, L. A.

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Ischemic stroke in Ukrainian population: possible involvement of the F2 G20210A, F5G1691A and MTHFR C677T gene variants von Tatarskyy, P F, Kucherenko, A M, Kravchenko, S A, Shulzhenko, D V, Kuznetsova, S M, Livshits, L A

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Clinical genealogical and molecular genetic study of patients with mental retardation von Hryshchenko, N. V., Bychkova, G. M., Livshyts, G. B., Kravchenko, S. A., Pampukha, V. M., Soloviov, O. O., Kucherenko, A. M., Tatarskyy, P. F., Afanasieva, N. O., Dubrovska, I. V., Patskun, E. J., Zymak-Zakutnia, N. O., Nikitchina, T. V., Lohush, S. Yu, Livshits, L. A.

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Molecular-genetics analysis of natural and stimulated ovulation impairment von Livshyts, G. B., Kravchenko, S. A., Tatarskyy, P. F., Sudoma, I. A., Livshits, L. A.

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Noncoding deletions reveal a gene that is critical for intestinal function von Oz-Levi, D, Olender, T, Bar-Joseph, I, Zhu, Y, Marek-Yagel, D, Barozzi, I, Osterwalder, M, Alkelai, A, Ruzzo, EK, Han, Y, Vos, ESM, Reznik-Wolf, H, Hartman, C, Shamir, R, Weiss, B, Shapiro, R, Pode-Shakked, B, Tatarskyy, P, Milgrom, R, Schvimer, M, Barshack, I, Imai, DM, Coleman-Derr, D, Dickel, DE, Nord, AS, Afzal, V, van Bueren, KL, Barnes, RM, Black, BL, Mayhew, CN, Kuhar, MF, Pitstick, A, Tekman, M, Stanescu, HC, Wells, JM, Kleta, R, de laat, W, Goldstein, DB, Pras, E, Visel, A, Lancet, D, Anikster, Y, Pennacchio, LA

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New insights into tardive dyskinesia genetics: Implementation of whole-exome sequencing approach von Alkelai, Anna, Greenbaum, Lior, Heinzen, Erin L., Baugh, Evan H., Teitelbaum, Alexander, Zhu, Xiaolin, Strous, Rael D., Tatarskyy, Pavel, Zai, Clement C., Tiwari, Arun K., Tampakeras, Maria, Freeman, Natalie, Müller, Daniel J., Voineskos, Aristotle N., Lieberman, Jeffrey A., Delaney, Shannon L., Meltzer, Herbert Y., Remington, Gary, Kennedy, James L., Pulver, Ann E., Peabody, Emma P., Levy, Deborah L., Lerer, Bernard

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