Search Results - "ALKELAI, A"

A role for TENM1 mutations in congenital general anosmia by 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.

“…Congenital general anosmia (CGA) is a neurological disorder entailing a complete innate inability to sense odors. While the mechanisms underlying vertebrate…”
Get full text

Support for association of HSPG2 with tardive dyskinesia in Caucasian populations by Greenbaum, L, Alkelai, A, Zozulinsky, P, Kohn, Y, Lerer, B

“…Tardive dyskinesia (TD) is a severe adverse effect of chronic antipsychotic drug treatment. In addition to clinical risk factors, TD susceptibility is…”
Get full text

Convergent lines of evidence support CAMKK2 as a schizophrenia susceptibility gene by Luo, X-j, Li, M, Huang, L, Steinberg, S, Mattheisen, M, Liang, G, Donohoe, G, Shi, Y, Chen, C, Yue, W, Alkelai, A, Lerer, B, Li, Z, Yi, Q, Rietschel, M, Cichon, S, Collier, D A, Tosato, S, Suvisaari, J, Rujescu, Dan, Golimbet, V, Silagadze, T, Durmishi, N, Milovancevic, M P, Stefansson, H, Schulze, T G, Nöthen, M M, Chen, C, Lyne, R, Morris, D W, Gill, M, Corvin, A, Zhang, D, Dong, Q, Moyzis, R K, Stefansson, K, Sigurdsson, E, Hu, F, Su, B, Gan, L

“…Genes that are differentially expressed between schizophrenia patients and healthy controls may have key roles in the pathogenesis of schizophrenia. We…”
Get full text

The CC2D1A, a member of a new gene family with C2 domains, is involved in autosomal recessive non-syndromic mental retardation by Basel-Vanagaite, L, Attia, R, Yahav, M, Ferland, R J, Anteki, L, Walsh, C A, Olender, T, Straussberg, R, Magal, N, Taub, E, Drasinover, V, Alkelai, A, Bercovich, D, Rechavi, G, Simon, A J, Shohat, M

“…Background: The molecular basis of autosomal recessive non-syndromic mental retardation (NSMR) is poorly understood, mostly owing to heterogeneity and absence…”
Get full text

Evidence for an interaction of schizophrenia susceptibility loci on chromosome 6q23.3 and 10q24.33-q26.13 in Arab Israeli families by Alkelai, A., Kohn, Y., Olender, T., Sarner-Kanyas, K., Rigbi, A., Hamdan, A., Ben-Asher, E., Lancet, D., Lerer, B.

“…A genome scan for schizophrenia related loci in Arab Israeli families by Lerer et al. [Lerer et al. (2003); Mol Psychiatry 8:488–498] detected significant…”
Get full text

P.1.01 An association of the glial cell line-derived neurotrophic factor family receptor alpha-1 gene with schizophrenia by Alkelai, A, Kohn, Y, Lupoli, S, Olender, T, Sarner-Kanyas, K, Ben-Asher, E, Lancet, D, Macciardi, F, Lerer, B

Get full text

Mapping of a new locus for autosomal recessive non-syndromic mental retardation in the chromosomal region 19p13.12-p13.2: further genetic heterogeneity by Basel-Vanagaite, L, Alkelai, A, Straussberg, R, Magal, N, Inbar, D, Mahajna, M, Shohat, M

“…Objective: To identify and clinically evaluate four consanguineous families of Israeli Arab origin with non-syndromic mental retardation (NSMR), comprising a…”
Get full text

A role for TENM1 mutations in congenital general anosmia: A role for TENM1 mutations in CGA by 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.

Get full text

Convergent Lines of Evidence Support LRP8 as a Susceptibility Gene for Psychosis by Li, Ming, Huang, Liang, Grigoroiu-Serbanescu, Maria, Bergen, Sarah E., Landén, Mikael, Hultman, Christina M., Forstner, Andreas J., Strohmaier, Jana, Hecker, Julian, Schulze, Thomas G., Müller-Myhsok, Bertram, Reif, Andreas, Mitchell, Philip B., Martin, Nicholas G., Cichon, Sven, Nöthen, Markus M., Alkelai, Anna, Lerer, Bernard, Jamain, Stéphane, Leboyer, Marion, Bellivier, Frank, Etain, Bruno, Kahn, Jean-Pierre, Henry, Chantal, Rietschel, Marcella

“…Reelin (RELN) is identified as a risk gene for major psychiatric disorders such as schizophrenia (SCZ) and bipolar disorder (BPD). However, the role of its…”
Get full text

Convergent lines of evidence support CAMKK2 as a schizophrenia susceptibility gene by LUO, X-J, LI, M, ALKELAI, A, LERER, B, LI, Z, YI, Q, RIETSCHEL, M, CICHON, S, COLLIER, D. A, TOSATO, S, SUVISAARI, J, RUJESCU, Dan, HUANG, L, GOLIMBET, V, SILAGADZE, T, DURMISHI, N, MILOVANCEVIC, M. P, STEFANSSON, H, SCHULZE, T. G, NÖTHEN, M. M, CHEN, C, LYNE, R, MORRIS, D. W, STEINBERG, S, GILL, M, CORVIN, A, ZHANG, D, DONG, Q, MOYZIS, R. K, STEFANSSON, K, SIGURDSSON, E, HU, F, SU, B, GAN, L, MATTHEISEN, M, LIANG, G, DONOHOE, G, SHI, Y, CHEN, C, YUE, W

Get full text

Mapping of a new locus for autosomal recessive non-syndromic mental retardation in the chromosomal region 19p13.12-p 13.2: further genetic heterogeneity by Basel-Vanagaite, L, Alkelai, A, Straussberg, R, Magal, N, Inbar, D, Mahajna, M, Shohat, M

Get full text

Mapping of a new locus for autosomal recessive non-syn romic mental retardation in the chromosomal region 19p13.12-p13.2: further genetic heterogeneity by BASEL-VANAGAITE, L, ALKELAI, A, STRAUSSBERG, R, MAGAL, N, INBAR, D, MAHAJNA, M, SHOHAT, M

Get full text