A role for TENM1 mutations in congenital general anosmia
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.
Published in Clinical genetics (01.09.2016)
Published in Clinical genetics (01.09.2016)
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Support for association of HSPG2 with tardive dyskinesia in Caucasian populations
Greenbaum, L, Alkelai, A, Zozulinsky, P, Kohn, Y, Lerer, B
Published in The pharmacogenomics journal (01.12.2012)
Published in The pharmacogenomics journal (01.12.2012)
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Journal Article
Convergent lines of evidence support CAMKK2 as a schizophrenia susceptibility gene
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
Published in Molecular psychiatry (01.07.2014)
Published in Molecular psychiatry (01.07.2014)
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Journal Article
The CC2D1A, a member of a new gene family with C2 domains, is involved in autosomal recessive non-syndromic mental retardation
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
Published in Journal of medical genetics (01.03.2006)
Published in Journal of medical genetics (01.03.2006)
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Journal Article
Evidence for an interaction of schizophrenia susceptibility loci on chromosome 6q23.3 and 10q24.33-q26.13 in Arab Israeli families
Alkelai, A., Kohn, Y., Olender, T., Sarner-Kanyas, K., Rigbi, A., Hamdan, A., Ben-Asher, E., Lancet, D., Lerer, B.
Published in American journal of medical genetics. Part B, Neuropsychiatric genetics (05.10.2009)
Published in American journal of medical genetics. Part B, Neuropsychiatric genetics (05.10.2009)
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Journal Article
P.1.01 An association of the glial cell line-derived neurotrophic factor family receptor alpha-1 gene with schizophrenia
Alkelai, A, Kohn, Y, Lupoli, S, Olender, T, Sarner-Kanyas, K, Ben-Asher, E, Lancet, D, Macciardi, F, Lerer, B
Published in European neuropsychopharmacology (2009)
Published in European neuropsychopharmacology (2009)
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Journal Article
Mapping of a new locus for autosomal recessive non-syndromic mental retardation in the chromosomal region 19p13.12-p13.2: further genetic heterogeneity
Basel-Vanagaite, L, Alkelai, A, Straussberg, R, Magal, N, Inbar, D, Mahajna, M, Shohat, M
Published in Journal of medical genetics (01.10.2003)
Published in Journal of medical genetics (01.10.2003)
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Journal Article
A role for TENM1 mutations in congenital general anosmia: A role for TENM1 mutations in CGA
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.
Published in Clinical genetics (01.09.2016)
Published in Clinical genetics (01.09.2016)
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Journal Article
Convergent Lines of Evidence Support LRP8 as a Susceptibility Gene for Psychosis
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
Published in Molecular neurobiology (01.12.2016)
Published in Molecular neurobiology (01.12.2016)
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Journal Article
Convergent lines of evidence support CAMKK2 as a schizophrenia susceptibility gene
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
Published in Molecular psychiatry (2014)
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Published in Molecular psychiatry (2014)
Journal Article
Mapping of a new locus for autosomal recessive non-syndromic mental retardation in the chromosomal region 19p13.12-p 13.2: further genetic heterogeneity
Basel-Vanagaite, L, Alkelai, A, Straussberg, R, Magal, N, Inbar, D, Mahajna, M, Shohat, M
Published in Journal of medical genetics (01.10.2003)
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Published in Journal of medical genetics (01.10.2003)
Journal Article
Mapping of a new locus for autosomal recessive non-syn romic mental retardation in the chromosomal region 19p13.12-p13.2: further genetic heterogeneity
BASEL-VANAGAITE, L, ALKELAI, A, STRAUSSBERG, R, MAGAL, N, INBAR, D, MAHAJNA, M, SHOHAT, M
Published in Journal of medical genetics (2003)
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Published in Journal of medical genetics (2003)
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