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Anna Alkelai
Anna Alkelai
Research Scientist, Institute for Genomic Medicine Columbia University
在 cumc.columbia.edu 的电子邮件经过验证
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引用次数
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The CC2D1A, a member of a new gene family with C2 domains, is involved in autosomal recessive non-syndromic mental retardation
L Basel-Vanagaite, R Attia, M Yahav, RJ Ferland, L Anteki, CA Walsh, ...
Journal of medical genetics 43 (3), 203-210, 2006
2132006
VarElect: the phenotype-based variation prioritizer of the GeneCards Suite
G Stelzer, I Plaschkes, D Oz-Levi, A Alkelai, T Olender, S Zimmerman, ...
BMC genomics 17, 195-206, 2016
2072016
Mutation in TECPR2 reveals a role for autophagy in hereditary spastic paraparesis
D Oz-Levi, B Ben-Zeev, EK Ruzzo, Y Hitomi, A Gelman, K Pelak, ...
The American Journal of Human Genetics 91 (6), 1065-1072, 2012
1772012
The human olfactory transcriptome
T Olender, I Keydar, JM Pinto, P Tatarskyy, A Alkelai, MS Chien, ...
BMC genomics 17, 1-18, 2016
1212016
Association of the Type 2 Diabetes Mellitus Susceptibility Gene, TCF7L2, with Schizophrenia in an Arab-Israeli Family Sample
A Alkelai, L Greenbaum, S Lupoli, Y Kohn, K Sarner-Kanyas, E Ben-Asher, ...
PloS one 7 (1), e29228, 2012
772012
Genome-wide association study of antipsychotic-induced parkinsonism severity among schizophrenia patients
A Alkelai, L Greenbaum, A Rigbi, K Kanyas, B Lerer
Psychopharmacology 206, 491-499, 2009
722009
DOCK4 and CEACAM21 as novel schizophrenia candidate genes in the Jewish population
A Alkelai, S Lupoli, L Greenbaum, Y Kohn, K Kanyas-Sarner, E Ben-Asher, ...
International Journal of Neuropsychopharmacology 15 (4), 459-469, 2012
682012
A role for TENM1 mutations in congenital general anosmia
A Alkelai, T Olender, R Haffner‐Krausz, MM Tsoory, V Boyko, P Tatarskyy, ...
Clinical genetics 90 (3), 211-219, 2016
652016
Preliminary evidence that a functional polymorphism in type 1 deiodinase is associated with enhanced potentiation of the antidepressant effect of sertraline by triiodothyronine
R Cooper-Kazaz, WM van der Deure, M Medici, TJ Visser, A Alkelai, ...
Journal of affective disorders 116 (1-2), 113-116, 2009
652009
Identification of a Functional Risk Variant for Pemphigus Vulgaris in the ST18 Gene
D Vodo, O Sarig, S Geller, E Ben-Asher, T Olender, R Bochner, I Goldberg, ...
PLoS genetics 12 (5), e1006008, 2016
562016
Convergent lines of evidence support CAMKK2 as a schizophrenia susceptibility gene
XJ Luo, M Li, L Huang, S Steinberg, M Mattheisen, G Liang, G Donohoe, ...
Molecular psychiatry 19 (7), 774-783, 2014
542014
Evidence for association of the GLI2 gene with tardive dyskinesia in patients with chronic schizophrenia
L Greenbaum, A Alkelai, A Rigbi, Y Kohn, B Lerer
Movement disorders 25 (16), 2809-2817, 2010
492010
Fine mapping of AHI1 as a schizophrenia susceptibility gene: from association to evolutionary evidence
F Torri, A Akelai, S Lupoli, M Sironi, D Amann Zalcenstein, M Fumagalli, ...
The FASEB journal 24 (8), 3066-3082, 2010
482010
Support for association of HSPG2 with tardive dyskinesia in Caucasian populations
L Greenbaum, A Alkelai, P Zozulinsky, Y Kohn, B Lerer
The pharmacogenomics journal 12 (6), 513-520, 2012
422012
Identification of new schizophrenia susceptibility loci in an ethnically homogeneous, family‐based, Arab‐Israeli sample
A Alkelai, S Lupoli, L Greenbaum, I Giegling, Y Kohn, K Sarner‐Kanyas, ...
The FASEB Journal 25 (11), 4011-4023, 2011
402011
High-impact rare genetic variants in severe schizophrenia
AW Zoghbi, RS Dhindsa, TE Goldberg, A Mehralizade, JE Motelow, ...
Proceedings of the National Academy of Sciences 118 (51), e2112560118, 2021
382021
Mapping of a new locus for autosomal recessive non-syndromic mental retardation in the chromosomal region 19p13. 12-p13. 2: further genetic heterogeneity
L Basel-Vanagaite, A Alkelai, R Straussberg, N Magal, D Inbar, ...
Journal of medical genetics 40 (10), 729-732, 2003
332003
Phenotypic expansion of CACNA1C-associated disorders to include isolated neurological manifestations
LH Rodan, RC Spillmann, HT Kurata, SM Lamothe, J Maghera, RA Jamra, ...
Genetics in medicine 23 (10), 1922-1932, 2021
302021
Noncoding deletions reveal a gene that is critical for intestinal function
D Oz-Levi, T Olender, I Bar-Joseph, Y Zhu, D Marek-Yagel, I Barozzi, ...
Nature 571 (7763), 107-111, 2019
292019
Convergent lines of evidence support LRP8 as a susceptibility gene for psychosis
M Li, L Huang, M Grigoroiu-Serbanescu, SE Bergen, M Landén, ...
Molecular neurobiology 53, 6608-6619, 2016
262016
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