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Journal of Human Genetics|September 19, 2020
Expansion of the GRIA2 phenotypic representation: a novel de novo loss of function mutation in a case with childhood onset schizophreniaAnna Alkelai, Shahar Shohat, Lior Greenbaum, et al.Drug Discovery Today|October 26, 2001
Population-based gene discovery in the post-genomic eraNaomi B. Zak, Sagiv Shifman, Anne Shalom, et al.Molecular and Cellular Probes|December 20, 2002
Quantitative technologies for allele frequency estimation of SNPs in DNA poolsSagiv Shifman, Anne Pisanté-Shalom, Benjamin Yakir, et al.Schizophrenia Research|January 16, 2023
Genetic insights into childhood-onset schizophrenia: The yield of clinical exome sequencingAnna Alkelai, Lior Greenbaum, Shahar Shohat, et al.The Israel Medical Association Journal : IMAJ|June 21, 2002
Genetic dissection of common diseasesNaomi B Zak, Sagiv Shifman, Anne Shalom, et al.Schizophrenia Research|January 18, 2005
A survey of the 22q11 microdeletion in a large cohort of schizophrenia patientsAnat Horowitz, Sagiv Shifman, Nechama Rivlin, et al.Human Molecular Genetics|March 26, 2003
Linkage disequilibrium patterns of the human genome across populationsSagiv Shifman, Jane Kuypers, Mark Kokoris, et al.Cancer Research|August 16, 2014
Transcriptional dynamics in colorectal carcinogenesis: new insights into the role of c-Myc and miR17 in benign to cancer transformationEyal Ben-David, Assaf C Bester, Sagiv Shifman, et al.Psychiatric Genetics|August 12, 2005
Further tests of the association between schizophrenia and single nucleotide polymorphism markers at the catechol-O-methyltransferase locus in an Askenazi Jewish population using microsatellite markersAnat Horowitz, Sagiv Shifman, Nehama Rivlin, et al.Cells|March 27, 2024
Analyses of Conditional Knockout Mice for Pogz, a Gene Responsible for Neurodevelopmental Disorders in Excitatory and Inhibitory Neurons in the BrainNanako Hamada, Takuma Nishijo, Ikuko Iwamoto, et al.Pageof 7