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Lior Greenbaum

Showing results (51-60 of 103) with videos related to

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Pharmacogenetics and Genomics|June 15, 2007
Association of the RGS2 gene with extrapyramidal symptoms induced by treatment with antipsychotic medicationLior Greenbaum, Rael D Strous, Kyra Kanyas, et al.
Frontiers in Aging Neuroscience|February 23, 2023
Neural correlates of subjective cognitive decline in adults at high risk for Alzheimer's diseaseLiat Ben-Ami, Ramit Ravona-Springer, Galia Tsarfaty, et al.
International Journal of Geriatric Psychiatry|September 22, 2015
Ethnicity/culture modulates the relationships of the haptoglobin (Hp) 1-1 phenotype with cognitive function in older individuals with type 2 diabetesElizabeth Guerrero-Berroa, Ramit Ravona-Springer, Anthony Heymann, et al.
European Neuropsychopharmacology : the Journal of the European College of Neuropsychopharmacology|July 22, 2014
The TOMM40 poly-T rs10524523 variant is associated with cognitive performance among non-demented elderly with type 2 diabetesLior Greenbaum, Ramit Ravona Springer, Michael W Lutz, et al.
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.
European Journal of Human Genetics : EJHG|December 20, 2017
Next-generation sequencing of patients with congenital anosmiaAnna Alkelai, Tsviya Olender, Catherine Dode, et al.
Parkinsonism & Related Disorders|January 19, 2024
Are LRRK2 p.G2019S or GBA1 variants associated with long-term outcomes of deep brain stimulation for Parkinson's disease?Saar Anis, Tomer Goldberg, Ethan Shvueli, et al.
Neurology. Genetics|March 25, 2021
Mild Phenotype of Wolfram Syndrome Associated With a Common Pathogenic Variant Is Predicted by a Structural Model of WolframinAdi Wilf-Yarkoni, Oded Shor, Avi Fellner, 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.
Genes|March 28, 2026
Broadening the Phenotypic Spectrum of <i>MAFB</i>-Related Disease: Renal, Auricular, Ocular, and Nervous System InvolvementAviva Eliyahu, Danit Atias-Varon, Ortal Barel, et al.
Pageof 11

Showing results (51-60 of 103) with videos related to

Sort By:
Pageof 11
Pharmacogenetics and Genomics|June 15, 2007
Association of the RGS2 gene with extrapyramidal symptoms induced by treatment with antipsychotic medicationLior Greenbaum, Rael D Strous, Kyra Kanyas, et al.
Frontiers in Aging Neuroscience|February 23, 2023
Neural correlates of subjective cognitive decline in adults at high risk for Alzheimer's diseaseLiat Ben-Ami, Ramit Ravona-Springer, Galia Tsarfaty, et al.
International Journal of Geriatric Psychiatry|September 22, 2015
Ethnicity/culture modulates the relationships of the haptoglobin (Hp) 1-1 phenotype with cognitive function in older individuals with type 2 diabetesElizabeth Guerrero-Berroa, Ramit Ravona-Springer, Anthony Heymann, et al.
European Neuropsychopharmacology : the Journal of the European College of Neuropsychopharmacology|July 22, 2014
The TOMM40 poly-T rs10524523 variant is associated with cognitive performance among non-demented elderly with type 2 diabetesLior Greenbaum, Ramit Ravona Springer, Michael W Lutz, et al.
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.
European Journal of Human Genetics : EJHG|December 20, 2017
Next-generation sequencing of patients with congenital anosmiaAnna Alkelai, Tsviya Olender, Catherine Dode, et al.
Parkinsonism & Related Disorders|January 19, 2024
Are LRRK2 p.G2019S or GBA1 variants associated with long-term outcomes of deep brain stimulation for Parkinson's disease?Saar Anis, Tomer Goldberg, Ethan Shvueli, et al.
Neurology. Genetics|March 25, 2021
Mild Phenotype of Wolfram Syndrome Associated With a Common Pathogenic Variant Is Predicted by a Structural Model of WolframinAdi Wilf-Yarkoni, Oded Shor, Avi Fellner, 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.
Genes|March 28, 2026
Broadening the Phenotypic Spectrum of <i>MAFB</i>-Related Disease: Renal, Auricular, Ocular, and Nervous System InvolvementAviva Eliyahu, Danit Atias-Varon, Ortal Barel, et al.
Pageof 11