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Maria Isabel Alvarez-Mora

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Genes|November 11, 2022
Special Issue: Genetics of Psychiatric Disease and the Basics of NeurobiologyLaia Rodriguez-Revenga, Maria Isabel Alvarez-Mora
Frontiers in Psychiatry|November 1, 2021
Neuroimaging Insight Into Fragile X-Associated Neuropsychiatric Disorders: Literature ReviewAndrea Elias-Mas, Maria Isabel Alvarez-Mora, Conxita Caro-Benito, et al.
American Journal of Medical Genetics. Part A|August 18, 2017
Paternal transmission of a FMR1 full mutation alleleMaria Isabel Alvarez-Mora, Miriam Guitart, Laia Rodriguez-Revenga, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 16, 2013
High apolipoprotein E4 allele frequency in FXTAS patientsFrancisca Silva, Laia Rodriguez-Revenga, Irene Madrigal, et al.
Genes|April 30, 2021
Novel Compound Heterozygous Mutation in <i>TRAPPC9</i> Gene: The Relevance of Whole Genome SequencingMaria Isabel Alvarez-Mora, Jordi Corominas, Christian Gilissen, et al.
Neuro-Degenerative Diseases|November 27, 2015
Skewed X Inactivation in Women Carrying the FMR1 Premutation and Its Relation with Fragile-X-Associated Tremor/Ataxia SyndromeMaria Isabel Alvarez-Mora, Laia Rodriguez-Revenga, Aina Feliu, et al.
Molecular Neurobiology|January 3, 2022
Reduced mtDNA Copy Number in the Prefrontal Cortex of C9ORF72 PatientsMaria Isabel Alvarez-Mora, Petar Podlesniy, Teresa Riazuelo, et al.
Neurobiology of Disease|January 15, 2014
Blood expression profiles of fragile X premutation carriers identify candidate genes involved in neurodegenerative and infertility phenotypesElisabet Mateu-Huertas, Laia Rodriguez-Revenga, Maria Isabel Alvarez-Mora, et al.
European Journal of Human Genetics : EJHG|January 7, 2016
A novel splicing mutation in the IQSEC2 gene that modulates the phenotype severity in a family with intellectual disabilityIrene Madrigal, Maria Isabel Alvarez-Mora, Jordi Rosell, et al.
Clinical Genetics|July 3, 2020
An exome-wide exploration of cases of primary ovarian insufficiency uncovers novel sequence variants and candidate genesMaria Isabel Alvarez-Mora, Anne-Laure Todeschini, Sandrine Caburet, et al.
Pageof 3

Showing results (1-10 of 29) with videos related to

Sort By:
Pageof 3
Genes|November 11, 2022
Special Issue: Genetics of Psychiatric Disease and the Basics of NeurobiologyLaia Rodriguez-Revenga, Maria Isabel Alvarez-Mora
Frontiers in Psychiatry|November 1, 2021
Neuroimaging Insight Into Fragile X-Associated Neuropsychiatric Disorders: Literature ReviewAndrea Elias-Mas, Maria Isabel Alvarez-Mora, Conxita Caro-Benito, et al.
American Journal of Medical Genetics. Part A|August 18, 2017
Paternal transmission of a FMR1 full mutation alleleMaria Isabel Alvarez-Mora, Miriam Guitart, Laia Rodriguez-Revenga, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 16, 2013
High apolipoprotein E4 allele frequency in FXTAS patientsFrancisca Silva, Laia Rodriguez-Revenga, Irene Madrigal, et al.
Genes|April 30, 2021
Novel Compound Heterozygous Mutation in <i>TRAPPC9</i> Gene: The Relevance of Whole Genome SequencingMaria Isabel Alvarez-Mora, Jordi Corominas, Christian Gilissen, et al.
Neuro-Degenerative Diseases|November 27, 2015
Skewed X Inactivation in Women Carrying the FMR1 Premutation and Its Relation with Fragile-X-Associated Tremor/Ataxia SyndromeMaria Isabel Alvarez-Mora, Laia Rodriguez-Revenga, Aina Feliu, et al.
Molecular Neurobiology|January 3, 2022
Reduced mtDNA Copy Number in the Prefrontal Cortex of C9ORF72 PatientsMaria Isabel Alvarez-Mora, Petar Podlesniy, Teresa Riazuelo, et al.
Neurobiology of Disease|January 15, 2014
Blood expression profiles of fragile X premutation carriers identify candidate genes involved in neurodegenerative and infertility phenotypesElisabet Mateu-Huertas, Laia Rodriguez-Revenga, Maria Isabel Alvarez-Mora, et al.
European Journal of Human Genetics : EJHG|January 7, 2016
A novel splicing mutation in the IQSEC2 gene that modulates the phenotype severity in a family with intellectual disabilityIrene Madrigal, Maria Isabel Alvarez-Mora, Jordi Rosell, et al.
Clinical Genetics|July 3, 2020
An exome-wide exploration of cases of primary ovarian insufficiency uncovers novel sequence variants and candidate genesMaria Isabel Alvarez-Mora, Anne-Laure Todeschini, Sandrine Caburet, et al.
Pageof 3