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Alexandra M Lopes

Showing results (31-40 of 47) with videos related to

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Human Reproduction (Oxford, England)|May 10, 2022
Actionable secondary findings following exome sequencing of 836 non-obstructive azoospermia cases and their value in patient managementLaura Kasak, Kristiina Lillepea, Liina Nagirnaja, et al.
Journal of Alzheimer'S Disease : JAD|February 1, 2021
Risk Variants in Three Alzheimer's Disease Genes Show Association with EEG EndophenotypesAna Macedo, Carlos Gómez, Miguel Ângelo Rebelo, et al.
Human Reproduction (Oxford, England)|February 2, 2024
Changes in environmental exposures over decades may influence the genetic architecture of severe spermatogenic failureMiriam Cerván-Martín, Sara González-Muñoz, Andrea Guzmán-Jiménez, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 4, 2020
Genetic dissection of spermatogenic arrest through exome analysis: clinical implications for the management of azoospermic menCsilla Krausz, Antoni Riera-Escamilla, Daniel Moreno-Mendoza, et al.
The New England Journal of Medicine|August 4, 2021
Variant <i>PNLDC1</i>, Defective piRNA Processing, and AzoospermiaLiina Nagirnaja, Nina Mørup, John E Nielsen, et al.
Communications Biology|April 5, 2025
Trans-ethnic GWAS meta-analysis of idiopathic spermatogenic failure highlights the immune-mediated nature of Sertoli cell-only syndromeSara González-Muñoz, Yichen Long, Andrea Guzmán-Jiménez, et al.
Human Molecular Genetics|January 8, 2025
Diminished DNA binding affinity of DMRT1 caused by heterozygous DM domain mutations is a cause of male infertilityTihana Marić, Helen Castillo-Madeen, Monika Logara Klarić, et al.
Plos Genetics|April 5, 2013
Human spermatogenic failure purges deleterious mutation load from the autosomes and both sex chromosomes, including the gene DMRT1Alexandra M Lopes, Kenneth I Aston, Emma Thompson, et al.
Fertility and Sterility|July 22, 2020
Intronic variation of the SOHLH2 gene confers risk to male reproductive impairmentMiriam Cerván-Martín, M Irene Suazo-Sánchez, Rocío Rivera-Egea, et al.
Frontiers in Cell and Developmental Biology|January 2, 2023
Contribution of <i>TEX15</i> genetic variants to the risk of developing severe non-obstructive oligozoospermiaAndrea Guzmán-Jiménez, Sara González-Muñoz, Miriam Cerván-Martín, et al.
Pageof 5

Showing results (31-40 of 47) with videos related to

Sort By:
Pageof 5
Human Reproduction (Oxford, England)|May 10, 2022
Actionable secondary findings following exome sequencing of 836 non-obstructive azoospermia cases and their value in patient managementLaura Kasak, Kristiina Lillepea, Liina Nagirnaja, et al.
Journal of Alzheimer'S Disease : JAD|February 1, 2021
Risk Variants in Three Alzheimer's Disease Genes Show Association with EEG EndophenotypesAna Macedo, Carlos Gómez, Miguel Ângelo Rebelo, et al.
Human Reproduction (Oxford, England)|February 2, 2024
Changes in environmental exposures over decades may influence the genetic architecture of severe spermatogenic failureMiriam Cerván-Martín, Sara González-Muñoz, Andrea Guzmán-Jiménez, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 4, 2020
Genetic dissection of spermatogenic arrest through exome analysis: clinical implications for the management of azoospermic menCsilla Krausz, Antoni Riera-Escamilla, Daniel Moreno-Mendoza, et al.
The New England Journal of Medicine|August 4, 2021
Variant <i>PNLDC1</i>, Defective piRNA Processing, and AzoospermiaLiina Nagirnaja, Nina Mørup, John E Nielsen, et al.
Communications Biology|April 5, 2025
Trans-ethnic GWAS meta-analysis of idiopathic spermatogenic failure highlights the immune-mediated nature of Sertoli cell-only syndromeSara González-Muñoz, Yichen Long, Andrea Guzmán-Jiménez, et al.
Human Molecular Genetics|January 8, 2025
Diminished DNA binding affinity of DMRT1 caused by heterozygous DM domain mutations is a cause of male infertilityTihana Marić, Helen Castillo-Madeen, Monika Logara Klarić, et al.
Plos Genetics|April 5, 2013
Human spermatogenic failure purges deleterious mutation load from the autosomes and both sex chromosomes, including the gene DMRT1Alexandra M Lopes, Kenneth I Aston, Emma Thompson, et al.
Fertility and Sterility|July 22, 2020
Intronic variation of the SOHLH2 gene confers risk to male reproductive impairmentMiriam Cerván-Martín, M Irene Suazo-Sánchez, Rocío Rivera-Egea, et al.
Frontiers in Cell and Developmental Biology|January 2, 2023
Contribution of <i>TEX15</i> genetic variants to the risk of developing severe non-obstructive oligozoospermiaAndrea Guzmán-Jiménez, Sara González-Muñoz, Miriam Cerván-Martín, et al.
Pageof 5