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Tatiana Maroilley

Showing results (1-10 of 18) with videos related to

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Methods in Molecular Biology (Clifton, N.J.)|August 30, 2025
Detection of Complex Genomic Rearrangements Using Short-Read Whole Genome Sequencing in C. elegansTatiana Maroilley, Maja Tarailo-Graovac
Genes|April 17, 2019
Uncovering Missing Heritability in Rare DiseasesTatiana Maroilley, Maja Tarailo-Graovac
Micropublication Biology|June 14, 2023
Molecular basis of essential and morphological variations across 12 balancer strains in <i>C. elegans</i>Filip Cotra, Tatiana Maroilley, Maja Tarailo-Graovac
Genes|January 21, 2023
The Power of Clinical Diagnosis for Deciphering Complex Genetic Mechanisms in Rare DiseasesLi Shu, Tatiana Maroilley, Maja Tarailo-Graovac
Orphanet Journal of Rare Diseases|February 23, 2022
Rare disorders have many faces: in silico characterization of rare disorder spectrumSimona D Frederiksen, Vladimir Avramović, Tatiana Maroilley, et al.
Scientific Reports|September 15, 2021
Deciphering complex genome rearrangements in C. elegans using short-read whole genome sequencingTatiana Maroilley, Xiao Li, Matthew Oldach, et al.
BMC Genomics|November 14, 2021
Whole genome sequencing facilitates intragenic variant interpretation following modifier screening in C. elegansFrancesca Jean, Susan Stasiuk, Tatiana Maroilley, et al.
Life Science Alliance|January 22, 2024
Single variant, yet "double trouble": TSC and KBG syndrome because of a large de novo inversionVictoria Rodrigues Alves Barbosa, Tatiana Maroilley, Catherine Diao, et al.
G3 (Bethesda, Md.)|August 16, 2023
Model Organism Modifier (MOM): a user-friendly Galaxy workflow to detect modifiers from genome sequencing data using Caenorhabditis elegansTatiana Maroilley, K M Tahsin Hassan Rahit, Afiya Razia Chida, et al.
Epilepsia Open|February 5, 2023
A novel FAME1 repeat configuration in a European family identified using a combined genomics approachTatiana Maroilley, Meng-Han Tsai, Rumika Mascarenhas, et al.
Pageof 2

Showing results (1-10 of 18) with videos related to

Sort By:
Pageof 2
Methods in Molecular Biology (Clifton, N.J.)|August 30, 2025
Detection of Complex Genomic Rearrangements Using Short-Read Whole Genome Sequencing in C. elegansTatiana Maroilley, Maja Tarailo-Graovac
Genes|April 17, 2019
Uncovering Missing Heritability in Rare DiseasesTatiana Maroilley, Maja Tarailo-Graovac
Micropublication Biology|June 14, 2023
Molecular basis of essential and morphological variations across 12 balancer strains in <i>C. elegans</i>Filip Cotra, Tatiana Maroilley, Maja Tarailo-Graovac
Genes|January 21, 2023
The Power of Clinical Diagnosis for Deciphering Complex Genetic Mechanisms in Rare DiseasesLi Shu, Tatiana Maroilley, Maja Tarailo-Graovac
Orphanet Journal of Rare Diseases|February 23, 2022
Rare disorders have many faces: in silico characterization of rare disorder spectrumSimona D Frederiksen, Vladimir Avramović, Tatiana Maroilley, et al.
Scientific Reports|September 15, 2021
Deciphering complex genome rearrangements in C. elegans using short-read whole genome sequencingTatiana Maroilley, Xiao Li, Matthew Oldach, et al.
BMC Genomics|November 14, 2021
Whole genome sequencing facilitates intragenic variant interpretation following modifier screening in C. elegansFrancesca Jean, Susan Stasiuk, Tatiana Maroilley, et al.
Life Science Alliance|January 22, 2024
Single variant, yet "double trouble": TSC and KBG syndrome because of a large de novo inversionVictoria Rodrigues Alves Barbosa, Tatiana Maroilley, Catherine Diao, et al.
G3 (Bethesda, Md.)|August 16, 2023
Model Organism Modifier (MOM): a user-friendly Galaxy workflow to detect modifiers from genome sequencing data using Caenorhabditis elegansTatiana Maroilley, K M Tahsin Hassan Rahit, Afiya Razia Chida, et al.
Epilepsia Open|February 5, 2023
A novel FAME1 repeat configuration in a European family identified using a combined genomics approachTatiana Maroilley, Meng-Han Tsai, Rumika Mascarenhas, et al.
Pageof 2