Maja Tarailo-Graovac

Publication Activity (10 Years)

Years Active: 2021-2024
Publications (10 Years): 19

Top Topics

Escherichia Coli

Top Venues

Genome research

Life science alliance

This page only lists publications with an associated author ORCID identifier.

Publications

Victoria Rodrigues Alves Barbosa, Tatiana Maroilley, Catherine Diao, Leslie Colvin-James, Renee Perrier, Maja Tarailo-Graovac
Single variant, yet "double trouble": TSC and KBG syndrome because of a large de novo inversion. Life science alliance 7 (4) (2024)
Victoria Rodrigues Alves Barbosa, Tatiana Maroilley, Catherine Diao, Leslie Colvin-James, Renee Perrier, Maja Tarailo-Graovac
Single variant, yet "double trouble": TSC and KBG syndrome because of a large de novo inversion. Life science alliance 7 (4) (2024)
Victoria Rodrigues Alves Barbosa, Tatiana Maroilley, Catherine Diao, Leslie Colvin-James, Renee Perrier, Maja Tarailo-Graovac
Single variant, yet "double trouble": TSC and KBG syndrome because of a large de novo inversion. Life science alliance 7 (4) (2024)
Xiao Li, Ivette Maria Menendez Perdomo, Victoria Rodrigues Alves Barbosa, Catherine Diao, Maja Tarailo-Graovac
The critical role of the iron-sulfur cluster and CTC components in DOG-1/BRIP1 function in Caenorhabditis elegans. Nucleic acids research (2024)
Li Shu, Tatiana Maroilley, Maja Tarailo-Graovac
The Power of Clinical Diagnosis for Deciphering Complex Genetic Mechanisms in Rare Diseases. Genes 14 (1) (2023)
Li Shu, Tatiana Maroilley, Maja Tarailo-Graovac
The Power of Clinical Diagnosis for Deciphering Complex Genetic Mechanisms in Rare Diseases. Genes 14 (1) (2023)
Tatiana Maroilley, Meng-Han Tsai, Rumika Mascarenhas, Catherine Diao, Maryam Khanbabaei, Sabine Kaya, Christel Depienne, Maja Tarailo-Graovac, Karl Martin Klein
A novel FAME1 repeat configuration in a European family identified using a combined genomics approach. Epilepsia open (2023)
Li Shu, Tatiana Maroilley, Maja Tarailo-Graovac
The Power of Clinical Diagnosis for Deciphering Complex Genetic Mechanisms in Rare Diseases. Genes 14 (1) (2023)
Li Shu, Tatiana Maroilley, Maja Tarailo-Graovac
The Power of Clinical Diagnosis for Deciphering Complex Genetic Mechanisms in Rare Diseases. Genes 14 (1) (2023)
Tatiana Maroilley, Stephane Flibotte, Francesca Jean, Victoria Rodrigues Alves Barbosa, Andrew Galbraith, Afiya Razia Chida, Filip Cotra, Xiao Li, Larisa Oncea, Mark L Edgley, Don Moerman, Maja Tarailo-Graovac
Genome sequencing of C. elegans balancer strains reveals previously unappreciated complex genomic rearrangements. Genome research 33 (1) (2022)
Tatiana Maroilley, Stephane Flibotte, Francesca Jean, Victoria Rodrigues Alves Barbosa, Andrew Galbraith, Afiya Razia Chida, Filip Cotra, Xiao Li, Larisa Oncea, Mark L Edgley, Don Moerman, Maja Tarailo-Graovac
Genome sequencing of C. elegans balancer strains reveals previously unappreciated complex genomic rearrangements. Genome research 33 (1) (2022)
Tatiana Maroilley, Stephane Flibotte, Francesca Jean, Victoria Rodrigues Alves Barbosa, Andrew Galbraith, Afiya Razia Chida, Filip Cotra, Xiao Li, Larisa Oncea, Mark L Edgley, Don Moerman, Maja Tarailo-Graovac
Genome sequencing of C. elegans balancer strains reveals previously unappreciated complex genomic rearrangements. Genome research 33 (1) (2022)
Tatiana Maroilley, Stephane Flibotte, Francesca Jean, Victoria Rodrigues Alves Barbosa, Andrew Galbraith, Afiya Razia Chida, Filip Cotra, Xiao Li, Larisa Oncea, Mark L Edgley, Don Moerman, Maja Tarailo-Graovac
Genome sequencing of C. elegans balancer strains reveals previously unappreciated complex genomic rearrangements. Genome research (2022)
Tatiana Maroilley, Stephane Flibotte, Francesca Jean, Victoria Rodrigues Alves Barbosa, Andrew Galbraith, Afiya Razia Chida, Filip Cotra, Xiao Li, Larisa Oncea, Mark L Edgley, Don Moerman, Maja Tarailo-Graovac
Genome sequencing of C. elegans balancer strains reveals previously unappreciated complex genomic rearrangements. Genome research 33 (1) (2022)
Simona D Frederiksen, Vladimir Avramović, Tatiana Maroilley, Anna Lehman, Laura Arbour, Maja Tarailo-Graovac
Rare disorders have many faces: in silico characterization of rare disorder spectrum. Orphanet journal of rare diseases 17 (1) (2022)
Tatiana Maroilley, Stephane Flibotte, Francesca Jean, Victoria Rodrigues Alves Barbosa, Andrew Galbraith, Afiya Razia Chida, Filip Cotra, Xiao Li, Larisa Oncea, Mark L Edgley, Donald G Moerman, Maja Tarailo-Graovac
Genome sequencing of C. elegans balancer strains reveals previously unappreciated complex genomic rearrangements. Genome research (2022)
Tatiana Maroilley, Stephane Flibotte, Francesca Jean, Victoria Rodrigues Alves Barbosa, Andrew Galbraith, Afiya Razia Chida, Filip Cotra, Xiao Li, Larisa Oncea, Mark L Edgley, Don Moerman, Maja Tarailo-Graovac
Genome sequencing of C. elegans balancer strains reveals previously unappreciated complex genomic rearrangements. Genome research 33 (1) (2022)
Vladimir Avramović, Simona Denise Frederiksen, Marjana Brkić, Maja Tarailo-Graovac
Driving mosaicism: somatic variants in reference population databases and effect on variant interpretation in rare genetic disease. Human genomics 15 (1) (2021)
Clara D van Karnebeek, Ingrid Blydt-Hansen, Allison M Matthews, Vladimir Avramovic, Magda Price, Britt Drogemoller, Casper Shyr, Jessica Lee, Jill Mwenifumbo, Aisha Ghani, Sylvia Stockler, Jan M Friedman, Anna Lehman, null null, Colin J Ross, Wyeth W Wasserman, Maja Tarailo-Graovac, Gabriella A Horvath
Secondary biogenic amine deficiencies: genetic etiology, therapeutic interventions, and clinical effects. Neurogenetics 22 (4) (2021)