Mos1-mediated transgenesis to probe consequences of single gene mutations in variation-rich isolates of Caenorhabditis elegans.

by Maja Tarailo-Graovac, Nansheng Chen
Published 2012-01-01

Uncovering Missing Heritability in Rare Diseases

by Tatiana Maroilley, Maja Tarailo-Graovac
Published 2019-04-01

Dissecting the Genetic and Etiological Causes of Primary Microcephaly

by Francesca Jean, Francesca Jean, Francesca Jean, Amanda Stuart, Amanda Stuart, Amanda Stuart, Maja Tarailo-Graovac, Maja Tarailo-Graovac, Maja Tarailo-Graovac
Published 2020-10-01

Genetic Modifiers and Rare Mendelian Disease

by K. M. Tahsin Hassan Rahit, Maja Tarailo-Graovac
Published 2020-02-01

Deciphering complex genome rearrangements in C. elegans using short-read whole genome sequencing

by Tatiana Maroilley, Xiao Li, Matthew Oldach, Francesca Jean, Susan J. Stasiuk, Maja Tarailo-Graovac
Published 2021-09-01

Correction to: FLAGS, frequently mutated genes in public exomes

by Casper Shyr, Maja Tarailo-Graovac, Michael Gottlieb, Jessica JY Lee, Clara van Karnebeek, Wyeth W Wasserman
Published 2017-11-01

De novo pathogenic DNM1L variant in a patient diagnosed with atypical hereditary sensory and autonomic neuropathy

by Maja Tarailo‐Graovac, Farah R. Zahir, Irena Zivkovic, Michelle Moksa, Kathryn Selby, Sunita Sinha, Corey Nislow, Sylvia G. Stockler‐Ipsiroglu, Ruth Sheffer, Ann Saada‐Reisch, Jan M. Friedman, Clara D. M. vanKarnebeek, Gabriella A. Horvath
Published 2019-10-01

Further Validation of the c.151+1G>T Mutation as Cause of Distal Hereditary Motor Neuropathy

by Jessica J. Y. Lee BSc, Clara D. M. van Karnebeek MD, PhD, Britt Drögemoller PhD, Casper Shyr PhD, Maja Tarailo-Graovac PhD, Patrice Eydoux PhD, Colin J. Ross PhD, Wyeth W. Wasserman PhD, Bruce Björnson MD, John K. Wu MD
Published 2016-09-01