Proper Cyclin B3 Dosage Is Important for Precision of Metaphase-to-Anaphase Onset Timing in Caenorhabditis elegans

door Tarailo-Graovac, Maja, Chen, Nansheng
Gepubliceerd in 2012

Mos1-Mediated Transgenesis to Probe Consequences of Single Gene Mutations in Variation-Rich Isolates of Caenorhabditis elegans

door Tarailo-Graovac, Maja, Chen, Nansheng
Gepubliceerd in 2012

Uncovering Missing Heritability in Rare Diseases

door Maroilley, Tatiana, Tarailo-Graovac, Maja
Gepubliceerd in Genes (Basel) (2019)

Dissecting the Genetic and Etiological Causes of Primary Microcephaly

door Jean, Francesca, Stuart, Amanda, Tarailo-Graovac, Maja
Gepubliceerd in Front Neurol (2020)

Genetic Modifiers and Rare Mendelian Disease

door Rahit, K. M. Tahsin Hassan, Tarailo-Graovac, Maja
Gepubliceerd in Genes (Basel) (2020)

Spindle assembly checkpoint genes reveal distinct as well as overlapping expression that implicates MDF-2/Mad2 in postembryonic seam cell proliferation in Caenorhabditis elegans

door Tarailo-Graovac, Maja, Wang, Jun, Chu, Jeffrey SC, Tu, Domena, Baillie, David L, Chen, Nansheng
Gepubliceerd in 2010

FLAGS, frequently mutated genes in public exomes

door Shyr, Casper, Tarailo-Graovac, Maja, Gottlieb, Michael, Lee, Jessica JY, van Karnebeek, Clara, Wasserman, Wyeth W
Gepubliceerd in BMC Med Genomics (2014)

Correction to: FLAGS, frequently mutated genes in public exomes

door Shyr, Casper, Tarailo-Graovac, Maja, Gottlieb, Michael, Lee, Jessica JY, van Karnebeek, Clara, Wasserman, Wyeth W
Gepubliceerd in BMC Med Genomics (2017)

Assessment of the ExAC data set for the presence of individuals with pathogenic genotypes implicated in severe Mendelian pediatric disorders

door Tarailo-Graovac, Maja, Zhu, Jing Yun Alice, Matthews, Allison, van Karnebeek, Clara D M, Wasserman, Wyeth W
Gepubliceerd in Genet Med (2017)

Spectrum of variations in dog-1/FANCJ and mdf-1/MAD1 defective Caenorhabditis elegans strains after long-term propagation

door Tarailo-Graovac, Maja, Wong, Tammy, Qin, Zhaozhao, Flibotte, Stephane, Taylor, Jon, Moerman, Donald G, Rose, Ann M, Chen, Nansheng
Gepubliceerd in BMC Genomics (2015)

Cyclin B3 and dynein heavy chain cooperate to increase fitness in the absence of mdf-1/MAD1 in Caenorhabditis elegans

door Tarailo-Graovac, Maja, Wong, Tammy, Qin, Zhaozhao, Flibotte, Stephane, Taylor, Jon, Moerman, Donald G, Rose, Ann M, Chen, Nansheng
Gepubliceerd in Cell Cycle (2014)

Polymorphic segmental duplication in the nematode <it>Caenorhabditis elegans</it>

door Baillie David L, Johnsen Robert C, Tarailo-Graovac Maja, Huang Jim C, Mah Allan K, Vergara Ismael A, Chen Nansheng
Gepubliceerd in 2009-07-01

Polymorphic segmental duplication in the nematode Caenorhabditis elegans

door Vergara, Ismael A, Mah, Allan K, Huang, Jim C, Tarailo-Graovac, Maja, Johnsen, Robert C, Baillie, David L, Chen, Nansheng
Gepubliceerd in 2009

Fine tuning of RFX/DAF-19-regulated target gene expression through binding to multiple sites in Caenorhabditis elegans

door Chu, Jeffery S. C., Tarailo-Graovac, Maja, Zhang, Di, Wang, Jun, Uyar, Bora, Tu, Domena, Trinh, Joanne, Baillie, David L., Chen, Nansheng
Gepubliceerd in 2012

De novo dominant variants affecting the motor domain of KIF1A are a cause of PEHO syndrome

door Langlois, Sylvie, Tarailo-Graovac, Maja, Sayson, Bryan, Drögemöller, Britt, Swenerton, Anne, Ross, Colin JD, Wasserman, Wyeth W, van Karnebeek, Clara DM
Gepubliceerd in Eur J Hum Genet (2016)

Genome-wide variations in a natural isolate of the nematode Caenorhabditis elegans

door Vergara, Ismael A, Tarailo-Graovac, Maja, Frech, Christian, Wang, Jun, Qin, Zhaozhao, Zhang, Ting, She, Rong, Chu, Jeffrey SC, Wang, Ke, Chen, Nansheng
Gepubliceerd in 2014

Mitochondrial Complex III Deficiency with Ketoacidosis and Hyperglycemia Mimicking Neonatal Diabetes

door Anastasio, Natascia, Tarailo-Graovac, Maja, Al-Khalifah, Reem, Legault, Laurent, Drogemoller, Britt, Ross, Colin J.D., Wasserman, Wyeth W., van Karnebeek, Clara, Buhas, Daniela
Gepubliceerd in JIMD Rep (2016)

Further Validation of the SIGMAR1 c.151+1G>T Mutation as Cause of Distal Hereditary Motor Neuropathy

door Lee, Jessica J. Y., van Karnebeek, Clara D. M., Drögemoller, Britt, Shyr, Casper, Tarailo-Graovac, Maja, Eydoux, Patrice, Ross, Colin J., Wasserman, Wyeth W., Björnson, Bruce, Wu, John K.
Gepubliceerd in Child Neurol Open (2016)

Identification of a large intronic transposal insertion in SLC17A5 causing sialic acid storage disease

door Tarailo-Graovac, Maja, Drögemöller, Britt I., Wasserman, Wyeth W., Ross, Colin J. D., van den Ouweland, Ans M. W., Darin, Niklas, Kollberg, Gittan, van Karnebeek, Clara D. M., Blomqvist, Maria
Gepubliceerd in Orphanet J Rare Dis (2017)

Integration of genomics and metabolomics for prioritization of rare disease variants: a 2018 literature review

door Graham, Emma, Lee, Jessica, Price, Magda, Tarailo-Graovac, Maja, Matthews, Allison, Engelke, Udo, Tang, Jeffrey, Kluijtmans, Leo A. J., Wevers, Ron A., Wasserman, Wyeth W., van Karnebeek, Clara D. M., Mostafavi, Sara
Gepubliceerd in J Inherit Metab Dis (2018)