Calvin Mok Ph.D.
Education outreach and Bioinformatician
B. Math University of Waterloo, Faculty of Mathematics, 2005
Ph.D. University of Toronto, Institute of Medical Science, 2012
Publications:
High-throughput phenotyping of infection by diverse microsporidia species reveals a wild C. elegans strain with opposing resistance and susceptibility traits.
Mok, C, Xiao, MA, Wan, YC, Zhao, W, Ahmed, SM, Luallen, RJ, Reinke, AW.
PLoS Pathog.19,2023. PubMed PMID:36893187
An intestinally secreted host factor promotes microsporidia invasion of C. elegans.
Tamim El Jarkass, H, Mok, C, Schertzberg, MR, Fraser, AG, Troemel, ER, Reinke, AW.
Elife.11,2022. PubMed PMID:34994689
PhenoMIP: High-Throughput Phenotyping of Diverse Caenorhabditis elegans Populations via Molecular Inversion Probes.
Mok, C, Belmarez, G, Edgley, ML, Moerman, DG, Waterston, RH.
G3 (Bethesda).10,2020. PubMed PMID:32868407
Challenges and Approaches to Genotyping Repetitive DNA.
Morton, EA, Hall, AN, Kwan, E, Mok, C, Queitsch, K, Nandakumar, V, Stamatoyannopoulos, J, Brewer, BJ, Waterston, R, Queitsch, C.
G3 (Bethesda).10,2020. PubMed PMID:31757929
MIP-MAP: High-Throughput Mapping of Caenorhabditis elegans Temperature-Sensitive Mutants via Molecular Inversion Probes.
Mok, CA, Au, V, Thompson, OA, Edgley, ML, Gevirtzman, L, Yochem, J, Lowry, J, Memar, N, Wallenfang, MR, Rasoloson, D, Bowerman, B, Schnabel, R, Seydoux, G, Moerman, DG, Waterston, RH.
Genetics.207,2017. PubMed PMID:28827289
Caenorhabditis elegans as a model organism for ciliopathies and related forms of photoreceptor degeneration.
Mok, CA, Héon, E.
Adv Exp Med Biol.723,2012. PubMed PMID:22183374
Mutations in a guanylate cyclase GCY-35/GCY-36 modify Bardet-Biedl syndrome-associated phenotypes in Caenorhabditis elegans.
Mok, CA, Healey, MP, Shekhar, T, Leroux, MR, Héon, E, Zhen, M.
PLoS Genet.7,2011. PubMed PMID:22022287
Ciliary dysfunction and obesity.
Mok, CA, Héon, E, Zhen, M.
Clin Genet.77,2010. PubMed PMID:19968672
BBS7 and TTC8 (BBS8) mutations play a minor role in the mutational load of Bardet-Biedl syndrome in a multiethnic population.
Bin, J, Madhavan, J, Ferrini, W, Mok, CA, Billingsley, G, Héon, E.
Hum Mutat.30,2009. PubMed PMID:19402160
An essential role for DYF-11/MIP-T3 in assembling functional intraflagellar transport complexes.
Li, C, Inglis, PN, Leitch, CC, Efimenko, E, Zaghloul, NA, Mok, CA, Davis, EE, Bialas, NJ, Healey, MP, Héon, E, Zhen, M, Swoboda, P, Katsanis, N, Leroux, MR.
PLoS Genet.4,2008. PubMed PMID:18369462
CRYBB1 mutation associated with congenital cataract and microcornea.
Willoughby, CE, Shafiq, A, Ferrini, W, Chan, LL, Billingsley, G, Priston, M, Mok, C, Chandna, A, Kaye, S, Héon, E.
Mol Vis.11,2005. PubMed PMID:16110300