BMP-mediated specification of the erythroid lineage suppresses endothelial development in blood island precursors

le Myers, Candace T., Krieg, Paul A.
Foilsithe 2013

Advancing epilepsy genetics in the genomic era

le Myers, Candace T., Mefford, Heather C.
Foilsithe in Genome Med (2015)

Regulation of endothelial cell development by ETS transcription factors

le Meadows, Stryder M., Myers, Candace T., Krieg, Paul A.
Foilsithe 2011

The ETS family protein, ETV2, is required for initiation of the endothelial lineage but not the hematopoietic lineage in the Xenopus embryo

le Salanga, Matthew C., Meadows, Stryder M., Myers, Candace T., Krieg, Paul A.
Foilsithe 2010

Hedgehog regulates angiogenesis of intersegmental vessels through the VEGF signaling pathway

le Moran, Carlos M., Myers, Candace T., Lewis, Cristy M., Krieg, Paul A.
Foilsithe in Dev Dyn (2012)

Prospective functional outcomes in sequential population based cohorts of stage III/ IV oropharyngeal carcinoma patients treated with 3D conformal vs. intensity modulated radiother...

le Kerr, Paul, Myers, Candace L, Butler, James, Alessa, Mohamed, Lambert, Pascal, Cooke, Andrew L
Foilsithe in J Otolaryngol Head Neck Surg (2015)

Hominids adapted to metabolize ethanol long before human-directed fermentation

le Carrigan, Matthew A., Uryasev, Oleg, Frye, Carole B., Eckman, Blair L., Myers, Candace R., Hurley, Thomas D., Benner, Steven A.
Foilsithe in Proc Natl Acad Sci U S A (2015)

p.P1379S, a benign variant with reduced ATP7B protein level in Wilson Disease

le Yi, Fan, Poskanzer, Sheri A., Myers, Candace T., Thies, Jenny, Collins, Christopher J., Dayuha, Remwilyn, Duong, Phi, Houwen, Roderick, Hahn, Si Houn
Foilsithe in JIMD Rep (2020)

Cyclic Nucleotide Gated Channels 7 and 8 Are Essential for Male Reproductive Fertility

le Tunc-Ozdemir, Meral, Rato, Claudia, Brown, Elizabeth, Rogers, Stephanie, Mooneyham, Amanda, Frietsch, Sabine, Myers, Candace T., Poulsen, Lisbeth Rosager, Malhó, Rui, Harper, Jeffrey F.
Foilsithe 2013

The co‐occurrence of Wilson disease and X‐linked agammaglobulinemia in one family highlights the promising diagnostic potential of proteolytic analysis

le Poskanzer, Sheri A., Thies, Jenny, Collins, Christopher J., Myers, Candace T., Dayuha, Remwilyn, Duong, Phi, Yi, Fan, Chang, Irene J., Ochs, Hans D., Torgerson, Troy R., Hahn, Si Houn
Foilsithe in Mol Genet Genomic Med (2020)

A Cyclic Nucleotide-Gated Channel (CNGC16) in Pollen Is Critical for Stress Tolerance in Pollen Reproductive Development(1)([W])([OA])

le Tunc-Ozdemir, Meral, Tang, Chong, Ishka, Maryam Rahmati, Brown, Elizabeth, Groves, Norman R., Myers, Candace T., Rato, Claudia, Poulsen, Lisbeth R., McDowell, Stephen, Miller, Gad, Mittler, Ron, Harper, Jeffrey F.
Foilsithe 2013

A population-based cost-effectiveness study of early genetic testing in severe epilepsies of infancy

le Howell, Katherine B., Eggers, Stefanie, Dalziel, Kim, Riseley, Jessica, Mandelstam, Simone, Myers, Candace T., McMahon, Jacinta M., Gen Couns, Amy Schneider M, Carvill, Gemma L., Mefford, Heather C, Scheffer, Ingrid E., Harvey, A. Simon
Foilsithe in Epilepsia (2018)

Parental Mosaicism in “De Novo” Epileptic Encephalopathies

le Myers, Candace T., Hollingsworth, Georgina, Muir, Alison M., Schneider, Amy L., Thuesmunn, Zoe, Knupp, Allison, King, Chontelle, Lacroix, Amy, Mehaffey, Michele G., Berkovic, Samuel F., Carvill, Gemma L., Sadleir, Lynette G., Scheffer, Ingrid E., Mefford, Heather C.
Foilsithe in N Engl J Med (2018)

Not all SCN1A epileptic encephalopathies are Dravet syndrome: Early profound Thr226Met phenotype

le Sadleir, Lynette G., Mountier, Emily I., Gill, Deepak, Davis, Suzanne, Joshi, Charuta, DeVile, Catherine, Kurian, Manju A., Mandelstam, Simone, Wirrell, Elaine, Nickels, Katherine C., Murali, Hema R., Carvill, Gemma, Myers, Candace T., Mefford, Heather C., Scheffer, Ingrid E.
Foilsithe in Neurology (2017)

Reanalysis and optimisation of bioinformatic pipelines is critical for mutation detection

le Cowley, Mark J, Liu, Yu‐Chi, Oliver, Karen L., Carvill, Gemma, Myers, Candace T., Gayevskiy, Velimir, Delatycki, Martin, Vlaskamp, Danique R.M., Zhu, Ying, Mefford, Heather, Buckley, Michael F., Bahlo, Melanie, Scheffer, Ingrid E., Dinger, Marcel E., Roscioli, Tony
Foilsithe in Hum Mutat (2019)

Simultaneous impairment of neuronal and metabolic function of mutated gephyrin in a patient with epileptic encephalopathy

le Dejanovic, Borislav, Djémié, Tania, Grünewald, Nora, Suls, Arvid, Kress, Vanessa, Hetsch, Florian, Craiu, Dana, Zemel, Matthew, Gormley, Padhraig, Lal, Dennis, Myers, Candace T, Mefford, Heather C, Palotie, Aarno, Helbig, Ingo, Meier, Jochen C, De Jonghe, Peter, Weckhuysen, Sarah, Schwarz, Guenter
Foilsithe in EMBO Mol Med (2015)

Simultaneous impairment of neuronal and metabolic function of mutated gephyrin in a patient with epileptic encephalopathy

le Dejanovic, Borislav, Djémié, Tania, Grünewald, Nora, Suls, Arvid, Kress, Vanessa, Hetsch, Florian, Craiu, Dana, Zemel, Matthew, Gormley, Padhraig, Lal, Dennis, Myers, Candace T, Mefford, Heather C, Palotie, Aarno, Helbig, Ingo, Meier, Jochen C, De Jonghe, Peter, Weckhuysen, Sarah, Schwarz, Guenter
Foilsithe in EMBO Mol Med (2017)

A targeted resequencing gene panel for focal epilepsy

le Hildebrand, Michael S., Myers, Candace T., Carvill, Gemma L., Regan, Brigid M., Damiano, John A., Mullen, Saul A., Newton, Mark R., Nair, Umesh, Gazina, Elena V., Milligan, Carol J., Reid, Christopher A., Petrou, Steven, Scheffer, Ingrid E., Berkovic, Samuel F., Mefford, Heather C.
Foilsithe in Neurology (2016)

Dominant KCNA2 mutation causes episodic ataxia and pharmacoresponsive epilepsy

le Corbett, Mark A., Bellows, Susannah T., Li, Melody, Carroll, Renée, Micallef, Silvana, Carvill, Gemma L., Myers, Candace T., Howell, Katherine B., Maljevic, Snezana, Lerche, Holger, Gazina, Elena V., Mefford, Heather C., Bahlo, Melanie, Berkovic, Samuel F., Petrou, Steven, Scheffer, Ingrid E., Gecz, Jozef
Foilsithe in Neurology (2016)

Contribution of ultrarare variants in mTOR pathway genes to sporadic focal epilepsies

le Pippucci, Tommaso, Licchetta, Laura, Baldassari, Sara, Marconi, Caterina, De Luise, Monica, Myers, Candace, Nardi, Elena, Provini, Federica, Cameli, Cinzia, Minardi, Raffaella, Bacchelli, Elena, Giordano, Lucio, Crichiutti, Giovanni, d'Orsi, Giuseppe, Seri, Marco, Gasparre, Giuseppe, Mefford, Heather C., Tinuper, Paolo, Bisulli, Francesca
Foilsithe in Ann Clin Transl Neurol (2019)