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Candace T. Myers, Ph.D. - Publications

Affiliations: 
2013 Molecular & Cellular Biology University of Arizona, Tucson, AZ 
Area:
Molecular Biology, Human Development
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32 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2020 Carvill GL, Helbig KL, Myers CT, Scala M, Huether R, Lewis S, Kruer TN, Guida BS, Bakhtiari S, Sebe J, Tang S, Stickney H, Oktay SU, Bhandiwad AA, Ramsey K, et al. Damaging de novo missense variants in EEF1A2 lead to a developmental and degenerative epileptic-dyskinetic encephalopathy. Human Mutation. PMID 32196822 DOI: 10.1002/Humu.24015  0.349
2019 Scheffer IE, Boysen KE, Schneider AL, Myers CT, Mehaffey MG, Rochtus AM, Yuen YP, Ronen G, Chak WK, Gill D, Poduri A, Mefford HC. BRAT1 encephalopathy: a recessive cause of epilepsy of infancy with migrating focal seizures. Developmental Medicine and Child Neurology. PMID 31868227 DOI: 10.1111/Dmcn.14428  0.307
2019 Bar C, Barcia G, Jennesson M, Le Guyader G, Schneider A, Mignot C, Lesca G, Breuillard D, Montomoli M, Keren B, Doummar D, de Villemeur TB, Afenjar A, Marey I, Gerard M, ... ... Myers CT, et al. Expanding the genetic and phenotypic relevance of KCNB1 variants in developmental and epileptic encephalopathies: 27 new patients and overview of the literature. Human Mutation. PMID 31513310 DOI: 10.1002/Humu.23915  0.326
2019 Salpietro V, Dixon CL, Guo H, Bello OD, Vandrovcova J, Efthymiou S, Maroofian R, Heimer G, Burglen L, Valence S, Torti E, Hacke M, Rankin J, Tariq H, Colin E, ... ... Myers CT, et al. AMPA receptor GluA2 subunit defects are a cause of neurodevelopmental disorders. Nature Communications. 10: 3094. PMID 31300657 DOI: 10.1038/S41467-019-10910-W  0.324
2019 Bisulli F, Licchetta L, Baldassari S, Muccioli L, Marconi C, Cantalupo G, Myers C, Menghi V, Minardi R, Caporali L, Marini C, Guerrini R, Mefford HC, Tinuper P, Pippucci T. SCN1A mutations in focal epilepsy with auditory features: widening the spectrum of GEFS plus. Epileptic Disorders : International Epilepsy Journal With Videotape. PMID 30977726 DOI: 10.1684/Epd.2019.1046  0.364
2019 Pippucci T, Licchetta L, Baldassari S, Marconi C, De Luise M, Myers C, Nardi E, Provini F, Cameli C, Minardi R, Bacchelli E, Giordano L, Crichiutti G, d'Orsi G, Seri M, et al. Contribution of ultrarare variants in mTOR pathway genes to sporadic focal epilepsies. Annals of Clinical and Translational Neurology. 6: 475-485. PMID 30911571 DOI: 10.1002/Acn3.722  0.323
2018 Vlaskamp DRM, Shaw BJ, Burgess R, Mei D, Montomoli M, Xie H, Myers CT, Bennett MF, XiangWei W, Williams D, Maas SM, Brooks AS, Mancini GMS, van de Laar IMBH, van Hagen JM, et al. encephalopathy: A distinctive generalized developmental and epileptic encephalopathy. Neurology. PMID 30541864 DOI: 10.1212/Wnl.0000000000006729  0.317
2018 Gregor A, Sadleir LG, Asadollahi R, Azzarello-Burri S, Battaglia A, Ousager LB, Boonsawat P, Bruel AL, Buchert R, Calpena E, Cogné B, Dallapiccola B, Distelmaier F, Elmslie F, Faivre L, ... ... Myers CT, et al. De Novo Variants in the F-Box Protein FBXO11 in 20 Individuals with a Variable Neurodevelopmental Disorder. American Journal of Human Genetics. PMID 30057029 DOI: 10.1016/J.Ajhg.2018.07.003  0.363
2018 Di Donato N, Timms AE, Aldinger KA, Mirzaa GM, Bennett JT, Collins S, Olds C, Mei D, Chiari S, Carvill G, Myers CT, Rivière JB, Zaki MS, Gleeson JG, et al. Analysis of 17 genes detects mutations in 81% of 811 patients with lissencephaly. Genetics in Medicine : Official Journal of the American College of Medical Genetics. PMID 29671837 DOI: 10.1038/Gim.2018.8  0.317
2018 Johannesen KM, Gardella E, Linnankivi T, Courage C, de Saint Martin A, Lehesjoki AE, Mignot C, Afenjar A, Lesca G, Abi-Warde MT, Chelly J, Piton A, Merritt JL, Rodan LH, Tan WH, ... ... Myers CT, et al. Defining the phenotypic spectrum of SLC6A1 mutations. Epilepsia. PMID 29315614 DOI: 10.1111/Epi.13986  0.315
2017 Hamdan FF, Myers CT, Cossette P, Lemay P, Spiegelman D, Laporte AD, Nassif C, Diallo O, Monlong J, Cadieux-Dion M, Dobrzeniecka S, Meloche C, Retterer K, Cho MT, Rosenfeld JA, et al. High Rate of Recurrent De Novo Mutations in Developmental and Epileptic Encephalopathies. American Journal of Human Genetics. 101: 664-685. PMID 29100083 DOI: 10.1016/J.Ajhg.2017.09.008  0.352
2017 Myers CT, Stong N, Mountier EI, Helbig KL, Freytag S, Sullivan JE, Ben Zeev B, Nissenkorn A, Tzadok M, Heimer G, Shinde DN, Rezazadeh A, Regan BM, Oliver KL, Ernst ME, et al. De Novo Mutations in PPP3CA Cause Severe Neurodevelopmental Disease with Seizures. American Journal of Human Genetics. PMID 28942967 DOI: 10.1016/J.Ajhg.2017.08.013  0.353
2016 Myers CT, McMahon JM, Schneider AL, Petrovski S, Allen AS, Carvill GL, Zemel M, Saykally JE, LaCroix AJ, Heinzen EL, Hollingsworth G, Nikanorova M, Corbett M, Gecz J, Coman D, et al. De Novo Mutations in SLC1A2 and CACNA1A Are Important Causes of Epileptic Encephalopathies American Journal of Human Genetics. 99: 287-298. PMID 27476654 DOI: 10.1016/J.Ajhg.2016.06.003  0.348
2016 Djémié T, Weckhuysen S, von Spiczak S, Carvill GL, Jaehn J, Anttonen AK, Brilstra E, Caglayan HS, de Kovel CG, Depienne C, Gaily E, Gennaro E, Giraldez BG, Gormley P, Guerrero-López R, ... ... Myers CT, et al. Pitfalls in genetic testing: the story of missed SCN1A mutations. Molecular Genetics & Genomic Medicine. 4: 457-64. PMID 27465585 DOI: 10.1002/Mgg3.217  0.309
2016 de Lange IM, Helbig KL, Weckhuysen S, Møller RS, Velinov M, Dolzhanskaya N, Marsh E, Helbig I, Devinsky O, Tang S, Mefford HC, Myers CT, van Paesschen W, Striano P, van Gassen K, et al. De novo mutations of KIAA2022 in females cause intellectual disability and intractable epilepsy. Journal of Medical Genetics. PMID 27358180 DOI: 10.1136/Jmedgenet-2016-103909  0.305
2016 Rudolf G, Lesca G, Mehrjouy MM, Labalme A, Salmi M, Bache I, Bruneau N, Pendziwiat M, Fluss J, de Bellescize J, Scholly J, Møller RS, Craiu D, Tommerup N, Valenti-Hirsch MP, ... ... Myers CT, et al. Loss of function of the retinoid-related nuclear receptor (RORB) gene and epilepsy. European Journal of Human Genetics : Ejhg. PMID 27352968 DOI: 10.1038/Ejhg.2016.80  0.35
2016 Myers CT, Mefford HC. Genetic investigations of the epileptic encephalopathies: Recent advances. Progress in Brain Research. 226: 35-60. PMID 27323938 DOI: 10.1016/Bs.Pbr.2016.04.006  0.364
2016 Tsai MH, Kuo PW, Myers CT, Li SW, Lin WC, Fu TY, Chang HY, Mefford HC, Chang YC, Tsai JW. A novel DCX missense mutation in a family with X-linked lissencephaly and subcortical band heterotopia syndrome inherited from a low-level somatic mosaic mother: Genetic and functional studies. European Journal of Paediatric Neurology : Ejpn : Official Journal of the European Paediatric Neurology Society. PMID 27292316 DOI: 10.1016/J.Ejpn.2016.05.010  0.307
2016 Mastrangelo M, Scheffer IE, Bramswig NC, Nair LD, Myers CT, Dentici ML, Korenke GC, Schoch K, Campeau PM, White SM, Shashi V, Kansagra S, Van Essen AJ, Leuzzi V. Epilepsy in KCNH1-related syndromes. Epileptic Disorders : International Epilepsy Journal With Videotape. PMID 27267311 DOI: 10.1684/Epd.2016.0830  0.305
2016 Petrovski S, Küry S, Myers CT, Anyane-Yeboa K, Cogné B, Bialer M, Xia F, Hemati P, Riviello J, Mehaffey M, Besnard T, Becraft E, Wadley A, Politi AR, Colombo S, et al. Germline De Novo Mutations in GNB1 Cause Severe Neurodevelopmental Disability, Hypotonia, and Seizures. American Journal of Human Genetics. PMID 27108799 DOI: 10.1016/J.Ajhg.2016.03.011  0.357
2016 Hildebrand MS, Myers CT, Carvill GL, Regan BM, Damiano JA, Mullen SA, Newton MR, Nair U, Gazina EV, Milligan CJ, Reid CA, Petrou S, Scheffer IE, Berkovic SF, Mefford HC. A targeted resequencing gene panel for focal epilepsy. Neurology. PMID 27029629 DOI: 10.1212/Wnl.0000000000002608  0.32
2016 Mignot C, von Stülpnagel C, Nava C, Ville D, Sanlaville D, Lesca G, Rastetter A, Gachet B, Marie Y, Korenke GC, Borggraefe I, Hoffmann-Zacharska D, Szczepanik E, Rudzka-Dybała M, Yiş U, ... ... Myers CT, et al. Genetic and neurodevelopmental spectrum of SYNGAP1-associated intellectual disability and epilepsy. Journal of Medical Genetics. PMID 26989088 DOI: 10.1136/Jmedgenet-2015-103451  0.334
2015 Dejanovic B, Djémié T, Grünewald N, Suls A, Kress V, Hetsch F, Craiu D, Zemel M, Gormley P, Lal D, Myers CT, Mefford HC, Palotie A, Helbig I, et al. Simultaneous impairment of neuronal and metabolic function of mutated gephyrin in a patient with epileptic encephalopathy. Embo Molecular Medicine. PMID 26613940 DOI: 10.15252/Emmm.201505323  0.327
2015 Myers CT, Mefford HC. Advancing epilepsy genetics in the genomic era. Genome Medicine. 7: 91. PMID 26302787 DOI: 10.1186/S13073-015-0214-7  0.342
2015 Galizia EC, Myers CT, Leu C, de Kovel CG, Afrikanova T, Cordero-Maldonado ML, Martins TG, Jacmin M, Drury S, Krishna Chinthapalli V, Muhle H, Pendziwiat M, Sander T, Ruppert AK, Møller RS, et al. CHD2 variants are a risk factor for photosensitivity in epilepsy. Brain : a Journal of Neurology. 138: 1198-207. PMID 25783594 DOI: 10.1093/Brain/Awv052  0.322
2014 Myers CT, Appleby SC, Krieg PA. Use of small molecule inhibitors of the Wnt and Notch signaling pathways during Xenopus development. Methods (San Diego, Calif.). 66: 380-9. PMID 24036250 DOI: 10.1016/J.Ymeth.2013.08.036  0.571
2013 Myers CT, Krieg PA. BMP-mediated specification of the erythroid lineage suppresses endothelial development in blood island precursors. Blood. 122: 3929-39. PMID 24100450 DOI: 10.1182/Blood-2013-03-490045  0.62
2013 Tunc-Ozdemir M, Rato C, Brown E, Rogers S, Mooneyham A, Frietsch S, Myers CT, Poulsen LR, Malhó R, Harper JF. Cyclic nucleotide gated channels 7 and 8 are essential for male reproductive fertility. Plos One. 8: e55277. PMID 23424627 DOI: 10.1371/Journal.Pone.0055277  0.318
2012 Moran CM, Myers CT, Lewis CM, Krieg PA. Hedgehog regulates angiogenesis of intersegmental vessels through the VEGF signaling pathway. Developmental Dynamics : An Official Publication of the American Association of Anatomists. 241: 1034-42. PMID 22513894 DOI: 10.1002/Dvdy.23795  0.603
2011 Meadows SM, Myers CT, Krieg PA. Regulation of endothelial cell development by ETS transcription factors. Seminars in Cell & Developmental Biology. 22: 976-84. PMID 21945894 DOI: 10.1016/J.Semcdb.2011.09.009  0.712
2010 Salanga MC, Meadows SM, Myers CT, Krieg PA. ETS family protein ETV2 is required for initiation of the endothelial lineage but not the hematopoietic lineage in the Xenopus embryo. Developmental Dynamics : An Official Publication of the American Association of Anatomists. 239: 1178-87. PMID 20235229 DOI: 10.1002/Dvdy.22277  0.613
2009 Myers C, Romanowsky SM, Barron YD, Garg S, Azuse CL, Curran A, Davis RM, Hatton J, Harmon AC, Harper JF. Calcium-dependent protein kinases regulate polarized tip growth in pollen tubes. The Plant Journal : For Cell and Molecular Biology. 59: 528-39. PMID 19392698 DOI: 10.1111/J.1365-313X.2009.03894.X  0.315
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