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Cynthia Morton, Ed.D. - Publications

Affiliations: 
2010 Education Walden University, Minneapolis, MN, United States 
Area:
Elementary Education, Teacher Training Education, Leadership Education
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26 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
2023 David D, Fino J, Oliveira R, Dória S, Morton CC. Balanced chromosomal rearrangements implicate YIPF5 and SPATC1L in non-obstructive oligoasthenozoospermia and oligozoospermia and of a derivative chromosome 22 in recurrent miscarriage. Gene. 147737. PMID 37625567 DOI: 10.1016/j.gene.2023.147737  0.352
2020 David D, Freixo JP, Fino J, Carvalho I, Marques M, Cardoso M, Piña-Aguilar RE, Morton CC. Comprehensive clinically oriented workflow for nucleotide level resolution and interpretation in prenatal diagnosis of de novo apparently balanced chromosomal translocations in their genomic landscape. Human Genetics. PMID 32030560 DOI: 10.1007/s00439-020-02121-x  0.311
2019 Wang H, Dong Z, Zhang R, Chau MHK, Yang Z, Tsang KYC, Wong HK, Gui B, Meng Z, Xiao K, Zhu X, Wang Y, Chen S, Leung TY, Cheung SW, ... Morton CC, et al. Low-pass genome sequencing versus chromosomal microarray analysis: implementation in prenatal diagnosis. Genetics in Medicine : Official Journal of the American College of Medical Genetics. PMID 31447483 DOI: 10.1038/s41436-019-0634-7  0.321
2018 Wilch ES, Morton CC. Historical and Clinical Perspectives on Chromosomal Translocations. Advances in Experimental Medicine and Biology. 1044: 1-14. PMID 29956287 DOI: 10.1007/978-981-13-0593-1_1  0.363
2018 Dong Z, Ye L, Yang Z, Chen H, Yuan J, Wang H, Guo X, Li Y, Wang J, Chen F, Cheung SW, Morton CC, Jiang H, Choy KW. Balanced Chromosomal Rearrangement Detection by Low-Pass Whole-Genome Sequencing. Current Protocols in Human Genetics. 96: 8.18.1-8.18.16. PMID 29364520 DOI: 10.1002/cphg.51  0.343
2018 Zepeda-Mendoza CJ, Bardon A, Kammin T, Harris DJ, Cox H, Redin C, Ordulu Z, Talkowski ME, Morton CC. Phenotypic interpretation of complex chromosomal rearrangements informed by nucleotide-level resolution and structural organization of chromatin. European Journal of Human Genetics : Ejhg. PMID 29321672 DOI: 10.1038/S41431-017-0068-0  0.338
2017 Dong Z, Wang H, Chen H, Jiang H, Yuan J, Yang Z, Wang WJ, Xu F, Guo X, Cao Y, Zhu Z, Geng C, Cheung WC, Kwok YK, Yang H, ... Morton CC, et al. Identification of balanced chromosomal rearrangements previously unknown among participants in the 1000 Genomes Project: implications for interpretation of structural variation in genomes and the future of clinical cytogenetics. Genetics in Medicine : Official Journal of the American College of Medical Genetics. PMID 29095815 DOI: 10.1038/gim.2017.170  0.314
2017 Zepeda-Mendoza CJ, Ibn-Salem J, Kammin T, Harris DJ, Rita D, Gripp KW, MacKenzie JJ, Gropman A, Graham B, Shaheen R, Alkuraya FS, Brasington CK, Spence EJ, Masser-Frye D, Bird LM, ... Morton CC, et al. Computational Prediction of Position Effects of Apparently Balanced Human Chromosomal Rearrangements. American Journal of Human Genetics. PMID 28735859 DOI: 10.1016/J.Ajhg.2017.06.011  0.301
2016 Redin C, Brand H, Collins RL, Kammin T, Mitchell E, Hodge JC, Hanscom C, Pillalamarri V, Seabra CM, Abbott MA, Abdul-Rahman OA, Aberg E, Adley R, Alcaraz-Estrada SL, Alkuraya FS, ... Morton CC, et al. The genomic landscape of balanced cytogenetic abnormalities associated with human congenital anomalies. Nature Genetics. PMID 27841880 DOI: 10.1038/Ng.3720  0.332
2016 Ordulu Z, Kammin T, Brand H, Pillalamarri V, Redin CE, Collins RL, Blumenthal I, Hanscom C, Pereira S, Bradley I, Crandall BF, Gerrol P, Hayden MA, Hussain N, Kanengisser-Pines B, ... Morton CC, et al. Structural Chromosomal Rearrangements Require Nucleotide-Level Resolution: Lessons from Next-Generation Sequencing in Prenatal Diagnosis. American Journal of Human Genetics. PMID 27745839 DOI: 10.1016/J.Ajhg.2016.08.022  0.323
2016 Giersch AB, Bieber FR, Dubuc AM, Fletcher JA, Ligon AH, Mason-Suares H, Morton CC, Weremowicz S, Xiao S, Dal Cin P. Reporting of Diagnostic Cytogenetic Results. Current Protocols in Human Genetics / Editorial Board, Jonathan L. Haines ... [Et Al.]. 89: A.1D.1-A.1D.23. PMID 27037490 DOI: 10.1002/0471142905.hg01ds89  0.342
2014 Ordulu Z, Wong KE, Currall BB, Ivanov AR, Pereira S, Althari S, Gusella JF, Talkowski ME, Morton CC. Describing sequencing results of structural chromosome rearrangements with a suggested next-generation cytogenetic nomenclature. American Journal of Human Genetics. 94: 695-709. PMID 24746958 DOI: 10.1016/J.Ajhg.2014.03.020  0.307
2012 Chiang C, Jacobsen JC, Ernst C, Hanscom C, Heilbut A, Blumenthal I, Mills RE, Kirby A, Lindgren AM, Rudiger SR, McLaughlan CJ, Bawden CS, Reid SJ, Faull RL, Snell RG, ... Morton CC, et al. Complex reorganization and predominant non-homologous repair following chromosomal breakage in karyotypically balanced germline rearrangements and transgenic integration. Nature Genetics. 44: 390-7, S1. PMID 22388000 DOI: 10.1038/Ng.2202  0.468
2011 Ligon AH, Morton CC, Bieber FR, Fletcher JA, Giersch AB, Kantarci S, Leach N, Lee C, Sandstrom M, Weremowicz S, Xiao S, Dal Cin P. Reporting of diagnostic cytogenetic results. Current Protocols in Human Genetics / Editorial Board, Jonathan L. Haines ... [Et Al.]. 1D. PMID 21735374 DOI: 10.1002/0471142905.hga01ds70  0.443
2011 Poitras JL, Costa D, Kluk MJ, Amrein PC, Stone RM, Lee C, Dal Cin P, Morton CC. Genomic alterations in myeloid neoplasms with novel, apparently balanced translocations. Cancer Genetics. 204: 68-76. PMID 21504705 DOI: 10.1016/J.Cancergen.2010.12.005  0.473
2010 Ligon AH, Morton CC, Bieber FR, Fletcher JA, Giersch AB, Kantarci S, Leach N, Lee C, Sandstrom M, Weremowicz S, Xiao S, Dal Cin P. Reporting of diagnostic cytogenetic results. Current Protocols in Human Genetics / Editorial Board, Jonathan L. Haines ... [Et Al.]. 1D.1-23. PMID 20891028 DOI: 10.1002/0471142905.hga01ds67  0.443
2010 Ordulu Z, Dal Cin P, Chong WW, Choy KW, Lee C, Muto MG, Quade BJ, Morton CC. Disseminated peritoneal leiomyomatosis after laparoscopic supracervical hysterectomy with characteristic molecular cytogenetic findings of uterine leiomyoma. Genes, Chromosomes & Cancer. 49: 1152-60. PMID 20842731 DOI: 10.1002/gcc.20824  0.34
2009 Brown KK, Alkuraya FS, Matos M, Robertson RL, Kimonis VE, Morton CC. NR2F1 deletion in a patient with a de novo paracentric inversion, inv(5)(q15q33.2), and syndromic deafness. American Journal of Medical Genetics. Part A. 149: 931-8. PMID 19353646 DOI: 10.1002/ajmg.a.32764  0.325
2008 Higgins AW, Alkuraya FS, Bosco AF, Brown KK, Bruns GA, Donovan DJ, Eisenman R, Fan Y, Farra CG, Ferguson HL, Gusella JF, Harris DJ, Herrick SR, Kelly C, Kim HG, ... Morton CC, et al. Characterization of apparently balanced chromosomal rearrangements from the developmental genome anatomy project. American Journal of Human Genetics. 82: 712-22. PMID 18319076 DOI: 10.1016/J.Ajhg.2008.01.011  0.339
2008 Lee C, Morton CC. Structural genomic variation and personalized medicine. The New England Journal of Medicine. 358: 740-1. PMID 18272898 DOI: 10.1056/NEJMcibr0708452  0.351
2007 Hodge JC, Morton CC. Genetic heterogeneity among uterine leiomyomata: insights into malignant progression. Human Molecular Genetics. 16: R7-13. PMID 17613550 DOI: 10.1093/Hmg/Ddm043  0.301
2007 Williamson RE, Darrow KN, Michaud S, Jacobs JS, Jones MC, Eberl DF, Maas RL, Liberman MC, Morton CC. Methylthioadenosine phosphorylase (MTAP) in hearing: gene disruption by chromosomal rearrangement in a hearing impaired individual and model organism analysis. American Journal of Medical Genetics. Part A. 143: 1630-9. PMID 17534888 DOI: 10.1002/Ajmg.A.31724  0.304
2004 Ligon AH, Morton CC, Bieber FR, Fletcher JA, Giersch AB, Lee C, Sandstrom M, Weremowicz S, Xiao S, Dal Cin P. Reporting of diagnostic cytogenetic results. Current Protocols in Human Genetics / Editorial Board, Jonathan L. Haines ... [Et Al.]. Appendix 1D. PMID 18428350 DOI: 10.1002/0471142905.hga01ds43  0.443
2004 Roberts AE, Irons MB, Kimonis VE, Mulliken JB, Morton CC, Lee C, Listewnik M. Description of a case of distal 2p trisomy by array-based comparative genomic hybridization: a high resolution genome-wide investigation for chromosomal aneuploidy in a single assay. American Journal of Medical Genetics. Part A. 130: 204-7. PMID 15372522 DOI: 10.1002/Ajmg.A.30223  0.46
2002 Picker JD, Cox GF, Fan YS, Fowler DJ, Weremowicz S, Morton CC, Lee C. Multicolor karyotypic interpretation of a heterochromatin-associated marker chromosome in a dysmorphic girl with developmental delay. American Journal of Medical Genetics. 110: 393-6. PMID 12116216 DOI: 10.1002/ajmg.10477  0.44
2002 Zhu C, Mills KD, Ferguson DO, Lee C, Manis J, Fleming J, Gao Y, Morton CC, Alt FW. Unrepaired DNA breaks in p53-deficient cells lead to oncogenic gene amplification subsequent to translocations. Cell. 109: 811-21. PMID 12110179 DOI: 10.1016/S0092-8674(02)00770-5  0.467
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