Debra J. Mathews, Ph.D.
Affiliations: | 2003 | Case Western Reserve University School of Medicine, Cleveland, OH, United States |
Area:
GeneticsGoogle:
"Debra Mathews"Parents
Sign in to add mentor| Aravinda Chakravarti | grad student | 2003 | Case Western Medical School | |
| (Intra- and intergenic variation on the human X chromosome.) | ||||
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Publications
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| Smith G, Mathews D, Sander-Effron S, et al. (2021) Microsatellite Markers in Biobanking: A New Multiplexed Assay. Biopreservation and Biobanking |
| Peppercorn J, Campbell E, Isakoff S, et al. (2019) Patient Preferences for Use of Archived Biospecimens from Oncology Trials When Adequacy of Informed Consent Is Unclear. The Oncologist |
| Stuttgen K, Dvoskin R, Bollinger J, et al. (2018) Risk perception before and after presymptomatic genetic testing for Huntington's disease: Not always what one might expect. Molecular Genetics & Genomic Medicine |
| Fiallos K, Applegate C, Mathews DJ, et al. (2017) Choices for return of primary and secondary genomic research results of 790 members of families with Mendelian disease. European Journal of Human Genetics : Ejhg |
| Chan S, Donovan PJ, Douglas T, et al. (2015) Genome Editing Technologies and Human Germline Genetic Modification: The Hinxton Group Consensus Statement. The American Journal of Bioethics : Ajob. 15: 42-7 |
| Chong JX, Buckingham KJ, Jhangiani SN, et al. (2015) The Genetic Basis of Mendelian Phenotypes: Discoveries, Challenges, and Opportunities. American Journal of Human Genetics. 97: 199-215 |
| Chong JX, Buckingham KJ, Jhangiani SN, et al. (2015) The Genetic Basis of Mendelian Phenotypes: Discoveries, Challenges, and Opportunities American Journal of Human Genetics |
| Kalfoglou AL, Doksum T, Bernhardt B, et al. (2005) Opinions about new reproductive genetic technologies: hopes and fears for our genetic future. Fertility and Sterility. 83: 1612-21 |
| Cutler DJ, Zwick ME, Carrasquillo MM, et al. (2001) High-throughput variation detection and genotyping using microarrays. Genome Research. 11: 1913-25 |
| Mathews DJ, Kashuk C, Brightwell G, et al. (2001) Sequence variation within the fragile X locus. Genome Research. 11: 1382-91 |