D I. Rodenhiser
Affiliations: | The University of Western Ontario (Canada) |
Area:
Molecular Biology, Oncology, Cell BiologyGoogle:
"D Rodenhiser"Children
Sign in to add trainee| Debora Mancini DiNardo | grad student | 2000 | The University of Western Ontario (Canada) |
BETA: Related publications
See more...
Publications
|
You can help our author matching system! If you notice any publications incorrectly attributed to this author, please sign in and mark matches as correct or incorrect. |
| Aref-Eshghi E, Kerkhof J, Pedro VP, et al. (2021) Evaluation of DNA Methylation Episignatures for Diagnosis and Phenotype Correlations in 42 Mendelian Neurodevelopmental Disorders. American Journal of Human Genetics. 108: 1161-1163 |
| Aref-Eshghi E, Kerkhof J, Pedro VP, et al. (2020) Evaluation of DNA Methylation Episignatures for Diagnosis and Phenotype Correlations in 42 Mendelian Neurodevelopmental Disorders. American Journal of Human Genetics |
| Bend EG, Aref-Eshghi E, Everman DB, et al. (2019) Gene domain-specific DNA methylation episignatures highlight distinct molecular entities of ADNP syndrome. Clinical Epigenetics. 11: 64 |
| Aref-Eshghi E, Bend EG, Colaiacovo S, et al. (2019) Diagnostic Utility of Genome-wide DNA Methylation Testing in Genetically Unsolved Individuals with Suspected Hereditary Conditions. American Journal of Human Genetics |
| Sadikovic B, Aref-Eshghi E, Levy MA, et al. (2019) DNA methylation signatures in mendelian developmental disorders as a diagnostic bridge between genotype and phenotype. Epigenomics |
| Aref-Eshghi E, Bend EG, Hood RL, et al. (2018) BAFopathies' DNA methylation epi-signatures demonstrate diagnostic utility and functional continuum of Coffin-Siris and Nicolaides-Baraitser syndromes. Nature Communications. 9: 4885 |
| Aref-Eshghi E, Schenkel LC, Ainsworth P, et al. (2018) Genomic DNA Methylation-Derived Algorithm Enables Accurate Detection of Malignant Prostate Tissues. Frontiers in Oncology. 8: 100 |
| Schenkel LC, Aref-Eshghi E, Skinner C, et al. (2018) Peripheral blood epi-signature of Claes-Jensen syndrome enables sensitive and specific identification of patients and healthy carriers with pathogenic mutations in. Clinical Epigenetics. 10: 21 |
| Aref-Eshghi E, Rodenhiser DI, Schenkel LC, et al. (2018) Genomic DNA Methylation Signatures Enable Concurrent Diagnosis and Clinical Genetic Variant Classification in Neurodevelopmental Syndromes. American Journal of Human Genetics. 102: 156-174 |
| Aref-Eshghi E, Schenkel LC, Lin H, et al. (2017) The defining DNA methylation signature of Kabuki syndrome enables functional assessment of genetic variants of unknown clinical significance. Epigenetics. 0 |