Fernandez, Conrad V.
Dalhousie University · Izaak Walton Killam Health Centre
4 papers on CoChatORCID 0000-0002-0746-8306
Most cited papers
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Mutations in mitochondrial carrier family gene SLC25A38 cause nonsyndromic autosomal recessive congenital sideroblastic anemia
Guernsey, D. L., Jiang, H., Campagna, D. R., Evans, S. C., Ferguson, M., Kellogg, M. D., Lachance, M., Matsuoka, M., Nightingale, M., Rideout, A., et al. (2009) · Nature Genetics
Iron Metabolism and DisordersHemoglobinopathies and Related Disorders
Cited by 244
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A comparison of journal instructions regarding institutional review board approval and conflict-of-interest disclosure between 1995 and 2005
Rowan-Legg, A., Weijer, C., Gao, J., & Fernandez, C. (2009) · Journal of Medical Ethics
Pharmaceutical industry and healthcareAcademic integrity and plagiarism
Cited by 64
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Genome-wide sequencing in acutely ill infants: genomic medicine’s critical application?
Friedman, J. M., Bombard, Y., Cornel, M. C., Fernandez, C. V., Junker, A. K., Plon, S. E., Stark, Z., & Knoppers, B. M. (2019) · Genetics in Medicine
Genomics and Rare DiseasesMetabolism and Genetic Disorders
Cited by 44
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Circulating Tumor DNA as a Biomarker in Patients With Stage III and IV Wilms Tumor: Analysis From a Children's Oncology Group Trial, AREN0533
Madanat-Harjuoja, L. M., Renfro, L. A., Klega, K., Tornwall, B., Thorner, A. R., Nag, A., Dix, D., Dome, J. S., Diller, L. R., Fernandez, C. V., et al. (2022) · Journal of Clinical Oncology
Renal and related cancersCancer Genomics and Diagnostics
Cited by 41
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