Magera, Mark J.
Mayo Clinic
5 papers on CoChatORCID 0000-0002-3323-3105
Most cited papers
- Verified
Improved specificity of newborn screening for congenital adrenal hyperplasia by second-tier steroid profiling using tandem mass spectrometry
Lacey, J. M., Minutti, C. Z., Magera, M. J., Tauscher, A. L., Casetta, B., McCann, M., Lymp, J., Hahn, S. H., Rinaldo, P., & Matern, D. (2004) · Clinical Chemistry
Sexual Differentiation and DisordersAdrenal Hormones and Disorders
Cited by 216
- Verified
Steroid profiling by tandem mass spectrometry improves the positive predictive value of newborn screening for congenital adrenal hyperplasia
Minutti, C. Z., Lacey, J. M., Magera, M. J., Hahn, S. H., McCann, M., Schulze, A., Cheillan, D., Dorche, C., Chace, D. H., Lymp, J. F., et al. (2004) · The Journal of Clinical Endocrinology & Metabolism
Sexual Differentiation and DisordersMetabolism and Genetic Disorders
Cited by 154
- Verified
Combined Newborn Screening for Succinylacetone, Amino Acids, and Acylcarnitines in Dried Blood Spots
Turgeon, C., Magera, M. J., Allard, P., Tortorelli, S., Gavrilov, D., Oglesbee, D., Raymond, K., Rinaldo, P., & Matern, D. (2008) · Clinical Chemistry
Metabolism and Genetic DisordersMetabolomics and Mass Spectrometry Studies
Cited by 145
- Verified
Diagnosis of Very Long Chain Acyl-Dehydrogenase Deficiency From an Infant's Newborn Screening Card
Wood, J. C., Magera, M. J., Rinaldo, P., Seashore, M. R., Strauss, A. W., & Friedman, A. (2001) · Pediatrics
Metabolism and Genetic DisordersGenomics and Rare Diseases
Cited by 62
- Verified
Streamlined determination of lysophosphatidylcholines in dried blood spots for newborn screening of X-linked adrenoleukodystrophy
Turgeon, C. T., Moser, A. B., Mørkrid, L., Magera, M. J., Gavrilov, D. K., Oglesbee, D., Raymond, K., Rinaldo, P., Matern, D., & Tortorelli, S. (2015) · Molecular Genetics and Metabolism
Metabolism and Genetic DisordersLysosomal Storage Disorders Research
Cited by 60
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