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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)

Dietrich Matern

Biochemical Genetics Laboratory

Division of Laboratory Genetics

Department of Laboratory Medicine and Pathology

Mayo Clinic



Name/email consistency: high



  • Biochemical Genetics Laboratory, Division of Laboratory Genetics, Department of Laboratory Medicine and Pathology, Mayo Clinic, USA. 2001 - 2008
  • Biochemical Genetics Laboratory, Mayo Clinic College of Medicine, Rochester, Minnesota 55905, USA. 2001 - 2007


  1. Newborn screening for lysosomal storage disorders. Matern, D. Acta. Paediatr. Suppl (2008) [Pubmed]
  2. Reduction of the false-positive rate in newborn screening by implementation of MS/MS-based second-tier tests: the Mayo Clinic experience (2004-2007). Matern, D., Tortorelli, S., Oglesbee, D., Gavrilov, D., Rinaldo, P. J. Inherit. Metab. Dis. (2007) [Pubmed]
  3. Prospective diagnosis of 2-methylbutyryl-CoA dehydrogenase deficiency in the Hmong population by newborn screening using tandem mass spectrometry. Matern, D., He, M., Berry, S.A., Rinaldo, P., Whitley, C.B., Madsen, P.P., van Calcar, S.C., Lussky, R.C., Andresen, B.S., Wolff, J.A., Vockley, J. Pediatrics (2003) [Pubmed]
  4. Glycogen storage disease type I: diagnosis and phenotype/genotype correlation. Matern, D., Seydewitz, H.H., Bali, D., Lang, C., Chen, Y.T. Eur. J. Pediatr. (2002) [Pubmed]
  5. Placental floor infarction complicating the pregnancy of a fetus with long-chain 3-hydroxyacyl-CoA dehydrogenase (LCHAD) deficiency. Matern, D., Schehata, B.M., Shekhawa, P., Strauss, A.W., Bennett, M.J., Rinaldo, P. Mol. Genet. Metab. (2001) [Pubmed]
  6. Mass spectrometry methods for metabolic and health assessment. Matern, D., Magera, M.J. J. Nutr. (2001) [Pubmed]
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