Lagerstedt SA - Search Results

1

Gender differences in C-reactive protein concentrations-confirmation with two sensitive methods.

McConnell JP, Branum EL, Ballman KV, Lagerstedt SA, Katzmann JA, Jaffe AS. McConnell JP, et al. Among authors: lagerstedt sa. Clin Chem Lab Med. 2002 Jan;40(1):56-9. doi: 10.1515/CCLM.2002.011. Clin Chem Lab Med. 2002. PMID: 11916271

2

Quantitative determination of plasma c8-c26 total fatty acids for the biochemical diagnosis of nutritional and metabolic disorders.

Lagerstedt SA, Hinrichs DR, Batt SM, Magera MJ, Rinaldo P, McConnell JP. Lagerstedt SA, et al. Mol Genet Metab. 2001 May;73(1):38-45. doi: 10.1006/mgme.2001.3170. Mol Genet Metab. 2001. PMID: 11350181

3

Measurement of plasma free metanephrine and normetanephrine by liquid chromatography-tandem mass spectrometry for diagnosis of pheochromocytoma.

Lagerstedt SA, O'Kane DJ, Singh RJ. Lagerstedt SA, et al. Clin Chem. 2004 Mar;50(3):603-11. doi: 10.1373/clinchem.2003.024703. Epub 2004 Jan 15. Clin Chem. 2004. PMID: 14726465

4

UGT1A1 genetic analysis as a diagnostic aid for individuals with unconjugated hyperbilirubinemia.

Skierka JM, Kotzer KE, Lagerstedt SA, O'Kane DJ, Baudhuin LM. Skierka JM, et al. Among authors: lagerstedt sa. J Pediatr. 2013 Jun;162(6):1146-52, 1152.e1-2. doi: 10.1016/j.jpeds.2012.11.042. Epub 2013 Jan 4. J Pediatr. 2013. PMID: 23290513

5

Decreased frequency of FBN1 missense variants in Ghent criteria-positive Marfan syndrome and characterization of novel FBN1 variants.

Baudhuin LM, Kotzer KE, Lagerstedt SA. Baudhuin LM, et al. Among authors: lagerstedt sa. J Hum Genet. 2015 May;60(5):241-52. doi: 10.1038/jhg.2015.10. Epub 2015 Feb 5. J Hum Genet. 2015. PMID: 25652356

6

Genetic and biochemical analyses in dyslipidemic patients undergoing LDL apheresis.

Donato LJ, Saenger AK, Train LJ, Kotzer KE, Lagerstedt SA, Hornseth JM, Basu A, Winters JL, Baudhuin LM. Donato LJ, et al. Among authors: lagerstedt sa. J Clin Apher. 2014 Oct;29(5):256-65. doi: 10.1002/jca.21317. Epub 2014 Jan 13. J Clin Apher. 2014. PMID: 24420163

7

Increased frequency of FBN1 truncating and splicing variants in Marfan syndrome patients with aortic events.

Baudhuin LM, Kotzer KE, Lagerstedt SA. Baudhuin LM, et al. Among authors: lagerstedt sa. Genet Med. 2015 Mar;17(3):177-87. doi: 10.1038/gim.2014.91. Epub 2014 Aug 7. Genet Med. 2015. PMID: 25101912 Free article.

8

Preemptive Pharmacogenomic Testing for Precision Medicine: A Comprehensive Analysis of Five Actionable Pharmacogenomic Genes Using Next-Generation DNA Sequencing and a Customized CYP2D6 Genotyping Cascade.

Ji Y, Skierka JM, Blommel JH, Moore BE, VanCuyk DL, Bruflat JK, Peterson LM, Veldhuizen TL, Fadra N, Peterson SE, Lagerstedt SA, Train LJ, Baudhuin LM, Klee EW, Ferber MJ, Bielinski SJ, Caraballo PJ, Weinshilboum RM, Black JL 3rd. Ji Y, et al. Among authors: lagerstedt sa. J Mol Diagn. 2016 May;18(3):438-445. doi: 10.1016/j.jmoldx.2016.01.003. Epub 2016 Mar 3. J Mol Diagn. 2016. PMID: 26947514 Free PMC article.

9

Variability in gene-based knowledge impacts variant classification: an analysis of FBN1 missense variants in ClinVar.

Baudhuin LM, Kluge ML, Kotzer KE, Lagerstedt SA. Baudhuin LM, et al. Among authors: lagerstedt sa. Eur J Hum Genet. 2019 Oct;27(10):1550-1560. doi: 10.1038/s41431-019-0440-3. Epub 2019 Jun 21. Eur J Hum Genet. 2019. PMID: 31227806 Free PMC article.

10

Confirming Variants in Next-Generation Sequencing Panel Testing by Sanger Sequencing.

Baudhuin LM, Lagerstedt SA, Klee EW, Fadra N, Oglesbee D, Ferber MJ. Baudhuin LM, et al. Among authors: lagerstedt sa. J Mol Diagn. 2015 Jul;17(4):456-61. doi: 10.1016/j.jmoldx.2015.03.004. Epub 2015 May 8. J Mol Diagn. 2015. PMID: 25960255 Free article.

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