UGT1A1 Genetic Analysis as a Diagnostic Aid for Individuals with Unconjugated Hyperbilirubinemia by Skierka, Jennifer M., BS, Kotzer, Katrina E., MS, Lagerstedt, Susan A., BS, O'Kane, Dennis J., PhD, Baudhuin, Linnea M., PhD

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Decreased frequency of FBN1 missense variants in Ghent criteria-positive Marfan syndrome and characterization of novel FBN1 variants by Baudhuin, Linnea M, Kotzer, Katrina E, Lagerstedt, Susan A

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Variability in gene-based knowledge impacts variant classification: an analysis of FBN1 missense variants in ClinVar by Baudhuin, Linnea M, Kluge, Michelle L, Kotzer, Katrina E, Lagerstedt, Susan A

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Measurement of Plasma Free Metanephrine and Normetanephrine by Liquid Chromatography-Tandem Mass Spectrometry for Diagnosis of Pheochromocytoma by Lagerstedt, Susan A, O'Kane, Dennis J, Singh, Ravinder J

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Genetic and biochemical analyses in dyslipidemic patients undergoing LDL apheresis by Donato, Leslie J., Saenger, Amy K., Train, Laura J., Kotzer, Katrina E., Lagerstedt, Susan A., Hornseth, Jean M., Basu, Ananda, Winters, Jeffrey L., Baudhuin, Linnea M.

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LDLR promoter variant and exon 14 mutation on the same chromosome are associated with an unusually severe FH phenotype and treatment resistance by Snozek, Christine LH, Lagerstedt, Susan A, Khoo, Teck K, Rubenfire, Melvyn, Isley, William L, Train, Laura J, Baudhuin, Linnea M

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Analysis of complement gene variants in the clinical laboratory: Comparison of Next-Generation Sequencing (NGS) and Sanger methods by Lagerstedt, Susan A., Csuka, Dorottya, Szilágyi, Ágnes, Prohászka, Zoltán, Abraham, Roshini S.

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Quantitative Determination of Plasma C8–C26 Total Fatty Acids for the Biochemical Diagnosis of Nutritional and Metabolic Disorders by Lagerstedt, Susan A., Hinrichs, Dallas R., Batt, Susan M., Magera, Mark J., Rinaldo, Piero, McConnell, Joseph P.

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Genetic and biochemical analyses in dyslipidemic patients undergoing LDL apheresis: Analysis of Dyslipidemic LDL Apheresis Patients by Donato, Leslie J., Saenger, Amy K., Train, Laura J., Kotzer, Katrina E., Lagerstedt, Susan A., Hornseth, Jean M., Basu, Ananda, Winters, Jeffrey L., Baudhuin, Linnea M.

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Variation in the risk of colorectal cancer in families with Lynch syndrome: a retrospective cohort study by Dowty, James G., Lee, Grant, Templeton, Allyson S., Alvarez, Karin, Ankathil, Ravindran, Austin, Rachel, Barca-Tierno, Verónica, Berthet, Pascaline, Boisjoli, Talya, Briollais, Laurent, Brunet, Joan, Bucksch, Karolin, Buettner, Reinhard, Burn, John, Caldés, Trinidad, Casey, Graham, Chew, Min H., Choi, Yun-hee, Church, James, Clendenning, Mark, Colas, Chrystelle, Coupier, Isabelle, de la Chapelle, Albert, Dębniak, Tadeusz, Della Valle, Adriana, Dominguez-Valentin, Mev, Engel, Christoph, Esperon, Patricia, Foulkes, William, Frebourg, Thierry, Gallinger, Steven, Garre, Pilar, Genuardi, Maurizio, Giraud, Sophie, Goodwin, Annabel, Green, Kate, Guindalini, Rodrigo S.C., Half, Elizabeth E., Hampel, Heather, Ho, Judy W.C., Hoogerbrugge, Nicoline, Hüneburg, Robert, Huntley, Vanessa, Jensen, Uffe B, Juhari, Wan K.W., Kloor, Matthias, Kupfer, Sonia S., Lagerstedt-Robinson, Kristina, Lalloo, Fiona, Lautrup, Charlotte K., Leggett, Barbara A., Lejeune, Sophie, Lindor, Noralane, Loeffler, Markus, Lucassen, Anneke M, Lynch, Patrick M., Møller, Pål, Navarro, Matilde, Neffa, Florencia, Neklason, Deborah, Nixon, Dawn M., Palmero, Edenir I., Pande, Mala, Parry, Susan, Pineda, Marta, Qiu, Jay, Ramesar, Raj, Rasmussen, Lene J., Redler, Silke, Ricciardiello, Luigi, Schulmann, Karsten, Schuster, Helène, Senter, Leigha, Seppälä, Toni T, Shtoyerman, Rakefet, Sijmons, Rolf H., Soto, Jose Luis, Spigelman, Allan, Steinke-Lange, Verena, Stoffel, Elena M., Strassburg, Christian P., Sunde, Lone, Therkildsen, Christina, Thibodeau, Steve, Tucker, Katherine M., Tunca, Berrin, Uhrhammer, Nancy, Vaccaro, Carlos, van Duijnhoven, Fränzel J.B., van Wanzeele, Meghan J., Vasen, Hans F.A., von Knebel Doeberitz, Magnus, von Salomé, Jenny, Ward, Robyn L., Wise, Paul E., Yamaguchi, Tatsuro, Zahary, Mohd N., Hopper, John L., Haile, Robert W., Jenkins, Mark A.

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