Jeannette Klein

Most-cited papers

1. Newborn screening for sickle cell disease in Europe: recommendations from a Pan‐European Consensus Conference

   S. Lobitz, P. Telfer, E. Cela, Bichr Allaf +41 more

   2018British Journal of Haematology135 citations Open access

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2. Features and outcome of galactokinase deficiency in children diagnosed by newborn screening

   J. Hennermann, P. Schadewaldt, Barbara Vetter, Y. Shin +2 more

   2011Journal of Inherited Metabolic Disease57 citations

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3. Competitive Inhibition of Amino Acid Uptake Suppresses Chlamydial Growth: Involvement of the Chlamydial Amino Acid Transporter BrnQ

   Peter R. Braun, Hesham M. Al-Younes, Joscha Gussmann, Jeannette Klein +2 more

   2007Journal of Bacteriology40 citations Open access

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4. Does the aromatic L-amino acid decarboxylase contribute to thyronamine biosynthesis?

   C. S. Hoefig, K. Renko, S. Piehl, T. Scanlan +7 more

   2012Molecular and Cellular Endocrinology38 citations

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5. Newborn Screening for SCID and Other Severe Primary Immunodeficiency in the Polish-German Transborder Area: Experience From the First 14 Months of Collaboration

   M. Giżewska, K. Durda, T. Winter, I. Ostrowska +16 more

   2020Frontiers in Immunology34 citations Open access

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6. Incidence of sickle cell disease in an unselected cohort of neonates born in Berlin, Germany

   S. Lobitz, Claudia Frömmel, Annemarie Brose, Jeannette Klein +1 more

   2014European Journal of Human Genetics28 citations Open access

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7. Newborn screening by tandem mass spectrometry confirms the high prevalence of sickle cell disease among German newborns

   S. Lobitz, Jeannette Klein, Annemarie Brose, O. Blankenstein +1 more

   2018Annals of Hematology26 citations

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8. Newborn Screening for Sickle Cell Disease: Technical and Legal Aspects of a German Pilot Study with 38,220 Participants

   Claudia Frömmel, Annemarie Brose, Jeannette Klein, O. Blankenstein +1 more

   2014BioMed Research International22 citations Open access

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9. Genotype and residual enzyme activity in medium‐chain acyl‐CoA dehydrogenase (MCAD) deficiency: Are predictions possible?

   S. Tucci, Christine Wagner, S. Grünert, U. Matysiak +10 more

   2021Journal of Inherited Metabolic Disease16 citations Open access

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10. False-positive newborn screening mimicking glutaric aciduria type I in infants with renal insufficiency

    J. Hennermann, S. Roloff, J. Gellermann, A. Grüters +1 more

    2009Journal of Inherited Metabolic Disease16 citations

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11. Newborn screening from an international perspective--different countries, different approaches.

    Jeannette Klein

    2011Clinical Biochemistry7 citations

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12. Simultaneous newborn screening for sickle cell disease, biotinidase deficiency, and hereditary tyrosinemia type 1 with an optimized tandem mass spectrometry protocol

    S. Lobitz, Claudia Frömmel, Annemarie Brose, O. Blankenstein +4 more

    2022Annals of Hematology4 citations Open access

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13. Newborn Screening for Familial Hypercholesterolemia Using LC-MS/MS-Based Free Cholesterol Measurements.

    Anke Hannemann, Theresa Winter, Elisabeth Steinhagen-Thiessen, M. Giżewska +9 more

    2026Jornal de Pediatria1 citations Open access

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14. Excavating the goddess in the nineties: feminist performance and video in Southern California

    Jeannette Klein

    20011 citations

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