Ralph Fingerhut

Klinikum Weiden — Germany

Biochemistry, Genetics and Molecular Biology · Life Sciences

36h-index4.2kcitations126works0.32yr avg
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Research Topics

Metabolism and Genetic Disorders(71), Neonatal Health and Biochemistry(27), Mitochondrial Function and Pathology(20), Amino Acid Enzymes and Metabolism(19), Cystic Fibrosis Research Advances(15)

Publications126 total

A 25-Year Retrospective on Bavaria’s Newborn Screening Programme: Achievements, Challenges and Long-Term Follow-Up
International Journal of Neonatal Screening·2025Open Access
Iron status in women of reproductive age in Switzerland: the role of inflammation and ferritin thresholds for the prevalence of iron deficiency–a cross-sectional study
Universität Zürich, ZORA·2025Open Access
Ten-Year Anniversary of the International Journal of Neonatal Screening: Revisiting Its Scope
International Journal of Neonatal Screening·2025Open Access
The effects of age and sex on reference intervals for cobalamin, homocysteine, and serum and urinary methylmalonic acid in healthy adult dogs
Journal of Veterinary Internal Medicine·2024· 1 citedOpen Access
Prevalence of Transient Hypothyroidism in Children Diagnosed with Congenital Hypothyroidism between 2000 and 2016
International Journal of Molecular Sciences·2023· 8 citedOpen Access
Immunoreactive trypsinogen in healthy newborns and infants with cystic fibrosis
Archives of Disease in Childhood Fetal & Neonatal·2022· 9 cited
Update Neugeborenenscreening: Neue Zielkrankheiten
Trillium Diagnostik·2022
Newborn Screening for Inborn Errors of Metabolism
2022· 1 cited
Correction: Spenger et al. Glutaric Aciduria Type I Missed by Newborn Screening: Report of Four Cases from Three Families. Int. J. Neonatal Screen. 2021, 7, 32
International Journal of Neonatal Screening·2021Open Access
The Editor’s Choice for Issue 3, Volume 7
International Journal of Neonatal Screening·2021Open Access
Newborn Screening for Congenital Hypothyroidism-Clinical Evaluation and Comparison of Two Different Test Kits for the Determination of TSH in Dried Blood Samples on Two Different Platforms
International Journal of Neonatal Screening·2021· 2 citedOpen Access
Glutaric Aciduria Type I Missed by Newborn Screening: Report of Four Cases from Three Families
International Journal of Neonatal Screening·2021· 12 citedOpen Access
IJNS Turns Seven—High Impact for Neonatal Screening
International Journal of Neonatal Screening·2021· 1 citedOpen Access
Neonatal Screening in Europe Revisited: An ISNS Perspective on the Current State and Developments Since 2010
International Journal of Neonatal Screening·2021· 222 citedOpen Access
P018 Follow-up of children with Cystic Fibrosis Screen Positive, Inconclusive Diagnosis (CFSPID) in Switzerland
Journal of Cystic Fibrosis·2021· 1 cited
Decrease of disease‐related metabolites upon fasting in a hemizygous knock‐in mouse model (<scp><i>Mut</i></scp>‐ko/ki) of methylmalonic aciduria
JIMD Reports·2020· 3 citedOpen Access
Regulatory landscape of providing information on newborn screening to parents across Europe
European Journal of Human Genetics·2020· 21 citedOpen Access
Phosphoglucomutase-1 deficiency: Early presentation, metabolic management and detection in neonatal blood spots
Molecular Genetics and Metabolism·2020· 33 citedOpen Access
Swiss newborn screening for severe T and B cell deficiency with a combined TREC/KREC assay – management recommendations
Swiss Medical Weekly·2020· 33 citedOpen Access
Determining Reference Ranges for Total T4 in Dried Blood Samples for Newborn Screening
International Journal of Neonatal Screening·2020· 6 citedOpen Access
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Frequent Co-authors

Bernhard Olgemöller(11), Adelbert A. Roscher(11), Bernhard Liebl(8), Matthias R. Baumgartner(6), Beat Thöny(5), Wulf Röschinger(5), Ernst Conzelmann(4), Ania C. Muntau(4), Michael Zimmermann(4), Maria Andersson(4), Gabriella Allegri(3), Johannes Häberle(3), Laura Vilarinho(3), Raquel Yahyaoui(3), Werner Schmitz(3), Esther M. Maier(3), Uta Nennstiel(3), Rüdiger von Kries(3), Alfried Kohlschütter(3), Stefan Kölker(3)