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Genomics|July 19, 2011
Influence of sex and genetic variability on expression of X-linked genes in human monocytesRaphaële Castagné, Tanja Zeller, Maxime Rotival, et al.Neurology|July 12, 2019
Quantitative MR neurography biomarkers in 5q-linked spinal muscular atrophyJennifer Kollmer, Tim Hilgenfeld, Andreas Ziegler, et al.Biomolecules|March 28, 2026
Urinary Metabolomics Predict Acute Kidney Injury in Very-Low-Birth-Weight Infants with Patent Ductus ArteriosusMoritz Niesert, Claire Cannet, Alexander Fichtner, et al.Pediatric Diabetes|October 11, 2018
Psychosocial benefits of insulin pump therapy in children with diabetes type 1 and their families: The pumpkin multicenter randomized controlled trialEsther Mueller-Godeffroy, Reinhard Vonthein, Carmen Ludwig-Seibold, et al.Archives of Dermatological Research|October 31, 2006
Variations of the melanocortin-1 receptor and the glutathione-S transferase T1 and M1 genes in cutaneous malignant melanomaRotraut Mössner, Nils Anders, Inke R König, et al.Journal of Neurochemistry|January 7, 2020
Cerebrospinal fluid proteomic profiling in nusinersen-treated patients with spinal muscular atrophyTobias Kessler, Pauline Latzer, Dominic Schmid, et al.Journal of Medical Genetics|December 8, 2009
FCGR2A functional genetic variant associated with susceptibility to severe malarial anaemia in Ghanaian childrenKathrin Schuldt, Claudia Esser, Jennifer Evans, et al.Human Heredity|May 4, 2005
Developmental dyslexia--recurrence risk estimates from a german bi-center study using the single proband sib pair designAndreas Ziegler, Inke R König, Wolfgang Deimel, et al.International Journal of Molecular Sciences|May 27, 2026
Interpretation of Pharmacometabolomics Results: Fingerprint of Drug Exposure or Confounder Effects? Insights from a Urinary Metabolomics Study with Voriconazole in Healthy ParticipantsKristine Chobanyan-Jürgens, Amin Muhareb, Moritz Niesert, et al.Zeitschrift Fur Arztliche Fortbildung Und Qualitatssicherung|June 19, 2002
[Familial pancreatic cancer--concept for study of the National Case Collection and early diagnosis program for high risk people]Berthold Gerdes, Ralf Kress, Harald Rieder, et al.Pageof 43