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American Journal of Medical Genetics. Part A|February 28, 2006
NTNG1 mutations are a rare cause of Rett syndromeHayley L Archer, Julie C Evans, David S Millar, et al.The American Journal of the Medical Sciences|February 4, 2015
Homoarginine in patients with primary hyperparathyroidismAndreas Tomaschitz, Nicolas Verheyen, Martin Gaksch, et al.Trends in Psychiatry and Psychotherapy|June 17, 2022
Human social isolation and stress: a systematic review of different contexts and recommendations for future studiesAndré Comiran Tonon, Ana Carolina O V de Abreu, Mariana Mendonça da Silva, et al.Circulation|March 19, 2003
Mutations in the human muscle LIM protein gene in families with hypertrophic cardiomyopathyChristian Geier, Andreas Perrot, Cemil Ozcelik, et al.Nature Communications|August 8, 2019
Aortic pathology from protein kinase G activation is prevented by an antioxidant vitamin B12 analogGerburg K Schwaerzer, Hema Kalyanaraman, Darren E Casteel, et al.Journal of the American Society of Nephrology : JASN|January 9, 2015
Galectin-3, Renal Function, and Clinical Outcomes: Results from the LURIC and 4D StudiesChristiane Drechsler, Graciela Delgado, Christoph Wanner, et al.Psychoneuroendocrinology|February 13, 2018
The relationship between inflammatory state and quantity of affective episodes in bipolar disorderRobert Queissner, René Pilz, Nina Dalkner, et al.The Journal of Allergy and Clinical Immunology|November 13, 2025
Neutralizing IL-22RA1 improves histologic and molecular alterations associated with atopic dermatitis pathogenesisSophia Wasserer, Thomas Litman, Josephine Hebsgaard, et al.Nature Communications|November 28, 2025
Genome-wide gene-environment interaction study uncovers 162 vitamin D status variants using a precise ambient UVB measureRasha Shraim, Maria Timofeeva, Cathy Wyse, et al.Nature Communications|December 13, 2022
Spatial transcriptomics landscape of lesions from non-communicable inflammatory skin diseasesA Schäbitz, C Hillig, M Mubarak, et al.Pageof 177