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Deletion of 16q22.2q23.3 in a Boy with a Phenotype Reminiscent of Silver-Russell Syndrome2021 Molecular Syndromology article Biochemistry, Genetics and Molecular Biology Genomic variations and chromosomal abnormalities Open access
Anna Lengyel, Éva Pinti, Thomas Eggermann, György Fekete, Irén Haltrich
8citations -
Re-focusing sampling, design and experimental methods to assess rapid evolution by non-native plant species2024 Biological Invasions article Biochemistry, Genetics and Molecular Biology Evolution and Genetic Dynamics Open access
Marília Souza Lucas, Isabell Hensen, Christopher D. Barratt, Ragan M. Callaway, Walter Durka, Ylva Lekberg, +6 more
25citations -
Temporal niche differentiation often leads to priority effects rather than coexistence: Lessons from a marine midge2025 Journal of Animal Ecology article Medicine Mathematical and Theoretical Epidemiology and Ecology Models Open access
Runa K. Ekrem, Charlotte de Vries, Tobias S. Kaiser, Hanna Kokko
4citations -
Sympathetic and Vagal Nerve Activity in COPD: Pathophysiology, Presumed Determinants and Underappreciated Therapeutic Potential2022 Frontiers in Physiology article Medicine Chronic Obstructive Pulmonary Disease (COPD) Research Open access
Jens Spießhoefer, Binaya Regmi, Matteo Maria Ottaviani, Florian Kahles, Alberto Giannoni, Chiara Borrelli, +3 more
30citations -
Nutrimetric Validation of Solanidine as Dietary‐Derived CYP2D6 Activity Marker In Vivo2023 Clinical Pharmacology & Therapeutics article Pharmacology, Toxicology and Pharmaceutics Pharmacogenetics and Drug Metabolism Open access
Julian Peter Müller, Jens Andreas Sarömba, Patrick Ziegler, Roman Tremmel, Jens Rengelshausen, Elke Schaeffeler, +4 more
15citations -
Effects of hyperventilation length on muscle sympathetic nerve activity in healthy humans simulating periodic breathing2022 Frontiers in Physiology article Medicine Heart Rate Variability and Autonomic Control Open access
Jens Spießhoefer, Alberto Giannoni, Chiara Borrelli, Paolo Sciarrone, Imke Husstedt, Michele Emdin, +8 more
8citations -
Development of autonomic innervation at the venous pole of the heart: bridging the gap from mice to human2025 Journal of Translational Medicine article Medicine Heart Rate Variability and Autonomic Control Open access
Fleur Zwanenburg, Arend D.J. ten Harkel, Monique C. Haak, Nathan D. Hahurij, Robert E. Poelmann, Conny J. van Munsteren, +4 more
3citations -
Amlodipine limits microglia activation and cognitive dysfunction in aged hypertensive mice2023 Journal of Hypertension article Neuroscience Neuroinflammation and Neurodegeneration Mechanisms Open access
Daniëlle Kerkhofs, Robin Helgers, Denise J. H. P. Hermes, H.P. Steinbusch, Helma van Essen, Peter J. A. Leenders, +5 more
32citations -
Gain and loss of TASK3 channel function and its regulation by novel variation cause KCNK9 imprinting syndrome2022 Genome Medicine article Biochemistry, Genetics and Molecular Biology Ion channel regulation and function Open access
Margot A. Cousin, Emma L. Veale, Nikita R. Dsouza, Swarnendu Tripathi, Robyn G. Holden, Maria Arélin, +64 more
25citations -
ANK3 related neurodevelopmental disorders: expanding the spectrum of heterozygous loss-of-function variants2021 Neurogenetics article Biochemistry, Genetics and Molecular Biology Genetics and Neurodevelopmental Disorders Open access
Katja Kloth, Bernarda Lozić, Julia Tagoe, Mariëtte J.V. Hoffer, Amelie T. van der Ven, Hölger Thiele, +6 more
28citations -
Triplications of chromosome 1p36.3, including the genes GABRD and SKI, are associated with a developmental disorder and a facial gestalt2023 American Journal of Medical Genetics Part A article Biochemistry, Genetics and Molecular Biology Genomic variations and chromosomal abnormalities Open access
Elise Pelgrims, Sally Ann Lynch, Laurens Hannes, Mariëtte J.V. Hoffer, Cindy Melotte, Arie van Haeringen, +2 more
1citations -
ATR-16 syndrome: mechanisms linking monosomy to phenotype2020 Journal of Medical Genetics article Biochemistry, Genetics and Molecular Biology Genomic variations and chromosomal abnormalities Open access
Christian Babbs, Jill M. Brown, Sharon W. Horsley, Joanne Slater, Evie Maifoshie, Shiwangini Kumar, +7 more
10citations -
Four groups of type 2 diabetes contribute to the etiological and clinical heterogeneity in newly diagnosed individuals: An IMI DIRECT study2022 Cell Reports Medicine article Medicine Diabetes, Cardiovascular Risks, and Lipoproteins Open access cited by 1 patent
Agata Wesolowska‐Andersen, Caroline Brorsson, Roberto Bizzotto, Andrea Mari, Andrea Tura, Robert Wilhelm Koivula, +54 more
94citations -
Biallelic PRMT7 pathogenic variants are associated with a recognizable syndromic neurodevelopmental disorder with short stature, obesity, and craniofacial and digital abnormalities2022 Genetics in Medicine article Biochemistry, Genetics and Molecular Biology Genetics and Neurodevelopmental Disorders Open access
Elisa Calì, Mohnish Suri, Marcello Scala, Matteo Paolo Ferla, Shahryar Alavi, Eissa Faqeih, +60 more
9citations