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Journal of Community Genetics|July 23, 2025
Age-specific uptake of non-invasive prenatal tests (NIPT) in Germany: a decision theory-based analysisMichael Krawczak, Bernd Eiben, Sebastian Sendel, et al.
Plos One|April 27, 2023
The role of PEEP for cannulation of the subclavian vein: A prospective observational studyChristine Eimer, Knut G Rump, Gunnar Elke, et al.
Annals of Vascular Surgery|April 27, 2021
Sexual Dysfunction Before and after Treatment of Infrarenal Aortic Aneurysm PatientsAndreas Bayer, Mark Kaschwich, Amke Caliebe, et al.
Clinical Neurology and Neurosurgery|August 2, 2023
Surgical approach for convexity meningiomas: An analysis of the preoperative clinical signs, radiological features and surgical outcomes of these tumorsHajrullah Ahmeti, Amke Caliebe, Nourane Trigui, et al.
Langmuir : the ACS Journal of Surfaces and Colloids|September 9, 2020
Operando X-ray Absorption Spectroscopy (XAS) Observation of Photoinduced Oxidation in FeNi (Oxy)hydroxide Overlayers on Hematite (α-Fe<sub>2</sub>O<sub>3</sub>) Photoanodes for Solar Water SplittingAnton Tsyganok, Paolo Ghigna, Alessandro Minguzzi, et al.
Anesthesia and Analgesia|February 25, 2005
Sevoflurane but not propofol preserves myocardial function during minimally invasive direct coronary artery bypass surgeryBerthold Bein, Jochen Renner, Dorothee Caliebe, et al.
European Journal of Medical Genetics|June 25, 2011
A de novo 1.1Mb microdeletion of chromosome 19p13.11 provides indirect evidence for EPS15L1 to be a strong candidate for split hand split foot malformationSusanne Bens, Andrea Haake, Holger Tönnies, et al.
Lupus|October 21, 2017
Low copy numbers of complement C4 and homozygous deficiency of C4A may predispose to severe disease and earlier disease onset in patients with systemic lupus erythematosusM Jüptner, F Flachsbart, A Caliebe, et al.
Clinical Dysmorphology|July 31, 2010
A de novo unbalanced translocation leading to partial monosomy 9p23-pter and partial trisomy 15q25.3-qter associated with 46,XY complete gonadal dysgenesis, tall stature and mental retardationLoukas Argyriou, Olaf Hiort, Peter Meinecke, et al.
European Journal of Medical Genetics|September 11, 2016
Do the exome: A case of Williams-Beuren syndrome with severe epilepsy due to a truncating de novo variant in GABRA1Bernt Popp, Regina Trollmann, Christian Büttner, et al.
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