Most cited papers from Kreiskliniken Reutlingen

Kreiskliniken Reutlingen

What are the most cited papers from Kreiskliniken Reutlingen?

The most cited paper from Kreiskliniken Reutlingen is "Senescence surveillance of pre-malignant hepatocytes limits liver cancer development" (Tae-Won Kang et al., 2011), with 1,629 citations. Next come "Genetic diagnosis of Mendelian disorders via RNA sequencing" (615) and "Apoptotic cell death and tissue remodelling during mouse mammary gland involution" (546).

Published TypeFieldAccessAuthorsCitations

Showing 50 of 58 papers. Every paper with more than 79 citations is listed.

Most cited papers, sortable by citations and release date
#	Paper
1	Senescence surveillance of pre-malignant hepatocytes limits liver cancer development Tae-Won Kang et al. · Nature	Nov 2011	1,629
2	Genetic diagnosis of Mendelian disorders via RNA sequencing Laura Sophie Kremer et al. · Nature Communications Open access	12 Jun 2017	615
3	Apoptotic cell death and tissue remodelling during mouse mammary gland involution Robert Strange, Feng Li, Susanne Saurer et al. · Development	May 1992	546
4	Glucose transporter-1 deficiency syndrome: the expanding clinical and genetic spectrum of a treatable disorder Willemijn G. Leen et al. · Brain Open access	2 Feb 2010	422
5	Implementing TIMERS: the race against hard-to-heal wounds Leanne Atkin, Zofia Bućko, Elena Conde Montero et al. · Journal of Wound Care Open access	Mar 2019	371
6	Efficacy of sapropterin dihydrochloride (tetrahydrobiopterin, 6R-BH4) for reduction of phenylalanine concentration in patients with phenylketonuria: a phase III randomised placebo-controlled study Harvey L. Levy, Andrzej Milanowski, Anupam Chakrapani et al. · The Lancet	Aug 2007	319
7	Thoracic Ultrasound for Diagnosing Pulmonary Embolism Gebhard Mathis, Wolfgang A Blank, Angelika Reißig et al. · CHEST Journal	Sep 2005	309
8	Reversal of Profound, High-dose Rocuronium-induced Neuromuscular Blockade by Sugammadex at Two Different Time Points: An International, Multicenter, Randomized, Dose-finding, Safety Assessor-blinded, Phase II Trial F. Pühringer, Christopher S. Rex, Andreas Wilhelm Sielenkämper et al. · Anesthesiology	Aug 2008	242
9	The surgical treatment of bony metastases of the spine and limbs Paul M. Böhm, Juliusz Huber · Journal of Bone and Joint Surgery - British Volume Open access	May 2002	229
10	Clinical implementation of RNA sequencing for Mendelian disease diagnostics Vicente A. Yépez et al. · Genome Medicine Open access	4 Apr 2022	219
11	EWMA Document: Negative Pressure Wound Therapy Jan Apelqvist, Christian Willy, Ann‐Mari Fagerdahl et al. · Journal of Wound Care	Mar 2017	215
12	Autologous chondrocyte implantation (ACI) for cartilage defects of the knee: A guideline by the working group “Clinical Tissue Regeneration” of the German Society of Orthopaedics and Trauma (DGOU) Philipp Niemeyer et al. · The Knee	5 Mar 2016	204
13	Efficacy of Sapropterin Dihydrochloride in Increasing Phenylalanine Tolerance in Children with Phenylketonuria: A Phase III, Randomized, Double-Blind, Placebo-Controlled Study Friedrich K. Trefz, Barbara K. Burton, Nicola Longo et al. · The Journal of Pediatrics	5 Mar 2009	196
14	Effectiveness of triclosan-coated PDS Plus versus uncoated PDS II sutures for prevention of surgical site infection after abdominal wall closure: the randomised controlled PROUD trial Markus K. Diener et al. · The Lancet Open access	7 Apr 2014	191
15	Viral Infection of Tumors Overcomes Resistance to PD-1-immunotherapy by Broadening Neoantigenome-directed T-cell Responses Norman Woller, Engin Gürlevik, Bettina Fleischmann-Mundt et al. · Molecular Therapy Open access	26 Jun 2015	189
16	Molecular diagnosis in mitochondrial complex I deficiency using exome sequencing Tobias B. Haack et al. · Journal of Medical Genetics Open access	Apr 2012	188
17	Efficacy and outcome of expanded newborn screening for metabolic diseases - Report of 10 years from South-West Germany * Martin S. Lindner, Gwendolyn Gramer, Gisela Haege et al. · Orphanet Journal of Rare Diseases Open access	20 Jun 2011	184
18	Mutations in FBXL4, Encoding a Mitochondrial Protein, Cause Early-Onset Mitochondrial Encephalomyopathy Xiaowu Gai et al. · The American Journal of Human Genetics Open access	29 Aug 2013	183
19	Tumor-Specific Vascularization Pattern of Liver Metastasis, Hepatocellular Carcinoma, Hemangioma and Focal Nodular Hyperplasia in the Differential Diagnosis of 1349 Liver Lesions in Contrast-Enhanced Ultrasound (CEUS) Deike D. Strobel, Karlheinz Seitz, Wolfgang A Blank et al. · Ultraschall in der Medizin - European Journal of Ultrasound	17 Aug 2009	177
20	Contrast-Enhanced Ultrasound (CEUS) for the Characterization of Focal Liver Lesions in Clinical Practice (DEGUM Multicenter Trial): CEUS vs. MRI – a Prospective Comparison in 269 Patients Karlheinz Seitz, Thomas Bernatik, Deike D. Strobel et al. · Ultraschall in der Medizin - European Journal of Ultrasound	22 Jul 2010	176
21	Mitochondrial Protein Lipoylation and the 2-Oxoglutarate Dehydrogenase Complex Controls HIF1α Stability in Aerobic Conditions Stephen P. Burr, Ana S.H. Costa, Guinevere L. Grice et al. · Cell Metabolism Open access	27 Oct 2016	174
22	Clinical presentation and outcome in a series of 88 patients with the cblC defect Sabine Fischer et al. · Journal of Inherited Metabolic Disease Open access	5 Mar 2014	174
23	Mutations in GTPBP3 Cause a Mitochondrial Translation Defect Associated with Hypertrophic Cardiomyopathy, Lactic Acidosis, and Encephalopathy Robert Kopajtich et al. · The American Journal of Human Genetics Open access	26 Nov 2014	163
24	Impaired complex I repair causes recessive Leber’s hereditary optic neuropathy Sarah L. Stenton et al. · Journal of Clinical Investigation Open access	19 Jan 2021	154
25	ELAC2 Mutations Cause a Mitochondrial RNA Processing Defect Associated with Hypertrophic Cardiomyopathy Tobias B. Haack, Robert Kopajtich, Peter Freisinger et al. · The American Journal of Human Genetics Open access	11 Jul 2013	151
26	Contrast-Enhanced Ultrasound (CEUS) for the Characterization of Focal Liver Lesions – Prospective Comparison in Clinical Practice: CEUS vs. CT (DEGUM Multicenter Trial) Parts of this Manuscript were presented at the Ultrasound Dreiländertreffen 2008, Davos Karlheinz Seitz, Deike D. Strobel, Thomas Bernatik et al. · Ultraschall in der Medizin - European Journal of Ultrasound	17 Aug 2009	150
27	Rationale for the German recommendations for phenylalanine level control in phenylketonuria 1997 P. Burgard, H. J. Bremer, Peter Bührdel et al. · European Journal of Pediatrics	1999	147
28	S2k-Leitlinie zur Diagnostik und Therapie von Patienten mit Asthma Deutsche Gesellschaft für Arbeitsmedizin und Umweltmedizin e. V. et al. · Pneumologie Open access	Dec 2017	143
29	Optimizing the use of sapropterin (BH4) in the management of phenylketonuria Nenad Blau, Amaya Bélanger‐Quintana, Mübeccel Demirkol et al. · Molecular Genetics and Metabolism	9 Feb 2009	140
30	Challenges and Pitfalls in the Management of Phenylketonuria François Feillet, Francjan J. van Spronsen, Anita MacDonald et al. · PEDIATRICS	13 Jul 2010	135
31	Cross-sectional study of 168 patients with hepatorenal tyrosinaemia and implications for clinical practice Sebene Mayorandan et al. · Orphanet Journal of Rare Diseases Open access	31 Jul 2014	135
32	Disturbed mitochondrial and peroxisomal dynamics due to loss of MFF causes Leigh-like encephalopathy, optic atrophy and peripheral neuropathy Johannes Koch, René Günther Feichtinger, Peter Freisinger et al. · Journal of Medical Genetics	18 Jan 2016	129
33	Incidence and duration of residual paralysis at the end of surgery after multiple administrations of cisatracurium and rocuronium Dirk M. Maybauer, Götz Geldner, Manfred Blobner et al. · Anaesthesia	6 Dec 2006	128
34	Diagnostic Accuracy of CEUS in the Differential Diagnosis of Small (≤ 20 mm) and Subcentimetric (≤ 10 mm) Focal Liver Lesions in Comparison with Histology Deike D. Strobel, Thomas Bernatik, Wolfgang A Blank et al. · Ultraschall in der Medizin - European Journal of Ultrasound	Dec 2011	128
35	An overview of L-2-hydroxyglutarate dehydrogenase gene (L2HGDH) variants: a genotype-phenotype study Marjan E. Steenweg et al. · Human Mutation Open access	5 Jan 2010	126
36	Thiamine Pyrophosphokinase Deficiency in Encephalopathic Children with Defects in the Pyruvate Oxidation Pathway Johannes Adalbert Mayr, Peter Freisinger, Kurt Schlachter et al. · The American Journal of Human Genetics Open access	Dec 2011	124
37	Evaluation of remifentanil as single drug for awake fiberoptic intubation Wolfgang Puchner, Matthias Egger, F. Pühringer et al. · Acta Anaesthesiologica Scandinavica	Apr 2002	122
38	Deficiency of ECHS 1 causes mitochondrial encephalopathy with cardiac involvement Tobias B. Haack et al. · Annals of Clinical and Translational Neurology Open access	13 Mar 2015	121
39	Spectrum of combined respiratory chain defects Johannes Adalbert Mayr, Tobias B. Haack, Peter Freisinger et al. · Journal of Inherited Metabolic Disease Open access	16 Mar 2015	117
40	Mutations in ATP6V1E1 or ATP6V1A Cause Autosomal-Recessive Cutis Laxa Tim Van Damme et al. · The American Journal of Human Genetics Open access	6 Jan 2017	114
41	COQ4 Mutations Cause a Broad Spectrum of Mitochondrial Disorders Associated with CoQ10 Deficiency Gloria Brea‐Calvo et al. · The American Journal of Human Genetics Open access	Feb 2015	110
42	Mutations in SLC33A1 Cause a Lethal Autosomal-Recessive Disorder with Congenital Cataracts, Hearing Loss, and Low Serum Copper and Ceruloplasmin Peter Huppke, Cornelia A. Brendel, Vera M. Kalscheuer et al. · The American Journal of Human Genetics Open access	2012	106
43	Guideline on positioning and early mobilisation in the critically ill by an expert panel Stefan Josef Schaller, Flora T. Scheffenbichler, Thomas Bein et al. · Intensive Care Medicine Open access	29 Jul 2024	101
44	Statement and Recommendations on Interventional Ultrasound as a Thyroid Diagnostic and Treatment Procedure Christoph Frank Dietrich, Thomas Müller, Jörg Bojunga et al. · Ultrasound in Medicine & Biology	7 Nov 2017	100
45	Clinical, biochemical, and genetic spectrum of seven patients with NFU1 deficiency Uwe Ahting et al. · Frontiers in Genetics Open access	13 Apr 2015	98
46	Impact of age at onset and newborn screening on outcome in organic acidurias Jana Herınger, Vassili Valayannopoulos, Allan Meldgaard Lund et al. · Journal of Inherited Metabolic Disease Open access	21 Dec 2015	96
47	Clinical, biochemical and genetic spectrum of 70 patients with ACAD9 deficiency: is riboflavin supplementation effective? Birgit Repp et al. · Orphanet Journal of Rare Diseases Open access	19 Jul 2018	94
48	Impaired riboflavin transport due to missense mutations in SLC52A2 causes Brown‐Vialetto‐Van Laere syndrome Tobias B. Haack, Christine C. Makowski, Yoshiaki Yao et al. · Journal of Inherited Metabolic Disease Open access	2 Aug 2012	94
49	Homozygous missense mutation in BOLA3 causes multiple mitochondrial dysfunctions syndrome in two siblings Tobias B. Haack, Boris Rolinski, Birgit Haberberger et al. · Journal of Inherited Metabolic Disease	4 May 2012	94
50	High-risk additional chromosomal abnormalities at low blast counts herald death by CML Rüdiger Hehlmann et al. · Leukemia Open access254 authors	7 May 2020	93

Citations are OpenAlex's own counts, from its 2026-09-23 snapshot, so the ranking can differ from Google Scholar or Web of Science. A paper is listed for an institution when any of its authors gave it as an affiliation; retracted papers and papers whose citation count cannot be traced to citing works are left out, and a preprint and the article it became are shown once. Release dates are OpenAlex's: where a source gave only a month or a year, that is what is shown. How the lists are chosen.