Most cited papers from Cnopf´sche Kinderklinik

Cnopf´sche Kinderklinik

What are the most cited papers from Cnopf´sche Kinderklinik?

The most cited paper from Cnopf´sche Kinderklinik is "DNA methylation-based classification of central nervous system tumours" (David Capper et al., 2018), with 3,228 citations. Next come "Driver mutations in histone H3.3 and chromatin remodelling genes in paediatric glioblastoma" (2,736) and "Hotspot Mutations in H3F3A and IDH1 Define Distinct Epigenetic and Biological Subgroups of Glioblastoma" (1,881).

Published TypeFieldAccessAuthorsCitations

Showing 50 of 60 papers. Every paper with more than 40 citations is listed.

Most cited papers, sortable by citations and release date
#	Paper
1	DNA methylation-based classification of central nervous system tumours David Capper et al. · Nature Open access143 authors	13 Mar 2018	3,228
2	Driver mutations in histone H3.3 and chromatin remodelling genes in paediatric glioblastoma Jeremy Schwartzentruber et al. · Nature	27 Jan 2012	2,736
3	Hotspot Mutations in H3F3A and IDH1 Define Distinct Epigenetic and Biological Subgroups of Glioblastoma Dominik Sturm et al. · Cancer Cell Open access	Oct 2012	1,881
4	New Brain Tumor Entities Emerge from Molecular Classification of CNS-PNETs Dominik Sturm et al. · Cell Open access110 authors	Feb 2016	1,028
5	Subgroup-specific structural variation across 1,000 medulloblastoma genomes Paul A. Northcott et al. · Nature Open access135 authors	24 Jul 2012	936
6	Genome Sequencing of Pediatric Medulloblastoma Links Catastrophic DNA Rearrangements with TP53 Mutations Tobias Rausch et al. · Cell Open access	2012	890
7	Dissecting the genomic complexity underlying medulloblastoma David Jones et al. · Nature Open access	24 Jul 2012	884
8	Recurrent somatic alterations of FGFR1 and NTRK2 in pilocytic astrocytoma David Jones et al. · Nature Genetics Open access	30 Jun 2013	847
9	Incidence of severe critical events in paediatric anaesthesia (APRICOT): a prospective multicentre observational study in 261 hospitals in Europe Walid Habre et al. · The Lancet Respiratory Medicine Open access1,004 authors	28 Mar 2017	826
10	Genome Sequencing of SHH Medulloblastoma Predicts Genotype-Related Response to Smoothened Inhibition Marcel Kool et al. · Cancer Cell Open access	Mar 2014	788
11	Enhancer hijacking activates GFI1 family oncogenes in medulloblastoma Paul A. Northcott et al. · Nature Open access	20 Jun 2014	684
12	BRAF gene duplication constitutes a mechanism of MAPK pathway activation in low-grade astrocytomas Stefan M. Pfister et al. · Journal of Clinical Investigation Open access	15 Apr 2008	526
13	Decoding the regulatory landscape of medulloblastoma using DNA methylation sequencing Volker Hovestadt et al. · Nature Open access	18 May 2014	474
14	Spectrum and prevalence of genetic predisposition in medulloblastoma: a retrospective genetic study and prospective validation in a clinical trial cohort Sebastian M. Waszak et al. · The Lancet Oncology Open access	9 May 2018	410
15	Mutations in STRA6 Cause a Broad Spectrum of Malformations Including Anophthalmia, Congenital Heart Defects, Diaphragmatic Hernia, Alveolar Capillary Dysplasia, Lung Hypoplasia, and Mental Retardation Francesca Pasutto et al. · The American Journal of Human Genetics Open access	5 Feb 2007	363
16	Outcome Prediction in Pediatric Medulloblastoma Based on DNA Copy-Number Aberrations of Chromosomes 6q and 17q and the MYC and MYCN Loci Stefan M. Pfister, Marc Remke, Axel Benner et al. · Journal of Clinical Oncology Open access	2 Mar 2009	295
17	tRNA splicing endonuclease mutations cause pontocerebellar hypoplasia Birgit Susanne Budde et al. · Nature Genetics	17 Aug 2008	260
18	Genotype-phenotype correlations in Noonan syndrome Martin Zenker, Gernot Buheitel, Ralf Rauch et al. · The Journal of Pediatrics	Mar 2004	249
19	Oncogenic FAM131B–BRAF fusion resulting from 7q34 deletion comprises an alternative mechanism of MAPK pathway activation in pilocytic astrocytoma Huriye Cin et al. · Acta Neuropathologica	19 Mar 2011	240
20	Sedation and analgesia practices in neonatal intensive care units (EUROPAIN): results from a prospective cohort study Ricardo Carbajal et al. · The Lancet Respiratory Medicine Open access	24 Sep 2015	198
21	Morbidity and mortality after anaesthesia in early life: results of the European prospective multicentre observational study, neonate and children audit of anaesthesia practice in Europe (NECTARINE) Nicola Massimo Disma et al. · British Journal of Anaesthesia Open access480 authors	Apr 2021	180
22	Adult and Pediatric Medulloblastomas Are Genetically Distinct and Require Different Algorithms for Molecular Risk Stratification Andrey Korshunov, Marc Remke, Wiebke Werft et al. · Journal of Clinical Oncology	18 May 2010	165
23	General anaesthetics and the developing brain: an overview Barbara Sinner, Karin Becke, Kristin Engelhard · Anaesthesia Open access	14 May 2014	162
24	Assessment of continuous pain in newborns admitted to NICU s in 18 E uropean countries Kanwaljeet J. S. Anand et al. · Acta Paediatrica Open access	3 Mar 2017	141
25	Validation of a predictive model for identifying an increased risk for thromboembolism in children with acute lymphoblastic leukemia: results of a multicenter cohort study Lesley Gayle Mitchell, Moritz Lambers, Silke Flege et al. · Blood Open access	25 Mar 2010	127
26	Perioperative intravenous fluid therapy in children: guidelines from the Association of the Scientific Medical Societies in Germany Robert Sümpelmann, Karin Becke, Sebastian Brenner et al. · Pediatric Anesthesia	17 Oct 2016	125
27	Anesthesia and the developing brain: A way forward for laboratory and clinical research Nicola Massimo Disma, James D. O’Leary, Andreas W. Loepke et al. · Pediatric Anesthesia Open access	16 Aug 2018	105
28	A Defect in Dolichol Phosphate Biosynthesis Causes a New Inherited Disorder with Death in Early Infancy Christian Kranz, Christoph Jungeblut, Jonas Denecke et al. · The American Journal of Human Genetics Open access	5 Feb 2007	104
29	Translocation breakpoints in three patients with campomelic dysplasia and autosomal sex reversal map more than 130 kb from SOX9 Jutta Wirth, Thomas Wagner, Jobst Meyer et al. · Human Genetics	Feb 1996	97
30	European consensus statement for intraoperative fluid therapy in children Robert Sümpelmann, Karin Becke, Peter M. Crean et al. · European Journal of Anaesthesiology	7 Jun 2011	96
31	Therapiestudie BFM 79/81 zur Behandlung der akuten lymphoblastischen Leukämie bei Kindern und Jugendlichen: intensivierte Reinduktionstherapie für Patientengruppen mit unterschiedlichem Rezidivrisiko Guenter Henze et al. · Klinische Pädiatrie	Jul 1982	94
32	Sorafenib and cisplatin/doxorubicin (PLADO) in pediatric hepatocellular carcinoma Irene Schmid, Beate Häberle, Michael H. Albert et al. · Pediatric Blood & Cancer	15 Sep 2011	93
33	An update on the perioperative management of children with upper respiratory tract infections Adrian Regli, Karin Becke, Britta Sylvia von Ungern-Sternberg · Current Opinion in Anaesthesiology	11 Mar 2017	92
34	Activating mutations in the calcium-sensing receptor: genetic and clinical spectrum in 25 patients with autosomal dominant hypocalcaemia - a German survey Friedhelm Raue, Josef Pichl, Helmuth-G. Dörr et al. · Clinical Endocrinology	6 Jun 2011	92
35	Genotyping circulating tumor DNA of pediatric Hodgkin lymphoma Ann-Kathrin Desch et al. · Leukemia	20 Aug 2019	86
36	1,25-Dihydroxyvitamin D Resistance, Rickets, and Alopecia: Analysis of Receptors and Bioresponse in Cultured Fibroblasts from Patients and Parents* Theresa L. Chen, MARGARET A. HIRST, Charlotte M. Cone et al. · The Journal of Clinical Endocrinology & Metabolism	Sep 1984	86
37	Impact of clear fluid fasting on pulmonary aspiration in children undergoing general anesthesia: Results of the German prospective multicenter observational (NiKs) study Christiane E. Beck et al. · Pediatric Anesthesia Open access	13 Jun 2020	85
38	Anesthesia in children with a cold Karin Becke · Current Opinion in Anaesthesiology	12 Apr 2012	81
39	“ADAM complex” (amniotic deformity, adhesions, mutilations)—A pattern of craniofacial and limb defects Henry Keller, Gerhard Neuhäuser, M. Virginia Durkin‐Stamm et al. · American Journal of Medical Genetics	1978	79
40	Biological and clinical heterogeneity of MYCN-amplified medulloblastoma Andrey Korshunov et al. · Acta Neuropathologica Open access	8 Dec 2011	77
41	Supratentorial primitive neuroectodermal tumors of the central nervous system frequently harbor deletions of the CDKN2A locus and other genomic aberrations distinct from medulloblastomas Stefan M. Pfister, Marc Remke, Grischa Toedt et al. · Genes Chromosomes and Cancer	25 Jun 2007	77
42	Patient-controlled analgesia with remifentanil versus alternative parenteral methods for pain management in labour Stephanie Weibel, Yvonne Jelting, Arash J. Afshari et al. · Cochrane Database of Systematic Reviews Open access	13 Apr 2017	74
43	Diagnosis and treatment of Hymenoptera venom allergy Franziska Ruëff et al. · Allergologie select Open access	2023	71
44	De novo 13q deletions in two patients with mild anorectal malformations as part of VATER/VACTERL and VATER/VACTERL‐like association and analysis of EFNB2 in patients with anorectal malformations Gabriel C. Dworschak et al. · American Journal of Medical Genetics Part A	16 Aug 2013	66
45	Treatment of the bone marrow failure in Fanconi anemia patients with danazol Kathrin Scheckenbach, Mary Anne M. Morgan, Judith Filger-Brillinger et al. · Blood Cells Molecules and Diseases	16 Dec 2011	64
46	Lethal cutis laxa with contractural arachnodactyly, overgrowth and soft tissue bleeding due to a novel homozygous fibulin‐4 gene mutation Juliane Hoyer, Cornelia S. Kraus, G. Hammersen et al. · Clinical Genetics	3 Aug 2009	63
47	Pseudohypoaldosteronism in Eight Families: Different Forms of Inheritance Are Evidence for Various Genetic Defects Ursula Kuhnle, Meta Damkjær Nielsen, H. U. Tietze et al. · The Journal of Clinical Endocrinology & Metabolism	Mar 1990	63
48	Bladder augmentation with small intestinal submucosa leads to unsatisfactory long-term results Michelle Schaefer, Annette Kaiser, Maximilian Stehr et al. · Journal of Pediatric Urology	16 Jan 2013	61
49	Peanut‐induced anaphylaxis in children and adolescents: Data from the European Anaphylaxis Registry Ioana Maris et al. · Allergy Open access	4 Dec 2020	59
50	Five Patients with a Biotin-Responsive Defect in Holocarboxylase Formation: Evaluation of Responsiveness to Biotin Therapy in Vivo and Comparative Biochemical Studies in Vi1 Terttu Suormala, Brian Fowler, Marinus Durán et al. · Pediatric Research	May 1997	55

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.