Most cited papers from Universitätskinderklinik

Universitätskinderklinik

What are the most cited papers from Universitätskinderklinik?

The most cited paper from Universitätskinderklinik is "Perzentile für den Body-mass-Index für das Kindes- und Jugendalter unter Heranziehung verschiedener deutscher Stichproben" (Katrin Kromeyer-Hauschild et al., 2001), with 2,200 citations. Next come "Truncating mutations of hSNF5/INI1 in aggressive paediatric cancer" (1,561) and "Estimation of Small Percentages of Fœtal Hæmoglobin" (1,017).

Published TypeFieldAccessAuthorsCitations

Showing 50 of 60 papers. Every paper with more than 189 citations is listed.

Most cited papers, sortable by citations and release date
#	Paper
1	Perzentile für den Body-mass-Index für das Kindes- und Jugendalter unter Heranziehung verschiedener deutscher Stichproben Katrin Kromeyer-Hauschild et al. · Monatsschrift Kinderheilkunde Open access	Aug 2001	2,200
2	Truncating mutations of hSNF5/INI1 in aggressive paediatric cancer Isabella Versteege, Nicolas Sévenet, Julian Lange et al. · Nature	Jul 1998	1,561
3	Estimation of Small Percentages of Fœtal Hæmoglobin Klaus Betke, Hanna Marti, Irmgard Schlicht · Nature	Dec 1959	1,017
4	Gene Therapy for Immunodeficiency Due to Adenosine Deaminase Deficiency Alessandro Aiuti et al. · New England Journal of Medicine Open access	28 Jan 2009	1,009
5	Detection of intracellular cytokines by flow cytometry Thomas Jung, Uwe Schauer, Christoph Heusser et al. · Journal of Immunological Methods	Feb 1993	990
6	Mutations in the DAX-1 gene give rise to both X-linked adrenal hypoplasia congenita and hypogonadotropic hypogonadism Françoise Muscatelli, Tim Matthias Strom, Ann P. Walker et al. · Nature	Dec 1994	776
7	RANDOMISED TRIAL OF FENTANYL ANAESTHESIA IN PRETERM BABIES UNDERGOING SURGERY: EFFECTS ON THE STRESS RESPONSE Kanwaljeet J. S. Anand, Wolfgang G. Sippell, Albert Aynsley-Green · The Lancet	1987	751
8	Worldwide variations in prevalence of symptoms of allergic rhinoconjunctivitis in children: the International Study of Asthma and Allergies in Childhood (ISAAC) David Peter Strachan et al. · Pediatric Allergy and Immunology	Nov 1997	656
9	Barttin is a Cl- channel β-subunit crucial for renal Cl- reabsorption and inner ear K+ secretion Raúl Estévez, Thomas Boettger, Valentin Stein et al. · Nature	29 Nov 2001	579
10	Mucopolysaccharidosis type II (Hunter syndrome): a clinical review and recommendations for treatment in the era of enzyme replacement therapy James Edmond Wraith, Maurizio Scarpa, Michael Beck et al. · European Journal of Pediatrics Open access	22 Nov 2007	537
11	Indoor allergen exposure is a risk factor for sensitization during the first three years of life Ulrich Wahn, Susanne Lau, Renate L. Bergmann et al. · Journal of Allergy and Clinical Immunology	Jun 1997	524
12	Reexpression of Cartilage-Specific Genes by Dedifferentiated Human Articular Chondrocytes Cultured in Alginate Beads Jacky Bonaventure, N. Kadhom, L Cohen-Solal et al. · Experimental Cell Research	May 1994	524
13	Epstein-Barr virus-associated Hodgkin's disease: Epidemiologic characteristics in international data Sally Louise Glaser, Ruby J. Lin, SUSAN LEROY STEWART et al. · International Journal of Cancer Open access	7 Feb 1997	501
14	Interleukin‐6 and α‐2‐macroglobulin indicate an acute‐phase state in Alzheimer's disease cortices Joachim Bauer, Sylvia Strauss, Ursula Schreiter-Gasser et al. · FEBS Letters Open access	8 Jul 1991	484
15	A gene (RPGR) with homology to the RCC1 guanine nucleotide exchange factor is mutated in X–linked retinitis pigmentosa (RP3) A Meindl, Katherine L. Dry, Karin Anna Herrmann et al. · Nature Genetics	May 1996	483
16	Regulation of chondrocyte differentiation by Cbfa1 I.S Kim, F Otto, Bernhard Zabel et al. · Mechanisms of Development Open access	Feb 1999	460
17	Cleidocranial dysplasia: clinical and molecular genetics Stefan Mundlos · Journal of Medical Genetics Open access	Mar 1999	420
18	Creatine Deficiency in the Brain: A New, Treatable Inborn Error of Metabolism Sylvia Stöckler, Ulrike Holzbach, Folker A. Hanefeld et al. · Pediatric Research	Sep 1994	419
19	Anaphylaxis: Case definition and guidelines for data collection, analysis, and presentation of immunization safety data Jens U. Rüggeberg, Michael Gold, José-María Bayas et al. · Vaccine	13 Mar 2007	387
20	THALIDOMIDE AND CONGENITAL ABNORMALITIES Widukind Lenz, RudolfA. Pfeiffer, Wilhelm Kosenow et al. · The Lancet	1962	379
21	Long-term results of the co-operative German–Austrian–Swiss osteosarcoma study group’s protocol COSS-86 of intensive multidrug chemotherapy and surgery for osteosarcoma of the limbs Nicola Fuchs, Stefan S. Bielack, D. Epler et al. · Annals of Oncology Open access	Aug 1998	349
22	Early Treatment With Alglucosidase Alfa Prolongs Long-Term Survival of Infants With Pompe Disease Priya Sunil Kishnani, Deya Corzo, Nancy D. Leslie et al. · Pediatric Research Open access	11 Aug 2009	348
23	Mutant chromatin remodeling protein SMARCAL1 causes Schimke immuno-osseous dysplasia Cornelius F. Boerkoel et al. · Nature Genetics	22 Jan 2002	334
24	SLC39A8 Deficiency: A Disorder of Manganese Transport and Glycosylation Julien H. Park et al. · The American Journal of Human Genetics Open access	Dec 2015	323
25	Population-based epidemiologic data on brain tumors in German children Peter Kaatsch, Christian H. Rickert, Joachim K�hl et al. · Cancer Open access	2001	311
26	Effects of an artificial magnetic field on serotonin N-acetyltransferase activity and melatonin content of the rat pineal gland Horst A. Welker, Peter Semm, Rolf Peter Willig et al. · Experimental Brain Research	May 1983	284
27	Atypical X-Linked Severe Combined Immunodeficiency Due to Possible Spontaneous Reversion of the Genetic Defect in T Cells Volker Stephan, Volker Wahn, Françoise Le Deist et al. · New England Journal of Medicine	21 Nov 1996	272
28	Congenital disorders of glycosylation (CDG): Quo vadis? Romain Péanne, Pascale de Lonlay, François Foulquier et al. · European Journal of Medical Genetics Open access	25 Oct 2017	271
29	TRAIL induced survival and proliferation in cancer cells resistant towards TRAIL-induced apoptosis mediated by NF-κB Harald Ehrhardt, Simone Fulda, Irene Schmid et al. · Oncogene	17 Jun 2003	270
30	Insulin sensitivity and secretion in normal children related to size at birth, postnatal growth, and plasma insulin-like growth factor-I levels Ken K. Ong, Clive J. Petry, Pauline M. Emmett et al. · Diabetologia Open access	19 May 2004	268
31	Die Corticosteroid-abhängige Dezimierung der Leukämiezellzahl im Blut als Prognosefaktor bei der akuten lymphoblastischen Leukämie im Kindesalter (Therapiestudie ALL-BFM 83) H. Riehm, Alfred Reiter, Martin Schrappe et al. · Klinische Pädiatrie	May 1987	265
32	Distinct spectrum of CFTR gene mutations in congenital absence of vas deferens Thilo Dörk, Bernd Dworniczak, C. Aulehla‐Scholz et al. · Human Genetics	4 Aug 1997	257
33	The type II collagenopathies: A spectrum of chondrodysplasias Jürgen W. Spranger, Andreas Winterpacht, Bernhard Zabel · European Journal of Pediatrics	Feb 1994	254
34	Malformations in newborn: results based on 30940 infants and fetuses from the Mainz congenital birth defect monitoring system (1990-1998) Annette Queißer‐Luft, Gabriela Stolz, Awi Wiesel et al. · Archives of Gynecology and Obstetrics	Jul 2002	254
35	Testosterone Substitution Normalizes Elevated Serum Leptin Levels in Hypogonadal Men Friedrich Jockenhövel, Werner Friedrich Blum, Elisabeth Vogel et al. · The Journal of Clinical Endocrinology & Metabolism	Aug 1997	251
36	Blood pressure in childhood: pooled findings of six European studies Robert A de Man, J Andr, H. Bachmann et al. · Journal of Hypertension	Feb 1991	246
37	Heterozygous mutations in ANKH, the human ortholog of the mouse progressive ankylosis gene, result in craniometaphyseal dysplasia Peter Nürnberg, Hölger Thiele, David Chandler et al. · Nature Genetics	May 2001	244
38	A Homozygous Mutation in Human PRICKLE1 Causes an Autosomal-Recessive Progressive Myoclonus Epilepsy-Ataxia Syndrome Alexander G. Bassuk et al. · The American Journal of Human Genetics Open access	31 Oct 2008	242
39	The role of the iminosugar N‐butyldeoxynojirimycin (miglustat) in the management of type I (non‐neuronopathic) Gaucher disease: A position statement Timothy Martin Cox, Johannes M. F. G. Aerts, Generoso Andria et al. · Journal of Inherited Metabolic Disease	Sep 2003	239
40	Die Thalidomid-Embryopathie * Widukind Lenz, Klaus Knapp · DMW - Deutsche Medizinische Wochenschrift	Jun 1962	236
41	WNT10A Mutations Are a Frequent Cause of a Broad Spectrum of Ectodermal Dysplasias with Sex-Biased Manifestation Pattern in Heterozygotes Axel Bohring, Thomas Stamm, Christiane Spaich et al. · The American Journal of Human Genetics Open access	26 Jun 2009	235
42	Prognostic significance of tumor volume in localized Ewing's sarcoma of bone in children and adolescents Verena G�bel, H. J�rgens, G. Etsp�ler et al. · Journal of Cancer Research and Clinical Oncology Open access	Apr 1987	233
43	Noonan syndrome: growth and clinical manifestations in 144 cases Michael B. Ranke, P. H. Heidemann, C. Knupfer et al. · European Journal of Pediatrics	Dec 1988	229
44	Primary immunodeficiency diseases: An update from the International Union of Immunological Societies Primary Immunodeficiency Diseases Classification Committee Meeting in Budapest, 2005 Luigi D. Notarangelo, Jean‐Laurent Casanova, Mary Ellen Conley et al. · Journal of Allergy and Clinical Immunology Open access	Apr 2006	227
45	Pertussis in adults: frequency of transmission after household exposure Carl Heinz Wirsing von König, S Postels-Multan, H.-J. Schmitt et al. · The Lancet	Nov 1995	225
46	Fatty acid composition of mature human milk in Germany Berthold V Koletzko, Maria Mrotzek, HJ Bremer · American Journal of Clinical Nutrition	Jun 1988	222
47	Spirometric reference values for white European children and adolescents: Polgar revisited Ph. H. Quanjer, G. J. J. M. Borsboom, Bert Brunekreef et al. · Pediatric Pulmonology Open access	Feb 1995	221
48	Ankyrin–1 mutations are a major cause of dominant and recessive hereditary spherocytosis Stefan Eber, Jennifer M. Reingle González, Marcia L. Lux et al. · Nature Genetics	Jun 1996	220
49	Defizienz an den kurzen Armen eines Chromosomes Nr. 4 Ulrich M. Wolf, H. Reinwein, Renate Porsch et al. · Human Genetics	1965	212
50	The diagnosis of coeliac disease. A commentary on the current practices of members of the European Society for Paediatric Gastroenterology and Nutrition (ESPGAN). Alexander S. McNeish, Hinrich Karsten Harms, J-B Rey et al. · Archives of Disease in Childhood Open access	Oct 1979	211

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.