PubRank

S Weidinger

Author PubWeight™ 38.91‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Diagnosis and treatment of atopic dermatitis in children and adults: European Academy of Allergology and Clinical Immunology/American Academy of Allergy, Asthma and Immunology/PRACTALL Consensus Report. Allergy 2006 1.54
2 Common variants in FCER1A influence total serum IgE levels from cord blood up to six years of life. Allergy 2009 1.54
3 Microheterogeneity of serum glycoproteins and their liver precursors in patients with carbohydrate-deficient glycoprotein syndrome type I: apparent deficiencies in clusterin and serum amyloid P. J Lab Clin Med 1997 1.42
4 Invasion of human keratinocytes by Staphylococcus aureus and intracellular bacterial persistence represent haemolysin-independent virulence mechanisms that are followed by features of necrotic and apoptotic keratinocyte cell death. Br J Dermatol 2002 1.42
5 Putative association of a TLR9 promoter polymorphism with atopic eczema. Allergy 2007 1.39
6 Stratum corneum lipids, skin barrier function and filaggrin mutations in patients with atopic eczema. Allergy 2010 1.19
7 A leucine-to-proline substitution causes a defective alpha 1-antichymotrypsin allele associated with familial obstructive lung disease. Genomics 1993 1.15
8 Alpha-1-antitrypsin: evidence for a fifth PI M subtype and a new deficiency allele PI*Z augsburg. Hum Genet 1985 1.11
9 Analysis of the high affinity IgE receptor genes reveals epistatic effects of FCER1A variants on eczema risk. Allergy 2009 1.01
10 Oral mannose therapy persistently corrects the severe clinical symptoms and biochemical abnormalities of phosphomannose isomerase deficiency. Acta Paediatr 2002 1.01
11 Role of Staphylococcus aureus surface-associated proteins in the attachment to cultured HaCaT keratinocytes in a new adhesion assay. J Invest Dermatol 1998 1.00
12 Agarose gel isoelectrofocusing of UDP-galactose pyrophosphorylase and galactose-1-phosphate uridyltransferase. Developmental aspect of UDP-galactose pyrophosphorylase. Clin Chim Acta 1987 0.97
13 Mis-sense mutation of alpha 1-antichymotrypsin gene associated with chronic lung disease. Lancet 1992 0.95
14 Allotypes of alpha 1-antitrypsin in patients with cystic fibrosis, homozygous and heterozygous for deltaF508. Pediatr Pulmonol 1994 0.95
15 Association of single nucleotide polymorphisms in the diamine oxidase gene with diamine oxidase serum activities. Allergy 2011 0.92
16 Identification and DNA sequence analysis of 15 new alpha 1-antitrypsin variants, including two PI*Q0 alleles and one deficient PI*M allele. Am J Hum Genet 1994 0.91
17 Integrative genetic and metabolite profiling analysis suggests altered phosphatidylcholine metabolism in asthma. Allergy 2013 0.89
18 The course of eczema in children aged 5-7 years and its relation to atopy: differences between boys and girls. Br J Dermatol 2006 0.89
19 The deficient alpha-I-antitrypsin phenotype PI P is associated with an A-to-T transversion in exon III of the gene. Am J Hum Genet 1989 0.89
20 Psychoendocrine and psychoneuroimmunological mechanisms in the comorbidity of atopic eczema and attention deficit/hyperactivity disorder. Psychoneuroendocrinology 2012 0.89
21 Monocyte-derived dendritic cells from highly atopic individuals are not impaired in their pro-inflammatory response to toll-like receptor ligands. Clin Exp Allergy 2007 0.83
22 Alpha1-antitrypsin: evidence for a fourth PiM allele. Distribution of the PiM subtypes in Southern Germany. Z Rechtsmed 1982 0.83
23 Molecular characterisation of the defective alpha 1-antitrypsin alleles PI Mwurzburg (Pro369Ser), Mheerlen (Pro369Leu), and Q0lisbon (Thr68Ile). Eur J Hum Genet 1999 0.83
24 DNA polymorphisms associated with a new alpha 1-antitrypsin PIQ0 variant (PIQ0riedenburg). Hum Genet 1991 0.82
25 Epidemiology of urticaria in infants and young children in Germany--results from the German LISAplus and GINIplus Birth Cohort Studies. Pediatr Allergy Immunol 2013 0.81
26 Two new Bf S subtypes revealed by isoelectric focusing and immunofixation. Hum Genet 1984 0.80
27 Sequence data of the rare deficient alpha 1-antitrypsin variant PI Zaugsburg. Am J Hum Genet 1990 0.80
28 Properdin factor B-polymorphism. An indication for the existence of a Bf O-allele. Z Rechtsmed 1979 0.80
29 Increased efficacy of omalizumab in atopic dermatitis patients with wild-type filaggrin status and higher serum levels of phosphatidylcholines. Allergy 2013 0.80
30 Identification and molecular characterization of the new alpha-1-antitrypsin deficient allele PI Y barcelona (Asp256-->Val and Pro391-->His). Mutations in brief no. 174. Online. Hum Mutat 1998 0.79
31 Itches and scratches – is there a link between eczema, ADHD, sleep disruption and food hypersensitivity? Allergy 2011 0.79
32 [Diagnosis and nosology of glycanosis CDG ("carbohydrate deficient glycoprotein syndrome")]. Monatsschr Kinderheilkd 1992 0.78
33 Orosomucoid system: 17 additional orosomucoid variants and proposal for a new nomenclature. Vox Sang 1993 0.78
34 What is Pi (proteinase inhibitor) null or PiQO?: a problem highlighted by the alpha 1 antitrypsin Mheerlen mutation. J Med Genet 1992 0.78
35 GSTM1, GSTT1 and GSTP1 gene polymorphism in polymorphous light eruption. J Eur Acad Dermatol Venereol 2012 0.77
36 Isoelectric focusing with immobilized pH gradients for the analysis of transferrin (Tf) subtypes and variants. Hum Genet 1983 0.77
37 AIDS: no association with the genetic systems GC (D-binding protein), ORM (orosomucoid = alpha-1-acid glycoprotein), and A2HS (alpha-2-HS-glycoprotein). Infection 1988 0.77
38 Characterisation of the alpha-1-antitrypsin M3 gene, a normal variant. Hum Genet 1990 0.77
39 A common atopy-associated variant in the Th2 cytokine locus control region impacts transcriptional regulation and alters SMAD3 and SP1 binding. Allergy 2014 0.76
40 Characterization of the normal alpha 1-antitrypsin allele Vmunich: a variant associated with a unique protein isoelectric focusing pattern. Am J Hum Genet 1990 0.76
41 Genetic polymorphism in the Garfagnana population (Tuscany). Gene Geogr 1993 0.76
42 A "new" allele of esterase D in a retinoblastoma family. Hum Genet 1988 0.75
43 [Early childhood oligoarthritis (antinuclear antibody positive) in alpha 1-antitrypsin deficiency of the PiIZ type]. Monatsschr Kinderheilkd 1989 0.75
44 Variation of alpha 1-antitrypsin glycoprotein microheterogeneity in hepatic postresuscitation disease. Eur J Pediatr 1990 0.75
45 Alpha-1-antitrypsin deficiency in children: liver disease is not reflected by low serum levels of alpha-1-antitrypsin - a study on 48 pediatric patients. Eur J Med Res 2005 0.75
46 Description of a new variant in the glutamate-oxaloacetate transaminase system by thin-layer agarose gel isoelectric focusing. Electrophoresis 1991 0.75
47 A1/A2 blood group variant due to fucosylation deficiency in carbohydrate deficient glycoprotein syndrome type I? Eur J Pediatr 1999 0.75
48 Genetic study of orosomucoid by isoelectric focusing and immunoprinting in patients with carcinoma. Electrophoresis 1993 0.75
49 Hypothyroidism phenocopy in glycanosis CDG (carbohydrate-deficient glycoprotein syndrome) Eur J Pediatr 1994 0.75
50 Apolipoprotein J deficiency in types I and IV carbohydrate-deficient glycoprotein syndrome (glycanosis CDG) Eur J Pediatr 1997 0.75
51 Extended polymorphism of the human esterase D isozyme system: description of a "new" allele EsD*11. Hum Genet 1986 0.75
52 PGM1 subtypes determined by agarose gel isoelectrofocusing. Z Rechtsmed 1980 0.75
53 Plasminogen (PLG): a useful genetic marker for paternity examinations. Z Rechtsmed 1985 0.75
54 Pericardial effusion in glycanosis CDG type I (MIM 212 065): an inflammatory endoplasmic reticulum overload response? Eur J Pediatr 1998 0.75
55 PI Scologne: a new variant in the alpha-1-antitrypsin system. Hum Genet 1988 0.75
56 [New insights into the pathogenesis of sensitive skin]. Hautarzt 2011 0.75
57 New mutation versus exclusion at the alpha-1-antitrypsin locus: a multifaceted approach in a problematical paternity case. Hum Hered 1991 0.75
58 [Demonstration of glyoxalase I (EC 4.4.1.5) in starch gel electrophoresis]. Med Lab (Stuttg) 1976 0.75
59 [Detection of tyrosinase mRNA using reverse transcription/polymerase chain reaction with fine needle punctures of melanoma metastases]. Hautarzt 1996 0.75
60 Transferrin variants in Tuscany (Italy). Evidence for two "new" Tf alleles. Hum Genet 1985 0.75
61 A case of junctional epidermolysis bullosa with prurigo-like lesions and reduction of collagen XVII and filaggrin. Br J Dermatol 2013 0.75
62 [Genome-associated studies in chronic inflammatory dermatoses]. Internist (Berl) 2014 0.75
63 Pi subtyping by isoelectric focusing: further genetic studies and application to paternity examinations. Z Rechtsmed 1980 0.75
64 [Genetics of common chronic inflammatory skin diseases : An update on atopic dermatitis and psoriasis]. Hautarzt 2011 0.75
65 Transferrin subtypes and variants in Germany; further evidence for a Tf null allele. Hum Genet 1984 0.75
66 [Dynamic measurement of pressure distribution on the foot sole of diabetic patients and a comparison group]. Wien Klin Wochenschr 1991 0.75
67 Association between atopy and cryptorchidism. J Allergy Clin Immunol 2004 0.75
68 Genetic polymorphism of alpha-2-HS-glycoprotein in a Spanish population. Hum Hered 1991 0.75
69 Classification of transferrin (Tf) subtypes by isoelectric focusing. Z Rechtsmed 1980 0.75
70 Distribution of C3 and Bf allotypes in Tuscany (Italy). Hum Hered 1986 0.75
71 PGD Port Elizabeth: a new variant found in South Africa. Hum Genet 1992 0.75
72 High-dose intravenous melphalan in a patient with multiple myeloma and oliguric renal failure. Clin Investig 1994 0.75
73 Subtyping of orosomucoid 1 (ORM1) by isoelectric focusing in agarose and polyacrylamide gels. Electrophoresis 1988 0.75
74 "New" phenotypes in the human red cell isozyme system ADA. Z Rechtsmed 1986 0.75
75 Evidence for a new allele at the esterase D (E.C.3.1.1.1) locus. Hum Hered 1988 0.75
76 Transient aberrancy of alpha 1-antitrypsin glycoprotein microheterogeneity in Pseudomonas aeruginosa septicaemia. Infection 1991 0.75
77 [Alcoholic ketoacidosis--3 episodes in one patient]. Wien Klin Wochenschr 1992 0.75
78 [Genetics of atopic eczema. An update]. Hautarzt 2015 0.75