A citation-based method for searching scientific literature

E L Wakeling, M Hitchins, P Stanier, D Monk, G E Moore, M A Preece. J Med Genet 2000
Times Cited: 19







List of co-cited articles
181 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


Variants of STAT6 (signal transducer and activator of transcription 6) in atopic asthma.
P S Gao, X Q Mao, M H Roberts, Y Arinobu, M Akaiwa, T Enomoto, Y Dake, M Kawai, S Sasaki, N Hamasaki,[...]. J Med Genet 2000
67
73

The association of atopy with a gain-of-function mutation in the alpha subunit of the interleukin-4 receptor.
G K Hershey, M F Friedrich, L A Esswein, M L Thomas, T A Chatila. N Engl J Med 1997
570
36

Essential role of Stat6 in IL-4 signalling.
K Takeda, T Tanaka, W Shi, M Matsumoto, M Minami, S Kashiwamura, K Nakanishi, N Yoshida, T Kishimoto, S Akira. Nature 1996
36

Cutting edge: dominant effect of Ile50Val variant of the human IL-4 receptor alpha-chain in IgE synthesis.
H Mitsuyasu, Y Yanagihara, X Q Mao, P S Gao, Y Arinobu, K Ihara, A Takabayashi, T Hara, T Enomoto, S Sasaki,[...]. J Immunol 1999
138
31



A cluster of seven tightly linked polymorphisms in the IL-13 gene is associated with total serum IgE levels in three populations of white children.
P E Graves, M Kabesch, M Halonen, C J Holberg, M Baldini, C Fritzsch, S K Weiland, R P Erickson, E von Mutius, F D Martinez. J Allergy Clin Immunol 2000
312
26

Variation in the interleukin 4-receptor alpha gene confers susceptibility to asthma and atopy in ethnically diverse populations.
C Ober, S A Leavitt, A Tsalenko, T D Howard, D M Hoki, R Daniel, D L Newman, X Wu, R Parry, L A Lester,[...]. Am J Hum Genet 2000
207
26

Genetic variants of IL-13 signalling and human asthma and atopy.
A Heinzmann, X Q Mao, M Akaiwa, R T Kreomer, P S Gao, K Ohshima, R Umeshita, Y Abe, S Braun, T Yamashita,[...]. Hum Mol Genet 2000
332
26

Lack of IL-4-induced Th2 response and IgE class switching in mice with disrupted Stat6 gene.
K Shimoda, J van Deursen, M Y Sangster, S R Sarawar, R T Carson, R A Tripp, C Chu, F W Quelle, T Nosaka, D A Vignali,[...]. Nature 1996
26

Novel dinucleotide repeat polymorphism in the first exon of the STAT-6 gene is associated with allergic diseases.
K Tamura, H Arakawa, M Suzuki, Y Kobayashi, H Mochizuki, M Kato, K Tokuyama, A Morikawa. Clin Exp Allergy 2001
63
26


Identification of the Meg1/Grb10 imprinted gene on mouse proximal chromosome 11, a candidate for the Silver-Russell syndrome gene.
N Miyoshi, Y Kuroiwa, T Kohda, H Shitara, H Yonekawa, T Kawabe, H Hasegawa, S C Barton, M A Surani, T Kaneko-Ishino,[...]. Proc Natl Acad Sci U S A 1998
127
21

Maternal uniparental disomy 7 in Silver-Russell syndrome.
M A Preece, S M Price, V Davies, L Clough, P Stanier, R C Trembath, G E Moore. J Med Genet 1997
136
21

Uniparental disomy 7 in Silver-Russell syndrome and primordial growth retardation.
D Kotzot, S Schmitt, F Bernasconi, W P Robinson, I W Lurie, H Ilyina, K Méhes, B C Hamel, B J Otten, M Hergersberg. Hum Mol Genet 1995
248
21

An analysis of the distribution of hetero- and isodisomic regions of chromosome 7 in five mUPD7 Silver-Russell syndrome probands.
M A Preece, S N Abu-Amero, Z Ali, K K Abu-Amero, E L Wakeling, P Stanier, G E Moore. J Med Genet 1999
44
21


Ile50Val variant of IL4R alpha upregulates IgE synthesis and associates with atopic asthma.
H Mitsuyasu, K Izuhara, X Q Mao, P S Gao, Y Arinobu, T Enomoto, M Kawai, S Sasaki, Y Dake, N Hamasaki,[...]. Nat Genet 1998
290
21



An IL-13 promoter polymorphism associated with increased risk of allergic asthma.
T C van der Pouw Kraan, A van Veen, L C Boeije, S A van Tuyl, E R de Groot, S O Stapel, A Bakker, C L Verweij, L A Aarden, J S van der Zee. Genes Immun 1999
216
21

Maternal uniparental disomy 7--review and further delineation of the phenotype.
D Kotzot, D Balmer, A Baumer, K Chrzanowska, B C Hamel, H Ilyina, M Krajewska-Walasek, I W Lurie, B J Otten, E Schoenle,[...]. Eur J Pediatr 2000
49
21

A gain-of-function mutation in STAT6.
C Daniel, A Salvekar, U Schindler. J Biol Chem 2000
49
21

STAT6 as an asthma candidate gene: polymorphism-screening, association and haplotype analysis in a Caucasian sib-pair study.
Gabriele Duetsch, Thomas Illig, Sabine Loesgen, Klaus Rohde, Norman Klopp, Nicole Herbon, Henning Gohlke, Janine Altmueller, Matthias Wjst. Hum Mol Genet 2002
80
21

An interstitial deletion of proximal 8q (q11-q13) in a girl with Silver-Russell syndrome-like features.
A A Schinzel, W P Robinson, F Binkert, A Fanconi. Clin Dysmorphol 1994
31
15

Biallelic expression of IGFBP1 and IGFBP3, two candidate genes for the Silver-Russell syndrome.
E L Wakeling, M P Hitchins, S N Abu-Amero, P Stanier, G E Moore, M A Preece. J Med Genet 2000
21
15



Distinct 15q genotypes in Russell-Silver and ring 15 syndromes.
P K Rogan, J R Seip, D J Driscoll, P R Papenhausen, V P Johnson, S Raskin, A L Woodward, M G Butler. Am J Med Genet 1996
39
15



Linkage analysis of IL4 and other chromosome 5q31.1 markers and total serum immunoglobulin E concentrations.
D G Marsh, J D Neely, D R Breazeale, B Ghosh, L R Freidhoff, E Ehrlich-Kautzky, C Schou, G Krishnaswamy, T H Beaty. Science 1994
853
15

Atopy and asthma: genetic variants of IL-4 and IL-13 signalling.
I Shirakawa, K A Deichmann, I Izuhara, I Mao, C N Adra, J M Hopkin. Immunol Today 2000
213
15

Interleukin-13: central mediator of allergic asthma.
M Wills-Karp, J Luyimbazi, X Xu, B Schofield, T Y Neben, C L Karp, D D Donaldson. Science 1998
15

Association between a C+33T polymorphism in the IL-4 promoter region and total serum IgE levels.
I Suzuki, N Hizawa, E Yamaguchi, Y Kawakami. Clin Exp Allergy 2000
56
15


Lack of association of atopy/asthma and the interleukin-4 receptor alpha gene in Japanese.
E Noguchi, M Shibasaki, T Arinami, K Takeda, Y Yokouchi, K Kobayashi, N Imoto, S Nakahara, A Matsui, H Hamaguchi. Clin Exp Allergy 1999
35
15

Localization of the human stat6 gene to chromosome 12q13.3-q14.1, a region implicated in multiple solid tumors.
B K Patel, C L Keck, R S O'Leary, N C Popescu, W J LaRochelle. Genomics 1998
40
15


The spectrum of Silver-Russell syndrome: a clinical and molecular genetic study and new diagnostic criteria.
S M Price, R Stanhope, C Garrett, M A Preece, R C Trembath. J Med Genet 1999
175
15

Isoform-specific imprinting of the human PEG1/MEST gene.
K Kosaki, R Kosaki, W J Craigen, N Matsuo. Am J Hum Genet 2000
61
15


Duplication of 7p11.2-p13, including GRB10, in Silver-Russell syndrome.
D Monk, E L Wakeling, V Proud, M Hitchins, S N Abu-Amero, P Stanier, M A Preece, G E Moore. Am J Hum Genet 2000
106
15

Uniparental isodisomy for paternal 7p and maternal 7q in a child with growth retardation.
F A Eggerding, S A Schonberg, F F Chehab, M E Norton, V A Cox, C J Epstein. Am J Hum Genet 1994
76
15



Paternal isodisomy of chromosome 7 associated with complete situs inversus and immotile cilia.
Y Pan, C D McCaskill, K H Thompson, J Hicks, B Casey, L G Shaffer, W J Craigen. Am J Hum Genet 1998
65
15

Human EGFR, a candidate gene for the Silver-Russell syndrome, is biallelically expressed in a wide range of fetal tissues.
E L Wakeling, S N Abu-Amero, P Stanier, M A Preece, G E Moore. Eur J Hum Genet 1998
34
15


Biparental expression of IGFBP1 and IGFBP3 renders their involvement in the etiology of Silver-Russell syndrome unlikely.
K Eggermann, H A Wollmann, G Binder, P Kaiser, M B Ranke, T Eggermann. Ann Genet 1999
10
30


Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.