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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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.