A citation-based method for searching scientific literature

S Saitoh, N Harada, Y Jinno, K Hashimoto, K Imaizumi, Y Kuroki, Y Fukushima, T Sugimoto, M Renedo, J Wagstaff. Am J Med Genet 1994
Times Cited: 72







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



Times Cited
  Times     Co-cited
Similarity



Angelman syndrome: consensus for diagnostic criteria. Angelman Syndrome Foundation.
C A Williams, H Angelman, J Clayton-Smith, D J Driscoll, J E Hendrickson, J H Knoll, R E Magenis, A Schinzel, J Wagstaff, E M Whidden. Am J Med Genet 1995
252
36

UBE3A/E6-AP mutations cause Angelman syndrome.
T Kishino, M Lalande, J Wagstaff. Nat Genet 1997
877
34

Clinical features in 27 patients with Angelman syndrome resulting from DNA deletion.
A Smith, C Wiles, E Haan, J McGill, G Wallace, J Dixon, R Selby, A Colley, R Marks, R J Trent. J Med Genet 1996
80
34

De novo truncating mutations in E6-AP ubiquitin-protein ligase gene (UBE3A) in Angelman syndrome.
T Matsuura, J S Sutcliffe, P Fang, R J Galjaard, Y H Jiang, C S Benton, J M Rommens, A L Beaudet. Nat Genet 1997
607
29

Distinct phenotypes distinguish the molecular classes of Angelman syndrome.
A C Lossie, M M Whitney, D Amidon, H J Dong, P Chen, D Theriaque, A Hutson, R D Nicholls, R T Zori, C A Williams,[...]. J Med Genet 2001
228
26

Angelman syndrome.
J Clayton-Smith, M E Pembrey. J Med Genet 1992
150
25

Angelman syndrome due to paternal uniparental disomy of chromosome 15: a milder phenotype?
A Bottani, W P Robinson, C D DeLozier-Blanchet, E Engel, M A Morris, B Schmitt, L Thun-Hohenstein, A Schinzel. Am J Med Genet 1994
95
23

The EEG in early diagnosis of the Angelman (happy puppet) syndrome.
S G Boyd, A Harden, M A Patton. Eur J Pediatr 1988
174
22

Angelman and Prader-Willi syndromes share a common chromosome 15 deletion but differ in parental origin of the deletion.
J H Knoll, R D Nicholls, R E Magenis, J M Graham, M Lalande, S A Latt. Am J Med Genet 1989
452
22

Inherited microdeletions in the Angelman and Prader-Willi syndromes define an imprinting centre on human chromosome 15.
K Buiting, S Saitoh, S Gross, B Dittrich, S Schwartz, R D Nicholls, B Horsthemke. Nat Genet 1995
470
22

Angelman syndrome: clinical profile.
R T Zori, J Hendrickson, S Woolven, E M Whidden, B Gray, C A Williams. J Child Neurol 1992
71
21

Clinical profile of Angelman syndrome at different ages.
I M Buntinx, R C Hennekam, O F Brouwer, H Stroink, J Beuten, K Mangelschots, J P Fryns. Am J Med Genet 1995
104
20

Mutations of the P gene in oculocutaneous albinism, ocular albinism, and Prader-Willi syndrome plus albinism.
S T Lee, R D Nicholls, S Bundey, R Laxova, M Musarella, R A Spritz. N Engl J Med 1994
164
20

Hypopigmentation in the Prader-Willi syndrome correlates with P gene deletion but not with haplotype of the hemizygous P allele.
R A Spritz, T Bailin, R D Nicholls, S T Lee, S K Park, M J Mascari, M G Butler. Am J Med Genet 1997
75
20

Uniparental paternal disomy in Angelman's syndrome.
S Malcolm, J Clayton-Smith, M Nichols, S Robb, T Webb, J A Armour, A J Jeffreys, M E Pembrey. Lancet 1991
263
20

Gene structure, DNA methylation, and imprinted expression of the human SNRPN gene.
C C Glenn, S Saitoh, M T Jong, M M Filbrandt, U Surti, D J Driscoll, R D Nicholls. Am J Hum Genet 1996
191
19

A gene for the mouse pink-eyed dilution locus and for human type II oculocutaneous albinism.
E M Rinchik, S J Bultman, B Horsthemke, S T Lee, K M Strunk, R A Spritz, K M Avidano, M T Jong, R D Nicholls. Nature 1993
323
19

Deletions of a differentially methylated CpG island at the SNRPN gene define a putative imprinting control region.
J S Sutcliffe, M Nakao, S Christian, K H Orstavik, N Tommerup, D H Ledbetter, A L Beaudet. Nat Genet 1994
369
18


Angelman syndrome 2005: updated consensus for diagnostic criteria.
Charles A Williams, Arthur L Beaudet, Jill Clayton-Smith, Joan H Knoll, Martin Kyllerman, Laura A Laan, R Ellen Magenis, Ann Moncla, Albert A Schinzel, Jane A Summers,[...]. Am J Med Genet A 2006
332
18

Molecular mechanisms in Angelman syndrome: a survey of 93 patients.
C T Chan, J Clayton-Smith, X J Cheng, J Buxton, T Webb, M E Pembrey, S Malcolm. J Med Genet 1993
57
21

Imprinting in Prader-Willi and Angelman syndromes.
R D Nicholls, S Saitoh, B Horsthemke. Trends Genet 1998
308
16

Angelman syndrome: correlations between epilepsy phenotypes and genotypes.
B A Minassian, T M DeLorey, R W Olsen, M Philippart, Y Bronstein, Q Zhang, R Guerrini, P Van Ness, M O Livet, A V Delgado-Escueta. Ann Neurol 1998
136
16

The 'happy puppet' syndrome of Angelman: review of the clinical features.
S A Robb, K R Pohl, M Baraitser, J Wilson, E M Brett. Arch Dis Child 1989
54
20

Paternal uniparental disomy in a child with a balanced 15;15 translocation and Angelman syndrome.
S B Freeman, K M May, D Pettay, P M Fernhoff, T J Hassold. Am J Med Genet 1993
50
22


Diagnosis of Angelman syndrome in infants.
J S Fryburg, W R Breg, V Lindgren. Am J Med Genet 1991
65
16

Imprinting mutations suggested by abnormal DNA methylation patterns in familial Angelman and Prader-Willi syndromes.
A Reis, B Dittrich, V Greger, K Buiting, M Lalande, G Gillessen-Kaesbach, M Anvret, B Horsthemke. Am J Hum Genet 1994
188
15

Modification of 15q11-q13 DNA methylation imprints in unique Angelman and Prader-Willi patients.
C C Glenn, R D Nicholls, W P Robinson, S Saitoh, N Niikawa, A Schinzel, B Horsthemke, D J Driscoll. Hum Mol Genet 1993
122
15

Molecular diagnosis of the Prader-Willi and Angelman syndromes by detection of parent-of-origin specific DNA methylation in 15q11-13.
B Dittrich, W P Robinson, H Knoblauch, K Buiting, K Schmidt, G Gillessen-Kaesbach, B Horsthemke. Hum Genet 1992
187
15

Mice lacking the beta3 subunit of the GABAA receptor have the epilepsy phenotype and many of the behavioral characteristics of Angelman syndrome.
T M DeLorey, A Handforth, S G Anagnostaras, G E Homanics, B A Minassian, A Asatourian, M S Fanselow, A Delgado-Escueta, G D Ellison, R W Olsen. J Neurosci 1998
327
13

Novel mutations of the P gene in type II oculocutaneous albinism (OCA2).
R A Spritz, S T Lee, K Fukai, K Brondum-Nielsen, D Chitayat, M H Lipson, M A Musarella, A Rosenmann, R G Weleber. Hum Mutat 1997
26
38






Association of the FcepsilonRIbeta gene with bronchial hyper-responsiveness in an Italian population.
E Trabetti, V Cusin, G Malerba, L C Martinati, A Casartelli, A L Boner, P F Pignatti. J Med Genet 1998
33
27

Hearing loss in Townes-Brocks syndrome.
D R Rossmiller, T R Pasic. Otolaryngol Head Neck Surg 1994
27
33



Variability of biochemical and clinical phenotype in X-linked liver glycogenosis with mutations in the phosphorylase kinase PHKA2 gene.
B Burwinkel, L Amat, R G Gray, N Matsuo, K Muroya, K Narisawa, R J Sokol, M A Vilaseca, M W Kilimann. Hum Genet 1998
46
19

Evidence that WT1 mutations in Denys-Drash syndrome patients may act in a dominant-negative fashion.
M H Little, K A Williamson, M Mannens, A Kelsey, C Gosden, N D Hastie, V van Heyningen. Hum Mol Genet 1993
127
12


Townes-Brocks syndrome in two mentally retarded youngsters.
T H Cameron, A M Lachiewicz, A S Aylsworth. Am J Med Genet 1991
31
29


p53 abnormalities in B-cell prolymphocytic leukemia.
D Lens, P J De Schouwer, R A Hamoudi, M Abdul-Rauf, N Farahat, E Matutes, T Crook, M J Dyer, D Catovsky. Blood 1997
78
12

STAT6: its role in interleukin 4-mediated biological functions.
K Takeda, T Kishimoto, S Akira. J Mol Med (Berl) 1997
96
12



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.