A citation-based method for searching scientific literature

S L Christian, W P Robinson, B Huang, A Mutirangura, M R Line, M Nakao, U Surti, A Chakravarti, D H Ledbetter. Am J Hum Genet 1995
Times Cited: 157







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



Times Cited
  Times     Co-cited
Similarity


Chromosome breakage in the Prader-Willi and Angelman syndromes involves recombination between large, transcribed repeats at proximal and distal breakpoints.
J M Amos-Landgraf, Y Ji, W Gottlieb, T Depinet, A E Wandstrat, S B Cassidy, D J Driscoll, P K Rogan, S Schwartz, R D Nicholls. Am J Hum Genet 1999
200
49

Autism or atypical autism in maternally but not paternally derived proximal 15q duplication.
E H Cook, V Lindgren, B L Leventhal, R Courchesne, A Lincoln, C Shulman, C Lord, E Courchesne. Am J Hum Genet 1997
469
31

Behavioral differences among subjects with Prader-Willi syndrome and type I or type II deletion and maternal disomy.
Merlin G Butler, Douglas C Bittel, Nataliya Kibiryeva, Zohreh Talebizadeh, Travis Thompson. Pediatrics 2004
171
29

Large genomic duplicons map to sites of instability in the Prader-Willi/Angelman syndrome chromosome region (15q11-q13).
S L Christian, J A Fantes, S K Mewborn, B Huang, D H Ledbetter. Hum Mol Genet 1999
192
28

Refined molecular characterization of the breakpoints in small inv dup(15) chromosomes.
B Huang, J A Crolla, S L Christian, M E Wolf-Ledbetter, M E Macha, P N Papenhausen, D H Ledbetter. Hum Genet 1997
93
30

Inherited interstitial duplications of proximal 15q: genotype-phenotype correlations.
C E Browne, N R Dennis, E Maher, F L Long, J C Nicholson, J Sillibourne, J C Barber. Am J Hum Genet 1997
160
26


Angelman syndrome: three molecular classes identified with chromosome 15q11q13-specific DNA markers.
J H Knoll, R D Nicholls, R E Magenis, K Glatt, J M Graham, L Kaplan, M Lalande. Am J Hum Genet 1990
131
23

Imprinting-mutation mechanisms in Prader-Willi syndrome.
T Ohta, T A Gray, P K Rogan, K Buiting, J M Gabriel, S Saitoh, B Muralidhar, B Bilienska, M Krajewska-Walasek, D J Driscoll,[...]. Am J Hum Genet 1999
186
23

Interstitial duplications of chromosome region 15q11q13: clinical and molecular characterization.
G M Repetto, L M White, P J Bader, D Johnson, J H Knoll. Am J Med Genet 1998
92
23

Prader-Willi syndrome: consensus diagnostic criteria.
V A Holm, S B Cassidy, M G Butler, J M Hanchett, L R Greenswag, B Y Whitman, F Greenberg. Pediatrics 1993
862
22


Intrachromosomal triplication of 15q11-q13.
A A Schinzel, L Brecevic, F Bernasconi, F Binkert, F Berthet, A Wuilloud, W P Robinson. J Med Genet 1994
88
23


Molecular cytogenetic analysis of inv dup(15) chromosomes, using probes specific for the Prader-Willi/Angelman syndrome region: clinical implications.
J Leana-Cox, L Jenkins, C G Palmer, R Plattner, L Sheppard, W L Flejter, J Zackowski, F Tsien, S Schwartz. Am J Hum Genet 1994
102
19


The mechanisms involved in formation of deletions and duplications of 15q11-q13.
W P Robinson, F Dutly, R D Nicholls, F Bernasconi, M Peñaherrera, R C Michaelis, D Abeliovich, A A Schinzel. J Med Genet 1998
82
23


Autism and maternally derived aberrations of chromosome 15q.
R J Schroer, M C Phelan, R C Michaelis, E C Crawford, S A Skinner, M Cuccaro, R J Simensen, J Bishop, C Skinner, D Fender,[...]. Am J Med Genet 1998
273
17

Duplication of the 15q11-13 region in a patient with autism, epilepsy and ataxia.
S Bundey, C Hardy, S Vickers, M W Kilpatrick, J A Corbett. Dev Med Child Neurol 1994
121
17

The phenotypic manifestations of interstitial duplications of proximal 15q with special reference to the autistic spectrum disorders.
P F Bolton, N R Dennis, C E Browne, N S Thomas, M W Veltman, R J Thompson, P Jacobs. Am J Med Genet 2001
154
17

Genome organization, function, and imprinting in Prader-Willi and Angelman syndromes.
R D Nicholls, J L Knepper. Annu Rev Genomics Hum Genet 2001
411
17


Paternally derived de novo interstitial duplication of proximal 15q in a patient with developmental delay.
T K Mohandas, J P Park, R A Spellman, J J Filiano, A C Mamourian, A B Hawk, D R Belloni, W W Noll, J B Moeschler. Am J Med Genet 1999
76
21

Comparison of phenotype between patients with Prader-Willi syndrome due to deletion 15q and uniparental disomy 15.
S B Cassidy, M Forsythe, S Heeger, R D Nicholls, N Schork, P Benn, S Schwartz. Am J Med Genet 1997
144
15

Genetic imprinting suggested by maternal heterodisomy in nondeletion Prader-Willi syndrome.
R D Nicholls, J H Knoll, M G Butler, S Karam, M Lalande. Nature 1989
660
15

Molecular characterisation of four cases of intrachromosomal triplication of chromosome 15q11-q14.
P Ungaro, S L Christian, J A Fantes, A Mutirangura, S Black, J Reynolds, S Malcolm, W B Dobyns, D H Ledbetter. J Med Genet 2001
61
24


Prader-Willi phenotype caused by paternal deficiency for the HBII-85 C/D box small nucleolar RNA cluster.
Trilochan Sahoo, Daniela del Gaudio, Jennifer R German, Marwan Shinawi, Sarika U Peters, Richard E Person, Adolfo Garnica, Sau Wai Cheung, Arthur L Beaudet. Nat Genet 2008
371
15

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
74
18

Cytogenetic and molecular analysis of inv dup(15) chromosomes observed in two patients with autistic disorder and mental retardation.
W L Flejter, P E Bennett-Baker, M Ghaziuddin, M McDonald, S Sheldon, J L Gorski. Am J Med Genet 1996
70
20


Characterisation of interstitial duplications and triplications of chromosome 15q11-q13.
Siân E Roberts, Nicholas R Dennis, Caroline E Browne, Lionel Willatt, GeoffreyC Woods, Ian Cross, Patricia A Jacobs, SimonN Thomas. Hum Genet 2002
81
17

Psychotic illness in people with Prader Willi syndrome due to chromosome 15 maternal uniparental disomy.
Harm Boer, Anthony Holland, Joyce Whittington, Jill Butler, Tessa Webb, David Clarke. Lancet 2002
176
14

Intellectual characteristics of Prader-Willi syndrome: comparison of genetic subtypes.
E Roof, W Stone, W MacLean, I D Feurer, T Thompson, M G Butler. J Intellect Disabil Res 2000
111
14

Maternal origin of inv dup(15) chromosomes in infantile autism.
T Martinsson, T Johannesson, M Vujic, A Sjöstedt, S Steffenburg, C Gillberg, J Wahlström. Eur Child Adolesc Psychiatry 1996
39
33

Prader-Willi syndrome: intellectual abilities and behavioural features by genetic subtype.
Katja M Milner, Ellen E Craig, Russell J Thompson, Marijcke W M Veltman, N Simon Thomas, Sian Roberts, Margaret Bellamy, Sarah R Curran, Caroline M J Sporikou, Patrick F Bolton. J Child Psychol Psychiatry 2005
105
13

Prader-Willi syndrome.
Suzanne B Cassidy, Daniel J Driscoll. Eur J Hum Genet 2009
337
13



Subtle chromosomal rearrangements in children with unexplained mental retardation.
S J Knight, R Regan, A Nicod, S W Horsley, L Kearney, T Homfray, R M Winter, P Bolton, J Flint. Lancet 1999
360
12



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
324
12

Autism as a strongly genetic disorder: evidence from a British twin study.
A Bailey, A Le Couteur, I Gottesman, P Bolton, E Simonoff, E Yuzda, M Rutter. Psychol Med 1995
12

How commonly are known medical conditions associated with autism?
M Barton, F Volkmar. J Autism Dev Disord 1998
71
16

Prader-Willi syndrome.
S B Cassidy. J Med Genet 1997
290
12

Prader-Willi syndrome--a study comparing deletion and uniparental disomy cases with reference to autism spectrum disorders.
Marijcke W M Veltman, Russell J Thompson, Sian E Roberts, N Simon Thomas, Joyce Whittington, Patrick F Bolton. Eur Child Adolesc Psychiatry 2004
86
13

Methylation-specific PCR simplifies imprinting analysis.
T Kubota, S Das, S L Christian, S B Baylin, J G Herman, D H Ledbetter. Nat Genet 1997
200
11

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
11


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.