A citation-based method for searching scientific literature

S Soni, J Whittington, A J Holland, T Webb, E N Maina, H Boer, D Clarke. Psychol Med 2008
Times Cited: 74







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



Times Cited
  Times     Co-cited
Similarity


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
54

The course and outcome of psychiatric illness in people with Prader-Willi syndrome: implications for management and treatment.
S Soni, J Whittington, A J Holland, T Webb, E Maina, H Boer, D Clarke. J Intellect Disabil Res 2007
89
47

Chromosome 15 maternal uniparental disomy and psychosis in Prader-Willi syndrome.
A Vogels, G Matthijs, E Legius, K Devriendt, J-P Fryns. J Med Genet 2003
76
31



Prader-Willi syndrome.
Suzanne B Cassidy, Daniel J Driscoll. Eur J Hum Genet 2009
337
25

Psychotic disorders in Prader-Willi syndrome.
A Vogels, M De Hert, M J Descheemaeker, V Govers, K Devriendt, E Legius, P Prinzie, J P Fryns. Am J Med Genet A 2004
59
30

Recommendations for the diagnosis and management of Prader-Willi syndrome.
A P Goldstone, A J Holland, B P Hauffa, A C Hokken-Koelega, M Tauber. J Clin Endocrinol Metab 2008
278
24

Psychiatric illness in a cohort of adults with Prader-Willi syndrome.
Margje Sinnema, Harm Boer, Philippe Collin, Marian A Maaskant, Kees E P van Roozendaal, Constance T R M Schrander-Stumpel, Leopold M G Curfs. Res Dev Disabil 2011
50
34

Behavior in Prader-Willi syndrome: relationship to genetic subtypes and age.
Elisabeth M Dykens, Elizabeth Roof. J Child Psychol Psychiatry 2008
77
21

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
172
20

Prader-Willi syndrome, compulsive and ritualistic behaviours: the first population-based survey.
D J Clarke, H Boer, J Whittington, A Holland, J Butler, T Webb. Br J Psychiatry 2002
91
18

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
867
18

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
373
18

Prader-Willi syndrome.
Suzanne B Cassidy, Stuart Schwartz, Jennifer L Miller, Daniel J Driscoll. Genet Med 2012
618
18

Cognitive abilities and genotype in a population-based sample of people with Prader-Willi syndrome.
J Whittington, A Holland, T Webb, J Butler, D Clarke, H Boer. J Intellect Disabil Res 2004
107
17

In search of the psychosis gene in people with Prader-Willi syndrome.
Tessa Webb, Esther N Maina, Sarita Soni, Joyce Whittington, Harm Boer, David Clarke, Anthony Holland. Am J Med Genet A 2008
23
56

Minimum prevalence, birth incidence and cause of death for Prader-Willi syndrome in Flanders.
Annick Vogels, Jenneke Van Den Ende, Kathelijne Keymolen, Geert Mortier, Koen Devriendt, E Legius, J P Fryns. Eur J Hum Genet 2004
115
16

Birth prevalence of Prader-Willi syndrome in Australia.
A Smith, J Egan, G Ridley, E Haan, P Montgomery, K Williams, E Elliott. Arch Dis Child 2003
80
16

Maladaptive behaviors and risk factors among the genetic subtypes of Prader-Willi syndrome.
Sigan L Hartley, William E Maclean, Merlin G Butler, Jennifer Zarcone, Travis Thompson. Am J Med Genet A 2005
69
15

Obsessions and compulsions in Prader-Willi syndrome.
E M Dykens, J F Leckman, S B Cassidy. J Child Psychol Psychiatry 1996
175
14

Prader-Willi syndrome: clinical genetics, cytogenetics and molecular biology.
Douglas C Bittel, Merlin G Butler. Expert Rev Mol Med 2005
182
14

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
14

Large recurrent microdeletions associated with schizophrenia.
Hreinn Stefansson, Dan Rujescu, Sven Cichon, Olli P H Pietil√§inen, Andres Ingason, Stacy Steinberg, Ragnheidur Fossdal, Engilbert Sigurdsson, Thordur Sigmundsson, Jacobine E Buizer-Voskamp,[...]. Nature 2008
14

Disruption of the mouse Necdin gene results in hypothalamic and behavioral alterations reminiscent of the human Prader-Willi syndrome.
F Muscatelli, D N Abrous, A Massacrier, I Boccaccio, M Le Moal, P Cau, H Cremer. Hum Mol Genet 2000
234
14

Prader-Willi syndrome: the psychopathological phenotype in uniparental disomy.
W M A Verhoeven, S Tuinier, L M G Curfs. J Med Genet 2003
36
30

Behavioral phenotype in adults with Prader-Willi syndrome.
Margje Sinnema, Stewart L Einfeld, Constance T R M Schrander-Stumpel, Marian A Maaskant, Harm Boer, Leopold M G Curfs. Res Dev Disabil 2011
45
24


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

Loss of the imprinted snoRNA mbii-52 leads to increased 5htr2c pre-RNA editing and altered 5HT2CR-mediated behaviour.
Christine M Doe, Dinko Relkovic, Alastair S Garfield, Jeffrey W Dalley, David E H Theobald, Trevor Humby, Lawrence S Wilkinson, Anthony R Isles. Hum Mol Genet 2009
123
13

Deletions of chromosome 15 as a cause of the Prader-Willi syndrome.
D H Ledbetter, V M Riccardi, S D Airhart, R J Strobel, B S Keenan, J D Crawford. N Engl J Med 1981
488
13

Prader-Willi syndrome.
S B Cassidy. J Med Genet 1997
292
12



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
12

SnoRNA Snord116 (Pwcr1/MBII-85) deletion causes growth deficiency and hyperphagia in mice.
Feng Ding, Hong Hua Li, Shengwen Zhang, Nicola M Solomon, Sally A Camper, Pinchas Cohen, Uta Francke. PLoS One 2008
190
12


Affective psychosis and Prader-Willi syndrome.
A Beardsmore, T Dorman, S A Cooper, T Webb. J Intellect Disabil Res 1998
43
20

Psychiatric illness and intellectual disability in the Prader-Willi syndrome with different molecular defects--a meta analysis.
Lin Yang, Guo-dong Zhan, Jun-jie Ding, Hui-jun Wang, Duan Ma, Guo-ying Huang, Wen-hao Zhou. PLoS One 2013
33
27

Genome organization, function, and imprinting in Prader-Willi and Angelman syndromes.
R D Nicholls, J L Knepper. Annu Rev Genomics Hum Genet 2001
411
10

The changing purpose of Prader-Willi syndrome clinical diagnostic criteria and proposed revised criteria.
M Gunay-Aygun, S Schwartz, S Heeger, M A O'Riordan, S B Cassidy. Pediatrics 2001
262
10

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
10

Pervasive developmental disorders in Prader-Willi syndrome: the Leuven experience in 59 subjects and controls.
Mie-Jef Descheemaeker, Veerle Govers, Peter Vermeulen, Jean-Pierre Fryns. Am J Med Genet A 2006
55
14

The relationship between compulsive behaviour and academic achievement across the three genetic subtypes of Prader-Willi syndrome.
J Zarcone, D Napolitano, C Peterson, J Breidbord, S Ferraioli, M Caruso-Anderson, L Holsen, M G Butler, T Thompson. J Intellect Disabil Res 2007
40
20

The Angelman Syndrome protein Ube3A regulates synapse development by ubiquitinating arc.
Paul L Greer, Rikinari Hanayama, Brenda L Bloodgood, Alan R Mardinly, David M Lipton, Steven W Flavell, Tae-Kyung Kim, Eric C Griffith, Zachary Waldon, Rene Maehr,[...]. Cell 2010
403
10


Association between microdeletion and microduplication at 16p11.2 and autism.
Lauren A Weiss, Yiping Shen, Joshua M Korn, Dan E Arking, David T Miller, Ragnheidur Fossdal, Evald Saemundsen, Hreinn Stefansson, Manuel A R Ferreira, Todd Green,[...]. N Engl J Med 2008
9

Intracranial abnormalities detected by three-dimensional magnetic resonance imaging in Prader-Willi syndrome.
Jennifer L Miller, Jessica A Couch, Ilona Schmalfuss, Guojun He, Yijun Liu, Daniel J Driscoll. Am J Med Genet A 2007
64
10

Gastric rupture and necrosis in Prader-Willi syndrome.
David A Stevenson, Janalee Heinemann, Moris Angulo, Merlin G Butler, Jim Loker, Norma Rupe, Patrick Kendell, Suzanne B Cassidy, Ann Scheimann. J Pediatr Gastroenterol Nutr 2007
62
11

Prevalence of, and risk factors for, physical ill-health in people with Prader-Willi syndrome: a population-based study.
J V Butler, J E Whittington, A J Holland, H Boer, D Clarke, T Webb. Dev Med Child Neurol 2002
189
9


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.