A citation-based method for searching scientific literature

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
Times Cited: 40







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



Times Cited
  Times     Co-cited
Similarity


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
80

Prader-Willi syndrome: clinical genetics, cytogenetics and molecular biology.
Douglas C Bittel, Merlin G Butler. Expert Rev Mol Med 2005
182
60

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
45

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
42

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
42

Behavior in Prader-Willi syndrome: relationship to genetic subtypes and age.
Elisabeth M Dykens, Elizabeth Roof. J Child Psychol Psychiatry 2008
77
42

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
40



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
35

Prader-Willi syndrome.
Suzanne B Cassidy, Stuart Schwartz, Jennifer L Miller, Daniel J Driscoll. Genet Med 2012
609
32

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
30

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
30


Array comparative genomic hybridization (aCGH) analysis in Prader-Willi syndrome.
Merlin G Butler, William Fischer, Nataliya Kibiryeva, Douglas C Bittel. Am J Med Genet A 2008
57
27


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
27

Nutritional phases in Prader-Willi syndrome.
Jennifer L Miller, Christy H Lynn, Danielle C Driscoll, Anthony P Goldstone, June-Anne Gold, Virginia Kimonis, Elisabeth Dykens, Merlin G Butler, Jonathan J Shuster, Daniel J Driscoll. Am J Med Genet A 2011
195
27

Are jigsaw puzzle skills 'spared' in persons with Prader-Willi syndrome?
Elisabeth M Dykens. J Child Psychol Psychiatry 2002
75
25

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
25

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
25

Obsessions and compulsions in Prader-Willi syndrome.
E M Dykens, J F Leckman, S B Cassidy. J Child Psychol Psychiatry 1996
175
25

Prader-Willi syndrome: a review of clinical, genetic, and endocrine findings.
M A Angulo, M G Butler, M E Cataletto. J Endocrinol Invest 2015
222
25


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
88
22



Methylation-specific multiplex ligation-dependent probe amplification and identification of deletion genetic subtypes in Prader-Willi syndrome.
Rebecca S Henkhaus, Soo-Jeong Kim, Virginia E Kimonis, June-Anne Gold, Elisabeth M Dykens, Daniel J Driscoll, Merlin G Butler. Genet Test Mol Biomarkers 2012
23
39


Autism spectrum disorders in Prader-Willi and Angelman syndromes: a systematic review.
Marijcke W M Veltman, Ellen E Craig, Patrick F Bolton. Psychiatr Genet 2005
128
20

The phenomenology and diagnosis of psychiatric illness in people with Prader-Willi syndrome.
S Soni, J Whittington, A J Holland, T Webb, E N Maina, H Boer, D Clarke. Psychol Med 2008
74
20

Molecular characterization of two proximal deletion breakpoint regions in both Prader-Willi and Angelman syndrome patients.
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
157
20


Prader-Willi Syndrome: Clinical and Genetic Findings.
Merlin G Butler, Travis Thompson. Endocrinologist 2000
59
20

Epimutations in Prader-Willi and Angelman syndromes: a molecular study of 136 patients with an imprinting defect.
Karin Buiting, Stephanie Gross, Christina Lich, Gabriele Gillessen-Kaesbach, Osman el-Maarri, Bernhard Horsthemke. Am J Hum Genet 2003
176
20



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

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
17

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
17


Microdeletion/microduplication of proximal 15q11.2 between BP1 and BP2: a susceptibility region for neurological dysfunction including developmental and language delay.
Rachel D Burnside, Romela Pasion, Fady M Mikhail, Andrew J Carroll, Nathaniel H Robin, Erin L Youngs, Inder K Gadi, Elizabeth Keitges, Vikram L Jaswaney, Peter R Papenhausen,[...]. Hum Genet 2011
159
17

Is gestation in Prader-Willi syndrome affected by the genetic subtype?
Merlin G Butler, Jennifer Sturich, Susan E Myers, June-Anne Gold, Virginia Kimonis, Daniel J Driscoll. J Assist Reprod Genet 2009
30
23

Unique and atypical deletions in Prader-Willi syndrome reveal distinct phenotypes.
Soo-Jeong Kim, Jennifer L Miller, Paul J Kuipers, Jennifer Ruth German, Arthur L Beaudet, Trilochan Sahoo, Daniel J Driscoll. Eur J Hum Genet 2012
62
17

Single Gene and Syndromic Causes of Obesity: Illustrative Examples.
Merlin G Butler. Prog Mol Biol Transl Sci 2016
26
26

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
15

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
15


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
15

Management of obesity in Prader-Willi syndrome.
Merlin G Butler. Nat Clin Pract Endocrinol Metab 2006
34
17


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.