A citation-based method for searching scientific literature

Merlin G Butler, Jennifer Sturich, Susan E Myers, June-Anne Gold, Virginia Kimonis, Daniel J Driscoll. J Assist Reprod Genet 2009
Times Cited: 30







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



Times Cited
  Times     Co-cited
Similarity


Prader-Willi syndrome.
Suzanne B Cassidy, Stuart Schwartz, Jennifer L Miller, Daniel J Driscoll. Genet Med 2012
614
63

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
196
46

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
43

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
40

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
261
36

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
36

Prader-Willi syndrome: clinical genetics, cytogenetics and molecular biology.
Douglas C Bittel, Merlin G Butler. Expert Rev Mol Med 2005
182
36

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
33


Growth standards of infants with Prader-Willi syndrome.
Merlin G Butler, Jennifer Sturich, Jaehoon Lee, Susan E Myers, Barbara Y Whitman, June-Anne Gold, Virginia Kimonis, Ann Scheimann, Norma Terrazas, Daniel J Driscoll. Pediatrics 2011
31
33

Prader-Willi syndrome: a review of clinical, genetic, and endocrine findings.
M A Angulo, M G Butler, M E Cataletto. J Endocrinol Invest 2015
224
33

Prader-Willi syndrome.
Suzanne B Cassidy, Daniel J Driscoll. Eur J Hum Genet 2009
337
30


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
372
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
30


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
865
26


Growth charts for non-growth hormone treated Prader-Willi syndrome.
Merlin G Butler, Jaehoon Lee, Ann M Manzardo, June-Anne Gold, Jennifer L Miller, Virginia Kimonis, Daniel J Driscoll. Pediatrics 2015
29
27

Management of obesity in Prader-Willi syndrome.
Merlin G Butler. Nat Clin Pract Endocrinol Metab 2006
34
23

Are jigsaw puzzle skills 'spared' in persons with Prader-Willi syndrome?
Elisabeth M Dykens. J Child Psychol Psychiatry 2002
75
23

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
23

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
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

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
23

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
177
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
23

GrowthHormone Research Society workshop summary: consensus guidelines for recombinant human growth hormone therapy in Prader-Willi syndrome.
Cheri L Deal, Michèle Tony, Charlotte Höybye, David B Allen, Maïthé Tauber, Jens Sandahl Christiansen. J Clin Endocrinol Metab 2013
169
23


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
20

A deletion of the HBII-85 class of small nucleolar RNAs (snoRNAs) is associated with hyperphagia, obesity and hypogonadism.
Adam J de Smith, Carolin Purmann, Robin G Walters, Richard J Ellis, Susan E Holder, Mieke M Van Haelst, Angela F Brady, Una L Fairbrother, Mehul Dattani, Julia M Keogh,[...]. Hum Mol Genet 2009
173
20


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
20

Paternally inherited microdeletion at 15q11.2 confirms a significant role for the SNORD116 C/D box snoRNA cluster in Prader-Willi syndrome.
Angela L Duker, Blake C Ballif, Erawati V Bawle, Richard E Person, Sangeetha Mahadevan, Sarah Alliman, Regina Thompson, Ryan Traylor, Bassem A Bejjani, Lisa G Shaffer,[...]. Eur J Hum Genet 2010
215
20

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
20


Trisomy 15 with loss of the paternal 15 as a cause of Prader-Willi syndrome due to maternal disomy.
S B Cassidy, L W Lai, R P Erickson, L Magnuson, E Thomas, R Gendron, J Herrmann. Am J Hum Genet 1992
145
20

Changing rates of genetic subtypes of Prader-Willi syndrome in the UK.
Joyce E Whittington, Jill V Butler, Anthony J Holland. Eur J Hum Genet 2007
41
20

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
26

Energy expenditure and physical activity in Prader-Willi syndrome: comparison with obese subjects.
Merlin G Butler, Mariana F Theodoro, Douglas C Bittel, Joseph E Donnelly. Am J Med Genet A 2007
101
16

Genome organization, function, and imprinting in Prader-Willi and Angelman syndromes.
R D Nicholls, J L Knepper. Annu Rev Genomics Hum Genet 2001
411
16

Prader-Willi Syndrome: Clinical and Genetic Findings.
Merlin G Butler, Travis Thompson. Endocrinologist 2000
59
16



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
160
16

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
16

Genomic imprinting disorders in humans: a mini-review.
Merlin G Butler. J Assist Reprod Genet 2009
107
16

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
16

Long-term growth hormone therapy changes the natural history of body composition and motor function in children with prader-willi syndrome.
Aaron L Carrel, Susan E Myers, Barbara Y Whitman, Jens Eickhoff, David B Allen. J Clin Endocrinol Metab 2010
104
16

Mental and motor development before and during growth hormone treatment in infants and toddlers with Prader-Willi syndrome.
D A M Festen, M Wevers, A C Lindgren, B Böhm, B J Otten, J M Wit, H J Duivenvoorden, A C S Hokken-Koelega. Clin Endocrinol (Oxf) 2008
88
16


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.