A citation-based method for searching scientific literature

Merlin G Butler. Curr Genomics 2011
Times Cited: 140







List of co-cited articles
789 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
631
53

Prader-Willi syndrome: a review of clinical, genetic, and endocrine findings.
M A Angulo, M G Butler, M E Cataletto. J Endocrinol Invest 2015
235
30


Prader-Willi syndrome: clinical genetics, cytogenetics and molecular biology.
Douglas C Bittel, Merlin G Butler. Expert Rev Mol Med 2005
182
24

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
200
22

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
284
19

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
178
17

Prader-Willi syndrome.
Suzanne B Cassidy, Daniel J Driscoll. Eur J Hum Genet 2009
341
15

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
191
13

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
869
13

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
374
13

Prader-Willi Syndrome: Clinical and Genetic Findings.
Merlin G Butler, Travis Thompson. Endocrinologist 2000
61
19

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
661
11

Endocrine manifestations and management of Prader-Willi syndrome.
Jill E Emerick, Karen S Vogt. Int J Pediatr Endocrinol 2013
58
18

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
104
11

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
11

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


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
10

Single Gene and Syndromic Causes of Obesity: Illustrative Examples.
Merlin G Butler. Prog Mol Biol Transl Sci 2016
28
35

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
15

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
64
14

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
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
174
9

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

Thyroid function studies in Prader-Willi syndrome.
Merlin G Butler, Mariana Theodoro, Jennifer D Skouse. Am J Med Genet A 2007
33
24

Benefits of long-term GH therapy in Prader-Willi syndrome: a 4-year study.
Aaron L Carrel, Susan E Myers, Barbara Y Whitman, David B Allen. J Clin Endocrinol Metab 2002
136
8

Clinical management of behavioral characteristics of Prader-Willi syndrome.
Alan Y Ho, Anastasia Dimitropoulos. Neuropsychiatr Dis Treat 2010
42
19

Congenital leptin deficiency is associated with severe early-onset obesity in humans.
C T Montague, I S Farooqi, J P Whitehead, M A Soos, H Rau, N J Wareham, C P Sewter, J E Digby, S N Mohammed, J A Hurst,[...]. Nature 1997
8

Genetics of Obesity: What have we Learned?
Hélène Choquet, David Meyre. Curr Genomics 2011
110
8


Cause of sudden, unexpected death of Prader-Willi syndrome patients with or without growth hormone treatment.
T Nagai, K Obata, H Tonoki, S Temma, N Murakami, Y Katada, A Yoshino, S Sakazume, E Takahashi, R Sakuta,[...]. Am J Med Genet A 2005
67
11

Review of 64 cases of death in children with Prader-Willi syndrome (PWS).
M Tauber, G Diene, C Molinas, M Hébert. Am J Med Genet A 2008
117
8

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
34

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
8


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
22

Mortality in Prader-Willi syndrome.
Stewart L Einfeld, Sophie J Kavanagh, Arabella Smith, Elizabeth J Evans, Bruce J Tonge, John Taffe. Am J Ment Retard 2006
69
10

The human MAGEL2 gene and its mouse homologue are paternally expressed and mapped to the Prader-Willi region.
I Boccaccio, H Glatt-Deeley, F Watrin, N Roëckel, M Lalande, F Muscatelli. Hum Mol Genet 1999
134
7

Whole genome microarray analysis of gene expression in Prader-Willi syndrome.
Douglas C Bittel, Nataliya Kibiryeva, Susan M Sell, Theresa V Strong, Merlin G Butler. Am J Med Genet A 2007
52
13

Prader-Willi syndrome: causes of death in an international series of 27 cases.
Constance Th R M Schrander-Stumpel, Leopold M G Curfs, Prapto Sastrowijoto, Suzanne B Cassidy, Jaap J P Schrander, Jean-Pierre Fryns. Am J Med Genet A 2004
117
7

Beneficial effects of growth hormone treatment on cognition in children with Prader-Willi syndrome: a randomized controlled trial and longitudinal study.
Elbrich P C Siemensma, Roderick F A Tummers-de Lind van Wijngaarden, Dederieke A M Festen, Zyrhea C E Troeman, A A E M Janielle van Alfen-van der Velden, Barto J Otten, Joost Rotteveel, Roelof J H Odink, G C B Karen Bindels-de Heus, Mariette van Leeuwen,[...]. J Clin Endocrinol Metab 2012
91
7

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
41
17

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
7

Molecular genetic classification in Prader-Willi syndrome: a multisite cohort study.
Merlin G Butler, Samantha N Hartin, Waheeda A Hossain, Ann M Manzardo, Virginia Kimonis, Elisabeth Dykens, June Anne Gold, Soo-Jeong Kim, Nicolette Weisensel, Roy Tamura,[...]. J Med Genet 2019
48
14

Prader-Willi Syndrome - Clinical Genetics, Diagnosis and Treatment Approaches: An Update.
Merlin G Butler, Jennifer L Miller, Janice L Forster. Curr Pediatr Rev 2019
50
14

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
106
6

Effects of growth hormone treatment in adults with Prader-Willi syndrome.
M G Butler, B K Smith, J Lee, C Gibson, C Schmoll, W V Moore, J E Donnelly. Growth Horm IGF Res 2013
31
19

Development of the eating behaviour in Prader-Willi Syndrome: advances in our understanding.
C J McAllister, J E Whittington, A J Holland. Int J Obes (Lond) 2011
49
12

Truncating mutations of MAGEL2 cause Prader-Willi phenotypes and autism.
Christian P Schaaf, Manuel L Gonzalez-Garay, Fan Xia, Lorraine Potocki, Karen W Gripp, Baili Zhang, Brock A Peters, Mark A McElwain, Radoje Drmanac, Arthur L Beaudet,[...]. Nat Genet 2013
167
6


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.