A citation-based method for searching scientific literature

Merlin G Butler, Ann M Manzardo, Janice L Forster. Curr Pediatr Rev 2016
Times Cited: 33







List of co-cited articles
159 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
57

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
48



Causes of death in Prader-Willi syndrome: Prader-Willi Syndrome Association (USA) 40-year mortality survey.
Merlin G Butler, Ann M Manzardo, Janalee Heinemann, Carolyn Loker, James Loker. Genet Med 2017
54
21

Prader-Willi syndrome.
Suzanne B Cassidy, Daniel J Driscoll. Eur J Hum Genet 2009
341
18

Prader-Willi syndrome: clinical genetics, cytogenetics and molecular biology.
Douglas C Bittel, Merlin G Butler. Expert Rev Mol Med 2005
182
18

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
18


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
15

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
15

Prader Willi Syndrome: Genetics, Metabolomics, Hormonal Function, and New Approaches to Therapy.
Krystal A Irizarry, Mark Miller, Michael Freemark, Andrea M Haqq. Adv Pediatr 2016
42
15

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
15

Obesity management in Prader-Willi syndrome: current perspectives.
Antonino Crinò, Danilo Fintini, Sarah Bocchini, Graziano Grugni. Diabetes Metab Syndr Obes 2018
40
15

Prader-Willi Syndrome: A spectrum of anatomical and clinical features.
Bradley J Hurren, Natasha A M S Flack. Clin Anat 2016
16
25

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
12

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
12

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
12

Deaths due to choking in Prader-Willi syndrome.
David A Stevenson, Janalee Heinemann, Moris Angulo, Merlin G Butler, Jim Loker, Norma Rupe, Patrick Kendell, Carol L Clericuzio, Ann O Scheimann. Am J Med Genet A 2007
37
12

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
12

Survival trends from the Prader-Willi Syndrome Association (USA) 40-year mortality survey.
Ann M Manzardo, James Loker, Janalee Heinemann, Carolyn Loker, Merlin G Butler. Genet Med 2018
23
17

Physical health problems in adults with Prader-Willi syndrome.
Margje Sinnema, Marian A Maaskant, Henny M J van Schrojenstein Lantman-de Valk, I Caroline van Nieuwpoort, Madeleine L Drent, Leopold M G Curfs, Constance T R M Schrander-Stumpel. Am J Med Genet A 2011
56
12

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
12

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
12

Early diagnosis and care is achieved but should be improved in infants with Prader-Willi syndrome.
Céline Bar, Gwenaelle Diene, Catherine Molinas, Eric Bieth, Charlotte Casper, Maithé Tauber. Orphanet J Rare Dis 2017
39
12

Behavior in Prader-Willi syndrome: relationship to genetic subtypes and age.
Elisabeth M Dykens, Elizabeth Roof. J Child Psychol Psychiatry 2008
78
12

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
12

The human necdin gene, NDN, is maternally imprinted and located in the Prader-Willi syndrome chromosomal region.
P Jay, C Rougeulle, A Massacrier, A Moncla, M G Mattei, P Malzac, N Roëckel, S Taviaux, J L Lefranc, P Cau,[...]. Nat Genet 1997
197
9


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
9

Growth Charts for Prader-Willi Syndrome During Growth Hormone Treatment.
Merlin G Butler, Jaehoon Lee, Devin M Cox, Ann M Manzardo, June-Anne Gold, Jennifer L Miller, Elizabeth Roof, Elisabeth Dykens, Virginia Kimonis, Daniel J Driscoll. Clin Pediatr (Phila) 2016
17
17

Single Gene and Syndromic Causes of Obesity: Illustrative Examples.
Merlin G Butler. Prog Mol Biol Transl Sci 2016
28
10

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
9


Endocrine manifestations and management of Prader-Willi syndrome.
Jill E Emerick, Karen S Vogt. Int J Pediatr Endocrinol 2013
58
9

Cognitive profile in a large French cohort of adults with Prader-Willi syndrome: differences between genotypes.
P Copet, J Jauregi, V Laurier, V Ehlinger, C Arnaud, A-M Cobo, C Molinas, M Tauber, D Thuilleaux. J Intellect Disabil Res 2010
41
9

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
13

The High Direct Medical Costs of Prader-Willi Syndrome.
Andrew J Shoffstall, Julia A Gaebler, Nerissa C Kreher, Timothy Niecko, Diah Douglas, Theresa V Strong, Jennifer L Miller, Diane E Stafford, Merlin G Butler. J Pediatr 2016
18
16

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
9

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
9

Two years of growth hormone therapy in young children with Prader-Willi syndrome: physical and neurodevelopmental benefits.
Susan E Myers, Barbara Y Whitman, Aaron L Carrel, Victoria Moerchen, M Tracy Bekx, David B Allen. Am J Med Genet A 2007
94
9

Metabolic syndrome in adult patients with Prader-Willi syndrome.
G Grugni, A Crinò, G Bedogni, M Cappa, A Sartorio, A Corrias, S Di Candia, L Gargantini, L Iughetti, C Pagano,[...]. Nutr Metab Cardiovasc Dis 2013
34
9

A double-blind randomized controlled trial of oxytocin nasal spray in Prader Willi syndrome.
Stewart L Einfeld, Ellie Smith, Iain S McGregor, Kate Steinbeck, John Taffe, Lauren J Rice, Siân K Horstead, Naomi Rogers, M Antoinette Hodge, Adam J Guastella. Am J Med Genet A 2014
70
9

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
9

Review of Prader-Willi syndrome: the endocrine approach.
Ryan Heksch, Manmohan Kamboj, Kathryn Anglin, Kathryn Obrynba. Transl Pediatr 2017
36
9

The Italian National Survey for Prader-Willi syndrome: an epidemiologic study.
Graziano Grugni, Antonino Crinò, Laura Bosio, Andrea Corrias, Marina Cuttini, Teresa De Toni, Eliana Di Battista, Adriana Franzese, Luigi Gargantini, Nella Greggio,[...]. Am J Med Genet A 2008
63
9



Analysis of the Prader-Willi syndrome imprinting center using droplet digital PCR and next-generation whole-exome sequencing.
Samantha N Hartin, Waheeda A Hossain, David Francis, David E Godler, Sangjucta Barkataki, Merlin G Butler. Mol Genet Genomic Med 2019
10
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
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.