A citation-based method for searching scientific literature

Merlin G Butler, Jennifer L Miller, Janice L Forster. Curr Pediatr Rev 2019
Times Cited: 50







List of co-cited articles
423 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
40

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
32

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

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
28

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
22

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
21

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
18


Obesity management in Prader-Willi syndrome: current perspectives.
Antonino Crinò, Danilo Fintini, Sarah Bocchini, Graziano Grugni. Diabetes Metab Syndr Obes 2018
40
20

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
14

Diagnosis and treatment of GH deficiency in Prader-Willi syndrome.
Graziano Grugni, Paolo Marzullo. Best Pract Res Clin Endocrinol Metab 2016
27
25

Endocrine manifestations and management of Prader-Willi syndrome.
Jill E Emerick, Karen S Vogt. Int J Pediatr Endocrinol 2013
58
14


Hypothalamic loss of Snord116 recapitulates the hyperphagia of Prader-Willi syndrome.
Joseph Polex-Wolf, Brian Yh Lam, Rachel Larder, John Tadross, Debra Rimmington, Fàtima Bosch, Verónica Jiménez Cenzano, Eduard Ayuso, Marcella Kl Ma, Kara Rainbow,[...]. J Clin Invest 2018
42
16

Highly restricted deletion of the SNORD116 region is implicated in Prader-Willi Syndrome.
Eric Bieth, Sanaa Eddiry, Véronique Gaston, Françoise Lorenzini, Alexandre Buffet, Françoise Conte Auriol, Catherine Molinas, Dorothée Cailley, Caroline Rooryck, Benoit Arveiler,[...]. Eur J Hum Genet 2015
82
14

A multidisciplinary approach to the clinical management of Prader-Willi syndrome.
Jessica Duis, Pieter J van Wattum, Ann Scheimann, Parisa Salehi, Elly Brokamp, Laura Fairbrother, Anna Childers, Althea Robinson Shelton, Nathan C Bingham, Ashley H Shoemaker,[...]. Mol Genet Genomic Med 2019
23
30

Prader- Willi syndrome: An uptodate on endocrine and metabolic complications.
Giovanna Muscogiuri, Gloria Formoso, Gabriella Pugliese, Rosaria Maddalena Ruggeri, Elisabetta Scarano, Annamaria Colao. Rev Endocr Metab Disord 2019
26
26

Medical, psychological and social features in a large cohort of adults with Prader-Willi syndrome: experience from a dedicated centre in France.
V Laurier, A Lapeyrade, P Copet, G Demeer, M Silvie, E Bieth, M Coupaye, C Poitou, F Lorenzini, F Labrousse,[...]. J Intellect Disabil Res 2015
36
19

Deficiency in prohormone convertase PC1 impairs prohormone processing in Prader-Willi syndrome.
Lisa C Burnett, Charles A LeDuc, Carlos R Sulsona, Daniel Paull, Richard Rausch, Sanaa Eddiry, Jayne F Martin Carli, Michael V Morabito, Alicja A Skowronski, Gabriela Hubner,[...]. J Clin Invest 2017
69
14

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
12

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
12

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
12


Disorders of glucose metabolism in Prader-Willi syndrome: Results of a multicenter Italian cohort study.
D Fintini, G Grugni, S Bocchini, C Brufani, S Di Candia, A Corrias, M Delvecchio, A Salvatoni, L Ragusa, N Greggio,[...]. Nutr Metab Cardiovasc Dis 2016
31
19


Prader-Willi syndrome.
Suzanne B Cassidy, Daniel J Driscoll. Eur J Hum Genet 2009
341
12

A Prader-Willi locus lncRNA cloud modulates diurnal genes and energy expenditure.
Weston T Powell, Rochelle L Coulson, Florence K Crary, Spencer S Wong, Robert A Ach, Peter Tsang, N Alice Yamada, Dag H Yasui, Janine M Lasalle. Hum Mol Genet 2013
94
12


Prader-Willi Syndrome: Clinical Genetics and Diagnostic Aspects with Treatment Approaches.
Merlin G Butler, Ann M Manzardo, Janice L Forster. Curr Pediatr Rev 2016
33
15

Elevated ratio of acylated to unacylated ghrelin in children and young adults with Prader-Willi syndrome.
R J Kuppens, G Diène, N E Bakker, C Molinas, S Faye, M Nicolino, D Bernoux, P J D Delhanty, A J van der Lely, S Allas,[...]. Endocrine 2015
45
11

Growth hormone therapy for Prader-willi syndrome: challenges and solutions.
Graziano Grugni, Alessandro Sartorio, Antonino Crinò. Ther Clin Risk Manag 2016
38
13

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
10

High levels of caregiver burden in Prader-Willi syndrome.
Nathalie Kayadjanian, Lauren Schwartz, Evan Farrar, Katherine Anne Comtois, Theresa V Strong. PLoS One 2018
20
25

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
191
10

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
216
10

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
174
10

Eight years of growth hormone treatment in children with Prader-Willi syndrome: maintaining the positive effects.
N E Bakker, R J Kuppens, E P C Siemensma, R F A Tummers-de Lind van Wijngaarden, D A M Festen, G C B Bindels-de Heus, G Bocca, D A J P Haring, J J G Hoorweg-Nijman, E C A M Houdijk,[...]. J Clin Endocrinol Metab 2013
73
10

Effect of Genotype and Previous GH Treatment on Adiposity in Adults With Prader-Willi Syndrome.
Muriel Coupaye, Maithé Tauber, Laurence Cuisset, Virginie Laurier, Eric Bieth, Jean-Marc Lacorte, Jean-Michel Oppert, Karine Clément, Christine Poitou. J Clin Endocrinol Metab 2016
23
21

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
10

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
10

Prader-Willi-Like Phenotype Caused by an Atypical 15q11.2 Microdeletion.
Qiming Tan, Kathryn J Potter, Lisa Cole Burnett, Camila E Orsso, Mark Inman, Davis C Ryman, Andrea M Haqq. Genes (Basel) 2020
13
38



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
10

Management of obesity in Prader-Willi syndrome.
Merlin G Butler. Nat Clin Pract Endocrinol Metab 2006
34
11

Impact of genetic subtypes of Prader-Willi syndrome with growth hormone therapy on intelligence and body mass index.
Merlin G Butler, Naomi A Matthews, Nidhi Patel, Abhilasha Surampalli, June-Anne Gold, Manaswitha Khare, Travis Thompson, Suzanne B Cassidy, Virginia E Kimonis. Am J Med Genet A 2019
13
30

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
10

Review of Prader-Willi syndrome: the endocrine approach.
Ryan Heksch, Manmohan Kamboj, Kathryn Anglin, Kathryn Obrynba. Transl Pediatr 2017
36
11

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

Prader-Willi syndrome and early-onset morbid obesity NIH rare disease consortium: A review of natural history study.
Merlin G Butler, Virginia Kimonis, Elisabeth Dykens, June A Gold, Jennifer Miller, Roy Tamura, Daniel J Driscoll. Am J Med Genet A 2018
16
25


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.