A citation-based method for searching scientific literature

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, Jennifer L Miller, Daniel J Driscoll. J Med Genet 2019
Times Cited: 45







List of co-cited articles
343 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
609
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
222
42

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
31


Prader-Willi Syndrome - Clinical Genetics, Diagnosis and Treatment Approaches: An Update.
Merlin G Butler, Jennifer L Miller, Janice L Forster. Curr Pediatr Rev 2019
40
27

Single Gene and Syndromic Causes of Obesity: Illustrative Examples.
Merlin G Butler. Prog Mol Biol Transl Sci 2016
26
38

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
22

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
46
20

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
22
36

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
80

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
80
17

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
168
17

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
17

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
274
17

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

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
15


Prader-Willi syndrome.
Suzanne B Cassidy, Daniel J Driscoll. Eur J Hum Genet 2009
337
15

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
15

Prader-Willi Syndrome: Clinical and Genetic Findings.
Merlin G Butler, Travis Thompson. Endocrinologist 2000
59
15

Obesity management in Prader-Willi syndrome: current perspectives.
Antonino Crinò, Danilo Fintini, Sarah Bocchini, Graziano Grugni. Diabetes Metab Syndr Obes 2018
36
19

Diagnosis and treatment of GH deficiency in Prader-Willi syndrome.
Graziano Grugni, Paolo Marzullo. Best Pract Res Clin Endocrinol Metab 2016
23
30

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

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
13

Three siblings with Prader-Willi syndrome caused by imprinting center microdeletions and review.
Samantha N Hartin, Waheeda A Hossain, Nicolette Weisensel, Merlin G Butler. Am J Med Genet A 2018
11
54


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
37

Contributing factors of mortality in Prader-Willi syndrome.
Jennifer Proffitt, Kathryn Osann, Barbara McManus, Virginia E Kimonis, Janalee Heinemann, Merlin G Butler, David A Stevenson, June-Anne Gold. Am J Med Genet A 2019
19
31

Prader-Willi syndrome genetic subtypes and clinical neuropsychiatric diagnoses in residential care adults.
A M Manzardo, N Weisensel, S Ayala, W Hossain, M G Butler. Clin Genet 2018
12
50

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
13

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
100
11

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
36
13

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
11

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
165
11

Management of obesity in Prader-Willi syndrome.
Merlin G Butler. Nat Clin Pract Endocrinol Metab 2006
34
14

A mouse model for Prader-Willi syndrome imprinting-centre mutations.
T Yang, T E Adamson, J L Resnick, S Leff, R Wevrick, U Francke, N A Jenkins, N G Copeland, C I Brannan. Nat Genet 1998
238
11

Growth hormone therapy for Prader-willi syndrome: challenges and solutions.
Graziano Grugni, Alessandro Sartorio, Antonino Crinò. Ther Clin Risk Manag 2016
35
14

Prader-Willi syndrome: clinical genetics, cytogenetics and molecular biology.
Douglas C Bittel, Merlin G Butler. Expert Rev Mol Med 2005
182
11

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
39
12

Appetite hormones and the transition to hyperphagia in children with Prader-Willi syndrome.
A P Goldstone, A J Holland, J V Butler, J E Whittington. Int J Obes (Lond) 2012
39
12



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
8

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
23

Reactivation of maternal SNORD116 cluster via SETDB1 knockdown in Prader-Willi syndrome iPSCs.
Estela Cruvinel, Tara Budinetz, Noelle Germain, Stormy Chamberlain, Marc Lalande, Kristen Martins-Taylor. Hum Mol Genet 2014
34
11

Prader-Willi syndrome and Angelman syndrome.
Karin Buiting. Am J Med Genet C Semin Med Genet 2010
181
8

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
8

Psychiatric illness and intellectual disability in the Prader-Willi syndrome with different molecular defects--a meta analysis.
Lin Yang, Guo-dong Zhan, Jun-jie Ding, Hui-jun Wang, Duan Ma, Guo-ying Huang, Wen-hao Zhou. PLoS One 2013
33
12

The noncoding RNA IPW regulates the imprinted DLK1-DIO3 locus in an induced pluripotent stem cell model of Prader-Willi syndrome.
Yonatan Stelzer, Ido Sagi, Ofra Yanuka, Rachel Eiges, Nissim Benvenisty. Nat Genet 2014
88
8

Hyperghrelinemia precedes obesity in Prader-Willi syndrome.
Eva Feigerlová, Gwenaëlle Diene, Françoise Conte-Auriol, Catherine Molinas, Isabelle Gennero, Jean-Pierre Salles, Catherine Arnaud, Maïthé Tauber. J Clin Endocrinol Metab 2008
83
8


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.