A citation-based method for searching scientific literature

R D Nicholls, J H Knoll, M G Butler, S Karam, M Lalande. Nature 1989
Times Cited: 660







List of co-cited articles
811 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
37

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
32


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

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
21

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

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
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
195
17

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
15

Inherited microdeletions in the Angelman and Prader-Willi syndromes define an imprinting centre on human chromosome 15.
K Buiting, S Saitoh, S Gross, B Dittrich, S Schwartz, R D Nicholls, B Horsthemke. Nat Genet 1995
467
15

Prader-Willi syndrome.
Suzanne B Cassidy, Daniel J Driscoll. Eur J Hum Genet 2009
337
14


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
14

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
13

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

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
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
12

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
12


Autism spectrum disorders in Prader-Willi and Angelman syndromes: a systematic review.
Marijcke W M Veltman, Ellen E Craig, Patrick F Bolton. Psychiatr Genet 2005
128
12


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
11

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
176
11

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
188
11

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
27

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
11

Clinical and genetic aspects of Angelman syndrome.
Charles A Williams, Daniel J Driscoll, Aditi I Dagli. Genet Med 2010
158
10

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
10

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


Comparison of phenotype between patients with Prader-Willi syndrome due to deletion 15q and uniparental disomy 15.
S B Cassidy, M Forsythe, S Heeger, R D Nicholls, N Schork, P Benn, S Schwartz. Am J Med Genet 1997
144
9

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
115
9

Is gestation in Prader-Willi syndrome affected by the genetic subtype?
Merlin G Butler, Jennifer Sturich, Susan E Myers, June-Anne Gold, Virginia Kimonis, Daniel J Driscoll. J Assist Reprod Genet 2009
30
30

Behavior in Prader-Willi syndrome: relationship to genetic subtypes and age.
Elisabeth M Dykens, Elizabeth Roof. J Child Psychol Psychiatry 2008
77
11

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
89
10

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
9

Genomic imprinting disorders in humans: a mini-review.
Merlin G Butler. J Assist Reprod Genet 2009
107
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
39

Minimum prevalence, birth incidence and cause of death for Prader-Willi syndrome in Flanders.
Annick Vogels, Jenneke Van Den Ende, Kathelijne Keymolen, Geert Mortier, Koen Devriendt, E Legius, J P Fryns. Eur J Hum Genet 2004
114
8

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
88
9

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
8

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

Clinical-etiologic correlation in children with Prader-Willi syndrome (PWS): an interdisciplinary study.
Maria Torrado, Veronica Araoz, Edgardo Baialardo, Karina Abraldes, Carmen Mazza, Gabriela Krochik, Blanca Ozuna, Vivian Leske, Silvia Caino, Virginia Fano,[...]. Am J Med Genet A 2007
40
20

Topoisomerase inhibitors unsilence the dormant allele of Ube3a in neurons.
Hsien-Sung Huang, John A Allen, Angela M Mabb, Ian F King, Jayalakshmi Miriyala, Bonnie Taylor-Blake, Noah Sciaky, J Walter Dutton, Hyeong-Min Lee, Xin Chen,[...]. Nature 2011
225
8


Uniparental disomy as a mechanism for human genetic disease.
J E Spence, R G Perciaccante, G M Greig, H F Willard, D H Ledbetter, J F Hejtmancik, M S Pollack, W E O'Brien, A L Beaudet. Am J Hum Genet 1988
393
8

UBE3A/E6-AP mutations cause Angelman syndrome.
T Kishino, M Lalande, J Wagstaff. Nat Genet 1997
869
8


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