A citation-based method for searching scientific literature


List of co-cited articles
102 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


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
180
87

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
75

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
75


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
62

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
62

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
62

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
62

Prader-Willi syndrome.
Suzanne B Cassidy, Stuart Schwartz, Jennifer L Miller, Daniel J Driscoll. Genet Med 2012
631
62


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
62

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
50


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
50


Prader-Willi syndrome: clinical genetics, cytogenetics and molecular biology.
Douglas C Bittel, Merlin G Butler. Expert Rev Mol Med 2005
182
50

Prader-Willi Syndrome: Clinical and Genetic Findings.
Merlin G Butler, Travis Thompson. Endocrinologist 2000
61
50

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
50

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
50

Are jigsaw puzzle skills 'spared' in persons with Prader-Willi syndrome?
Elisabeth M Dykens. J Child Psychol Psychiatry 2002
75
37

Cognitive abilities and genotype in a population-based sample of people with Prader-Willi syndrome.
J Whittington, A Holland, T Webb, J Butler, D Clarke, H Boer. J Intellect Disabil Res 2004
108
37

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
37


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
37

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
37

Thyroid function studies in Prader-Willi syndrome.
Merlin G Butler, Mariana Theodoro, Jennifer D Skouse. Am J Med Genet A 2007
33
37

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
37

Genomic imprinting disorders in humans: a mini-review.
Merlin G Butler. J Assist Reprod Genet 2009
111
37

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
37

Effects of recombinant human growth hormone therapy in adults with Prader-Willi syndrome: a meta-analysis.
Ruth Sanchez-Ortiga, Anne Klibanski, Nicholas A Tritos. Clin Endocrinol (Oxf) 2012
56
37

A 5-year-old white girl with Prader-Willi syndrome and a submicroscopic deletion of chromosome 15q11q13.
M G Butler, S L Christian, T Kubota, D H Ledbetter. Am J Med Genet 1996
25
37

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
37

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
37

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
37


Decreased bone mineral density in Prader-Willi syndrome: comparison with obese subjects.
M G Butler, L Haber, R Mernaugh, M G Carlson, R Price, I D Feurer. Am J Med Genet 2001
43
37

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
37

Clinical and genetic aspects of Angelman syndrome.
Charles A Williams, Daniel J Driscoll, Aditi I Dagli. Genet Med 2010
164
37

UPD detection using homozygosity profiling with a SNP genotyping microarray.
Peter Papenhausen, Stuart Schwartz, Hiba Risheg, Elisabeth Keitges, Inder Gadi, Rachel D Burnside, Vikram Jaswaney, John Pappas, Romela Pasion, Kenneth Friedman,[...]. Am J Med Genet A 2011
88
37

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
37

Single Gene and Syndromic Causes of Obesity: Illustrative Examples.
Merlin G Butler. Prog Mol Biol Transl Sci 2016
28
37

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
37

Prader-Willi syndrome.
Suzanne B Cassidy, Daniel J Driscoll. Eur J Hum Genet 2009
341
25

Large genomic duplicons map to sites of instability in the Prader-Willi/Angelman syndrome chromosome region (15q11-q13).
S L Christian, J A Fantes, S K Mewborn, B Huang, D H Ledbetter. Hum Mol Genet 1999
192
25

Imprinting mutations suggested by abnormal DNA methylation patterns in familial Angelman and Prader-Willi syndromes.
A Reis, B Dittrich, V Greger, K Buiting, M Lalande, G Gillessen-Kaesbach, M Anvret, B Horsthemke. Am J Hum Genet 1994
188
25


Hypopigmentation in the Prader-Willi syndrome correlates with P gene deletion but not with haplotype of the hemizygous P allele.
R A Spritz, T Bailin, R D Nicholls, S T Lee, S K Park, M J Mascari, M G Butler. Am J Med Genet 1997
75
25

Breakage in the SNRPN locus in a balanced 46,XY,t(15;19) Prader-Willi syndrome patient.
Y Sun, R D Nicholls, M G Butler, S Saitoh, B E Hainline, C G Palmer. Hum Mol Genet 1996
62
25


Chromosome breakage in the Prader-Willi and Angelman syndromes involves recombination between large, transcribed repeats at proximal and distal breakpoints.
J M Amos-Landgraf, Y Ji, W Gottlieb, T Depinet, A E Wandstrat, S B Cassidy, D J Driscoll, P K Rogan, S Schwartz, R D Nicholls. Am J Hum Genet 1999
200
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.