A citation-based method for searching scientific literature

Douglas C Bittel, Nataliya Kibiryeva, Merlin G Butler. Genet Test 2007
Times Cited: 33







List of co-cited articles
259 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
618
42

Prader-Willi syndrome: clinical genetics, cytogenetics and molecular biology.
Douglas C Bittel, Merlin G Butler. Expert Rev Mol Med 2005
182
39

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
172
36


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
52

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
373
33


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
30

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
178
27

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
27

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

Prader-Willi syndrome: a review of clinical, genetic, and endocrine findings.
M A Angulo, M G Butler, M E Cataletto. J Endocrinol Invest 2015
227
27

Genome organization, function, and imprinting in Prader-Willi and Angelman syndromes.
R D Nicholls, J L Knepper. Annu Rev Genomics Hum Genet 2001
411
24


Methylation-specific MLPA (MS-MLPA): simultaneous detection of CpG methylation and copy number changes of up to 40 sequences.
Anders O H Nygren, Najim Ameziane, Helena M B Duarte, Raymon N C P Vijzelaar, Quinten Waisfisz, Corine J Hess, Jan P Schouten, Abdellatif Errami. Nucleic Acids Res 2005
277
24


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
24

Single Gene and Syndromic Causes of Obesity: Illustrative Examples.
Merlin G Butler. Prog Mol Biol Transl Sci 2016
27
29

Quantification of the methylation status of the PWS/AS imprinted region: comparison of two approaches based on bisulfite sequencing and methylation-sensitive MLPA.
Nicola Dikow, Anders Oh Nygren, Jan P Schouten, Carolin Hartmann, Nikola Krämer, Bart Janssen, Johannes Zschocke. Mol Cell Probes 2007
43
21

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
21

Prader-Willi syndrome.
Suzanne B Cassidy, Daniel J Driscoll. Eur J Hum Genet 2009
337
21

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
867
21

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
21

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
189
21

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
21

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
196
21

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
21

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
18


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
278
18

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
24

Are jigsaw puzzle skills 'spared' in persons with Prader-Willi syndrome?
Elisabeth M Dykens. J Child Psychol Psychiatry 2002
75
18

Prader-Willi Syndrome: Clinical and Genetic Findings.
Merlin G Butler, Travis Thompson. Endocrinologist 2000
59
18

Microdeletion/microduplication of proximal 15q11.2 between BP1 and BP2: a susceptibility region for neurological dysfunction including developmental and language delay.
Rachel D Burnside, Romela Pasion, Fady M Mikhail, Andrew J Carroll, Nathaniel H Robin, Erin L Youngs, Inder K Gadi, Elizabeth Keitges, Vikram L Jaswaney, Peter R Papenhausen,[...]. Hum Genet 2011
161
18

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
18

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
15

Clinical and genetic aspects of Angelman syndrome.
Charles A Williams, Daniel J Driscoll, Aditi I Dagli. Genet Med 2010
161
15

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
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

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
15

Genomic imprinting disorders in humans: a mini-review.
Merlin G Butler. J Assist Reprod Genet 2009
109
15

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
16

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
17


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
12



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
190
12

Neural mechanisms underlying hyperphagia in Prader-Willi syndrome.
Laura M Holsen, Jennifer R Zarcone, William M Brooks, Merlin G Butler, Travis I Thompson, Jasjit S Ahluwalia, Nicole L Nollen, Cary R Savage. Obesity (Silver Spring) 2006
108
12

Molecular characterization of two proximal deletion breakpoint regions in both Prader-Willi and Angelman syndrome patients.
S L Christian, W P Robinson, B Huang, A Mutirangura, M R Line, M Nakao, U Surti, A Chakravarti, D H Ledbetter. Am J Hum Genet 1995
157
12


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.