A citation-based method for searching scientific literature

M C Varela, F Kok, N Setian, C A Kim, C P Koiffmann. Clin Genet 2005
Times Cited: 70







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



Times Cited
  Times     Co-cited
Similarity


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
51

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
50

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
40

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
31

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
145
24

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
24

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
22

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
22

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
23

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
21


Genome organization, function, and imprinting in Prader-Willi and Angelman syndromes.
R D Nicholls, J L Knepper. Annu Rev Genomics Hum Genet 2001
411
20

Genotype-phenotype correlation in a series of 167 deletion and non-deletion patients with Prader-Willi syndrome.
G Gillessen-Kaesbach, W Robinson, D Lohmann, S Kaya-Westerloh, E Passarge, B Horsthemke. Hum Genet 1995
86
20


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

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
107
18

Prader-Willi syndrome.
Suzanne B Cassidy, Stuart Schwartz, Jennifer L Miller, Daniel J Driscoll. Genet Med 2012
618
18

Prader-Willi syndrome--a study comparing deletion and uniparental disomy cases with reference to autism spectrum disorders.
Marijcke W M Veltman, Russell J Thompson, Sian E Roberts, N Simon Thomas, Joyce Whittington, Patrick F Bolton. Eur Child Adolesc Psychiatry 2004
86
17



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
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
373
17

Are jigsaw puzzle skills 'spared' in persons with Prader-Willi syndrome?
Elisabeth M Dykens. J Child Psychol Psychiatry 2002
75
15


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
14

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
14

Prader-Willi syndrome: causes of death in an international series of 27 cases.
Constance Th R M Schrander-Stumpel, Leopold M G Curfs, Prapto Sastrowijoto, Suzanne B Cassidy, Jaap J P Schrander, Jean-Pierre Fryns. Am J Med Genet A 2004
115
14

Hypogonadism and pubertal development in Prader-Willi syndrome.
A Crinò, R Schiaffini, P Ciampalini, S Spera, L Beccaria, F Benzi, L Bosio, A Corrias, L Gargantini, A Salvatoni,[...]. Eur J Pediatr 2003
93
14

Electroclinical characteristics of seizures-comparing Prader--Willi syndrome with Angelman syndrome.
Pen-Jung Wang, Jia-Woei Hou, Whey-Chen Sue, Wang-Tso Lee. Brain Dev 2005
20
50



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

Prader-Willi syndrome.
S B Cassidy. J Med Genet 1997
292
12

Elevated plasma ghrelin levels in Prader Willi syndrome.
David E Cummings, Karine Clement, Jonathan Q Purnell, Christian Vaisse, Karen E Foster, R Scott Frayo, Michael W Schwartz, Arnaud Basdevant, David S Weigle. Nat Med 2002
417
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
12

Chromosome 15 maternal uniparental disomy and psychosis in Prader-Willi syndrome.
A Vogels, G Matthijs, E Legius, K Devriendt, J-P Fryns. J Med Genet 2003
76
12

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
115
12

Prader-Willi syndrome, compulsive and ritualistic behaviours: the first population-based survey.
D J Clarke, H Boer, J Whittington, A Holland, J Butler, T Webb. Br J Psychiatry 2002
91
12

Prader-Willi and Angelman syndromes: sister imprinted disorders.
S B Cassidy, E Dykens, C A Williams. Am J Med Genet 2000
173
12


Intracranial abnormalities detected by three-dimensional magnetic resonance imaging in Prader-Willi syndrome.
Jennifer L Miller, Jessica A Couch, Ilona Schmalfuss, Guojun He, Yijun Liu, Daniel J Driscoll. Am J Med Genet A 2007
64
14

Behavior in Prader-Willi syndrome: relationship to genetic subtypes and age.
Elisabeth M Dykens, Elizabeth Roof. J Child Psychol Psychiatry 2008
77
12

Characteristics and frequency of seizure disorder in 56 patients with Prader-Willi syndrome.
Zheng Fan, Robert Greenwood, Amy Fisher, Surekha Pendyal, Cynthia M Powell. Am J Med Genet A 2009
19
47

Obsessions and compulsions in Prader-Willi syndrome.
E M Dykens, J F Leckman, S B Cassidy. J Child Psychol Psychiatry 1996
175
11

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
137
11

Behavioural and emotional disturbances in people with Prader-Willi Syndrome.
H-C Steinhausen, U Eiholzer, B P Hauffa, Z Malin. J Intellect Disabil Res 2004
43
18

Psychotic disorders in Prader-Willi syndrome.
A Vogels, M De Hert, M J Descheemaeker, V Govers, K Devriendt, E Legius, P Prinzie, J P Fryns. Am J Med Genet A 2004
59
13


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
470
11


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.