A citation-based method for searching scientific literature

Heather J Stalker, Kory L Keller, Brian A Gray, Roberto T Zori. Am J Med Genet A 2003
Times Cited: 14







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



Times Cited
  Times     Co-cited
Similarity


1p36 deletion syndrome associated with Prader-Willi-like phenotype.
Yu Tsuyusaki, Hiroshi Yoshihashi, Noritaka Furuya, Masanori Adachi, Hitoshi Osaka, Kayono Yamamoto, Kenji Kurosawa. Pediatr Int 2010
26
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
867
42

Prader-Willi-like phenotype: investigation of 1p36 deletion in 41 patients with delayed psychomotor development, hypotonia, obesity and/or hyperphagia, learning disabilities and behavioral problems.
Carla S D'Angelo, José A Da Paz, Chong A Kim, Débora R Bertola, Claudia I E Castro, Monica C Varela, Célia P Koiffmann. Eur J Med Genet 2006
39
42

Detailed phenotype-genotype study in five patients with chromosome 6q16 deletion: narrowing the critical region for Prader-Willi-like phenotype.
Maria Clara Bonaglia, Roberto Ciccone, Giorgio Gimelli, Stefania Gimelli, Susan Marelli, Joke Verheij, Roberto Giorda, Rita Grasso, Renato Borgatti, Filomena Pagone,[...]. Eur J Hum Genet 2008
61
42


Prader-Willi-like phenotype in fragile X syndrome.
C Schrander-Stumpel, W J Gerver, H Meyer, J Engelen, H Mulder, J P Fryns. Clin Genet 1994
38
35

The Prader-Willi phenotype of fragile X syndrome.
Stephen T Nowicki, Flora Tassone, Michele Y Ono, Jessica Ferranti, Marie Francoise Croquette, Beth Goodlin-Jones, Randi J Hagerman. J Dev Behav Pediatr 2007
83
35

Prader-Willi-like syndrome in a patient with an Xq23q25 duplication.
K G Monaghan, D L Van Dyke, G L Feldman. Am J Med Genet 1998
21
35

Early-onset obesity and paternal 2pter deletion encompassing the ACP1, TMEM18, and MYT1L genes.
Martine Doco-Fenzy, Camille Leroy, Anouck Schneider, Florence Petit, Marie-Ange Delrue, Joris Andrieux, Laurence Perrin-Sabourin, Emilie Landais, Azzedine Aboura, Jacques Puechberty,[...]. Eur J Hum Genet 2014
35
35

Endocrine phenotype of 6q16.1-q21 deletion involving SIM1 and Prader-Willi syndrome-like features.
Kosuke Izumi, Ryan Housam, Chirag Kapadia, Virginia A Stallings, Livija Medne, Tamim H Shaikh, Bassil M Kublaoui, Elaine H Zackai, Adda Grimberg. Am J Med Genet A 2013
23
35


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
201
28

A new case of interstitial 6q16.2 deletion in a patient with Prader-Willi-like phenotype and investigation of SIM1 gene deletion in 87 patients with syndromic obesity.
Monica C Varela, Alex Y Simões-Sato, Chong A Kim, Débora R Bertola, Claudia I E De Castro, Celia P Koiffmann. Eur J Med Genet 2006
43
28

Interstitial 6q deletion with a Prader-Willi-like phenotype: a new case and review of the literature.
H J Gilhuis, C M van Ravenswaaij, B J Hamel, F J Gabreëls. Eur J Paediatr Neurol 2000
50
28

Maternal uniparental disomy 14 syndrome demonstrates prader-willi syndrome-like phenotype.
Kana Hosoki, Masayo Kagami, Touju Tanaka, Masaya Kubota, Kenji Kurosawa, Mitsuhiro Kato, Kimiaki Uetake, Jun Tohyama, Tsutomu Ogata, Shinji Saitoh. J Pediatr 2009
42
28

Prader-Willi syndrome phenocopy due to duplication of Xq21.1-q21.31, with array CGH of the critical region.
M T Gabbett, G B Peters, J M Carmichael, A P Darmanian, F A Collins. Clin Genet 2008
19
28

Prader-Willi syndrome.
Suzanne B Cassidy, Stuart Schwartz, Jennifer L Miller, Daniel J Driscoll. Genet Med 2012
691
28

Clinical and molecular studies in fragile X patients with a Prader-Willi-like phenotype.
B B de Vries, J P Fryns, M G Butler, F Canziani, E Wesby-van Swaay, J O van Hemel, B A Oostra, D J Halley, M F Niermeijer. J Med Genet 1993
70
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
263
21

Genome organization, function, and imprinting in Prader-Willi and Angelman syndromes.
R D Nicholls, J L Knepper. Annu Rev Genomics Hum Genet 2001
418
21

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
239
21

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
474
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
188
21

Inactivation of the mouse Magel2 gene results in growth abnormalities similar to Prader-Willi syndrome.
Jocelyn M Bischof, Colin L Stewart, Rachel Wevrick. Hum Mol Genet 2007
125
21


Deletion of the SIM1 gene (6q16.2) in a patient with a Prader-Willi-like phenotype.
L Faivre, V Cormier-Daire, J M Lapierre, L Colleaux, S Jacquemont, D Geneviéve, P Saunier, A Munnich, C Turleau, S Romana,[...]. J Med Genet 2002
87
21

Is there a higher incidence of maternal uniparental disomy 14 [upd(14)mat]? Detection of 10 new patients by methylation-specific PCR.
Diana Mitter, Karin Buiting, Ferdinand von Eggeling, Alma Kuechler, Thomas Liehr, Ulrike Angelika Mau-Holzmann, Eva-Christina Prott, Dagmar Wieczorek, Gabriele Gillessen-Kaesbach. Am J Med Genet A 2006
54
21

Obesity with associated developmental delay and/or learning disability in patients exhibiting additional features: report of novel pathogenic copy number variants.
Carla Sustek D'Angelo, Ilana Kohl, Monica Castro Varela, Cláudia Irene Emílio de Castro, Chong Ae Kim, Débora Romeo Bertola, Charles Marques Lourenço, Ana Beatriz Alvarez Perez, Celia Priszkulnik Koiffmann. Am J Med Genet A 2013
22
21

De novo paracentric inversion (X)(q26q28) with features mimicking Prader-Willi syndrome.
Luisa Florez, Mary Anderson, Yves Lacassie. Am J Med Genet A 2003
5
60

Genotype/phenotype correlations in two patients with 12q subtelomere deletions.
Dmitriy M Niyazov, Zafar Nawaz, April N Justice, Helga V Toriello, Christa Lese Martin, Margaret P Adam. Am J Med Genet A 2007
16
21



Loss-of-function mutations in SIM1 contribute to obesity and Prader-Willi-like features.
Amélie Bonnefond, Anne Raimondo, Fanny Stutzmann, Maya Ghoussaini, Shwetha Ramachandrappa, David C Bersten, Emmanuelle Durand, Vincent Vatin, Beverley Balkau, Olivier Lantieri,[...]. J Clin Invest 2013
73
21




CYFIP/Sra-1 controls neuronal connectivity in Drosophila and links the Rac1 GTPase pathway to the fragile X protein.
Annette Schenck, Barbara Bardoni, Caillin Langmann, Nicholas Harden, Jean Louis Mandel, Angela Giangrande. Neuron 2003
246
14

Biochemical and genetic interaction between the fragile X mental retardation protein and the microRNA pathway.
Peng Jin, Daniela C Zarnescu, Stephanie Ceman, Mika Nakamoto, Julie Mowrey, Thomas A Jongens, David L Nelson, Kevin Moses, Stephen T Warren. Nat Neurosci 2004
463
14

Methylation-specific PCR simplifies imprinting analysis.
T Kubota, S Das, S L Christian, S B Baylin, J G Herman, D H Ledbetter. Nat Genet 1997
203
14

Prader-Willi syndrome.
Daniel J Wattendorf, Maximilian Muenke. Am Fam Physician 2005
20
14

De novo deletions of SNRPN exon 1 in early human and mouse embryos result in a paternal to maternal imprint switch.
B Bielinska, S M Blaydes, K Buiting, T Yang, M Krajewska-Walasek, B Horsthemke, C I Brannan. Nat Genet 2000
127
14

An imprinted, mammalian bicistronic transcript encodes two independent proteins.
T A Gray, S Saitoh, R D Nicholls. Proc Natl Acad Sci U S A 1999
130
14

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
181
14

Deletions of a differentially methylated CpG island at the SNRPN gene define a putative imprinting control region.
J S Sutcliffe, M Nakao, S Christian, K H Orstavik, N Tommerup, D H Ledbetter, A L Beaudet. Nat Genet 1994
372
14

The IC-SNURF-SNRPN transcript serves as a host for multiple small nucleolar RNA species and as an antisense RNA for UBE3A.
M Runte, A Hüttenhofer, S Gross, M Kiefmann, B Horsthemke, K Buiting. Hum Mol Genet 2001
266
14

Minimal definition of the imprinting center and fixation of chromosome 15q11-q13 epigenotype by imprinting mutations.
S Saitoh, K Buiting, P K Rogan, J L Buxton, D J Driscoll, J Arnemann, R König, S Malcolm, B Horsthemke, R D Nicholls. Proc Natl Acad Sci U S A 1996
139
14

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
14

The human MAGEL2 gene and its mouse homologue are paternally expressed and mapped to the Prader-Willi region.
I Boccaccio, H Glatt-Deeley, F Watrin, N Roëckel, M Lalande, F Muscatelli. Hum Mol Genet 1999
136
14

Identification of brain-specific and imprinted small nucleolar RNA genes exhibiting an unusual genomic organization.
J Cavaillé, K Buiting, M Kiefmann, M Lalande, C I Brannan, B Horsthemke, J P Bachellerie, J Brosius, A Hüttenhofer. Proc Natl Acad Sci U S A 2000
428
14


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.