A citation-based method for searching scientific literature

Angela L Duker, Blake C Ballif, Erawati V Bawle, Richard E Person, Sangeetha Mahadevan, Sarah Alliman, Regina Thompson, Ryan Traylor, Bassem A Bejjani, Lisa G Shaffer, Jill A Rosenfeld, Allen N Lamb, Trilochan Sahoo. Eur J Hum Genet 2010
Times Cited: 221







List of co-cited articles
1078 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


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
381
71

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
177
59

Highly restricted deletion of the SNORD116 region is implicated in Prader-Willi Syndrome.
Eric Bieth, Sanaa Eddiry, Véronique Gaston, Françoise Lorenzini, Alexandre Buffet, Françoise Conte Auriol, Catherine Molinas, Dorothée Cailley, Caroline Rooryck, Benoit Arveiler,[...]. Eur J Hum Genet 2015
87
59

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
194
48

Prader-Willi syndrome.
Suzanne B Cassidy, Stuart Schwartz, Jennifer L Miller, Daniel J Driscoll. Genet Med 2012
674
44

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
32

Deletion of the MBII-85 snoRNA gene cluster in mice results in postnatal growth retardation.
Boris V Skryabin, Leonid V Gubar, Birte Seeger, Jana Pfeiffer, Sergej Handel, Thomas Robeck, Elena Karpova, Timofey S Rozhdestvensky, Jürgen Brosius. PLoS Genet 2007
128
30


Snord116 is critical in the regulation of food intake and body weight.
Yue Qi, Louise Purtell, Melissa Fu, Nicola J Lee, Julia Aepler, Lei Zhang, Kim Loh, Ronaldo F Enriquez, Paul A Baldock, Sergei Zolotukhin,[...]. Sci Rep 2016
50
48

A Prader-Willi locus lncRNA cloud modulates diurnal genes and energy expenditure.
Weston T Powell, Rochelle L Coulson, Florence K Crary, Spencer S Wong, Robert A Ach, Peter Tsang, N Alice Yamada, Dag H Yasui, Janine M Lasalle. Hum Mol Genet 2013
96
22

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
263
21

Prader-Willi syndrome: a review of clinical, genetic, and endocrine findings.
M A Angulo, M G Butler, M E Cataletto. J Endocrinol Invest 2015
257
21

Hypothalamic loss of Snord116 recapitulates the hyperphagia of Prader-Willi syndrome.
Joseph Polex-Wolf, Brian Yh Lam, Rachel Larder, John Tadross, Debra Rimmington, Fàtima Bosch, Verónica Jiménez Cenzano, Eduard Ayuso, Marcella Kl Ma, Kara Rainbow,[...]. J Clin Invest 2018
47
42

Long noncoding RNAs with snoRNA ends.
Qing-Fei Yin, Li Yang, Yang Zhang, Jian-Feng Xiang, Yue-Wei Wu, Gordon G Carmichael, Ling-Ling Chen. Mol Cell 2012
274
19

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
18

Deficiency in prohormone convertase PC1 impairs prohormone processing in Prader-Willi syndrome.
Lisa C Burnett, Charles A LeDuc, Carlos R Sulsona, Daniel Paull, Richard Rausch, Sanaa Eddiry, Jayne F Martin Carli, Michael V Morabito, Alicja A Skowronski, Gabriela Hubner,[...]. J Clin Invest 2017
76
23

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
177
16

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
63
25

Mouse models of Prader-Willi Syndrome: a systematic review.
Sandrina Bervini, Herbert Herzog. Front Neuroendocrinol 2013
55
29

Long nuclear-retained non-coding RNAs and allele-specific higher-order chromatin organization at imprinted snoRNA gene arrays.
Patrice Vitali, Hélène Royo, Virginie Marty, Marie-Line Bortolin-Cavaillé, Jérôme Cavaillé. J Cell Sci 2010
47
31


A paternal deletion of MKRN3, MAGEL2 and NDN does not result in Prader-Willi syndrome.
Deniz Kanber, Jacques Giltay, Dagmar Wieczorek, Corinna Zogel, Ron Hochstenbach, Almuth Caliebe, Alma Kuechler, Bernhard Horsthemke, Karin Buiting. Eur J Hum Genet 2009
78
19


Loss of the imprinted snoRNA mbii-52 leads to increased 5htr2c pre-RNA editing and altered 5HT2CR-mediated behaviour.
Christine M Doe, Dinko Relkovic, Alastair S Garfield, Jeffrey W Dalley, David E H Theobald, Trevor Humby, Lawrence S Wilkinson, Anthony R Isles. Hum Mol Genet 2009
125
15

Prader-Willi syndrome and Angelman syndrome.
Karin Buiting. Am J Med Genet C Semin Med Genet 2010
191
14

The noncoding RNA IPW regulates the imprinted DLK1-DIO3 locus in an induced pluripotent stem cell model of Prader-Willi syndrome.
Yonatan Stelzer, Ido Sagi, Ofra Yanuka, Rachel Eiges, Nissim Benvenisty. Nat Genet 2014
91
15

Exclusion of the C/D box snoRNA gene cluster HBII-52 from a major role in Prader-Willi syndrome.
Maren Runte, Raymonda Varon, Denise Horn, Bernhard Horsthemke, Karin Buiting. Hum Genet 2005
71
18

Evidence for the role of PWCR1/HBII-85 C/D box small nucleolar RNAs in Prader-Willi syndrome.
Renata C Gallagher, Birgit Pils, Mohammed Albalwi, Uta Francke. Am J Hum Genet 2002
87
14

ADAR2-mediated editing of RNA substrates in the nucleolus is inhibited by C/D small nucleolar RNAs.
Patrice Vitali, Eugenia Basyuk, Elodie Le Meur, Edouard Bertrand, Françoise Muscatelli, Jérôme Cavaillé, Alexander Huttenhofer. J Cell Biol 2005
167
13

SNORD116 deletions cause Prader-Willi syndrome with a mild phenotype and macrocephaly.
P Fontana, M Grasso, F Acquaviva, E Gennaro, M L Galli, M Falco, F Scarano, G Scarano, F Lonardo. Clin Genet 2017
17
76

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
187
12

The snoRNA MBII-52 (SNORD 115) is processed into smaller RNAs and regulates alternative splicing.
Shivendra Kishore, Amit Khanna, Zhaiyi Zhang, Jingyi Hui, Piotr J Balwierz, Mihaela Stefan, Carol Beach, Robert D Nicholls, Mihaela Zavolan, Stefan Stamm. Hum Mol Genet 2010
199
12

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
12

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
124
12

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
215
12

Unusual Processing Generates SPA LncRNAs that Sequester Multiple RNA Binding Proteins.
Huang Wu, Qing-Fei Yin, Zheng Luo, Run-Wen Yao, Chuan-Chuan Zheng, Jun Zhang, Jian-Feng Xiang, Li Yang, Ling-Ling Chen. Mol Cell 2016
75
16

Deletion of the Snord116/SNORD116 Alters Sleep in Mice and Patients with Prader-Willi Syndrome.
Glenda Lassi, Lorenzo Priano, Silvia Maggi, Celina Garcia-Garcia, Edoardo Balzani, Nadia El-Assawy, Marco Pagani, Federico Tinarelli, Daniela Giardino, Alessandro Mauro,[...]. Sleep 2016
39
30

Increased alternate splicing of Htr2c in a mouse model for Prader-Willi syndrome leads disruption of 5HT2C receptor mediated appetite.
Alastair S Garfield, Jennifer R Davies, Luke K Burke, Hannah V Furby, Lawrence S Wilkinson, Lora K Heisler, Anthony R Isles. Mol Brain 2016
32
37

Snord116-dependent diurnal rhythm of DNA methylation in mouse cortex.
Rochelle L Coulson, Dag H Yasui, Keith W Dunaway, Benjamin I Laufer, Annie Vogel Ciernia, Yihui Zhu, Charles E Mordaunt, Theresa S Totah, Janine M LaSalle. Nat Commun 2018
31
38

Prader-Willi syndrome.
Suzanne B Cassidy, Daniel J Driscoll. Eur J Hum Genet 2009
351
11


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
264
11

snoTARGET shows that human orphan snoRNA targets locate close to alternative splice junctions.
Peter S Bazeley, Valery Shepelev, Zohreh Talebizadeh, Merlin G Butler, Larisa Fedorova, Vadim Filatov, Alexei Fedorov. Gene 2008
64
17

Targeting the histone methyltransferase G9a activates imprinted genes and improves survival of a mouse model of Prader-Willi syndrome.
Yuna Kim, Hyeong-Min Lee, Yan Xiong, Noah Sciaky, Samuel W Hulbert, Xinyu Cao, Jeffrey I Everitt, Jian Jin, Bryan L Roth, Yong-Hui Jiang. Nat Med 2017
59
18

Cognitive deficits in the Snord116 deletion mouse model for Prader-Willi syndrome.
Anna Adhikari, Nycole A Copping, Beth Onaga, Michael C Pride, Rochelle L Coulson, Mu Yang, Dag H Yasui, Janine M LaSalle, Jill L Silverman. Neurobiol Learn Mem 2019
31
35

Molecular breakpoint cloning and gene expression studies of a novel translocation t(4;15)(q27;q11.2) associated with Prader-Willi syndrome.
Birgitt Schüle, Mohammed Albalwi, Emma Northrop, David I Francis, Margaret Rowell, Howard R Slater, R J McKinlay Gardner, Uta Francke. BMC Med Genet 2005
47
21

The imprinted gene Magel2 regulates normal circadian output.
Serguei V Kozlov, James W Bogenpohl, Maureen P Howell, Rachel Wevrick, Satchin Panda, John B Hogenesch, Louis J Muglia, Russell N Van Gelder, Erik D Herzog, Colin L Stewart. Nat Genet 2007
128
10

Reactivation of maternal SNORD116 cluster via SETDB1 knockdown in Prader-Willi syndrome iPSCs.
Estela Cruvinel, Tara Budinetz, Noelle Germain, Stormy Chamberlain, Marc Lalande, Kristen Martins-Taylor. Hum Mol Genet 2014
38
26

Differential regulation of non-protein coding RNAs from Prader-Willi Syndrome locus.
Chenna R Galiveti, Carsten A Raabe, Zoltán Konthur, Timofey S Rozhdestvensky. Sci Rep 2014
30
33

Maternal transcription of non-protein coding RNAs from the PWS-critical region rescues growth retardation in mice.
Timofey S Rozhdestvensky, Thomas Robeck, Chenna R Galiveti, Carsten A Raabe, Birte Seeger, Anna Wolters, Leonid V Gubar, Jürgen Brosius, Boris V Skryabin. Sci Rep 2016
14
71


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.