A citation-based method for searching scientific literature

Ferdinand Althammer, Francoise Muscatelli, Valery Grinevich, Christian P Schaaf. Transl Psychiatry 2022
Times Cited: 2







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



Times Cited
  Times     Co-cited
Similarity


A single postnatal injection of oxytocin rescues the lethal feeding behaviour in mouse newborns deficient for the imprinted Magel2 gene.
Fabienne Schaller, Françoise Watrin, Rachel Sturny, Annick Massacrier, Pierre Szepetowski, Françoise Muscatelli. Hum Mol Genet 2010
133
100

Magel2 knockout mice manifest altered social phenotypes and a deficit in preference for social novelty.
M D Fountain, H Tao, C-A Chen, J Yin, C P Schaaf. Genes Brain Behav 2017
26
50

Phylogenetic Analysis of the SNORD116 Locus.
Deborah J Good, Matthew A Kocher. Genes (Basel) 2017
7
50


Clinical phenotypes of MAGEL2 mutations and deletions.
Karin Buiting, Nataliya Di Donato, Jasmin Beygo, Susanne Bens, Maja von der Hagen, Karl Hackmann, Bernhard Horsthemke. Orphanet J Rare Dis 2014
19
50

SNORD116 and SNORD115 change expression of multiple genes and modify each other's activity.
Marina Falaleeva, Justin Surface, Manli Shen, Pierre de la Grange, Stefan Stamm. Gene 2015
42
50

Disruption of the mouse Necdin gene results in hypothalamic and behavioral alterations reminiscent of the human Prader-Willi syndrome.
F Muscatelli, D N Abrous, A Massacrier, I Boccaccio, M Le Moal, P Cau, H Cremer. Hum Mol Genet 2000
240
50

Neural representations of hunger and satiety in Prader-Willi syndrome.
E C Hinton, A J Holland, M S N Gellatly, S Soni, M Patterson, M A Ghatei, A M Owen. Int J Obes (Lond) 2006
75
50

Paternally inherited microdeletion at 15q11.2 confirms a significant role for the SNORD116 C/D box snoRNA cluster in Prader-Willi syndrome.
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,[...]. Eur J Hum Genet 2010
226
50

Unexpectedly increased anorexigenic postprandial responses of PYY and GLP-1 to fast ice cream consumption in adult patients with Prader-Willi syndrome.
A E Rigamonti, S Bini, G Grugni, F Agosti, A De Col, M Mallone, S G Cella, A Sartorio. Clin Endocrinol (Oxf) 2014
10
50


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
182
50

Autism spectrum disorder in Prader-Willi syndrome: A systematic review.
Jeffrey A Bennett, Tamara Germani, Andrea M Haqq, Lonnie Zwaigenbaum. Am J Med Genet A 2015
65
50

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
231
50

Mutations in TrkA Causing Congenital Insensitivity to Pain with Anhidrosis (CIPA) Induce Misfolding, Aggregation, and Mutation-dependent Neurodegeneration by Dysfunction of the Autophagic Flux.
María Luisa Franco, Cristina Melero, Esther Sarasola, Paloma Acebo, Alfonso Luque, Isabel Calatayud-Baselga, María García-Barcina, Marçal Vilar. J Biol Chem 2016
20
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
863
50

An investigation into food preferences and the neural basis of food-related incentive motivation in Prader-Willi syndrome.
E C Hinton, A J Holland, M S N Gellatly, S Soni, A M Owen. J Intellect Disabil Res 2006
32
50

In vivo neuroimaging evidence of hypothalamic alteration in Prader-Willi syndrome.
Stephanie S G Brown, Katherine E Manning, Paul Fletcher, Anthony Holland. Brain Commun 2022
1
100

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
390
50

Growth hormone, gender and face shape in Prader-Willi syndrome.
Mauren Abreu de Souza, Catherine McAllister, Michael Suttie, Concetta Perrotta, Teresa Mattina, Francesca Faravelli, Francesca Forzano, Anthony Holland, Peter Hammond. Am J Med Genet A 2013
14
50

Hypothalamus Specific Re-Introduction of SNORD116 into Otherwise Snord116 Deficient Mice Increased Energy Expenditure.
Y Qi, L Purtell, M Fu, L Zhang, S Zolotukhin, L Campbell, H Herzog. J Neuroendocrinol 2017
6
50

Necdin shapes serotonergic development and SERT activity modulating breathing in a mouse model for Prader-Willi syndrome.
Valéry Matarazzo, Laura Caccialupi, Fabienne Schaller, Yuri Shvarev, Nazim Kourdougli, Alessandra Bertoni, Clément Menuet, Nicolas Voituron, Evan Deneris, Patricia Gaspar,[...]. Elife 2017
21
50

A review of clinical trials of oxytocin in Prader-Willi syndrome.
Lauren J Rice, Stewart L Einfeld, Nan Hu, C Sue Carter. Curr Opin Psychiatry 2018
28
50

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
184
50

The C15orf2 gene in the Prader-Willi syndrome region is subject to genomic imprinting and positive selection.
Michaela Wawrzik, Unga Arifa Unmehopa, Dick Frans Swaab, Johannes van de Nes, Karin Buiting, Bernhard Horsthemke. Neurogenetics 2010
16
50

The paradox of Prader-Willi syndrome revisited: Making sense of the phenotype.
Anthony Holland, Katie Manning, Joyce Whittington. EBioMedicine 2022
1
100

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
83
50

Oxytocin is an age-specific circulating hormone that is necessary for muscle maintenance and regeneration.
Christian Elabd, Wendy Cousin, Pavan Upadhyayula, Robert Y Chen, Marc S Chooljian, Ju Li, Sunny Kung, Kevin P Jiang, Irina M Conboy. Nat Commun 2014
224
50

Oxytocin affects nitric oxide and cytokine production by sepsis-sensitized macrophages.
Gabriela Ravanelli Oliveira-Pelegrin, Rafael Simone Saia, Evelin Capellari Cárnio, Maria José Alves Rocha. Neuroimmunomodulation 2013
33
50

Oxytocin: A Potential Therapeutic for Obesity.
Soo Min Hong, Jeong-Kyung Ko, Jung-Joon Moon, Youl-Ri Kim. J Obes Metab Syndr 2021
2
50


Oxytocin administration suppresses hypothalamic activation in response to visual food cues.
Agatha A van der Klaauw, Hisham Ziauddeen, Julia M Keogh, Elana Henning, Sekesai Dachi, Paul C Fletcher, I Sadaf Farooqi. Sci Rep 2017
25
50



The neuroanatomical distribution of oxytocin receptor binding and mRNA in the male rhesus macaque (Macaca mulatta).
Sara M Freeman, Kiyoshi Inoue, Aaron L Smith, Mark M Goodman, Larry J Young. Psychoneuroendocrinology 2014
146
50

Targeting the Oxytocinergic System: A Possible Pharmacological Strategy for the Treatment of Inflammation Occurring in Different Chronic Diseases.
Marzia Friuli, Barbara Eramo, Marta Valenza, Caterina Scuderi, Gustavo Provensi, Adele Romano. Int J Mol Sci 2021
7
50

The effect of acute stress exposure on ischemia and reperfusion injury in rat heart: role of oxytocin.
Maryam Moghimian, Mahdieh Faghihi, Seyed Morteza Karimian, Alireza Imani. Stress 2012
19
50

Impaired thermoregulatory ability of oxytocin-deficient mice during cold-exposure.
Yoshiyuki Kasahara, Yuki Takayanagi, Teruo Kawada, Keiichi Itoi, Katsuhiko Nishimori. Biosci Biotechnol Biochem 2007
57
50

Oxytocin treatment attenuates amygdala activity in autism: a treatment-mechanism study with long-term follow-up.
Sylvie Bernaerts, Bart Boets, Jean Steyaert, Nicole Wenderoth, Kaat Alaerts. Transl Psychiatry 2020
11
50

Caffeine inhibits hypothalamic A1R to excite oxytocin neuron and ameliorate dietary obesity in mice.
Liufeng Wu, Jia Meng, Qing Shen, Yi Zhang, Susu Pan, Zhuo Chen, Ling-Qiang Zhu, Youming Lu, Yuan Huang, Guo Zhang. Nat Commun 2017
43
50

Oxytocin, A Possible Treatment for Covid-19? Everything to Gain, Nothing to Lose.
Phuoc-Tan Diep, Benjamin Buemann, Kerstin Uvnäs-Moberg. Clin Neuropsychiatry 2020
3
50

Central effects of oxytocin.
P Richard, F Moos, M J Freund-Mercier. Physiol Rev 1991
314
50


Oxytocin can regulate myometrial smooth muscle excitability by inhibiting the Na+ -activated K+ channel, Slo2.1.
Juan J Ferreira, Alice Butler, Richard Stewart, Ana Laura Gonzalez-Cota, Pascale Lybaert, Chinwendu Amazu, Erin L Reinl, Monali Wakle-Prabagaran, Lawrence Salkoff, Sarah K England,[...]. J Physiol 2019
18
50

An Early Postnatal Oxytocin Treatment Prevents Social and Learning Deficits in Adult Mice Deficient for Magel2, a Gene Involved in Prader-Willi Syndrome and Autism.
Hamid Meziane, Fabienne Schaller, Sylvian Bauer, Claude Villard, Valery Matarazzo, Fabrice Riet, Gilles Guillon, Daniel Lafitte, Michel G Desarmenien, Maithé Tauber,[...]. Biol Psychiatry 2015
103
50

The effects of chronic oxytocin administration on body weight and food intake in DHT-induced PCOS model rats.
Takeshi Iwasa, Toshiya Matsuzaki, Yiliyasi Mayila, Takako Kawakita, Rie Yanagihara, Minoru Irahara. Gynecol Endocrinol 2020
9
50


CD38 is critical for social behaviour by regulating oxytocin secretion.
Duo Jin, Hong-Xiang Liu, Hirokazu Hirai, Takashi Torashima, Taku Nagai, Olga Lopatina, Natalia A Shnayder, Kiyofumi Yamada, Mami Noda, Toshihiro Seike,[...]. Nature 2007
462
50

Early life oxytocin treatment improves thermo-sensory reactivity and maternal behavior in neonates lacking the autism-associated gene Magel2.
Laura Caccialupi Da Prato, Ugo Zayan, Dina Abdallah, Vanessa Point, Fabienne Schaller, Emilie Pallesi-Pocachard, Aurélie Montheil, Stéphane Canaan, Jean-Luc Gaiarsa, Françoise Muscatelli,[...]. Neuropsychopharmacology 2022
1
100


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.