A citation-based method for searching scientific literature

Flavia Niccolini, Niccolo E Mencacci, Tayyabah Yousaf, Eugenii A Rabiner, Vincenzo Salpietro, Gennaro Pagano, Bettina Balint, Stephanie Efthymiou, Henry Houlden, Roger N Gunn, Nicholas Wood, Kailash P Bhatia, Marios Politis. Mov Disord 2018
Times Cited: 19







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



Times Cited
  Times     Co-cited
Similarity


De Novo Mutations in PDE10A Cause Childhood-Onset Chorea with Bilateral Striatal Lesions.
Niccolò E Mencacci, Erik-Jan Kamsteeg, Kosuke Nakashima, Lea R'Bibo, David S Lynch, Bettina Balint, Michèl A A P Willemsen, Matthew E Adams, Sarah Wiethoff, Kazunori Suzuki,[...]. Am J Hum Genet 2016
64
63

Biallelic Mutations in PDE10A Lead to Loss of Striatal PDE10A and a Hyperkinetic Movement Disorder with Onset in Infancy.
Christine P Diggle, Stacey J Sukoff Rizzo, Michael Popiolek, Reetta Hinttala, Jan-Philip Schülke, Manju A Kurian, Ian M Carr, Alexander F Markham, David T Bonthron, Christopher Watson,[...]. Am J Hum Genet 2016
43
57

A homozygous loss-of-function mutation in PDE2A associated to early-onset hereditary chorea.
Vincenzo Salpietro, Belen Perez-Dueñas, Kosuke Nakashima, Victoria San Antonio-Arce, Andreea Manole, Stephanie Efthymiou, Jana Vandrovcova, Conceicao Bettencourt, Niccolò E Mencacci, Christine Klein,[...]. Mov Disord 2018
24
57

Gain-of-function ADCY5 mutations in familial dyskinesia with facial myokymia.
Ying-Zhang Chen, Jennifer R Friedman, Dong-Hui Chen, Guy C-K Chan, Cinnamon S Bloss, Fuki M Hisama, Sarah E Topol, Andrew R Carson, Phillip H Pham, Emily S Bonkowski,[...]. Ann Neurol 2014
81
52


Phenotypic insights into ADCY5-associated disease.
Florence C F Chang, Ana Westenberger, Russell C Dale, Martin Smith, Hardev S Pall, Belen Perez-Dueñas, Padraic Grattan-Smith, Robert A Ouvrier, Neil Mahant, Bernadette C Hanna,[...]. Mov Disord 2016
75
42

A PDE10A de novo mutation causes childhood-onset chorea with diurnal fluctuations.
Silvia Esposito, Miryam Carecchio, Davide Tonduti, Veronica Saletti, Celeste Panteghini, Luisa Chiapparini, Giovanna Zorzi, Chiara Pantaleoni, Barbara Garavaglia, Dimitri Krainc,[...]. Mov Disord 2017
10
60

ADCY5-related dyskinesia: Broader spectrum and genotype-phenotype correlations.
Dong-Hui Chen, Aurélie Méneret, Jennifer R Friedman, Olena Korvatska, Alona Gad, Emily S Bonkowski, Holly A Stessman, Diane Doummar, Cyril Mignot, Mathieu Anheim,[...]. Neurology 2015
74
31

ADCY5-related movement disorders: Frequency, disease course and phenotypic variability in a cohort of paediatric patients.
Miryam Carecchio, Niccolò E Mencacci, Alessandro Iodice, Roser Pons, Celeste Panteghini, Giovanna Zorzi, Federica Zibordi, Anastasios Bonakis, Argyris Dinopoulos, Joseph Jankovic,[...]. Parkinsonism Relat Disord 2017
44
31

Familial choreoathetosis due to novel heterozygous mutation in PDE10A.
Dhanya L Narayanan, Dipti Deshpande, Aneek Das Bhowmik, Dandu R Varma, Ashwin Dalal. Am J Med Genet A 2018
8
75

A de novo ADCY5 mutation causes early-onset autosomal dominant chorea and dystonia.
Raphael Carapito, Nicodème Paul, Meiggie Untrau, Marion Le Gentil, Louise Ott, Ghada Alsaleh, Pierre Jochem, Mirjana Radosavljevic, Cédric Le Caignec, Albert David,[...]. Mov Disord 2015
49
31

Mutations in GNAL cause primary torsion dystonia.
Tania Fuchs, Rachel Saunders-Pullman, Ikuo Masuho, Marta San Luciano, Deborah Raymond, Stewart Factor, Anthony E Lang, Tsao-Wei Liang, Richard M Trosch, Sierra White,[...]. Nat Genet 2013
196
26

Loss of phosphodiesterase 10A expression is associated with progression and severity in Parkinson's disease.
Flavia Niccolini, Thomas Foltynie, Tiago Reis Marques, Nils Muhlert, Andri C Tziortzi, Graham E Searle, Sridhar Natesan, Shitij Kapur, Eugenii A Rabiner, Roger N Gunn,[...]. Brain 2015
72
26

ADCY5 mutation carriers display pleiotropic paroxysmal day and nighttime dyskinesias.
Jennifer R Friedman, Aurélie Méneret, Dong-Hui Chen, Oriane Trouillard, Marie Vidailhet, Wendy H Raskind, Emmanuel Roze. Mov Disord 2016
34
26

ADCY5 mutations are another cause of benign hereditary chorea.
Niccolo E Mencacci, Roberto Erro, Sarah Wiethoff, Joshua Hersheson, Mina Ryten, Bettina Balint, Christos Ganos, Maria Stamelou, Niall Quinn, Henry Houlden,[...]. Neurology 2015
51
26

The clinical and genetic heterogeneity of paroxysmal dyskinesias.
Alice R Gardiner, Fatima Jaffer, Russell C Dale, Robyn Labrum, Roberto Erro, Esther Meyer, Georgia Xiromerisiou, Maria Stamelou, Matthew Walker, Dimitri Kullmann,[...]. Brain 2015
78
26

Biallelic PDE2A variants: a new cause of syndromic paroxysmal dyskinesia.
Diane Doummar, Christel Dentel, Romane Lyautey, Julia Metreau, Boris Keren, Nathalie Drouot, Ludivine Malherbe, Viviane Bouilleret, Jérémie Courraud, Maria Paola Valenti-Hirsch,[...]. Eur J Hum Genet 2020
9
55

Cyclic nucleotide phosphodiesterases: molecular regulation to clinical use.
Andrew T Bender, Joseph A Beavo. Pharmacol Rev 2006
21

Mutations in GNAL: a novel cause of craniocervical dystonia.
Kishore R Kumar, Katja Lohmann, Ikuo Masuho, Ryosuke Miyamoto, Andreas Ferbert, Thora Lohnau, Meike Kasten, Johann Hagenah, Norbert Brüggemann, Julia Graf,[...]. JAMA Neurol 2014
48
21

Change in PDE10 across early Huntington disease assessed by [18F]MNI-659 and PET imaging.
David S Russell, Danna L Jennings, Olivier Barret, Gilles D Tamagnan, Vincent M Carroll, Fabien Caillé, David Alagille, Thomas J Morley, Caroline Papin, John P Seibyl,[...]. Neurology 2016
44
21

Movement disorder in GNAO1 encephalopathy associated with gain-of-function mutations.
Huijie Feng, Benita Sjögren, Behirda Karaj, Vincent Shaw, Aysegul Gezer, Richard R Neubig. Neurology 2017
37
21

Galpha(olf) is necessary for coupling D1 and A2a receptors to adenylyl cyclase in the striatum.
J C Corvol, J M Studler, J S Schonn, J A Girault, D Hervé. J Neurochem 2001
148
21

Loss of extra-striatal phosphodiesterase 10A expression in early premanifest Huntington's disease gene carriers.
Heather Wilson, Flavia Niccolini, Salman Haider, Tiago Reis Marques, Gennaro Pagano, Christopher Coello, Sridhar Natesan, Shitij Kapur, Eugenii A Rabiner, Roger N Gunn,[...]. J Neurol Sci 2016
25
21


Definition and classification of hyperkinetic movements in childhood.
Terence D Sanger, Daofen Chen, Darcy L Fehlings, Mark Hallett, Anthony E Lang, Jonathan W Mink, Harvey S Singer, Katharine Alter, Hilla Ben-Pazi, Erin E Butler,[...]. Mov Disord 2010
212
21

Motor dysfunction in type 5 adenylyl cyclase-null mice.
Tamio Iwamoto, Satoshi Okumura, Kousaku Iwatsubo, Jun-Ichi Kawabe, Koji Ohtsu, Ikuko Sakai, Yoko Hashimoto, Aki Izumitani, Kazunori Sango, Kyoko Ajiki,[...]. J Biol Chem 2003
80
21

Treatment of ADCY5-Associated Dystonia, Chorea, and Hyperkinetic Disorders With Deep Brain Stimulation: A Multicenter Case Series.
Marisela E Dy, Florence C F Chang, Sol De Jesus, Irina Anselm, Neil Mahant, Pamela Zeilman, Lance H Rodan, Kelly D Foote, Wen-Hann Tan, Emad Eskandar,[...]. J Child Neurol 2016
26
21

Caffeine and the Dyskinesia Related to Mutations in the ADCY5 Gene.
Aurélie Méneret, Domitille Gras, Eavan McGovern, Emmanuel Roze. Ann Intern Med 2019
13
30

Is Benign Hereditary Chorea Really Benign? Brain-Lung-Thyroid Syndrome Caused by NKX2-1 Mutations.
Mered Parnes, Hassaan Bashir, Joseph Jankovic. Mov Disord Clin Pract 2018
8
50

Autosomal recessive inheritance of ADCY5-related generalized dystonia and myoclonus.
Matthew J Barrett, Eli S Williams, Chelsea Chambers, Radhika Dhamija. Neurol Genet 2017
12
33

Autosomal dominant familial dyskinesia and facial myokymia: single exome sequencing identifies a mutation in adenylyl cyclase 5.
Ying-Zhang Chen, Mark M Matsushita, Peggy Robertson, Mark Rieder, Santhosh Girirajan, Francesca Antonacci, Hillary Lipe, Evan E Eichler, Deborah A Nickerson, Thomas D Bird,[...]. Arch Neurol 2012
78
21

Clinical exome sequencing in early-onset generalized dystonia and large-scale resequencing follow-up.
Michael Zech, Sylvia Boesch, Angela Jochim, Sandrina Weber, Tobias Meindl, Barbara Schormair, Thomas Wieland, Christian Lunetta, Valeria Sansone, Michael Messner,[...]. Mov Disord 2017
67
21

Altered PDE10A expression detectable early before symptomatic onset in Huntington's disease.
Flavia Niccolini, Salman Haider, Tiago Reis Marques, Nils Muhlert, Andri C Tziortzi, Graham E Searle, Sridhar Natesan, Paola Piccini, Shitij Kapur, Eugenii A Rabiner,[...]. Brain 2015
62
21

Successful treatment of disabling paroxysmal nonkinesigenic dyskinesia with deep brain stimulation of the globus pallidus internus.
Riaan van Coller, Pieter Slabbert, Janardan Vaidyanathan, Clara Schutte. Stereotact Funct Neurosurg 2014
17
23

Triheptanoin dramatically reduces paroxysmal motor disorder in patients with GLUT1 deficiency.
Fanny Mochel, Elodie Hainque, Domitille Gras, Isaac M Adanyeguh, Samantha Caillet, Bénédicte Héron, Agathe Roubertie, Elsa Kaphan, Romain Valabregue, Daisy Rinaldi,[...]. J Neurol Neurosurg Psychiatry 2016
56
21

Dopamine dysregulation in a mouse model of paroxysmal nonkinesigenic dyskinesia.
Hsien-yang Lee, Junko Nakayama, Ying Xu, Xueliang Fan, Maha Karouani, Yiguo Shen, Emmanuel N Pothos, Ellen J Hess, Ying-Hui Fu, Robert H Edwards,[...]. J Clin Invest 2012
34
21


Benign infantile seizures and paroxysmal dyskinesia caused by an SCN8A mutation.
Elena Gardella, Felicitas Becker, Rikke S Møller, Julian Schubert, Johannes R Lemke, Line H G Larsen, Hans Eiberg, Michael Nothnagel, Holger Thiele, Janine Altmüller,[...]. Ann Neurol 2016
106
21


The evolving spectrum of PRRT2-associated paroxysmal diseases.
Darius Ebrahimi-Fakhari, Afshin Saffari, Ana Westenberger, Christine Klein. Brain 2015
143
21

PRRT2 Regulates Synaptic Fusion by Directly Modulating SNARE Complex Assembly.
Jeff Coleman, Ouardane Jouannot, Sathish K Ramakrishnan, Maria N Zanetti, Jing Wang, Vincenzo Salpietro, Henry Houlden, James E Rothman, Shyam S Krishnakumar. Cell Rep 2018
37
21

Clinical Course of Six Children With GNAO1 Mutations Causing a Severe and Distinctive Movement Disorder.
Amitha L Ananth, Amy Robichaux-Viehoever, Young-Min Kim, Andrea Hanson-Kahn, Rachel Cox, Gregory M Enns, Jonathan Strober, Marcia Willing, Bradley L Schlaggar, Yvonne W Wu,[...]. Pediatr Neurol 2016
49
21

PET imaging shows loss of striatal PDE10A in patients with Huntington disease.
Rawaha Ahmad, Sophie Bourgeois, Andrey Postnov, Mark E Schmidt, Guy Bormans, Koen Van Laere, Wim Vandenberghe. Neurology 2014
54
15

Current Understanding of PDE10A in the Modulation of Basal Ganglia Circuitry.
Jan-Philip Schülke, Nicholas J Brandon. Adv Neurobiol 2017
7
42

Phosphodiesterase 10A Inhibition Improves Cortico-Basal Ganglia Function in Huntington's Disease Models.
Vahri Beaumont, Sheng Zhong, Hai Lin, WenJin Xu, Amyaouch Bradaia, Esther Steidl, Melanie Gleyzes, Kristian Wadel, Bruno Buisson, Fernando E Padovan-Neto,[...]. Neuron 2016
59
15

Mutant huntingtin affects the rate of transcription of striatum-specific isoforms of phosphodiesterase 10A.
Haibei Hu, Elizabeth A McCaw, Andrea L O Hebb, Geraldine T Gomez, Eileen M Denovan-Wright. Eur J Neurosci 2004
60
15

Inhibition of the striatal specific phosphodiesterase PDE10A ameliorates striatal and cortical pathology in R6/2 mouse model of Huntington's disease.
Carmela Giampà, Daunia Laurenti, Serenella Anzilotti, Giorgio Bernardi, Frank S Menniti, Francesca Romana Fusco. PLoS One 2010
138
15

Distinct roles of PDE4 and PDE10A in the regulation of cAMP/PKA signaling in the striatum.
Akinori Nishi, Mahomi Kuroiwa, Diane B Miller, James P O'Callaghan, Helen S Bateup, Takahide Shuto, Naoki Sotogaku, Takaichi Fukuda, Nathaniel Heintz, Paul Greengard,[...]. J Neurosci 2008
192
15

PDE10 inhibition increases GluA1 and CREB phosphorylation and improves spatial and recognition memories in a Huntington's disease mouse model.
Albert Giralt, Ana Saavedra, Olga Carretón, Helena Arumí, Shiraz Tyebji, Jordi Alberch, Esther Pérez-Navarro. Hippocampus 2013
55
15



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.