A citation-based method for searching scientific literature

Dong-Hui Chen, Aurélie Méneret, Jennifer R Friedman, Olena Korvatska, Alona Gad, Emily S Bonkowski, Holly A Stessman, Diane Doummar, Cyril Mignot, Mathieu Anheim, Saunder Bernes, Marie Y Davis, Nathalie Damon-Perrière, Bertrand Degos, David Grabli, Domitille Gras, Fuki M Hisama, Katherine M Mackenzie, Phillip D Swanson, Christine Tranchant, Marie Vidailhet, Steven Winesett, Oriane Trouillard, Laura M Amendola, Michael O Dorschner, Michael Weiss, Evan E Eichler, Ali Torkamani, Emmanuel Roze, Thomas D Bird, Wendy H Raskind. Neurology 2015
Times Cited: 76







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



Times Cited
  Times     Co-cited
Similarity


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
82
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
76
51

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
81
38

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
51
50

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
35
71

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
45

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
47

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
27
62

ADCY5-related dyskinesia presenting as familial myoclonus-dystonia.
Andrew G L Douglas, Gaia Andreoletti, Kevin Talbot, Simon R Hammans, Jaspal Singh, Andrea Whitney, Sarah Ennis, Nicola C Foulds. Neurogenetics 2017
25
68

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
68
23

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
199
17

Phenomenology and classification of dystonia: a consensus update.
Alberto Albanese, Kailash Bhatia, Susan B Bressman, Mahlon R Delong, Stanley Fahn, Victor S C Fung, Mark Hallett, Joseph Jankovic, Hyder A Jinnah, Christine Klein,[...]. Mov Disord 2013
17

Familial dyskinesia and facial myokymia (FDFM): a novel movement disorder.
M Fernandez, W Raskind, J Wolff, M Matsushita, E Yuen, W Graf, H Lipe, T Bird. Ann Neurol 2001
30
40

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
45
26

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
66
18

Alternating Hemiplegia of Childhood as a New Presentation of Adenylate Cyclase 5-Mutation-Associated Disease: A Report of Two Cases.
Ana Westenberger, Christoph Max, Norbert Brüggemann, Aloysius Domingo, Karen Grütz, Heike Pawlack, Anne Weissbach, Andrea A Kühn, Juliane Spiegler, Anthony E Lang,[...]. J Pediatr 2017
17
70


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
112
14

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
81
14

The evolving spectrum of PRRT2-associated paroxysmal diseases.
Darius Ebrahimi-Fakhari, Afshin Saffari, Ana Westenberger, Christine Klein. Brain 2015
149
14

Deep Brain Stimulation in an Additional Patient With ADCY5-Related Movement Disorder.
Inge A Meijer, Joan Miravite, Brian H Kopell, Naomi Lubarr. J Child Neurol 2017
14
78

Phenotypic spectrum of GNAO1 variants: epileptic encephalopathy to involuntary movements with severe developmental delay.
Hirotomo Saitsu, Ryoko Fukai, Bruria Ben-Zeev, Yasunari Sakai, Masakazu Mimaki, Nobuhiko Okamoto, Yasuhiro Suzuki, Yukifumi Monden, Hiroshi Saito, Barak Tziperman,[...]. Eur J Hum Genet 2016
67
14

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
13

Paroxysmal dyskinesias: clinical features and classification.
M Demirkiran, J Jankovic. Ann Neurol 1995
356
11

Exome sequencing identifies truncating mutations in PRRT2 that cause paroxysmal kinesigenic dyskinesia.
Wan-Jin Chen, Yu Lin, Zhi-Qi Xiong, Wei Wei, Wang Ni, Guo-He Tan, Shun-Ling Guo, Jin He, Ya-Fang Chen, Qi-Jie Zhang,[...]. Nat Genet 2011
312
11

Homozygous GNAL mutation associated with familial childhood-onset generalized dystonia.
Ikuo Masuho, Mingyan Fang, Chunyu Geng, Jianguo Zhang, Hui Jiang, Riza Köksal Özgul, Didem Yücel Yılmaz, Dilek Yalnızoğlu, Deniz Yüksel, Anna Yarrow,[...]. Neurol Genet 2016
17
52

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
41
21

Autosomal recessive inheritance of ADCY5-related generalized dystonia and myoclonus.
Matthew J Barrett, Eli S Williams, Chelsea Chambers, Radhika Dhamija. Neurol Genet 2017
13
69

Caffeine and the Dyskinesia Related to Mutations in the ADCY5 Gene.
Aurélie Méneret, Domitille Gras, Eavan McGovern, Emmanuel Roze. Ann Intern Med 2019
15
60

Role of Gα(olf) in familial and sporadic adult-onset primary dystonia.
Satya R Vemula, Andreas Puschmann, Jianfeng Xiao, Yu Zhao, Monika Rudzińska, Karen P Frei, Daniel D Truong, Zbigniew K Wszolek, Mark S LeDoux. Hum Mol Genet 2013
78
10

De Novo mutations in GNAO1, encoding a Gαo subunit of heterotrimeric G proteins, cause epileptic encephalopathy.
Kazuyuki Nakamura, Hirofumi Kodera, Tenpei Akita, Masaaki Shiina, Mitsuhiro Kato, Hideki Hoshino, Hiroshi Terashima, Hitoshi Osaka, Shinichi Nakamura, Jun Tohyama,[...]. Am J Hum Genet 2013
127
10

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.
Sue Richards, Nazneen Aziz, Sherri Bale, David Bick, Soma Das, Julie Gastier-Foster, Wayne W Grody, Madhuri Hegde, Elaine Lyon, Elaine Spector,[...]. Genet Med 2015
10

Nomenclature of genetic movement disorders: Recommendations of the international Parkinson and movement disorder society task force.
Connie Marras, Anthony Lang, Bart P van de Warrenburg, Carolyn M Sue, Sarah J Tabrizi, Lars Bertram, Saadet Mercimek-Mahmutoglu, Darius Ebrahimi-Fakhari, Thomas T Warner, Alexandra Durr,[...]. Mov Disord 2016
137
10

Expanding the ADCY5 phenotype toward spastic paraparesis: A mutation in the M2 domain.
Anne J E Waalkens, Fleur Vansenne, Annemarie H van der Hout, Rodi Zutt, Jeroen Mourmans, Eduardo Tolosa, Tom J de Koning, Marina A J Tijssen. Neurol Genet 2018
10
80

ADCY5-Related Dyskinesia: Improving Clinical Detection of an Evolving Disorder.
Nirosen Vijiaratnam, Kailash P Bhatia, Anthony E Lang, Wendy H Raskind, Alberto J Espay. Mov Disord Clin Pract 2019
18
44

Severe phenotypic spectrum of biallelic mutations in PRRT2 gene.
Marion Delcourt, Florence Riant, Josette Mancini, Mathieu Milh, Vincent Navarro, Emmanuel Roze, Véronique Humbertclaude, Christian Korff, Vincent Des Portes, Pierre Szepetowski,[...]. J Neurol Neurosurg Psychiatry 2015
50
14

Differential expression of type I, II, and V adenylyl cyclase gene in the postnatal developing rat brain.
I Matsuoka, Y Suzuki, N Defer, H Nakanishi, J Hanoune. J Neurochem 1997
97
9

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
52
13



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
41

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
58
12

Familial paroxysmal exercise-induced dystonia: atypical presentation of autosomal dominant GTP-cyclohydrolase 1 deficiency.
Russell C Dale, Anna Melchers, Victor S C Fung, Padraic Grattan-Smith, Henry Houlden, John Earl. Dev Med Child Neurol 2010
34
20

The phenotypic spectrum of DYT24 due to ANO3 mutations.
Maria Stamelou, Gavin Charlesworth, Carla Cordivari, Susanne A Schneider, Georg Kägi, Una-Marie Sheerin, Ignacio Rubio-Agusti, Amit Batla, Henry Houlden, Nicholas W Wood,[...]. Mov Disord 2014
70
10

Paroxysmal exercise-induced dystonia within the phenotypic spectrum of ECHS1 deficiency.
Simone Olgiati, Matej Skorvanek, Marialuisa Quadri, Michelle Minneboo, Josja Graafland, Guido J Breedveld, Ramon Bonte, Zeliha Ozgur, Mirjam C G N van den Hout, Kees Schoonderwoerd,[...]. Mov Disord 2016
38
18

Mutations in the histone methyltransferase gene KMT2B cause complex early-onset dystonia.
Esther Meyer, Keren J Carss, Julia Rankin, John M E Nichols, Detelina Grozeva, Agnel P Joseph, Niccolo E Mencacci, Apostolos Papandreou, Joanne Ng, Serena Barral,[...]. Nat Genet 2017
118
9

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
150
9

A post hoc study on gene panel analysis for the diagnosis of dystonia.
Martje E van Egmond, Coen H A Lugtenberg, Oebele F Brouwer, Maria Fiorella Contarino, Victor S C Fung, M Rebecca Heiner-Fokkema, Jacobus J van Hilten, Annemarie H van der Hout, Kathryn J Peall, Richard J Sinke,[...]. Mov Disord 2017
39
17

GNAO1 encephalopathy: Broadening the phenotype and evaluating treatment and outcome.
Federica Rachele Danti, Serena Galosi, Marta Romani, Martino Montomoli, Keren J Carss, F Lucy Raymond, Elena Parrini, Claudia Bianchini, Tony McShane, Russell C Dale,[...]. Neurol Genet 2017
48
14

Facial twitches in ADCY5-associated disease - Myokymia or myoclonus? An electromyography study.
Sinem Tunc, Norbert Brüggemann, Magdalena K Baaske, Corinna Hartmann, Karen Grütz, Ana Westenberger, Christine Klein, Alexander Münchau, Tobias Bäumer. Parkinsonism Relat Disord 2017
13
53


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.