A citation-based method for searching scientific literature

Niccolo E Mencacci, Roberto Erro, Sarah Wiethoff, Joshua Hersheson, Mina Ryten, Bettina Balint, Christos Ganos, Maria Stamelou, Niall Quinn, Henry Houlden, Nicholas W Wood, Kailash P Bhatia. Neurology 2015
Times Cited: 51







List of co-cited articles
423 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
81
54

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
49

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
47

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
48

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
45

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
27

Benign hereditary chorea: phenotype, prognosis, therapeutic outcome and long term follow-up in a large series with new mutations in the TITF1/NKX2-1 gene.
Domitille Gras, Laurence Jonard, Emmanuel Roze, Sandra Chantot-Bastaraud, Jeanette Koht, Jacques Motte, Diana Rodriguez, Malek Louha, Isabelle Caubel, Isabelle Kemlin,[...]. J Neurol Neurosurg Psychiatry 2012
67
25

Mutations in TITF-1 are associated with benign hereditary chorea.
Guido J Breedveld, Jeroen W F van Dongen, Cesare Danesino, Andrea Guala, Alan K Percy, Leon S Dure, Peter Harper, Lazarus P Lazarou, Herma van der Linde, Marijke Joosse,[...]. Hum Mol Genet 2002
146
23

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

Benign Hereditary Chorea: An Update.
Kathryn J Peall, Manju A Kurian. Tremor Other Hyperkinet Mov (N Y) 2015
23
52

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
35

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
27

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
42

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
64

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
24
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
25

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
19

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
19

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
15


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
16

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
66
15

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
57

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
61

Benign hereditary chorea related to NKX2.1: expansion of the genotypic and phenotypic spectrum.
Kathryn J Peall, Daniel Lumsden, Rachel Kneen, Rajesh Madhu, Deirdre Peake, Frances Gibbon, Hilary Lewis, Tammy Hedderly, Esther Meyer, Stephanie A Robb,[...]. Dev Med Child Neurol 2014
29
24

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
96
13

C9orf72 expansions are the most common genetic cause of Huntington disease phenocopies.
Davina J Hensman Moss, Mark Poulter, Jon Beck, Jason Hehir, James M Polke, Tracy Campbell, Garry Adamson, Ese Mudanohwo, Peter McColgan, Andrea Haworth,[...]. Neurology 2014
128
13

Progressive Movement Disorder in Brothers Carrying a GNAO1 Mutation Responsive to Deep Brain Stimulation.
Neil Kulkarni, Sha Tang, Ratan Bhardwaj, Saunder Bernes, Theresa A Grebe. J Child Neurol 2016
40
17

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
122
13

A missense mutation in KCTD17 causes autosomal dominant myoclonus-dystonia.
Niccolo E Mencacci, Ignacio Rubio-Agusti, Anselm Zdebik, Friedrich Asmus, Marthe H R Ludtmann, Mina Ryten, Vincent Plagnol, Ann-Kathrin Hauser, Sara Bandres-Ciga, Conceição Bettencourt,[...]. Am J Hum Genet 2015
69
11


The differential diagnosis of Huntington's disease-like syndromes: 'red flags' for the clinician.
Davide Martino, Maria Stamelou, Kailash P Bhatia. J Neurol Neurosurg Psychiatry 2013
38
15

Recent advances in genetics of chorea.
Niccolò E Mencacci, Miryam Carecchio. Curr Opin Neurol 2016
17
35

A case of severe movement disorder with GNAO1 mutation responsive to topiramate.
Saori Sakamoto, Yukifumi Monden, Ryoko Fukai, Noriko Miyake, Hiroshi Saito, Akihiko Miyauchi, Ayumi Matsumoto, Masako Nagashima, Hitoshi Osaka, Naomichi Matsumoto,[...]. Brain Dev 2017
15
40

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
16

GNAO1-related movement disorder with life-threatening exacerbations: movement phenomenology and response to DBS.
Michaela Waak, Shekeeb S Mohammad, David Coman, Kate Sinclair, Lisa Copeland, Peter Silburn, Terry Coyne, Jim McGill, Mary O'Regan, Richard Selway,[...]. J Neurol Neurosurg Psychiatry 2018
30
20


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
77
9

Impaired D2 dopamine receptor function in mice lacking type 5 adenylyl cyclase.
Ko-Woon Lee, Jang-Hee Hong, In Young Choi, Yongzhe Che, Ja-Kyeong Lee, Sung-Don Yang, Chang-Woo Song, Ho Sung Kang, Jae-Heun Lee, Jai Sung Noh,[...]. J Neurosci 2002
112
9

H-ABC syndrome and DYT4: Variable expressivity or pleiotropy of TUBB4 mutations?
Roberto Erro, Joshua Hersheson, Christos Ganos, Niccoló E Mencacci, Maria Stamelou, Amit Batla, Stefanie Catherine Thust, Jose M Bras, Rita J Guerreiro, John Hardy,[...]. Mov Disord 2015
33
15

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
9

Huntington disease phenocopy is a familial prion disease.
R C Moore, F Xiang, J Monaghan, D Han, Z Zhang, L Edström, M Anvret, S B Prusiner. Am J Hum Genet 2001
88
9

Junctophilin 3 (JPH3) expansion mutations causing Huntington disease like 2 (HDL2) are common in South African patients with African ancestry and a Huntington disease phenotype.
Amanda Krause, Claire Mitchell, Fahmida Essop, Susan Tager, James Temlett, Giovanni Stevanin, Christopher Ross, Dobrila Rudnicki, Russell Margolis. Am J Med Genet B Neuropsychiatr Genet 2015
30
16

Identification of a human synaptotagmin-1 mutation that perturbs synaptic vesicle cycling.
Kate Baker, Sarah L Gordon, Detelina Grozeva, Margriet van Kogelenberg, Nicola Y Roberts, Michael Pike, Edward Blair, Matthew E Hurles, W Kling Chong, Torsten Baldeweg,[...]. J Clin Invest 2015
60
9

Deleterious mutation in GPR88 is associated with chorea, speech delay, and learning disabilities.
Fadi Alkufri, Avraham Shaag, Bassam Abu-Libdeh, Orly Elpeleg. Neurol Genet 2016
27
18

A novel de novo mutation of the TITF1/NKX2-1 gene causing ataxia, benign hereditary chorea, hypothyroidism and a pituitary mass in a UK family and review of the literature.
Liana Veneziano, Michael H Parkinson, Elide Mantuano, Marina Frontali, Kailash P Bhatia, Paola Giunti. Cerebellum 2014
19
26

Recurrent GNAO1 Mutations Associated With Developmental Delay and a Movement Disorder.
Leonie A Menke, Marc Engelen, Mariel Alders, Vincent J J Odekerken, Frank Baas, Jan M Cobben. J Child Neurol 2016
24
20

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
16
31

GNAO1-associated epileptic encephalopathy and movement disorders: c.607G>A variant represents a probable mutation hotspot with a distinct phenotype.
Ravindra Arya, Christine Spaeth, Donald L Gilbert, James L Leach, Katherine D Holland. Epileptic Disord 2017
19
26

Expanding Phenotype of De Novo Mutations in GNAO1: Four New Cases and Review of Literature.
David C Schorling, Tobias Dietel, Christina Evers, Katrin Hinderhofer, Rudolf Korinthenberg, Daniel Ezzo, Carsten G Bönnemann, Janbernd Kirschner. Neuropediatrics 2017
20
25


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.