A citation-based method for searching scientific literature

H A Jinnah, Yan V Sun. Neurobiol Dis 2019
Times Cited: 23







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



Times Cited
  Times     Co-cited
Similarity


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
73

Dystonia.
Bettina Balint, Niccolò E Mencacci, Enza Maria Valente, Antonio Pisani, John Rothwell, Joseph Jankovic, Marie Vidailhet, Kailash P Bhatia. Nat Rev Dis Primers 2018
99
56

Dopa-responsive dystonia--clinical and genetic heterogeneity.
Subhashie Wijemanne, Joseph Jankovic. Nat Rev Neurol 2015
116
30

Update on the Genetics of Dystonia.
Katja Lohmann, Christine Klein. Curr Neurol Neurosci Rep 2017
67
30

Striatal cholinergic dysfunction as a unifying theme in the pathophysiology of dystonia.
K L Eskow Jaunarajs, P Bonsi, M F Chesselet, D G Standaert, A Pisani. Prog Neurobiol 2015
87
26

Dystonia: diagnosis and management.
A Albanese, M Di Giovanni, S Lalli. Eur J Neurol 2019
32
21

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
126
21

A new knock-in mouse model of l-DOPA-responsive dystonia.
Samuel J Rose, Xin Y Yu, Ann K Heinzer, Porter Harrast, Xueliang Fan, Robert S Raike, Valerie B Thompson, Jean-Francois Pare, David Weinshenker, Yoland Smith,[...]. Brain 2015
30
17

Assessment of patients with isolated or combined dystonia: an update on dystonia syndromes.
Victor S C Fung, H A Jinnah, Kailash Bhatia, Marie Vidailhet. Mov Disord 2013
60
17

The Dystonias.
H A Jinnah. Continuum (Minneap Minn) 2019
9
44

Longitudinal studies of botulinum toxin in cervical dystonia: Why do patients discontinue therapy?
H A Jinnah, Cynthia L Comella, Joel Perlmutter, Codrin Lungu, Mark Hallett. Toxicon 2018
25
17

Dystonia treatment: Patterns of medication use in an international cohort.
Sarah Pirio Richardson, Ashley R Wegele, Betty Skipper, Amanda Deligtisch, H A Jinnah. Neurology 2017
24
17

Dystonia and dopamine: From phenomenology to pathophysiology.
Bastien Ribot, Jérome Aupy, Marie Vidailhet, Joachim Mazère, Antonio Pisani, Erwan Bezard, Dominique Guehl, Pierre Burbaud. Prog Neurobiol 2019
18
22

Dystonia as a network disorder: a concept in evolution.
Tommaso Schirinzi, Giuseppe Sciamanna, Nicola B Mercuri, Antonio Pisani. Curr Opin Neurol 2018
29
17

Dystonia genes functionally converge in specific neurons and share neurobiology with psychiatric disorders.
Niccolò E Mencacci, Regina Reynolds, Sonia Garcia Ruiz, Jana Vandrovcova, Paola Forabosco, Alvaro Sánchez-Ferrer, Viola Volpato, Michael E Weale, Kailash P Bhatia, Caleb Webber,[...]. Brain 2020
15
26

The functional neuroanatomy of dystonia.
Vladimir K Neychev, Robert E Gross, Stephane Lehéricy, Ellen J Hess, H A Jinnah. Neurobiol Dis 2011
266
17

Clinical and genetic features of cervical dystonia in a large multicenter cohort.
Mark S LeDoux, Satya R Vemula, Jianfeng Xiao, Misty M Thompson, Joel S Perlmutter, Laura J Wright, H A Jinnah, Ami R Rosen, Peter Hedera, Cynthia L Comella,[...]. Neurol Genet 2016
26
17

Psychiatric associations of adult-onset focal dystonia phenotypes.
Brian D Berman, Johanna Junker, Erika Shelton, Stefan H Sillau, H A Jinnah, Joel S Perlmutter, Alberto J Espay, Joseph Jankovic, Marie Vidailhet, Cecilia Bonnet,[...]. J Neurol Neurosurg Psychiatry 2017
45
13

Dystonia: Are animal models relevant in therapeutics?
M Meringolo, A Tassone, P Imbriani, G Ponterio, A Pisani. Rev Neurol (Paris) 2018
7
42

The Anatomical Basis for Dystonia: The Motor Network Model.
H A Jinnah, Vladimir Neychev, Ellen J Hess. Tremor Other Hyperkinet Mov (N Y) 2017
49
13

It's not just the basal ganglia: Cerebellum as a target for dystonia therapeutics.
Ambika Tewari, Rachel Fremont, Kamran Khodakhah. Mov Disord 2017
48
13



Wilson's disease and other neurological copper disorders.
Oliver Bandmann, Karl Heinz Weiss, Stephen G Kaler. Lancet Neurol 2015
311
13

Mutations in SLC39A14 disrupt manganese homeostasis and cause childhood-onset parkinsonism-dystonia.
Karin Tuschl, Esther Meyer, Leonardo E Valdivia, Ningning Zhao, Chris Dadswell, Alaa Abdul-Sada, Christina Y Hung, Michael A Simpson, W K Chong, Thomas S Jacques,[...]. Nat Commun 2016
134
13

Mutations in SLC30A10 cause parkinsonism and dystonia with hypermanganesemia, polycythemia, and chronic liver disease.
Marialuisa Quadri, Antonio Federico, Tianna Zhao, Guido J Breedveld, Carla Battisti, Cathérine Delnooz, Lies-Anne Severijnen, Lara Di Toro Mammarella, Andrea Mignarri, Lucia Monti,[...]. Am J Hum Genet 2012
226
13

Botulinum toxin treatment failures in cervical dystonia: causes, management, and outcomes.
H A Jinnah, Emily Goodmann, Ami R Rosen, Marian Evatt, Alan Freeman, Stewart Factor. J Neurol 2016
27
13

Psychiatric comorbidities in dystonia: emerging concepts.
Mateusz Zurowski, William M McDonald, Susan Fox, Laura Marsh. Mov Disord 2013
53
13

Treatable inherited rare movement disorders.
H A Jinnah, Alberto Albanese, Kailash P Bhatia, Francisco Cardoso, Gustavo Da Prat, Tom J de Koning, Alberto J Espay, Victor Fung, Pedro J Garcia-Ruiz, Oscar Gershanik,[...]. Mov Disord 2018
45
13

The neurobiological basis for novel experimental therapeutics in dystonia.
Anthony M Downs, Kaitlyn M Roman, Simone A Campbell, Antonio Pisani, Ellen J Hess, Paola Bonsi. Neurobiol Dis 2019
11
27

Functional Genomic Analyses of Mendelian and Sporadic Disease Identify Impaired eIF2α Signaling as a Generalizable Mechanism for Dystonia.
Joseph E Rittiner, Zachary F Caffall, Ricardo Hernández-Martinez, Sydney M Sanderson, James L Pearson, Kaylin K Tsukayama, Anna Y Liu, Changrui Xiao, Samantha Tracy, Miranda K Shipman,[...]. Neuron 2016
42
13

An anticholinergic reverses motor control and corticostriatal LTD deficits in Dyt1 ΔGAG knock-in mice.
Mai T Dang, Fumiaki Yokoi, Chad C Cheetham, Jun Lu, Viet Vo, David M Lovinger, Yuqing Li. Behav Brain Res 2012
65
13

The focal dystonias: current views and challenges for future research.
H A Jinnah, Alfredo Berardelli, Cynthia Comella, Giovanni Defazio, Mahlon R Delong, Stewart Factor, Wendy R Galpern, Mark Hallett, Christy L Ludlow, Joel S Perlmutter,[...]. Mov Disord 2013
126
13

Negative allosteric modulation of mGlu5 receptor rescues striatal D2 dopamine receptor dysfunction in rodent models of DYT1 dystonia.
G Sciamanna, G Ponterio, A Tassone, M Maltese, G Madeo, G Martella, S Poli, T Schirinzi, P Bonsi, A Pisani. Neuropharmacology 2014
20
15

Hyperkinetic disorders and loss of synaptic downscaling.
Paolo Calabresi, Antonio Pisani, John Rothwell, Veronica Ghiglieri, Josè A Obeso, Barbara Picconi. Nat Neurosci 2016
64
13

The early-onset torsion dystonia gene (DYT1) encodes an ATP-binding protein.
L J Ozelius, J W Hewett, C E Page, S B Bressman, P L Kramer, C Shalish, D de Leon, M F Brin, D Raymond, D P Corey,[...]. Nat Genet 1997
750
13

Abnormal striatal and thalamic dopamine neurotransmission: Genotype-related features of dystonia.
M Carbon, M Niethammer, S Peng, D Raymond, V Dhawan, T Chaly, Y Ma, S Bressman, D Eidelberg. Neurology 2009
74
13

EFNS guidelines on diagnosis and treatment of primary dystonias.
A Albanese, F Asmus, K P Bhatia, A E Elia, B Elibol, G Filippini, T Gasser, J K Krauss, N Nardocci, A Newton,[...]. Eur J Neurol 2011
239
13

Monogenic variants in dystonia: an exome-wide sequencing study.
Michael Zech, Robert Jech, Sylvia Boesch, Matej Škorvánek, Sandrina Weber, Matias Wagner, Chen Zhao, Angela Jochim, Ján Necpál, Yasemin Dincer,[...]. Lancet Neurol 2020
32
13

Exome sequencing and network analysis identifies shared mechanisms underlying spinocerebellar ataxia.
Esther A R Nibbeling, Anna Duarri, Corien C Verschuuren-Bemelmans, Michiel R Fokkens, Juha M Karjalainen, Cleo J L M Smeets, Jelkje J de Boer-Bergsma, Gerben van der Vries, Dennis Dooijes, Giovana B Bampi,[...]. Brain 2017
57
13

The neural substrates of rapid-onset Dystonia-Parkinsonism.
D Paola Calderon, Rachel Fremont, Franca Kraenzlin, Kamran Khodakhah. Nat Neurosci 2011
148
13

Mutations in ANO3 cause dominant craniocervical dystonia: ion channel implicated in pathogenesis.
Gavin Charlesworth, Vincent Plagnol, Kira M Holmström, Jose Bras, Una-Marie Sheerin, Elisavet Preza, Ignacio Rubio-Agusti, Mina Ryten, Susanne A Schneider, Maria Stamelou,[...]. Am J Hum Genet 2012
151
13

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
13

Heterozygous Gnal Mice Are a Novel Animal Model with Which to Study Dystonia Pathophysiology.
Assunta Pelosi, Fabien Menardy, Daniela Popa, Jean-Antoine Girault, Denis Hervé. J Neurosci 2017
20
15

Diverse Mechanisms Lead to Common Dysfunction of Striatal Cholinergic Interneurons in Distinct Genetic Mouse Models of Dystonia.
Karen L Eskow Jaunarajs, Mariangela Scarduzio, Michelle E Ehrlich, Lori L McMahon, David G Standaert. J Neurosci 2019
14
21

Abnormalities of motor function, transcription and cerebellar structure in mouse models of THAP1 dystonia.
Marta Ruiz, Georgina Perez-Garcia, Maitane Ortiz-Virumbrales, Aurelie Méneret, Andrika Morant, Jessica Kottwitz, Tania Fuchs, Justine Bonet, Pedro Gonzalez-Alegre, Patrick R Hof,[...]. Hum Mol Genet 2015
31
13

Loss of the dystonia gene Thap1 leads to transcriptional deficits that converge on common pathogenic pathways in dystonic syndromes.
Natalie M Frederick, Parth V Shah, Alessandro Didonna, Monica R Langley, Anumantha G Kanthasamy, Puneet Opal. Hum Mol Genet 2019
15
20

Mutations in THAP1/DYT6 reveal that diverse dystonia genes disrupt similar neuronal pathways and functions.
Zuchra Zakirova, Tomas Fanutza, Justine Bonet, Ben Readhead, Weijia Zhang, Zhengzi Yi, Genevieve Beauvais, Thomas P Zwaka, Laurie J Ozelius, Robert D Blitzer,[...]. PLoS Genet 2018
33
13

Mutations in the THAP1 gene are responsible for DYT6 primary torsion dystonia.
Tania Fuchs, Sophie Gavarini, Rachel Saunders-Pullman, Deborah Raymond, Michelle E Ehrlich, Susan B Bressman, Laurie J Ozelius. Nat Genet 2009
211
13

Mutations in THAP1 (DYT6) in early-onset dystonia: a genetic screening study.
Susan B Bressman, Deborah Raymond, Tania Fuchs, Gary A Heiman, Laurie J Ozelius, Rachel Saunders-Pullman. Lancet Neurol 2009
119
13


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.