A citation-based method for searching scientific literature

O Zhuchenko, J Bailey, P Bonnen, T Ashizawa, D W Stockton, C Amos, W B Dobyns, S H Subramony, H Y Zoghbi, C C Lee. Nat Genet 1997
Times Cited: 978







List of co-cited articles
1925 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


SEIZURES INDUCED BY MOVEMENT: A FORM OF REFLEX EPILEPSY.
C W WHITTY, W A LISHMAN, J P FITZGIBBON. Lancet 1964
28
3

Missense Variants in RHOBTB2 Cause a Developmental and Epileptic Encephalopathy in Humans, and Altered Levels Cause Neurological Defects in Drosophila.
Jonas Straub, Enrico D H Konrad, Johanna Grüner, Annick Toutain, Levinus A Bok, Megan T Cho, Heather P Crawford, Holly Dubbs, Ganka Douglas, Rebekah Jobling,[...]. Am J Hum Genet 2018
25
4

Factors in the disease severity of ATP1A3 mutations: Impairment, misfolding, and allele competition.
Elena Arystarkhova, Ihtsham U Haq, Timothy Luebbert, Fanny Mochel, Rachel Saunders-Pullman, Susan B Bressman, Polina Feschenko, Cynthia Salazar, Jared F Cook, Scott Demarest,[...]. Neurobiol Dis 2019
12
8

Alternating hemiplegia of childhood: clinical manifestations and long-term outcome.
M A Mikati, U Kramer, M L Zupanc, R J Shanahan. Pediatr Neurol 2000
106
1

Movement disorders in patients with alternating hemiplegia: "Soft" and "stiff" at the same time.
Eleni Panagiotakaki, Diane Doummar, Erika Nogue, Nicolas Nagot, Gaetan Lesca, Florence Riant, Sophie Nicole, Charlene Delaygue, Marie Anne Barthez, Marie Cécile Nassogne,[...]. Neurology 2020
4
25

Motor function domains in alternating hemiplegia of childhood.
Melanie Masoud, Kelly Gordon, Amanda Hall, Joan Jasien, Kara Lardinois, Julie Uchitel, Melissa Mclean, Lyndsey Prange, Jeffrey Wuchich, Mohamad A Mikati. Dev Med Child Neurol 2017
18
5


The epileptology of alternating hemiplegia of childhood.
Julie Uchitel, Ashley Helseth, Lyndsey Prange, Melissa McLean, Ryan Ghusayni, Monisha Sachdev, Arsen Hunanyan, Mohamad A Mikati. Neurology 2019
18
5

Defective glucose transport across the blood-brain barrier as a cause of persistent hypoglycorrhachia, seizures, and developmental delay.
D C De Vivo, R R Trifiletti, R I Jacobson, G M Ronen, R A Behmand, S I Harik. N Engl J Med 1991
383
1

Cortical spreading depression modulates the caudate nucleus activity.
M Seghatoleslam, M Khaleghi Ghadiri, N Ghaffarian, E-J Speckmann, A Gorji. Neuroscience 2014
15
6


Functional consequences of SLC1A3 mutations associated with episodic ataxia 6.
Aparna S Chivukula, Mariia Suslova, Daniel Kortzak, Peter Kovermann, Christoph Fahlke. Hum Mutat 2020
7
14

Ictal 99mTc ECD SPECT in paroxysmal kinesigenic choreoathetosis.
Chun-Hung Ko, Chi-Keung Kong, Wai-Tat Ngai, Kwok-Man Ma. Pediatr Neurol 2001
1
100

Alternating hemiplegia of childhood.
M Mikati. Pediatr Neurol 1999
3
33

Ictal (99m)Tc ECD SPECT in paroxysmal kinesigenic choreoathetosis.
C H Ko, C K Kong, W T Ngai, K M Ma. Pediatr Neurol 2001
32
3


Drug-induced cerebellar ataxia: a systematic review.
J van Gaalen, F G Kerstens, R P P W M Maas, L Härmark, B P C van de Warrenburg. CNS Drugs 2014
27
3


Tics induced by antiepileptic drugs: a pragmatic review.
James Peters, Nirosen Vijiaratnam, Heather Angus-Leppan. J Neurol 2021
1
100

Drug-induced tremors.
John C Morgan, Kapil D Sethi. Lancet Neurol 2005
72
1



Drug-induced movement disorders.
Shyamal H Mehta, John C Morgan, Kapil D Sethi. Neurol Clin 2015
26
3

A syndrome of autosomal dominant alternating hemiplegia: clinical presentation mimicking intractable epilepsy; chromosomal studies; and physiologic investigations.
M A Mikati, H Maguire, C F Barlow, L Ozelius, X O Breakefield, S M Klauck, B Korf, S L O'Tuama, F Dangond. Neurology 1992
48
2

Severe paroxysmal dyskinesias without epilepsy in a RHOBTB2 mutation carrier.
Ján Necpál, Michael Zech, Alica Valachová, Zdeněk Sedláček, Šárka Bendová, Miroslava Hančárová, Katarína Okáľová, Juliane Winkelmann, Robert Jech. Parkinsonism Relat Disord 2020
2
50

Compound heterozygosity with PRRT2: Pushing the phenotypic envelope in genetic epilepsies.
Christelle Moufawad El Achkar, Beth Rosen Sheidley, Declan O'Rourke, Masanori Takeoka, Annapurna Poduri. Epilepsy Behav Case Rep 2017
4
25

Functional analysis of a novel potassium channel (KCNA1) mutation in hereditary myokymia.
Haijun Chen, Christian von Hehn, Leonard K Kaczmarek, Laura R Ment, Barbara R Pober, Fuki M Hisama. Neurogenetics 2007
21
4

A case of dyskinesia after levetiracetam administration.
Soo Hwan Yim, Yun Ho Choi, Kyoung Heo, Kyoo Ho Cho. BMC Neurol 2019
2
50

Clinical profile of patients with ATP1A3 mutations in Alternating Hemiplegia of Childhood-a study of 155 patients.
Eleni Panagiotakaki, Elisa De Grandis, Michela Stagnaro, Erin L Heinzen, Carmen Fons, Sanjay Sisodiya, Boukje de Vries, Christophe Goubau, Sarah Weckhuysen, David Kemlink,[...]. Orphanet J Rare Dis 2015
76
1

Epileptic encephalopathy with features of rapid-onset dystonia Parkinsonism and alternating hemiplegia of childhood: a novel combination phenotype associated with ATP1A3 mutation.
Linh Tran, Jason Richards, Marie McDonald, Allyn McConkie-Rosell, Nicholas Stong, Joan Jasien, Vandana Shashi, Mohamad A Mikati. Epileptic Disord 2020
4
25

Adverse motor effects induced by antiepileptic drugs.
G Zaccara, M Cincotta, A Borgheresi, F Balestrieri. Epileptic Disord 2004
41
2

Phenytoin Induced Chorea: A Case Report.
Dalvir Gill, Mitchell Lyons, Fatme Allam. Am J Ther 2018
3
33

Alternating hemiplegia of childhood.
Sujay Kansagra, Mohamad A Mikati, Federico Vigevano. Handb Clin Neurol 2013
19
5

High-resolution molecular genomic autopsy reveals complex sudden unexpected death in epilepsy risk profile.
Tara L Klassen, Valerie C Bomben, Ankita Patel, Janice Drabek, Tim T Chen, Wenli Gu, Feng Zhang, Kevin Chapman, James R Lupski, Jeffrey L Noebels,[...]. Epilepsia 2014
52
1

Survival and Prognostic Factors in C9orf72 Repeat Expansion Carriers: A Systematic Review and Meta-analysis.
Stella A Glasmacher, Charis Wong, Iona E Pearson, Suvankar Pal. JAMA Neurol 2020
5
20

A Māori specific RFC1 pathogenic repeat configuration in CANVAS, likely due to a founder allele.
Sarah J Beecroft, Andrea Cortese, Roisin Sullivan, Wai Yan Yau, Zoe Dyer, Teddy Y Wu, Eoin Mulroy, Luciana Pelosi, Miriam Rodrigues, Rachael Taylor,[...]. Brain 2020
3
33

Long-read sequencing identifies the pathogenic nucleotide repeat expansion in RFC1 in a Japanese case of CANVAS.
Haruko Nakamura, Hiroshi Doi, Satomi Mitsuhashi, Satoko Miyatake, Kazutaka Katoh, Martin C Frith, Tetsuya Asano, Yosuke Kudo, Takuya Ikeda, Shun Kubota,[...]. J Hum Genet 2020
8
12

Long-read sequencing identified repeat expansions in the 5'UTR of the NOTCH2NLC gene from Chinese patients with neuronal intranuclear inclusion disease.
Jianwen Deng, Muliang Gu, Yu Miao, Sheng Yao, Min Zhu, Pu Fang, Xuefan Yu, Pidong Li, Yanan Su, Jian Huang,[...]. J Med Genet 2019
25
4

Pentanucleotide repeat-primed PCR for genetic diagnosis of spinocerebellar ataxia type 31.
Takayuki Ishige, Setsu Sawai, Sakae Itoga, Kenichi Sato, Emi Utsuno, Minako Beppu, Kazuaki Kanai, Motoi Nishimura, Kazuyuki Matsushita, Satoshi Kuwabara,[...]. J Hum Genet 2012
7
14


Epigenetics in nucleotide repeat expansion disorders.
Fang He, Peter K Todd. Semin Neurol 2011
24
4

Parkinsonism in spinocerebellar ataxia.
Hyeyoung Park, Han-Joon Kim, Beom S Jeon. Biomed Res Int 2015
37
2


Accurate, scalable and integrative haplotype estimation.
Olivier Delaneau, Jean-François Zagury, Matthew R Robinson, Jonathan L Marchini, Emmanouil T Dermitzakis. Nat Commun 2019
24
4

CGG expansion in NOTCH2NLC is associated with oculopharyngodistal myopathy with neurological manifestations.
Masashi Ogasawara, Aritoshi Iida, Theerawat Kumutpongpanich, Ayami Ozaki, Yasushi Oya, Hirofumi Konishi, Akinori Nakamura, Ryuta Abe, Hiroshi Takai, Ritsuko Hanajima,[...]. Acta Neuropathol Commun 2020
3
33

Finding and extending ancient simple sequence repeat-derived regions in the human genome.
Jonathan A Shortt, Robert P Ruggiero, Corey Cox, Aaron C Wacholder, David D Pollock. Mob DNA 2020
3
33

A novel polyalanine expansion in FOXL2: the first evidence for a recessive form of the blepharophimosis syndrome (BPES) associated with ovarian dysfunction.
Jeyabalan Nallathambi, Lara Moumné, Elfride De Baere, Diane Beysen, Kim Usha, Periasamy Sundaresan, Reiner A Veitia. Hum Genet 2007
40
2

Mentally ill West Indian immigrants.
E B Gordon. Br J Psychiatry 1965
40
2

Cerebellar ataxia, neuropathy, and vestibular areflexia syndrome: a slowly progressive disorder with stereotypical presentation.
Daniele Cazzato, Eleonora Dalla Bella, Patrizia Dacci, Caterina Mariotti, Giuseppe Lauria. J Neurol 2016
11
9

Analysis of short tandem repeat expansions and their methylation state with nanopore sequencing.
Pay Giesselmann, Björn Brändl, Etienne Raimondeau, Rebecca Bowen, Christian Rohrandt, Rashmi Tandon, Helene Kretzmer, Günter Assum, Christina Galonska, Reiner Siebert,[...]. Nat Biotechnol 2019
22
4


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.