A citation-based method for searching scientific literature

Zheyu Xu, Che-Kang Lim, Louis C S Tan, Eng-King Tan. Curr Neurol Neurosci Rep 2019
Times Cited: 4







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



Times Cited
  Times     Co-cited
Similarity


PRRT2 mutations and paroxysmal disorders.
A Méneret, C Gaudebout, F Riant, M Vidailhet, C Depienne, E Roze. Eur J Neurol 2013
67
75

Identification of PRRT2 as the causative gene of paroxysmal kinesigenic dyskinesias.
Jun-Ling Wang, Li Cao, Xun-Hua Li, Zheng-Mao Hu, Jia-Da Li, Jian-Guo Zhang, Yu Liang, San-A, Nan Li, Su-Qin Chen,[...]. Brain 2011
195
75

Paroxysmal movement disorders: An update.
A Méneret, E Roze. Rev Neurol (Paris) 2016
30
50

Paroxysmal choreoathetosis/spasticity (DYT9) is caused by a GLUT1 defect.
Y G Weber, C Kamm, A Suls, J Kempfle, K Kotschet, R Schüle, T V Wuttke, S Maljevic, J Liebrich, T Gasser,[...]. Neurology 2011
56
50

The spectrum of movement disorders in Glut-1 deficiency.
Roser Pons, Abbie Collins, Michael Rotstein, Kristin Engelstad, Darryl C De Vivo. Mov Disord 2010
93
50

Paroxysmal dyskinesias: clinical features and classification.
M Demirkiran, J Jankovic. Ann Neurol 1995
349
50


Paroxysmal kinesigenic choreoathetosis: a report of 26 patients.
M K Houser, V L Soland, K P Bhatia, N P Quinn, C D Marsden. J Neurol 1999
83
50

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
292
50

Clinical evaluation of idiopathic paroxysmal kinesigenic dyskinesia: new diagnostic criteria.
M K Bruno, M Hallett, K Gwinn-Hardy, B Sorensen, E Considine, S Tucker, D R Lynch, K D Mathews, K J Swoboda, J Harris,[...]. Neurology 2004
234
50

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
36
50


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
50

PRRT2-related disorders: further PKD and ICCA cases and review of the literature.
Felicitas Becker, Julian Schubert, Pasquale Striano, Anna-Kaisa Anttonen, Elina Liukkonen, Eija Gaily, Christian Gerloff, Stephan Müller, Nicole Heußinger, Christoph Kellinghaus,[...]. J Neurol 2013
43
50

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
77
50

The mutational constraint spectrum quantified from variation in 141,456 humans.
Konrad J Karczewski, Laurent C Francioli, Grace Tiao, Beryl B Cummings, Jessica Alföldi, Qingbo Wang, Ryan L Collins, Kristen M Laricchia, Andrea Ganna, Daniel P Birnbaum,[...]. Nature 2020
25

Parallel mapping and simultaneous sequencing reveals deletions in BCAN and FAM83H associated with discrete inherited disorders in a domestic dog breed.
Oliver P Forman, Jacques Penderis, Claudia Hartley, Louisa J Hayward, Sally L Ricketts, Cathryn S Mellersh. PLoS Genet 2012
45
25

Glycogen storage disease type III: modified Atkins diet improves myopathy.
Sebene Mayorandan, Uta Meyer, Hans Hartmann, Anibh Martin Das. Orphanet J Rare Dis 2014
28
25

Novel homozygous PCK1 mutation causing cytosolic phosphoenolpyruvate carboxykinase deficiency presenting as childhood hypoglycemia, an abnormal pattern of urine metabolites and liver dysfunction.
Päivi Vieira, Jessie Cameron, Elisa Rahikkala, Riikka Keski-Filppula, Lin-Hua Zhang, Saikat Santra, Allison Matthews, Päivi Myllynen, Matti Nuutinen, Jukka S Moilanen,[...]. Mol Genet Metab 2017
12
25

Clinical characteristics of Scottie Cramp in 31 cases.
G Urkasemsin, N J Olby. J Small Anim Pract 2015
8
25


A program for annotating and predicting the effects of single nucleotide polymorphisms, SnpEff: SNPs in the genome of Drosophila melanogaster strain w1118; iso-2; iso-3.
Pablo Cingolani, Adrian Platts, Le Lily Wang, Melissa Coon, Tung Nguyen, Luan Wang, Susan J Land, Xiangyi Lu, Douglas M Ruden. Fly (Austin) 2012
25

Mitochondrial phosphoenolpyruvate carboxykinase deficiency.
J V Leonard, K Hyland, N Furukawa, P T Clayton. Eur J Pediatr 1991
12
25

Mitochondrial phosphoenolpyruvate carboxykinase deficiency.
P T Clayton, K Hyland, M Brand, J V Leonard. Eur J Pediatr 1986
24
25

A homozygous PIGN missense mutation in Soft-Coated Wheaten Terriers with a canine paroxysmal dyskinesia.
Ana L Kolicheski, Gary S Johnson, Tendai Mhlanga-Mutangadura, Jeremy F Taylor, Robert D Schnabel, Taroh Kinoshita, Yoshiko Murakami, Dennis P O'Brien. Neurogenetics 2017
11
25

Regulation of the mitochondrial ATP-synthase in human fibroblasts.
A M Das, D J Byrd, J Brodehl. Clin Chim Acta 1994
22
25

Serotonin release varies with brain tryptophan levels.
J D Schaechter, R J Wurtman. Brain Res 1990
111
25

Phenotypic characterisation of canine epileptoid cramping syndrome in the Border terrier.
V Black, L Garosi, M Lowrie, R J Harvey, J Gale. J Small Anim Pract 2014
27
25

Dyskinesia in an adult bichon frise.
J Penderis, R J Franklin. J Small Anim Pract 2001
19
25

GLUT-1 deficiency syndrome caused by haploinsufficiency of the blood-brain barrier hexose carrier.
G Seidner, M G Alvarez, J I Yeh, K R O'Driscoll, J Klepper, T S Stump, D Wang, N B Spinner, M J Birnbaum, D C De Vivo. Nat Genet 1998
259
25

Implications of altered NAD metabolism in metabolic disorders.
Keisuke Okabe, Keisuke Yaku, Kazuyuki Tobe, Takashi Nakagawa. J Biomed Sci 2019
50
25

Echocardiographic parameters and indices in the normal beagle dog.
L Crippa, E Ferro, E Melloni, P Brambilla, E Cavalletti. Lab Anim 1992
44
25

Paroxysmal dyskinesia in the bichon frise.
Mark Lowrie, Artur S P Varejão. Vet Rec 2018
1
100

Muscle pain, cramps and hypertonicity.
G Diane Shelton. Vet Clin North Am Small Anim Pract 2004
20
25

Phosphoenolpyruvate cycling via mitochondrial phosphoenolpyruvate carboxykinase links anaplerosis and mitochondrial GTP with insulin secretion.
Romana Stark, Francisco Pasquel, Adina Turcu, Rebecca L Pongratz, Michael Roden, Gary W Cline, Gerald I Shulman, Richard G Kibbey. J Biol Chem 2009
89
25

Phenotypic characterization of paroxysmal dyskinesia in Maltese dogs.
Dakir Polidoro, Luc Van Ham, Patrick Santens, Ine Cornelis, Marios Charalambous, Bart J G Broeckx, Sofie F M Bhatti. J Vet Intern Med 2020
8
25

Ketone body turnover and net hepatic ketone production in fasted and diabetic dogs.
U Keller, A D Cherrington, J E Liljenquist. Am J Physiol 1978
95
25

Structural insights into the mechanism of PEPCK catalysis.
Todd Holyoak, Sarah M Sullivan, Thomas Nowak. Biochemistry 2006
51
25


Characterization of Paroxysmal Gluten-Sensitive Dyskinesia in Border Terriers Using Serological Markers.
M Lowrie, O A Garden, M Hadjivassiliou, D S Sanders, R Powell, L Garosi. J Vet Intern Med 2018
12
25

Three rare diseases in one Sib pair: RAI1, PCK1, GRIN2B mutations associated with Smith-Magenis Syndrome, cytosolic PEPCK deficiency and NMDA receptor glutamate insensitivity.
David R Adams, Hongjie Yuan, Todd Holyoak, Katrina H Arajs, Parvin Hakimi, Thomas C Markello, Lynne A Wolfe, Thierry Vilboux, Barbara K Burton, Karin Fuentes Fajardo,[...]. Mol Genet Metab 2014
35
25



Acetazolamide-responsive paroxysmal dyskinesia in a 12-week-old female golden retriever dog.
Emilie Royaux, Sofie Bhatti, Robert Harvey, Laurent Garosi, G Diane Shelton, Luc Van Ham. Vet Q 2016
5
25

Tetrahydrobiopterin biosynthesis, regeneration and functions.
B Thöny, G Auerbach, N Blau. Biochem J 2000
566
25

Cerebral Gluconeogenesis and Diseases.
James Yip, Xiaokun Geng, Jiamei Shen, Yuchuan Ding. Front Pharmacol 2017
30
25


A movement disorder in boxer pups.
I K Ramsey, K E Chandler, R J Franklin. Vet Rec 1999
19
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.