A citation-based method for searching scientific literature

Gerard Saranza, Karen Grütz, Christine Klein, Ana Westenberger, Anthony E Lang. Brain 2020
Times Cited: 6







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



Times Cited
  Times     Co-cited
Similarity


Biallelic MYORG mutation carriers exhibit primary brain calcification with a distinct phenotype.
Lou Grangeon, David Wallon, Camille Charbonnier, Olivier Quenez, Anne-Claire Richard, Stéphane Rousseau, Clara Budowski, Thibaud Lebouvier, Anne-Gaëlle Corbille, Marie Vidailhet,[...]. Brain 2019
36
66

Biallelic Mutations in MYORG Cause Autosomal Recessive Primary Familial Brain Calcification.
Xiang-Ping Yao, Xuewen Cheng, Chong Wang, Miao Zhao, Xin-Xin Guo, Hui-Zhen Su, Lu-Lu Lai, Xiao-Huan Zou, Xue-Jiao Chen, Yuying Zhao,[...]. Neuron 2018
80
50

MYORG Mutation Heterozygosity Is Associated With Brain Calcification.
You Chen, Zhidong Cen, Xinhui Chen, Haotian Wang, Si Chen, Dehao Yang, Feng Fu, Lebo Wang, Peng Liu, Hongwei Wu,[...]. Mov Disord 2020
6
33


Murine Placental-Fetal Phosphate Dyshomeostasis Caused by an Xpr1 Deficiency Accelerates Placental Calcification and Restricts Fetal Growth in Late Gestation.
Xuan Xu, Xiunan Li, Hao Sun, Zhijian Cao, Ruixi Gao, Tingting Niu, Yanli Wang, Tingbin Ma, Rui Chen, Cheng Wang,[...]. J Bone Miner Res 2020
11
33

Familial IBGC caused by SLC20A2 mutation presenting as paroxysmal kinesigenic dyskinesia.
Min Zhu, Xuan Zhu, Hui Wan, Daojun Hong. Parkinsonism Relat Disord 2014
23
33

MYORG Mutations: a Major Cause of Recessive Primary Familial Brain Calcification.
Max Bauer, Dolev Rahat, Elad Zisman, Yuval Tabach, Alexander Lossos, Vardiella Meiner, David Arkadir. Curr Neurol Neurosci Rep 2019
13
33

Evaluation of MYORG mutations as a novel cause of primary familial brain calcification.
You Chen, Feng Fu, Si Chen, Zhidong Cen, Haiyan Tang, Jinxiu Huang, Fei Xie, Xiaosheng Zheng, Dehao Yang, Haotian Wang,[...]. Mov Disord 2019
20
33

Endothelium-specific ablation of PDGFB leads to pericyte loss and glomerular, cardiac and placental abnormalities.
Mattias Bjarnegård, Maria Enge, Jenny Norlin, Sigrun Gustafsdottir, Simon Fredriksson, Alexandra Abramsson, Minoru Takemoto, Erika Gustafsson, Reinhard Fässler, Christer Betsholtz. Development 2004
243
16


Microangiopathy in primary familial brain calcification: Evidence from skin biopsies.
Gaël Nicolas, Florent Marguet, Annie Laquerrière, João Ricardo Mendes de Oliveira, Didier Hannequin. Neurol Genet 2017
8
16

Lack of Major Ophthalmic Findings in Patients with Primary Familial Brain Calcification Linked to SLC20A2 and PDGFB.
Rayssa Leal Borges-Medeiros, Laura Durão Ferreira, João Ricardo Mendes de Oliveira. J Mol Neurosci 2019
4
25

Slc20a2, Encoding the Phosphate Transporter PiT2, Is an Important Genetic Determinant of Bone Quality and Strength.
Sarah Beck-Cormier, Christopher J Lelliott, John G Logan, David T Lafont, Laure Merametdjian, Victoria D Leitch, Natalie C Butterfield, Hayley J Protheroe, Peter I Croucher, Paul A Baldock,[...]. J Bone Miner Res 2019
18
16

Proteomics. Tissue-based map of the human proteome.
Mathias Uhlén, Linn Fagerberg, Björn M Hallström, Cecilia Lindskog, Per Oksvold, Adil Mardinoglu, Åsa Sivertsson, Caroline Kampf, Evelina Sjöstedt, Anna Asplund,[...]. Science 2015
16

Mutations in SLC20A2 link familial idiopathic basal ganglia calcification with phosphate homeostasis.
Cheng Wang, Yulei Li, Lei Shi, Jie Ren, Monica Patti, Tao Wang, João R M de Oliveira, María-Jesús Sobrido, Beatriz Quintáns, Miguel Baquero,[...]. Nat Genet 2012
259
16

XPR1 mutations are a rare cause of primary familial brain calcification.
Mathieu Anheim, Uriel López-Sánchez, Donatella Giovannini, Anne-Claire Richard, Jawida Touhami, Ludovic N'Guyen, Gabrielle Rudolf, Anne Thibault-Stoll, Thierry Frebourg, Didier Hannequin,[...]. J Neurol 2016
38
16

The emerging importance of the SPX domain-containing proteins in phosphate homeostasis.
David Secco, Chuang Wang, Bulak A Arpat, Zhiye Wang, Yves Poirier, Stephen D Tyerman, Ping Wu, Huixia Shou, James Whelan. New Phytol 2012
160
16


Mutations in XPR1 cause primary familial brain calcification associated with altered phosphate export.
Andrea Legati, Donatella Giovannini, Gaël Nicolas, Uriel López-Sánchez, Beatriz Quintáns, João R M Oliveira, Renee L Sears, Eliana Marisa Ramos, Elizabeth Spiteri, María-Jesús Sobrido,[...]. Nat Genet 2015
170
16

Characterization of XPR1/SLC53A1 variants located outside of the SPX domain in patients with primary familial brain calcification.
Uriel López-Sánchez, Gaël Nicolas, Anne-Claire Richard, David Maltête, Mahmoud Charif, Xavier Ayrignac, Cyril Goizet, Jawida Touhami, Gilles Labesse, Jean-Luc Battini,[...]. Sci Rep 2019
7
16

Primary brain calcification: an international study reporting novel variants and associated phenotypes.
Eliana Marisa Ramos, Miryam Carecchio, Roberta Lemos, Joana Ferreira, Andrea Legati, Renee Louise Sears, Sandy Chan Hsu, Celeste Panteghini, Luca Magistrelli, Ettore Salsano,[...]. Eur J Hum Genet 2018
34
16


Receptors for polytropic and xenotropic mouse leukaemia viruses encoded by a single gene at Rmc1.
Y L Yang, L Guo, S Xu, C A Holland, T Kitamura, K Hunter, J M Cunningham. Nat Genet 1999
113
16

Mutation of the PDGFRB gene as a cause of idiopathic basal ganglia calcification.
Gaël Nicolas, Cyril Pottier, David Maltête, Sophie Coutant, Anne Rovelet-Lecrux, Solenn Legallic, Stéphane Rousseau, Yvan Vaschalde, Lucie Guyant-Maréchal, Jérôme Augustin,[...]. Neurology 2013
182
16

A PDGFB mutation causes paroxysmal nonkinesigenic dyskinesia with brain calcification.
Cheng Wang, Xixiang Ma, Xuan Xu, Benyan Huang, Hao Sun, Lulu Li, Min Zhang, Jing Yu Liu. Mov Disord 2017
10
16

Estimation of minimal disease prevalence from population genomic data: Application to primary familial brain calcification.
Gaël Nicolas, Camille Charbonnier, Dominique Campion, Joris A Veltman. Am J Med Genet B Neuropsychiatr Genet 2018
19
16


Mutations in the gene encoding PDGF-B cause brain calcifications in humans and mice.
Annika Keller, Ana Westenberger, Maria J Sobrido, Maria García-Murias, Aloysius Domingo, Renee L Sears, Roberta R Lemos, Andres Ordoñez-Ugalde, Gael Nicolas, José E Gomes da Cunha,[...]. Nat Genet 2013
209
16

Paroxysmal Dyskinesias Revealing 3-Hydroxy-Isobutyryl-CoA Hydrolase (HIBCH) Deficiency.
Marie-Aude Spitz, Guy Lenaers, Majida Charif, Thomas Wirth, Jameleddine Chelly, Marie-Thérèse Abi-Warde, Pierre Meyer, Nicolas Leboucq, Elise Schaefer, Mathieu Anheim,[...]. Neuropediatrics 2021
1
100

The PNKD gene is associated with Tourette Disorder or Tic disorder in a multiplex family.
N Sun, C Nasello, L Deng, N Wang, Y Zhang, Z Xu, Z Song, K Kwan, R A King, Z P Pang,[...]. Mol Psychiatry 2018
20
16

Functional jerks, tics, and paroxysmal movement disorders.
Y E M Dreissen, D C Cath, M A J Tijssen. Handb Clin Neurol 2016
9
16

Cerebrospinal fluid analysis in the workup of GLUT1 deficiency syndrome: a systematic review.
Wilhelmina G Leen, Ron A Wevers, Erik-Jan Kamsteeg, Hans Scheffer, Marcel M Verbeek, Michèl A Willemsen. JAMA Neurol 2013
66
16

Atypical Manifestations in Glut1 Deficiency Syndrome.
V De Giorgis, C Varesio, C Baldassari, E Piazza, S Olivotto, J Macasaet, U Balottin, P Veggiotti. J Child Neurol 2016
20
16

Rapid-onset dystonia-parkinsonism with ATP1A3 mutation and left lower limb paroxysmal dystonia.
Shohei Nomura, Mitsuru Kashiwagi, Takuya Tanabe, Chizu Oba, Kumiko Yanagi, Tadashi Kaname, Nobuhiko Okamoto, Akira Ashida. Brain Dev 2021
3
33

Paroxysmal dyskinesias: clinical features and classification.
M Demirkiran, J Jankovic. Ann Neurol 1995
356
16

From nocturnal paroxysmal dystonia to nocturnal frontal lobe epilepsy.
F Provini, G Plazzi, E Lugaresi. Clin Neurophysiol 2000
53
16


PRRT2 mutations and paroxysmal disorders.
A Méneret, C Gaudebout, F Riant, M Vidailhet, C Depienne, E Roze. Eur J Neurol 2013
72
16

Genetics of Movement Disorders and the Practicing Clinician; Who and What to Test for?
Alessio Di Fonzo, Edoardo Monfrini, Roberto Erro. Curr Neurol Neurosci Rep 2018
16
16

TBC1D24-TLDc-related epilepsy exercise-induced dystonia: rescue by antioxidants in a disease model.
Kevin Lüthy, Davide Mei, Baptiste Fischer, Maurizio De Fusco, Jef Swerts, Jone Paesmans, Elena Parrini, Naomi Lubarr, Inge A Meijer, Katherine M Mackenzie,[...]. Brain 2019
27
16

Expanding the phenotypic spectrum of Allan-Herndon-Dudley syndrome in patients with SLC16A2 mutations.
Ganaelle Remerand, Odile Boespflug-Tanguy, Davide Tonduti, Renaud Touraine, Diana Rodriguez, Aurore Curie, Nathalie Perreton, Vincent Des Portes, Catherine Sarret. Dev Med Child Neurol 2019
27
16

Pyruvate dehydrogenase complex deficiency: four neurological phenotypes with differing pathogenesis.
Christine Barnerias, Jean-Marie Saudubray, Guy Touati, Pascale De Lonlay, Olivier Dulac, Gerard Ponsot, Cécile Marsac, Michèle Brivet, Isabelle Desguerre. Dev Med Child Neurol 2010
97
16

A Japanese family with primary familial brain calcification presenting with paroxysmal kinesigenic dyskinesia - A comprehensive mutational analysis.
Akihiko Mitsutake, Takashi Matsukawa, Kristine Joyce L Porto, Tatsuya Sato, Junko Katsumata, Tomonari Seki, Risa Maekawa, Takuto Hideyama, Masaki Tanaka, Hiroyuki Ishiura,[...]. J Neurol Sci 2020
2
50

Genotype-phenotype correlation of paroxysmal nonkinesigenic dyskinesia.
M K Bruno, H-Y Lee, G W J Auburger, A Friedman, J E Nielsen, A E Lang, E Bertini, P Van Bogaert, Y Averyanov, M Hallett,[...]. Neurology 2007
91
16

Neurologic phenotypes associated with acanthocytosis.
R H Walker, H H Jung, C Dobson-Stone, L Rampoldi, A Sano, F Tison, A Danek. Neurology 2007
67
16

Oxcarbazepine-responsive paroxysmal kinesigenic dyskinesia in Wilson disease.
Federico Micheli, Lorena Tschopp, Maria Graciela Cersosimo. Clin Neuropharmacol 2011
9
16

Clinical and biochemical characterization of 3-hydroxyisobutyryl-CoA hydrolase (HIBCH) deficiency that causes Leigh-like disease and ketoacidosis.
Kenichiro Yamada, Misako Naiki, Shin Hoshino, Yasuyuki Kitaura, Yusuke Kondo, Noriko Nomura, Reiko Kimura, Daisuke Fukushi, Yasukazu Yamada, Nobuyuki Shimozawa,[...]. Mol Genet Metab Rep 2014
24
16

Pyruvate dehydrogenase complex-E2 deficiency causes paroxysmal exercise-induced dyskinesia.
Jennifer Friedman, Annette Feigenbaum, Nathaniel Chuang, Jennifer Silhavy, Joseph G Gleeson. Neurology 2017
16
16


A case of Wilson's disease presenting with paroxysmal dystonia.
Hyun Jae Kim, Jung Han Yoon. Neurol Sci 2017
4
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.