A citation-based method for searching scientific literature

Cheng Wang, Xixiang Ma, Xuan Xu, Benyan Huang, Hao Sun, Lulu Li, Min Zhang, Jing Yu Liu. Mov Disord 2017
Times Cited: 10







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



Times Cited
  Times     Co-cited
Similarity


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
90

Familial IBGC caused by SLC20A2 mutation presenting as paroxysmal kinesigenic dyskinesia.
Min Zhu, Xuan Zhu, Hui Wan, Daojun Hong. Parkinsonism Relat Disord 2014
23
80

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
184
70

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
262
70

Phenotypic spectrum of probable and genetically-confirmed idiopathic basal ganglia calcification.
Gaël Nicolas, Cyril Pottier, Camille Charbonnier, Lucie Guyant-Maréchal, Isabelle Le Ber, Jérémie Pariente, Pierre Labauge, Xavier Ayrignac, Luc Defebvre, David Maltête,[...]. Brain 2013
138
60

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
36
60

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
81
60

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
60

Brain calcification process and phenotypes according to age and sex: Lessons from SLC20A2, PDGFB, and PDGFRB mutation carriers.
Gaël Nicolas, Camille Charbonnier, Roberta Rodrigues de Lemos, Anne-Claire Richard, Olivier Guillin, David Wallon, Andrea Legati, Daniel Geschwind, Giovanni Coppola, Thierry Frebourg,[...]. Am J Med Genet B Neuropsychiatr Genet 2015
63
50

Mutations in SLC20A2 are a major cause of familial idiopathic basal ganglia calcification.
Sandy Chan Hsu, Renee L Sears, Roberta R Lemos, Beatriz Quintáns, Alden Huang, Elizabeth Spiteri, Lisette Nevarez, Catherine Mamah, Mayana Zatz, Kerrie D Pierce,[...]. Neurogenetics 2013
107
50

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
40

Functional Characterization of Germline Mutations in PDGFB and PDGFRB in Primary Familial Brain Calcification.
Michael Vanlandewijck, Thibaud Lebouvier, Maarja Andaloussi Mäe, Khayrun Nahar, Simone Hornemann, David Kenkel, Sara I Cunha, Johan Lennartsson, Andreas Boss, Carl-Henrik Heldin,[...]. PLoS One 2015
62
40

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
40

Novel SLC20A2 mutations identified in southern Chinese patients with idiopathic basal ganglia calcification.
Wan-Jin Chen, Xiang-Ping Yao, Qi-Jie Zhang, Wang Ni, Jin He, Hong-Fu Li, Xin-Yi Liu, Gui-Xian Zhao, Shen-Xing Murong, Ning Wang,[...]. Gene 2013
37
30

Novel mutations of PDGFRB cause primary familial brain calcification in Chinese families.
Chong Wang, Xiang-Ping Yao, Hai-Ting Chen, Jing-Hui Lai, Xin-Xin Guo, Hui-Zhen Su, En-Lin Dong, Qi-Jie Zhang, Ning Wang, Wan-Jin Chen. J Hum Genet 2017
10
30


Evaluation of SLC20A2 mutations that cause idiopathic basal ganglia calcification in Japan.
Megumi Yamada, Masaki Tanaka, Mari Takagi, Seiju Kobayashi, Yoshiharu Taguchi, Shutaro Takashima, Kortaro Tanaka, Tetsuo Touge, Hiroyuki Hatsuta, Shigeo Murayama,[...]. Neurology 2014
58
30

A de novo nonsense PDGFB mutation causing idiopathic basal ganglia calcification with laryngeal dystonia.
Gaël Nicolas, Agnès Jacquin, Christel Thauvin-Robinet, Anne Rovelet-Lecrux, Olivier Rouaud, Cyril Pottier, Marie-Hélène Aubriot-Lorton, Stéphane Rousseau, David Wallon, Christian Duvillard,[...]. Eur J Hum Genet 2014
40
30

Deconstructing Fahr's disease/syndrome of brain calcification in the era of new genes.
Amit Batla, Xin You Tai, Lucia Schottlaender, Robert Erro, Bettina Balint, Kailash P Bhatia. Parkinsonism Relat Disord 2017
45
30

Primary familial brain calcification with known gene mutations: a systematic review and challenges of phenotypic characterization.
Vera Tadic, Ana Westenberger, Aloysius Domingo, Daniel Alvarez-Fischer, Christine Klein, Meike Kasten. JAMA Neurol 2015
53
30

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
30

Update and Mutational Analysis of SLC20A2: A Major Cause of Primary Familial Brain Calcification.
Roberta R Lemos, Eliana M Ramos, Andrea Legati, Gaël Nicolas, Emma M Jenkinson, John H Livingston, Yanick J Crow, Dominique Campion, Giovanni Coppola, João R M Oliveira. Hum Mutat 2015
56
30


Primary familial brain calcifications: genetic and clinical update.
Ana Westenberger, Alexander Balck, Christine Klein. Curr Opin Neurol 2019
28
30


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
254
30

Identification of a novel genetic locus on chromosome 8p21.1-q11.23 for idiopathic basal ganglia calcification.
Xiaohua Dai, Yong Gao, Zhenping Xu, Xiaoniu Cui, Juan Liu, Yulei Li, Haibo Xu, Mugen Liu, Qing K Wang, Jing Yu Liu. Am J Med Genet B Neuropsychiatr Genet 2010
40
20

Slc20a2 is critical for maintaining a physiologic inorganic phosphate level in cerebrospinal fluid.
Nina Jensen, Jacob Kwasi Autzen, Lene Pedersen. Neurogenetics 2016
36
20


Mutation screening of PDGFB gene in Chinese population with primary familial brain calcification.
Xiang-Ping Yao, Chong- Wang, Hui-Zhen Su, Xin-Xin Guo, Ying-Qian Lu, Miao Zhao, Yao-Bin Liu, Jing-Hui Lai, Hai-Ting Chen, Ning Wang,[...]. Gene 2016
8
25


Brain Calcification and Movement Disorders.
Vladimir S Kostić, Igor N Petrović. Curr Neurol Neurosci Rep 2017
15
20

Mutations at the SLC20A2 gene and brain resilience in families with idiopathic basal ganglia calcification ("Fahr's disease").
Danyllo F de Oliveira, Roberta R de Lemos, João R M de Oliveira. Front Hum Neurosci 2013
7
28

Idiopathic basal ganglia calcification-associated PDGFRB mutations impair the receptor signalling.
Florence A Arts, Amélie I Velghe, Monique Stevens, Jean-Christophe Renauld, Ahmed Essaghir, Jean-Baptiste Demoulin. J Cell Mol Med 2015
39
20

SLC20A2 Deficiency in Mice Leads to Elevated Phosphate Levels in Cerbrospinal Fluid and Glymphatic Pathway-Associated Arteriolar Calcification, and Recapitulates Human Idiopathic Basal Ganglia Calcification.
Mary Catherine Wallingford, Jia Jun Chia, Elizabeth M Leaf, Suhaib Borgeia, Nicholas W Chavkin, Chenphop Sawangmake, Ken Marro, Timothy C Cox, Mei Y Speer, Cecilia M Giachelli. Brain Pathol 2017
44
20

Neuroradiologic evidence of pre-synaptic and post-synaptic nigrostriatal dopaminergic dysfunction in idiopathic Basal Ganglia calcification: a case report.
Takahiro Saito, Mitsuru Nakamura, Teruhiko Shimizu, Keiichi Oda, Kiichi Ishiwata, Kenji Ishii, Kunihiro Isse. J Neuroimaging 2010
9
22

Overall mutational spectrum of SLC20A2, PDGFB and PDGFRB in idiopathic basal ganglia calcification.
Gaël Nicolas, Anne-Claire Richard, Cyril Pottier, Christophe Verny, Franck Durif, Emmanuel Roze, Pascal Favrole, Gabrielle Rudolf, Mathieu Anheim, Christine Tranchant,[...]. Neurogenetics 2014
16
20


The genetics of primary familial brain calcifications.
Ana Westenberger, Christine Klein. Curr Neurol Neurosci Rep 2014
33
20

First Japanese family with primary familial brain calcification due to a mutation in the PDGFB gene: an exome analysis study.
Teruo Hayashi, Andrea Legati, Tadashi Nishikawa, Giovanni Coppola. Psychiatry Clin Neurosci 2015
19
20


Identification of partial SLC20A2 deletions in primary brain calcification using whole-exome sequencing.
Stéphanie David, Joana Ferreira, Olivier Quenez, Anne Rovelet-Lecrux, Anne-Claire Richard, Marc Vérin, Snejana Jurici, Isabelle Le Ber, Anne Boland, Jean-François Deleuze,[...]. Eur J Hum Genet 2016
18
20

Severe vascular disturbance in a case of familial brain calcinosis.
Judit Miklossy, Ian R Mackenzie, Katerina Dorovini-Zis, Donald B Calne, Zbigniew K Wszolek, Andis Klegeris, Patrick L McGeer. Acta Neuropathol 2005
50
20

The Need for Consensus on Primary Familial Brain Calcification Nomenclature.
Laura Durão Ferreira, João Ricardo Mendes de Oliveira. J Neuropsychiatry Clin Neurosci 2018
3
66

Clinical heterogeneity of primary familial brain calcification due to a novel mutation in PDGFB.
Michael J Keogh, Angela Pyle, Daniyal Daud, Helen Griffin, Konstantinos Douroudis, Gail Eglon, James Miller, Rita Horvath, Patrick F Chinnery. Neurology 2015
11
20

2q37 as a susceptibility locus for idiopathic basal ganglia calcification (IBGC) in a large South Tyrolean family.
Claudia Béu Volpato, Alessandro De Grandi, Ebba Buffone, Maurizio Facheris, Uwe Gebert, Günther Schifferle, Rudolf Schönhuber, Andrew Hicks, Peter P Pramstaller. J Mol Neurosci 2009
33
20

High frequency of calcification in basal ganglia on brain computed tomography images in Japanese older adults.
Megumi Yamada, Takahiko Asano, Kouichirou Okamoto, Yuichi Hayashi, Masayuki Kanematsu, Hiroaki Hoshi, Yasuhisa Akaiwa, Takayoshi Shimohata, Masatoyo Nishizawa, Takashi Inuzuka,[...]. Geriatr Gerontol Int 2013
50
20

Primary Brain Calcification Causal PiT2 Transport-Knockout Variants can Exert Dominant Negative Effects on Wild-Type PiT2 Transport Function in Mammalian Cells.
Frederik Tibert Larsen, Nina Jensen, Jacob Kwasi Autzen, Iben Boutrup Kongsfelt, Lene Pedersen. J Mol Neurosci 2017
20
20

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
20

Primary familial brain calcification: Genetic analysis and clinical spectrum.
Ilaria Taglia, Andrea Mignarri, Simone Olgiati, Elisabetta Menci, Patrizia L Petrocelli, Guido J Breedveld, Cesa Scaglione, Paolo Martinelli, Antonio Federico, Vincenzo Bonifati,[...]. Mov Disord 2014
23
20


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.