A citation-based method for searching scientific literature

Benjamin Roeben, Dominik Blum, Heinz Gabriel, Matthis Synofzik. J Neurol 2019
Times Cited: 1







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



Times Cited
  Times     Co-cited
Similarity


Copy Number Variant in the Region of Adenosine Kinase (ADK) and Its Possible Contribution to Schizophrenia Susceptibility.
Hiroki Kimura, Itaru Kushima, Akira Yohimi, Branko Aleksic, Norio Ozaki. Int J Neuropsychopharmacol 2018
2
100

Phase determination using chromosomal microarray and fluorescence in situ hybridization in a patient with early onset Parkinson disease and two deletions in PRKN.
Eli S Williams, Matthew J Barrett, Radhika Dhamija, Lisa Toran, Chelsea Chambers, Mani S Mahadevan, Wendy L Golden. Mol Genet Genomic Med 2018
3
100

Epidemiology of Alzheimer disease.
Richard Mayeux, Yaakov Stern. Cold Spring Harb Perspect Med 2012
408
100

A Meta-Analysis of α-Synuclein Multiplication in Familial Parkinsonism.
Adam Book, Ilaria Guella, Tara Candido, Alexis Brice, Nobutaka Hattori, Beomseok Jeon, Matthew J Farrer. Front Neurol 2018
32
100

Identification of a Large DNAJB2 Deletion in a Family with Spinal Muscular Atrophy and Parkinsonism.
Elena Sanchez, Hossein Darvish, Roxana Mesias, Shaghyegh Taghavi, Saghar Ghasemi Firouzabadi, Ruth H Walker, Abbas Tafakhori, Coro Paisán-Ruiz. Hum Mutat 2016
22
100


Successful GPi stimulation in genetic Parkinson's disease caused by mosaicism of alpha-synuclein gene duplication: first description.
C Perandones, N Aráoz Olivos, G B Raina, L A Pellene, J C Giugni, D S Calvo, M Radrizzani, F Piedimonte, F E Micheli. J Neurol 2015
7
100

Neurons with Complex Karyotypes Are Rare in Aged Human Neocortex.
William D Chronister, Ian E Burbulis, Margaret B Wierman, Matthew J Wolpert, Mark F Haakenson, Aiden C B Smith, Joel E Kleinman, Thomas M Hyde, Daniel R Weinberger, Stefan Bekiranov,[...]. Cell Rep 2019
21
100

Mosaicism of alpha-synuclein gene rearrangements: report of two unrelated cases of early-onset parkinsonism.
C Perandones, J C Giugni, D S Calvo, G B Raina, L De Jorge Lopez, V Volpini, C P Zabetian, I F Mata, M Caputo, D Corach,[...]. Parkinsonism Relat Disord 2014
11
100

NeuroArray, A Custom CGH Microarray to Decipher Copy Number Variants in Alzheimer's Disease.
Denis Cuccaro, Maria Guarnaccia, Rosario Iemmolo, Velia D'Agata, Sebastiano Cavallaro. Curr Genomics 2018
1
100

Splicing: is there an alternative contribution to Parkinson's disease?
Valentina La Cognata, Velia D'Agata, Francesca Cavalcanti, Sebastiano Cavallaro. Neurogenetics 2015
36
100

The epidemiology of ALS and the role of population-based registries.
Ettore Beghi, Giancarlo Logroscino, Adriano Chiò, Orla Hardiman, Douglas Mitchell, Robert Swingler, Bryan J Traynor. Biochim Biophys Acta 2006
144
100

Ageing and neurodegenerative diseases.
Chia-Wei Hung, Yu-Chih Chen, Wan-Ling Hsieh, Shih-Hwa Chiou, Chung-Lan Kao. Ageing Res Rev 2010
107
100

Neuroimaging, genetic, and enzymatic study in a Japanese family with a GBA gross deletion.
Yuta Ichinose, Hiroyuki Ishiura, Masaki Tanaka, Jun Yoshimura, Koichiro Doi, Takako Umeda, Hajime Yamauchi, Mai Tsuchiya, Kishin Koh, Nobuo Yamashiro,[...]. Parkinsonism Relat Disord 2019
4
100


Deletion of exons 9 and 10 of the Presenilin 1 gene in a patient with Early-onset Alzheimer Disease generates longer amyloid seeds.
Kilan Le Guennec, Sarah Veugelen, Olivier Quenez, Maria Szaruga, Stéphane Rousseau, Gaël Nicolas, David Wallon, Frédérique Fluchere, Thierry Frébourg, Bart De Strooper,[...]. Neurobiol Dis 2017
13
100

Copy number variability in Parkinson's disease: assembling the puzzle through a systems biology approach.
Valentina La Cognata, Giovanna Morello, Velia D'Agata, Sebastiano Cavallaro. Hum Genet 2017
24
100

Sulfotransferase 1A3/4 copy number variation is associated with neurodegenerative disease.
N J Butcher, M K Horne, G D Mellick, C J Fowler, C L Masters, R F Minchin. Pharmacogenomics J 2018
6
100

A Clinical and Molecular Genetic Study of 50 Families with Autosomal Recessive Parkinsonism Revealed Known and Novel Gene Mutations.
Shaghayegh Taghavi, Rita Chaouni, Abbas Tafakhori, Luis J Azcona, Saghar Ghasemi Firouzabadi, Mir Davood Omrani, Javad Jamshidi, Babak Emamalizadeh, Gholam Ali Shahidi, Mona Ahmadi,[...]. Mol Neurobiol 2018
39
100

Novel compound heterozygous mutations in the PARK2 gene identified in a Chinese pedigree with early-onset Parkinson's disease.
Yingying Shi, Hideshi Kawakami, Weizhou Zang, Gang Li, Jiewen Zhang, Changshui Xu. Brain Behav 2017
5
100


Genome-wide survey of copy number variants finds MAPT duplications in progressive supranuclear palsy.
Zhongbo Chen, Jason A Chen, Aleksey Shatunov, Ashley R Jones, Stephanie N Kravitz, Alden Y Huang, Lauren Lawrence, Jennifer K Lowe, Cathryn M Lewis, Christine A M Payan,[...]. Mov Disord 2019
7
100

Identification of a large homozygous VPS13C deletion in a patient with early-onset Parkinsonism.
Hossein Darvish, Paloma Bravo, Abbas Tafakhori, Luis J Azcona, Sakineh Ranji-Burachaloo, Amir Hossein Johari, Coro Paisán-Ruiz. Mov Disord 2018
17
100

Cerebrospinal fluid levels of complement proteins C3, C4 and CR1 in Alzheimer's disease.
Jonny Daborg, Ulf Andreasson, Marcela Pekna, Ronald Lautner, Eric Hanse, Lennart Minthon, Kaj Blennow, Oskar Hansson, Henrik Zetterberg. J Neural Transm (Vienna) 2012
42
100

Copy number variation and susceptibility to complex traits.
Cesar P Canales, Katherina Walz. EMBO Mol Med 2011
8
100

Variable PARK2 Mutations Cause Early-Onset Parkinson's Disease in a Small Restricted Population.
Shay Ben-Shachar, Zaid Afawi, Rafik Masalha, Samih Badarny, Tova Neiman, Dina Pavzner, Anat Bar-Shira, Avi Orr-Urtreger. J Mol Neurosci 2017
1
100

The Database of Genomic Variants: a curated collection of structural variation in the human genome.
Jeffrey R MacDonald, Robert Ziman, Ryan K C Yuen, Lars Feuk, Stephen W Scherer. Nucleic Acids Res 2014
632
100

An approach to finding brain-situated mutations in sporadic Parkinson's disease.
Roger Pamphlett, Julia M Morahan, Natasha Luquin, Bing Yu. Parkinsonism Relat Disord 2012
4
100

22q11.2 Deletion Syndrome-Associated Parkinson's Disease.
Erik Boot, Anne S Bassett, Connie Marras. Mov Disord Clin Pract 2018
9
100

Compound heterozygous mutations in PARK2 causing early-onset Parkinson disease: A case report.
Yu-Qing Fang, Fei Mao, Mei-Jia Zhu, Xiu-Hua Li. Medicine (Baltimore) 2019
5
100

Quantitative evaluation of iron content in idiopathic rapid eye movement sleep behavior disorder.
Junyan Sun, Zhaoyu Lai, Jinghong Ma, Linlin Gao, Meijie Chen, Jie Chen, Jiliang Fang, Yangyang Fan, Yan Bao, Dongling Zhang,[...]. Mov Disord 2020
9
100

A Case of Parkinson's Disease with No Lewy Body Pathology due to a Homozygous Exon Deletion in Parkin.
Krisztina Kunszt Johansen, Sverre Helge Torp, Matthew J Farrer, Emil K Gustavsson, Jan O Aasly. Case Rep Neurol Med 2018
18
100

Analysis of copy number variation in Alzheimer's disease in a cohort of clinically characterized and neuropathologically verified individuals.
Shanker Swaminathan, Matthew J Huentelman, Jason J Corneveaux, Amanda J Myers, Kelley M Faber, Tatiana Foroud, Richard Mayeux, Li Shen, Sungeun Kim, Mari Turk,[...]. PLoS One 2012
29
100

Typical features of Parkinson disease and diagnostic challenges with microdeletion 22q11.2.
Erik Boot, Nancy J Butcher, Sean Udow, Connie Marras, Kin Y Mok, Satoshi Kaneko, Matthew J Barrett, Paolo Prontera, Brian D Berman, Mario Masellis,[...]. Neurology 2018
19
100

The impact of human copy number variation on gene expression.
Eric R Gamazon, Barbara E Stranger. Brief Funct Genomics 2015
59
100

Exonic rearrangements in the known Parkinson's disease-causing genes are a rare cause of the disease in South African patients.
Celia van der Merwe, Jonathan Carr, Brigitte Glanzmann, Soraya Bardien. Neurosci Lett 2016
5
100

Somatic copy number gains of α-synuclein (SNCA) in Parkinson's disease and multiple system atrophy brains.
Katya Mokretar, Daniel Pease, Jan-Willem Taanman, Aynur Soenmez, Ayesha Ejaz, Tammaryn Lashley, Helen Ling, Steve Gentleman, Henry Houlden, Janice L Holton,[...]. Brain 2018
25
100

Large 3-Mb deletions at 22q11.2 locus in Parkinson's disease and schizophrenia.
Jia Nee Foo, Jimmy Lee, Louis C Tan, Jianjun Liu, Eng-King Tan. Mov Disord 2016
6
100

Genetic compendium of 1511 human brains available through the UK Medical Research Council Brain Banks Network Resource.
Michael J Keogh, Wei Wei, Ian Wilson, Jon Coxhead, Sarah Ryan, Sara Rollinson, Helen Griffin, Marzena Kurzawa-Akanbi, Mauro Santibanez-Koref, Kevin Talbot,[...]. Genome Res 2017
29
100

Concurrent AFG3L2 and SPG7 mutations associated with syndromic parkinsonism and optic atrophy with aberrant OPA1 processing and mitochondrial network fragmentation.
Stefania Magri, Valentina Fracasso, Massimo Plumari, Enrico Alfei, Daniele Ghezzi, Cinzia Gellera, Paola Rusmini, Angelo Poletti, Daniela Di Bella, Antonio E Elia,[...]. Hum Mutat 2018
15
100

Association of MAPT haplotypes with Alzheimer's disease risk and MAPT brain gene expression levels.
Mariet Allen, Michaela Kachadoorian, Zachary Quicksall, Fanggeng Zou, High Seng Chai, Curtis Younkin, Julia E Crook, V Shane Pankratz, Minerva M Carrasquillo, Siddharth Krishnan,[...]. Alzheimers Res Ther 2014
71
100

17q21.31 duplication causes prominent tau-related dementia with increased MAPT expression.
K Le Guennec, O Quenez, G Nicolas, D Wallon, S Rousseau, A-C Richard, J Alexander, P Paschou, C Charbonnier, C Bellenguez,[...]. Mol Psychiatry 2017
32
100

Heterozygous Deletion of Chorein Exons 70-73 and GNA14 Exons 3-7 in a Brazilian Patient Presenting With Probable Tau-Negative Early-Onset Alzheimer Disease.
Maciej J Lazarczyk, Sven Haller, Armand Savioz, Stefania Gimelli, Frédérique Bena, Panteleimon Giannakopoulos. Alzheimer Dis Assoc Disord 2017
2
100

Identification of mutations in the PARK2 gene in Serbian patients with Parkinson's disease.
M Z Jankovic, V Dobricic, N Kresojevic, V Markovic, I Petrovic, M Svetel, T Pekmezovic, I Novakovic, V Kostic. J Neurol Sci 2018
3
100

Increasing the Coding Potential of Genomes Through Alternative Splicing: The Case of PARK2 Gene.
Valentina La Cognata, Rosario Iemmolo, Velia D'Agata, Soraya Scuderi, Filippo Drago, Mario Zappia, Sebastiano Cavallaro. Curr Genomics 2014
22
100

Peripheral clearance of amyloid beta peptide by complement C3-dependent adherence to erythrocytes.
Joseph Rogers, Rena Li, Diego Mastroeni, Andrew Grover, Brian Leonard, Geoffrey Ahern, Phillip Cao, Heather Kolody, Linda Vedders, William P Kolb,[...]. Neurobiol Aging 2006
118
100

Translational Medicine in Neurological Disorders: A Genomic Perspective.
Giulia Gentile, Sebastiano Cavallaro. Curr Genomics 2019
1
100

Copy Number Variants in Alzheimer's Disease.
Denis Cuccaro, Elvira Valeria De Marco, Rita Cittadella, Sebastiano Cavallaro. J Alzheimers Dis 2017
19
100

Bidirectional interactions between indomethacin and the murine intestinal microbiota.
Xue Liang, Kyle Bittinger, Xuanwen Li, Darrell R Abernethy, Frederic D Bushman, Garret A FitzGerald. Elife 2015
50
100

Whole-genome sequencing suggests mechanisms for 22q11.2 deletion-associated Parkinson's disease.
Nancy J Butcher, Daniele Merico, Mehdi Zarrei, Lucas Ogura, Christian R Marshall, Eva W C Chow, Anthony E Lang, Stephen W Scherer, Anne S Bassett. PLoS One 2017
10
100


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.