A citation-based method for searching scientific literature

Laurie A Robak, Iris E Jansen, Jeroen van Rooij, André G Uitterlinden, Robert Kraaij, Joseph Jankovic, Peter Heutink, Joshua M Shulman. Brain 2017
Times Cited: 207







List of co-cited articles
1595 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


Multicenter analysis of glucocerebrosidase mutations in Parkinson's disease.
E Sidransky, M A Nalls, J O Aasly, J Aharon-Peretz, G Annesi, E R Barbosa, A Bar-Shira, D Berg, J Bras, A Brice,[...]. N Engl J Med 2009
38

A meta-analysis of genome-wide association studies identifies 17 new Parkinson's disease risk loci.
Diana Chang, Mike A Nalls, Ingileif B Hallgrímsdóttir, Julie Hunkapiller, Marcel van der Brug, Fang Cai, Geoffrey A Kerchner, Gai Ayalon, Baris Bingol, Morgan Sheng,[...]. Nat Genet 2017
583
30

Gaucher disease glucocerebrosidase and α-synuclein form a bidirectional pathogenic loop in synucleinopathies.
Joseph R Mazzulli, You-Hai Xu, Ying Sun, Adam L Knight, Pamela J McLean, Guy A Caldwell, Ellen Sidransky, Gregory A Grabowski, Dimitri Krainc. Cell 2011
877
29

Identification of novel risk loci, causal insights, and heritable risk for Parkinson's disease: a meta-analysis of genome-wide association studies.
Mike A Nalls, Cornelis Blauwendraat, Costanza L Vallerga, Karl Heilbron, Sara Bandres-Ciga, Diana Chang, Manuela Tan, Demis A Kia, Alastair J Noyce, Angli Xue,[...]. Lancet Neurol 2019
591
22

Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease.
Mike A Nalls, Nathan Pankratz, Christina M Lill, Chuong B Do, Dena G Hernandez, Mohamad Saad, Anita L DeStefano, Eleanna Kara, Jose Bras, Manu Sharma,[...]. Nat Genet 2014
22

Is Parkinson's disease a lysosomal disorder?
Andrés D Klein, Joseph R Mazzulli. Brain 2018
83
20

Reversible Conformational Conversion of α-Synuclein into Toxic Assemblies by Glucosylceramide.
Friederike Zunke, Alexandra C Moise, Nandkishore R Belur, Eilrayna Gelyana, Iva Stojkovska, Haris Dzaferbegovic, Nicholas J Toker, Sohee Jeon, Kristina Fredriksen, Joseph R Mazzulli. Neuron 2018
124
17

The genetic architecture of Parkinson's disease.
Cornelis Blauwendraat, Mike A Nalls, Andrew B Singleton. Lancet Neurol 2020
276
17

Mutation in the alpha-synuclein gene identified in families with Parkinson's disease.
M H Polymeropoulos, C Lavedan, E Leroy, S E Ide, A Dehejia, A Dutra, B Pike, H Root, J Rubenstein, R Boyer,[...]. Science 1997
16

Staging of brain pathology related to sporadic Parkinson's disease.
Heiko Braak, Kelly Del Tredici, Udo Rüb, Rob A I de Vos, Ernst N H Jansen Steur, Eva Braak. Neurobiol Aging 2003
16

Impaired degradation of mutant alpha-synuclein by chaperone-mediated autophagy.
Ana Maria Cuervo, Leonidas Stefanis, Ross Fredenburg, Peter T Lansbury, David Sulzer. Science 2004
15

Glucocerebrosidase activity in Parkinson's disease with and without GBA mutations.
Roy N Alcalay, Oren A Levy, Cheryl C Waters, Stanley Fahn, Blair Ford, Sheng-Han Kuo, Pietro Mazzoni, Michael W Pauciulo, William C Nichols, Ziv Gan-Or,[...]. Brain 2015
229
15

Alpha-synuclein in Lewy bodies.
M G Spillantini, M L Schmidt, V M Lee, J Q Trojanowski, R Jakes, M Goedert. Nature 1997
15

Glucocerebrosidase deficiency in substantia nigra of parkinson disease brains.
Matthew E Gegg, Derek Burke, Simon J R Heales, J Mark Cooper, John Hardy, Nicholas W Wood, Anthony H V Schapira. Ann Neurol 2012
380
15

Glucocerebrosidase mutations in clinical and pathologically proven Parkinson's disease.
Juliane Neumann, Jose Bras, Emma Deas, Sean S O'Sullivan, Laura Parkkinen, Robin H Lachmann, Abi Li, Janice Holton, Rita Guerreiro, Reema Paudel,[...]. Brain 2009
457
15

Phenotype, genotype, and worldwide genetic penetrance of LRRK2-associated Parkinson's disease: a case-control study.
Daniel G Healy, Mario Falchi, Sean S O'Sullivan, Vincenzo Bonifati, Alexandra Durr, Susan Bressman, Alexis Brice, Jan Aasly, Cyrus P Zabetian, Stefano Goldwurm,[...]. Lancet Neurol 2008
986
15

Cysteine cathepsins are essential in lysosomal degradation of α-synuclein.
Ryan P McGlinchey, Jennifer C Lee. Proc Natl Acad Sci U S A 2015
107
14

SMPD1 mutations, activity, and α-synuclein accumulation in Parkinson's disease.
Roy N Alcalay, Victoria Mallett, Benoît Vanderperre, Omid Tavassoly, Yves Dauvilliers, Richard Y J Wu, Jennifer A Ruskey, Claire S Leblond, Amirthagowri Ambalavanan, Sandra B Laurent,[...]. Mov Disord 2019
44
31

Reduced glucocerebrosidase is associated with increased α-synuclein in sporadic Parkinson's disease.
Karen E Murphy, Amanda M Gysbers, Sarah K Abbott, Nahid Tayebi, Woojin S Kim, Ellen Sidransky, Antony Cooper, Brett Garner, Glenda M Halliday. Brain 2014
322
14

Parkinson's disease.
Lorraine V Kalia, Anthony E Lang. Lancet 2015
13

Activation of β-Glucocerebrosidase Reduces Pathological α-Synuclein and Restores Lysosomal Function in Parkinson's Patient Midbrain Neurons.
Joseph R Mazzulli, Friederike Zunke, Taiji Tsunemi, Nicholas J Toker, Sohee Jeon, Lena F Burbulla, Samarjit Patnaik, Ellen Sidransky, Juan J Marugan, Carolyn M Sue,[...]. J Neurosci 2016
158
13

Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathology.
Alexander Zimprich, Saskia Biskup, Petra Leitner, Peter Lichtner, Matthew Farrer, Sarah Lincoln, Jennifer Kachergus, Mary Hulihan, Ryan J Uitti, Donald B Calne,[...]. Neuron 2004
13

MDS clinical diagnostic criteria for Parkinson's disease.
Ronald B Postuma, Daniela Berg, Matthew Stern, Werner Poewe, C Warren Olanow, Wolfgang Oertel, José Obeso, Kenneth Marek, Irene Litvan, Anthony E Lang,[...]. Mov Disord 2015
13

Hereditary parkinsonism with dementia is caused by mutations in ATP13A2, encoding a lysosomal type 5 P-type ATPase.
Alfredo Ramirez, André Heimbach, Jan Gründemann, Barbara Stiller, Dan Hampshire, L Pablo Cid, Ingrid Goebel, Ammar F Mubaidin, Abdul-Latif Wriekat, Jochen Roeper,[...]. Nat Genet 2006
796
12


Penetrance of Parkinson disease in glucocerebrosidase gene mutation carriers.
M Anheim, A Elbaz, S Lesage, A Durr, C Condroyer, F Viallet, P Pollak, B Bonaïti, C Bonaïti-Pellié, A Brice. Neurology 2012
151
12

Cathepsin D expression level affects alpha-synuclein processing, aggregation, and toxicity in vivo.
Valerie Cullen, Maria Lindfors, Juliana Ng, Anders Paetau, Erika Swinton, Piotr Kolodziej, Heather Boston, Paul Saftig, John Woulfe, Mel B Feany,[...]. Mol Brain 2009
190
12

Differential effects of severe vs mild GBA mutations on Parkinson disease.
Ziv Gan-Or, Idan Amshalom, Laura L Kilarski, Anat Bar-Shira, Mali Gana-Weisz, Anat Mirelman, Karen Marder, Susan Bressman, Nir Giladi, Avi Orr-Urtreger. Neurology 2015
198
12

Web-based genome-wide association study identifies two novel loci and a substantial genetic component for Parkinson's disease.
Chuong B Do, Joyce Y Tung, Elizabeth Dorfman, Amy K Kiefer, Emily M Drabant, Uta Francke, Joanna L Mountain, Samuel M Goldman, Caroline M Tanner, J William Langston,[...]. PLoS Genet 2011
377
12

Lysosomal storage diseases.
Frances M Platt, Alessandra d'Azzo, Beverly L Davidson, Elizabeth F Neufeld, Cynthia J Tifft. Nat Rev Dis Primers 2018
291
12

Ambroxol for the Treatment of Patients With Parkinson Disease With and Without Glucocerebrosidase Gene Mutations: A Nonrandomized, Noncontrolled Trial.
Stephen Mullin, Laura Smith, Katherine Lee, Gayle D'Souza, Philip Woodgate, Josh Elflein, Jenny Hällqvist, Marco Toffoli, Adam Streeter, Joanne Hosking,[...]. JAMA Neurol 2020
125
12

Genome-wide association study reveals genetic risk underlying Parkinson's disease.
Javier Simón-Sánchez, Claudia Schulte, Jose M Bras, Manu Sharma, J Raphael Gibbs, Daniela Berg, Coro Paisan-Ruiz, Peter Lichtner, Sonja W Scholz, Dena G Hernandez,[...]. Nat Genet 2009
11

Lysosomal Dysfunction and α-Synuclein Aggregation in Parkinson's Disease: Diagnostic Links.
Tim Moors, Silvia Paciotti, Davide Chiasserini, Paolo Calabresi, Lucilla Parnetti, Tommaso Beccari, Wilma D J van de Berg. Mov Disord 2016
90
12

Gaucher disease: mutation and polymorphism spectrum in the glucocerebrosidase gene (GBA).
Kathleen S Hruska, Mary E LaMarca, C Ronald Scott, Ellen Sidransky. Hum Mutat 2008
405
11

Glucosylsphingosine Promotes α-Synuclein Pathology in Mutant GBA-Associated Parkinson's Disease.
Yumiko V Taguchi, Jun Liu, Jiapeng Ruan, Joshua Pacheco, Xiaokui Zhang, Justin Abbasi, Joan Keutzer, Pramod K Mistry, Sreeganga S Chandra. J Neurosci 2017
126
11

No evidence for substrate accumulation in Parkinson brains with GBA mutations.
Matthew E Gegg, Lindsay Sweet, Bing H Wang, Lamya S Shihabuddin, Sergio Pablo Sardi, Anthony H V Schapira. Mov Disord 2015
90
12

Survival and dementia in GBA-associated Parkinson's disease: The mutation matters.
Roberto Cilia, Sara Tunesi, Giorgio Marotta, Emanuele Cereda, Chiara Siri, Silvana Tesei, Anna L Zecchinelli, Margherita Canesi, Claudio B Mariani, Nicoletta Meucci,[...]. Ann Neurol 2016
200
11

Parkinson disease.
Werner Poewe, Klaus Seppi, Caroline M Tanner, Glenda M Halliday, Patrik Brundin, Jens Volkmann, Anette-Eleonore Schrag, Anthony E Lang. Nat Rev Dis Primers 2017
11

alpha-Synuclein locus triplication causes Parkinson's disease.
A B Singleton, M Farrer, J Johnson, A Singleton, S Hague, J Kachergus, M Hulihan, T Peuralinna, A Dutra, R Nussbaum,[...]. Science 2003
11

Cloning of the gene containing mutations that cause PARK8-linked Parkinson's disease.
Coro Paisán-Ruíz, Shushant Jain, E Whitney Evans, William P Gilks, Javier Simón, Marcel van der Brug, Adolfo López de Munain, Silvia Aparicio, Angel Martínez Gil, Naheed Khan,[...]. Neuron 2004
11

The endocytic membrane trafficking pathway plays a major role in the risk of Parkinson's disease.
Sara Bandres-Ciga, Sara Saez-Atienzar, Luis Bonet-Ponce, Kimberley Billingsley, Dan Vitale, Cornelis Blauwendraat, Jesse Raphael Gibbs, Lasse Pihlstrøm, Ziv Gan-Or, Mark R Cookson,[...]. Mov Disord 2019
40
25

LIMP-2 is a receptor for lysosomal mannose-6-phosphate-independent targeting of beta-glucocerebrosidase.
David Reczek, Michael Schwake, Jenny Schröder, Heather Hughes, Judith Blanz, Xiaoying Jin, William Brondyk, Scott Van Patten, Tim Edmunds, Paul Saftig. Cell 2007
343
10

Alpha-synuclein blocks ER-Golgi traffic and Rab1 rescues neuron loss in Parkinson's models.
Antony A Cooper, Aaron D Gitler, Anil Cashikar, Cole M Haynes, Kathryn J Hill, Bhupinder Bhullar, Kangning Liu, Kexiang Xu, Katherine E Strathearn, Fang Liu,[...]. Science 2006
997
10

Lewy pathology in Parkinson's disease consists of crowded organelles and lipid membranes.
Sarah H Shahmoradian, Amanda J Lewis, Christel Genoud, Jürgen Hench, Tim E Moors, Paula P Navarro, Daniel Castaño-Díez, Gabriel Schweighauser, Alexandra Graff-Meyer, Kenneth N Goldie,[...]. Nat Neurosci 2019
344
10

The p.L302P mutation in the lysosomal enzyme gene SMPD1 is a risk factor for Parkinson disease.
Ziv Gan-Or, Laurie J Ozelius, Anat Bar-Shira, Rachel Saunders-Pullman, Anat Mirelman, Ruth Kornreich, Mali Gana-Weisz, Deborah Raymond, Liron Rozenkrantz, Andres Deik,[...]. Neurology 2013
114
10

ER Stress and Autophagic Perturbations Lead to Elevated Extracellular α-Synuclein in GBA-N370S Parkinson's iPSC-Derived Dopamine Neurons.
Hugo J R Fernandes, Elizabeth M Hartfield, Helen C Christian, Evangelia Emmanoulidou, Ying Zheng, Heather Booth, Helle Bogetofte, Charmaine Lang, Brent J Ryan, S Pablo Sardi,[...]. Stem Cell Reports 2016
197
10

VPS35 mutations in Parkinson disease.
Carles Vilariño-Güell, Christian Wider, Owen A Ross, Justus C Dachsel, Jennifer M Kachergus, Sarah J Lincoln, Alexandra I Soto-Ortolaza, Stephanie A Cobb, Greggory J Wilhoite, Justin A Bacon,[...]. Am J Hum Genet 2011
566
10

Genetic modifiers of risk and age at onset in GBA associated Parkinson's disease and Lewy body dementia.
Cornelis Blauwendraat, Xylena Reed, Lynne Krohn, Karl Heilbron, Sara Bandres-Ciga, Manuela Tan, J Raphael Gibbs, Dena G Hernandez, Ravindran Kumaran, Rebekah Langston,[...]. Brain 2020
83
12

Reduced sphingolipid hydrolase activities, substrate accumulation and ganglioside decline in Parkinson's disease.
Mylene Huebecker, Elizabeth B Moloney, Aarnoud C van der Spoel, David A Priestman, Ole Isacson, Penelope J Hallett, Frances M Platt. Mol Neurodegener 2019
59
16

Specifically neuropathic Gaucher's mutations accelerate cognitive decline in Parkinson's.
Ganqiang Liu, Brendon Boot, Joseph J Locascio, Iris E Jansen, Sophie Winder-Rhodes, Shirley Eberly, Alexis Elbaz, Alexis Brice, Bernard Ravina, Jacobus J van Hilten,[...]. Ann Neurol 2016
152
9


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.