A citation-based method for searching scientific literature

Brian M Schilder, Towfique Raj. Hum Mol Genet 2022
Times Cited: 4







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



Times Cited
  Times     Co-cited
Similarity


Partitioning heritability by functional annotation using genome-wide association summary statistics.
Hilary K Finucane, Brendan Bulik-Sullivan, Alexander Gusev, Gosia Trynka, Yakir Reshef, Po-Ru Loh, Verneri Anttila, Han Xu, Chongzhi Zang, Kyle Farh,[...]. Nat Genet 2015
891
75

Common genetic variation in the HLA region is associated with late-onset sporadic Parkinson's disease.
Taye H Hamza, Cyrus P Zabetian, Albert Tenesa, Alain Laederach, Jennifer Montimurro, Dora Yearout, Denise M Kay, Kimberly F Doheny, Justin Paschall, Elizabeth Pugh,[...]. Nat Genet 2010
531
75

Dysregulation of mitochondrial and proteolysosomal genes in Parkinson's disease myeloid cells.
Elisa Navarro, Evan Udine, Katia de Paiva Lopes, Madison Parks, Giulietta Riboldi, Brian M Schilder, Jack Humphrey, Gijsje J L Snijders, Ricardo A Vialle, Maojuan Zhuang,[...]. Nat Aging 2021
3
66

Linkage disequilibrium in humans: models and data.
J K Pritchard, M Przeworski. Am J Hum Genet 2001
769
50

Direct Identification of Hundreds of Expression-Modulating Variants using a Multiplexed Reporter Assay.
Ryan Tewhey, Dylan Kotliar, Daniel S Park, Brandon Liu, Sarah Winnicki, Steven K Reilly, Kristian G Andersen, Tarjei S Mikkelsen, Eric S Lander, Stephen F Schaffner,[...]. Cell 2018
22
50

FINEMAP: efficient variable selection using summary data from genome-wide association studies.
Christian Benner, Chris C A Spencer, Aki S Havulinna, Veikko Salomaa, Samuli Ripatti, Matti Pirinen. Bioinformatics 2016
241
50


Evaluating the informativeness of deep learning annotations for human complex diseases.
Kushal K Dey, Bryce van de Geijn, Samuel Sungil Kim, Farhad Hormozdiari, David R Kelley, Alkes L Price. Nat Commun 2020
8
50


Prospects of Fine-Mapping Trait-Associated Genomic Regions by Using Summary Statistics from Genome-wide Association Studies.
Christian Benner, Aki S Havulinna, Marjo-Riitta Järvelin, Veikko Salomaa, Samuli Ripatti, Matti Pirinen. Am J Hum Genet 2017
83
50

Single-cell epigenomic analyses implicate candidate causal variants at inherited risk loci for Alzheimer's and Parkinson's diseases.
M Ryan Corces, Anna Shcherbina, Soumya Kundu, Michael J Gloudemans, Laure Frésard, Jeffrey M Granja, Bryan H Louie, Tiffany Eulalio, Shadi Shams, S Tansu Bagdatli,[...]. Nat Genet 2020
65
50


Functionally informed fine-mapping and polygenic localization of complex trait heritability.
Omer Weissbrod, Farhad Hormozdiari, Christian Benner, Ran Cui, Jacob Ulirsch, Steven Gazal, Armin P Schoech, Bryce van de Geijn, Yakir Reshef, Carla Márquez-Luna,[...]. Nat Genet 2020
39
50

Improved methods for multi-trait fine mapping of pleiotropic risk loci.
Gleb Kichaev, Megan Roytman, Ruth Johnson, Eleazar Eskin, Sara Lindström, Peter Kraft, Bogdan Pasaniuc. Bioinformatics 2017
57
50

Fine-mapping genetic associations.
Anna Hutchinson, Jennifer Asimit, Chris Wallace. Hum Mol Genet 2020
9
50

Bayesian test for colocalisation between pairs of genetic association studies using summary statistics.
Claudia Giambartolomei, Damjan Vukcevic, Eric E Schadt, Lude Franke, Aroon D Hingorani, Chris Wallace, Vincent Plagnol. PLoS Genet 2014
768
50

The UK Biobank resource with deep phenotyping and genomic data.
Clare Bycroft, Colin Freeman, Desislava Petkova, Gavin Band, Lloyd T Elliott, Kevin Sharp, Allan Motyer, Damjan Vukcevic, Olivier Delaneau, Jared O'Connell,[...]. Nature 2018
50

Sequential regulatory activity prediction across chromosomes with convolutional neural networks.
David R Kelley, Yakir A Reshef, Maxwell Bileschi, David Belanger, Cory Y McLean, Jasper Snoek. Genome Res 2018
101
50

From genome-wide associations to candidate causal variants by statistical fine-mapping.
Daniel J Schaid, Wenan Chen, Nicholas B Larson. Nat Rev Genet 2018
254
50

Brain cell type-specific enhancer-promoter interactome maps and disease-risk association.
Alexi Nott, Inge R Holtman, Nicole G Coufal, Johannes C M Schlachetzki, Miao Yu, Rong Hu, Claudia Z Han, Monique Pena, Jiayang Xiao, Yin Wu,[...]. Science 2019
182
50

A single-cell atlas of the human substantia nigra reveals cell-specific pathways associated with neurological disorders.
Devika Agarwal, Cynthia Sandor, Viola Volpato, Tara M Caffrey, Jimena Monzón-Sandoval, Rory Bowden, Javier Alegre-Abarrategui, Richard Wade-Martins, Caleb Webber. Nat Commun 2020
52
50

Modeling the complex genetic architectures of brain disease.
Michael B Fernando, Tim Ahfeldt, Kristen J Brennand. Nat Genet 2020
23
50

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
50

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
50

Excessive burden of lysosomal storage disorder gene variants in Parkinson's disease.
Laurie A Robak, Iris E Jansen, Jeroen van Rooij, André G Uitterlinden, Robert Kraaij, Joseph Jankovic, Peter Heutink, Joshua M Shulman. Brain 2017
198
50

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
50

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
37
50

Genetics of Parkinson's disease: An introspection of its journey towards precision medicine.
Sara Bandres-Ciga, Monica Diez-Fairen, Jonggeol Jeff Kim, Andrew B Singleton. Neurobiol Dis 2020
112
50

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
50

Characterizing the Genetic Architecture of Parkinson's Disease in Latinos.
Douglas P Loesch, Andrea R V R Horimoto, Karl Heilbron, Elif I Sarihan, Miguel Inca-Martinez, Emily Mason, Mario Cornejo-Olivas, Luis Torres, Pilar Mazzetti, Carlos Cosentino,[...]. Ann Neurol 2021
12
50

The genetic architecture of Parkinson's disease.
Cornelis Blauwendraat, Mike A Nalls, Andrew B Singleton. Lancet Neurol 2020
248
50

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
50

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
536
50

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
559
50

Large-scale pathway specific polygenic risk and transcriptomic community network analysis identifies novel functional pathways in Parkinson disease.
S Bandres-Ciga, S Saez-Atienzar, J J Kim, M B Makarious, F Faghri, M Diez-Fairen, H Iwaki, H Leonard, J Botia, M Ryten,[...]. Acta Neuropathol 2020
26
50

Inflammatory dysregulation of blood monocytes in Parkinson's disease patients.
Veselin Grozdanov, Corinna Bliederhaeuser, Wolfgang P Ruf, Valerie Roth, Kathrin Fundel-Clemens, Lisa Zondler, David Brenner, Ana Martin-Villalba, Bastian Hengerer, Jan Kassubek,[...]. Acta Neuropathol 2014
145
50

Heritability of Parkinson disease in Swedish twins: a longitudinal study.
Karin Wirdefeldt, Margaret Gatz, Chandra A Reynolds, Carol A Prescott, Nancy L Pedersen. Neurobiol Aging 2011
66
50

Concordance for Parkinson's disease in twins: A 20-year update.
Samuel M Goldman, Kenneth Marek, Ruth Ottman, Cheryl Meng, Kathleen Comyns, Piu Chan, Jinghong Ma, Connie Marras, J William Langston, G Webster Ross,[...]. Ann Neurol 2019
28
50

Using genome-wide complex trait analysis to quantify 'missing heritability' in Parkinson's disease.
Margaux F Keller, Mohamad Saad, Jose Bras, Francesco Bettella, Nayia Nicolaou, Javier Simón-Sánchez, Florian Mittag, Finja Büchel, Manu Sharma, J Raphael Gibbs,[...]. Hum Mol Genet 2012
132
50

Infiltration of CD4+ lymphocytes into the brain contributes to neurodegeneration in a mouse model of Parkinson disease.
Vanessa Brochard, Béhazine Combadière, Annick Prigent, Yasmina Laouar, Aline Perrin, Virginie Beray-Berthat, Olivia Bonduelle, Daniel Alvarez-Fischer, Jacques Callebert, Jean-Marie Launay,[...]. J Clin Invest 2009
696
50


Parkinson-associated risk variant in distal enhancer of α-synuclein modulates target gene expression.
Frank Soldner, Yonatan Stelzer, Chikdu S Shivalila, Brian J Abraham, Jeanne C Latourelle, M Inmaculada Barrasa, Johanna Goldmann, Richard H Myers, Richard A Young, Rudolf Jaenisch. Nature 2016
325
50

Genetic identification of cell types underlying brain complex traits yields insights into the etiology of Parkinson's disease.
Julien Bryois, Nathan G Skene, Thomas Folkmann Hansen, Lisette J A Kogelman, Hunna J Watson, Zijing Liu, Leo Brueggeman, Gerome Breen, Cynthia M Bulik, Ernest Arenas,[...]. Nat Genet 2020
83
50

Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci.
Kyle J Gaulton, Teresa Ferreira, Yeji Lee, Anne Raimondo, Reedik Mägi, Michael E Reschen, Anubha Mahajan, Adam Locke, N William Rayner, Neil Robertson,[...]. Nat Genet 2015
259
25


Mapping identifiers for the integration of genomic datasets with the R/Bioconductor package biomaRt.
Steffen Durinck, Paul T Spellman, Ewan Birney, Wolfgang Huber. Nat Protoc 2009
25

Bayesian refinement of association signals for 14 loci in 3 common diseases.
Julian B Maller, Gilean McVean, Jake Byrnes, Damjan Vukcevic, Kimmo Palin, Zhan Su, Joanna M M Howson, Adam Auton, Simon Myers, Andrew Morris,[...]. Nat Genet 2012
283
25

Linkage disequilibrium-dependent architecture of human complex traits shows action of negative selection.
Steven Gazal, Hilary K Finucane, Nicholas A Furlotte, Po-Ru Loh, Pier Francesco Palamara, Xuanyao Liu, Armin Schoech, Brendan Bulik-Sullivan, Benjamin M Neale, Alexander Gusev,[...]. Nat Genet 2017
146
25

The NIH Roadmap Epigenomics Mapping Consortium.
Bradley E Bernstein, John A Stamatoyannopoulos, Joseph F Costello, Bing Ren, Aleksandar Milosavljevic, Alexander Meissner, Manolis Kellis, Marco A Marra, Arthur L Beaudet, Joseph R Ecker,[...]. Nat Biotechnol 2010
25

Fine-mapping and functional studies highlight potential causal variants for rheumatoid arthritis and type 1 diabetes.
Harm-Jan Westra, Marta Martínez-Bonet, Suna Onengut-Gumuscu, Annette Lee, Yang Luo, Nikola Teslovich, Jane Worthington, Javier Martin, Tom Huizinga, Lars Klareskog,[...]. Nat Genet 2018
75
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.