A citation-based method for searching scientific literature

Marcus Tuke, Jessica Tyrrell, Katherine S Ruth, Robin N Beaumont, Andrew R Wood, Anna Murray, Timothy M Frayling, Michael N Weedon, Caroline F Wright. Am J Hum Genet 2020
Times Cited: 1







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



Times Cited
  Times     Co-cited
Similarity


Insufficient evidence for pathogenicity of SNCA His50Gln (H50Q) in Parkinson's disease.
Cornelis Blauwendraat, Demis A Kia, Lasse Pihlstrøm, Ziv Gan-Or, Suzanne Lesage, J Raphael Gibbs, Jinhui Ding, Roy N Alcalay, Sharon Hassin-Baer, Alan M Pittman,[...]. Neurobiol Aging 2018
18
100

Copy number variation in familial Parkinson disease.
Nathan Pankratz, Alexandra Dumitriu, Kurt N Hetrick, Mei Sun, Jeanne C Latourelle, Jemma B Wilk, Cheryl Halter, Kimberly F Doheny, James F Gusella, William C Nichols,[...]. PLoS One 2011
45
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

Structures of fibrils formed by α-synuclein hereditary disease mutant H50Q reveal new polymorphs.
David R Boyer, Binsen Li, Chuanqi Sun, Weijia Fan, Michael R Sawaya, Lin Jiang, David S Eisenberg. Nat Struct Mol Biol 2019
38
100

Parkinson's disease age at onset genome-wide association study: Defining heritability, genetic loci, and α-synuclein mechanisms.
Cornelis Blauwendraat, Karl Heilbron, Costanza L Vallerga, Sara Bandres-Ciga, Rainer von Coelln, Lasse Pihlstrøm, Javier Simón-Sánchez, Claudia Schulte, Manu Sharma, Lynne Krohn,[...]. Mov Disord 2019
100
100

Monogenic and polygenic inheritance become instruments for clonal selection.
Po-Ru Loh, Giulio Genovese, Steven A McCarroll. Nature 2020
25
100

ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data.
Kai Wang, Mingyao Li, Hakon Hakonarson. Nucleic Acids Res 2010
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

The mutational constraint spectrum quantified from variation in 141,456 humans.
Konrad J Karczewski, Laurent C Francioli, Grace Tiao, Beryl B Cummings, Jessica Alföldi, Qingbo Wang, Ryan L Collins, Kristen M Laricchia, Andrea Ganna, Daniel P Birnbaum,[...]. Nature 2020
100

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
100

A comprehensive analysis of SNCA-related genetic risk in sporadic parkinson disease.
Lasse Pihlstrøm, Cornelis Blauwendraat, Chiara Cappelletti, Victoria Berge-Seidl, Margrete Langmyhr, Sandra Pilar Henriksen, Wilma D J van de Berg, J Raphael Gibbs, Mark R Cookson, Andrew B Singleton,[...]. Ann Neurol 2018
20
100

Schizophrenia as a prodromal symptom in a patient harboring SNCA duplication.
Shogo Takamura, Aya Ikeda, Kenya Nishioka, Hirokazu Furuya, Mari Tashiro, Takashi Matsushima, Yuanzhe Li, Hiroyo Yoshino, Manabu Funayama, Shigeru Morinobu,[...]. Parkinsonism Relat Disord 2016
6
100

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
289
100

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
310
100

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
100

Autosomal dominant Parkinson's disease caused by SNCA duplications.
Takuya Konno, Owen A Ross, Andreas Puschmann, Dennis W Dickson, Zbigniew K Wszolek. Parkinsonism Relat Disord 2016
81
100

Clonal myelopoiesis in the UK Biobank cohort: ASXL1 mutations are strongly associated with smoking.
Ahmed A Z Dawoud, William J Tapper, Nicholas C P Cross. Leukemia 2020
17
100

Different Effects of α-Synuclein Mutants on Lipid Binding and Aggregation Detected by Single Molecule Fluorescence Spectroscopy and ThT Fluorescence-Based Measurements.
Viktoria C Ruf, Georg S Nübling, Sophia Willikens, Song Shi, Felix Schmidt, Johannes Levin, Kai Bötzel, Frits Kamp, Armin Giese. ACS Chem Neurosci 2019
18
100

Update of the MDS research criteria for prodromal Parkinson's disease.
Sebastian Heinzel, Daniela Berg, Thomas Gasser, Honglei Chen, Chun Yao, Ronald B Postuma. Mov Disord 2019
118
100

Mechanisms of mosaicism, chimerism and uniparental disomy identified by single nucleotide polymorphism array analysis.
Laura K Conlin, Brian D Thiel, Carsten G Bonnemann, Livija Medne, Linda M Ernst, Elaine H Zackai, Matthew A Deardorff, Ian D Krantz, Hakon Hakonarson, Nancy B Spinner. Hum Mol Genet 2010
265
100

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
100

Insights into clonal haematopoiesis from 8,342 mosaic chromosomal alterations.
Po-Ru Loh, Giulio Genovese, Robert E Handsaker, Hilary K Finucane, Yakir A Reshef, Pier Francesco Palamara, Brenda M Birmann, Michael E Talkowski, Samuel F Bakhoum, Steven A McCarroll,[...]. Nature 2018
99
100

Second-generation PLINK: rising to the challenge of larger and richer datasets.
Christopher C Chang, Carson C Chow, Laurent Cam Tellier, Shashaank Vattikuti, Shaun M Purcell, James J Lee. Gigascience 2015
100

Investigation of somatic CNVs in brains of synucleinopathy cases using targeted SNCA analysis and single cell sequencing.
Diego Perez-Rodriguez, Maria Kalyva, Melissa Leija-Salazar, Tammaryn Lashley, Maxime Tarabichi, Viorica Chelban, Steve Gentleman, Lucia Schottlaender, Hannah Franklin, George Vasmatzis,[...]. Acta Neuropathol Commun 2019
12
100

Alpha-synuclein locus duplication as a cause of familial Parkinson's disease.
Marie-Christine Chartier-Harlin, Jennifer Kachergus, Christophe Roumier, Vincent Mouroux, Xavier Douay, Sarah Lincoln, Clotilde Levecque, Lydie Larvor, Joris Andrieux, Mary Hulihan,[...]. Lancet 2004
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.