A citation-based method for searching scientific literature

Hanna Julienne, Vincent Laville, Zachary R McCaw, Zihuai He, Vincent Guillemot, Carla Lasry, Andrey Ziyatdinov, Cyril Nerin, Amaury Vaysse, Pierre Lechat, Hervé Ménager, Wilfried Le Goff, Marie-Pierre Dube, Peter Kraft, Iuliana Ionita-Laza, Bjarni J Vilhjálmsson, Hugues Aschard. PLoS Genet 2021
Times Cited: 3







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



Times Cited
  Times     Co-cited
Similarity


Mixed-model association for biobank-scale datasets.
Po-Ru Loh, Gleb Kichaev, Steven Gazal, Armin P Schoech, Alkes L Price. Nat Genet 2018
246
66

Multi-trait analysis of genome-wide association summary statistics using MTAG.
Patrick Turley, Raymond K Walters, Omeed Maghzian, Aysu Okbay, James J Lee, Mark Alan Fontana, Tuan Anh Nguyen-Viet, Robbee Wedow, Meghan Zacher, Nicholas A Furlotte,[...]. Nat Genet 2018
323
66

10 Years of GWAS Discovery: Biology, Function, and Translation.
Peter M Visscher, Naomi R Wray, Qian Zhang, Pamela Sklar, Mark I McCarthy, Matthew A Brown, Jian Yang. Am J Hum Genet 2017
66

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
66

A global overview of pleiotropy and genetic architecture in complex traits.
Kyoko Watanabe, Sven Stringer, Oleksandr Frei, Maša Umićević Mirkov, Christiaan de Leeuw, Tinca J C Polderman, Sophie van der Sluis, Ole A Andreassen, Benjamin M Neale, Danielle Posthuma. Nat Genet 2019
350
66

Introduction to Danish (nationwide) registers on health and social issues: structure, access, legislation, and archiving.
Lau Caspar Thygesen, Camilla Daasnes, Ivan Thaulow, Henrik Brønnum-Hansen. Scand J Public Health 2011
653
33

Genome-wide association analyses of chronotype in 697,828 individuals provides insights into circadian rhythms.
Samuel E Jones, Jacqueline M Lane, Andrew R Wood, Vincent T van Hees, Jessica Tyrrell, Robin N Beaumont, Aaron R Jeffries, Hassan S Dashti, Melvyn Hillsdon, Katherine S Ruth,[...]. Nat Commun 2019
221
33

A catalog of genetic loci associated with kidney function from analyses of a million individuals.
Matthias Wuttke, Yong Li, Man Li, Karsten B Sieber, Mary F Feitosa, Mathias Gorski, Adrienne Tin, Lihua Wang, Audrey Y Chu, Anselm Hoppmann,[...]. Nat Genet 2019
272
33

Case-control association mapping by proxy using family history of disease.
Jimmy Z Liu, Yaniv Erlich, Joseph K Pickrell. Nat Genet 2017
110
33

Mixed model with correction for case-control ascertainment increases association power.
Tristan J Hayeck, Noah A Zaitlen, Po-Ru Loh, Bjarni Vilhjalmsson, Samuela Pollack, Alexander Gusev, Jian Yang, Guo-Bo Chen, Michael E Goddard, Peter M Visscher,[...]. Am J Hum Genet 2015
38
33

Human longevity: 25 genetic loci associated in 389,166 UK biobank participants.
Luke C Pilling, Chia-Ling Kuo, Kamil Sicinski, Jone Tamosauskaite, George A Kuchel, Lorna W Harries, Pamela Herd, Robert Wallace, Luigi Ferrucci, David Melzer. Aging (Albany NY) 2017
90
33

The Heritability of Autism Spectrum Disorder.
Sven Sandin, Paul Lichtenstein, Ralf Kuja-Halkola, Christina Hultman, Henrik Larsson, Abraham Reichenberg. JAMA 2017
264
33

Efficient toolkit implementing best practices for principal component analysis of population genetic data.
Florian Privé, Keurcien Luu, Michael G B Blum, John J McGrath, Bjarni J Vilhjálmsson. Bioinformatics 2020
20
33

Analysis of time-to-event for observational studies: Guidance to the use of intensity models.
Per Kragh Andersen, Maja Pohar Perme, Hans C van Houwelingen, Richard J Cook, Pierre Joly, Torben Martinussen, Jeremy M G Taylor, Michal Abrahamowicz, Terry M Therneau. Stat Med 2021
13
33

Efficient analysis of large-scale genome-wide data with two R packages: bigstatsr and bigsnpr.
Florian Privé, Hugues Aschard, Andrey Ziyatdinov, Michael G B Blum. Bioinformatics 2018
96
33

Utility of polygenic embryo screening for disease depends on the selection strategy.
Todd Lencz, Daniel Backenroth, Einat Granot-Hershkovitz, Adam Green, Kyle Gettler, Judy H Cho, Omer Weissbrod, Or Zuk, Shai Carmi. Elife 2021
16
33

Cox regression increases power to detect genotype-phenotype associations in genomic studies using the electronic health record.
Jacob J Hughey, Seth D Rhoades, Darwin Y Fu, Lisa Bastarache, Joshua C Denny, Qingxia Chen. BMC Genomics 2019
11
33

Risk of Early-Onset Depression Associated With Polygenic Liability, Parental Psychiatric History, and Socioeconomic Status.
Esben Agerbo, Betina B Trabjerg, Anders D Børglum, Andrew J Schork, Bjarni J Vilhjálmsson, Carsten B Pedersen, Christian Hakulinen, Clara Albiñana, David M Hougaard, Jakob Grove,[...]. JAMA Psychiatry 2021
14
33

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
647
33

RICOPILI: Rapid Imputation for COnsortias PIpeLIne.
Max Lam, Swapnil Awasthi, Hunna J Watson, Jackie Goldstein, Georgia Panagiotaropoulou, Vassily Trubetskoy, Robert Karlsson, Oleksander Frei, Chun-Chieh Fan, Ward De Witte,[...]. Bioinformatics 2020
76
33

Genetic associations with human longevity at the APOE and ACE loci.
F Schächter, L Faure-Delanef, F Guénot, H Rouger, P Froguel, L Lesueur-Ginot, D Cohen. Nat Genet 1994
863
33

The iPSYCH2012 case-cohort sample: new directions for unravelling genetic and environmental architectures of severe mental disorders.
C B Pedersen, J Bybjerg-Grauholm, M G Pedersen, J Grove, E Agerbo, M Bækvad-Hansen, J B Poulsen, C S Hansen, J J McGrath, T D Als,[...]. Mol Psychiatry 2018
134
33

A multiple-phenotype imputation method for genetic studies.
Andrew Dahl, Valentina Iotchkova, Amelie Baud, Åsa Johansson, Ulf Gyllensten, Nicole Soranzo, Richard Mott, Andreas Kranis, Jonathan Marchini. Nat Genet 2016
43
33

Identification of 15 new psoriasis susceptibility loci highlights the role of innate immunity.
Lam C Tsoi, Sarah L Spain, Jo Knight, Eva Ellinghaus, Philip E Stuart, Francesca Capon, Jun Ding, Yanming Li, Trilokraj Tejasvi, Johann E Gudjonsson,[...]. Nat Genet 2012
652
33

Age-of-onset information helps identify 76 genetic variants associated with allergic disease.
Manuel A R Ferreira, Judith M Vonk, Hansjörg Baurecht, Ingo Marenholz, Chao Tian, Joshua D Hoffman, Quinta Helmer, Annika Tillander, Vilhelmina Ullemar, Yi Lu,[...]. PLoS Genet 2020
9
33

A Fast and Accurate Method for Genome-Wide Time-to-Event Data Analysis and Its Application to UK Biobank.
Wenjian Bi, Lars G Fritsche, Bhramar Mukherjee, Sehee Kim, Seunggeun Lee. Am J Hum Genet 2020
20
33

Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations.
Ming-Huei Chen, Laura M Raffield, Abdou Mousas, Saori Sakaue, Jennifer E Huffman, Arden Moscati, Bhavi Trivedi, Tao Jiang, Parsa Akbari, Dragana Vuckovic,[...]. Cell 2020
136
33


Epidemiology and Heritability of Major Depressive Disorder, Stratified by Age of Onset, Sex, and Illness Course in Generation Scotland: Scottish Family Health Study (GS:SFHS).
Ana Maria Fernandez-Pujals, Mark James Adams, Pippa Thomson, Andrew G McKechanie, Douglas H R Blackwood, Blair H Smith, Anna F Dominiczak, Andrew D Morris, Keith Matthews, Archie Campbell,[...]. PLoS One 2015
60
33



A mixed-model approach for genome-wide association studies of correlated traits in structured populations.
Arthur Korte, Bjarni J Vilhjálmsson, Vincent Segura, Alexander Platt, Quan Long, Magnus Nordborg. Nat Genet 2012
238
33

Fine-mapping type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps.
Anubha Mahajan, Daniel Taliun, Matthias Thurner, Neil R Robertson, Jason M Torres, N William Rayner, Anthony J Payne, Valgerdur Steinthorsdottir, Robert A Scott, Niels Grarup,[...]. Nat Genet 2018
719
33

Conditional and joint multiple-SNP analysis of GWAS summary statistics identifies additional variants influencing complex traits.
Jian Yang, Teresa Ferreira, Andrew P Morris, Sarah E Medland, Pamela A F Madden, Andrew C Heath, Nicholas G Martin, Grant W Montgomery, Michael N Weedon, Ruth J Loos,[...]. Nat Genet 2012
764
33

Estimating missing heritability for disease from genome-wide association studies.
Sang Hong Lee, Naomi R Wray, Michael E Goddard, Peter M Visscher. Am J Hum Genet 2011
676
33

The Danish Psychiatric Central Research Register.
Ole Mors, Gurli P Perto, Preben Bo Mortensen. Scand J Public Health 2011
33

Association studies of up to 1.2 million individuals yield new insights into the genetic etiology of tobacco and alcohol use.
Mengzhen Liu, Yu Jiang, Robbee Wedow, Yue Li, David M Brazel, Fang Chen, Gargi Datta, Jose Davila-Velderrain, Daniel McGuire, Chao Tian,[...]. Nat Genet 2019
626
33

Polygenic Risk and Progression to Bipolar or Psychotic Disorders Among Individuals Diagnosed With Unipolar Depression in Early Life.
Katherine L Musliner, Morten D Krebs, Clara Albiñana, Bjarni Vilhjalmsson, Esben Agerbo, Peter P Zandi, David M Hougaard, Merete Nordentoft, Anders D Børglum, Thomas Werge,[...]. Am J Psychiatry 2020
23
33

Genome-wide association meta-analysis in 269,867 individuals identifies new genetic and functional links to intelligence.
Jeanne E Savage, Philip R Jansen, Sven Stringer, Kyoko Watanabe, Julien Bryois, Christiaan A de Leeuw, Mats Nagel, Swapnil Awasthi, Peter B Barr, Jonathan R I Coleman,[...]. Nat Genet 2018
426
33

Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals.
James J Lee, Robbee Wedow, Aysu Okbay, Edward Kong, Omeed Maghzian, Meghan Zacher, Tuan Anh Nguyen-Viet, Peter Bowers, Julia Sidorenko, Richard Karlsson Linnér,[...]. Nat Genet 2018
812
33

Efficiently controlling for case-control imbalance and sample relatedness in large-scale genetic association studies.
Wei Zhou, Jonas B Nielsen, Lars G Fritsche, Rounak Dey, Maiken E Gabrielsen, Brooke N Wolford, Jonathon LeFaive, Peter VandeHaar, Sarah A Gagliano, Aliya Gifford,[...]. Nat Genet 2018
372
33

Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression.
Naomi R Wray, Stephan Ripke, Manuel Mattheisen, Maciej Trzaskowski, Enda M Byrne, Abdel Abdellaoui, Mark J Adams, Esben Agerbo, Tracy M Air, Till M F Andlauer,[...]. Nat Genet 2018
33

Liability threshold modeling of case-control status and family history of disease increases association power.
Margaux L A Hujoel, Steven Gazal, Po-Ru Loh, Nick Patterson, Alkes L Price. Nat Genet 2020
18
33

Contrasting genetic architectures of schizophrenia and other complex diseases using fast variance-components analysis.
Po-Ru Loh, Gaurav Bhatia, Alexander Gusev, Hilary K Finucane, Brendan K Bulik-Sullivan, Samuela J Pollack, Teresa R de Candia, Sang Hong Lee, Naomi R Wray, Kenneth S Kendler,[...]. Nat Genet 2015
240
33

Risk prediction of late-onset Alzheimer's disease implies an oligogenic architecture.
Qian Zhang, Julia Sidorenko, Baptiste Couvy-Duchesne, Riccardo E Marioni, Margaret J Wright, Alison M Goate, Edoardo Marcora, Kuan-Lin Huang, Tenielle Porter, Simon M Laws,[...]. Nat Commun 2020
53
33

A resource-efficient tool for mixed model association analysis of large-scale data.
Longda Jiang, Zhili Zheng, Ting Qi, Kathryn E Kemper, Naomi R Wray, Peter M Visscher, Jian Yang. Nat Genet 2019
119
33

Genome-wide meta-analysis identifies new loci and functional pathways influencing Alzheimer's disease risk.
Iris E Jansen, Jeanne E Savage, Kyoko Watanabe, Julien Bryois, Dylan M Williams, Stacy Steinberg, Julia Sealock, Ida K Karlsson, Sara Hägg, Lavinia Athanasiu,[...]. Nat Genet 2019
843
33


The Danish Civil Registration System.
Carsten Bøcker Pedersen. Scand J Public Health 2011
33



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.