A citation-based method for searching scientific literature

Tinca J C Polderman, Beben Benyamin, Christiaan A de Leeuw, Patrick F Sullivan, Arjen van Bochoven, Peter M Visscher, Danielle Posthuma. Nat Genet 2015
Times Cited: 648







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



Times Cited
  Times     Co-cited
Similarity


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
481
17

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
847
15


LD Score regression distinguishes confounding from polygenicity in genome-wide association studies.
Brendan K Bulik-Sullivan, Po-Ru Loh, Hilary K Finucane, Stephan Ripke, Jian Yang, Nick Patterson, Mark J Daly, Alkes L Price, Benjamin M Neale. Nat Genet 2015
15

The nature of nurture: Effects of parental genotypes.
Augustine Kong, Gudmar Thorleifsson, Michael L Frigge, Bjarni J Vilhjalmsson, Alexander I Young, Thorgeir E Thorgeirsson, Stefania Benonisdottir, Asmundur Oddsson, Bjarni V Halldorsson, Gisli Masson,[...]. Science 2018
216
14

Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder.
Ditte Demontis, Raymond K Walters, Joanna Martin, Manuel Mattheisen, Thomas D Als, Esben Agerbo, Gísli Baldursson, Rich Belliveau, Jonas Bybjerg-Grauholm, Marie Bækvad-Hansen,[...]. Nat Genet 2019
514
13

Genome-wide association study identifies 30 loci associated with bipolar disorder.
Eli A Stahl, Gerome Breen, Andreas J Forstner, Andrew McQuillin, Stephan Ripke, Vassily Trubetskoy, Manuel Mattheisen, Yunpeng Wang, Jonathan R I Coleman, Héléna A Gaspar,[...]. Nat Genet 2019
408
13

Analysis of shared heritability in common disorders of the brain.
Verneri Anttila, Brendan Bulik-Sullivan, Hilary K Finucane, Raymond K Walters, Jose Bras, Laramie Duncan, Valentina Escott-Price, Guido J Falcone, Padhraig Gormley, Rainer Malik,[...]. Science 2018
622
13

An atlas of genetic correlations across human diseases and traits.
Brendan Bulik-Sullivan, Hilary K Finucane, Verneri Anttila, Alexander Gusev, Felix R Day, Po-Ru Loh, Laramie Duncan, John R B Perry, Nick Patterson, Elise B Robinson,[...]. Nat Genet 2015
13

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
12

Genome-wide meta-analysis of depression identifies 102 independent variants and highlights the importance of the prefrontal brain regions.
David M Howard, Mark J Adams, Toni-Kim Clarke, Jonathan D Hafferty, Jude Gibson, Masoud Shirali, Jonathan R I Coleman, Saskia P Hagenaars, Joey Ward, Eleanor M Wigmore,[...]. Nat Neurosci 2019
361
11

Heritability in the genomics era--concepts and misconceptions.
Peter M Visscher, William G Hill, Naomi R Wray. Nat Rev Genet 2008
806
11


Comparing Within- and Between-Family Polygenic Score Prediction.
Saskia Selzam, Stuart J Ritchie, Jean-Baptiste Pingault, Chandra A Reynolds, Paul F O'Reilly, Robert Plomin. Am J Hum Genet 2019
51
19

Identification of common genetic risk variants for autism spectrum disorder.
Jakob Grove, Stephan Ripke, Thomas D Als, Manuel Mattheisen, Raymond K Walters, Hyejung Won, Jonatan Pallesen, Esben Agerbo, Ole A Andreassen, Richard Anney,[...]. Nat Genet 2019
437
10

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
10

Genomic structural equation modelling provides insights into the multivariate genetic architecture of complex traits.
Andrew D Grotzinger, Mijke Rhemtulla, Ronald de Vlaming, Stuart J Ritchie, Travis T Mallard, W David Hill, Hill F Ip, Riccardo E Marioni, Andrew M McIntosh, Ian J Deary,[...]. Nat Hum Behav 2019
117
10

OpenMx 2.0: Extended Structural Equation and Statistical Modeling.
Michael C Neale, Michael D Hunter, Joshua N Pritikin, Mahsa Zahery, Timothy R Brick, Robert M Kirkpatrick, Ryne Estabrook, Timothy C Bates, Hermine H Maes, Steven M Boker. Psychometrika 2016
341
9

Classical twin studies and beyond.
Dorret Boomsma, Andreas Busjahn, Leena Peltonen. Nat Rev Genet 2002
620
8

Research review: Polygenic methods and their application to psychiatric traits.
Naomi R Wray, Sang Hong Lee, Divya Mehta, Anna A E Vinkhuyzen, Frank Dudbridge, Christel M Middeldorp. J Child Psychol Psychiatry 2014
306
8

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
322
8

Genetic influences on measures of the environment: a systematic review.
Kenneth S Kendler, Jessica H Baker. Psychol Med 2007
365
7

Finding the missing heritability of complex diseases.
Teri A Manolio, Francis S Collins, Nancy J Cox, David B Goldstein, Lucia A Hindorff, David J Hunter, Mark I McCarthy, Erin M Ramos, Lon R Cardon, Aravinda Chakravarti,[...]. Nature 2009
7

Relatedness disequilibrium regression estimates heritability without environmental bias.
Alexander I Young, Michael L Frigge, Daniel F Gudbjartsson, Gudmar Thorleifsson, Gyda Bjornsdottir, Patrick Sulem, Gisli Masson, Unnur Thorsteinsdottir, Kari Stefansson, Augustine Kong. Nat Genet 2018
41
17

The Nature of Nurture: Using a Virtual-Parent Design to Test Parenting Effects on Children's Educational Attainment in Genotyped Families.
Timothy C Bates, Brion S Maher, Sarah E Medland, Kerrie McAloney, Margaret J Wright, Narelle K Hansell, Kenneth S Kendler, Nicholas G Martin, Nathan A Gillespie. Twin Res Hum Genet 2018
53
13

Comparison of Adopted and Nonadopted Individuals Reveals Gene-Environment Interplay for Education in the UK Biobank.
Rosa Cheesman, Avina Hunjan, Jonathan R I Coleman, Yasmin Ahmadzadeh, Robert Plomin, Tom A McAdams, Thalia C Eley, Gerome Breen. Psychol Sci 2020
22
31

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
262
7

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
151
7

Genetic epidemiology of major depression: review and meta-analysis.
P F Sullivan, M C Neale, K S Kendler. Am J Psychiatry 2000
6

No Support for Historical Candidate Gene or Candidate Gene-by-Interaction Hypotheses for Major Depression Across Multiple Large Samples.
Richard Border, Emma C Johnson, Luke M Evans, Andrew Smolen, Noah Berley, Patrick F Sullivan, Matthew C Keller. Am J Psychiatry 2019
155
6

Common SNPs explain a large proportion of the heritability for human height.
Jian Yang, Beben Benyamin, Brian P McEvoy, Scott Gordon, Anjali K Henders, Dale R Nyholt, Pamela A Madden, Andrew C Heath, Nicholas G Martin, Grant W Montgomery,[...]. Nat Genet 2010
6

Deconstructing the sources of genotype-phenotype associations in humans.
Alexander I Young, Stefania Benonisdottir, Molly Przeworski, Augustine Kong. Science 2019
29
20

Top 10 Replicated Findings From Behavioral Genetics.
Robert Plomin, John C DeFries, Valerie S Knopik, Jenae M Neiderhiser. Perspect Psychol Sci 2016
102
6

Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection.
Antonio F Pardiñas, Peter Holmans, Andrew J Pocklington, Valentina Escott-Price, Stephan Ripke, Noa Carrera, Sophie E Legge, Sophie Bishop, Darren Cameron, Marian L Hamshere,[...]. Nat Genet 2018
506
6

Causal associations between risk factors and common diseases inferred from GWAS summary data.
Zhihong Zhu, Zhili Zheng, Futao Zhang, Yang Wu, Maciej Trzaskowski, Robert Maier, Matthew R Robinson, John J McGrath, Peter M Visscher, Naomi R Wray,[...]. Nat Commun 2018
223
6

Common polygenic variation contributes to risk of schizophrenia and bipolar disorder.
Shaun M Purcell, Naomi R Wray, Jennifer L Stone, Peter M Visscher, Michael C O'Donovan, Patrick F Sullivan, Pamela Sklar. Nature 2009
6

Genome-wide association study of cognitive functions and educational attainment in UK Biobank (N=112 151).
G Davies, R E Marioni, D C Liewald, W D Hill, S P Hagenaars, S E Harris, S J Ritchie, M Luciano, C Fawns-Ritchie, D Lyall,[...]. Mol Psychiatry 2016
173
6

Principal components analysis corrects for stratification in genome-wide association studies.
Alkes L Price, Nick J Patterson, Robert M Plenge, Michael E Weinblatt, Nancy A Shadick, David Reich. Nat Genet 2006
6

A combined analysis of genetically correlated traits identifies 187 loci and a role for neurogenesis and myelination in intelligence.
W D Hill, R E Marioni, O Maghzian, S J Ritchie, S P Hagenaars, A M McIntosh, C R Gale, G Davies, I J Deary. Mol Psychiatry 2019
92
6

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
207
6

Genetic correlations of polygenic disease traits: from theory to practice.
Wouter van Rheenen, Wouter J Peyrot, Andrew J Schork, S Hong Lee, Naomi R Wray. Nat Rev Genet 2019
53
11

Cohort Profile Update: The Norwegian Mother and Child Cohort Study (MoBa).
Per Magnus, Charlotte Birke, Kristine Vejrup, Anita Haugan, Elin Alsaker, Anne Kjersti Daltveit, Marte Handal, Margaretha Haugen, Gudrun Høiseth, Gun Peggy Knudsen,[...]. Int J Epidemiol 2016
294
5

Accounting for genetic and environmental confounds in associations between parent and child characteristics: a systematic review of children-of-twins studies.
Tom A McAdams, Jenae M Neiderhiser, Fruhling V Rijsdijk, Jurgita Narusyte, Paul Lichtenstein, Thalia C Eley. Psychol Bull 2014
69
7

A reference panel of 64,976 haplotypes for genotype imputation.
Shane McCarthy, Sayantan Das, Warren Kretzschmar, Olivier Delaneau, Andrew R Wood, Alexander Teumer, Hyun Min Kang, Christian Fuchsberger, Petr Danecek, Kevin Sharp,[...]. Nat Genet 2016
969
5

The contribution of common genetic risk variants for ADHD to a general factor of childhood psychopathology.
Isabell Brikell, Henrik Larsson, Yi Lu, Erik Pettersson, Qi Chen, Ralf Kuja-Halkola, Robert Karlsson, Benjamin B Lahey, Paul Lichtenstein, Joanna Martin. Mol Psychiatry 2020
47
10

Influence of life stress on depression: moderation by a polymorphism in the 5-HTT gene.
Avshalom Caspi, Karen Sugden, Terrie E Moffitt, Alan Taylor, Ian W Craig, HonaLee Harrington, Joseph McClay, Jonathan Mill, Judy Martin, Antony Braithwaite,[...]. Science 2003
5


Human Demographic History Impacts Genetic Risk Prediction across Diverse Populations.
Alicia R Martin, Christopher R Gignoux, Raymond K Walters, Genevieve L Wojcik, Benjamin M Neale, Simon Gravel, Mark J Daly, Carlos D Bustamante, Eimear E Kenny. Am J Hum Genet 2017
400
5

Clinical use of current polygenic risk scores may exacerbate health disparities.
Alicia R Martin, Masahiro Kanai, Yoichiro Kamatani, Yukinori Okada, Benjamin M Neale, Mark J Daly. Nat Genet 2019
393
5

The heritability of general cognitive ability increases linearly from childhood to young adulthood.
C M A Haworth, M J Wright, M Luciano, N G Martin, E J C de Geus, C E M van Beijsterveldt, M Bartels, D Posthuma, D I Boomsma, O S P Davis,[...]. Mol Psychiatry 2010
249
5


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.