A citation-based method for searching scientific literature

Peter Kraft, David J Hunter. N Engl J Med 2009
Times Cited: 288







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



Times Cited
  Times     Co-cited
Similarity


Common genetic variation and human traits.
David B Goldstein. N Engl J Med 2009
617
27


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
20

Performance of common genetic variants in breast-cancer risk models.
Sholom Wacholder, Patricia Hartge, Ross Prentice, Montserrat Garcia-Closas, Heather Spencer Feigelson, W Ryan Diver, Michael J Thun, David G Cox, Susan E Hankinson, Peter Kraft,[...]. N Engl J Med 2010
324
13

PLINK: a tool set for whole-genome association and population-based linkage analyses.
Shaun Purcell, Benjamin Neale, Kathe Todd-Brown, Lori Thomas, Manuel A R Ferreira, David Bender, Julian Maller, Pamela Sklar, Paul I W de Bakker, Mark J Daly,[...]. Am J Hum Genet 2007
12

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
10

Genomewide association studies and human disease.
John Hardy, Andrew Singleton. N Engl J Med 2009
478
8

Potential etiologic and functional implications of genome-wide association loci for human diseases and traits.
Lucia A Hindorff, Praveen Sethupathy, Heather A Junkins, Erin M Ramos, Jayashri P Mehta, Francis S Collins, Teri A Manolio. Proc Natl Acad Sci U S A 2009
8

Genome-wide association studies for complex traits: consensus, uncertainty and challenges.
Mark I McCarthy, Gonçalo R Abecasis, Lon R Cardon, David B Goldstein, Julian Little, John P A Ioannidis, Joel N Hirschhorn. Nat Rev Genet 2008
8


Hundreds of variants clustered in genomic loci and biological pathways affect human height.
Hana Lango Allen, Karol Estrada, Guillaume Lettre, Sonja I Berndt, Michael N Weedon, Fernando Rivadeneira, Cristen J Willer, Anne U Jackson, Sailaja Vedantam, Soumya Raychaudhuri,[...]. Nature 2010
8

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
8


Five years of GWAS discovery.
Peter M Visscher, Matthew A Brown, Mark I McCarthy, Jian Yang. Am J Hum Genet 2012
8

Multifactor-dimensionality reduction reveals high-order interactions among estrogen-metabolism genes in sporadic breast cancer.
M D Ritchie, L W Hahn, N Roodi, L R Bailey, W D Dupont, F F Parl, J H Moore. Am J Hum Genet 2001
8



Genetic heterogeneity in human disease.
Jon McClellan, Mary-Claire King. Cell 2010
649
7


Polygenes, risk prediction, and targeted prevention of breast cancer.
Paul D P Pharoah, Antonis C Antoniou, Douglas F Easton, Bruce A J Ponder. N Engl J Med 2008
403
7

Projecting the performance of risk prediction based on polygenic analyses of genome-wide association studies.
Nilanjan Chatterjee, Bill Wheeler, Joshua Sampson, Patricia Hartge, Stephen J Chanock, Ju-Hyun Park. Nat Genet 2013
215
7

Genome-wide strategies for detecting multiple loci that influence complex diseases.
Jonathan Marchini, Peter Donnelly, Lon R Cardon. Nat Genet 2005
608
7


BOOST: A fast approach to detecting gene-gene interactions in genome-wide case-control studies.
Xiang Wan, Can Yang, Qiang Yang, Hong Xue, Xiaodan Fan, Nelson L S Tang, Weichuan Yu. Am J Hum Genet 2010
243
7


Initial sequencing and analysis of the human genome.
E S Lander, L M Linton, B Birren, C Nusbaum, M C Zody, J Baldwin, K Devon, K Dewar, M Doyle, W FitzHugh,[...]. Nature 2001
6

Bayesian inference analyses of the polygenic architecture of rheumatoid arthritis.
Eli A Stahl, Daniel Wegmann, Gosia Trynka, Javier Gutierrez-Achury, Ron Do, Benjamin F Voight, Peter Kraft, Robert Chen, Henrik J Kallberg, Fina A S Kurreeman,[...]. Nat Genet 2012
286
6

Prediction of individual genetic risk to disease from genome-wide association studies.
Naomi R Wray, Michael E Goddard, Peter M Visscher. Genome Res 2007
388
6

Estimation of effect size distribution from genome-wide association studies and implications for future discoveries.
Ju-Hyun Park, Sholom Wacholder, Mitchell H Gail, Ulrike Peters, Kevin B Jacobs, Stephen J Chanock, Nilanjan Chatterjee. Nat Genet 2010
447
6

Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease.
Heribert Schunkert, Inke R König, Sekar Kathiresan, Muredach P Reilly, Themistocles L Assimes, Hilma Holm, Michael Preuss, Alexandre F R Stewart, Maja Barbalic, Christian Gieger,[...]. Nat Genet 2011
6

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
654
6

The NHGRI GWAS Catalog, a curated resource of SNP-trait associations.
Danielle Welter, Jacqueline MacArthur, Joannella Morales, Tony Burdett, Peggy Hall, Heather Junkins, Alan Klemm, Paul Flicek, Teri Manolio, Lucia Hindorff,[...]. Nucleic Acids Res 2014
6

Interpretation of genetic association studies: markers with replicated highly significant odds ratios may be poor classifiers.
Johanna Jakobsdottir, Michael B Gorin, Yvette P Conley, Robert E Ferrell, Daniel E Weeks. PLoS Genet 2009
183
5

A map of human genome variation from population-scale sequencing.
Gonçalo R Abecasis, David Altshuler, Adam Auton, Lisa D Brooks, Richard M Durbin, Richard A Gibbs, Matt E Hurles, Gil A McVean. Nature 2010
5

A HapMap harvest of insights into the genetics of common disease.
Teri A Manolio, Lisa D Brooks, Francis S Collins. J Clin Invest 2008
628
5

Beyond missing heritability: prediction of complex traits.
Robert Makowsky, Nicholas M Pajewski, Yann C Klimentidis, Ana I Vazquez, Christine W Duarte, David B Allison, Gustavo de los Campos. PLoS Genet 2011
173
5

Biological, clinical and population relevance of 95 loci for blood lipids.
Tanya M Teslovich, Kiran Musunuru, Albert V Smith, Andrew C Edmondson, Ioannis M Stylianou, Masahiro Koseki, James P Pirruccello, Samuli Ripatti, Daniel I Chasman, Cristen J Willer,[...]. Nature 2010
5


Genotype score in addition to common risk factors for prediction of type 2 diabetes.
James B Meigs, Peter Shrader, Lisa M Sullivan, Jarred B McAteer, Caroline S Fox, Josée Dupuis, Alisa K Manning, Jose C Florez, Peter W F Wilson, Ralph B D'Agostino,[...]. N Engl J Med 2008
538
5

Rare-variant association testing for sequencing data with the sequence kernel association test.
Michael C Wu, Seunggeun Lee, Tianxi Cai, Yun Li, Michael Boehnke, Xihong Lin. Am J Hum Genet 2011
5

GCTA: a tool for genome-wide complex trait analysis.
Jian Yang, S Hong Lee, Michael E Goddard, Peter M Visscher. Am J Hum Genet 2011
5


Polygenic modeling with bayesian sparse linear mixed models.
Xiang Zhou, Peter Carbonetto, Matthew Stephens. PLoS Genet 2013
372
5

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
5

Predicting genetic predisposition in humans: the promise of whole-genome markers.
Gustavo de los Campos, Daniel Gianola, David B Allison. Nat Rev Genet 2010
166
5


Complement factor H polymorphism in age-related macular degeneration.
Robert J Klein, Caroline Zeiss, Emily Y Chew, Jen-Yue Tsai, Richard S Sackler, Chad Haynes, Alice K Henning, John Paul SanGiovanni, Shrikant M Mane, Susan T Mayne,[...]. Science 2005
5


Predictive rule inference for epistatic interaction detection in genome-wide association studies.
Xiang Wan, Can Yang, Qiang Yang, Hong Xue, Nelson L S Tang, Weichuan Yu. Bioinformatics 2010
78
6



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.