A citation-based method for searching scientific literature

A Cecile J W Janssens, Cornelia M van Duijn. Hum Mol Genet 2008
Times Cited: 214







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



Times Cited
  Times     Co-cited
Similarity


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
17

Genetic risk prediction in complex disease.
Luke Jostins, Jeffrey C Barrett. Hum Mol Genet 2011
119
10

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
10

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
9

Predictive testing for complex diseases using multiple genes: fact or fiction?
A Cecile J W Janssens, Yurii S Aulchenko, Stefano Elefante, Gerard J J M Borsboom, Ewout W Steyerberg, Cornelia M van Duijn. Genet Med 2006
169
9


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
9

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

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
405
7



Risk prediction using genome-wide association studies.
Charles Kooperberg, Michael LeBlanc, Valerie Obenchain. Genet Epidemiol 2010
84
8

Association between a literature-based genetic risk score and cardiovascular events in women.
Nina P Paynter, Daniel I Chasman, Guillaume Paré, Julie E Buring, Nancy R Cook, Joseph P Miletich, Paul M Ridker. JAMA 2010
255
7

ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing.
Robert C Green, Jonathan S Berg, Wayne W Grody, Sarah S Kalia, Bruce R Korf, Christa L Martin, Amy L McGuire, Robert L Nussbaum, Julianne M O'Daniel, Kelly E Ormond,[...]. Genet Med 2013
7

The mystery of missing heritability: Genetic interactions create phantom heritability.
Or Zuk, Eliana Hechter, Shamil R Sunyaev, Eric S Lander. Proc Natl Acad Sci U S A 2012
918
6

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
325
6

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
217
6

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
6

Rare and common variants: twenty arguments.
Greg Gibson. Nat Rev Genet 2012
709
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
184
6

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
543
6

A HapMap harvest of insights into the genetics of common disease.
Teri A Manolio, Lisa D Brooks, Francis S Collins. J Clin Invest 2008
629
5



Effects of communicating DNA-based disease risk estimates on risk-reducing behaviours.
Theresa M Marteau, David P French, Simon J Griffin, A T Prevost, Stephen Sutton, Clare Watkinson, Sophie Attwood, Gareth J Hollands. Cochrane Database Syst Rev 2010
200
5

Inclusion of gene-gene and gene-environment interactions unlikely to dramatically improve risk prediction for complex diseases.
Hugues Aschard, Jinbo Chen, Marilyn C Cornelis, Lori B Chibnik, Elizabeth W Karlson, Peter Kraft. Am J Hum Genet 2012
63
7

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
5

Pathway analysis of GWAS provides new insights into genetic susceptibility to 3 inflammatory diseases.
Hariklia Eleftherohorinou, Victoria Wright, Clive Hoggart, Anna-Liisa Hartikainen, Marjo-Riitta Jarvelin, David Balding, Lachlan Coin, Michael Levin. PLoS One 2009
109
5

Effect of direct-to-consumer genomewide profiling to assess disease risk.
Cinnamon S Bloss, Nicholas J Schork, Eric J Topol. N Engl J Med 2011
352
5

Prediction of individual genetic risk to disease from genome-wide association studies.
Naomi R Wray, Michael E Goddard, Peter M Visscher. Genome Res 2007
392
5


Evaluation of polygenic risk scores for predicting breast and prostate cancer risk.
Mitchell J Machiela, Chia-Yen Chen, Constance Chen, Stephen J Chanock, David J Hunter, Peter Kraft. Genet Epidemiol 2011
59
8

Missing heritability and strategies for finding the underlying causes of complex disease.
Evan E Eichler, Jonathan Flint, Greg Gibson, Augustine Kong, Suzanne M Leal, Jason H Moore, Joseph H Nadeau. Nat Rev Genet 2010
5

Prediction of individual genetic risk of complex disease.
Naomi R Wray, Michael E Goddard, Peter M Visscher. Curr Opin Genet Dev 2008
109
5

A second generation human haplotype map of over 3.1 million SNPs.
Kelly A Frazer, Dennis G Ballinger, David R Cox, David A Hinds, Laura L Stuve, Richard A Gibbs, John W Belmont, Andrew Boudreau, Paul Hardenbol, Suzanne M Leal,[...]. Nature 2007
5

A new initiative on precision medicine.
Francis S Collins, Harold Varmus. N Engl J Med 2015
5


SLCO1B1 variants and statin-induced myopathy--a genomewide study.
E Link, S Parish, J Armitage, L Bowman, S Heath, F Matsuda, I Gut, M Lathrop, R Collins. N Engl J Med 2008
4

Gene ontology: tool for the unification of biology. The Gene Ontology Consortium.
M Ashburner, C A Ball, J A Blake, D Botstein, H Butler, J M Cherry, A P Davis, K Dolinski, S S Dwight, J T Eppig,[...]. Nat Genet 2000
4

Clinical assessment incorporating a personal genome.
Euan A Ashley, Atul J Butte, Matthew T Wheeler, Rong Chen, Teri E Klein, Frederick E Dewey, Joel T Dudley, Kelly E Ormond, Aleksandra Pavlovic, Alexander A Morgan,[...]. Lancet 2010
468
4

Genomic and personalized medicine: foundations and applications.
Geoffrey S Ginsburg, Huntington F Willard. Transl Res 2009
271
4

A genome-wide association study identifies novel risk loci for type 2 diabetes.
Robert Sladek, Ghislain Rocheleau, Johan Rung, Christian Dina, Lishuang Shen, David Serre, Philippe Boutin, Daniel Vincent, Alexandre Belisle, Samy Hadjadj,[...]. Nature 2007
4

A large-scale genome-wide association study of Asian populations uncovers genetic factors influencing eight quantitative traits.
Yoon Shin Cho, Min Jin Go, Young Jin Kim, Jee Yeon Heo, Ji Hee Oh, Hyo-Jeong Ban, Dankyu Yoon, Mi Hee Lee, Dong-Joon Kim, Miey Park,[...]. Nat Genet 2009
714
4

Genome-wide association study identifies eight loci associated with blood pressure.
Christopher Newton-Cheh, Toby Johnson, Vesela Gateva, Martin D Tobin, Murielle Bochud, Lachlan Coin, Samer S Najjar, Jing Hua Zhao, Simon C Heath, Susana Eyheramendy,[...]. Nat Genet 2009
884
4

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
658
4


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
4

Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants.
Sekar Kathiresan, Benjamin F Voight, Shaun Purcell, Kiran Musunuru, Diego Ardissino, Pier M Mannucci, Sonia Anand, James C Engert, Nilesh J Samani, Heribert Schunkert,[...]. Nat Genet 2009
831
4

Managing incidental findings and research results in genomic research involving biobanks and archived data sets.
Susan M Wolf, Brittney N Crock, Brian Van Ness, Frances Lawrenz, Jeffrey P Kahn, Laura M Beskow, Mildred K Cho, Michael F Christman, Robert C Green, Ralph Hall,[...]. Genet Med 2012
306
4



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.