A citation-based method for searching scientific literature

Loubna Jouan, Julie Gauthier, Patrick A Dion, Guy A Rouleau. Hum Hered 2012
Times Cited: 4







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



Times Cited
  Times     Co-cited
Similarity


Identification of rare variants from exome sequence in a large pedigree with autism.
E E Marchani, N H Chapman, C Y K Cheung, K Ankenman, I B Stanaway, H H Coon, D Nickerson, R Bernier, Z Brkanac, E M Wijsman. Hum Hered 2012
8
50


DNA sequencing with chain-terminating inhibitors.
F Sanger, S Nicklen, A R Coulson. Proc Natl Acad Sci U S A 1977
50

Optimal tests for rare variant effects in sequencing association studies.
Seunggeun Lee, Michael C Wu, Xihong Lin. Biostatistics 2012
388
25

SNP set association analysis for familial data.
Elizabeth D Schifano, Michael P Epstein, Lawrence F Bielak, Min A Jhun, Sharon L R Kardia, Patricia A Peyser, Xihong Lin. Genet Epidemiol 2012
81
25

Comprehensive approach to analyzing rare genetic variants.
Thomas J Hoffmann, Nicholas J Marini, John S Witte. PLoS One 2010
103
25

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
25

Sequence kernel association test for quantitative traits in family samples.
Han Chen, James B Meigs, Josée Dupuis. Genet Epidemiol 2013
155
25

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
25



Haplotype sharing analysis using mantel statistics.
L Beckmann, D C Thomas, C Fischer, J Chang-Claude. Hum Hered 2005
39
25

Replication validity of genetic association studies.
J P Ioannidis, E E Ntzani, T A Trikalinos, D G Contopoulos-Ioannidis. Nat Genet 2001
25

Haplotype-based association analysis via variance-components score test.
Jung-Ying Tzeng, Daowen Zhang. Am J Hum Genet 2007
61
25


Association studies for next-generation sequencing.
Li Luo, Eric Boerwinkle, Momiao Xiong. Genome Res 2011
71
25

Assessment of rare BRCA1 and BRCA2 variants of unknown significance using hierarchical modeling.
Marinela Capanu, Patrick Concannon, Robert W Haile, Leslie Bernstein, Kathleen E Malone, Charles F Lynch, Xiaolin Liang, Sharon N Teraoka, Anh T Diep, Duncan C Thomas,[...]. Genet Epidemiol 2011
14
25

Linkage analysis in the next-generation sequencing era.
Joan E Bailey-Wilson, Alexander F Wilson. Hum Hered 2011
67
25

Incorporating model uncertainty in detecting rare variants: the Bayesian risk index.
Melanie A Quintana, Jonine L Berstein, Duncan C Thomas, David V Conti. Genet Epidemiol 2011
35
25

Testing for an unusual distribution of rare variants.
Benjamin M Neale, Manuel A Rivas, Benjamin F Voight, David Altshuler, Bernie Devlin, Marju Orho-Melander, Sekar Kathiresan, Shaun M Purcell, Kathryn Roeder, Mark J Daly. PLoS Genet 2011
419
25

Rare variant association analysis methods for complex traits.
Jennifer Asimit, Eleftheria Zeggini. Annu Rev Genet 2010
173
25

Gene set enrichment analysis: a knowledge-based approach for interpreting genome-wide expression profiles.
Aravind Subramanian, Pablo Tamayo, Vamsi K Mootha, Sayan Mukherjee, Benjamin L Ebert, Michael A Gillette, Amanda Paulovich, Scott L Pomeroy, Todd R Golub, Eric S Lander,[...]. Proc Natl Acad Sci U S A 2005
25



Studying gene and gene-environment effects of uncommon and common variants on continuous traits: a marker-set approach using gene-trait similarity regression.
Jung-Ying Tzeng, Daowen Zhang, Monnat Pongpanich, Chris Smith, Mark I McCarthy, Michèle M Sale, Bradford B Worrall, Fang-Chi Hsu, Duncan C Thomas, Patrick F Sullivan. Am J Hum Genet 2011
58
25

Methodological Issues in Multistage Genome-wide Association Studies.
Duncan C Thomas, Graham Casey, David V Conti, Robert W Haile, Juan Pablo Lewinger, Daniel O Stram. Stat Sci 2009
34
25

Genomic screening and replication using the same data set in family-based association testing.
Kristel Van Steen, Matthew B McQueen, Alan Herbert, Benjamin Raby, Helen Lyon, Dawn L Demeo, Amy Murphy, Jessica Su, Soma Datta, Carsten Rosenow,[...]. Nat Genet 2005
142
25

Analysing biological pathways in genome-wide association studies.
Kai Wang, Mingyao Li, Hakon Hakonarson. Nat Rev Genet 2010
562
25





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
25

Could inbred cases identified in GWAS data succeed in detecting rare recessive variants where affected sib-pairs have failed?
Emmanuelle Génin, Mourad Sahbatou, Steven Gazal, Marie-Claude Babron, Hervé Perdry, Anne-Louise Leutenegger. Hum Hered 2012
6
25

A groupwise association test for rare mutations using a weighted sum statistic.
Bo Eskerod Madsen, Sharon R Browning. PLoS Genet 2009
758
25


Next generation analytic tools for large scale genetic epidemiology studies of complex diseases.
Leah E Mechanic, Huann-Sheng Chen, Christopher I Amos, Nilanjan Chatterjee, Nancy J Cox, Rao L Divi, Ruzong Fan, Emily L Harris, Kevin Jacobs, Peter Kraft,[...]. Genet Epidemiol 2012
46
25

Genotype imputation.
Yun Li, Cristen Willer, Serena Sanna, Gonçalo Abecasis. Annu Rev Genomics Hum Genet 2009
742
25

Population genetics of rare variants and complex diseases.
M Cyrus Maher, Lawrence H Uricchio, Dara G Torgerson, Ryan D Hernandez. Hum Hered 2012
37
25

Hierarchical Bayes prioritization of marker associations from a genome-wide association scan for further investigation.
Juan Pablo Lewinger, David V Conti, James W Baurley, Timothy J Triche, Duncan C Thomas. Genet Epidemiol 2007
57
25

Rare variant association testing for next-generation sequencing data via hierarchical clustering.
Ioanna Tachmazidou, Andrew Morris, Eleftheria Zeggini. Hum Hered 2012
3
33

Detecting rare variants for complex traits using family and unrelated data.
Xiaofeng Zhu, Tao Feng, Yali Li, Qing Lu, Robert C Elston. Genet Epidemiol 2010
97
25

Using affected sib-pairs to uncover rare disease variants.
Hervé Perdry, Bertram Müller-Myhsok, Françoise Clerget-Darpoux. Hum Hered 2012
6
25

Single-variant and multi-variant trend tests for genetic association with next-generation sequencing that are robust to sequencing error.
Wonkuk Kim, Douglas Londono, Lisheng Zhou, Jinchuan Xing, Alejandro Q Nato, Anthony Musolf, Tara C Matise, Stephen J Finch, Derek Gordon. Hum Hered 2012
4
25


Optimal unified approach for rare-variant association testing with application to small-sample case-control whole-exome sequencing studies.
Seunggeun Lee, Mary J Emond, Michael J Bamshad, Kathleen C Barnes, Mark J Rieder, Deborah A Nickerson, David C Christiani, Mark M Wurfel, Xihong Lin. Am J Hum Genet 2012
521
25

In silico method for inferring genotypes in pedigrees.
Joshua T Burdick, Wei-Min Chen, Gonçalo R Abecasis, Vivian G Cheung. Nat Genet 2006
97
25

Rare and common variants: twenty arguments.
Greg Gibson. Nat Rev Genet 2012
691
25

Efficient genome-wide association testing of gene-environment interaction in case-parent trios.
W James Gauderman, Duncan C Thomas, Cassandra E Murcray, David Conti, Dalin Li, Juan Pablo Lewinger. Am J Epidemiol 2010
29
25

Detecting rare variants.
Tao Feng, Xiaofeng Zhu. Methods Mol Biol 2012
6
25


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.