A citation-based method for searching scientific literature

Ellen M Wijsman. Hum Genet 2012
Times Cited: 73







List of co-cited articles
441 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
23

Merlin--rapid analysis of dense genetic maps using sparse gene flow trees.
Gonçalo R Abecasis, Stacey S Cherny, William O Cookson, Lon R Cardon. Nat Genet 2002
21

Linkage analysis in the next-generation sequencing era.
Joan E Bailey-Wilson, Alexander F Wilson. Hum Hered 2011
68
20

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
17

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
17


GIGI: an approach to effective imputation of dense genotypes on large pedigrees.
Charles Y K Cheung, Elizabeth A Thompson, Ellen M Wijsman. Am J Hum Genet 2013
43
27

Construction of multilocus genetic linkage maps in humans.
E S Lander, P Green. Proc Natl Acad Sci U S A 1987
15

Sequence kernel association test for quantitative traits in family samples.
Han Chen, James B Meigs, Josée Dupuis. Genet Epidemiol 2013
156
15



The Genome Analysis Toolkit: a MapReduce framework for analyzing next-generation DNA sequencing data.
Aaron McKenna, Matthew Hanna, Eric Banks, Andrey Sivachenko, Kristian Cibulskis, Andrew Kernytsky, Kiran Garimella, David Altshuler, Stacey Gabriel, Mark Daly,[...]. Genome Res 2010
13

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
13


In silico method for inferring genotypes in pedigrees.
Joshua T Burdick, Wei-Min Chen, Gonçalo R Abecasis, Vivian G Cheung. Nat Genet 2006
98
12

A method and server for predicting damaging missense mutations.
Ivan A Adzhubei, Steffen Schmidt, Leonid Peshkin, Vasily E Ramensky, Anna Gerasimova, Peer Bork, Alexey S Kondrashov, Shamil R Sunyaev. Nat Methods 2010
12

A general framework for estimating the relative pathogenicity of human genetic variants.
Martin Kircher, Daniela M Witten, Preti Jain, Brian J O'Roak, Gregory M Cooper, Jay Shendure. Nat Genet 2014
12

Rare and common variants: twenty arguments.
Greg Gibson. Nat Rev Genet 2012
702
10

An integrated map of genetic variation from 1,092 human genomes.
Goncalo R Abecasis, Adam Auton, Lisa D Brooks, Mark A DePristo, Richard M Durbin, Robert E Handsaker, Hyun Min Kang, Gabor T Marth, Gil A McVean. Nature 2012
10


A global reference for human genetic variation.
Adam Auton, Lisa D Brooks, Richard M Durbin, Erik P Garrison, Hyun Min Kang, Jan O Korbel, Jonathan L Marchini, Shane McCarthy, Gil A McVean, Gonçalo R Abecasis. Nature 2015
10

Genetic linkage analysis in the age of whole-genome sequencing.
Jurg Ott, Jing Wang, Suzanne M Leal. Nat Rev Genet 2015
136
10





Parametric and nonparametric linkage analysis: a unified multipoint approach.
L Kruglyak, M J Daly, M P Reeve-Daly, E S Lander. Am J Hum Genet 1996
9

Family-based designs for genome-wide association studies.
Jurg Ott, Yoichiro Kamatani, Mark Lathrop. Nat Rev Genet 2011
171
9


ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data.
Kai Wang, Mingyao Li, Hakon Hakonarson. Nucleic Acids Res 2010
9

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
549
8

A second-generation combined linkage physical map of the human genome.
Tara C Matise, Fang Chen, Wenwei Chen, Francisco M De La Vega, Mark Hansen, Chunsheng He, Fiona C L Hyland, Giulia C Kennedy, Xiangyang Kong, Sarah S Murray,[...]. Genome Res 2007
249
8


MaCH: using sequence and genotype data to estimate haplotypes and unobserved genotypes.
Yun Li, Cristen J Willer, Jun Ding, Paul Scheet, Gonçalo R Abecasis. Genet Epidemiol 2010
8

Statistical analysis strategies for association studies involving rare variants.
Vikas Bansal, Ondrej Libiger, Ali Torkamani, Nicholas J Schork. Nat Rev Genet 2010
323
8

SIFT: Predicting amino acid changes that affect protein function.
Pauline C Ng, Steven Henikoff. Nucleic Acids Res 2003
8

Inferring rare disease risk variants based on exact probabilities of sharing by multiple affected relatives.
Alexandre Bureau, Samuel G Younkin, Margaret M Parker, Joan E Bailey-Wilson, Mary L Marazita, Jeffrey C Murray, Elisabeth Mangold, Hasan Albacha-Hejazi, Terri H Beaty, Ingo Ruczinski. Bioinformatics 2014
21
28

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


Optimal tests for rare variant effects in sequencing association studies.
Seunggeun Lee, Michael C Wu, Xihong Lin. Biostatistics 2012
402
6

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
83
6



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
62

Incorporating linkage information into a common disease/rare variant framework.
Anthony L Hinrichs, Brian K Suarez. Genet Epidemiol 2011
12
41

Exome sequencing, ANGPTL3 mutations, and familial combined hypolipidemia.
Kiran Musunuru, James P Pirruccello, Ron Do, Gina M Peloso, Candace Guiducci, Carrie Sougnez, Kiran V Garimella, Sheila Fisher, Justin Abreu, Andrew J Barry,[...]. N Engl J Med 2010
434
6

Targeted capture and massively parallel sequencing of 12 human exomes.
Sarah B Ng, Emily H Turner, Peggy D Robertson, Steven D Flygare, Abigail W Bigham, Choli Lee, Tristan Shaffer, Michelle Wong, Arindam Bhattacharjee, Evan E Eichler,[...]. Nature 2009
6


Linkage and association of phospholipid transfer protein activity to LASS4.
Elisabeth A Rosenthal, James Ronald, Joseph Rothstein, Ramakrishnan Rajagopalan, Jane Ranchalis, G Wolfbauer, John J Albers, John D Brunzell, Arno G Motulsky, Mark J Rieder,[...]. J Lipid Res 2011
17
29



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.