Ellen M Wijsman. Hum Genet 2012
Times Cited: 73
Times Cited: 73
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
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
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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
Gonçalo R Abecasis, Stacey S Cherny, William O Cookson, Lon R Cardon. Nat Genet 2002
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Linkage analysis in the next-generation sequencing era.
Joan E Bailey-Wilson, Alexander F Wilson. Hum Hered 2011
Joan E Bailey-Wilson, Alexander F Wilson. Hum Hered 2011
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
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
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
40
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
Charles Y K Cheung, Elizabeth A Thompson, Ellen M Wijsman. Am J Hum Genet 2013
27
Construction of multilocus genetic linkage maps in humans.
E S Lander, P Green. Proc Natl Acad Sci U S A 1987
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
Han Chen, James B Meigs, Josée Dupuis. Genet Epidemiol 2013
15
Uncovering the roles of rare variants in common disease through whole-genome sequencing.
Elizabeth T Cirulli, David B Goldstein. Nat Rev Genet 2010
Elizabeth T Cirulli, David B Goldstein. Nat Rev Genet 2010
15
A groupwise association test for rare mutations using a weighted sum statistic.
Bo Eskerod Madsen, Sharon R Browning. PLoS Genet 2009
Bo Eskerod Madsen, Sharon R Browning. PLoS Genet 2009
13
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
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
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
Power of family-based association designs to detect rare variants in large pedigrees using imputed genotypes.
Mohamad Saad, Ellen M Wijsman. Genet Epidemiol 2014
Mohamad Saad, Ellen M Wijsman. Genet Epidemiol 2014
45
In silico method for inferring genotypes in pedigrees.
Joshua T Burdick, Wei-Min Chen, Gonçalo R Abecasis, Vivian G Cheung. Nat Genet 2006
Joshua T Burdick, Wei-Min Chen, Gonçalo R Abecasis, Vivian G Cheung. Nat Genet 2006
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
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
Martin Kircher, Daniela M Witten, Preti Jain, Brian J O'Roak, Gregory M Cooper, Jay Shendure. Nat Genet 2014
12
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
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
Methods for detecting associations with rare variants for common diseases: application to analysis of sequence data.
Bingshan Li, Suzanne M Leal. Am J Hum Genet 2008
Bingshan Li, Suzanne M Leal. Am J Hum Genet 2008
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
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
Jurg Ott, Jing Wang, Suzanne M Leal. Nat Rev Genet 2015
10
Lessons learned from Genetic Analysis Workshop 17: transitioning from genome-wide association studies to whole-genome statistical genetic analysis.
Alexander F Wilson, Andreas Ziegler. Genet Epidemiol 2011
Alexander F Wilson, Andreas Ziegler. Genet Epidemiol 2011
41
Descent graphs in pedigree analysis: applications to haplotyping, location scores, and marker-sharing statistics.
E Sobel, K Lange. Am J Hum Genet 1996
E Sobel, K Lange. Am J Hum Genet 1996
9
Multilocus lod scores in large pedigrees: combination of exact and approximate calculations.
Liping Tong, Elizabeth Thompson. Hum Hered 2008
Liping Tong, Elizabeth Thompson. Hum Hered 2008
26
9
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
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
Jurg Ott, Yoichiro Kamatani, Mark Lathrop. Nat Rev Genet 2011
9
Fast and accurate short read alignment with Burrows-Wheeler transform.
Heng Li, Richard Durbin. Bioinformatics 2009
Heng Li, Richard Durbin. Bioinformatics 2009
9
ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data.
Kai Wang, Mingyao Li, Hakon Hakonarson. Nucleic Acids Res 2010
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
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
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
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
8
Multipoint linkage analysis with many multiallelic or dense diallelic markers: Markov chain-Monte Carlo provides practical approaches for genome scans on general pedigrees.
Ellen M Wijsman, Joseph H Rothstein, Elizabeth A Thompson. Am J Hum Genet 2006
Ellen M Wijsman, Joseph H Rothstein, Elizabeth A Thompson. Am J Hum Genet 2006
10
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
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
Vikas Bansal, Ondrej Libiger, Ali Torkamani, Nicholas J Schork. Nat Rev Genet 2010
8
SIFT: Predicting amino acid changes that affect protein function.
Pauline C Ng, Steven Henikoff. Nucleic Acids Res 2003
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
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
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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
Alkes L Price, Nick J Patterson, Robert M Plenge, Michael E Weinblatt, Nancy A Shadick, David Reich. Nat Genet 2006
6
Markov chain Monte Carlo segregation and linkage analysis for oligogenic models.
S C Heath. Am J Hum Genet 1997
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Optimal tests for rare variant effects in sequencing association studies.
Seunggeun Lee, Michael C Wu, Xihong Lin. Biostatistics 2012
Seunggeun Lee, Michael C Wu, Xihong Lin. Biostatistics 2012
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
Elizabeth D Schifano, Michael P Epstein, Lawrence F Bielak, Min A Jhun, Sharon L R Kardia, Patricia A Peyser, Xihong Lin. Genet Epidemiol 2012
6
A strategy to discover genes that carry multi-allelic or mono-allelic risk for common diseases: a cohort allelic sums test (CAST).
Stephan Morgenthaler, William G Thilly. Mutat Res 2007
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6
Study designs for identification of rare disease variants in complex diseases: the utility of family-based designs.
Iuliana Ionita-Laza, Ruth Ottman. Genetics 2011
Iuliana Ionita-Laza, Ruth Ottman. Genetics 2011
17
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
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
62
Incorporating linkage information into a common disease/rare variant framework.
Anthony L Hinrichs, Brian K Suarez. Genet Epidemiol 2011
Anthony L Hinrichs, Brian K Suarez. Genet Epidemiol 2011
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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
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
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
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
Genetic analysis of simulated oligogenic traits in nuclear and extended pedigrees: summary of GAW10 contributions.
E M Wijsman, C I Amos. Genet Epidemiol 1997
E M Wijsman, C I Amos. Genet Epidemiol 1997
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
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
29
Differential confounding of rare and common variants in spatially structured populations.
Iain Mathieson, Gil McVean. Nat Genet 2012
Iain Mathieson, Gil McVean. Nat Genet 2012
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.