A citation-based method for searching scientific literature

John J Connolly, Joseph T Glessner, Berta Almoguera, David R Crosslin, Gail P Jarvik, Patrick M Sleiman, Hakon Hakonarson. Front Genet 2014
Times Cited: 8







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



Times Cited
  Times     Co-cited
Similarity


The Electronic Medical Records and Genomics (eMERGE) Network: past, present, and future.
Omri Gottesman, Helena Kuivaniemi, Gerard Tromp, W Andrew Faucett, Rongling Li, Teri A Manolio, Saskia C Sanderson, Joseph Kannry, Randi Zinberg, Melissa A Basford,[...]. Genet Med 2013
404
50

EMR-linked GWAS study: investigation of variation landscape of loci for body mass index in children.
Bahram Namjou, Mehdi Keddache, Keith Marsolo, Michael Wagner, Todd Lingren, Beth Cobb, Cassandra Perry, Stephanie Kennebeck, Ingrid A Holm, Rongling Li,[...]. Front Genet 2013
31
37

Genomic analyses with biofilter 2.0: knowledge driven filtering, annotation, and model development.
Sarah A Pendergrass, Alex Frase, John Wallace, Daniel Wolfe, Neerja Katiyar, Carrie Moore, Marylyn D Ritchie. BioData Min 2013
35
25

Systematic comparison of phenome-wide association study of electronic medical record data and genome-wide association study data.
Joshua C Denny, Lisa Bastarache, Marylyn D Ritchie, Robert J Carroll, Raquel Zink, Jonathan D Mosley, Julie R Field, Jill M Pulley, Andrea H Ramirez, Erica Bowton,[...]. Nat Biotechnol 2013
453
25

Quality control procedures for genome-wide association studies.
Stephen Turner, Loren L Armstrong, Yuki Bradford, Christopher S Carlson, Dana C Crawford, Andrew T Crenshaw, Mariza de Andrade, Kimberly F Doheny, Jonathan L Haines, Geoffrey Hayes,[...]. Curr Protoc Hum Genet 2011
175
25

Return of results in the genomic medicine projects of the eMERGE network.
Iftikhar J Kullo, Ra'ad Haddad, Cynthia A Prows, Ingrid Holm, Saskia C Sanderson, Nanibaa' A Garrison, Richard R Sharp, Maureen E Smith, Helena Kuivaniemi, Erwin P Bottinger,[...]. Front Genet 2014
31
25

Imputation and quality control steps for combining multiple genome-wide datasets.
Shefali S Verma, Mariza de Andrade, Gerard Tromp, Helena Kuivaniemi, Elizabeth Pugh, Bahram Namjou-Khales, Shubhabrata Mukherjee, Gail P Jarvik, Leah C Kottyan, Amber Burt,[...]. Front Genet 2014
78
25

Origins and functional impact of copy number variation in the human genome.
Donald F Conrad, Dalila Pinto, Richard Redon, Lars Feuk, Omer Gokcumen, Yujun Zhang, Jan Aerts, T Daniel Andrews, Chris Barnes, Peter Campbell,[...]. Nature 2010
25

Two new Loci for body-weight regulation identified in a joint analysis of genome-wide association studies for early-onset extreme obesity in French and german study groups.
André Scherag, Christian Dina, Anke Hinney, Vincent Vatin, Susann Scherag, Carla I G Vogel, Timo D Müller, Harald Grallert, H-Erich Wichmann, Beverley Balkau,[...]. PLoS Genet 2010
217
12

A genome-wide association study identifies novel alleles associated with hair color and skin pigmentation.
Jiali Han, Peter Kraft, Hongmei Nan, Qun Guo, Constance Chen, Abrar Qureshi, Susan E Hankinson, Frank B Hu, David L Duffy, Zhen Zhen Zhao,[...]. PLoS Genet 2008
329
12

Knowledge-driven multi-locus analysis reveals gene-gene interactions influencing HDL cholesterol level in two independent EMR-linked biobanks.
Stephen D Turner, Richard L Berg, James G Linneman, Peggy L Peissig, Dana C Crawford, Joshua C Denny, Dan M Roden, Catherine A McCarty, Marylyn D Ritchie, Russell A Wilke. PLoS One 2011
50
12

Genetic variants that confer resistance to malaria are associated with red blood cell traits in African-Americans: an electronic medical record-based genome-wide association study.
Keyue Ding, Mariza de Andrade, Teri A Manolio, Dana C Crawford, Laura J Rasmussen-Torvik, Marylyn D Ritchie, Joshua C Denny, Daniel R Masys, Hayan Jouni, Jennifer A Pachecho,[...]. G3 (Bethesda) 2013
24
12


Admixture mapping and subsequent fine-mapping suggests a biologically relevant and novel association on chromosome 11 for type 2 diabetes in African Americans.
Janina M Jeff, Loren L Armstrong, Marylyn D Ritchie, Joshua C Denny, Abel N Kho, Melissa A Basford, Wendy A Wolf, Jennifer A Pacheco, Rongling Li, Rex L Chisholm,[...]. PLoS One 2014
10
12

Merging and emerging cohorts: necessary but not sufficient.
Francis S Collins, Teri A Manolio. Nature 2007
49
12

Generalization of variants identified by genome-wide association studies for electrocardiographic traits in African Americans.
Janina M Jeff, Marylyn D Ritchie, Joshua C Denny, Abel N Kho, Andrea H Ramirez, David Crosslin, Loren Armstrong, Melissa A Basford, Wendy A Wolf, Jennifer A Pacheco,[...]. Ann Hum Genet 2013
24
12

The metabochip, a custom genotyping array for genetic studies of metabolic, cardiovascular, and anthropometric traits.
Benjamin F Voight, Hyun Min Kang, Jun Ding, Cameron D Palmer, Carlo Sidore, Peter S Chines, Noël P Burtt, Christian Fuchsberger, Yanming Li, Jeanette Erdmann,[...]. PLoS Genet 2012
373
12

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
12

The eMERGE Network: a consortium of biorepositories linked to electronic medical records data for conducting genomic studies.
Catherine A McCarty, Rex L Chisholm, Christopher G Chute, Iftikhar J Kullo, Gail P Jarvik, Eric B Larson, Rongling Li, Daniel R Masys, Marylyn D Ritchie, Dan M Roden,[...]. BMC Med Genomics 2011
449
12

Next-generation analysis of cataracts: determining knowledge driven gene-gene interactions using Biofilter, and gene-environment interactions using the PhenX Toolkit.
Sarah A Pendergrass, Shefali S Verma, Emily R Holzinger, Carrie B Moore, John Wallace, Scott M Dudek, Wayne Huggins, Terrie Kitchner, Carol Waudby, Richard Berg,[...]. Pac Symp Biocomput 2013
14
12

Environment-wide association study (EWAS) for type 2 diabetes in the Marshfield Personalized Medicine Research Project Biobank.
Molly A Hall, Scott M Dudek, Robert Goodloe, Dana C Crawford, Sarah A Pendergrass, Peggy Peissig, Murray Brilliant, Catherine A McCarty, Marylyn D Ritchie. Pac Symp Biocomput 2014
28
12

Several common variants modulate heart rate, PR interval and QRS duration.
Hilma Holm, Daniel F Gudbjartsson, David O Arnar, Gudmar Thorleifsson, Gudmundur Thorgeirsson, Hrafnhildur Stefansdottir, Sigurjon A Gudjonsson, Aslaug Jonasdottir, Ellisiv B Mathiesen, Inger Njølstad,[...]. Nat Genet 2010
268
12

Genes, environment and the value of prospective cohort studies.
Teri A Manolio, Joan E Bailey-Wilson, Francis S Collins. Nat Rev Genet 2006
216
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
12

Web-based, participant-driven studies yield novel genetic associations for common traits.
Nicholas Eriksson, J Michael Macpherson, Joyce Y Tung, Lawrence S Hon, Brian Naughton, Serge Saxonov, Linda Avey, Anne Wojcicki, Itsik Pe'er, Joanna Mountain. PLoS Genet 2010
277
12

Genome-wide association studies identify several new loci associated with pigmentation traits and skin cancer risk in European Americans.
Mingfeng Zhang, Fengju Song, Liming Liang, Hongmei Nan, Jiangwen Zhang, Hongliang Liu, Li-E Wang, Qingyi Wei, Jeffrey E Lee, Christopher I Amos,[...]. Hum Mol Genet 2013
77
12

Genotyping technologies for genetic research.
Jiannis Ragoussis. Annu Rev Genomics Hum Genet 2009
121
12

Genetic variants associated with the white blood cell count in 13,923 subjects in the eMERGE Network.
David R Crosslin, Andrew McDavid, Noah Weston, Sarah C Nelson, Xiuwen Zheng, Eugene Hart, Mariza de Andrade, Iftikhar J Kullo, Catherine A McCarty, Kimberly F Doheny,[...]. Hum Genet 2012
88
12

Genome-wide association study of PR interval.
Arne Pfeufer, Charlotte van Noord, Kristin D Marciante, Dan E Arking, Martin G Larson, Albert Vernon Smith, Kirill V Tarasov, Martina Müller, Nona Sotoodehnia, Moritz F Sinner,[...]. Nat Genet 2010
316
12

Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease.
Adam C Naj, Gyungah Jun, Gary W Beecham, Li-San Wang, Badri Narayan Vardarajan, Jacqueline Buros, Paul J Gallins, Joseph D Buxbaum, Gail P Jarvik, Paul K Crane,[...]. Nat Genet 2011
12

High density GWAS for LDL cholesterol in African Americans using electronic medical records reveals a strong protective variant in APOE.
Laura J Rasmussen-Torvik, Jennifer A Pacheco, Russell A Wilke, William K Thompson, Marylyn D Ritchie, Abel N Kho, Arun Muthalagu, M Geoff Hayes, Loren L Armstrong, Douglas A Scheftner,[...]. Clin Transl Sci 2012
34
12

Genome-wide association studies in diverse populations.
Noah A Rosenberg, Lucy Huang, Ethan M Jewett, Zachary A Szpiech, Ivana Jankovic, Michael Boehnke. Nat Rev Genet 2010
360
12

Novel associations for hypothyroidism include known autoimmune risk loci.
Nicholas Eriksson, Joyce Y Tung, Amy K Kiefer, David A Hinds, Uta Francke, Joanna L Mountain, Chuong B Do. PLoS One 2012
93
12

Use of diverse electronic medical record systems to identify genetic risk for type 2 diabetes within a genome-wide association study.
Abel N Kho, M Geoffrey Hayes, Laura Rasmussen-Torvik, Jennifer A Pacheco, William K Thompson, Loren L Armstrong, Joshua C Denny, Peggy L Peissig, Aaron W Miller, Wei-Qi Wei,[...]. J Am Med Inform Assoc 2012
187
12

Genetic variation associated with circulating monocyte count in the eMERGE Network.
David R Crosslin, Andrew McDavid, Noah Weston, Xiuwen Zheng, Eugene Hart, Mariza de Andrade, Iftikhar J Kullo, Catherine A McCarty, Kimberly F Doheny, Elizabeth Pugh,[...]. Hum Mol Genet 2013
44
12

Genetic variation in SCN10A influences cardiac conduction.
John C Chambers, Jing Zhao, Cesare M N Terracciano, Connie R Bezzina, Weihua Zhang, Riyaz Kaba, Manoraj Navaratnarajah, Amol Lotlikar, Joban S Sehmi, Manraj K Kooner,[...]. Nat Genet 2010
193
12

Genetic Loci implicated in erythroid differentiation and cell cycle regulation are associated with red blood cell traits.
Keyue Ding, Khader Shameer, Hayan Jouni, Daniel R Masys, Gail P Jarvik, Abel N Kho, Marylyn D Ritchie, Catherine A McCarty, Christopher G Chute, Teri A Manolio,[...]. Mayo Clin Proc 2012
32
12

PheWAS: demonstrating the feasibility of a phenome-wide scan to discover gene-disease associations.
Joshua C Denny, Marylyn D Ritchie, Melissa A Basford, Jill M Pulley, Lisa Bastarache, Kristin Brown-Gentry, Deede Wang, Dan R Masys, Dan M Roden, Dana C Crawford. Bioinformatics 2010
551
12

Validation of electronic medical record-based phenotyping algorithms: results and lessons learned from the eMERGE network.
Katherine M Newton, Peggy L Peissig, Abel Ngo Kho, Suzette J Bielinski, Richard L Berg, Vidhu Choudhary, Melissa Basford, Christopher G Chute, Iftikhar J Kullo, Rongling Li,[...]. J Am Med Inform Assoc 2013
220
12

Pleiotropy in complex traits: challenges and strategies.
Nadia Solovieff, Chris Cotsapas, Phil H Lee, Shaun M Purcell, Jordan W Smoller. Nat Rev Genet 2013
534
12

Biofilter: a knowledge-integration system for the multi-locus analysis of genome-wide association studies.
William S Bush, Scott M Dudek, Marylyn D Ritchie. Pac Symp Biocomput 2009
91
12

Complement receptor 1 gene variants are associated with erythrocyte sedimentation rate.
Iftikhar J Kullo, Keyue Ding, Khader Shameer, Catherine A McCarty, Gail P Jarvik, Joshua C Denny, Marylyn D Ritchie, Zi Ye, David R Crosslin, Rex L Chisholm,[...]. Am J Hum Genet 2011
51
12

The NCBI dbGaP database of genotypes and phenotypes.
Matthew D Mailman, Michael Feolo, Yumi Jin, Masato Kimura, Kimberly Tryka, Rinat Bagoutdinov, Luning Hao, Anne Kiang, Justin Paschall, Lon Phan,[...]. Nat Genet 2007
672
12

The PhenX Toolkit: get the most from your measures.
Carol M Hamilton, Lisa C Strader, Joseph G Pratt, Deborah Maiese, Tabitha Hendershot, Richard K Kwok, Jane A Hammond, Wayne Huggins, Dean Jackman, Huaqin Pan,[...]. Am J Epidemiol 2011
286
12

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
12

A genome- and phenome-wide association study to identify genetic variants influencing platelet count and volume and their pleiotropic effects.
Khader Shameer, Joshua C Denny, Keyue Ding, Hayan Jouni, David R Crosslin, Mariza de Andrade, Christopher G Chute, Peggy Peissig, Jennifer A Pacheco, Rongling Li,[...]. Hum Genet 2014
95
12

Electronic medical records for genetic research: results of the eMERGE consortium.
Abel N Kho, Jennifer A Pacheco, Peggy L Peissig, Luke Rasmussen, Katherine M Newton, Noah Weston, Paul K Crane, Jyotishman Pathak, Christopher G Chute, Suzette J Bielinski,[...]. Sci Transl Med 2011
227
12

Replication of SCN5A Associations with Electrocardio-graphic Traits in African Americans from Clinical and Epidemiologic Studies.
Janina M Jeff, Kristin Brown-Gentry, Robert Goodloe, Marylyn D Ritchie, Joshua C Denny, Abel N Kho, Loren L Armstrong, Bob McClellan, Ping Mayo, Melissa Allen,[...]. Evol Comput Mach Learn Data Min Bioinform 2014
2
50

Abundant pleiotropy in human complex diseases and traits.
Shanya Sivakumaran, Felix Agakov, Evropi Theodoratou, James G Prendergast, Lina Zgaga, Teri Manolio, Igor Rudan, Paul McKeigue, James F Wilson, Harry Campbell. Am J Hum Genet 2011
309
12



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.