A citation-based method for searching scientific literature

Alan E Guttmacher, Francis S Collins. N Engl J Med 2002
Times Cited: 350







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



Times Cited
  Times     Co-cited
Similarity


Genomic medicine--an updated primer.
W Gregory Feero, Alan E Guttmacher, Francis S Collins. N Engl J Med 2010
280
21

The sequence of the human genome.
J C Venter, M D Adams, E W Myers, P W Li, R J Mural, G G Sutton, H O Smith, M Yandell, C A Evans, R A Holt,[...]. Science 2001
11

Nurses transforming health care using genetics and genomics.
Kathleen A Calzone, Ann Cashion, Suzanne Feetham, Jean Jenkins, Cynthia A Prows, Janet K Williams, Shu-Fen Wung. Nurs Outlook 2010
95
10

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
10

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
8

A new initiative on precision medicine.
Francis S Collins, Harold Varmus. N Engl J Med 2015
8

A vision for the future of genomics research.
Francis S Collins, Eric D Green, Alan E Guttmacher, Mark S Guyer. Nature 2003
998
7



Five years of GWAS discovery.
Peter M Visscher, Matthew A Brown, Mark I McCarthy, Jian Yang. Am J Hum Genet 2012
7


Genetics education for primary-care providers.
Wylie Burke, Jon Emery. Nat Rev Genet 2002
76
6

Getting ready for gene-based medicine.
Harold Varmus. N Engl J Med 2002
56
8

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
5


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

Prediction of total genetic value using genome-wide dense marker maps.
T H Meuwissen, B J Hayes, M E Goddard. Genetics 2001
5

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
5

Survey of nursing integration of genomics into nursing practice.
Kathleen A Calzone, Jean Jenkins, Jan Yates, Georgie Cusack, Gwenyth R Wallen, David J Liewehr, Seth M Steinberg, Colleen McBride. J Nurs Scholarsh 2012
41
12

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
5

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
5

Exome sequencing identifies the cause of a mendelian disorder.
Sarah B Ng, Kati J Buckingham, Choli Lee, Abigail W Bigham, Holly K Tabor, Karin M Dent, Chad D Huff, Paul T Shannon, Ethylin Wang Jabs, Deborah A Nickerson,[...]. Nat Genet 2010
5

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.
Sue Richards, Nazneen Aziz, Sherri Bale, David Bick, Soma Das, Julie Gastier-Foster, Wayne W Grody, Madhuri Hegde, Elaine Lyon, Elaine Spector,[...]. Genet Med 2015
5

Implementing genomic medicine in the clinic: the future is here.
Teri A Manolio, Rex L Chisholm, Brad Ozenberger, Dan M Roden, Marc S Williams, Richard Wilson, David Bick, Erwin P Bottinger, Murray H Brilliant, Charis Eng,[...]. Genet Med 2013
337
5

Ten years on--the human genome and medicine.
Harold Varmus. N Engl J Med 2010
54
7

A HapMap harvest of insights into the genetics of common disease.
Teri A Manolio, Lisa D Brooks, Francis S Collins. J Clin Invest 2008
622
4

Personalized medicine: progress and promise.
Isaac S Chan, Geoffrey S Ginsburg. Annu Rev Genomics Hum Genet 2011
135
4

Making a definitive diagnosis: successful clinical application of whole exome sequencing in a child with intractable inflammatory bowel disease.
Elizabeth A Worthey, Alan N Mayer, Grant D Syverson, Daniel Helbling, Benedetta B Bonacci, Brennan Decker, Jaime M Serpe, Trivikram Dasu, Michael R Tschannen, Regan L Veith,[...]. Genet Med 2011
476
4



Predicting genetic predisposition in humans: the promise of whole-genome markers.
Gustavo de los Campos, Daniel Gianola, David B Allison. Nat Rev Genet 2010
163
4

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
4

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
211
4

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
402
4

Exome sequencing as a tool for Mendelian disease gene discovery.
Michael J Bamshad, Sarah B Ng, Abigail W Bigham, Holly K Tabor, Mary J Emond, Deborah A Nickerson, Jay Shendure. Nat Rev Genet 2011
4


Relevance of genomics to healthcare and nursing practice.
Kathleen A Calzone, Jean Jenkins, Nick Nicol, Heather Skirton, W Gregory Feero, Eric D Green. J Nurs Scholarsh 2013
40
10

Faculty Performance on the Genomic Nursing Concept Inventory.
Catherine Y Read, Linda D Ward. J Nurs Scholarsh 2016
21
19

Development and psychometric evaluation of the genomic nursing concept inventory.
Linda D Ward, Mel Haberman, Celestina Barbosa-Leiker. J Nurs Educ 2014
15
26

A blueprint for genomic nursing science.
Kathleen A Calzone, Jean Jenkins, Alexis D Bakos, Ann K Cashion, Nancy Donaldson, W Gregory Feero, Suzanne Feetham, Patricia A Grady, Ada Sue Hinshaw, Ann R Knebel,[...]. J Nurs Scholarsh 2013
56
7

A gene-expression signature as a predictor of survival in breast cancer.
Marc J van de Vijver, Yudong D He, Laura J van't Veer, Hongyue Dai, Augustinus A M Hart, Dorien W Voskuil, George J Schreiber, Johannes L Peterse, Chris Roberts, Matthew J Marton,[...]. N Engl J Med 2002
3

A map of human genome sequence variation containing 1.42 million single nucleotide polymorphisms.
R Sachidanandam, D Weissman, S C Schmidt, J M Kakol, L D Stein, G Marth, S Sherry, J C Mullikin, B J Mortimore, D L Willey,[...]. Nature 2001
3



Educating health-care professionals about genetics and genomics.
Alan E Guttmacher, Mary E Porteous, Joseph D McInerney. Nat Rev Genet 2007
195
3

Reconsidering the family history in primary care.
Eugene C Rich, Wylie Burke, Caryl J Heaton, Susanne Haga, Linda Pinsky, M Priscilla Short, Louise Acheson. J Gen Intern Med 2004
229
3

The Personalized Medicine Coalition: goals and strategies.
Edward Abrahams, Geoffrey S Ginsburg, Mike Silver. Am J Pharmacogenomics 2005
65
4

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
3

Advanced sequencing technologies: methods and goals.
Jay Shendure, Robi D Mitra, Chris Varma, George M Church. Nat Rev Genet 2004
308
3

Cytochrome p-450 polymorphisms and response to clopidogrel.
Jessica L Mega, Sandra L Close, Stephen D Wiviott, Lei Shen, Richard D Hockett, John T Brandt, Joseph R Walker, Elliott M Antman, William Macias, Eugene Braunwald,[...]. N Engl J Med 2009
3


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.