A citation-based method for searching scientific literature

Razib Khan, David Mittelman. Genome Biol 2018
Times Cited: 44







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



Times Cited
  Times     Co-cited
Similarity


Identity inference of genomic data using long-range familial searches.
Yaniv Erlich, Tal Shor, Itsik Pe'er, Shai Carmi. Science 2018
104
18

Genome-wide polygenic scores for common diseases identify individuals with risk equivalent to monogenic mutations.
Amit V Khera, Mark Chaffin, Krishna G Aragam, Mary E Haas, Carolina Roselli, Seung Hoan Choi, Pradeep Natarajan, Eric S Lander, Steven A Lubitz, Patrick T Ellinor,[...]. Nat Genet 2018
15

Genealogy databases and the future of criminal investigation.
Natalie Ram, Christi J Guerrini, Amy L McGuire. Science 2018
35
17

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
13

False-positive results released by direct-to-consumer genetic tests highlight the importance of clinical confirmation testing for appropriate patient care.
Stephany Tandy-Connor, Jenna Guiltinan, Kate Krempely, Holly LaDuca, Patrick Reineke, Stephanie Gutierrez, Phillip Gray, Brigette Tippin Davis. Genet Med 2018
131
13

Cryptic distant relatives are common in both isolated and cosmopolitan genetic samples.
Brenna M Henn, Lawrence Hon, J Michael Macpherson, Nick Eriksson, Serge Saxonov, Itsik Pe'er, Joanna L Mountain. PLoS One 2012
99
11


The UK Biobank resource with deep phenotyping and genomic data.
Clare Bycroft, Colin Freeman, Desislava Petkova, Gavin Band, Lloyd T Elliott, Kevin Sharp, Allan Motyer, Damjan Vukcevic, Olivier Delaneau, Jared O'Connell,[...]. Nature 2018
11

Identifying personal genomes by surname inference.
Melissa Gymrek, Amy L McGuire, David Golan, Eran Halperin, Yaniv Erlich. Science 2013
493
9


Routes for breaching and protecting genetic privacy.
Yaniv Erlich, Arvind Narayanan. Nat Rev Genet 2014
156
9

Human Demographic History Impacts Genetic Risk Prediction across Diverse Populations.
Alicia R Martin, Christopher R Gignoux, Raymond K Walters, Genevieve L Wojcik, Benjamin M Neale, Simon Gravel, Mark J Daly, Carlos D Bustamante, Eimear E Kenny. Am J Hum Genet 2017
544
9


The personal and clinical utility of polygenic risk scores.
Ali Torkamani, Nathan E Wineinger, Eric J Topol. Nat Rev Genet 2018
566
9

Consumer use and response to online third-party raw DNA interpretation services.
Catharine Wang, Tiernan J Cahill, Andrew Parlato, Blake Wertz, Qiankun Zhong, Tricia Norkunas Cunningham, James J Cummings. Mol Genet Genomic Med 2018
22
18

Privacy and genetic genealogy data.
Ellen M Greytak, David H Kaye, Bruce Budowle, CeCe Moore, Steven L Armentrout. Science 2018
15
26

Forensic genealogy: Some serious concerns.
Denise Syndercombe Court. Forensic Sci Int Genet 2018
24
16

Direct-to-Consumer Testing 2.0: Emerging Models of Direct-to-Consumer Genetic Testing.
Megan A Allyse, David H Robinson, Matthew J Ferber, Richard R Sharp. Mayo Clin Proc 2018
66
9

Direct-to-Consumer Genetic Testing: User Motivations, Decision Making, and Perceived Utility of Results.
J Scott Roberts, Michele C Gornick, Deanna Alexis Carere, Wendy R Uhlmann, Mack T Ruffin, Robert C Green. Public Health Genomics 2017
71
9

Consumer Perceptions of Interactions With Primary Care Providers After Direct-to-Consumer Personal Genomic Testing.
Cathelijne H van der Wouden, Deanna Alexis Carere, Anke H Maitland-van der Zee, Mack T Ruffin, J Scott Roberts, Robert C Green. Ann Intern Med 2016
71
9


Maximum-likelihood estimation of recent shared ancestry (ERSA).
Chad D Huff, David J Witherspoon, Tatum S Simonson, Jinchuan Xing, W Scott Watkins, Yuhua Zhang, Therese M Tuohy, Deborah W Neklason, Randall W Burt, Stephen L Guthery,[...]. Genome Res 2011
89
6

Whole population, genome-wide mapping of hidden relatedness.
Alexander Gusev, Jennifer K Lowe, Markus Stoffel, Mark J Daly, David Altshuler, Jan L Breslow, Jeffrey M Friedman, Itsik Pe'er. Genome Res 2009
276
6

DNA.Land is a framework to collect genomes and phenomes in the era of abundant genetic information.
Jie Yuan, Assaf Gordon, Daniel Speyer, Richard Aufrichtig, Dina Zielinski, Joseph Pickrell, Yaniv Erlich. Nat Genet 2018
12
25

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
6


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
6

The Clinical Sequencing Evidence-Generating Research Consortium: Integrating Genomic Sequencing in Diverse and Medically Underserved Populations.
Laura M Amendola, Jonathan S Berg, Carol R Horowitz, Frank Angelo, Jeannette T Bensen, Barbara B Biesecker, Leslie G Biesecker, Gregory M Cooper, Kelly East, Kelly Filipski,[...]. Am J Hum Genet 2018
64
6

Blockchain distributed ledger technologies for biomedical and health care applications.
Tsung-Ting Kuo, Hyeon-Eui Kim, Lucila Ohno-Machado. J Am Med Inform Assoc 2017
142
6

The Impact of Whole-Genome Sequencing on the Primary Care and Outcomes of Healthy Adult Patients: A Pilot Randomized Trial.
Jason L Vassy, Kurt D Christensen, Erica F Schonman, Carrie L Blout, Jill O Robinson, Joel B Krier, Pamela M Diamond, Matthew Lebo, Kalotina Machini, Danielle R Azzariti,[...]. Ann Intern Med 2017
113
6

The dawn of consumer-directed testing.
Erica Ramos, Scott M Weissman. Am J Med Genet C Semin Med Genet 2018
32
9

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
6


Is It Ethical to Use Genealogy Data to Solve Crimes?
Benjamin E Berkman, Wynter K Miller, Christine Grady. Ann Intern Med 2018
11
27

Genetic genealogy for cold case and active investigations.
Ellen M Greytak, CeCe Moore, Steven L Armentrout. Forensic Sci Int 2019
31
9

Robust relationship inference in genome-wide association studies.
Ani Manichaikul, Josyf C Mychaleckyj, Stephen S Rich, Kathy Daly, Michèle Sale, Wei-Min Chen. Bioinformatics 2010
6

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
6

UK biobank: an open access resource for identifying the causes of a wide range of complex diseases of middle and old age.
Cathie Sudlow, John Gallacher, Naomi Allen, Valerie Beral, Paul Burton, John Danesh, Paul Downey, Paul Elliott, Jane Green, Martin Landray,[...]. PLoS Med 2015
6

Common polygenic variation contributes to risk of schizophrenia and bipolar disorder.
Shaun M Purcell, Naomi R Wray, Jennifer L Stone, Peter M Visscher, Michael C O'Donovan, Patrick F Sullivan, Pamela Sklar. Nature 2009
6

10 Years of GWAS Discovery: Biology, Function, and Translation.
Peter M Visscher, Naomi R Wray, Qian Zhang, Pamela Sklar, Mark I McCarthy, Matthew A Brown, Jian Yang. Am J Hum Genet 2017
6

Privacy Risks from Genomic Data-Sharing Beacons.
Suyash S Shringarpure, Carlos D Bustamante. Am J Hum Genet 2015
86
6


Who's on third? Regulation of third-party genetic interpretation services.
Christi J Guerrini, Jennifer K Wagner, Sarah C Nelson, Gail H Javitt, Amy L McGuire. Genet Med 2020
17
17

The geography of recent genetic ancestry across Europe.
Peter Ralph, Graham Coop. PLoS Biol 2013
159
4

Policy implications for familial searching.
Joyce Kim, Danny Mammo, Marni B Siegel, Sara H Katsanis. Investig Genet 2011
17
11

Quantitative analysis of population-scale family trees with millions of relatives.
Joanna Kaplanis, Assaf Gordon, Tal Shor, Omer Weissbrod, Dan Geiger, Mary Wahl, Michael Gershovits, Barak Markus, Mona Sheikh, Melissa Gymrek,[...]. Science 2018
78
4

Evaluation of massively parallel sequencing for forensic DNA methylation profiling.
Rebecca Richards, Jayshree Patel, Kate Stevenson, SallyAnn Harbison. Electrophoresis 2018
9
22

Sequence-based US population data for the SE33 locus.
Lisa A Borsuk, Katherine B Gettings, Carolyn R Steffen, Kevin M Kiesler, Peter M Vallone. Electrophoresis 2018
15
13


Developmental validation studies of epigenetic DNA methylation markers for the detection of blood, semen and saliva samples.
Deborah S B S Silva, Joana Antunes, Kuppareddi Balamurugan, George Duncan, Clarice S Alho, Bruce McCord. Forensic Sci Int Genet 2016
34
5


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.