A citation-based method for searching scientific literature

Eden V Haverfield, Edward D Esplin, Sienna J Aguilar, Kathryn E Hatchell, Kelly E Ormond, Andrea Hanson-Kahn, Paldeep S Atwal, Sarah Macklin-Mantia, Stephanie Hines, Caron W-M Sak, Steven Tucker, Steven B Bleyl, Peter J Hulick, Ora K Gordon, Lea Velsher, Jessica Y J Gu, Scott M Weissman, Teresa Kruisselbrink, Christopher Abel, Michele Kettles, Anne Slavotinek, Bryce A Mendelsohn, Robert C Green, Swaroop Aradhya, Robert L Nussbaum. BMC Med 2021
Times Cited: 3







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



Times Cited
  Times     Co-cited
Similarity


"Forward-Thinking" in U.S. Biobanking.
R Jean Cadigan, Teresa P Edwards, Dragana Lassiter, Arlene M Davis, Gail E Henderson. Genet Test Mol Biomarkers 2017
5
33

Models of consent to return of incidental findings in genomic research.
Paul S Appelbaum, Erik Parens, Cameron R Waldman, Robert Klitzman, Abby Fyer, Josue Martinez, W Nicholson Price, Wendy K Chung. Hastings Cent Rep 2014
51
33

Can I be sued for that? Liability risk and the disclosure of clinically significant genetic research findings.
Amy L McGuire, Bartha Maria Knoppers, Ma'n H Zawati, Ellen Wright Clayton. Genome Res 2014
21
33

Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2016 update (ACMG SF v2.0): a policy statement of the American College of Medical Genetics and Genomics.
Sarah S Kalia, Kathy Adelman, Sherri J Bale, Wendy K Chung, Christine Eng, James P Evans, Gail E Herman, Sophia B Hufnagel, Teri E Klein, Bruce R Korf,[...]. Genet Med 2017
902
33

The mutational constraint spectrum quantified from variation in 141,456 humans.
Konrad J Karczewski, Laurent C Francioli, Grace Tiao, Beryl B Cummings, Jessica Alföldi, Qingbo Wang, Ryan L Collins, Kristen M Laricchia, Andrea Ganna, Daniel P Birnbaum,[...]. Nature 2020
33

Genome-wide rare variant analysis for thousands of phenotypes in over 70,000 exomes from two cohorts.
Elizabeth T Cirulli, Simon White, Robert W Read, Gai Elhanan, William J Metcalf, Francisco Tanudjaja, Donna M Fath, Efren Sandoval, Magnus Isaksson, Karen A Schlauch,[...]. Nat Commun 2020
44
33

A state-based approach to genomics for rare disease and population screening.
Kelly M East, Whitley V Kelley, Ashley Cannon, Meagan E Cochran, Irene P Moss, Thomas May, Mariko Nakano-Okuno, Stephen O Sodeke, Jeffrey C Edberg, James J Cimino,[...]. Genet Med 2021
4
33

Budget impact analysis-principles of good practice: report of the ISPOR 2012 Budget Impact Analysis Good Practice II Task Force.
Sean D Sullivan, Josephine A Mauskopf, Federico Augustovski, J Jaime Caro, Karen M Lee, Mark Minchin, Ewa Orlewska, Pete Penna, Jose-Manuel Rodriguez Barrios, Wen-Yi Shau. Value Health 2014
483
33

Aggregate penetrance of genomic variants for actionable disorders in European and African Americans.
Pradeep Natarajan, Nina B Gold, Alexander G Bick, Heather McLaughlin, Peter Kraft, Heidi L Rehm, Gina M Peloso, James G Wilson, Adolfo Correa, Jonathan G Seidman,[...]. Sci Transl Med 2016
38
33

Validation of a decision regret scale.
Jamie C Brehaut, Annette M O'Connor, Timothy J Wood, Thomas F Hack, Laura Siminoff, Elisa Gordon, Deb Feldman-Stewart. Med Decis Making 2003
644
33

Return of genetic and genomic research findings: experience of a pediatric biorepository.
Tanya Papaz, Eriskay Liston, Laura Zahavich, Dimitri J Stavropoulos, Rebekah K Jobling, Raymond H Kim, Miriam Reuter, Anastasia Miron, Erwin Oechslin, Tapas Mondal,[...]. BMC Med Genomics 2019
10
33



Experiences and attitudes of genome investigators regarding return of individual genetic test results.
Rachel B Ramoni, Amy L McGuire, Jill Oliver Robinson, Debra S Morley, Sharon E Plon, Steven Joffe. Genet Med 2013
39
33

Implementation of Electronic Consent at a Biobank: An Opportunity for Precision Medicine Research.
Natalie T Boutin, Kathleen Mathieu, Alison G Hoffnagle, Nicole L Allen, Victor M Castro, Megan Morash, P Pearl O'Rourke, Elizabeth L Hohmann, Neil Herring, Lynn Bry,[...]. J Pers Med 2016
34
33

Participant choices for return of genomic results in the eMERGE Network.
Christin Hoell, Julia Wynn, Luke V Rasmussen, Keith Marsolo, Sharon A Aufox, Wendy K Chung, John J Connolly, Robert R Freimuth, David Kochan, Hakon Hakonarson,[...]. Genet Med 2020
11
33

Return of individual genomic research results: are laws and policies keeping step?
Adrian Thorogood, Gratien Dalpé, Bartha Maria Knoppers. Eur J Hum Genet 2019
42
33

The cost-effectiveness of returning incidental findings from next-generation genomic sequencing.
Caroline S Bennette, Carlos J Gallego, Wylie Burke, Gail P Jarvik, David L Veenstra. Genet Med 2015
68
33

Identifying rare, medically relevant variation via population-based genomic screening in Alabama: opportunities and pitfalls.
Kevin M Bowling, Michelle L Thompson, David E Gray, James M J Lawlor, Kelly Williams, Kelly M East, Whitley V Kelley, Irene P Moss, Devin M Absher, E Christopher Partridge,[...]. Genet Med 2021
3
33

Disclosure of clinically actionable genetic variants to thoracic aortic dissection biobank participants.
Adelyn Beil, Whitney Hornsby, Wendy R Uhlmann, Rajani Aatre, Patricia Arscott, Brooke Wolford, Kim A Eagle, Bo Yang, Jennifer McNamara, Cristen Willer,[...]. BMC Med Genomics 2021
3
33

Automatic Placement of Genomic Research Results in Medical Records: Do Researchers Have a Duty? Should Participants Have a Choice?
Anya E R Prince, John M Conley, Arlene M Davis, Gabriel Lázaro-Muñoz, R Jean Cadigan. J Law Med Ethics 2015
9
33

Generic consent for genetic screening.
S Elias, G J Annas. N Engl J Med 1994
114
33

Researchers' views on return of incidental genomic research results: qualitative and quantitative findings.
Robert Klitzman, Paul S Appelbaum, Abby Fyer, Josue Martinez, Brigitte Buquez, Julia Wynn, Cameron R Waldman, Jo Phelan, Erik Parens, Wendy K Chung. Genet Med 2013
86
33

Exome Sequencing-Based Screening for BRCA1/2 Expected Pathogenic Variants Among Adult Biobank Participants.
Kandamurugu Manickam, Adam H Buchanan, Marci L B Schwartz, Miranda L G Hallquist, Janet L Williams, Alanna Kulchak Rahm, Heather Rocha, Juliann M Savatt, Alyson E Evans, Loren M Butry,[...]. JAMA Netw Open 2018
90
33


Population genomic screening of all young adults in a health-care system: a cost-effectiveness analysis.
Lei Zhang, Yining Bao, Moeen Riaz, Jane Tiller, Danny Liew, Xun Zhuang, David J Amor, Aamira Huq, Lara Petelin, Mark Nelson,[...]. Genet Med 2019
32
33

Data in question: A survey of European biobank professionals on ethical, legal and societal challenges of biobank research.
Melanie Goisauf, Gillian Martin, Heidi Beate Bentzen, Isabelle Budin-Ljøsne, Lars Ursin, Anna Durnová, Liis Leitsalu, Katharine Smith, Sara Casati, Marialuisa Lavitrano,[...]. PLoS One 2019
7
33

Managing incidental findings and research results in genomic research involving biobanks and archived data sets.
Susan M Wolf, Brittney N Crock, Brian Van Ness, Frances Lawrenz, Jeffrey P Kahn, Laura M Beskow, Mildred K Cho, Michael F Christman, Robert C Green, Ralph Hall,[...]. Genet Med 2012
306
33

Population genetic screening efficiently identifies carriers of autosomal dominant diseases.
J J Grzymski, G Elhanan, J A Morales Rosado, E Smith, K A Schlauch, R Read, C Rowan, N Slotnick, S Dabe, W J Metcalf,[...]. Nat Med 2020
41
33

ClinGen Variant Curation Expert Panel experiences and standardized processes for disease and gene-level specification of the ACMG/AMP guidelines for sequence variant interpretation.
Edgar A Rivera-Muñoz, Laura V Milko, Steven M Harrison, Danielle R Azzariti, C Lisa Kurtz, Kristy Lee, Jessica L Mester, Meredith A Weaver, Erin Currey, William Craigen,[...]. Hum Mutat 2018
67
33

Genotype-first approach to the detection of hereditary breast and ovarian cancer risk, and effects of risk disclosure to biobank participants.
Liis Leitsalu, Marili Palover, Timo Tõnis Sikka, Anu Reigo, Mart Kals, Kalle Pärn, Tiit Nikopensius, Tõnu Esko, Andres Metspalu, Peeter Padrik,[...]. Eur J Hum Genet 2021
3
33

Clinical outcomes of a genomic screening program for actionable genetic conditions.
Adam H Buchanan, H Lester Kirchner, Marci L B Schwartz, Melissa A Kelly, Tara Schmidlen, Laney K Jones, Miranda L G Hallquist, Heather Rocha, Megan Betts, Rachel Schwiter,[...]. Genet Med 2020
24
33

A tiered-layered-staged model for informed consent in personal genome testing.
Eline M Bunnik, A Cecile J W Janssens, Maartje H N Schermer. Eur J Hum Genet 2013
60
33

Processes and preliminary outputs for identification of actionable genes as incidental findings in genomic sequence data in the Clinical Sequencing Exploratory Research Consortium.
Jonathan S Berg, Laura M Amendola, Christine Eng, Eliezer Van Allen, Stacy W Gray, Nikhil Wagle, Heidi L Rehm, Elizabeth T DeChene, Matthew C Dulik, Fuki M Hisama,[...]. Genet Med 2013
89
33

ClinVar: improving access to variant interpretations and supporting evidence.
Melissa J Landrum, Jennifer M Lee, Mark Benson, Garth R Brown, Chen Chao, Shanmuga Chitipiralla, Baoshan Gu, Jennifer Hart, Douglas Hoffman, Wonhee Jang,[...]. Nucleic Acids Res 2018
33

Potential impact of family history-based screening guidelines on the detection of early-onset colorectal cancer.
Samir Gupta, Balambal Bharti, Dennis J Ahnen, Daniel D Buchanan, Iona C Cheng, Michelle Cotterchio, Jane C Figueiredo, Steven J Gallinger, Robert W Haile, Mark A Jenkins,[...]. Cancer 2020
17
33

NCCN Guidelines Insights: Genetic/Familial High-Risk Assessment: Colorectal, Version 2.2019.
Samir Gupta, Dawn Provenzale, Xavier Llor, Amy L Halverson, William Grady, Daniel C Chung, Sigurdis Haraldsdottir, Arnold J Markowitz, Thomas P Slavin, Heather Hampel,[...]. J Natl Compr Canc Netw 2019
111
33

Public perspectives on informed consent for biobanking.
Juli Murphy, Joan Scott, David Kaufman, Gail Geller, Lisa LeRoy, Kathy Hudson. Am J Public Health 2009
116
33

Genetic identification of familial hypercholesterolemia within a single U.S. health care system.
Noura S Abul-Husn, Kandamurugu Manickam, Laney K Jones, Eric A Wright, Dustin N Hartzel, Claudia Gonzaga-Jauregui, Colm O'Dushlaine, Joseph B Leader, H Lester Kirchner, D'Andra M Lindbuchler,[...]. Science 2016
223
33

Genetic counseling for patients with positive genomic screening results: Considerations for when the genetic test comes first.
Marci L B Schwartz, Adam H Buchanan, Miranda L G Hallquist, Christopher M Haggerty, Amy C Sturm. J Genet Couns 2021
1
100

The "All of Us" Research Program.
Joshua C Denny, Joni L Rutter, David B Goldstein, Anthony Philippakis, Jordan W Smoller, Gwynne Jenkins, Eric Dishman. N Engl J Med 2019
276
33

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
33

Return of research results from genomic biobanks: cost matters.
Marianna J Bledsoe, Ellen Wright Clayton, Amy L McGuire, William E Grizzle, P Pearl O'Rourke, Nikolajs Zeps. Genet Med 2013
42
33


Use of SNP chips to detect rare pathogenic variants: retrospective, population based diagnostic evaluation.
Weedon Mn, Jackson L, Harrison Jw, Ruth Ks, Tyrrell J, Hattersley At, Wright Cf. BMJ 2021
9
33

Assessing the Pathogenicity, Penetrance, and Expressivity of Putative Disease-Causing Variants in a Population Setting.
Caroline F Wright, Ben West, Marcus Tuke, Samuel E Jones, Kashyap Patel, Thomas W Laver, Robin N Beaumont, Jessica Tyrrell, Andrew R Wood, Timothy M Frayling,[...]. Am J Hum Genet 2019
74
33

Preferences for Return of Genetic Results Among Participants in the Jackson Heart Study and Framingham Heart Study.
Steven Joffe, Deborah E Sellers, Lynette Ekunwe, Donna Antoine-Lavigne, Sarah McGraw, Daniel Levy, Greta Lee Splansky. Circ Genom Precis Med 2019
7
33

Evidence-based assessments of clinical actionability in the context of secondary findings: Updates from ClinGen's Actionability Working Group.
Elizabeth M Webber, Jessica Ezzell Hunter, Leslie G Biesecker, Adam H Buchanan, Elizabeth V Clarke, Erin Currey, Orit Dagan-Rosenfeld, Kristy Lee, Noralane M Lindor, Christa Lese Martin,[...]. Hum Mutat 2018
18
33

Precision Population Medicine in Primary Care: The Sanford Chip Experience.
Kurt D Christensen, Megan Bell, Carrie L B Zawatsky, Lauren N Galbraith, Robert C Green, Allison M Hutchinson, Leila Jamal, Jessica L LeBlanc, Jennifer R Leonhard, Michelle Moore,[...]. Front Genet 2021
8
33

Clinical Genetic Testing for Familial Hypercholesterolemia: JACC Scientific Expert Panel.
Amy C Sturm, Joshua W Knowles, Samuel S Gidding, Zahid S Ahmad, Catherine D Ahmed, Christie M Ballantyne, Seth J Baum, Mafalda Bourbon, Alain Carrié, Marina Cuchel,[...]. J Am Coll Cardiol 2018
196
33


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.