A citation-based method for searching scientific literature

Gabrielle M Christenhusz, Koenraad Devriendt, Kris Dierickx. Eur J Hum Genet 2013
Times Cited: 99







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



Times Cited
  Times     Co-cited
Similarity


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
86
4


Policy challenges of clinical genome sequencing.
Caroline F Wright, Anna Middleton, Hilary Burton, Fiona Cunningham, Steve E Humphries, Jane Hurst, Ewan Birney, Helen V Firth. BMJ 2013
36
11

The implications of familial incidental findings from exome sequencing: the NIH Undiagnosed Diseases Program experience.
Lauren Lawrence, Murat Sincan, Thomas Markello, David R Adams, Fred Gill, Rena Godfrey, Gretchen Golas, Catherine Groden, Dennis Landis, Michele Nehrebecky,[...]. Genet Med 2014
39
10

The full spectrum of ethical issues in dementia care: systematic qualitative review.
Daniel Strech, Marcel Mertz, Hannes Knüppel, Gerald Neitzke, Martina Schmidhuber. Br J Psychiatry 2013
32
12

Dynamic consent: a patient interface for twenty-first century research networks.
Jane Kaye, Edgar A Whitley, David Lund, Michael Morrison, Harriet Teare, Karen Melham. Eur J Hum Genet 2015
192
4


Processes and factors involved in decisions regarding return of incidental genomic findings in research.
Robert Klitzman, Brigitte Buquez, Paul S Appelbaum, Abby Fyer, Wendy K Chung. Genet Med 2014
22
18

Preferences for results delivery from exome sequencing/genome sequencing.
Martha F Wright, Katie L Lewis, Tyler C Fisher, Gillian W Hooker, Toby E Emanuel, Leslie G Biesecker, Barbara B Biesecker. Genet Med 2014
41
9

The unintended implications of blurring the line between research and clinical care in a genomic age.
Benjamin E Berkman, Sara Chandros Hull, Lisa Eckstein. Per Med 2014
23
17

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
47
8


Societal preferences for the return of incidental findings from clinical genomic sequencing: a discrete-choice experiment.
Dean A Regier, Stuart J Peacock, Reka Pataky, Kimberly van der Hoek, Gail P Jarvik, Jeffrey Hoch, David Veenstra. CMAJ 2015
47
8

Ethical signposts for clinical geneticists in secondary variant and incidental finding disclosure discussions.
Gabrielle M Christenhusz, Koenraad Devriendt, Hilde Van Esch, Kris Dierickx. Med Health Care Philos 2015
6
66

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
4


Current state of ethics literature synthesis: a systematic review of reviews.
Marcel Mertz, Hannes Kahrass, Daniel Strech. BMC Med 2016
22
18


Pre- and postnatal genetic testing by array-comparative genomic hybridization: genetic counseling perspectives.
Sandra Darilek, Patricia Ward, Amber Pursley, Katie Plunkett, Patti Furman, Pilar Magoulas, Ankita Patel, Sau Wai Cheung, Christine M Eng. Genet Med 2008
56
5

"What does it mean?": uncertainties in understanding results of chromosomal microarray testing.
Marian Reiff, Barbara A Bernhardt, Surabhi Mulchandani, Danielle Soucier, Diana Cornell, Reed E Pyeritz, Nancy B Spinner. Genet Med 2012
75
4


Copy number and SNP arrays in clinical diagnostics.
Christian P Schaaf, Joanna Wiszniewska, Arthur L Beaudet. Annu Rev Genomics Hum Genet 2011
93
3

ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data.
Kai Wang, Mingyao Li, Hakon Hakonarson. Nucleic Acids Res 2010
3

Exome sequencing: dual role as a discovery and diagnostic tool.
Chee-Seng Ku, David N Cooper, Constantin Polychronakos, Nasheen Naidoo, Mengchu Wu, Richie Soong. Ann Neurol 2012
111
3

Disease gene identification strategies for exome sequencing.
Christian Gilissen, Alexander Hoischen, Han G Brunner, Joris A Veltman. Eur J Hum Genet 2012
261
3

Target-enrichment strategies for next-generation sequencing.
Lira Mamanova, Alison J Coffey, Carol E Scott, Iwanka Kozarewa, Emily H Turner, Akash Kumar, Eleanor Howard, Jay Shendure, Daniel J Turner. Nat Methods 2010
627
3

Biobanks, consent and claims of consensus.
Zubin Master, Erin Nelson, Blake Murdoch, Timothy Caulfield. Nat Methods 2012
48
6

Ethical endgames: broad consent for narrow interests; open consent for closed minds.
Jan Reinert Karlsen, Jan Helge Solbakk, Søren Holm. Camb Q Healthc Ethics 2011
17
17

Active choice but not too active: public perspectives on biobank consent models.
Christian M Simon, Jamie L'heureux, Jeffrey C Murray, Patricia Winokur, George Weiner, Elizabeth Newbury, Laura Shinkunas, Bridget Zimmerman. Genet Med 2011
94
3


Can Broad Consent be Informed Consent?
Mark Sheehan. Public Health Ethics 2011
63
4

Individual genetic and genomic research results and the tradition of informed consent: exploring US review board guidance.
Christian Simon, Laura A Shinkunas, Debra Brandt, Janet K Williams. J Med Ethics 2012
16
18


The Centers for Mendelian Genomics: a new large-scale initiative to identify the genes underlying rare Mendelian conditions.
Michael J Bamshad, Jay A Shendure, David Valle, Ada Hamosh, James R Lupski, Richard A Gibbs, Eric Boerwinkle, Richard P Lifton, Mark Gerstein, Murat Gunel,[...]. Am J Med Genet A 2012
76
3


Racial differences in the use of BRCA1/2 testing among women with a family history of breast or ovarian cancer.
Katrina Armstrong, Ellyn Micco, Amy Carney, Jill Stopfer, Mary Putt. JAMA 2005
254
3

Sociocultural influences on participation in genetic risk assessment and testing among African American women.
Chanita Hughes, Grace Ann Fasaye, V Holland LaSalle, Clinton Finch. Patient Educ Couns 2003
71
4

Incidental findings of therapeutic misconception in biobank-based research.
Colin M E Halverson, Lainie Friedman Ross. Genet Med 2012
30
10

Patient reactions to personalized medicine vignettes: an experimental design.
Morgan Butrick, Debra Roter, Kimberly Kaphingst, Lori H Erby, Carlton Haywood, Mary Catherine Beach, Howard P Levy. Genet Med 2011
14
21

Whole exome and whole genome sequencing.
David Bick, David Dimmock. Curr Opin Pediatr 2011
86
3

Disclosing pathogenic genetic variants to research participants: quantifying an emerging ethical responsibility.
Christopher A Cassa, Sarah K Savage, Patrick L Taylor, Robert C Green, Amy L McGuire, Kenneth D Mandl. Genome Res 2012
67
4

An informatics approach to analyzing the incidentalome.
Jonathan S Berg, Michael Adams, Nassib Nassar, Chris Bizon, Kristy Lee, Charles P Schmitt, Kirk C Wilhelmsen, James P Evans. Genet Med 2013
101
3

Chromosomal microarray versus karyotyping for prenatal diagnosis.
Ronald J Wapner, Christa Lese Martin, Brynn Levy, Blake C Ballif, Christine M Eng, Julia M Zachary, Melissa Savage, Lawrence D Platt, Daniel Saltzman, William A Grobman,[...]. N Engl J Med 2012
597
3


Rapid whole-genome sequencing for genetic disease diagnosis in neonatal intensive care units.
Carol Jean Saunders, Neil Andrew Miller, Sarah Elizabeth Soden, Darrell Lee Dinwiddie, Aaron Noll, Noor Abu Alnadi, Nevene Andraws, Melanie LeAnn Patterson, Lisa Ann Krivohlavek, Joel Fellis,[...]. Sci Transl Med 2012
348
3

ACMG recommendations for standards for interpretation and reporting of sequence variations: Revisions 2007.
C Sue Richards, Sherri Bale, Daniel B Bellissimo, Soma Das, Wayne W Grody, Madhuri R Hegde, Elaine Lyon, Brian E Ward. Genet Med 2008
499
3

The advent of personal genome sequencing.
Radoje Drmanac. Genet Med 2011
37
8

Population studies: return of research results and incidental findings Policy Statement.
Bartha Maria Knoppers, Mylène Deschênes, Ma'n H Zawati, Anne Marie Tassé. Eur J Hum Genet 2013
66
4

Developing a policy for paediatric biobanks: principles for good practice.
Kristien Hens, Carla E Van El, Pascal Borry, Anne Cambon-Thomsen, Martina C Cornel, Francesca Forzano, Anneke Lucassen, Christine Patch, Lisbeth Tranebjaerg, Eric Vermeulen,[...]. Eur J Hum Genet 2013
39
7

Ethics of future disclosure of individual risk information in a genetic cohort study: a survey of donor preferences.
Kenji Matsui, Reidar K Lie, Yoshikuni Kita, Hirotsugu Ueshima. J Epidemiol 2008
16
18


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.