A citation-based method for searching scientific literature

McKinsey L Goodenberger, Brittany C Thomas, Karen E Wain. J Genet Couns 2015
Times Cited: 6







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



Times Cited
  Times     Co-cited
Similarity


Genetic counselor review of genetic test orders in a reference laboratory reduces unnecessary testing.
Christine E Miller, Patti Krautscheid, Erin E Baldwin, Tatiana Tvrdik, Amanda S Openshaw, Kim Hart, Danielle Lagrave. Am J Med Genet A 2014
64
66

Defining the role of laboratory genetic counselor.
Susan Christian, Margaret Lilley, Stacey Hume, Patrick Scott, Martin Somerville. J Genet Couns 2012
18
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
50

Genetic testing utilization and the role of the laboratory genetic counselor.
Katrina E Kotzer, Jacquelyn D Riley, Jessie H Conta, Claire M Anderson, Kimberly A Schahl, McKinsey L Goodenberger. Clin Chim Acta 2014
17
50

Further Defining the Role of the Laboratory Genetic Counselor.
Lindsey Waltman, Cassandra Runke, Jessica Balcom, Jacquelyn D Riley, Margaret Lilley, Susan Christian, Lindsay Zetzsche, McKinsey L Goodenberger. J Genet Couns 2016
22
50

Improving the value of costly genetic reference laboratory testing with active utilization management.
Jane A Dickerson, Bonnie Cole, Jessie H Conta, Monica Wellner, Stephanie E Wallace, Rhona M Jack, Joe Rutledge, Michael L Astion. Arch Pathol Lab Med 2014
34
50

Ethical and Professional Challenges Encountered by Laboratory Genetic Counselors.
Daniel Groepper, Patricia McCarthy Veach, Bonnie S LeRoy, Matthew Bower. J Genet Couns 2015
7
33

Looking back and moving forward: an historical perspective from laboratory genetic counselors.
Lindsay H Zetzsche, Katrina E Kotzer, Karen E Wain. J Genet Couns 2014
15
33

Improving Molecular Genetic Test Utilization through Order Restriction, Test Review, and Guidance.
Jacquelyn D Riley, Gary W Procop, Kandice Kottke-Marchant, Robert Wyllie, Felicitas L Lacbawan. J Mol Diagn 2015
24
33

Promoting appropriate genetic testing: the impact of a combined test review and consultative service.
Carlos J Suarez, Linbo Yu, Natalie Downs, Helio A Costa, David A Stevenson. Genet Med 2017
9
33

Preventing Genetic Testing Order Errors With a Laboratory Utilization Management Program.
Patrick C Mathias, Jessie H Conta, Eric Q Konnick, Darci L Sternen, Shannon M Stasi, Bonnie L Cole, Michael L Astion, Jane A Dickerson. Am J Clin Pathol 2016
13
33

Adding value to genetic testing through utilization management: Commercial laboratory's experience.
Gina K Londre, Christina A Zaleski, Jessie H Conta. Am J Med Genet A 2017
5
40

The half-truth of first-mover advantage.
Fernando Suarez, Gianvito Lanzolla. Harv Bus Rev 2005
3
33

Overview of the impact of noninvasive prenatal testing on diagnostic procedures.
Steven L Warsof, Sebastian Larion, Alfred Z Abuhamad. Prenat Diagn 2015
75
16

ACMG statement on noninvasive prenatal screening for fetal aneuploidy.
Anthony R Gregg, S J Gross, R G Best, K G Monaghan, K Bajaj, B G Skotko, B H Thompson, M S Watson. Genet Med 2013
175
16

ACMG position statement on prenatal/preconception expanded carrier screening.
Wayne W Grody, Barry H Thompson, Anthony R Gregg, Lora H Bean, Kristin G Monaghan, Adele Schneider, Roger V Lebo. Genet Med 2013
170
16

Genetic counselors: translating genomic science into clinical practice.
Robin L Bennett, Heather L Hampel, Jessica B Mandell, Joan H Marks. J Clin Invest 2003
24
16



Challenges in the clinical application of whole-genome sequencing.
Kelly E Ormond, Matthew T Wheeler, Louanne Hudgins, Teri E Klein, Atul J Butte, Russ B Altman, Euan A Ashley, Henry T Greely. Lancet 2010
151
16




Determinants of moral distress in medical and surgical nurses at an adult acute tertiary care hospital.
Elizabeth M Rice, Mohamed Y Rady, Arreta Hamrick, Joseph L Verheijde, Debra K Pendergast. J Nurs Manag 2008
111
16

Applying the four principles.
R Macklin. J Med Ethics 2003
28
16

Duty to re-contact.
K Hirschhorn, L D Fleisher, L Godmilow, R R Howell, R R Lebel, E R McCabe, M J McGinniss, A Milunsky, M Z Pelias, R E Pyeritz,[...]. Genet Med 1999
34
16

Comprehensive molecular screening of the FBN1 gene favors locus homogeneity of classical Marfan syndrome.
B Loeys, J De Backer, P Van Acker, K Wettinck, G Pals, L Nuytinck, P Coucke, A De Paepe. Hum Mutat 2004
141
16

Molecular testing: improving patient care through partnering with laboratory genetic counselors.
Cheryl Scacheri, Joy B Redman, Lisa Pike-Buchanan, Kelle Steenblock. Genet Med 2008
12
16

Genetic testing: practical, ethical, and counseling considerations.
Regina E Ensenauer, Virginia V Michels, Shanda S Reinke. Mayo Clin Proc 2005
34
16

Academic family physicians' perception of genetic testing and integration into practice: a CERA study.
Arch G Mainous, Sharleen P Johnson, Svetlana Chirina, Richard Baker. Fam Med 2013
31
16

A comparative analysis of ethical and professional challenges experienced by Australian and U.S. genetic counselors.
Sarah Alliman, Patricia McCarthy Veach, Dianne M Bartels, Fengqin Lian, Carolyn James, Bonnie S LeRoy. J Genet Couns 2009
17
16

Dilemmas of moral distress: moral responsibility and nursing practice.
A Jameton. AWHONNS Clin Issues Perinat Womens Health Nurs 1993
217
16

Ethical dilemmas associated with genetic testing: which are most commonly seen and how are they managed?
Natalie McLean, Martin B Delatycki, Ivan Macciocca, Rony E Duncan. Genet Med 2013
7
16




A survey of genetic counselors' strategies for addressing ethical and professional challenges in practice.
Matthew A Bower, Patricia McCarthy Veach, Dianne M Bartels, Bonnie S LeRoy. J Genet Couns 2002
36
16



Expansion of the fragile X CGG repeat in females with premutation or intermediate alleles.
Sarah L Nolin, W Ted Brown, Anne Glicksman, George E Houck, Alice D Gargano, Amy Sullivan, Valérie Biancalana, Karen Bröndum-Nielsen, Helle Hjalgrim, Elke Holinski-Feder,[...]. Am J Hum Genet 2003
240
16



Fragile X syndrome: diagnostic and carrier testing.
Stephanie Sherman, Beth A Pletcher, Deborah A Driscoll. Genet Med 2005
182
16

Genomic medicine and incidental findings: balancing actionability and patient autonomy.
Jennifer B McCormick, Richard R Sharp, Gianrico Farrugia, Noralane M Lindor, Dusica Babovic-Vuksanovic, Mitesh J Borad, Alan H Bryce, Richard J Caselli, Matthew J Ferber, Kiley J Johnson,[...]. Mayo Clin Proc 2014
10
16


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
16

Ethical and practical guidelines for reporting genetic research results to study participants: updated guidelines from a National Heart, Lung, and Blood Institute working group.
Richard R Fabsitz, Amy McGuire, Richard R Sharp, Mona Puggal, Laura M Beskow, Leslie G Biesecker, Ebony Bookman, Wylie Burke, Esteban Gonzalez Burchard, George Church,[...]. Circ Cardiovasc Genet 2010
280
16





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.