A citation-based method for searching scientific literature


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



Times Cited
  Times     Co-cited
Similarity


"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
78
63

Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies.
David T Miller, Margaret P Adam, Swaroop Aradhya, Leslie G Biesecker, Arthur R Brothman, Nigel P Carter, Deanna M Church, John A Crolla, Evan E Eichler, Charles J Epstein,[...]. Am J Hum Genet 2010
45

Physicians' perspectives on the uncertainties and implications of chromosomal microarray testing of children and families.
M Reiff, K Ross, S Mulchandani, K J Propert, R E Pyeritz, N B Spinner, B A Bernhardt. Clin Genet 2013
45
36


Uncertainty and perceived personal control among parents of children with rare chromosome conditions: the role of genetic counseling.
Shawn E Lipinski, Michael J Lipinski, Leslie G Biesecker, Barbara B Biesecker. Am J Med Genet C Semin Med Genet 2006
50
36

Preferences for results from genomic microarrays: comparing parents and health care providers.
E Turbitt, J L Halliday, D J Amor, S A Metcalfe. Clin Genet 2015
16
36

Variants of unknown significance on chromosomal microarray analysis: parental perspectives.
Stephanie Jez, Megan Martin, Sarah South, Rena Vanzo, Erin Rothwell. J Community Genet 2015
24
36

Clinical utility of chromosomal microarray analysis.
Jay W Ellison, J Britt Ravnan, Jill A Rosenfeld, S Annie Morton, Nicholas J Neill, Marc S Williams, Jodi Lewis, Beth S Torchia, Cathryn Walker, Ryan N Traylor,[...]. Pediatrics 2012
35
27

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
27

Whole genome scanning: resolving clinical diagnosis and management amidst complex data.
Sarah E Ali-Khan, Abdallah S Daar, Cheryl Shuman, Peter N Ray, Stephen W Scherer. Pediatr Res 2009
50
27

Phenotypic heterogeneity of genomic disorders and rare copy-number variants.
Santhosh Girirajan, Jill A Rosenfeld, Bradley P Coe, Sumit Parikh, Neil Friedman, Amy Goldstein, Robyn A Filipink, Juliann S McConnell, Brad Angle, Wendy S Meschino,[...]. N Engl J Med 2012
366
27

American College of Medical Genetics standards and guidelines for interpretation and reporting of postnatal constitutional copy number variants.
Hutton M Kearney, Erik C Thorland, Kerry K Brown, Fabiola Quintero-Rivera, Sarah T South. Genet Med 2011
558
27


A place for genetic uncertainty: parents valuing an unknown in the meaning of disease.
Ian Whitmarsh, Arlene M Davis, Debra Skinner, Donald B Bailey. Soc Sci Med 2007
46
27

Parental attitudes, values, and beliefs toward the return of results from exome sequencing in children.
J C Sapp, D Dong, C Stark, L E Ivey, G Hooker, L G Biesecker, B B Biesecker. Clin Genet 2014
89
27

Parents' Perspectives on Variants of Uncertain Significance from Chromosome Microarray Analysis.
Lesli A Kiedrowski, Kailey M Owens, Beverly M Yashar, Jane L Schuette. J Genet Couns 2016
34
27

Teaching genomic counseling: preparing the genetic counseling workforce for the genomic era.
Gillian W Hooker, Kelly E Ormond, Kevin Sweet, Barbara B Biesecker. J Genet Couns 2014
47
27

A genetic counselor's guide to using next-generation sequencing in clinical practice.
Flavia M Facio, Kristy Lee, Julianne M O'Daniel. J Genet Couns 2014
24
27

Genetics specialists' perspectives on disclosure of genomic incidental findings in the clinical setting.
Nancy R Downing, Janet K Williams, Sandra Daack-Hirsch, Martha Driessnack, Christian M Simon. Patient Educ Couns 2013
41
18

Incidental copy-number variants identified by routine genome testing in a clinical population.
Philip M Boone, Zachry T Soens, Ian M Campbell, Pawel Stankiewicz, Sau Wai Cheung, Ankita Patel, Arthur L Beaudet, Sharon E Plon, Chad A Shaw, Amy L McGuire,[...]. Genet Med 2013
32
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
58
18

Arrays in postnatal and prenatal diagnosis: An exploration of the ethics of consent.
Wybo Dondorp, Birgit Sikkema-Raddatz, Christine de Die-Smulders, Guido de Wert. Hum Mutat 2012
47
18



Parents' experiences of receiving their child's genetic diagnosis: a qualitative study to inform clinical genetics practice.
Setareh Ashtiani, Nancy Makela, Prescilla Carrion, Jehannine Austin. Am J Med Genet A 2014
29
18

Living without a diagnosis: the parental experience.
Celine Lewis, Heather Skirton, Ray Jones. Genet Test Mol Biomarkers 2010
39
18


Copy number variations and clinical cytogenetic diagnosis of constitutional disorders.
Charles Lee, A John Iafrate, Arthur R Brothman. Nat Genet 2007
269
18

How do research participants perceive "uncertainty" in genome sequencing?
Barbara B Biesecker, William Klein, Katie L Lewis, Tyler C Fisher, Martha Frances Wright, Leslie G Biesecker, Paul K Han. Genet Med 2014
50
18

What is a meaningful result? Disclosing the results of genomic research in autism to research participants.
Fiona Alice Miller, Robin Zoe Hayeems, Jessica Peace Bytautas. Eur J Hum Genet 2010
46
18


Psychological benefit of diagnostic certainty for mothers of children with disabilities: lessons from Down syndrome.
W Lenhard, E Breitenbach, H Ebert, H J Schindelhauer-Deutscher, W Henn. Am J Med Genet A 2005
60
18

Debating clinical utility.
Wylie Burke, A-M Laberge, N Press. Public Health Genomics 2010
48
18


Lynch syndrome patients' views of and preferences for return of results following whole exome sequencing.
Kelly Hitch, Galen Joseph, Jenna Guiltinan, Jessica Kianmahd, Janey Youngblom, Amie Blanco. J Genet Couns 2014
47
18

Next generation genetic counseling: introduction to the special issue.
Myra I Roche, Christina G S Palmer. J Genet Couns 2014
4
50

Evaluating a counselling strategy for diagnostic WES in paediatric neurology: an exploration of parents' information and communication needs.
L Krabbenborg, J Schieving, T Kleefstra, L E L M Vissers, M A Willemsen, J A Veltman, S van der Burg. Clin Genet 2016
16
18

22q11 deletion syndrome - the meaning of a diagnosis. A qualitative study on parental perspectives.
U Hallberg, S Oskarsdóttir, G Klingberg. Child Care Health Dev 2010
22
18

Informed consent for whole genome sequencing: a qualitative analysis of participant expectations and perceptions of risks, benefits, and harms.
Holly K Tabor, Jacquie Stock, Tracy Brazg, Margaret J McMillin, Karin M Dent, Joon-Ho Yu, Jay Shendure, Michael J Bamshad. Am J Med Genet A 2012
83
18

Factors associated with perceived uncertainty among parents of children with undiagnosed medical conditions.
Anne C Madeo, Kathleen E O'Brien, Barbara A Bernhardt, Barbara B Biesecker. Am J Med Genet A 2012
41
18

A qualitative study of healthcare providers' perspectives on the implications of genome-wide testing in pediatric clinical practice.
Marian Reiff, Rebecca Mueller, Surabhi Mulchandani, Nancy B Spinner, Reed E Pyeritz, Barbara A Bernhardt. J Genet Couns 2014
16
18

A prospective evaluation of whole-exome sequencing as a first-tier molecular test in infants with suspected monogenic disorders.
Zornitza Stark, Tiong Y Tan, Belinda Chong, Gemma R Brett, Patrick Yap, Maie Walsh, Alison Yeung, Heidi Peters, Dylan Mordaunt, Shannon Cowie,[...]. Genet Med 2016
219
18

Clinical and Counseling Experiences of Early Adopters of Whole Exome Sequencing.
Shubhangi Arora, Eden Haverfield, Gabriele Richard, Susanne B Haga, Rachel Mills. J Genet Couns 2016
13
18

Understanding the Psychosocial Effects of WES Test Results on Parents of Children with Rare Diseases.
Lotte Krabbenborg, L E L M Vissers, J Schieving, T Kleefstra, E J Kamsteeg, J A Veltman, M A Willemsen, S Van der Burg. J Genet Couns 2016
47
18

From genetic counseling to "genomic counseling".
Kelly E Ormond. Mol Genet Genomic Med 2013
48
18

Supervision of psychosocial skills in genetic counseling.
L DiAnne Borders, Sonja Eubanks, Nancy Callanan. J Genet Couns 2006
19
18


Illustrative case studies in the return of exome and genome sequencing results.
Laura M Amendola, Denise Lautenbach, Sarah Scollon, Barbara Bernhardt, Sawona Biswas, Kelly East, Jessica Everett, Marian J Gilmore, Patricia Himes, Victoria M Raymond,[...]. Per Med 2015
30
18


A new definition of Genetic Counseling: National Society of Genetic Counselors' Task Force report.
Robert Resta, Barbara Bowles Biesecker, Robin L Bennett, Sandra Blum, Susan Estabrooks Hahn, Michelle N Strecker, Janet L Williams. J Genet Couns 2006
400
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.