Joanna H Fanos. Genet Med 2012
Times Cited: 11
Times Cited: 11
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
Marian Reiff, Barbara A Bernhardt, Surabhi Mulchandani, Danielle Soucier, Diana Cornell, Reed E Pyeritz, Nancy B Spinner. Genet Med 2012
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
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
M Reiff, K Ross, S Mulchandani, K J Propert, R E Pyeritz, N B Spinner, B A Bernhardt. Clin Genet 2013
36
Array-based technology and recommendations for utilization in medical genetics practice for detection of chromosomal abnormalities.
Melanie Manning, Louanne Hudgins. Genet Med 2010
Melanie Manning, Louanne Hudgins. Genet Med 2010
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
Shawn E Lipinski, Michael J Lipinski, Leslie G Biesecker, Barbara B Biesecker. Am J Med Genet C Semin Med Genet 2006
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
E Turbitt, J L Halliday, D J Amor, S A Metcalfe. Clin Genet 2015
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
Stephanie Jez, Megan Martin, Sarah South, Rena Vanzo, Erin Rothwell. J Community Genet 2015
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
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
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
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
Sarah E Ali-Khan, Abdallah S Daar, Cheryl Shuman, Peter N Ray, Stephen W Scherer. Pediatr Res 2009
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
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
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
Hutton M Kearney, Erik C Thorland, Kerry K Brown, Fabiola Quintero-Rivera, Sarah T South. Genet Med 2011
27
Why do we need a diagnosis? A qualitative study of parents' experiences, coping and needs, when the newborn child is severely disabled.
A H Graungaard, L Skov. Child Care Health Dev 2007
A H Graungaard, L Skov. Child Care Health Dev 2007
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
Ian Whitmarsh, Arlene M Davis, Debra Skinner, Donald B Bailey. Soc Sci Med 2007
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
J C Sapp, D Dong, C Stark, L E Ivey, G Hooker, L G Biesecker, B B Biesecker. Clin Genet 2014
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
Lesli A Kiedrowski, Kailey M Owens, Beverly M Yashar, Jane L Schuette. J Genet Couns 2016
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
Gillian W Hooker, Kelly E Ormond, Kevin Sweet, Barbara B Biesecker. J Genet Couns 2014
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
Flavia M Facio, Kristy Lee, Julianne M O'Daniel. J Genet Couns 2014
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
Nancy R Downing, Janet K Williams, Sandra Daack-Hirsch, Martha Driessnack, Christian M Simon. Patient Educ Couns 2013
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
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
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
Sandra Darilek, Patricia Ward, Amber Pursley, Katie Plunkett, Patti Furman, Pilar Magoulas, Ankita Patel, Sau Wai Cheung, Christine M Eng. Genet Med 2008
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
Wybo Dondorp, Birgit Sikkema-Raddatz, Christine de Die-Smulders, Guido de Wert. Hum Mutat 2012
18
Genetic counseling, activism and 'genotype-first' diagnosis of developmental disorders.
Daniel Navon. J Genet Couns 2012
Daniel Navon. J Genet Couns 2012
50
Deploying whole genome sequencing in clinical practice and public health: meeting the challenge one bin at a time.
Jonathan S Berg, Muin J Khoury, James P Evans. Genet Med 2011
Jonathan S Berg, Muin J Khoury, James P Evans. Genet Med 2011
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
Setareh Ashtiani, Nancy Makela, Prescilla Carrion, Jehannine Austin. Am J Med Genet A 2014
18
Living without a diagnosis: the parental experience.
Celine Lewis, Heather Skirton, Ray Jones. Genet Test Mol Biomarkers 2010
Celine Lewis, Heather Skirton, Ray Jones. Genet Test Mol Biomarkers 2010
18
Clinical impact of copy number variation analysis using high-resolution microarray technologies: advantages, limitations and concerns.
Curtis R Coughlin, Gunter H Scharer, Tamim H Shaikh. Genome Med 2012
Curtis R Coughlin, Gunter H Scharer, Tamim H Shaikh. Genome Med 2012
18
Copy number variations and clinical cytogenetic diagnosis of constitutional disorders.
Charles Lee, A John Iafrate, Arthur R Brothman. Nat Genet 2007
Charles Lee, A John Iafrate, Arthur R Brothman. Nat Genet 2007
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
Barbara B Biesecker, William Klein, Katie L Lewis, Tyler C Fisher, Martha Frances Wright, Leslie G Biesecker, Paul K Han. Genet Med 2014
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
Fiona Alice Miller, Robin Zoe Hayeems, Jessica Peace Bytautas. Eur J Hum Genet 2010
18
Parental attitudes toward a diagnosis in children with unidentified multiple congenital anomaly syndromes.
E T Rosenthal, L G Biesecker, B B Biesecker. Am J Med Genet 2001
E T Rosenthal, L G Biesecker, B B Biesecker. Am J Med Genet 2001
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
W Lenhard, E Breitenbach, H Ebert, H J Schindelhauer-Deutscher, W Henn. Am J Med Genet A 2005
18
Parental perceived value of a diagnosis for intellectual disability (ID): a qualitative comparison of families with and without a diagnosis for their child's ID.
Nancy L Makela, Patricia H Birch, Jan M Friedman, Carlo A Marra. Am J Med Genet A 2009
Nancy L Makela, Patricia H Birch, Jan M Friedman, Carlo A Marra. Am J Med Genet A 2009
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
Kelly Hitch, Galen Joseph, Jenna Guiltinan, Jessica Kianmahd, Janey Youngblom, Amie Blanco. J Genet Couns 2014
18
Next generation genetic counseling: introduction to the special issue.
Myra I Roche, Christina G S Palmer. J Genet Couns 2014
Myra I Roche, Christina G S Palmer. J Genet Couns 2014
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
L Krabbenborg, J Schieving, T Kleefstra, L E L M Vissers, M A Willemsen, J A Veltman, S van der Burg. Clin Genet 2016
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
U Hallberg, S Oskarsdóttir, G Klingberg. Child Care Health Dev 2010
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
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
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
Anne C Madeo, Kathleen E O'Brien, Barbara A Bernhardt, Barbara B Biesecker. Am J Med Genet A 2012
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
Marian Reiff, Rebecca Mueller, Surabhi Mulchandani, Nancy B Spinner, Reed E Pyeritz, Barbara A Bernhardt. J Genet Couns 2014
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
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
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
Shubhangi Arora, Eden Haverfield, Gabriele Richard, Susanne B Haga, Rachel Mills. J Genet Couns 2016
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
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
18
Supervision of psychosocial skills in genetic counseling.
L DiAnne Borders, Sonja Eubanks, Nancy Callanan. J Genet Couns 2006
L DiAnne Borders, Sonja Eubanks, Nancy Callanan. J Genet Couns 2006
18
Genetic counselling in the era of genomic medicine. As we move towards personalized medicine, it becomes more important to help patients understand genetic tests and make complex decisions about their health.
Jon Weil. EMBO Rep 2002
Jon Weil. EMBO Rep 2002
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
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
18
Genomic Testing: a Genetic Counselor's Personal Reflection on Three Years of Consenting and Testing.
Julia Wynn. J Genet Couns 2016
Julia Wynn. J Genet Couns 2016
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
Robert Resta, Barbara Bowles Biesecker, Robin L Bennett, Sandra Blum, Susan Estabrooks Hahn, Michelle N Strecker, Janet L Williams. J Genet Couns 2006
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.