M Reiff, K Ross, S Mulchandani, K J Propert, R E Pyeritz, N B Spinner, B A Bernhardt. Clin Genet 2013
Times Cited: 45
Times Cited: 45
Times Cited
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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
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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
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Melanie Manning, Louanne Hudgins. Genet Med 2010
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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
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Pre- and postnatal genetic testing by array-comparative genomic hybridization: genetic counseling perspectives.
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Clinical genetics evaluation in identifying the etiology of autism spectrum disorders: 2013 guideline revisions.
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Clinical genetic testing for patients with autism spectrum disorders.
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Chromosome microarray in Australia: a guide for paediatricians.
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Whole-genome sequencing in health care: recommendations of the European Society of Human Genetics.
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15
American College of Medical Genetics standards and guidelines for interpretation and reporting of postnatal constitutional copy number variants.
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Hutton M Kearney, Erik C Thorland, Kerry K Brown, Fabiola Quintero-Rivera, Sarah T South. Genet Med 2011
13
Women's experiences receiving abnormal prenatal chromosomal microarray testing results.
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Arrays in postnatal and prenatal diagnosis: An exploration of the ethics of consent.
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Wybo Dondorp, Birgit Sikkema-Raddatz, Christine de Die-Smulders, Guido de Wert. Hum Mutat 2012
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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
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Uncertainty and perceived personal control among parents of children with rare chromosome conditions: the role of genetic counseling.
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Chromosomal microarray impacts clinical management.
E R Riggs, K E Wain, D Riethmaier, B Smith-Packard, W A Faucett, N Hoppman, E C Thorland, V C Patel, D T Miller. Clin Genet 2014
E R Riggs, K E Wain, D Riethmaier, B Smith-Packard, W A Faucett, N Hoppman, E C Thorland, V C Patel, D T Miller. Clin Genet 2014
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Genetic counselling and ethical issues with chromosome microarray analysis in prenatal testing.
George McGillivray, Jill A Rosenfeld, R J McKinlay Gardner, Lynn H Gillam. Prenat Diagn 2012
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Anne Townsend, Shelin Adam, Patricia H Birch, Zoe Lohn, Francois Rousseau, Jan M Friedman. Am J Med Genet A 2012
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Disclosure of incidental findings from next-generation sequencing in pediatric genomic research.
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Clinical utility of chromosomal microarray analysis.
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Phenotypic heterogeneity of genomic disorders and rare copy-number variants.
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The coming explosion in genetic testing--is there a duty to recontact?
Reed E Pyeritz. N Engl J Med 2011
Reed E Pyeritz. N Engl J Med 2011
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Informed consent for whole-genome sequencing studies in the clinical setting. Proposed recommendations on essential content and process.
Carmen Ayuso, José M Millán, Marta Mancheño, Rafael Dal-Ré. Eur J Hum Genet 2013
Carmen Ayuso, José M Millán, Marta Mancheño, Rafael Dal-Ré. Eur J Hum Genet 2013
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Autism genetic testing: a qualitative study of awareness, attitudes, and experiences among parents of children with autism spectrum disorders.
Lei-Shih Chen, Lei Xu, Tse-Yang Huang, Shweta U Dhar. Genet Med 2013
Lei-Shih Chen, Lei Xu, Tse-Yang Huang, Shweta U Dhar. Genet Med 2013
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Parental interest in a genetic risk assessment test for autism spectrum disorders.
Vivien Narcisa, Marie Discenza, Erica Vaccari, Beth Rosen-Sheidley, Antonio Y Hardan, Elizabeth Couchon. Clin Pediatr (Phila) 2013
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Primary-care providers' perceived barriers to integration of genetics services: a systematic review of the literature.
Natalie A Mikat-Stevens, Ingrid A Larson, Beth A Tarini. Genet Med 2015
Natalie A Mikat-Stevens, Ingrid A Larson, Beth A Tarini. Genet Med 2015
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Exploring concordance and discordance for return of incidental findings from clinical sequencing.
Robert C Green, Jonathan S Berg, Gerard T Berry, Leslie G Biesecker, David P Dimmock, James P Evans, Wayne W Grody, Madhuri R Hegde, Sarah Kalia, Bruce R Korf,[...]. Genet Med 2012
Robert C Green, Jonathan S Berg, Gerard T Berry, Leslie G Biesecker, David P Dimmock, James P Evans, Wayne W Grody, Madhuri R Hegde, Sarah Kalia, Bruce R Korf,[...]. Genet Med 2012
8
Unexpected findings in cancer predisposition genes detected by array comparative genomic hybridisation: what are the issues?
Gabriella Pichert, Shehla Nilofer Mohammed, Joo Wook Ahn, Caroline Mackie Ogilvie, Louise Izatt. J Med Genet 2011
Gabriella Pichert, Shehla Nilofer Mohammed, Joo Wook Ahn, Caroline Mackie Ogilvie, Louise Izatt. J Med Genet 2011
13
ACOG Committee Opinion No. 446: array comparative genomic hybridization in prenatal diagnosis.
. Obstet Gynecol 2009
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8
Opportunities and challenges for the integration of massively parallel genomic sequencing into clinical practice: lessons from the ClinSeq project.
Leslie G Biesecker. Genet Med 2012
Leslie G Biesecker. Genet Med 2012
8
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
12
Providing family guidance in rapidly shifting sand: informed consent for genetic testing.
Julie Cohen, Alec Hoon, Anna Maria Wilms Floet. Dev Med Child Neurol 2013
Julie Cohen, Alec Hoon, Anna Maria Wilms Floet. Dev Med Child Neurol 2013
57
New "first families": the psychosocial impact of new genetic technologies.
Joanna H Fanos. Genet Med 2012
Joanna H Fanos. Genet Med 2012
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Chromosomal microarray versus karyotyping for prenatal diagnosis.
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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
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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
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8
Managing incidental genomic findings: legal obligations of clinicians.
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Evaluating the utility of personal genomic information.
Morris W Foster, John J Mulvihill, Richard R Sharp. Genet Med 2009
Morris W Foster, John J Mulvihill, Richard R Sharp. Genet Med 2009
8
Key informants' perspectives of implementing chromosomal microarrays into clinical practice in Australia.
Erin Turbitt, Jane L Halliday, Sylvia A Metcalfe. Twin Res Hum Genet 2013
Erin Turbitt, Jane L Halliday, Sylvia A Metcalfe. Twin Res Hum Genet 2013
50
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
25
Capturing the clinical utility of genomic testing: medical recommendations following pediatric microarray.
Robin Z Hayeems, Ny Hoang, Sebastien Chenier, Dimitri J Stavropoulos, Shuye Pu, Rosanna Weksberg, Cheryl Shuman. Eur J Hum Genet 2015
Robin Z Hayeems, Ny Hoang, Sebastien Chenier, Dimitri J Stavropoulos, Shuye Pu, Rosanna Weksberg, Cheryl Shuman. Eur J Hum Genet 2015
26
Communicating genetic information: a difficult challenge for future pediatricians.
Eduardo Rosas-Blum, Pratibha Shirsat, Marie Leiner. BMC Med Educ 2007
Eduardo Rosas-Blum, Pratibha Shirsat, Marie Leiner. BMC Med Educ 2007
20
Physicians' preparedness for integration of genomic and pharmacogenetic testing into practice within a major healthcare system.
Christina G Selkirk, Scott M Weissman, Andy Anderson, Peter J Hulick. Genet Test Mol Biomarkers 2013
Christina G Selkirk, Scott M Weissman, Andy Anderson, Peter J Hulick. Genet Test Mol Biomarkers 2013
8
Parents' perceptions of the usefulness of chromosomal microarray analysis for children with autism spectrum disorders.
Marian Reiff, Ellen Giarelli, Barbara A Bernhardt, Ebony Easley, Nancy B Spinner, Pamela L Sankar, Surabhi Mulchandani. J Autism Dev Disord 2015
Marian Reiff, Ellen Giarelli, Barbara A Bernhardt, Ebony Easley, Nancy B Spinner, Pamela L Sankar, Surabhi Mulchandani. J Autism Dev Disord 2015
8
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
11
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
16
Do researchers have an obligation to actively look for genetic incidental findings?
Catherine Gliwa, Benjamin E Berkman. Am J Bioeth 2013
Catherine Gliwa, Benjamin E Berkman. Am J Bioeth 2013
6
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