Marian Reiff, Barbara A Bernhardt, Surabhi Mulchandani, Danielle Soucier, Diana Cornell, Reed E Pyeritz, Nancy B Spinner. Genet Med 2012
Times Cited: 75
Times Cited: 75
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.
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Physicians' perspectives on the uncertainties and implications of chromosomal microarray testing of children and families.
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ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing.
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Parents' Perspectives on Variants of Uncertain Significance from Chromosome Microarray Analysis.
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American College of Medical Genetics standards and guidelines for interpretation and reporting of postnatal constitutional copy number variants.
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Women's experiences receiving abnormal prenatal chromosomal microarray testing results.
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Barbara A Bernhardt, Danielle Soucier, Karen Hanson, Melissa S Savage, Laird Jackson, Ronald J Wapner. Genet Med 2013
16
Chromosomal microarray testing influences medical management.
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Michael E Coulter, David T Miller, David J Harris, Pamela Hawley, Jonathan Picker, Amy E Roberts, Magdi M Sobeih, Mira Irons. Genet Med 2011
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Clinical genetics evaluation in identifying the etiology of autism spectrum disorders: 2013 guideline revisions.
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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.
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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
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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
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The impact of chromosomal microarray on clinical management: a retrospective analysis.
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Parents' perceptions of the usefulness of chromosomal microarray analysis for children with autism spectrum disorders.
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22
Pre- and postnatal genetic testing by array-comparative genomic hybridization: genetic counseling perspectives.
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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.
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Nancy L Makela, Patricia H Birch, Jan M Friedman, Carlo A Marra. Am J Med Genet A 2009
21
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
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16
Confirmation of chromosomal microarray as a first-tier clinical diagnostic test for individuals with developmental delay, intellectual disability, autism spectrum disorders and dysmorphic features.
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Whole genome scanning: resolving clinical diagnosis and management amidst complex data.
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Sarah E Ali-Khan, Abdallah S Daar, Cheryl Shuman, Peter N Ray, Stephen W Scherer. Pediatr Res 2009
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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
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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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Clinical genetic testing for patients with autism spectrum disorders.
Yiping Shen, Kira A Dies, Ingrid A Holm, Carolyn Bridgemohan, Magdi M Sobeih, Elizabeth B Caronna, Karen J Miller, Jean A Frazier, Iris Silverstein, Jonathan Picker,[...]. Pediatrics 2010
Yiping Shen, Kira A Dies, Ingrid A Holm, Carolyn Bridgemohan, Magdi M Sobeih, Elizabeth B Caronna, Karen J Miller, Jean A Frazier, Iris Silverstein, Jonathan Picker,[...]. Pediatrics 2010
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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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Ella J Wilkins, Alison D Archibald, Margaret A Sahhar, Susan M White. Am J Med Genet A 2016
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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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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
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Chromosome microarray in Australia: a guide for paediatricians.
Elizabeth E Palmer, Greg B Peters, David Mowat. J Paediatr Child Health 2012
Elizabeth E Palmer, Greg B Peters, David Mowat. J Paediatr Child Health 2012
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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
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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
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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
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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
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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Comprehensive evaluation of the child with intellectual disability or global developmental delays.
John B Moeschler, Michael Shevell. Pediatrics 2014
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Association between microdeletion and microduplication at 16p11.2 and autism.
Lauren A Weiss, Yiping Shen, Joshua M Korn, Dan E Arking, David T Miller, Ragnheidur Fossdal, Evald Saemundsen, Hreinn Stefansson, Manuel A R Ferreira, Todd Green,[...]. N Engl J Med 2008
Lauren A Weiss, Yiping Shen, Joshua M Korn, Dan E Arking, David T Miller, Ragnheidur Fossdal, Evald Saemundsen, Hreinn Stefansson, Manuel A R Ferreira, Todd Green,[...]. N Engl J Med 2008
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Global variation in copy number in the human genome.
Richard Redon, Shumpei Ishikawa, Karen R Fitch, Lars Feuk, George H Perry, T Daniel Andrews, Heike Fiegler, Michael H Shapero, Andrew R Carson, Wenwei Chen,[...]. Nature 2006
Richard Redon, Shumpei Ishikawa, Karen R Fitch, Lars Feuk, George H Perry, T Daniel Andrews, Heike Fiegler, Michael H Shapero, Andrew R Carson, Wenwei Chen,[...]. Nature 2006
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A copy number variation morbidity map of developmental delay.
Gregory M Cooper, Bradley P Coe, Santhosh Girirajan, Jill A Rosenfeld, Tiffany H Vu, Carl Baker, Charles Williams, Heather Stalker, Rizwan Hamid, Vickie Hannig,[...]. Nat Genet 2011
Gregory M Cooper, Bradley P Coe, Santhosh Girirajan, Jill A Rosenfeld, Tiffany H Vu, Carl Baker, Charles Williams, Heather Stalker, Rizwan Hamid, Vickie Hannig,[...]. Nat Genet 2011
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Disclosure of incidental findings from next-generation sequencing in pediatric genomic research.
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Ruqayyah Abdul-Karim, Benjamin E Berkman, David Wendler, Annette Rid, Javed Khan, Tom Badgett, Sara Chandros Hull. Pediatrics 2013
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American College of Medical Genetics recommendations for the design and performance expectations for clinical genomic copy number microarrays intended for use in the postnatal setting for detection of constitutional abnormalities.
Hutton M Kearney, Sarah T South, Daynna J Wolff, Allen Lamb, Ada Hamosh, Kathleen W Rao. Genet Med 2011
Hutton M Kearney, Sarah T South, Daynna J Wolff, Allen Lamb, Ada Hamosh, Kathleen W Rao. Genet Med 2011
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An exploration of genetic counselors' needs and experiences with prenatal chromosomal microarray testing.
Barbara A Bernhardt, Katherine Kellom, Alexandra Barbarese, W Andrew Faucett, Ronald J Wapner. J Genet Couns 2014
Barbara A Bernhardt, Katherine Kellom, Alexandra Barbarese, W Andrew Faucett, Ronald J Wapner. J Genet Couns 2014
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Chromosomal microarray analysis of consecutive individuals with autism spectrum disorders or learning disability presenting for genetic services.
Jennifer L Roberts, Karine Hovanes, Majed Dasouki, Ann M Manzardo, Merlin G Butler. Gene 2014
Jennifer L Roberts, Karine Hovanes, Majed Dasouki, Ann M Manzardo, Merlin G Butler. Gene 2014
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The genetics of Autism Spectrum Disorders--a guide for clinicians.
Karsten M Heil, Christian P Schaaf. Curr Psychiatry Rep 2013
Karsten M Heil, Christian P Schaaf. Curr Psychiatry Rep 2013
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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
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The usefulness of whole-exome sequencing in routine clinical practice.
Alejandro Iglesias, Kwame Anyane-Yeboa, Julia Wynn, Ashley Wilson, Megan Truitt Cho, Edwin Guzman, Rebecca Sisson, Claire Egan, Wendy K Chung. Genet Med 2014
Alejandro Iglesias, Kwame Anyane-Yeboa, Julia Wynn, Ashley Wilson, Megan Truitt Cho, Edwin Guzman, Rebecca Sisson, Claire Egan, Wendy K Chung. Genet Med 2014
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ACMG Standards and Guidelines for constitutional cytogenomic microarray analysis, including postnatal and prenatal applications: revision 2013.
Sarah T South, Charles Lee, Allen N Lamb, Anne W Higgins, Hutton M Kearney. Genet Med 2013
Sarah T South, Charles Lee, Allen N Lamb, Anne W Higgins, Hutton M Kearney. Genet Med 2013
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Practice parameter for the assessment and treatment of children and adolescents with autism spectrum disorder.
Fred Volkmar, Matthew Siegel, Marc Woodbury-Smith, Bryan King, James McCracken, Matthew State. J Am Acad Child Adolesc Psychiatry 2014
Fred Volkmar, Matthew Siegel, Marc Woodbury-Smith, Bryan King, James McCracken, Matthew State. J Am Acad Child Adolesc Psychiatry 2014
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The Database of Genomic Variants: a curated collection of structural variation in the human genome.
Jeffrey R MacDonald, Robert Ziman, Ryan K C Yuen, Lars Feuk, Stephen W Scherer. Nucleic Acids Res 2014
Jeffrey R MacDonald, Robert Ziman, Ryan K C Yuen, Lars Feuk, Stephen W Scherer. Nucleic Acids Res 2014
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How physicians use array comparative genomic hybridization results to guide patient management in children with developmental delay.
Jennifer Saam, Jim Gudgeon, Emily Aston, Arthur R Brothman. Genet Med 2008
Jennifer Saam, Jim Gudgeon, Emily Aston, Arthur R Brothman. Genet Med 2008
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Clinical exome sequencing for genetic identification of rare Mendelian disorders.
Hane Lee, Joshua L Deignan, Naghmeh Dorrani, Samuel P Strom, Sibel Kantarci, Fabiola Quintero-Rivera, Kingshuk Das, Traci Toy, Bret Harry, Michael Yourshaw,[...]. JAMA 2014
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An evidence-based approach to establish the functional and clinical significance of copy number variants in intellectual and developmental disabilities.
Erin B Kaminsky, Vineith Kaul, Justin Paschall, Deanna M Church, Brian Bunke, Dawn Kunig, Daniel Moreno-De-Luca, Andres Moreno-De-Luca, Jennifer G Mulle, Stephen T Warren,[...]. Genet Med 2011
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6
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.