Marian Reiff, Ellen Giarelli, Barbara A Bernhardt, Ebony Easley, Nancy B Spinner, Pamela L Sankar, Surabhi Mulchandani. J Autism Dev Disord 2015
Times Cited: 49
Times Cited: 49
Times Cited
Times Co-cited
Similarity
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
46
Clinical genetics evaluation in identifying the etiology of autism spectrum disorders: 2013 guideline revisions.
G Bradley Schaefer, Nancy J Mendelsohn. Genet Med 2013
G Bradley Schaefer, Nancy J Mendelsohn. Genet Med 2013
40
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
30
Molecular Diagnostic Yield of Chromosomal Microarray Analysis and Whole-Exome Sequencing in Children With Autism Spectrum Disorder.
Kristiina Tammimies, Christian R Marshall, Susan Walker, Gaganjot Kaur, Bhooma Thiruvahindrapuram, Anath C Lionel, Ryan K C Yuen, Mohammed Uddin, Wendy Roberts, Rosanna Weksberg,[...]. JAMA 2015
Kristiina Tammimies, Christian R Marshall, Susan Walker, Gaganjot Kaur, Bhooma Thiruvahindrapuram, Anath C Lionel, Ryan K C Yuen, Mohammed Uddin, Wendy Roberts, Rosanna Weksberg,[...]. JAMA 2015
28
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
29
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
Vivien Narcisa, Marie Discenza, Erica Vaccari, Beth Rosen-Sheidley, Antonio Y Hardan, Elizabeth Couchon. Clin Pediatr (Phila) 2013
46
Comprehensive evaluation of the child with intellectual disability or global developmental delays.
John B Moeschler, Michael Shevell. Pediatrics 2014
John B Moeschler, Michael Shevell. Pediatrics 2014
24
Parents' Experience with Pediatric Microarray: Transferrable Lessons in the Era of Genomic Counseling.
R Z Hayeems, R Babul-Hirji, N Hoang, R Weksberg, C Shuman. J Genet Couns 2016
R Z Hayeems, R Babul-Hirji, N Hoang, R Weksberg, C Shuman. J Genet Couns 2016
46
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
20
The impact of chromosomal microarray on clinical management: a retrospective analysis.
Lindsay B Henderson, Carolyn D Applegate, Elizabeth Wohler, Molly B Sheridan, Julie Hoover-Fong, Denise A S Batista. Genet Med 2014
Lindsay B Henderson, Carolyn D Applegate, Elizabeth Wohler, Molly B Sheridan, Julie Hoover-Fong, Denise A S Batista. Genet Med 2014
20
In search of biomarkers for autism: scientific, social and ethical challenges.
Pat Walsh, Mayada Elsabbagh, Patrick Bolton, Ilina Singh. Nat Rev Neurosci 2011
Pat Walsh, Mayada Elsabbagh, Patrick Bolton, Ilina Singh. Nat Rev Neurosci 2011
20
Genetic testing and corresponding services among individuals with autism spectrum disorder (ASD).
Michael L Cuccaro, Kayla Czape, Michael Alessandri, Joycelyn Lee, Abigail Rupchock Deppen, Elise Bendik, Nicole Dueker, Laura Nations, Margaret Pericak-Vance, Susan Hahn. Am J Med Genet A 2014
Michael L Cuccaro, Kayla Czape, Michael Alessandri, Joycelyn Lee, Abigail Rupchock Deppen, Elise Bendik, Nicole Dueker, Laura Nations, Margaret Pericak-Vance, Susan Hahn. Am J Med Genet A 2014
47
"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
18
Recurrence risk for autism spectrum disorders: a Baby Siblings Research Consortium study.
Sally Ozonoff, Gregory S Young, Alice Carter, Daniel Messinger, Nurit Yirmiya, Lonnie Zwaigenbaum, Susan Bryson, Leslie J Carver, John N Constantino, Karen Dobkins,[...]. Pediatrics 2011
Sally Ozonoff, Gregory S Young, Alice Carter, Daniel Messinger, Nurit Yirmiya, Lonnie Zwaigenbaum, Susan Bryson, Leslie J Carver, John N Constantino, Karen Dobkins,[...]. Pediatrics 2011
18
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
18
Meta-analysis and multidisciplinary consensus statement: exome sequencing is a first-tier clinical diagnostic test for individuals with neurodevelopmental disorders.
Siddharth Srivastava, Jamie A Love-Nichols, Kira A Dies, David H Ledbetter, Christa L Martin, Wendy K Chung, Helen V Firth, Thomas Frazier, Robin L Hansen, Lisa Prock,[...]. Genet Med 2019
Siddharth Srivastava, Jamie A Love-Nichols, Kira A Dies, David H Ledbetter, Christa L Martin, Wendy K Chung, Helen V Firth, Thomas Frazier, Robin L Hansen, Lisa Prock,[...]. Genet Med 2019
18
Chromosomal microarray testing influences medical management.
Michael E Coulter, David T Miller, David J Harris, Pamela Hawley, Jonathan Picker, Amy E Roberts, Magdi M Sobeih, Mira Irons. Genet Med 2011
Michael E Coulter, David T Miller, David J Harris, Pamela Hawley, Jonathan Picker, Amy E Roberts, Magdi M Sobeih, Mira Irons. Genet Med 2011
16
Evidence report: Genetic and metabolic testing on children with global developmental delay: report of the Quality Standards Subcommittee of the American Academy of Neurology and the Practice Committee of the Child Neurology Society.
D J Michelson, M I Shevell, E H Sherr, J B Moeschler, A L Gropman, S Ashwal. Neurology 2011
D J Michelson, M I Shevell, E H Sherr, J B Moeschler, A L Gropman, S Ashwal. Neurology 2011
16
Autism genetic testing information needs among parents of affected children: A qualitative study.
Ming Li, Ann Amuta, Lei Xu, Shweta U Dhar, Divya Talwar, Eunju Jung, Lei-Shih Chen. Patient Educ Couns 2016
Ming Li, Ann Amuta, Lei Xu, Shweta U Dhar, Divya Talwar, Eunju Jung, Lei-Shih Chen. Patient Educ Couns 2016
57
Advancing the understanding of autism disease mechanisms through genetics.
Luis de la Torre-Ubieta, Hyejung Won, Jason L Stein, Daniel H Geschwind. Nat Med 2016
Luis de la Torre-Ubieta, Hyejung Won, Jason L Stein, Daniel H Geschwind. Nat Med 2016
16
Mothers' appreciation of chromosomal microarray analysis for autism spectrum disorder.
Ellen Giarelli, Marian Reiff. J Spec Pediatr Nurs 2015
Ellen Giarelli, Marian Reiff. J Spec Pediatr Nurs 2015
80
Utilization of genetic testing among children with developmental disabilities in the United States.
Bridget Kiely, Sujit Vettam, Andrew Adesman. Appl Clin Genet 2016
Bridget Kiely, Sujit Vettam, Andrew Adesman. Appl Clin Genet 2016
44
Underutilization of genetics services for autism: the importance of parental awareness and provider recommendation.
Kimberly Vande Wydeven, Andrea Kwan, Antonio Y Hardan, Jonathan A Bernstein. J Genet Couns 2012
Kimberly Vande Wydeven, Andrea Kwan, Antonio Y Hardan, Jonathan A Bernstein. J Genet Couns 2012
26
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
29
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
14
Whole-genome sequencing of quartet families with autism spectrum disorder.
Ryan K C Yuen, Bhooma Thiruvahindrapuram, Daniele Merico, Susan Walker, Kristiina Tammimies, Ny Hoang, Christina Chrysler, Thomas Nalpathamkalam, Giovanna Pellecchia, Yi Liu,[...]. Nat Med 2015
Ryan K C Yuen, Bhooma Thiruvahindrapuram, Daniele Merico, Susan Walker, Kristiina Tammimies, Ny Hoang, Christina Chrysler, Thomas Nalpathamkalam, Giovanna Pellecchia, Yi Liu,[...]. Nat Med 2015
14
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
14
Confirmation of chromosomal microarray as a first-tier clinical diagnostic test for individuals with developmental delay, intellectual disability, autism spectrum disorders and dysmorphic features.
Agatino Battaglia, Viola Doccini, Laura Bernardini, Antonio Novelli, Sara Loddo, Anna Capalbo, Tiziana Filippi, John C Carey. Eur J Paediatr Neurol 2013
Agatino Battaglia, Viola Doccini, Laura Bernardini, Antonio Novelli, Sara Loddo, Anna Capalbo, Tiziana Filippi, John C Carey. Eur J Paediatr Neurol 2013
14
Parents' perceptions of autism spectrum disorder etiology and recurrence risk and effects of their perceptions on family planning: Recommendations for genetic counselors.
Christina G Selkirk, Patricia McCarthy Veach, Fengqin Lian, Lisa Schimmenti, Bonnie S LeRoy. J Genet Couns 2009
Christina G Selkirk, Patricia McCarthy Veach, Fengqin Lian, Lisa Schimmenti, Bonnie S LeRoy. J Genet Couns 2009
14
Identification and evaluation of children with autism spectrum disorders.
Chris Plauché Johnson, Scott M Myers. Pediatrics 2007
Chris Plauché Johnson, Scott M Myers. Pediatrics 2007
14
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
17
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
12
Autistic phenotypes and genetic testing: state-of-the-art for the clinical geneticist.
C Lintas, A M Persico. J Med Genet 2009
C Lintas, A M Persico. J Med Genet 2009
12
Diagnostic yield of chromosomal microarray analysis in an autism primary care practice: which guidelines to implement?
Susan G McGrew, Brittany R Peters, Julie A Crittendon, Jeremy Veenstra-Vanderweele. J Autism Dev Disord 2012
Susan G McGrew, Brittany R Peters, Julie A Crittendon, Jeremy Veenstra-Vanderweele. J Autism Dev Disord 2012
15
Detection of clinically relevant genetic variants in autism spectrum disorder by whole-genome sequencing.
Yong-hui Jiang, Ryan K C Yuen, Xin Jin, Mingbang Wang, Nong Chen, Xueli Wu, Jia Ju, Junpu Mei, Yujian Shi, Mingze He,[...]. Am J Hum Genet 2013
Yong-hui Jiang, Ryan K C Yuen, Xin Jin, Mingbang Wang, Nong Chen, Xueli Wu, Jia Ju, Junpu Mei, Yujian Shi, Mingze He,[...]. Am J Hum Genet 2013
12
Parental attitudes, beliefs, and perceptions about genetic testing for FAP and colorectal cancer surveillance in minors.
Fallon R Levine, James E Coxworth, David A Stevenson, Thérèse Tuohy, Randall W Burt, Anita Y Kinney. J Genet Couns 2010
Fallon R Levine, James E Coxworth, David A Stevenson, Thérèse Tuohy, Randall W Burt, Anita Y Kinney. J Genet Couns 2010
22
Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk Loci.
Stephan J Sanders, Xin He, A Jeremy Willsey, A Gulhan Ercan-Sencicek, Kaitlin E Samocha, A Ercument Cicek, Michael T Murtha, Vanessa H Bal, Somer L Bishop, Shan Dong,[...]. Neuron 2015
Stephan J Sanders, Xin He, A Jeremy Willsey, A Gulhan Ercan-Sencicek, Kaitlin E Samocha, A Ercument Cicek, Michael T Murtha, Vanessa H Bal, Somer L Bishop, Shan Dong,[...]. Neuron 2015
12
Autism spectrum disorder in the genetics clinic: a review.
M T Carter, S W Scherer. Clin Genet 2013
M T Carter, S W Scherer. Clin Genet 2013
12
14
Clinical utility of genetic and genomic services: a position statement of the American College of Medical Genetics and Genomics.
. Genet Med 2015
. Genet Med 2015
10
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
13
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
10
The familial risk of autism.
Sven Sandin, Paul Lichtenstein, Ralf Kuja-Halkola, Henrik Larsson, Christina M Hultman, Abraham Reichenberg. JAMA 2014
Sven Sandin, Paul Lichtenstein, Ralf Kuja-Halkola, Henrik Larsson, Christina M Hultman, Abraham Reichenberg. JAMA 2014
10
Most genetic risk for autism resides with common variation.
Trent Gaugler, Lambertus Klei, Stephan J Sanders, Corneliu A Bodea, Arthur P Goldberg, Ann B Lee, Milind Mahajan, Dina Manaa, Yudi Pawitan, Jennifer Reichert,[...]. Nat Genet 2014
Trent Gaugler, Lambertus Klei, Stephan J Sanders, Corneliu A Bodea, Arthur P Goldberg, Ann B Lee, Milind Mahajan, Dina Manaa, Yudi Pawitan, Jennifer Reichert,[...]. Nat Genet 2014
10
Genetic testing and counseling in the case of an autism diagnosis: A caregivers perspective.
Kristien Hens, Hilde Peeters, Kris Dierickx. Eur J Med Genet 2016
Kristien Hens, Hilde Peeters, Kris Dierickx. Eur J Med Genet 2016
55
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
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
10
Autism genetics: opportunities and challenges for clinical translation.
Jacob A S Vorstman, Jeremy R Parr, Daniel Moreno-De-Luca, Richard J L Anney, John I Nurnberger, Joachim F Hallmayer. Nat Rev Genet 2017
Jacob A S Vorstman, Jeremy R Parr, Daniel Moreno-De-Luca, Richard J L Anney, John I Nurnberger, Joachim F Hallmayer. Nat Rev Genet 2017
10
Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2016 update (ACMG SF v2.0): a policy statement of the American College of Medical Genetics and Genomics.
Sarah S Kalia, Kathy Adelman, Sherri J Bale, Wendy K Chung, Christine Eng, James P Evans, Gail E Herman, Sophia B Hufnagel, Teri E Klein, Bruce R Korf,[...]. Genet Med 2017
Sarah S Kalia, Kathy Adelman, Sherri J Bale, Wendy K Chung, Christine Eng, James P Evans, Gail E Herman, Sophia B Hufnagel, Teri E Klein, Bruce R Korf,[...]. Genet Med 2017
10
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
10
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.