Literature DB >> 24036677

Genetic testing and genetic counseling among Medicaid-enrolled children with autism spectrum disorder in 2001 and 2007.

Lindsay Shea1, Craig J Newschaffer, Ming Xie, Scott M Myers, David S Mandell.   

Abstract

The rise in the prevalence of autism spectrum disorder (ASD) has resulted in increased efforts to understand the causes of this complex set of disorders that emerge early in childhood. Although research in this area is underway and yielding useful, but complex information about ASD, guidelines for the use of genetic testing and counseling among children with ASD conflict. The purpose of this study was to determine the frequency of use of genetic testing and counseling before the widespread implementation of clinical chromosomal microarray (CMA) to establish a baseline for the use of both services and to investigate potential disparities in the use of both services among children with ASD. We found that about two-thirds of children with ASD received genetic testing or counseling and the use of both services is increasing with time, even in the pre-CMA era. Being female and having a comorbid intellectual disability diagnosis both increased the likelihood of receiving genetic testing and genetic counseling. Initial discrepancies in the use of both services based on race/ethnicity suggest that troubling disparities observed in other services delivered to children with ASD and other mental health disorders persist in genetic testing and counseling as well. These results should incentivize further investigation of the impact of genetic testing and counseling on children with ASD and their families, and should drive efforts to explore and confront disparities in the delivery of these services, particularly with the advancing scientific research on this topic.

Entities:  

Mesh:

Year:  2013        PMID: 24036677      PMCID: PMC4765906          DOI: 10.1007/s00439-013-1362-8

Source DB:  PubMed          Journal:  Hum Genet        ISSN: 0340-6717            Impact factor:   4.132


  45 in total

Review 1.  The genetics of autism: key issues, recent findings, and clinical implications.

Authors:  Paul El-Fishawy; Matthew W State
Journal:  Psychiatr Clin North Am       Date:  2010-03

2.  Value for money? Array genomic hybridization for diagnostic testing for genetic causes of intellectual disability.

Authors:  Dean A Regier; Jan M Friedman; Carlo A Marra
Journal:  Am J Hum Genet       Date:  2010-04-15       Impact factor: 11.025

3.  What is a meaningful result? Disclosing the results of genomic research in autism to research participants.

Authors:  Fiona Alice Miller; Robin Zoe Hayeems; Jessica Peace Bytautas
Journal:  Eur J Hum Genet       Date:  2010-03-17       Impact factor: 4.246

Review 4.  Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies.

Authors:  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; W Andrew Faucett; Lars Feuk; Jan M Friedman; Ada Hamosh; Laird Jackson; Erin B Kaminsky; Klaas Kok; Ian D Krantz; Robert M Kuhn; Charles Lee; James M Ostell; Carla Rosenberg; Stephen W Scherer; Nancy B Spinner; Dimitri J Stavropoulos; James H Tepperberg; Erik C Thorland; Joris R Vermeesch; Darrel J Waggoner; Michael S Watson; Christa Lese Martin; David H Ledbetter
Journal:  Am J Hum Genet       Date:  2010-05-14       Impact factor: 11.025

5.  A recurrent 16p12.1 microdeletion supports a two-hit model for severe developmental delay.

Authors:  Santhosh Girirajan; Jill A Rosenfeld; Gregory M Cooper; Francesca Antonacci; Priscillia Siswara; Andy Itsara; Laura Vives; Tom Walsh; Shane E McCarthy; Carl Baker; Heather C Mefford; Jeffrey M Kidd; Sharon R Browning; Brian L Browning; Diane E Dickel; Deborah L Levy; Blake C Ballif; Kathryn Platky; Darren M Farber; Gordon C Gowans; Jessica J Wetherbee; Alexander Asamoah; David D Weaver; Paul R Mark; Jennifer Dickerson; Bhuwan P Garg; Sara A Ellingwood; Rosemarie Smith; Valerie C Banks; Wendy Smith; Marie T McDonald; Joe J Hoo; Beatrice N French; Cindy Hudson; John P Johnson; Jillian R Ozmore; John B Moeschler; Urvashi Surti; Luis F Escobar; Dima El-Khechen; Jerome L Gorski; Jennifer Kussmann; Bonnie Salbert; Yves Lacassie; Alisha Biser; Donna M McDonald-McGinn; Elaine H Zackai; Matthew A Deardorff; Tamim H Shaikh; Eric Haan; Kathryn L Friend; Marco Fichera; Corrado Romano; Jozef Gécz; Lynn E DeLisi; Jonathan Sebat; Mary-Claire King; Lisa G Shaffer; Evan E Eichler
Journal:  Nat Genet       Date:  2010-02-14       Impact factor: 38.330

Review 6.  Genetics of autistic disorders: review and clinical implications.

Authors:  Christine M Freitag; Wouter Staal; Sabine M Klauck; Eftichia Duketis; Regina Waltes
Journal:  Eur Child Adolesc Psychiatry       Date:  2009-11-26       Impact factor: 4.785

7.  Brief report: Under-representation of African americans in autism genetic research: a rationale for inclusion of subjects representing diverse family structures.

Authors:  Claudia L Hilton; Robert T Fitzgerald; Kelley M Jackson; Rolanda A Maxim; Christopher C Bosworth; Paul T Shattuck; Daniel H Geschwind; John N Constantino
Journal:  J Autism Dev Disord       Date:  2010-05

Review 8.  Advances in autism genetics: on the threshold of a new neurobiology.

Authors:  Brett S Abrahams; Daniel H Geschwind
Journal:  Nat Rev Genet       Date:  2008-05       Impact factor: 53.242

Review 9.  Autism spectrum disorders: clinical and research frontiers.

Authors:  E B Caronna; J M Milunsky; H Tager-Flusberg
Journal:  Arch Dis Child       Date:  2008-02-27       Impact factor: 3.791

10.  Clinical genetic testing for patients with autism spectrum disorders.

Authors:  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; Laura Weissman; Peter Raffalli; Shafali Jeste; Laurie A Demmer; Heather K Peters; Stephanie J Brewster; Sara J Kowalczyk; Beth Rosen-Sheidley; Caroline McGowan; Andrew W Duda; Sharyn A Lincoln; Kathryn R Lowe; Alison Schonwald; Michael Robbins; Fuki Hisama; Robert Wolff; Ronald Becker; Ramzi Nasir; David K Urion; Jeff M Milunsky; Leonard Rappaport; James F Gusella; Christopher A Walsh; Bai-Lin Wu; David T Miller
Journal:  Pediatrics       Date:  2010-03-15       Impact factor: 7.124

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  11 in total

1.  The effect of Medicaid waivers on ameliorating racial/ethnic disparities among children with autism.

Authors:  Michelle LaClair; David S Mandell; Andrew W Dick; Khaled Iskandarani; Bradley D Stein; Douglas L Leslie
Journal:  Health Serv Res       Date:  2019-05-27       Impact factor: 3.402

Review 2.  Genomic medicine for kidney disease.

Authors:  Emily E Groopman; Hila Milo Rasouly; Ali G Gharavi
Journal:  Nat Rev Nephrol       Date:  2018-01-08       Impact factor: 28.314

3.  Cryptic and complex chromosomal aberrations in early-onset neuropsychiatric disorders.

Authors:  Harrison Brand; Vamsee Pillalamarri; Ryan L Collins; Stacey Eggert; Colm O'Dushlaine; Ellen B Braaten; Matthew R Stone; Kimberly Chambert; Nathan D Doty; Carrie Hanscom; Jill A Rosenfeld; Hillary Ditmars; Jessica Blais; Ryan Mills; Charles Lee; James F Gusella; Steven McCarroll; Jordan W Smoller; Michael E Talkowski; Alysa E Doyle
Journal:  Am J Hum Genet       Date:  2014-10-02       Impact factor: 11.025

Review 4.  Heterogeneity in Autism Spectrum Disorder Case-Finding Algorithms in United States Health Administrative Database Analyses.

Authors:  Scott D Grosse; Phyllis Nichols; Kwame Nyarko; Matthew Maenner; Melissa L Danielson; Lindsay Shea
Journal:  J Autism Dev Disord       Date:  2021-09-28

Review 5.  Autism genetics: opportunities and challenges for clinical translation.

Authors:  Jacob A S Vorstman; Jeremy R Parr; Daniel Moreno-De-Luca; Richard J L Anney; John I Nurnberger; Joachim F Hallmayer
Journal:  Nat Rev Genet       Date:  2017-03-06       Impact factor: 53.242

6.  Experiences with offering pro bono medical genetics services in the West Indies: Benefits to patients, physicians, and the community.

Authors:  Andrew K Sobering; Dong Li; Jennifer S Beighley; John C Carey; Tyhiesia Donald; Sarah H Elsea; Karla P Figueroa; Jennifer Gerdts; Andre Hamlet; Ghayda M Mirzaa; Beverly Nelson; Stefan M Pulst; Janice L Smith; Flora Tassone; Helga V Toriello; Ruth H Walker; Katherine R Yearwood; Elizabeth J Bhoj
Journal:  Am J Med Genet C Semin Med Genet       Date:  2020-12-04       Impact factor: 3.908

7.  Families with complex needs: an inside perspective from young people, their carers, and healthcare providers.

Authors:  Mădălina Radu; Ramona Moldovan; Adriana Băban
Journal:  J Community Genet       Date:  2022-03-18

8.  Provision of Genetic Services for Autism and its Impact on Spanish Families.

Authors:  Marta Codina-Solà; Luis A Pérez-Jurado; Ivon Cuscó; Clara Serra-Juhé
Journal:  J Autism Dev Disord       Date:  2017-10

Review 9.  Tackling healthcare access barriers for individuals with autism from diagnosis to adulthood.

Authors:  Natasha Malik-Soni; Andrew Shaker; Helen Luck; Anne E Mullin; Ryan E Wiley; M E Suzanne Lewis; Joaquin Fuentes; Thomas W Frazier
Journal:  Pediatr Res       Date:  2021-03-25       Impact factor: 3.953

10.  Attitudes and Practices of Australian Nephrologists Toward Implementation of Clinical Genomics.

Authors:  Kushani Jayasinghe; Catherine Quinlan; Andrew J Mallett; Peter G Kerr; Belinda McClaren; Amy Nisselle; Amali Mallawaarachchi; Kevan R Polkinghorne; Chirag Patel; Stephanie Best; Zornitza Stark
Journal:  Kidney Int Rep       Date:  2020-11-10
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