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Strengthening Causal Inference in Exposomics Research: Application of Genetic Data and Methods.

Autor: Avery, Christy L.^1,2 Christy_avery@unc.edu, Howard, Annie Green^2,3, Ballou, Anna F.¹, Buchanan, Victoria L.¹, Collins, Jason M.¹, Downie, Carolina G.¹, Engel, Stephanie M.¹, Graff, Mariaelisa¹, Highland, Heather M.¹, Lee, Moa P.¹, Lilly, Adam G.^2,4, Kun Lu⁵, Rager, Julia E.⁵, Staley, Brooke S.¹, North, Kari E.¹, Gordon-Larsen, Penny^2,6

Publikováno v: Environmental Health Perspectives. May2022, Vol. 130 Issue 5, p055001-1-055001-9. 9p. 2 Diagrams, 1 Chart.

The Burden of COVID-19 on Caregivers of Children with Suspected Genetic Conditions: A Therapeutic Odyssey

Autor: Waltz, Margaret, Canter, Courtney, Bensen, Jeannette T., Berg, Jonathan S., Foreman, Ann Katherine M., Grant, Tracey L., Lich, Kristen Hassmiller, Navas, Angelo, O’Daniel, Julianne M., Powell, Bradford C., Rini, Christine M., Staley, Brooke S., Cadigan, R. Jean

Publikováno v: Physical & Occupational Therapy In Pediatrics. 43:257-271

Children with disabilities and rare or undiagnosed conditions and their families have faced numerous hardships of living during the COVID-19 pandemic. For those with undiagnosed conditions, the diagnostic odyssey can be long, expensive, and marked by

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::14bac9028f2e80e592d015ae73a02d51
https://doi.org/10.1080/01942638.2022.2138734

Evaluating the clinical utility of early exome sequencing in diverse pediatric outpatient populations in the North Carolina Clinical Genomic Evaluation of Next-generation Exome Sequencing (NCGENES) 2 study: a randomized controlled trial.

Autor: Staley, Brooke S.¹ (AUTHOR) bstaley@unc.edu, Milko, Laura V.² (AUTHOR), Waltz, Margaret³ (AUTHOR), Griesemer, Ida^4,5 (AUTHOR), Mollison, Lonna² (AUTHOR), Grant, Tracey L.² (AUTHOR), Farnan, Laura⁶ (AUTHOR), Roche, Myra^2,7 (AUTHOR), Navas, Angelo² (AUTHOR), Lightfoot, Alexandra^4,8 (AUTHOR), Foreman, Ann Katherine M.² (AUTHOR), O'Daniel, Julianne M.² (AUTHOR), O'Neill, Suzanne C.⁹ (AUTHOR), Lin, Feng-Chang¹⁰ (AUTHOR), Roman, Tamara S.² (AUTHOR), Brandt, Alicia² (AUTHOR), Powell, Bradford C.² (AUTHOR), Rini, Christine^11,12 (AUTHOR), Berg, Jonathan S.² (AUTHOR), Bensen, Jeannette T.¹ (AUTHOR)

Publikováno v: Trials. 6/14/2021, Vol. 22 Issue 1, p1-19. 19p. 1 Diagram, 5 Charts.

Additional file 1 of Evaluating the clinical utility of early exome sequencing in diverse pediatric outpatient populations in the North Carolina Clinical Genomic Evaluation of Next-generation Exome Sequencing (NCGENES) 2 study: a randomized controlled trial

Autor: Staley, Brooke S., Milko, Laura V., Waltz, Margaret, Griesemer, Ida, Mollison, Lonna, Grant, Tracey L., Farnan, Laura, Roche, Myra, Navas, Angelo, Lightfoot, Alexandra, Foreman, Ann Katherine M., O’Daniel, Julianne M., O’Neill, Suzanne C., Lin, Feng-Chang, Roman, Tamara S., Brandt, Alicia, Powell, Bradford C., Rini, Christine, Berg, Jonathan S., Bensen, Jeannette T.

Additional file 1: NCGENES 2 Clinical Criteria. Clinical screening criteria to determine pediatric patient NCGENES 2 eligibility. NOTE: Criteria evolve as new conditions and symptoms are identified in eligible patients through referral reason and med

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b5fed61b04c2e082f157682bd8ba2f87