The Experts below are selected from a list of 25497 Experts worldwide ranked by ideXlab platform

Ann M. Manzardo - One of the best experts on this subject based on the ideXlab platform.

  • Article High-Resolution Chromosome Ideogram Representation of Currently Recognized Genes for Autism Spectrum Disorders
    2016
    Co-Authors: Merlin G. Butler, Syed K. Rafi, Ann M. Manzardo
    Abstract:

    Abstract: Recently, autism-related research has focused on the identification of various genes and disturbed pathways causing the genetically heterogeneous group of autism spectrum disorders (ASD). The list of autism-related genes has significantly increased due to better awareness with advances in genetic technology and expanding searchable genomic databases. We compiled a master list of known and clinically relevant autism spectrum disorder genes identified with supporting evidence from peer-reviewed medical literature sources by searching key words related to autism and genetics and from authoritative autism-related public access websites, such as the Simons Foundation Autism Research Institute autism genomic database dedicated to gene discovery and characterization. Our list consists of 792 genes arranged in alphabetical order in tabular form with gene symbols placed on high-resolution human chromosome ideograms, thereby enabling clinical and laboratory geneticists and genetic counsellors to access convenient visual images of the location and distribution of ASD genes. Meaningful correlations of the observed phenotype in patients with suspected/confirmed ASD gene(s) at the chromosome region or breakpoint band site can be made to inform diagnosis and gene-based Personalized Care and provide genetic counselling for families

  • high resolution chromosome ideogram representation of currently recognized genes for autism spectrum disorders
    International Journal of Molecular Sciences, 2015
    Co-Authors: Merlin G. Butler, Syed K. Rafi, Ann M. Manzardo
    Abstract:

    Recently, autism-related research has focused on the identification of various genes and disturbed pathways causing the genetically heterogeneous group of autism spectrum disorders (ASD). The list of autism-related genes has significantly increased due to better awareness with advances in genetic technology and expanding searchable genomic databases. We compiled a master list of known and clinically relevant autism spectrum disorder genes identified with supporting evidence from peer-reviewed medical literature sources by searching key words related to autism and genetics and from authoritative autism-related public access websites, such as the Simons Foundation Autism Research Institute autism genomic database dedicated to gene discovery and characterization. Our list consists of 792 genes arranged in alphabetical order in tabular form with gene symbols placed on high-resolution human chromosome ideograms, thereby enabling clinical and laboratory geneticists and genetic counsellors to access convenient visual images of the location and distribution of ASD genes. Meaningful correlations of the observed phenotype in patients with suspected/confirmed ASD gene(s) at the chromosome region or breakpoint band site can be made to inform diagnosis and gene-based Personalized Care and provide genetic counselling for families.

Mollie A Ruben - One of the best experts on this subject based on the ideXlab platform.

  • integrating Personalized Care planning into primary Care a multiple case study of early adopting patient centered medical homes
    Journal of General Internal Medicine, 2020
    Co-Authors: Rendelle E Bolton, Barbara G Bokhour, Timothy P Hogan, Tana M Luger, Mollie A Ruben
    Abstract:

    Personalized Care planning is a patient-centered, whole-person approach to treatment planning. Personalized Care plans improve patient outcomes and are now mandated for chronic Care management reimbursement. Yet guidance on how to best implement Personalized Care planning in practice is limited. We examined the adoption of Personalized Care planning in patient-centered medical home (PCMH) clinics to identify processes and organizational characteristics that facilitated or hindered use in routine practice. Qualitative multiple-case study design. We conducted site visits at PCMH clinics in four US Veterans Health Administration (VHA) medical centers. Data included 10 general clinic observations, 34 direct observations of patient-provider clinical encounters, 60 key informant interviews, and a document review. Data were analyzed via qualitative content analysis using a priori and emergent coding. Employees and patients participating in clinical encounters in PCMH clinics at four VHA medical centers. Each clinic used a distinct approach to Personalized Care planning: (1) distributed tasks approach; (2) two-tiered approach; (3) health coaching approach; and (4) leveraging a village approach. Each varied in workflow, healthCare team utilization, and degree of integration into clinical Care. Across sites, critical components for implementation included expanding planning beyond initial assessment of patient priorities; framing the initiative for patients; using a team-based approach to Care plan development and updates; using communication mechanisms beyond the electronic health record; and engaging stakeholders in implementation planning. Personalized Care planning is a novel patient-centered practice, but complicated to implement. We found variation in effective implementation and identified critical components to structuring this practice in a manner that engages patients in treatment aligned with personal priorities. Primary Care practices seeking to implement Personalized Care planning must go beyond simply asking patients a series of questions to establish a plan. They must also engage team members in plan development, communication, and dissemination.

Merlin G. Butler - One of the best experts on this subject based on the ideXlab platform.

  • Article High-Resolution Chromosome Ideogram Representation of Currently Recognized Genes for Autism Spectrum Disorders
    2016
    Co-Authors: Merlin G. Butler, Syed K. Rafi, Ann M. Manzardo
    Abstract:

    Abstract: Recently, autism-related research has focused on the identification of various genes and disturbed pathways causing the genetically heterogeneous group of autism spectrum disorders (ASD). The list of autism-related genes has significantly increased due to better awareness with advances in genetic technology and expanding searchable genomic databases. We compiled a master list of known and clinically relevant autism spectrum disorder genes identified with supporting evidence from peer-reviewed medical literature sources by searching key words related to autism and genetics and from authoritative autism-related public access websites, such as the Simons Foundation Autism Research Institute autism genomic database dedicated to gene discovery and characterization. Our list consists of 792 genes arranged in alphabetical order in tabular form with gene symbols placed on high-resolution human chromosome ideograms, thereby enabling clinical and laboratory geneticists and genetic counsellors to access convenient visual images of the location and distribution of ASD genes. Meaningful correlations of the observed phenotype in patients with suspected/confirmed ASD gene(s) at the chromosome region or breakpoint band site can be made to inform diagnosis and gene-based Personalized Care and provide genetic counselling for families

  • high resolution chromosome ideogram representation of currently recognized genes for autism spectrum disorders
    International Journal of Molecular Sciences, 2015
    Co-Authors: Merlin G. Butler, Syed K. Rafi, Ann M. Manzardo
    Abstract:

    Recently, autism-related research has focused on the identification of various genes and disturbed pathways causing the genetically heterogeneous group of autism spectrum disorders (ASD). The list of autism-related genes has significantly increased due to better awareness with advances in genetic technology and expanding searchable genomic databases. We compiled a master list of known and clinically relevant autism spectrum disorder genes identified with supporting evidence from peer-reviewed medical literature sources by searching key words related to autism and genetics and from authoritative autism-related public access websites, such as the Simons Foundation Autism Research Institute autism genomic database dedicated to gene discovery and characterization. Our list consists of 792 genes arranged in alphabetical order in tabular form with gene symbols placed on high-resolution human chromosome ideograms, thereby enabling clinical and laboratory geneticists and genetic counsellors to access convenient visual images of the location and distribution of ASD genes. Meaningful correlations of the observed phenotype in patients with suspected/confirmed ASD gene(s) at the chromosome region or breakpoint band site can be made to inform diagnosis and gene-based Personalized Care and provide genetic counselling for families.

Rendelle E Bolton - One of the best experts on this subject based on the ideXlab platform.

  • integrating Personalized Care planning into primary Care a multiple case study of early adopting patient centered medical homes
    Journal of General Internal Medicine, 2020
    Co-Authors: Rendelle E Bolton, Barbara G Bokhour, Timothy P Hogan, Tana M Luger, Mollie A Ruben
    Abstract:

    Personalized Care planning is a patient-centered, whole-person approach to treatment planning. Personalized Care plans improve patient outcomes and are now mandated for chronic Care management reimbursement. Yet guidance on how to best implement Personalized Care planning in practice is limited. We examined the adoption of Personalized Care planning in patient-centered medical home (PCMH) clinics to identify processes and organizational characteristics that facilitated or hindered use in routine practice. Qualitative multiple-case study design. We conducted site visits at PCMH clinics in four US Veterans Health Administration (VHA) medical centers. Data included 10 general clinic observations, 34 direct observations of patient-provider clinical encounters, 60 key informant interviews, and a document review. Data were analyzed via qualitative content analysis using a priori and emergent coding. Employees and patients participating in clinical encounters in PCMH clinics at four VHA medical centers. Each clinic used a distinct approach to Personalized Care planning: (1) distributed tasks approach; (2) two-tiered approach; (3) health coaching approach; and (4) leveraging a village approach. Each varied in workflow, healthCare team utilization, and degree of integration into clinical Care. Across sites, critical components for implementation included expanding planning beyond initial assessment of patient priorities; framing the initiative for patients; using a team-based approach to Care plan development and updates; using communication mechanisms beyond the electronic health record; and engaging stakeholders in implementation planning. Personalized Care planning is a novel patient-centered practice, but complicated to implement. We found variation in effective implementation and identified critical components to structuring this practice in a manner that engages patients in treatment aligned with personal priorities. Primary Care practices seeking to implement Personalized Care planning must go beyond simply asking patients a series of questions to establish a plan. They must also engage team members in plan development, communication, and dissemination.

Syed K. Rafi - One of the best experts on this subject based on the ideXlab platform.

  • Article High-Resolution Chromosome Ideogram Representation of Currently Recognized Genes for Autism Spectrum Disorders
    2016
    Co-Authors: Merlin G. Butler, Syed K. Rafi, Ann M. Manzardo
    Abstract:

    Abstract: Recently, autism-related research has focused on the identification of various genes and disturbed pathways causing the genetically heterogeneous group of autism spectrum disorders (ASD). The list of autism-related genes has significantly increased due to better awareness with advances in genetic technology and expanding searchable genomic databases. We compiled a master list of known and clinically relevant autism spectrum disorder genes identified with supporting evidence from peer-reviewed medical literature sources by searching key words related to autism and genetics and from authoritative autism-related public access websites, such as the Simons Foundation Autism Research Institute autism genomic database dedicated to gene discovery and characterization. Our list consists of 792 genes arranged in alphabetical order in tabular form with gene symbols placed on high-resolution human chromosome ideograms, thereby enabling clinical and laboratory geneticists and genetic counsellors to access convenient visual images of the location and distribution of ASD genes. Meaningful correlations of the observed phenotype in patients with suspected/confirmed ASD gene(s) at the chromosome region or breakpoint band site can be made to inform diagnosis and gene-based Personalized Care and provide genetic counselling for families

  • high resolution chromosome ideogram representation of currently recognized genes for autism spectrum disorders
    International Journal of Molecular Sciences, 2015
    Co-Authors: Merlin G. Butler, Syed K. Rafi, Ann M. Manzardo
    Abstract:

    Recently, autism-related research has focused on the identification of various genes and disturbed pathways causing the genetically heterogeneous group of autism spectrum disorders (ASD). The list of autism-related genes has significantly increased due to better awareness with advances in genetic technology and expanding searchable genomic databases. We compiled a master list of known and clinically relevant autism spectrum disorder genes identified with supporting evidence from peer-reviewed medical literature sources by searching key words related to autism and genetics and from authoritative autism-related public access websites, such as the Simons Foundation Autism Research Institute autism genomic database dedicated to gene discovery and characterization. Our list consists of 792 genes arranged in alphabetical order in tabular form with gene symbols placed on high-resolution human chromosome ideograms, thereby enabling clinical and laboratory geneticists and genetic counsellors to access convenient visual images of the location and distribution of ASD genes. Meaningful correlations of the observed phenotype in patients with suspected/confirmed ASD gene(s) at the chromosome region or breakpoint band site can be made to inform diagnosis and gene-based Personalized Care and provide genetic counselling for families.