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  1. Article ; Online: An Unusual Cause of Diarrhea in Young Adulthood.

    Bejjani, Joseph / Allain, Dawn C / Hart, Phil A

    Gastroenterology

    2022  Volume 164, Issue 6, Page(s) e1–e2

    MeSH term(s) Humans ; Young Adult ; Adult ; Pancreas, Exocrine ; Lipase ; Diarrhea/etiology ; Exocrine Pancreatic Insufficiency
    Chemical Substances Lipase (EC 3.1.1.3)
    Language English
    Publishing date 2022-10-19
    Publishing country United States
    Document type Journal Article
    ZDB-ID 80112-4
    ISSN 1528-0012 ; 0016-5085
    ISSN (online) 1528-0012
    ISSN 0016-5085
    DOI 10.1053/j.gastro.2022.10.013
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  2. Article ; Online: Assessment of Interprofessional Competence of Leadership Education in Neurodevelopmental and Related Disabilities Trainees through a Virtual Standardized Patient Encounter.

    Barnhardt, Elizabeth W / Gonzalez, Alicia / Rabidoux, Paula / Allain, Dawn C

    Maternal and child health journal

    2023  Volume 28, Issue 1, Page(s) 44–51

    Abstract: Introduction: Leadership Education in Neurodevelopmental and Related Disabilities (LEND) programs have an emphasis on developing skills in providing family-centered and interdisciplinary care. Due to Coronavirus pandemic-related restrictions, ... ...

    Abstract Introduction: Leadership Education in Neurodevelopmental and Related Disabilities (LEND) programs have an emphasis on developing skills in providing family-centered and interdisciplinary care. Due to Coronavirus pandemic-related restrictions, opportunities for interdisciplinary education were limited for the 2020-2021 LEND Trainee cohort at The Ohio State University Nisonger Center. Standardized Patient (SP) encounters can be a mechanism for instruction and assessment of interprofessional competence.
    Methods: An SP encounter was developed for the The Ohio State University 2020-2021 LEND Cohort. Prior to the activity, participants (N = 11) were given clinic notes to review from their respective disciplines. During the activity, participants met virtually to develop collaborative recommendations which were then delivered to the SP who portrayed the mother of a young child receiving a new diagnosis of autism spectrum disorder. Following the encounter, 4 LEND faculty observers completed the Modified McMaster-Ottawa Team Rating Scale and participants completed the Interprofessional Collaboration Competency Attainment Scale-Revised (ICCAS-R).
    Results: Eleven LEND trainees completed the ICCAS-R with an overall increase in the mean score from 3.86 to 4.12. Four LEND faculty members completed the Modified McMaster-Ottawa Team Rating Scale, with the Communication domain demonstrating the highest level of competence.
    Discussion: This activity was well-received by both faculty and LEND trainees. Although delivered in virtual format, it could easily be transitioned to an in-person encounter for future LEND trainees. The success of this activity further supports that standardized patient encounters can be a feasible mechanism for instruction and assessment of interprofessional competencies and serve as a training mechanism for LEND programs.
    MeSH term(s) Humans ; Autism Spectrum Disorder/diagnosis ; Faculty ; Interdisciplinary Studies ; Interprofessional Relations ; Leadership ; Professional Competence ; Child, Preschool
    Language English
    Publishing date 2023-11-01
    Publishing country United States
    Document type Journal Article
    ZDB-ID 1339905-6
    ISSN 1573-6628 ; 1092-7875
    ISSN (online) 1573-6628
    ISSN 1092-7875
    DOI 10.1007/s10995-023-03798-y
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  3. Article ; Online: The Accreditation Council for Genetic Counseling's response to COVID-19 impact on genetic counseling programs.

    Allain, Dawn C / Randall Armel, Susan / Carmany, Erin P / Creswick, Heather / McBrien, Sarah B / Reed, E Kate / Williams, Janet L

    Journal of genetic counseling

    2021  Volume 30, Issue 4, Page(s) 1046–1056

    Language English
    Publishing date 2021-07-05
    Publishing country United States
    Document type Journal Article
    ZDB-ID 1117799-8
    ISSN 1573-3599 ; 1059-7700
    ISSN (online) 1573-3599
    ISSN 1059-7700
    DOI 10.1002/jgc4.1456
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  4. Article ; Online: A qualitative assessment of parental experiences with false-positive newborn screening for Krabbe disease.

    Peterson, Laiken / Siemon, Amy / Olewiler, Leah / McBride, Kim L / Allain, Dawn C

    Journal of genetic counseling

    2021  Volume 31, Issue 1, Page(s) 252–260

    Abstract: Numerous US states have implemented newborn screening for Krabbe disease (Krabbe NBS) as a result of legislative state mandates. While healthcare provider opinions toward Krabbe NBS have been documented, few studies have explored parental experiences and ...

    Abstract Numerous US states have implemented newborn screening for Krabbe disease (Krabbe NBS) as a result of legislative state mandates. While healthcare provider opinions toward Krabbe NBS have been documented, few studies have explored parental experiences and opinions regarding Krabbe NBS. Eleven families, who received a false-positive Krabbe NBS result and received genetic counseling at an institution in central Ohio, were consented to participate in semistructured interviews. Interviews explored parents' experiences throughout the NBS process and ascertained their opinions regarding Krabbe NBS. Three major themes emerged from thematic analysis: (1) improved understanding of the NBS process from a parent perspective, (2) the role of healthcare provider communication, and (3) the value of Krabbe NBS. Parents saw value in Krabbe NBS, despite many disclosing emotional distress and uncertainty throughout the NBS process. Parent experiences throughout the NBS process varied widely. Due to the expressed emotional distress, further research assessing effective communication during the NBS process is warranted. The researchers suggest additional NBS education for non-genetics healthcare providers (i.e., nurses or primary care physicians) and further participation of genetic counselors in the NBS process may benefit families with a positive Krabbe NBS result.
    MeSH term(s) Genetic Counseling ; Health Personnel/psychology ; Humans ; Infant, Newborn ; Leukodystrophy, Globoid Cell/diagnosis ; Neonatal Screening/psychology ; Parents/psychology
    Language English
    Publishing date 2021-07-15
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 1117799-8
    ISSN 1573-3599 ; 1059-7700
    ISSN (online) 1573-3599
    ISSN 1059-7700
    DOI 10.1002/jgc4.1480
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  5. Article: Presidential address 2003: NSGC living life forward.

    Allain, Dawn C

    Journal of genetic counseling

    2009  Volume 13, Issue 1, Page(s) 1–7

    MeSH term(s) Genetic Counseling/organization & administration ; Genetic Counseling/standards ; Genetic Counseling/trends ; Goals ; Humans ; Licensure ; Societies, Scientific/organization & administration ; Societies, Scientific/trends ; United States
    Language English
    Publishing date 2009-08-04
    Publishing country United States
    Document type Address
    ZDB-ID 1117799-8
    ISSN 1059-7700
    ISSN 1059-7700
    DOI 10.1023/b:jogc.0000013378.49516.4b
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  6. Article: KMT2D

    Dauch, Cara / Shim, Sharon / Cole, Matthew Wyatt / Pollock, Nijole C / Beer, Abigail J / Ramroop, Johnny / Klee, Victoria / Allain, Dawn C / Shakya, Reena / Knoblaugh, Sue E / Kulewsky, Jesse / Toland, Amanda Ewart

    American journal of cancer research

    2022  Volume 12, Issue 3, Page(s) 1309–1322

    Abstract: Cutaneous squamous cell carcinoma (cSCC) is the second most lethal skin cancer. Due to ultraviolet light-induced damage, cSCCs have a high mutation rate, but some genes are more frequently mutated in aggressive cSCCs. Lysine-specific histone ... ...

    Abstract Cutaneous squamous cell carcinoma (cSCC) is the second most lethal skin cancer. Due to ultraviolet light-induced damage, cSCCs have a high mutation rate, but some genes are more frequently mutated in aggressive cSCCs. Lysine-specific histone methyltransferase 2D (
    Language English
    Publishing date 2022-03-15
    Publishing country United States
    Document type Journal Article
    ZDB-ID 2589522-9
    ISSN 2156-6976
    ISSN 2156-6976
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  7. Article ; Online: Accreditation Council for Genetic Counseling Board of Directors Response to Myers et al 'A report of the AGCPD task force to evaluate associations between select admissions requirements, demographics, and performance on ABGC certification examination'.

    McGinniss, Molly A / Armel, Susan Randall / Mann, Sylvia / Carmany, Erin P / Creswick, Heather / McBrien, Sarah B / Reed, E Kate / Eichmeyer, Jennifer N / Allain, Dawn C

    Journal of genetic counseling

    2022  Volume 31, Issue 2, Page(s) 316–318

    MeSH term(s) Accreditation ; Certification ; Demography ; Education, Medical, Graduate ; Genetic Counseling ; Humans ; United States
    Language English
    Publishing date 2022-02-12
    Publishing country United States
    Document type Journal Article ; Comment
    ZDB-ID 1117799-8
    ISSN 1573-3599 ; 1059-7700
    ISSN (online) 1573-3599
    ISSN 1059-7700
    DOI 10.1002/jgc4.1563
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  8. Article ; Online: Age of onset and behavioral manifestations in Huntington's disease: An Enroll-HD cohort analysis.

    Ranganathan, Megha / Kostyk, Sandra K / Allain, Dawn C / Race, Jonathan A / Daley, Allison M

    Clinical genetics

    2020  Volume 99, Issue 1, Page(s) 133–142

    Abstract: Huntington's disease is associated with motor, cognitive and behavioral dysfunction. Behavioral symptoms may present before, after, or simultaneously with clinical disease manifestation. The relationship between age of onset and behavioral symptom ... ...

    Abstract Huntington's disease is associated with motor, cognitive and behavioral dysfunction. Behavioral symptoms may present before, after, or simultaneously with clinical disease manifestation. The relationship between age of onset and behavioral symptom presentation and severity was explored using the Enroll-HD database. Manifest individuals (n = 4469) were initially divided into three groups for preliminary analysis: early onset (<30 years; n = 479); mid-adult onset (30-59 years; n = 3478); and late onset (>59 years; n = 512). Incidence of behavioral symptoms reported at onset was highest in those with early onset symptoms at 26% (n = 126), compared with 19% (n = 678) for mid-adult onset and 11% (n = 56) for late onset (P < 0.0001). Refined analysis, looking across the continuum of ages rather than between categorical subgroups found that a one-year increase in age of onset was associated with a 5.6% decrease in the odds of behavioral symptoms being retrospectively reported as the presenting symptom (P < 0.0001). By the time of study enrollment, the odds of reporting severe behavioral symptoms decreased by 5.5% for each one-year increase in reported age of onset. Exploring environmental, genetic and epigenetic factors that affect age of onset and further characterizing types and severity of behavioral symptoms may improve treatment and understanding of Huntington's disease's impact on affected individuals.
    MeSH term(s) Adult ; Age of Onset ; Aged ; Behavioral Symptoms/epidemiology ; Behavioral Symptoms/genetics ; Behavioral Symptoms/physiopathology ; Cognitive Dysfunction/epidemiology ; Cognitive Dysfunction/genetics ; Cognitive Dysfunction/physiopathology ; Cohort Studies ; Disease Progression ; Epigenomics ; Female ; Humans ; Huntington Disease/epidemiology ; Huntington Disease/genetics ; Huntington Disease/physiopathology ; Male ; Middle Aged ; Retrospective Studies ; Severity of Illness Index
    Language English
    Publishing date 2020-10-16
    Publishing country Denmark
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 221209-2
    ISSN 1399-0004 ; 0009-9163
    ISSN (online) 1399-0004
    ISSN 0009-9163
    DOI 10.1111/cge.13857
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  9. Article: Genetic counseling and testing for common hereditary breast cancer syndromes: a paper from the 2007 William Beaumont hospital symposium on molecular pathology.

    Allain, Dawn C

    The Journal of molecular diagnostics : JMD

    2008  Volume 10, Issue 5, Page(s) 383–395

    Abstract: Throughout the past 15 years, the identification of several genes associated with hereditary breast cancer has fueled the growth of clinical genetic counseling and testing services. In addition, increased knowledge of the genetic and molecular pathways ... ...

    Abstract Throughout the past 15 years, the identification of several genes associated with hereditary breast cancer has fueled the growth of clinical genetic counseling and testing services. In addition, increased knowledge of the genetic and molecular pathways of the known hereditary breast cancer genes, as well as an increased understanding of the impact of testing on individuals has added to the ability to identify, manage, and provide psychosocial support for mutation carriers. This review provides an overview of the clinical features, cancer risks, causative genes, and management for hereditary breast and ovarian cancer syndrome, Cowden syndrome, and Li-Fraumeni syndrome. This article summarizes the genetic counseling process and genetic test result interpretation, including a review of the key elements involved in the provision of risk assessment and informed consent, as well as a review of the risks, benefits, and limitations of cancer susceptibility genetic testing.
    MeSH term(s) Breast Neoplasms/diagnosis ; Breast Neoplasms/genetics ; Female ; Genetic Counseling ; Genetic Testing ; Hamartoma Syndrome, Multiple/diagnosis ; Hamartoma Syndrome, Multiple/genetics ; Humans ; Li-Fraumeni Syndrome/diagnosis ; Li-Fraumeni Syndrome/genetics ; Ovarian Neoplasms/diagnosis ; Ovarian Neoplasms/genetics ; Syndrome
    Language English
    Publishing date 2008-08-07
    Publishing country United States
    Document type Journal Article ; Review
    ZDB-ID 2000060-1
    ISSN 1943-7811 ; 1525-1578
    ISSN (online) 1943-7811
    ISSN 1525-1578
    DOI 10.2353/jmoldx.2008.070161
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  10. Article ; Online: Models of service delivery for cancer genetic risk assessment and counseling.

    Trepanier, Angela M / Allain, Dawn C

    Journal of genetic counseling

    2013  Volume 23, Issue 2, Page(s) 239–253

    Abstract: Increasing awareness of and the potentially concomitant increasing demand for cancer genetic services is driving the need to explore more efficient models of service delivery. The aims of this study were to determine which service delivery models are ... ...

    Abstract Increasing awareness of and the potentially concomitant increasing demand for cancer genetic services is driving the need to explore more efficient models of service delivery. The aims of this study were to determine which service delivery models are most commonly used by genetic counselors, assess how often they are used, compare the efficiency of each model as well as impact on access to services, and investigate the perceived benefits and barriers of each. Full members of the NSGC Familial Cancer Special Interest Group who subscribe to its listserv were invited to participate in a web-based survey. Eligible respondents were asked which of ten defined service delivery models they use and specific questions related to aspects of model use. One-hundred ninety-two of the approximately 450 members of the listserv responded (42.7%); 177 (92.2%) had provided clinical service in the last year and were eligible to complete all sections of the survey. The four direct care models most commonly used were the (traditional) face-to-face pre- and post-test model (92.2%), the face-to-face pretest without face-to-face post-test model (86.5%), the post-test counseling only for complex results model (36.2%), and the post test counseling for all results model (18.3%). Those using the face-to-face pretest only, post-test all, and post-test complex models reported seeing more new patients than when they used the traditional model and these differences were statistically significantly. There were no significant differences in appointment wait times or distances traveled by patients when comparing use of the traditional model to the other three models. Respondents recognize that a benefit of using alternative service delivery models is increased access to services; however, some are concerned that this may affect quality of care.
    MeSH term(s) Adult ; Counseling ; Female ; Genetic Predisposition to Disease ; Humans ; Male ; Middle Aged ; Neoplasms/epidemiology ; Neoplasms/genetics ; Risk Assessment ; Young Adult
    Language English
    Publishing date 2013-10-26
    Publishing country United States
    Document type Journal Article
    ZDB-ID 1117799-8
    ISSN 1573-3599 ; 1059-7700
    ISSN (online) 1573-3599
    ISSN 1059-7700
    DOI 10.1007/s10897-013-9655-6
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