12 results on '"Susan Hiatt"'
Search Results
2. 338 The Alabama Genomic Health Initiative: Integrating Genomic Medicine into Primary Care
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Nita A Limdi, Devin Absher, Irf Asif, Lori Bateman, Greg Barsh, Kevin M. Bowling, Gregory M. Cooper, Brittney H. Davis, Kelly M. East, Candice R. Finnila, Blake Goff, Susan Hiatt, Melissa Kelly, Whitley V. Kelley, Bruce R. Korf, Donald R. Latner, James Lawlor, Thomas May, Matt Might, Irene P. Moss, Mariko Nakano-Okuno, Tiffany Osborne, Stephen Sodeke, Adriana Stout, and Michelle L. Thompson
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Medicine - Abstract
OBJECTIVES/GOALS: Supported by the State of Alabama, the Alabama Genomic Health Initiative (AGHI) is aimed at preventing and treating common conditions with a genetic basis. This joint UAB Medicine-HudsonAlpha Institute for Biotechnology effort provides genomic testing, interpretation, and counseling free of charge to residents in each of Alabama’s 67 counties. METHODS/STUDY POPULATION: Launched in 2017, as a state-wide population cohort, AGHI (1.0) enrolled 6,331 Alabamians and returned individual risk of disease(s) related to the ACMG SF v2.0 medically actionable genes. In 2021, the cohort was expanded to include a primary care cohort. AGHI (2.0) has enrolled 750 primary care patients, returning individual risk of disease(s) related to the ACMG SF v3.1 gene list and pre-emptive pharmacogenetics (PGx) to guide medication therapy. Genotyping is done on the Illumina Global Diversity Array with Sanger sequencing to confirm likely pathogenic / pathogenic variants in medically actionable genes and CYP2D6 copy number variants using Taqman assays, resulting in a CLIA-grade report. Disease risk results are returned by genetic counselors and Pharmacogenetics results are returned by Pharmacists. RESULTS/ANTICIPATED RESULTS: We have engaged a statewide community (>7000 participants), returning 94 disease risk genetic reports and 500 PGx reports. Disease risk reports include increased predisposition to cancers (n=38), cardiac diseases (n=33), metabolic (n=12), other (n=11). 100% of participants harbor an actionable PGx variant, 70% are on medication with PGx guidance, 48% harbor PGx variants and are taking medications affected. In 10% of participants, pharmacists sent an active alert to the provider to consider/ recommend alternative medication. Most commonly impacted medications included antidepressants, NSAIDS, proton-pump inhibitors and tramadol. To enable the EMR integration of genomic information, we have developed an automated transfer of reports into the EMR with Genetics Reports and PGx reports viewable in Cerner. DISCUSSION/SIGNIFICANCE: We share our experience on pre-emptive implementation of genetic risk and pharmacogenetic actionability at a population and clinic level. Both patients and providers are actively engaged, providing feedback to refine the return of results. Real time alerts with guidance at the time of prescription are needed to ensure future actionability and value.
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- 2023
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3. eP370: SouthSeq: Genome sequencing for a diverse population of hospitalized infants
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Donald Latner, Kevin Bowling, Michelle Thompson, Candice Finnila, Susan Hiatt, Michelle Amaral, James Lawlor, Kelly East, Meagan Cochran, Veronica Greve, Whitley V. Kelley, David Gray, Stephanie Felker, Hannah Meddaugh, Ashley Cannon, Amanda Luedecke, Kelly Jackson, Laura Hendon, Hillary Janani, Marla Johnston, Lee Ann Merin, Sarah Deans, Carly Tuura, Heather Williams, Kelly Laborde, Matthew Neu, Jessica Patrick-Esteve, Anna Hurst, Jegen Kandasamy, Waldemar Carlo, Kyle Brothers, Brian Kirmse, Renate Savich, Duane Superneau, Steven Spedale, Sara Knight, Gregory Barsh, Bruce Korf, and Gregory Cooper
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Genetics (clinical) - Published
- 2022
4. eP122: The clinical significance of poisoned splicing variants in early-onset neurodevelopmental disorders
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Stephanie Felker, James Lawlor, Donald Latner, Michelle Thompson, Kevin Bowling, Susan Hiatt, Candice Finnila, and Gregory Cooper
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Genetics (clinical) - Published
- 2022
5. eP144: Long-read genome sequencing secondary processing pipelines provide variant call accuracy that exceeds current clinical standards for short-read genome sequencing
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James Holt, Lori Handley, James Lawlor, Susan Hiatt, Gregory Cooper, Jane Grimwood, and Ghunwa Nakouzi
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Genetics (clinical) - Published
- 2022
6. eP425: Parental impact of genome sequencing during the neonatal period
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Kyle Brothers, Carla Rich, Emily Gimpel, Kelly East, Meagan Cochran, Veronica Greve, Whitley V. Kelley, Kelly Jackson, Laura Hendon, Amanda Luedecke, Hillary Janani, Hannah Meddaugh, Donald Latner, Kevin Bowling, Michelle Thompson, Candice Finnila, Susan Hiatt, Michelle Amaral, James Lawlor, David Gray, Stephanie Felker, Ashley Cannon, Marla Johnston, Lee Ann Merin, Sarah Deans, Carly Tuura, Heather Williams, Kelly Laborde, Matthew Neu, Jessica Patrick-Esteve, Anna Hurst, Jegen Kandasamy, Waldemar Carlo, Brian Kirmse, Renate Savich, Duane Superneau, Steven Spedale, Sara Knight, Gregory Barsh, Bruce Korf, and Gregory Cooper
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Genetics (clinical) - Published
- 2022
7. eP141: Expansion of long-read genome sequencing for the molecular diagnosis of neurodevelopmental disorders and multiple congenital anomalies
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Susan Hiatt, James Lawlor, Lori Handley, Zachary Bonnstetter, Jerry Jenkins, John Lovell, James Holt, Candice Finnila, Michelle Thompson, Donald Latner, Christopher Partridge, Christopher Plott, Lori Beth Boston, Melissa Williams, Kevin Bowling, Jane Grimwood, Jeremy Schmutz, and Gregory Cooper
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Genetics (clinical) - Published
- 2022
8. Correction: Variants in MED12L, encoding a subunit of the Mediator kinase module, are responsible for intellectual disability associated with transcriptional defect
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Mathilde Nizon, Vincent Laugel, Kevin M. Flanigan, Matthew Pastore, Megan A. Waldrop, Jill A. Rosenfeld, Ronit Marom, Rui Xiao, Amanda Gerard, Olivier Pichon, Cédric Le Caignec, Marion Gérard, Klaus Dieterich, Megan Truitt Cho, Kirsty McWalter, Susan Hiatt, Michelle L. Thompson, Stéphane Bézieau, Alexandrea Wadley, Klaas J. Wierenga, Jean-Marc Egly, Bertrand Isidor, Service de génétique médicale - Unité de génétique clinique [Nantes], Université de Nantes (UN)-Centre hospitalier universitaire de Nantes (CHU Nantes), Hôpital de Hautepierre [Strasbourg], Baylor College of Medicine (BCM), Baylor University, Gatonero SA, Centre hospitalier universitaire de Nantes (CHU Nantes), Service de Génétique [CHU Caen], Université de Caen Normandie (UNICAEN), Normandie Université (NU)-Normandie Université (NU)-CHU Caen, Normandie Université (NU)-Tumorothèque de Caen Basse-Normandie (TCBN)-Tumorothèque de Caen Basse-Normandie (TCBN), INSERM U836, équipe 4, Muscles et pathologies, Grenoble Institut des Neurosciences (GIN), Institut National de la Santé et de la Recherche Médicale (INSERM)-CHU Grenoble-Université Joseph Fourier - Grenoble 1 (UJF)-Institut National de la Santé et de la Recherche Médicale (INSERM)-CHU Grenoble-Université Joseph Fourier - Grenoble 1 (UJF), Service de Génétique, Institut de génétique et biologie moléculaire et cellulaire (IGBMC), Université Louis Pasteur - Strasbourg I-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS), unité de recherche de l'institut du thorax UMR1087 UMR6291 (ITX), Université de Nantes - UFR de Médecine et des Techniques Médicales (UFR MEDECINE), Université de Nantes (UN)-Université de Nantes (UN)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS), Nationwide Children's Hospital, Biologie, génétique et thérapies ostéoarticulaires et respiratoires (BIOTARGEN), Normandie Université (NU)-Normandie Université (NU), Pôle Couple-Enfant, Département de Génétique et Procréation, GeneDx [Gaithersburg, MD, USA], HudsonAlpha Genome Sequencing Center, University of Alabama in Huntsville (UAH), University of Oklahoma (OU), Mayo Clinic [Jacksonville], Richard, Nicolas, Unité de recherche de l'institut du thorax (ITX-lab), Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)-Université de Nantes - UFR de Médecine et des Techniques Médicales (UFR MEDECINE), and Université de Nantes (UN)-Université de Nantes (UN)
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MED12L ,corpus callosum ,[SDV.GEN]Life Sciences [q-bio]/Genetics ,[SDV.GEN.GH]Life Sciences [q-bio]/Genetics/Human genetics ,intellectual disability ,transcriptional defect ,[SDV.GEN] Life Sciences [q-bio]/Genetics ,[SDV.GEN.GH] Life Sciences [q-bio]/Genetics/Human genetics ,Article ,mediator complex ,Genetics (clinical) - Abstract
Purpose Mediator is a multiprotein complex that allows the transfer of genetic information from DNA binding proteins to the RNA polymerase II during transcription initiation. MED12L is a subunit of the kinase module, which is one of the four sub-complexes of the mediator complex. Other subunits of the kinase module have been already implicated in intellectual disability, namely MED12, MED13L, MED13 and CDK19. Methods We describe an international cohort of seven affected individuals harboring variants involving MED12L identified by array CGH, exome or genome sequencing. Results All affected individuals presented with intellectual disability and/or developmental delay, including speech impairment. Other features included autism spectrum disorder, aggressive behavior, corpus callosum abnormality and mild facial morphological features. Three individuals had a MED12L deletion or duplication. The other four individuals harbored single nucleotide variants (one nonsense, one frameshift and two splicing variants). Functional analysis confirmed a moderate and significant alteration of RNA synthesis in two individuals. Conclusion Overall data suggest that MED12L haploinsufficiency is responsible for intellectual disability and transcriptional defect. Our findings confirm that the integrity of this kinase module is a critical factor for neurological development.
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- 2019
9. Differences in program implementation between nurses and paraprofessionals providing home visits during pregnancy and infancy: a randomized trial
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Jon Korfmacher, David L. Olds, Susan Hiatt, and Ruth O'Brien
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Adult ,Gerontology ,medicine.medical_specialty ,Colorado ,Patient Dropouts ,Child Health Services ,Nurses ,law.invention ,Randomized controlled trial ,Pregnancy ,law ,Epidemiology ,Humans ,Medicine ,Maternal Health Services ,Least-Squares Analysis ,Poverty ,Socioeconomic status ,Community Health Workers ,business.industry ,Public health ,Health Plan Implementation ,Public Health, Environmental and Occupational Health ,Infant ,Physical health ,Professional-Patient Relations ,medicine.disease ,Home Care Services ,Logistic Models ,Home visits ,Patient Satisfaction ,Models, Organizational ,Family medicine ,Gestation ,Female ,business ,Research Article ,Program Evaluation - Abstract
OBJECTIVES: This study examined differences between nurses and paraprofessionals in implementation of a home visiting program for low-income, first-time parents during pregnancy and the first 2 years of the child's life. METHODS: Mothers were randomly assigned to either a nurse-visited (n = 236) or a paraprofessional-visited (n = 244) condition. Nurse- and paraprofessional-visited families were compared on number and length of visits, topics covered, number of program dropouts, and relationship with home visitor. RESULTS: On average, nurses completed more visits than paraprofessionals (28 vs 23; P < .001) and spent a greater proportion of time on physical health issues during pregnancy (38% vs 27%; P < .001) and on parenting issues during infancy (46% vs 32%; P < .001). Paraprofessionals conducted visits that lasted longer and spent a greater proportion of time on environmental health and safety issues (15% vs 7% pregnancy; 15% vs 8% infancy; P < .001). While home visitors were viewed equally positively by mothers, nurses had fewer dropouts than did paraprofessionals (38% vs 48%; P = .04). More paraprofessional-visited families than nurse-visited families experienced staff turnover. CONCLUSIONS: Nurses and paraprofessionals, even when using the same model, provide home visiting services in different ways.
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- 1999
10. Paraprofessional home visitation: Conceptual and pragmatic considerations
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Susan Hiatt, Diane Baird, and Darlene Sampson
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Medical education ,Social Psychology ,business.industry ,media_common.quotation_subject ,Empathy ,Acculturation ,Schedule (workplace) ,Identification (information) ,Nursing ,Formal education ,Credibility ,Home visitation ,Medicine ,business ,Adaptation (computer science) ,media_common - Abstract
The adaptation for paraprofessional visitors of a home visitation model originally developed for nurses is described. There are several hypothesized benefits of using paraprofessional home visitors, including power as role models and increased empathy with clients. Challenges inherent in employing paraprofessionals include limited formal education and resulting lack of credibility among professional care providers, difficulties in acculturation to the workplace, and learning how to effectively focus their commitment to and identification with the community. These challenges result in the need for unique training and sensitive and consistent supervision. Implementation data from the randomized trial of home visitation in Denver indicate that paraprofessional visitors conducted the program according to the prescribed visitation schedule and covered the material appropriately. Differences that emerged between nurse and paraprofessional visitors regarding content covered are discussed and suggestions are made for future programmatic considerations. © 1997 John Wiley & Sons, Inc.
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- 1997
11. Home visiting by paraprofessionals and by nurses: a randomized, controlled trial
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Rosanna K. Ng, Susan Hiatt, Ruth O'Brien, Lisa M. Pettitt, JoAnn Robinson, Ayelet Talmi, David L. Olds, Karen L. Sheff, Jon Korfmacher, Charles R. Henderson, and Dennis W. Luckey
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Gerontology ,medicine.medical_specialty ,media_common.quotation_subject ,Anger ,law.invention ,chemistry.chemical_compound ,Randomized controlled trial ,law ,House call ,medicine ,Humans ,Maternal Welfare ,media_common ,Maternal-Child Nursing ,Proportional Hazards Models ,Pregnancy ,business.industry ,Public health ,Infant Welfare ,Infant, Newborn ,Infant ,medicine.disease ,House Calls ,Outcome and Process Assessment, Health Care ,chemistry ,Pediatrics, Perinatology and Child Health ,Regression Analysis ,Temperament ,Female ,Cotinine ,business ,Medicaid ,Demography - Abstract
Objective. To examine the effectiveness of home visiting by paraprofessionals and by nurses as separate means of improving maternal and child health when both types of visitors are trained in a program model that has demonstrated effectiveness when delivered by nurses.Methods. A randomized, controlled trial was conducted in public- and private-care settings in Denver, Colorado. One thousand one hundred seventy-eight consecutive pregnant women with no previous live births who were eligible for Medicaid or who had no private health insurance were invited to participate. Seven hundred thirty-five women were randomized to control, paraprofessional, or nurse conditions.Nurses completed an average of 6.5 home visits during pregnancy and 21 visits from birth to the children’s second birthdays. Paraprofessionals completed an average of 6.3 home visits during pregnancy and 16 visits from birth to the children’s second birthdays.The main outcomes consisted of changes in women’s urine cotinine over the course of pregnancy; women’s use of ancillary services during pregnancy; subsequent pregnancies and births, educational achievement, workforce participation, and use of welfare; mother-infant responsive interaction; families’ home environments; infants’ emotional vulnerability in response to fear stimuli and low emotional vitality in response to joy and anger stimuli; and children’s language and mental development, temperament, and behavioral problems.Results. Paraprofessional-visited mother-child pairs in which the mother had low psychological resources interacted with one another more responsively than their control-group counterparts (99.45 vs 97.54 standard score points). There were no other statistically significant paraprofessional effects.In contrast to their control-group counterparts, nurse-visited smokers had greater reductions in cotinine levels from intake to the end of pregnancy (259.0 vs 12.32 ng/mL); by the study child’s second birthday, women visited by nurses had fewer subsequent pregnancies (29% vs 41%) and births (12% vs 19%); they delayed subsequent pregnancies for longer intervals; and during the second year after the birth of their first child, they worked more than women in the control group (6.83 vs 5.65 months).Nurse-visited mother-child pairs interacted with one another more responsively than those in the control group (100.31 vs 98.99 standard score points). At 6 months of age, nurse-visited infants, in contrast to their control-group counterparts, were less likely to exhibit emotional vulnerability in response to fear stimuli (16% vs 25%) and nurse-visited infants born to women with low psychological resources were less likely to exhibit low emotional vitality in response to joy and anger stimuli (24% vs 40% and 13% vs 33%). At 21 months, nurse-visited children born to women with low psychological resources were less likely to exhibit language delays (7% vs 18%); and at 24 months, they exhibited superior mental development (90.18 vs 86.20 Mental Development Index scores) than their control-group counterparts. There were no statistically significant program effects for the nurses on women’s use of ancillary prenatal services, educational achievement, use of welfare, or their children’s temperament or behavior problems.For most outcomes on which either visitor produced significant effects, the paraprofessionals typically had effects that were about half the size of those produced by nurses.Conclusions. When trained in a model program of prenatal and infancy home visiting, paraprofessionals produced small effects that rarely achieved statistical or clinical significance; the absence of statistical significance for some outcomes is probably attributable to limited statistical power to detect small effects. Nurses produced significant effects on a wide range of maternal and child outcomes.
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- 2002
12. Asymmetry of inference in the dishabituation paradigm.
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Jerome, Kagan, primary, Susan, Linn, additional, Robin, Mount, additional, Reznick, Steven J., additional, and Susan, Hiatt, additional
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- 1979
- Full Text
- View/download PDF
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