Search Results - Ingrid Holm

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  1. 1

    P415: Multi-dimensional and longitudinal impact of a genetic diagnosis for infants in an intensive care unit by Monica Wojcik, Maya del Rosario, Ingrid Holm

    Published in Genetics in Medicine Open (2023-01-01)
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  2. 2

    P517: An automated approach to report drafting for newborn genomic sequencing in the BabySeq Project by Anna Nagy, Eugene Mysen, Chungming Glendy Sun, Lisa Mahanta, Bethany Zettler, Alan Beggs, Ingrid Holm, Robert Green, Matthew Lebo, Hana Zouk

    Published in Genetics in Medicine Open (2023-01-01)
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  3. 3

    P858: Optimism and pessimism about genome sequencing in pediatric health care: Preliminary findings in the BabySeq Project* by Hadley Smith, Madison Hickingbotham, Bethany Zettler, Tanner Coleman, Kelly East, Stacey Pereira, Amy McGuire, Ingrid Holm, Robert Green, Kurt Christensen

    Published in Genetics in Medicine Open (2024-01-01)
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  4. 4

    P410: The effect of newborn genomic screening on downstream health care utilization and costs: Evidence from the BabySeq Project* by Hadley Smith, Pankaj Agrawal, Dmitry Dukhovny, Casie Genetti, Ingrid Holm, Amy McGuire, Stacey Pereira, Ann Wu, Alan Beggs, Robert Green, Richard Parad, Kurt Christensen

    Published in Genetics in Medicine Open (2023-01-01)
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  5. 5

    P491: Enrollment of a diverse population into a trial of newborn genomic sequencing: Preliminary data from the BabySeq Project by Kurt Christensen, Hadley Smith, Madison Hickingbotham, Bethany Zettler, Stacey Pereira, Bruce Korf, Bruce Gelb, Carol Horowitz, Ramin Homayouni, Amy McGuire, Ingrid Holm, Robert Green

    Published in Genetics in Medicine Open (2024-01-01)
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  6. 6

    P579: Multidimensional utility of genomic autopsy for infant mortality by Monica Wojcik, Casie Genetti, Malika Sud, Jill Madden, Kathleen Garvey, Ikeoluwa Osei-Owusu, Nicole Groussis, Sundos Al-Husayni, Pankaj Agrawal, Richard Goldstein, Heidi Rehm, Anne O'Donnell-Luria, Alan Beggs, Ingrid Holm

    Published in Genetics in Medicine Open (2025-01-01)
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  7. 7

    P408: Perspectives of rare disease experts on sequencing newborns for treatable genetic conditions* by Nidhi Shah, Nina Gold, Sophia Adelson, Shardae Williams, Sarah Bick, Jessica Gold, Alanna Strong, Rebecca Ganetzky, Amy Roberts, Melissa Walker, Alexander Holtz, Vijay Sankaran, Ottavia Delmonte, Weizhen Tan, Ingrid Holm, Jay Thiagarajah, Junne Kamihara, Jason Comander, Emily Place, Janey Wiggs, Robert Green

    Published in Genetics in Medicine Open (2023-01-01)
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