Clinical Management of Pediatric Genomic Testing

Por Holm, Ingrid A.
Publicado no Curr Genet Med Rep (2014)

Pediatric Issues in Return of Results and Incidental Findings: Weighing Autonomy and Best Interests

Por Holm, Ingrid A.
Publicado no Genet Test Mol Biomarkers (2017)

The Informed Cohort Oversight Board: From Values to Architecture

Por Holm, Ingrid A., Taylor, Patrick L.
Publicado em 2012

From Sequence Data to Returnable Results: Ethical Issues in Variant Calling and Interpretation

Por Holm, Ingrid A., Yu, Timothy W., Joffe, Steven
Publicado no Genet Test Mol Biomarkers (2017)

Data sharing in the Undiagnosed Diseases Network

Por Brownstein, Catherine A., Holm, Ingrid A., Ramoni, Rachel, Goldstein, David B.
Publicado no Hum Mutat (2015)

Genetic Factors Underlying Sudden Infant Death Syndrome

Por Keywan, Christine, Poduri, Annapurna H, Goldstein, Richard D, Holm, Ingrid A
Publicado no Appl Clin Genet (2021)

Expectation versus Reality: The Impact of Utility on Emotional Outcomes after Returning Individualized Genetic Research Results in Pediatric Rare Disease Research, a Qualitative In...

Por Cacioppo, Cara N., Chandler, Ariel E., Towne, Meghan C., Beggs, Alan H., Holm, Ingrid A.
Publicado no PLoS One (2016)

Returning a Genomic Result for an Adult-Onset Condition to the Parents of a Newborn: Insights From the BabySeq Project

Por Holm, Ingrid A., McGuire, Amy, Pereira, Stacey, Rehm, Heidi, Green, Robert C., Beggs, Alan H.
Publicado no Pediatrics (2019)

A CLINICIAN'S GUIDE TO X-LINKED HYPOPHOSPHATEMIA

Por Carpenter, Thomas O., Imel, Erik A., Holm, Ingrid A., Jan de Beur, Suzanne M., Insogna, Karl L.
Publicado em 2011

Inheritance of Febrile Seizures in Sudden Unexplained Death in Toddlers

Por Holm, Ingrid A., Poduri, Annapurna, Crandall, Laura, Haas, Elisabeth, Grafe, Marjorie R., Kinney, Hannah C., Krous, Henry F.
Publicado em 2012

Implementing the Single Institutional Review Board Model: Lessons from the Undiagnosed Diseases Network

Por Splinter, Kimberly, Hull, Sara Chandros, Holm, Ingrid A., McDonough, Tara L., Wise, Anastasia L., Ramoni, Rachel B.
Publicado no Clin Transl Sci (2017)

In the Early Postpartum Period, Parents are Interested in Newborn Genomic Testing

Por Waisbren, Susan E., Bäck, Danielle K., Liu, Christina, Kalia, Sarah S., Ringer, Steven A., Holm, Ingrid A., Green, Robert C.
Publicado no Genet Med (2014)

Parental Perception of Self-Empowerment in Pediatric Pharmacogenetic Testing: The Reactions of Parents to the Communication of Actual and Hypothetical CYP2D6 Test Results

Por Adelsperger, Sarah, Prows, Cynthia A., Myers, Melanie F., Perry, Cassandra L., Chandler, Ariel, Holm, Ingrid A., Lynch, John A.
Publicado no Health Commun (2016)

A de novo BRPF1 variant in a case of Sudden Unexplained Death in Childhood

Por Keywan, Christine, Holm, Ingrid A., Poduri, Annapurna, Brownstein, Catherine A., Alexandrescu, Sanda, Chen, Jennifer, Geffre, Christopher, Goldstein, Richard D.
Publicado no Eur J Med Genet (2020)

Parents’ Preferences for Return of Results in Pediatric Genomic Research

Por Ziniel, Sonja, Savage, Sarah K., Huntington, Noelle, Amatruda, Jonathan, Green, Robert C., Weitzman, Elissa R., Taylor, Patrick, Holm, Ingrid A.
Publicado em 2014

Impact of an electronic template on documentation of obesity in a primary care clinic

Por Thaker, Vidhu V., Lee, Felix, Bottino, Clement J., Perry, Cassandra L., Holm, Ingrid A., Hirschhorn, Joel N., Osganian, Stavroula K.
Publicado no Clin Pediatr (Phila) (2015)

Challenging the Current Recommendations for Carrier Testing in Children

Por VanNoy, Grace E., Genetti, Casie A., McGuire, Amy L., Green, Robert C., Beggs, Alan H., Holm, Ingrid A.
Publicado no Pediatrics (2019)

The role of sodium channels in sudden unexpected death in pediatrics

Por Rochtus, Anne M., Goldstein, Richard D., Holm, Ingrid A., Brownstein, Catherine A., Pérez‐Palma, Eduardo, Haynes, Robin, Lal, Dennis, Poduri, Annapurna H.
Publicado no Mol Genet Genomic Med (2020)

Prior opioid exposure influences parents’ sharing of their children's CYP2D6 research results

Por Myers, Melanie F, Zhang, Xue, McLaughlin, Brooke, Kissell, Diane, Perry, Cassandra L, Veerkamp, Matthew, Zhang, Kejian, Holm, Ingrid A, Prows, Cynthia A
Publicado no Pharmacogenomics (2017)

The Serotonin-Related FEV Gene Variant in the Sudden Infant Death Syndrome is a Common Polymorphism in the African–American Population

Por Broadbelt, Kevin G., Barger, Melissa A., Paterson, David S., Holm, Ingrid A., Haas, Elisabeth A., Krous, Henry F., Kinney, Hannah C., Markianos, Kyriacos, Beggs, Alan H.
Publicado em 2009