Výsledky vyhledávání - Prows, Cynthia A

Adolescents’ and Parents’ Genomic Testing Decisions: Associations with Age, Race, and Sex Autor Myers, Melanie F., Martin, Lisa J., Prows, Cynthia A.

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Establishing the Outcome Indicators for the Essential Nursing Competencies and Curricula Guidelines for Genetics and Genomics Autor Calzone, Kathleen A., Jenkins, Jean, Prows, Cynthia A., Masny, Agnes

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Decisional conflict among adolescents and parents making decisions about genomic sequencing results Autor Raghuram Pillai, Preethi, Prows, Cynthia A., Martin, Lisa J., Myers, Melanie F.

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Racial Differences in Escitalopram/Citalopram-Related Weight Gain in Children and Adolescents: A Natural Language Processing-Based Electronic Medical Record Study Autor Ramsey, Laura B., Aldrich, Stacey L., Poweleit, Ethan, Prows, Cynthia A., Martin, Lisa J., Strawn, Jeffrey R.

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Influence of CYP2D6 metabolizer status on ondansetron efficacy in pediatric patients undergoing hematopoietic stem cell transplantation: A case series Autor Edwards, Andrea, Teusink‐Cross, Ashley, Martin, Lisa J., Prows, Cynthia A., Mehta, Parinda A., Ramsey, Laura B.

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Nurses Transforming Health Care Using Genetics and Genomics Autor Calzone, Kathleen A., Cashion, Ann, Feetham, Suzanne, Jenkins, Jean, Prows, Cynthia A., Williams, Janet K., Wung, Shu-Fen

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Adolescent and Parental Attitudes about Return of Genomic Research Results: Focus Group Findings Regarding Decisional Preferences Autor McGowan, Michelle L., Prows, Cynthia A., DeJonckheere, Melissa, Brinkman, William B., Vaughn, Lisa, Myers, Melanie F.

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Influence of CYP2C19 Metabolizer Status on Escitalopram/Citalopram Tolerability and Response in Youth With Anxiety and Depressive Disorders Autor Aldrich, Stacey L., Poweleit, Ethan A., Prows, Cynthia A., Martin, Lisa J., Strawn, Jeffrey R., Ramsey, Laura B.

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Parental Perception of Self-Empowerment in Pediatric Pharmacogenetic Testing: The Reactions of Parents to the Communication of Actual and Hypothetical CYP2D6 Test Results Autor Adelsperger, Sarah, Prows, Cynthia A., Myers, Melanie F., Perry, Cassandra L., Chandler, Ariel, Holm, Ingrid A., Lynch, John A.

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Drug-Metabolizing Enzyme Genotypes and Aggressive Behavior Treatment Response in Hospitalized Pediatric Psychiatric Patients Autor Prows, Cynthia A., Nick, Todd G., Saldaña, Shannon N., Pathak, Sanjeev, Liu, Chunyan, Zhang, Kejian, Daniels, Zachary S., Vinks, Alexander A., Glauser, Tracy A.

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Prior opioid exposure influences parents’ sharing of their children's CYP2D6 research results Autor Myers, Melanie F, Zhang, Xue, McLaughlin, Brooke, Kissell, Diane, Perry, Cassandra L, Veerkamp, Matthew, Zhang, Kejian, Holm, Ingrid A, Prows, Cynthia A

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A mutation in FRIZZLED2 impairs Wnt signaling and causes autosomal dominant omodysplasia Autor Saal, Howard M., Prows, Cynthia A., Guerreiro, Iris, Donlin, Milene, Knudson, Luke, Sund, Kristen L., Chang, Ching-Fang, Brugmann, Samantha A., Stottmann, Rolf W.

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Implementation of Pharmacogenetics at Cincinnati Children’s Hospital Medical Center: Lessons learned over 14 years of personalizing medicine Autor Ramsey, Laura B., Prows, Cynthia A., Zhang, Kejian, Saldaña, Shannon N., Sorter, Michael T., Pestian, John P., Wenstrup, Richard J., Vinks, Alexander A., Glauser, Tracy A.

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Using human sequencing to guide craniofacial research Autor Liegel, Ryan P., Finnerty, Erin, Blizzard, Lauren, DiStasio, Andrew, Hufnagel, Robert B., Saal, Howard M., Sund, Kristen L., Prows, Cynthia A., Stottmann, Rolf W.

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Characteristics of successful recruitment in prospective pediatric pharmacogenetic studies Autor Saldaña, Shannon N., Hooper, David K., Froehlich, Tanya E., Campbell, Kathleen M., Prows, Cynthia A., Sadhasivam, Senthilkumar, Nick, Todd G., Seid, Michael, Vinks, Alexander A., Glauser, Tracy A.

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Clinical Pharmacogenetics Implementation Consortium (CPIC) Guideline for CYP2D6 Genotype and Use of Ondansetron and Tropisetron Autor Bell, Gillian C., Caudle, Kelly E., Whirl-Carrillo, Michelle, Gordon, Ronald J., Hikino, Keiko, Prows, Cynthia A., Gaedigk, Andrea, Agundez, Jose A.G., Sadhasivam, Senthilkumar, Klein, Teri E., Schwab, Matthias

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Copb2 is essential for embryogenesis and hypomorphic mutations cause human microcephaly Autor DiStasio, Andrew, Driver, Ashley, Sund, Kristen, Donlin, Milene, Muraleedharan, Ranjith M, Pooya, Shabnam, Kline-Fath, Beth, Kaufman, Kenneth M, Prows, Cynthia A, Schorry, Elizabeth, Dasgupta, Biplab, Stottmann, Rolf W

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Homozygous missense variant in BMPR1A resulting in BMPR signaling disruption and syndromic features Autor Russell, Bianca E., Rigueur, Diana, Weaver, Kathryn N., Sund, Kristen, Basil, Janet S., Hufnagel, Robert B., Prows, Cynthia A., Oestreich, Alan, Al‐Gazali, Lihadh, Hopkin, Robert J, Saal, Howard M., Lyons, Karen, Dauber, Andrew

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Healthcare provider education to support integration of pharmacogenomics in practice: the eMERGE Network experience Autor Rohrer Vitek, Carolyn R, Abul-Husn, Noura S, Connolly, John J, Hartzler, Andrea L, Kitchner, Terrie, Peterson, Josh F, Rasmussen, Luke V, Smith, Maureen E, Stallings, Sarah, Williams, Marc S, Wolf, Wendy A, Prows, Cynthia A

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Return of results in the genomic medicine projects of the eMERGE network Autor Kullo, Iftikhar J., Haddad, Ra'ad, Prows, Cynthia A., Holm, Ingrid, Sanderson, Saskia C., Garrison, Nanibaa' A., Sharp, Richard R., Smith, Maureen E., Kuivaniemi, Helena, Bottinger, Erwin P., Connolly, John J., Keating, Brendan J., McCarty, Catherine A., Williams, Marc S., Jarvik, Gail P.

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