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Multi-Institutional Implementation of Clinical Decision Support for APOL1, NAT2, and YEATS4 Genotyping in Antihypertensive Management.
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- Journal of Personalized Medicine, 2021, v. 11, n. 6, p. 480, doi. 10.3390/jpm11060480
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- Article
Pelizaeus-Merzbacher disease: a point mutation in exon 6 of the proteolipid protein ( PLP) gene.
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- Clinical Genetics, 1995, v. 47, n. 2, p. 99, doi. 10.1111/j.1399-0004.1995.tb03932.x
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- Article
Implementation of a Renal Precision Medicine Program: Clinician Attitudes and Acceptance.
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- Life (2075-1729), 2020, v. 10, n. 4, p. 32, doi. 10.3390/life10040032
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- Article
EVEN‐PLUS syndrome: A case report with novel variants in HSPA9 and evidence of HSPA9 gene dysfunction.
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- American Journal of Medical Genetics. Part A, 2020, v. 182, n. 11, p. 2501, doi. 10.1002/ajmg.a.61808
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- Article
An unusual cause for Coffin–Lowry syndrome: Three brothers with a novel microduplication in RPS6KA3.
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- American Journal of Medical Genetics. Part A, 2019, v. 179, n. 12, p. 2357, doi. 10.1002/ajmg.a.61353
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- Article
Mosaic isochromosome 15q and maternal uniparental isodisomy for chromosome 15 in a patient with morbid obesity and variant PWS-like phenotype.
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- American Journal of Medical Genetics. Part A, 2013, v. 161A, n. 7, p. 1695, doi. 10.1002/ajmg.a.35939
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- Article
Translating pharmacogenetics from research to routine clinical practice – a survey of the IGNITE Network.
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- Translational Medicine Communications, 2020, v. 5, n. 1, p. 1, doi. 10.1186/s41231-020-00057-y
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- Article
Challenges and strategies for implementing genomic services in diverse settings: experiences from the Implementing GeNomics In pracTicE (IGNITE) network.
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- BMC Medical Genomics, 2017, v. 10, p. 1, doi. 10.1186/s12920-017-0273-2
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- Article
Are We Ready for a Blood-Based Test to Detect Colon Cancer?
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- Clinical Chemistry, 2014, v. 60, n. 9, p. 1141, doi. 10.1373/clinchem.2014.227132
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- Article
Development of a Multifaceted Program for Pharmacogenetics Adoption at an Academic Medical Center: Practical Considerations and Lessons Learned.
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- Clinical Pharmacology & Therapeutics, 2024, v. 116, n. 4, p. 914, doi. 10.1002/cpt.3402
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- Article
PharmVar GeneFocus: CYP3A5.
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- Clinical Pharmacology & Therapeutics, 2022, v. 112, n. 6, p. 1159, doi. 10.1002/cpt.2563
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- Article
PharmVar GeneFocus: CYP2C9.
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- Clinical Pharmacology & Therapeutics, 2021, v. 110, n. 3, p. 662, doi. 10.1002/cpt.2333
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- Article
PharmVar GeneFocus: CYP2C19.
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- Clinical Pharmacology & Therapeutics, 2021, v. 109, n. 2, p. 352, doi. 10.1002/cpt.1973
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- Article
PharmVar and the Landscape of Pharmacogenetic Resources.
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- Clinical Pharmacology & Therapeutics, 2020, v. 107, n. 1, p. 43, doi. 10.1002/cpt.1654
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- Article
Multisite Investigation of Strategies for the Implementation of CYP2C19 Genotype‐Guided Antiplatelet Therapy.
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- Clinical Pharmacology & Therapeutics, 2018, v. 104, n. 4, p. 664, doi. 10.1002/cpt.1006
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- Article
FDA's draft guidance on laboratory-developed tests increases clinical and economic risk to adoption of pharmacogenetic testing.
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- Journal of Clinical Pharmacology, 2015, v. 55, n. 7, p. 725, doi. 10.1002/jcph.492
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- Article
Understanding Implications of the Proposed FDA Regulation of Laboratory Developed Tests.
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- Personalized Medicine in Oncology, 2015, v. 4, n. 3, p. 138
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- Article
Implementing a pragmatic clinical trial to tailor opioids for chronic pain on behalf of the IGNITE ADOPT PGx investigators.
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- CTS: Clinical & Translational Science, 2024, v. 17, n. 8, p. 1, doi. 10.1111/cts.70005
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- Article
Tracheal Aspirate as an Alternative Biologic Sample for Pharmacogenomics Testing in Mechanically Ventilated Pediatric Patients.
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- CTS: Clinical & Translational Science, 2021, v. 14, n. 2, p. 497, doi. 10.1111/cts.12847
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- Article
Bioelectronic Sensor Technology for Detection of Cystic Fibrosis and Hereditary Hemochromatosis Mutations.
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- Archives of Pathology & Laboratory Medicine, 2003, v. 127, n. 12, p. 1565, doi. 10.5858/2003-127-1565-bstfdo
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- Article
Cypiripi: exact genotyping of CYP2D6 using high-throughput sequencing data.
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- Bioinformatics, 2015, v. 31, n. 12, p. i27, doi. 10.1093/bioinformatics/btv232
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- Article
Genetics of Pelizaeus-Merzbacher Disease.
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- Developmental Neuroscience, 1993, v. 15, n. 6, p. 383, doi. 10.1159/000111361
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- Article