Items on this page may include news associated with the IGNITE network as well as other organizations in the field of human genetics and genomics.

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ADOPT PGx News ()
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December 13, 2022News,

PGx ECHO Program

The University of Minnesota College of Pharmacy invites all actively practicing clinicians to join their Pharmacogenomics (PGx) ECHO project. PGx ECHO aims to improve health professionals’ confidence in using PGx […]...

November 10, 2021Education, News

NHGRI Fact Sheets about Genomics

The National Human Genome Research Institute (NHGRI) has produced this series of fact sheets to explain complex concepts in genomics research to a non-scientific audience. Teachers, students and the general […]...

March 21, 2019News

Evaluating Genomic Medicine Interventions

The IGNITE I Network funded six genomic medicine projects. Through varied interventions, Lori Orlando, M.D., and team hypothesized that synergies across projects could be leveraged to better understand participants’ experiences […]...

General

  • CYP2D6 phenotype and post-surgical pain control with hydrocodone and oxycodone May 11, 2026
    Christelle Lteif; Larisa H. Cavallari DOI: 10.3389/fphar.2026.1817652 Article on Jama Network
  • ADOPT PGx Depression Manuscript Published May 6, 2026
    A new manuscript from the IGNITE Pragmatic Trials Network has been published in JAMA Network Open, describing results from the ADOPT PGx Depression trial. The randomized clinical trial evaluated whether genotype-guided prescribing of selective serotonin reuptake inhibitors (SSRIs) could improve outcomes for patients with depression. The study enrolled 1,460 adults and children receiving care in primary care, psychiatry, and family medicine clinics across the United States. Researchers examined whether pharmacogenetic information related to CYP2D6 and CYP2C19 — genes that influence how ...
  • Genotype-Guided Antidepressant Prescribing for Patients With Depression May 6, 2026
    Kathryn V. Blake, PharmD; Lindsay J. Hines, PhD; Michelle Liu, PharmD DOI: 10.1001/jamanetworkopen.2026.10609 Article on Jama Network
  • GUARDD-US APOL1 Genetic Testing Manuscript Published March 6, 2026
    A new manuscript from the IGNITE Pragmatic Trials Network has been published in JAMA Network Open, describing the primary results of the GUARDD-US study.  GUARDD-US is a randomized controlled trial examining the impact of returning APOL1 genetic risk results to patients with hypertension and their clinicians. The study explores whether knowledge of genetic risk for kidney disease can influence blood pressure management and chronic kidney disease (CKD) screening in routine clinical care.  GUARDD-US enrolled more than 6,700 participants with self-reported ...
  • Genetic Testing for APOL1 in Adults With Hypertension – The GUARDD-US Randomized Clinical Trial March 6, 2026
    Michael T. Eadon, MD; Kerri L. Cavanaugh, MD, MHS; Lilin She, PhD DOI: 10.1001/jamanetworkopen.2026.0528 Article on Jama Network
  • ADOPT-PGx Acute Pain Manuscript Published with Invited Commentary February 20, 2026
    The ADOPT-PGx study examined the impact of genotype-guided opioid prescribing on postoperative pain management. Results from the study were recently published in JAMA Network Open, accompanied by an invited commentary reflecting on the findings and their implications for pharmacogenetics in clinical care. ADOPT-PGx is a pragmatic, randomized clinical trial designed to evaluate whether CYP2D6-guided opioid prescribing improves pain outcomes following surgery compared with usual care. The study was conducted in real-world clinical settings to assess the feasibility and effectiveness of pharmacogenetic ...
  • CYP2D6-Guided Opioid Management and Postoperative Pain Control February 20, 2026
    Larisa H. Cavallari, PharmD1; Rachel A. Myers, PhD; Hrishikesh Chakraborty, DrPH DOI: 10.1001/jamanetworkopen.2025.58299 Article on Jama Network

ADOPT/GUARDD

  • New Leadership Announced for Coordinating Center February 4, 2022
    The Implementing GeNomics In practice (IGNITE) Pragmatic Clinical Trials Network is an NIH-funded network dedicated to supporting the implementation of genomics in healthcare. Effective January 2022, Christina Wyatt, MD, associate professor of medicine (Nephrology) and Scott Palmer, MD, MHS, professor of medicine (Pulmonary, Allergy, and Critical Care Medicine) will replace Geoff Ginsburg, MD, PhD, as principal investigators for the IGNITE Pragmatic Clinical Trials Network coordinating center. Ginsburg recently was announced as the National Institutes of Health (NIH) Chief Medical and Scientific Officer for the All ...
  • IGNITE Diversity & Inclusion Statement November 25, 2020
    The IGNITE Network Leadership calls for Diversity and Inclusion in the conduct of research We call on scientific and medical communities to acknowledge and work toward eliminating the injustices perpetuated through all forms of systemic racism and discrimination, both past and present, overt and covert. We condemn eugenic beliefs, policies, and practices. While ancestry has some genetic underpinnings, race is a social construct. Thus, we recognize the consequences of racism and bias on health, healthcare, and research. To provide more equitable care ...
  • IGNITE blazes the way for genomic medicine December 3, 2019
    Getting diagnosed with a disease can be scary. Health providers work to find the right treatment plan based on the current standard of care guidelines. But what if in addition to the current evidence, doctors could also factor in each patient’s unique genetic makeup to help them diagnose more quickly and accurately, create a tailored treatment plan, or better yet, learn which patients are at a higher risk for developing specific diseases and employ methods for prevention or earlier detection? ...
  • The Lancet publishes series of 5 papers featuring IGNITE researchers August 5, 2019
    Members of the IGNITE Network were involved in three of the five publications in this series. Genomic Medicine 1: Opportunities, resources and techniques for implementing genomics in clinical care describes the major types and measurement tools of genomic variation that are currently of clinical importance, reviews approaches to interpreting genomic sequence variants, identifies publicly available tools and resources for genomic test interpretation, and discusses several key barriers in using genomic information in routine clinical practice. Genomic Medicine 4: Family health history: Underused for ...
  • NIH funds clinical trials using genomics to treat chronic diseases June 5, 2019
    The National Institutes of Health will fund clinical trials to assess the benefits, applicability and efficacy of applying genomic medicine interventions to improve management of diseases such as high blood pressure, depression and chronic pain. The trials are part of the second phase of the Implementing Genomics in Practice (IGNITE) Network with a total investment of $42 million over five years, pending the availability of funds. The trials will begin in 2020. Read more
  • NHGRI publishes overview about IGNITE March 23, 2019
    The Implementing Genomic in Practice (IGNITE) Network was established in 2013 (RFA-HG-12-006, RFA-HG-12-007 and RFA-HG-13-004) to develop methods for incorporating genomic information into clinical care and explore the methods for effective implementation, diffusion, and sustainability in diverse clinical settings. The first phase of the network, IGNITE I, was a consortium of collaborative genomic medicine pilot Demonstration Projects designed to demonstrate the feasibility of, and develop methods for, incorporating an individual patient’s genomic findings into his or her clinical care. The next phase of IGNITE, IGNITE ...