Rachel Linnemann

Emory University School of Medicine

United States

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Articles (15)

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2025

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2025

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2025

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2024

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2023

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2022

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2022

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2022

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2021

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2021

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2021

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2021

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2021

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2020

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2020

Collaborators (10)

Kathryn Oliver

Assistant Professor

Emory University School of Medicine

UNITED STATES

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Stephanie DiFiglia

Research Assistant Professor

Albert Einstein College of Medicine

UNITED STATES

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Dana Albon

UNITED STATES

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Hari Polenakovik

Wright State University

UNITED STATES

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Rebekah Brown

Associate Professor of Pediatrics

Vanderbilt University Medical Center

UNITED STATES

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Eva Van Braeckel

Tenured Assistant Research Professor of Respiratory Medicine, respiratory infections and cystic fibrosis

Ghent University

BELGIUM

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Alex Gifford

Associate Professor

University Hospital

UNITED STATES

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Elizabeth Seng

Research Associate Professor

Albert Einstein College of Medicine

UNITED STATES

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Rossana Sanchez Russo

Assistant Professor of Human Genetics

Emory University

UNITED STATES

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Silvia Maria del Rocio Delgado Villalta

Clinical Assistant Professor

University of Florida

UNITED STATES

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Rachel Linnemann

Research Interests

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Articles (15)

Long-Term Safety and Efficacy of Elexacaftor/Tezacaftor/Ivacaftor in Adults and Adolescents with Cystic Fibrosis and at Least One F508del Allele: A Phase 3 Open-Label Extension Study

Evaluating Georgia’s Cystic Fibrosis Newborn Screening Algorithm to Inform Improvement Recommendations

CFTR Variant Frequencies and Newborn Screening Panel Performance in the Diverse CF Population Receiving Care in the State of Georgia

Palliative care needs among outpatient adults with cystic fibrosis: Baseline data from the Improving Life with CF trial

Long-term safety and efficacy of elexacaftor/tezacaftor/ivacaftor in people with cystic fibrosis and at least oneF508delallele: 144-week interim results from a 192-week open-label extension study

Discontinuation versus continuation of hypertonic saline or dornase alfa in modulator treated people with cystic fibrosis (SIMPLIFY): results from two parallel, multicentre, open-label, randomised, controlled, non-inferiority trials.

Cystic fibrosis learning network telehealth innovation lab during the COVID-19 pandemic: a success QI story for interdisciplinary care and agenda setting.

Serum anti-PAD4 autoantibodies are present in cystic fibrosis children and increase with age and lung disease severity.

A Randomized Clinical Trial of Antimicrobial Duration for Cystic Fibrosis Pulmonary Exacerbation Treatment.

Improving lung function in adolescents with CF by tracking annual rate of lung function decline.

Use of the NINJA (Nephrotoxic Injury Negated by Just-in-Time Action) Program to Identify Nephrotoxicity in Pediatric Patients with Cystic Fibrosis.

Long-term safety and efficacy of tezacaftor-ivacaftor in individuals with cystic fibrosis aged 12 years or older who are homozygous or heterozygous for Phe508del CFTR (EXTEND): an open-label extension study.

Safety and Efficacy of Elexacaftor/Tezacaftor/Ivacaftor for 24 Weeks or Longer in People with Cystic Fibrosis and One or More <i>F508del</i> Alleles: Interim Results of an Open-Label Phase 3 Clinical Trial.

IgA autoantibodies directed against self DNA are elevated in cystic fibrosis and associated with more severe lung dysfunction.

Trajectories of oral glucose tolerance testing in cystic fibrosis.

Collaborators (10)

Kathryn Oliver

Stephanie DiFiglia

Dana Albon

Hari Polenakovik

Rebekah Brown

Eva Van Braeckel

Alex Gifford

Elizabeth Seng

Rossana Sanchez Russo

Silvia Maria del Rocio Delgado Villalta

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