Deepika Polineni

Research output

Research output per year 2006 2018 2019 2020 2021 2023

• 16 Article
• 6 Review article
• 3 Letter
• 2 Editorial

Research output per year

Research output per year

Search results

• 2023

  Partners in research: The success with therapies research consortium and the CF community unite to improve self-management

  Sawicki, G. S., Goodman, A., Bacon, C., Collins, L., Greenberg, J., Duncan, C., Frederick, C., Luebbert, S., Mazuera, S., Polineni, D., Stark, L. L., George, C. & Riekert, K. A., 2023, (Accepted/In press) In: Journal of Cystic Fibrosis.

  Research output: Contribution to journal › Article › peer-review

  • Self-Management 100%
  • Cystic Fibrosis 90%
  • Research Personnel 16%
  • Therapeutics 15%
  • Caregivers 13%

• Sex and Gender in Lung Diseases and Sleep Disorders: A State-of-the-Art Review: Part 2

  Sodhi, A., Cox-Flaherty, K., Greer, M. K., Lat, T. I., Gao, Y., Polineni, D., Pisani, M. A., Bourjeily, G., Glassberg, M. K. & D'Ambrosio, C., Feb 2023, In: CHEST. 163, 2, p. 366-382 17 p.

  Research output: Contribution to journal › Review article › peer-review

  • Sleep Wake Disorders 100%
  • Lung Diseases 81%
  • Cystic Fibrosis 53%
  • Sarcoidosis 39%
  • Sex Characteristics 34%
  1 Scopus citations
• 2022

  Feasibility and acceptability of a CF-specific cognitive-behavioral preventive intervention for adults integrated into team-based care

  Friedman, D., Smith, B. A., Bruce, A., Schwartz, C. E., Lee, H., Pinsky, H., Gootkind, E., Hardcastle, M., Shea, N., Roach, C. M., Miller, C., Polineni, D., Salathe, M., Quittner, A. L. & Georgiopoulos, A. M., Nov 2022, In: Pediatric Pulmonology. 57, 11, p. 2781-2790 10 p.

  Research output: Contribution to journal › Article › peer-review

  • Cystic Fibrosis 100%
  • Depression 26%
  • Anxiety 22%
  • Mental Health 16%
  • Preventive Health Services 12%
  2 Scopus citations

• Trabecular bone score in people with cystic fibrosis

  Anabtawi, A., Holyoak, M., He, J., Cristiano, E., Polineni, D. & Graves, L., May 2022, In: Osteoporosis International. 33, 5, p. 1137-1145 9 p.

  Research output: Contribution to journal › Article › peer-review

  • Cancellous Bone 100%
  • Cystic Fibrosis 92%
  • Femur Neck 91%
  • Transplants 22%
  • Bone Density 21%
  1 Scopus citations
• 2021

  A pilot study of cystic fibrosis exacerbation response phenotypes reveals contrasting serum and sputum iron trends

  Gifford, A. H., Polineni, D., He, J., D’Amico, J. L., Dorman, D. B., Williams, M. A., Nymon, A. B., Balwan, A., Budden, T. & Zuckerman, J. B., Dec 2021, In: Scientific reports. 11, 1, 4897.

  Research output: Contribution to journal › Article › peer-review

  Open Access

  • Sputum 100%
  • Cystic Fibrosis 98%
  • Iron 84%
  • Phenotype 60%
  • Lung 54%
  1 Scopus citations

• Cystic fibrosis

  Shteinberg, M., Haq, I. J., Polineni, D. & Davies, J. C., Jun 5 2021, In: The Lancet. 397, 10290, p. 2195-2211 17 p.

  Research output: Contribution to journal › Review article › peer-review

  • Cystic Fibrosis 100%
  • lead chloride 26%
  • Mutation 24%
  • Exocrine Pancreatic Insufficiency 19%
  • Mucociliary Clearance 19%
  178 Scopus citations

• Safety and efficacy of elexacaftor/tezacaftor/ivacaftor for 24 weeks or longer in people with cystic fibrosis and one or more F508del alleles: Interim results of an open-label phase 3 clinical trial

  Griese, M., Costa, S., Linnemann, R. W., Mall, M. A., McKone, E. F., Polineni, D., Quon, B. S., Ringshausen, F. C., Taylor-Cousar, J. L., Withers, N. J., Moskowitz, S. M. & Daines, C. L., Feb 1 2021, In: American journal of respiratory and critical care medicine. 203, 3, p. 381-385 5 p.

  Research output: Contribution to journal › Letter › peer-review

  Open Access
  74 Scopus citations

• Triple therapy for cystic fibrosis Phe508del-gating and -residual function genotypes

  Barry, P. J., Mall, M. A., Álvarez, A., Colombo, C., de Winter-De Groot, K. M., Fajac, I., McBennett, K. A., McKone, E. F., Ramsey, B. W., Sutharsan, S., Taylor-Cousar, J. L., Tullis, E., Ahluwalia, N., Jun, L. S., Moskowitz, S. M., Prieto-Centurion, V., Tian, S., Waltz, D., Xuan, F., Zhang, Y., & 2 othersRowe, S. M. & Polineni, D., Aug 26 2021, In: New England Journal of Medicine. 385, 9, p. 815-825 11 p.

  Research output: Contribution to journal › Article › peer-review

  • tezacaftor; ivacaftor 100%
  • Cystic Fibrosis 46%
  • Genotype 34%
  • Cystic Fibrosis Transmembrane Conductance Regulator 30%
  • Confidence Intervals 17%
  66 Scopus citations
• 2020

  Gender Equity

  Polineni, D., Mar 2020, In: Journal of Cystic Fibrosis. 19, 2, p. 328-329 2 p.

  Research output: Contribution to journal › Letter › peer-review

  Open Access

• Losartan rescues inflammation-related mucociliary dysfunction in relevant models of cystic fibrosis

  Kim, M. D., Baumlin, N., Yoshida, M., Polineni, D., Salathe, S. F., David, J. K., Peloquin, C. A., Wanner, A., Dennis, J. S., Sailland, J., Whitney, P., Horrigan, F. T., Sabater, J. R., Abraham, W. M. & Salathe, M., Feb 1 2020, In: American journal of respiratory and critical care medicine. 201, 3, p. 313-324 12 p.

  Research output: Contribution to journal › Article › peer-review

  • Losartan 100%
  • Mucus 88%
  • Cystic Fibrosis 81%
  • Inflammation 48%
  • Sheep 45%
  25 Scopus citations

• Mining GWAS and eQTL data for CF lung disease modifiers by gene expression imputation

  Dang, H., Polineni, D., Pace, R. G., Stonebraker, J. R., Corvol, H., Cutting, G. R., Drumm, M. L., Strug, L. J., O’Neal, W. K. & Knowles, M. R., Nov 2020, In: PloS one. 15, 11 November, e0239189.

  Research output: Contribution to journal › Article › peer-review

  Open Access

  • Modifier Genes 100%
  • Genome-Wide Association Study 72%
  • Cystic Fibrosis 68%
  • Lung Diseases 62%
  • Gene Expression 41%
  5 Scopus citations
• 2019

  Aztreonam Lysine Inhalation Solution in Cystic Fibrosis

  Elson, E. C., Mermis, J., Polineni, D. & Oermann, C. M., Apr 1 2019, In: Clinical Medicine Insights: Circulatory, Respiratory and Pulmonary Medicine. 13

  Research output: Contribution to journal › Review article › peer-review

  Open Access

  • Aztreonam 100%
  • Cystic Fibrosis 71%
  • Lysine 71%
  • Inhalation 68%
  • Pseudomonas aeruginosa 27%
  10 Scopus citations

• Elexacaftor-tezacaftor-ivacaftor for cystic fibrosis with a single Phe508del allele

  VX17-445-102 Study Group, Nov 7 2019, In: New England Journal of Medicine. 381, 19, p. 1809-1819 11 p.

  Research output: Contribution to journal › Article › peer-review

  • tezacaftor; ivacaftor 100%
  • Cystic Fibrosis 46%
  • Cystic Fibrosis Transmembrane Conductance Regulator 40%
  • Alleles 34%
  • Placebos 14%
  844 Scopus citations

• Genetic association and transcriptome integration identify contributing genes and tissues at cystic fibrosis modifier loci

  Gong, J., Wang, F., Xiao, B., Panjwani, N., Lin, F., Keenan, K., Avolio, J., Esmaeili, M., Zhang, L., He, G., Soave, D., Mastromatteo, S., Baskurt, Z., Kim, S., O’Neal, W. K., Polineni, D., Blackman, S. M., Corvol, H., Cutting, G. R., Drumm, M., & 4 othersKnowles, M. R., Rommens, J. M., Sun, L. & Strug, L. J., Feb 2019, In: PLoS genetics. 15, 2, e1008007.

  Research output: Contribution to journal › Article › peer-review

  Open Access

  • Meconium Ileus 100%
  • cystic fibrosis 85%
  • modifiers (genes) 78%
  • intestinal obstruction 66%
  • chromosome 65%
  42 Scopus citations

• Perspectives on anemia and iron deficiency from the cystic fibrosis care community

  Garlow, G. M., Gettle, L. S., Felicetti, N. J., Polineni, D. & Gifford, A. H., Jul 2019, In: Pediatric Pulmonology. 54, 7, p. 939-940 2 p.

  Research output: Contribution to journal › Letter › peer-review
  5 Scopus citations

• Unraveling the CFTR function–phenotype connection for precision treatment in cystic fibrosis

  Zemanick, E. T. & Polineni, D., May 1 2019, In: American journal of respiratory and critical care medicine. 199, 9, p. 1053-1054 2 p.

  Research output: Contribution to journal › Editorial

  Open Access
• 2018

  Airway mucosal host defense is key to genomic regulation of cystic fibrosis lung disease severity

  Polineni, D., Dang, H., Gallins, P. J., Jones, L. C., Pace, R. G., Stonebraker, J. R., Commander, L. A., Krenicky, J. E., Zhou, Y. H., Corvol, H., Cutting, G. R., Drumm, M. L., Strug, L. J., Boyle, M. P., Durie, P. R., Chmiel, J. F., Zou, F., Wright, F. A., O’Neal, W. K. & Knowles, M. R., Jan 1 2018, In: American journal of respiratory and critical care medicine. 197, 1, p. 79-93 15 p.

  Research output: Contribution to journal › Article › peer-review

  • Cystic Fibrosis 100%
  • Lung Diseases 91%
  • Genome-Wide Association Study 58%
  • Gene Expression 33%
  • Cystic Fibrosis Transmembrane Conductance Regulator 23%
  33 Scopus citations

• Analysis of a large cohort of cystic fibrosis patients with severe liver disease indicates lung function decline does not significantly differ from that of the general cystic fibrosis population

  Polineni, D., Piccorelli, A. V., Hannah, W. B., Dalrymple, S. N., Pace, R. G., Durie, P. R., Ling, S. C., Knowles, M. R. & Stonebraker, J. R., Oct 2018, In: PloS one. 13, 10, e0205257.

  Research output: Contribution to journal › Article › peer-review

  Open Access

  • Cystic Fibrosis 100%
  • Liver Diseases 86%
  • Forced Expiratory Volume 76%
  • Lung 54%
  • Population 40%
  13 Scopus citations

• Chasing Zero: Increasing Infection Control Compliance on an Inpatient Cystic Fibrosis Unit

  Johnson, S., McNeal, M., Mermis, J., Polineni, D. & Burger, S., 2018, In: Journal of Nursing Care Quality. 33, 1, p. 67-71 5 p.

  Research output: Contribution to journal › Article › peer-review

  • Infection Control 100%
  • Cystic Fibrosis 96%
  • Compliance 89%
  • Inpatients 78%
  • Contracts 38%
  3 Scopus citations

• Diagnosis of primary ciliary dyskinesia: An official American thoracic society clinical practice guideline

  Shapiro, A. J., Davis, S. D., Polineni, D., Manion, M., Rosenfeld, M., Dell, S. D., Chilvers, M. A., Ferkol, T. W., Zariwala, M. A., Sagel, S. D., Josephson, M., Morgan, L., Yilmaz, O., Olivier, K. N., Milla, C., Pittman, J. E., Leigh Anne Daniels, M., Jones, M. H., Janahi, I. A., Ware, S. M., & 10 othersDaniel, S. J., Cooper, M. L., Nogee, L. M., Anton, B., Eastvold, T., Ehrne, L., Guadagno, E., Knowles, M. R., Leigh, M. W. & Lavergne, V., Jun 15 2018, In: American journal of respiratory and critical care medicine. 197, 12, p. e24-e39

  Research output: Contribution to journal › Article › peer-review

  • Ciliary Motility Disorders 100%
  • Routine Diagnostic Tests 64%
  • Practice Guidelines 63%
  • Thorax 46%
  • Health Equity 19%
  186 Scopus citations

• In statistics we trust: Towards the careful derivation and interpretation of meaningful survival estimates in cystic fibrosis

  Mayer-Hamblett, N., Polineni, D. & Heltshe, S. L., Mar 2018, In: Journal of Cystic Fibrosis. 17, 2, p. 133-134 2 p.

  Research output: Contribution to journal › Editorial

  Open Access

• Overcoming psychosocial challenges in cystic fibrosis: Promoting resilience

  Muther, E. F., Polineni, D. & Sawicki, G. S., Nov 2018, In: Pediatric Pulmonology. 53, p. S86-S92

  Research output: Contribution to journal › Review article › peer-review

  • Cystic Fibrosis 100%
  • Psychology 17%
  16 Scopus citations
• 2017

  Accuracy of nasal nitric oxide measurement as a diagnostic test for primary ciliary dyskinesia a systematic review and meta-analysis

  Shapiro, A. J., Josephson, M., Rosenfeld, M., Yilmaz, O., Davis, S. D., Polineni, D., Guadagno, E., Leigh, M. W. & Lavergne, V., Jul 2017, In: Annals of the American Thoracic Society. 14, 7, p. 1184-1196 13 p.

  Research output: Contribution to journal › Review article › peer-review

  • Ciliary Motility Disorders 100%
  • Routine Diagnostic Tests 64%
  • Nitric Oxide 55%
  • Nose 54%
  • Meta-Analysis 50%
  35 Scopus citations
• 2016

  Effect of extracorporeal photopheresis on lung function decline for severe bronchiolitis obliterans syndrome following allogeneic stem cell transplantation

  Brownback, K. R., Simpson, S. Q., Pitts, L. R., Polineni, D., McGuirk, J. P., Ganguly, S., Aljitawi, O. S., Lin, T. L., Singh, A. & Abhyankar, S., Aug 1 2016, In: Journal of Clinical Apheresis. 31, 4, p. 347-352 6 p.

  Research output: Contribution to journal › Article › peer-review

  • Photopheresis 100%
  • Bronchiolitis Obliterans 89%
  • Allogeneic Cells 70%
  • Forced Expiratory Volume 69%
  • Stem Cell Transplantation 68%
  15 Scopus citations

• Treatment recommendations in Primary Ciliary Dyskinesia

  Polineni, D., Davis, S. D. & Dell, S. D., Mar 1 2016, In: Paediatric Respiratory Reviews. 18, p. 39-45 7 p.

  Research output: Contribution to journal › Review article › peer-review

  • Ciliary Motility Disorders 100%
  • Bronchiectasis 16%
  • Lung 14%
  • Cystic Fibrosis 13%
  • Health Personnel 11%
  19 Scopus citations
• 2008

  Persistent activation of an innate immune response translates respiratory viral infection into chronic lung disease

  Kim, E. Y., Battaile, J. T., Patel, A. C., You, Y., Agapov, E., Grayson, M. H., Benoit, L. A., Byers, D. E., Alevy, Y., Tucker, J., Swanson, S., Tidwell, R., Tyner, J. W., Morton, J. D., Castro, M., Polineni, D., Patterson, G. A., Schwendener, R. A., Allard, J. D., Peltz, G., & 1 othersHoltzman, M. J., Jun 2008, In: Nature medicine. 14, 6, p. 633-640 8 p.

  Research output: Contribution to journal › Article › peer-review

  • Respiratory Tract Infections 100%
  • Innate Immunity 99%
  • Lung Diseases 96%
  • Chronic Disease 79%
  • Virus Diseases 79%
  425 Scopus citations
• 2006

  An interactive web-based curriculum on evidence-based medicine: Design and effectiveness

  Schilling, K., Wiecha, J., Polineni, D. & Khalil, S., Feb 2006, In: Family Medicine. 38, 2, p. 126-132 7 p.

  Research output: Contribution to journal › Article › peer-review

  • Evidence-Based Medicine 100%
  • Curriculum 86%
  • Students 61%
  • MEDLINE 44%
  • Learning 37%
  16 Scopus citations