Research output per year
Research output per year
- 1 - 50 out of 146 results
Search results
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2025
Genetic Testing Utilization in the U.S. Registry for Childhood Interstitial and Diffuse Lung Diseases
for the chILD Registry Collaborative, Apr 2025, In: Pediatric pulmonology. 60, 4, e71073.Research output: Contribution to journal › Article › peer-review
Open Access -
Interstitial Lung Disease and Lung Cancer Associated with a Monoallelic Novel Variant in SFTPB
Wambach, J. A., Nogee, L. M., Spielberg, D. R., Cole, F. S., Roberts, D. M., Murphy, S. & Garcia, C. K., Jun 1 2025, In: American journal of respiratory and critical care medicine. 211, 6, p. 1085-1088 4 p.Research output: Contribution to journal › Letter › peer-review
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2024
Children's interstitial lung disease (chILD): Less rare than we thought?
Bush, A. & Nogee, L., Aug 19 2024, In: Thorax. 79, 9, p. 807-808 2 p.Research output: Contribution to journal › Editorial › peer-review
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Erratum: Human inherited CCR2 deficiency underlies progressive polycystic lung disease (Cell (2024) 187(2) (390–408.e23), (S0092867423013235), (10.1016/j.cell.2023.11.036))
Neehus, A. L., Carey, B., Landekic, M., Panikulam, P., Deutsch, G., Ogishi, M., Arango-Franco, C. A., Philippot, Q., Modaresi, M., Mohammadzadeh, I., Berndt, M. C., Rinchai, D., Le Voyer, T., Rosain, J., Momenilandi, M., Martin-Fernandez, M., Khan, T., Bohlen, J., Han, J. E. & Deslys, A. & 54 others, , Jun 20 2024, In: Cell. 187, 13, p. 3460 1 p.Research output: Contribution to journal › Comment/debate › peer-review
Open Access -
Genetic testing for diffuse lung diseases in children
Hamvas, A., Chaudhari, B. P. & Nogee, L. M., Sep 2024, In: Pediatric pulmonology. 59, 9, p. 2286-2297 12 p.Research output: Contribution to journal › Article › peer-review
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Human inherited CCR2 deficiency underlies progressive polycystic lung disease
Neehus, A. L., Carey, B., Landekic, M., Panikulam, P., Deutsch, G., Ogishi, M., Arango-Franco, C. A., Philippot, Q., Modaresi, M., Mohammadzadeh, I., Corcini Berndt, M., Rinchai, D., Le Voyer, T., Rosain, J., Momenilandi, M., Martin-Fernandez, M., Khan, T., Bohlen, J., Han, J. E. & Deslys, A. & 52 others, , Jan 18 2024, In: Cell. 187, 2, p. 390-408.e23Research output: Contribution to journal › Article › peer-review
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Inherited Disorders of Surfactant Metabolism
Wambach, J. A., Nogee, L. M., Hamvas, A. & Cole, F. S., Jan 1 2024, Nelson Textbook of Pediatrics: Volume 1-2. Elsevier, p. 2686-2687.e1Research output: Chapter in Book/Report/Conference proceeding › Chapter
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Pulmonary Alveolar Proteinosis
Wambach, J. A., Nogee, L. M., Cole, F. S. & Hamvas, A., Jan 1 2024, Nelson Textbook of Pediatrics: Volume 1-2. Elsevier, p. 2686-2687.e1Research output: Chapter in Book/Report/Conference proceeding › Chapter
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The US national registry for childhood interstitial and diffuse lung disease: Report of study design and initial enrollment cohort
for the chILD Registry Collaborative, Sep 2024, In: Pediatric pulmonology. 59, 9, p. 2236-2246 11 p.Research output: Contribution to journal › Article › peer-review
Open Access -
2023
ATP binding cassette member A3 (ABCA3): Coming of age
Casey, A., Nogee, L. & Wambach, J., Jun 1 2023, In: Thorax. 78, 6, p. 533-534 2 p.Research output: Contribution to journal › Editorial › peer-review
Open Access -
Rare to “Ubiquitinous”: Alveolar Capillary Dysplasia, FOXF1, and a Sly Approach to Angiogenesis
Cornfield, D. N. & Nogee, L. M., Apr 15 2023, In: American journal of respiratory and critical care medicine. 207, 8, p. 969-971 3 p.Research output: Contribution to journal › Editorial › peer-review
Open Access -
2022
Accurate assignment of disease liability to genetic variants using only population data
Collaco, J. M., Raraigh, K. S., Betz, J., Aksit, M. A., Blau, N., Brown, J., Dietz, H. C., MacCarrick, G., Nogee, L. M., Sheridan, M. B., Vernon, H. J., Beaty, T. H., Louis, T. & Cutting, G. R., Jan 2022, In: Genetics in Medicine. 24, 1, p. 87-99 13 p.Research output: Contribution to journal › Article › peer-review
Open Access -
Biallelic variants of ATP13A3 cause dose-dependent childhood-onset pulmonary arterial hypertension characterised by extreme morbidity and mortality
NIHR Bioresource – Rare Diseases, Sep 2022, In: Journal of medical genetics. 59, 9, p. 906-911 6 p.Research output: Contribution to journal › Article › peer-review
Open Access -
Child Interstitial Lung Disease in an Infant with Surfactant Protein C Dysfunction due to c.202G>T Variant (p.V68F)
Park, H., Bidiwala, A., Conrad, L. A., Aborawi, N., Ewart, M., Josephson, M., Nogee, L. M. & Arens, R., Feb 2022, In: Lung. 200, 1, p. 67-71 5 p.Research output: Contribution to journal › Article › peer-review
Open Access -
First Steps toward Personalized Therapies for ABCA3 Deficiency
Wambach, J. A., Nogee, L. M. & Cole, F. S., Apr 2022, In: American journal of respiratory cell and molecular biology. 66, 4, p. 349-350 2 p.Research output: Contribution to journal › Editorial › peer-review
Open Access -
2021
Community-Onset Severe Acute Respiratory Syndrome Coronavirus 2 Infection in Young Infants: A Systematic Review
Mark, E. G., Golden, W. C., Gilmore, M. M., Sick-Samuels, A., Curless, M. S., Nogee, L. M., Milstone, A. M. & Johnson, J., Jan 2021, In: Journal of Pediatrics. 228, p. 94-100.e3Research output: Contribution to journal › Article › peer-review
Open Access2 Scopus citations -
Coronavirus Disease 2019 in Pregnancy and Outcomes among Pregnant Women and Neonates: A Literature Review
Mark, E. G., McAleese, S., Golden, W. C., Gilmore, M. M., Sick-Samuels, A., Curless, M. S., Nogee, L. M., Milstone, A. M. & Johnson, J., May 1 2021, In: Pediatric Infectious Disease Journal. 40, 5, p. 473-478 6 p.Research output: Contribution to journal › Review article › peer-review
Open Access1 Scopus citations -
Genetic testing for neonatal respiratory disease
Nogee, L. M. & Ryan, R. M., Mar 2021, In: Children. 8, 3, 216.Research output: Contribution to journal › Article › peer-review
Open Access -
2020
A lung tropic AAV vector improves survival in a mouse model of surfactant B deficiency
Kang, M. H., van Lieshout, L. P., Xu, L., Domm, J. M., Vadivel, A., Renesme, L., Mühlfeld, C., Hurskainen, M., Mižíková, I., Pei, Y., van Vloten, J. P., Thomas, S. P., Milazzo, C., Cyr-Depauw, C., Whitsett, J. A., Nogee, L. M., Wootton, S. K. & Thébaud, B., Dec 1 2020, In: Nature communications. 11, 1, 3929.Research output: Contribution to journal › Article › peer-review
Open Access2 Scopus citations -
Genetic testing for rare pediatric lung disorders: The promise and the pitfalls
Nogee, L. M., Mar 1 2020, In: Pediatric Investigation. 4, 1, p. 59-60 2 p.Research output: Contribution to journal › Editorial › peer-review
Open Access -
Neonatal respiratory failure due to novel compound heterozygous mutations in the ABCA3 lipid transporter
Oltvai, Z. N., Smith, E. A., Wiens, K., Nogee, L. M., Luquette, M., Nelson, A. C. & Wikenheiser-Brokamp, K. A., Feb 2020, In: Cold Spring Harbor Molecular Case Studies. 6, 3, a005074.Research output: Contribution to journal › Article › peer-review
Open Access -
Single-Center Outcome of Fetoscopic Tracheal Balloon Occlusion for Severe Congenital Diaphragmatic Hernia
Baschat, A. A., Rosner, M., Millard, S. E., Murphy, J. D., Blakemore, K. J., Keiser, A. M., Kearney, J., Bullard, J., Nogee, L. M., Bembea, M., Jelin, E. B. & Miller, J. L., Mar 1 2020, In: Obstetrics and gynecology. 135, 3, p. 511-521 11 p.Research output: Contribution to journal › Article › peer-review
3 Scopus citations -
The common K333Q polymorphism in long-chain acyl-CoA dehydrogenase (LCAD) reduces enzyme stability and function
Beck, M. E., Zhang, Y., Bharathi, S. S., Kosmider, B., Bahmed, K., Dahmer, M. K., Nogee, L. M. & Goetzman, E. S., Sep 1 2020, In: Molecular genetics and metabolism. 131, 1-2, p. 83-89 7 p.Research output: Contribution to journal › Article › peer-review
Open Access2 Scopus citations -
The past and future of genetics in pulmonary disease: You can teach an old dog new tricks
Nogee, L. M. & Hamvas, A., Jul 1 2020, In: Pediatric pulmonology. 55, 7, p. 1789-1793 5 p.Research output: Contribution to journal › Comment/debate › peer-review
Open Access -
2019
57 - Lung Diseases Associated With Disruption of Pulmonary Surfactant Homeostasis
Nogee, L. M. & Trapnell, B. C., 2019, Kendig's Disorders of the Respiratory Tract in Children. Elsevier Inc., p. 836-849.e5Research output: Chapter in Book/Report/Conference proceeding › Chapter
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A step toward treating a lethal neonatal lung disease: STAT3 and alveolar capillary dysplasia
Wambach, J. A. & Nogee, L. M., Oct 15 2019, In: American journal of respiratory and critical care medicine. 200, 8, p. 961-962 2 p.Research output: Contribution to journal › Editorial › peer-review
Open Access -
Genetic causes of surfactant protein abnormalities
Nogee, L. M., Jun 1 2019, In: Current opinion in pediatrics. 31, 3, p. 330-339 10 p.Research output: Contribution to journal › Review article › peer-review
7 Scopus citations -
2018
Current status and future opportunities in lung precision medicine research with a focus on biomarkers: An American Thoracic Society/National Heart, Lung, and Blood Institute Research Statement
Wu, A. C., Kiley, J. P., Noel, P. J., Amur, S., Burchard, E. G., Clancy, J. P., Galanter, J., Inada, M., Jones, T. K., Kropski, J. A., Loyd, J. E., Nogee, L. M., Raby, B. A., Rogers, A. J., Schwartz, D. A., Sin, D. D., Spira, A., Weiss, S. T., Young, L. R. & Himes, B. E., Dec 15 2018, In: American journal of respiratory and critical care medicine. 198, 12, p. E116-E136Research output: Contribution to journal › Article › peer-review
Open Access20 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 others, , Jun 15 2018, In: American journal of respiratory and critical care medicine. 197, 12, p. e24-e39Research output: Contribution to journal › Article › peer-review
100 Scopus citations -
Ethical considerations concerning amnioinfusions for treating fetal bilateral renal agenesis
Sugarman, J., Anderson, J., Baschat, A. A., Herrera Beutler, J., Bienstock, J. L., Bunchman, T. E., Desai, N. M., Gates, E., Goldberg, A., Grimm, P. C., Henry, L. M., Jelin, E. B., Johnson, E., Hertenstein, C. B., Mastroianni, A. C., Mercurio, M. R., Neu, A., Nogee, L. M., Polzin, W. J. & Ralston, S. J. & 5 others, , Jan 1 2018, In: Obstetrics and gynecology. 131, 1, p. 130-134 5 p.Research output: Contribution to journal › Article › peer-review
11 Scopus citations -
NHLRC2 variants identified in patients with fibrosis, neurodegeneration, and cerebral angiomatosis (FINCA): characterisation of a novel cerebropulmonary disease
Uusimaa, J., Kaarteenaho, R., Paakkola, T., Tuominen, H., Karjalainen, M. K., Nadaf, J., Varilo, T., Uusi-Mäkelä, M., Suo-Palosaari, M., Pietilä, I., Hiltunen, A. E., Ruddock, L., Alanen, H., Biterova, E., Miinalainen, I., Salminen, A., Soininen, R., Manninen, A., Sormunen, R. & Kaakinen, M. & 12 others, , May 1 2018, In: Acta neuropathologica. 135, 5, p. 727-742 16 p.Research output: Contribution to journal › Article › peer-review
6 Scopus citations -
Respiratory distress syndrome
Nogee, J. M. & Nogee, L. M., Jan 1 2018, The 5-Minute Pediatric Consult, 8th Edition. Wolters Kluwer Health, p. 780-781 2 p.Research output: Chapter in Book/Report/Conference proceeding › Chapter
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2017
A novel surfactant protein C gene mutation associated with progressive respiratory failure in infancy
Litao, M. K. S., Hayes, D., Chiwane, S., Nogee, L. M., Kurland, G. & Guglani, L., Jan 1 2017, In: Pediatric pulmonology. 52, 1, p. 57-68 12 p.Research output: Contribution to journal › Article › peer-review
18 Scopus citations -
Childhood interstitial lung diseases in immunocompetent children in Australia and New Zealand: A decade's experience
Saddi, V., Beggs, S., Bennetts, B., Harrison, J., Hime, N., Kapur, N., Lipsett, J., Nogee, L. M., Phu, A., Suresh, S., Schultz, A., Selvadurai, H., Sherrard, S., Strachan, R., Vyas, J., Zurynski, Y. & Jaffé, A., Jul 25 2017, In: Orphanet journal of rare diseases. 12, 1, 133.Research output: Contribution to journal › Article › peer-review
Open Access14 Scopus citations -
Delayed Presentation and Prolonged Survival of a Child with Surfactant Protein B Deficiency
López-Andreu, J. A., Hidalgo-Santos, A. D., Fuentes-Castelló, M. A., Mancheño-Franch, N., Cerón-Pérez, J. A., Esteban-Ricós, M. J., Pedrola-Vidal, L. & Nogee, L. M., Nov 2017, In: Journal of Pediatrics. 190, p. 268-270.e1Research output: Contribution to journal › Article › peer-review
3 Scopus citations -
Genetics and Physiology of Surfactant Protein Deficiencies
Nogee, L. M., Jan 1 2017, Fetal and Neonatal Physiology, 2-Volume Set. Elsevier, p. 843-854.e2Research output: Chapter in Book/Report/Conference proceeding › Chapter
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Interstitial lung disease in newborns
Nogee, L. M., Aug 2017, In: Seminars in Fetal and Neonatal Medicine. 22, 4, p. 227-233 7 p.Research output: Contribution to journal › Review article › peer-review
31 Scopus citations -
Premature Identical Twin Neonates with Sleep Apnea
Ramesh, A., Diaz, J., Nogee, L., Duis, J., Jang, D. S., Lawson, C. & Maegawa, G., Oct 1 2017, In: Clinical pediatrics. 56, 11, p. 1075-1078 4 p.Research output: Contribution to journal › Article › peer-review
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2016
Persistent lung disease in adults with NKX2.1 mutation and familial neuroendocrine cell hyperplasia of infancy
Nevel, R. J., Garnett, E. T., Worrell, J. A., Morton, R. L., Nogee, L. M., Blackwell, T. S. & Young, L. R., 2016, In: Annals of the American Thoracic Society. 13, 8, p. 1299-1304 6 p.Research output: Contribution to journal › Article › peer-review
Open Access21 Scopus citations -
Surfactant during lung development
Weaver, T. E., Nogee, L. & Jobe, A. H., Apr 18 2016, Fetal and Neonatal Lung Development: Clinical Correlates and Technologies for the Future. Cambridge University Press, p. 141-163 23 p.Research output: Chapter in Book/Report/Conference proceeding › Chapter
2 Scopus citations -
2015
A disorder of surfactant metabolism without identified genetic mutations
Montella, S., Vece, T. J., Langston, C., Carrera, P., Nogee, L. M., Hamvas, A., Manna, A., Cervasio, M. & Santamaria, F., Nov 25 2015, In: Italian Journal of Pediatrics. 41, 1, 93.Research output: Contribution to journal › Article › peer-review
Open Access5 Scopus citations -
Erratum: A disorder of surfactant metabolism without identified genetic mutations (Italian Journal of Pediatrics (2015) 41 (93))
Montella, S., Vece, T. J., Langston, C., Carrera, P., Nogee, L. M., Hamvas, A., Manna, A., Cervasio, M. & Santamaria, F., Dec 16 2015, In: Italian Journal of Pediatrics. 41, 1, 98.Research output: Contribution to journal › Comment/debate › peer-review
Open Access1 Scopus citations -
2014
Genotype-phenotype correlations for infants and children with ABCA3 deficiency
Wambach, J. A., Casey, A. M., Fishman, M. P., Wegner, D. J., Wert, S. E., Sessions Cole, F., Hamvas, A. & Nogee, L. M., Jun 15 2014, In: American journal of respiratory and critical care medicine. 189, 12, p. 1538-1543 6 p.Research output: Contribution to journal › Article › peer-review
Open Access84 Scopus citations -
Natural history of five children with surfactant protein C mutations and interstitial lung disease
Avital, A., Hevroni, A., Godfrey, S., Cohen, S., Maayan, C., Nusair, S., Nogee, L. M. & Springer, C., Nov 1 2014, In: Pediatric pulmonology. 49, 11, p. 1097-1105 9 p.Research output: Contribution to journal › Article › peer-review
41 Scopus citations -
The expanded spectrum of genetic surfactant dysfunction disorders
Gower, W. A., Collaco, J. M. & Nogee, L. M., Jan 14 2014, In: Clinical Pulmonary Medicine. 21, 1, p. 16-23 8 p.Research output: Contribution to journal › Review article › peer-review
2 Scopus citations -
2013
A mutation in TTF1/NKX2.1 is associated with familial neuroendocrine cell hyperplasia of infancy
Young, L. R., Deutsch, G. H., Bokulic, R. E., Brody, A. S. & Nogee, L. M., Oct 2013, In: CHEST. 144, 4, p. 1199-1206 8 p.Research output: Contribution to journal › Article › peer-review
Open Access48 Scopus citations -
An official american thoracic society clinical practice guideline: Classification, evaluation, and management of childhood interstitial lung disease in infancy
Kurland, G., Deterding, R. R., Hagood, J. S., Young, L. R., Brody, A. S., Castile, R. G., Dell, S., Fan, L. L., Hamvas, A., Hilman, B. C., Langston, C., Nogee, L. M. & Redding, G. J., Aug 1 2013, In: American journal of respiratory and critical care medicine. 188, 3, p. 376-394 19 p.Research output: Contribution to journal › Article › peer-review
210 Scopus citations -
Candidate gene analysis of the surfactant protein d gene in pediatric diffuse lung disease
Gower, W. A. & Nogee, L. M., Dec 2013, In: Journal of Pediatrics. 163, 6, p. 1778-1780 3 p.Research output: Contribution to journal › Article › peer-review
Open Access5 Scopus citations -
Heterogeneous pulmonary phenotypes associated with mutations in the thyroid transcription factor gene NKX2-1
Hamvas, A., Deterding, R. R., Wert, S. E., White, F. V., Dishop, M. K., Alfano, D. N., Halbower, A. C., Planer, B., Stephan, M. J., Uchida, D. A., Williames, L. D., Rosenfeld, J. A., Lebel, R. R., Young, L. R., Cole, F. S. & Nogee, L. M., Sep 2013, In: CHEST. 144, 3, p. 794-804 11 p.Research output: Contribution to journal › Article › peer-review
Open Access93 Scopus citations -
Large ABCA3 and SFTPC deletions resulting in lung disease
Henderson, L. B., Melton, K., Wert, S., Couriel, J., Bush, A., Ashworth, M. & Nogee, L. M., Dec 2013, In: Annals of the American Thoracic Society. 10, 6, p. 602-607 6 p.Research output: Contribution to journal › Article › peer-review
Open Access16 Scopus citations