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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2002 2
2003 2
2004 6
2005 2
2006 6
2007 7
2008 4
2009 2
2010 3
2011 4
2012 5
2013 7
2014 2
2015 2
2016 2
2017 4
2018 4
2019 2
2020 7
2021 4
2022 3
2023 4
2024 1

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78 results

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Page 1
Human inherited CCR2 deficiency underlies progressive polycystic lung disease.
Neehus AL, Carey B, Landekic M, Panikulam P, Deutsch G, Ogishi M, Arango-Franco CA, 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 JE, Deslys A, Bernard M, Gajardo-Carrasco T, Soudée C, Le Floc'h C, Migaud M, Seeleuthner Y, Jang MS, Nikolouli E, Seyedpour S, Begueret H, Emile JF, Le Guen P, Tavazzi G, Colombo CNJ, Marzani FC, Angelini M, Trespidi F, Ghirardello S, Alipour N, Molitor A, Carapito R, Mazloomrezaei M, Rokni-Zadeh H, Changi-Ashtiani M, Brouzes C, Vargas P, Borghesi A, Lachmann N, Bahram S, Crestani B, Pahari S, Schlesinger LS, Marr N, Bugonovic D, Boisson-Dupuis S, Béziat V, Abel L, Borie R, Young LR, Deterding R, Shahrooei M, Rezaei N, Parvaneh N, Craven D, Gros P, Malo D, Sepulveda FE, Nogee LM, Aladjidi N, Trapnell BC, Casanova JL, Bustamante J. Neehus AL, et al. Among authors: nogee lm. Cell. 2024 Jan 18;187(2):390-408.e23. doi: 10.1016/j.cell.2023.11.036. Epub 2023 Dec 28. Cell. 2024. PMID: 38157855 Free PMC article.
The US national registry for childhood interstitial and diffuse lung disease: Report of study design and initial enrollment cohort.
Nevel RJ, Deutsch GH, Craven D, Deterding R, Fishman MP, Wambach JA, Casey A, Krone K, Liptzin DR, O'Connor MG, Kurland G, Taylor JB, Gower WA, Hagood JS, Conrad C, Tam-Williams JB, Fiorino EK, Goldfarb S, Sadreameli SC, Nogee LM, Montgomery G, Hamvas A, Laguna TA, Bansal M, Lew C, Santiago M, Popova A, De A, Chan M, Powers MR, Josephson MB, Camburn D, Voss L, Li Y, Young LR; chILD Registry Collaborative. Nevel RJ, et al. Among authors: nogee lm. Pediatr Pulmonol. 2023 Jul 4:10.1002/ppul.26568. doi: 10.1002/ppul.26568. Online ahead of print. Pediatr Pulmonol. 2023. PMID: 37401889
Genetic testing for diffuse lung diseases in children.
Hamvas A, Chaudhari BP, Nogee LM. Hamvas A, et al. Among authors: nogee lm. Pediatr Pulmonol. 2023 May 16. doi: 10.1002/ppul.26447. Online ahead of print. Pediatr Pulmonol. 2023. PMID: 37191361
First Steps toward Personalized Therapies for ABCA3 Deficiency.
Wambach JA, Nogee LM, Cole FS. Wambach JA, et al. Among authors: nogee lm. Am J Respir Cell Mol Biol. 2022 Apr;66(4):349-350. doi: 10.1165/rcmb.2021-0405ED. Am J Respir Cell Mol Biol. 2022. PMID: 35077664 Free PMC article. No abstract available.
Accurate assignment of disease liability to genetic variants using only population data.
Collaco JM, Raraigh KS, Betz J, Aksit MA, Blau N, Brown J, Dietz HC, MacCarrick G, Nogee LM, Sheridan MB, Vernon HJ, Beaty TH, Louis TA, Cutting GR. Collaco JM, et al. Among authors: nogee lm. Genet Med. 2022 Jan;24(1):87-99. doi: 10.1016/j.gim.2021.08.012. Epub 2021 Nov 30. Genet Med. 2022. PMID: 34906463 Free PMC article.
Genetic Testing for Neonatal Respiratory Disease.
Nogee LM, Ryan RM. Nogee LM, et al. Children (Basel). 2021 Mar 11;8(3):216. doi: 10.3390/children8030216. Children (Basel). 2021. PMID: 33799761 Free PMC article. Review.
78 results