Skip to main page content
Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

My NCBI Filters
Results by year

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

Year Number of Results
2010 2
2011 4
2012 5
2013 1
2014 2
2015 3
2016 4
2017 6
2018 2
2019 3
2020 1
2021 3
Text availability
Article attribute
Article type
Publication date

Search Results

34 results
Results by year
Filters applied: . Clear all
Page 1
Exome sequencing links mutations in PARN and RTEL1 with familial pulmonary fibrosis and telomere shortening.
Stuart BD, Choi J, Zaidi S, Xing C, Holohan B, Chen R, Choi M, Dharwadkar P, Torres F, Girod CE, Weissler J, Fitzgerald J, Kershaw C, Klesney-Tait J, Mageto Y, Shay JW, Ji W, Bilguvar K, Mane S, Lifton RP, Garcia CK. Stuart BD, et al. Nat Genet. 2015 May;47(5):512-7. doi: 10.1038/ng.3278. Epub 2015 Apr 13. Nat Genet. 2015. PMID: 25848748 Free PMC article.
Whole-Exome Sequencing in Adults With Chronic Kidney Disease: A Pilot Study.
Lata S, Marasa M, Li Y, Fasel DA, Groopman E, Jobanputra V, Rasouly H, Mitrotti A, Westland R, Verbitsky M, Nestor J, Slater LM, D'Agati V, Zaniew M, Materna-Kiryluk A, Lugani F, Caridi G, Rampoldi L, Mattoo A, Newton CA, Rao MK, Radhakrishnan J, Ahn W, Canetta PA, Bomback AS, Appel GB, Antignac C, Markowitz GS, Garcia CK, Kiryluk K, Sanna-Cherchi S, Gharavi AG. Lata S, et al. Ann Intern Med. 2018 Jan 16;168(2):100-109. doi: 10.7326/M17-1319. Epub 2017 Dec 5. Ann Intern Med. 2018. PMID: 29204651 Free PMC article.
Genetic interstitial lung disease.
Devine MS, Garcia CK. Devine MS, et al. Clin Chest Med. 2012 Mar;33(1):95-110. doi: 10.1016/j.ccm.2011.11.001. Epub 2011 Dec 6. Clin Chest Med. 2012. PMID: 22365249 Free PMC article. Review.
Pulmonary fibrosis in the era of stratified medicine.
Mathai SK, Newton CA, Schwartz DA, Garcia CK. Mathai SK, et al. Thorax. 2016 Dec;71(12):1154-1160. doi: 10.1136/thoraxjnl-2016-209172. Epub 2016 Oct 31. Thorax. 2016. PMID: 27799632 Free PMC article. Review.
Homozygous Rare PARN Missense Mutation in Familial Pulmonary Fibrosis.
Zhang D, Zhou Z, Abu-Hijleh M, Batra K, Xing C, Garcia CK. Zhang D, et al. Am J Respir Crit Care Med. 2019 Mar 15;199(6):797-799. doi: 10.1164/rccm.201809-1632LE. Am J Respir Crit Care Med. 2019. PMID: 30525901 Free PMC article. No abstract available.
34 results
You have reached the last page of results. A maximum of 10,000 results are available.
Jump to page