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

Year Number of Results
1992 1
1993 1
1994 2
1995 2
1996 1
1997 3
1998 4
2000 1
2004 1
2005 1
2006 3
2007 3
2008 4
2009 6
2010 2
2011 4
2012 2
2013 1
2014 2
2015 4
2016 1
2017 2
2018 3
2019 3
2020 2
2021 3
2022 3
2023 6
2024 2

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69 results

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Page 1
The Genetic Landscape of Familial Pulmonary Fibrosis.
Liu Q, Zhou Y, Cogan JD, Mitchell DB, Sheng Q, Zhao S, Bai Y, Ciombor KK, Sabusap CM, Malabanan MM, Markin CR, Douglas K, Ding G, Banovich NE, Nickerson DA, Blue EE, Bamshad MJ, Brown KK, Schwartz DA, Phillips JA 3rd, Martinez-Barricarte R, Salisbury ML, Shyr Y, Loyd JE, Kropski JA, Blackwell TS. Liu Q, et al. Among authors: cogan jd. Am J Respir Crit Care Med. 2023 May 15;207(10):1345-1357. doi: 10.1164/rccm.202204-0781OC. Am J Respir Crit Care Med. 2023. PMID: 36622818
Heterozygous rare variants in NR2F2 cause a recognizable multiple congenital anomaly syndrome with developmental delays.
Ganapathi M, Matsuoka LS, March M, Li D, Brokamp E, Benito-Sanz S, White SM, Lachlan K, Ahimaz P, Sewda A, Bastarache L, Thomas-Wilson A, Stoler JM, Bramswig NC, Baptista J, Stals K, Demurger F, Cogne B, Isidor B, Bedeschi MF, Peron A, Amiel J, Zackai E, Schacht JP, Iglesias AD, Morton J, Schmetz A; Undiagnosed Diseases Network; Seidel V, Lucia S, Baskin SM, Thiffault I, Cogan JD, Gordon CT, Chung WK, Bowdin S, Bhoj E. Ganapathi M, et al. Among authors: cogan jd. Eur J Hum Genet. 2023 Oct;31(10):1117-1124. doi: 10.1038/s41431-023-01434-5. Epub 2023 Jul 27. Eur J Hum Genet. 2023. PMID: 37500725
Phenotypic heterogeneity of ZMPSTE24 deficiency.
Cassini TA, Robertson AK, Bican AG, Cogan JD, Hannig VL, Newman JH, Hamid R, Phillips JA 3rd; Undiagnosed Diseases Network. Cassini TA, et al. Among authors: cogan jd. Am J Med Genet A. 2018 May;176(5):1175-1179. doi: 10.1002/ajmg.a.38493. Epub 2018 Jan 17. Am J Med Genet A. 2018. PMID: 29341437 Free PMC article.
Low-grade albuminuria in pulmonary arterial hypertension.
Nickel NP, de Jesus Perez VA, Zamanian RT, Fessel JP, Cogan JD, Hamid R, West JD, de Caestecker MP, Yang H, Austin ED. Nickel NP, et al. Among authors: cogan jd. Pulm Circ. 2019 Apr-Jun;9(2):2045894018824564. doi: 10.1177/2045894018824564. Pulm Circ. 2019. PMID: 30632900 Free PMC article.
Probable digenic inheritance of Diamond-Blackfan anemia.
Furuta Y, Tinker RJ, Gulsevin A, Neumann SM, Hamid R, Cogan JD, Rives L, Liu Q, Chen HC, Joos KM, Phillips JA 3rd; Undiagnosed Diseases Network. Furuta Y, et al. Among authors: cogan jd. Am J Med Genet A. 2024 Mar;194(3):e63454. doi: 10.1002/ajmg.a.63454. Epub 2023 Oct 27. Am J Med Genet A. 2024. PMID: 37897121
GH1 gene deletions and IGHD type 1A.
Cogan JD, Phillips JA 3rd. Cogan JD, et al. Pediatr Endocrinol Rev. 2006 Aug;3 Suppl 3:480-8. Pediatr Endocrinol Rev. 2006. PMID: 17551470 Review.
Peripheral Blood Telomere Attrition in Persons at Risk for Familial Pulmonary Fibrosis.
Salisbury ML, Markin CR, Wu P, Cogan JD, Mitchell DB, Liu Q, Loyd JE, Lancaster LH, Kropski JA, Blackwell TS. Salisbury ML, et al. Among authors: cogan jd. Am J Respir Crit Care Med. 2023 Jan 15;207(2):208-211. doi: 10.1164/rccm.202204-0766LE. Am J Respir Crit Care Med. 2023. PMID: 36036734 Free PMC article. No abstract available.
The Association between Exposures and Disease Characteristics in Familial Pulmonary Fibrosis.
Copeland CR, Donnelly EF, Mehrad M, Ding G, Markin CR, Douglas K, Wu P, Cogan JD, Young LR, Bartholmai BJ, Martinez FJ, Flaherty KR, Loyd JE, Lancaster LH, Kropski JA, Blackwell TS, Salisbury ML. Copeland CR, et al. Among authors: cogan jd. Ann Am Thorac Soc. 2022 Dec;19(12):2003-2012. doi: 10.1513/AnnalsATS.202203-267OC. Ann Am Thorac Soc. 2022. PMID: 35877079 Free PMC article.
69 results