DeMeo DL - Search Results

1

Genetic variation in genes regulating skeletal muscle regeneration and tissue remodelling associated with weight loss in chronic obstructive pulmonary disease.

Lakshman Kumar P, Wilson AC, Rocco A, Cho MH, Wan E, Hobbs BD, Washko GR, Ortega VE, Christenson SA, Li X, Wells JM, Bhatt SP, DeMeo DL, Lutz SM, Rossiter H, Casaburi R, Rennard SI, Lomas DA, Labaki WW, Tal-Singer R, Bowler RP, Hersh CP, Tiwari HK, Dransfield M, Thalacker-Mercer A, Meyers DA, Silverman EK, McDonald MN; COPDGene, ECLIPSE and SPIROMICS investigators. Lakshman Kumar P, et al. Among authors: demeo dl. J Cachexia Sarcopenia Muscle. 2021 Dec;12(6):1803-1817. doi: 10.1002/jcsm.12782. Epub 2021 Sep 15. J Cachexia Sarcopenia Muscle. 2021. PMID: 34523824 Free PMC article.

2

Univariate and multivariate family-based association analysis of the IL-13 ARG130GLN polymorphism in the Childhood Asthma Management Program.

DeMeo DL, Lange C, Silverman EK, Senter JM, Drazen JM, Barth MJ, Laird N, Weiss ST. DeMeo DL, et al. Genet Epidemiol. 2002 Nov;23(4):335-48. doi: 10.1002/gepi.10182. Genet Epidemiol. 2002. PMID: 12432502

3

Using the noninformative families in family-based association tests: a powerful new testing strategy.

Lange C, DeMeo D, Silverman EK, Weiss ST, Laird NM. Lange C, et al. Am J Hum Genet. 2003 Oct;73(4):801-11. doi: 10.1086/378591. Epub 2003 Sep 18. Am J Hum Genet. 2003. PMID: 14502464 Free PMC article.

4

A new powerful non-parametric two-stage approach for testing multiple phenotypes in family-based association studies.

Lange C, Lyon H, DeMeo D, Raby B, Silverman EK, Weiss ST. Lange C, et al. Hum Hered. 2003;56(1-3):10-7. doi: 10.1159/000073728. Hum Hered. 2003. PMID: 14614234

5

PBAT: tools for family-based association studies.

Lange C, DeMeo D, Silverman EK, Weiss ST, Laird NM. Lange C, et al. Am J Hum Genet. 2004 Feb;74(2):367-9. doi: 10.1086/381563. Am J Hum Genet. 2004. PMID: 14740322 Free PMC article. No abstract available.

6

Alpha1-antitrypsin deficiency. 2: genetic aspects of alpha(1)-antitrypsin deficiency: phenotypes and genetic modifiers of emphysema risk.

DeMeo DL, Silverman EK. DeMeo DL, et al. Thorax. 2004 Mar;59(3):259-64. doi: 10.1136/thx.2003.006502. Thorax. 2004. PMID: 14985567 Free PMC article. Review.

7

Familial aggregation of FEF(25-75) and FEF(25-75)/FVC in families with severe, early onset COPD.

DeMeo DL, Carey VJ, Chapman HA, Reilly JJ, Ginns LC, Speizer FE, Weiss ST, Silverman EK. DeMeo DL, et al. Thorax. 2004 May;59(5):396-400. doi: 10.1136/thx.2003.012856. Thorax. 2004. PMID: 15115866 Free PMC article.

8

The transforming growth factor-beta1 (TGFB1) gene is associated with chronic obstructive pulmonary disease (COPD).

Celedón JC, Lange C, Raby BA, Litonjua AA, Palmer LJ, DeMeo DL, Reilly JJ, Kwiatkowski DJ, Chapman HA, Laird N, Sylvia JS, Hernandez M, Speizer FE, Weiss ST, Silverman EK. Celedón JC, et al. Among authors: demeo dl. Hum Mol Genet. 2004 Aug 1;13(15):1649-56. doi: 10.1093/hmg/ddh171. Epub 2004 Jun 2. Hum Mol Genet. 2004. PMID: 15175276

9

Genome-wide linkage of forced mid-expiratory flow in chronic obstructive pulmonary disease.

DeMeo DL, Celedón JC, Lange C, Reilly JJ, Chapman HA, Sylvia JS, Speizer FE, Weiss ST, Silverman EK. DeMeo DL, et al. Am J Respir Crit Care Med. 2004 Dec 15;170(12):1294-301. doi: 10.1164/rccm.200404-524OC. Epub 2004 Sep 3. Am J Respir Crit Care Med. 2004. PMID: 15347563

10

Smoke and mirrors: Mouse models as a reflection of human chronic obstructive pulmonary disease.

Shapiro SD, Demeo DL, Silverman EK. Shapiro SD, et al. Among authors: demeo dl. Am J Respir Crit Care Med. 2004 Nov 1;170(9):929-31. doi: 10.1164/rccm.2408007. Am J Respir Crit Care Med. 2004. PMID: 15504815 No abstract available.

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