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Nature Communications|April 16, 2015
Increased prevalence of EPAS1 variant in cattle with high-altitude pulmonary hypertensionJohn H Newman, Timothy N Holt, Joy D Cogan, et al.
Public Health Genomics|May 21, 2026
Sex-Based Disparities in Fabry Disease Cause Challenges in Newborn ScreeningYutaka Furuta, Neena S Agrawal, Natalie N Owen, et al.
Public Health Genomics|February 17, 2026
Sex-Specific Diagnostic Inequality in Fabry Disease: Lessons Learned from Analysis of Newborn Screening and Cascade Testing in Tennessee from 2017 to 2024Yutaka Furuta, Neena S Agrawal, Natalie N Owen, et al.
Human Genetics|January 20, 2021
Genetics of agenesis/hypoplasia of the uterus and vagina: narrowing down the number of candidate genes for Mayer-Rokitansky-Küster-Hauser SyndromeSasha Mikhael, Sonal Dugar, Madison Morton, et al.
The New England Journal of Medicine|March 30, 2007
Telomerase mutations in families with idiopathic pulmonary fibrosisMary Y Armanios, Julian J-L Chen, Joy D Cogan, et al.
Experimental Lung Research|March 8, 2012
Telomerase deficiency does not alter bleomycin-induced fibrosis in miceAmber L Degryse, Xiaochuan C Xu, J Luke Newman, et al.
American Journal of Respiratory and Critical Care Medicine|August 20, 2005
Clinical and pathologic features of familial interstitial pneumoniaMark P Steele, Marcy C Speer, James E Loyd, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 30, 2008
Short telomeres are a risk factor for idiopathic pulmonary fibrosisJonathan K Alder, Julian J-L Chen, Lisa Lancaster, et al.
Journal of the American College of Cardiology|June 15, 2004
Genetic basis of pulmonary arterial hypertension: current understanding and future directionsJohn H Newman, Richard C Trembath, Jane A Morse, et al.
American Journal of Medical Genetics. Part A|February 9, 2012
Phenotypic variability in hyperphosphatasia with seizures and neurologic deficit (Mabry syndrome)Miles D Thompson, Tony Roscioli, Carlo Marcelis, et al.
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