Exome sequencing links mutations in PARN and RTEL1 with familial pulmonary fibrosis and telomere shortening

An Official ATS/ERS/JRS/ALAT Statement: Idiopathic Pulmonary Fibrosis: Evidence-based Guidelines for Diagnosis and Management

Ganesh Raghu, Harold R. Collard, Jim Egan et al. · American Journal of Respiratory and Critical Care Medicine · 2011 · 7.3K citations · Full text

Medicine, Clinical Sciences, Internal Medicine +17

A second generation human haplotype map of over 3.1 million SNPs

Sarah S. Murray, Todd A. Johnson · Nature · 2007 · 4.6K citations · Full text

Life Sciences, Genetics, Molecular Genetics +11

An Official American Thoracic Society/European Respiratory Society Statement: Update of the International Multidisciplinary Classification of the Idiopathic Interstitial Pneumonias

William D. Travis, Ulrich Costabel, David M. Hansell et al. · American Journal of Respiratory and Critical Care Medicine · 2013 · 4.3K citations · Full text

Medicine, Internal Medicine, Pathology +14

De novo mutations revealed by whole-exome sequencing are strongly associated with autism

Stephan Sanders, Michael T. Murtha, Abha R. Gupta et al. · Nature · 2012 · 2.2K citations

Life Sciences, Genetics, Molecular Genetics +12

De Novo Gene Disruptions in Children on the Autistic Spectrum

Ivan Iossifov, Michael Ronemus, Dan Levy et al. · Neuron · 2012 · 1.5K citations · Full text

Life Sciences, Genetics, Molecular Genetics +14