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Prenatal Diagnosis|October 26, 2018
Reliable detection of subchromosomal deletions and duplications using cell-based noninvasive prenatal testingLiesbeth Vossaert, Qun Wang, Roseen Salman, et al.
The Journal of Biological Chemistry|July 16, 2010
Proinflammatory role for let-7 microRNAS in experimental asthmaSumanth Polikepahad, John M Knight, Arash O Naghavi, et al.
Genome Medicine|July 28, 2019
A clinical survey of mosaic single nucleotide variants in disease-causing genes detected by exome sequencingYe Cao, Mari J Tokita, Edward S Chen, et al.
Circulation|May 3, 2012
Human genome-wide association and mouse knockout approaches identify platelet supervillin as an inhibitor of thrombus formation under shear stressLeonard C Edelstein, Elizabeth J Luna, Ian B Gibson, et al.
Blood Cells, Molecules & Diseases|July 30, 2018
Effects of genetic variation in protease activated receptor 4 after an acute coronary syndrome: Analysis from the TRACER trialPierluigi Tricoci, Megan Neely, Michael J Whitley, et al.
Human Molecular Genetics|March 28, 2009
Complex rearrangements in patients with duplications of MECP2 can occur by fork stalling and template switchingClaudia M B Carvalho, Feng Zhang, Pengfei Liu, et al.
European Journal of Human Genetics : EJHG|May 23, 2013
Combined array CGH plus SNP genome analyses in a single assay for optimized clinical testingJoanna Wiszniewska, Weimin Bi, Chad Shaw, et al.
American Journal of Human Genetics|March 16, 2007
Characterization of Potocki-Lupski syndrome (dup(17)(p11.2p11.2)) and delineation of a dosage-sensitive critical interval that can convey an autism phenotypeLorraine Potocki, Weimin Bi, Diane Treadwell-Deering, et al.
Neoplasia (New York, N.Y.)|July 14, 2014
Pathway-centric integrative analysis identifies RRM2 as a prognostic marker in breast cancer associated with poor survival and tamoxifen resistanceNagireddy Putluri, Suman Maity, Ramakrishna Kommagani, et al.
Nucleic Acids Research|December 17, 2016
Homozygous and hemizygous CNV detection from exome sequencing data in a Mendelian disease cohortTomasz Gambin, Zeynep C Akdemir, Bo Yuan, et al.
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