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JAMA|July 14, 2015
Noninvasive Prenatal Testing and Incidental Detection of Occult Maternal MalignanciesDiana W Bianchi, Darya Chudova, Amy J Sehnert, et al.Obstetrics and Gynecology|January 9, 2015
Fetal sex chromosome testing by maternal plasma DNA sequencing: clinical laboratory experience and biologyDiana W Bianchi, Saba Parsa, Sucheta Bhatt, et al.Science Translational Medicine|September 1, 2017
Rare autosomal trisomies, revealed by maternal plasma DNA sequencing, suggest increased risk of feto-placental diseaseMark D Pertile, Meredith Halks-Miller, Nicola Flowers, et al.Personalized Medicine|May 20, 2018
Potential clinical utility of gene-expression profiling in identifying tumors of uncertain originMarianne Laouri, Meredith Halks-Miller, W David Henner, et al.Bioinformatics (Oxford, England)|September 24, 2009
Bayesian detection of non-sinusoidal periodic patterns in circadian expression dataDarya Chudova, Alexander Ihler, Kevin K Lin, et al.Proceedings of the National Academy of Sciences of the United States of America|November 3, 2004
Identification of hair cycle-associated genes from time-course gene expression profile data by using replicate varianceKevin K Lin, Darya Chudova, G Wesley Hatfield, et al.Trends in Molecular Medicine|June 27, 2021
Function Follows Form: Gene Expression and Prenatal ScreeningDiana W BianchiPrenatal Diagnosis|December 24, 2016
Should we 'open the kimono' to release the results of rare autosomal aneuploidies following noninvasive prenatal whole genome sequencing?Diana W BianchiNature Medicine|July 10, 2012
From prenatal genomic diagnosis to fetal personalized medicine: progress and challengesDiana W BianchiBest Practice & Research. Clinical Obstetrics & Gynaecology|December 8, 2004
Fetomaternal cell traffic, pregnancy-associated progenitor cells, and autoimmune diseaseDiana W BianchiPageof 22