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Neuron|June 11, 2011
Rare de novo and transmitted copy-number variation in autistic spectrum disordersDan Levy, Michael Ronemus, Boris Yamrom, et al.
Communications Biology|September 2, 2021
Rates of contributory de novo mutation in high and low-risk autism familiesSeungtai Yoon, Adriana Munoz, Boris Yamrom, et al.
Human Genetics|August 28, 2013
The contribution of de novo and rare inherited copy number changes to congenital heart disease in an unselected sample of children with conotruncal defects or hypoplastic left heart diseaseDorothy Warburton, Michael Ronemus, Jennie Kline, et al.
Genome Research|November 16, 2019
Copolymerization of single-cell nucleic acids into balls of acrylamide gelSiran Li, Jude Kendall, Sarah Park, et al.
NPJ Genomic Medicine|October 10, 2025
A ciliopathy combining Joubert syndrome and Oro-Facial-Digital syndrome caused by bi-allelic 5'-UTR loss-of-function CEP83 variantMatan M Jean, Anan Yunis, Tzofit Elbaz-Biton, et al.
The European Respiratory Journal|October 30, 2020
Validation of Lung EpiCheck, a novel methylation-based blood assay, for the detection of lung cancer in European and Chinese high-risk individualsMina Gaga, Joanna Chorostowska-Wynimko, Ildikó Horváth, et al.
Toxicological Sciences : an Official Journal of the Society of Toxicology|August 9, 2011
The safety and regulation of natural products used as foods and food ingredientsAli Abdel-Rahman, Njwen Anyangwe, Louis Carlacci, et al.
Rheumatology (Oxford, England)|May 11, 2021
Significance of Sjögren's syndrome and anti-cN1A antibody in myositis patientsDan Levy, Benoit Nespola, Margherita Giannini, et al.
Rheumatology (Oxford, England)|August 12, 2020
Refining myositis associated with primary Sjögren's syndrome: data from the prospective cohort ASSESSRenaud Felten, Margherita Giannini, Benoit Nespola, et al.
Genome Biology|September 27, 2025
Hybrid BAG-seq: DNA and RNA from the same single nucleus reveals interactions between genomic and transcriptomic landscapes in human tumor samplesSiran Li, Joan Alexander, Jude Kendall, et al.
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