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European Journal of Human Genetics : EJHG|December 24, 2015
Expansion of the spectrum of ITGB6-related disorders to adolescent alopecia, dentogingival abnormalities and intellectual disabilityMuhammad Ansar, Abid Jan, Regie Lyn P Santos-Cortez, et al.Science Translational Medicine|June 8, 2012
Noninvasive whole-genome sequencing of a human fetusJacob O Kitzman, Matthew W Snyder, Mario Ventura, et al.International Journal of Dermatology|November 19, 2015
Novel mutations in the genes TGM1 and ALOXE3 underlying autosomal recessive congenital ichthyosisRahim Ullah, Muhammad Ansar, Zaka Ullah Durrani, et al.Nature|August 25, 2022
Embryo model completes gastrulation to neurulation and organogenesisGianluca Amadei, Charlotte E Handford, Chengxiang Qiu, et al.Nature|January 15, 2025
Massively parallel characterization of transcriptional regulatory elementsVikram Agarwal, Fumitaka Inoue, Max Schubach, et al.Plos Genetics|June 13, 2020
Elevated exopolysaccharide levels in Pseudomonas aeruginosa flagellar mutants have implications for biofilm growth and chronic infectionsJoe J Harrison, Henrik Almblad, Yasuhiko Irie, et al.Nature Genetics|May 17, 2011
Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutationsBrian J O'Roak, Pelagia Deriziotis, Choli Lee, et al.Nature Protocols|July 10, 2020
lentiMPRA and MPRAflow for high-throughput functional characterization of gene regulatory elementsM Grace Gordon, Fumitaka Inoue, Beth Martin, et al.Circulation Research|July 23, 2011
Exome sequencing identifies SMAD3 mutations as a cause of familial thoracic aortic aneurysm and dissection with intracranial and other arterial aneurysmsEllen S Regalado, Dong-Chuan Guo, Carlos Villamizar, et al.Influenza and Other Respiratory Viruses|January 7, 2023
Results from a test-and-treat study for influenza among residents of homeless shelters in King County, WA: A stepped-wedge cluster-randomized trialJulia H Rogers, Amanda M Casto, Gift Nwanne, et al.Pageof 43