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G3 (Bethesda, Md.)|September 19, 2015
Whole-Genome Sequencing Suggests Schizophrenia Risk Mechanisms in Humans with 22q11.2 Deletion SyndromeDaniele Merico, Mehdi Zarrei, Gregory Costain, et al.Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|September 5, 2008
Immunohistochemical level of unsulfated chondroitin disaccharides in the cancer stroma is an independent predictor of prostate cancer relapseAndrew J Sakko, Miriam S Butler, Sharon Byers, et al.NPJ Genomic Medicine|March 28, 2026
A novel phenotype-guided genome analysis pipeline for variant discoveryLayla Ahmed, Erika Tavares, Janice Min Li, et al.Neurobiology of Aging|June 3, 2017
Functional neuroanatomy of speech signal decoding in primary progressive aphasiasChris J D Hardy, Jennifer L Agustus, Charles R Marshall, et al.Journal of Medical Genetics|September 17, 2009
Phenotypic spectrum associated with de novo and inherited deletions and duplications at 16p11.2 in individuals ascertained for diagnosis of autism spectrum disorderBridget A Fernandez, Wendy Roberts, Brian Chung, et al.Nature Chemistry|December 31, 2020
Screening and characterization of a diverse panel of metagenomic imine reductases for biocatalytic reductive aminationJames R Marshall, Peiyuan Yao, Sarah L Montgomery, et al.The Journal of Infectious Diseases|July 12, 2012
Serologic reactivity to the emerging pathogen Granulibacter bethesdensisDavid E Greenberg, Adam R Shoffner, Kimberly R Marshall-Batty, et al.Frontiers in Immunology|September 11, 2025
Reliable genetic diagnosis of NCF1 (p47phox)-deficient chronic granulomatous disease using high-throughput sequencingAmy P Hsu, Eric Karlins, Justin Lack, et al.HGG Advances|April 25, 2024
A systematic assessment of the impact of rare canonical splice site variants on splicing using functional and in silico methodsRachel Y Oh, Ali AlMail, David Cheerie, et al.Nature Immunology|April 26, 2016
Tcf1 and Lef1 transcription factors establish CD8(+) T cell identity through intrinsic HDAC activityShaojun Xing, Fengyin Li, Zhouhao Zeng, et al.Pageof 201