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Nature Communications|January 17, 2017
Massively parallel digital transcriptional profiling of single cellsGrace X Y Zheng, Jessica M Terry, Phillip Belgrader, et al.
Nature|August 9, 2023
Lactate limits CNS autoimmunity by stabilizing HIF-1α in dendritic cellsLiliana M Sanmarco, Joseph M Rone, Carolina M Polonio, et al.
Genes|August 29, 2024
A Genotype/Phenotype Study of KDM5B-Associated Disorders Suggests a Pathogenic Effect of Dominantly Inherited Missense VariantsMaria Carla Borroto, Coralie Michaud, Chloé Hudon, et al.
BMJ (Clinical Research Ed.)|August 19, 2017
Estimates of burden and consequences of infants born small for gestational age in low and middle income countries with INTERGROWTH-21st standard: analysis of CHERG datasetsAnne Cc Lee, Naoko Kozuki, Simon Cousens, et al.
American Journal of Human Genetics|February 17, 2015
De novo mutations in NALCN cause a syndrome characterized by congenital contractures of the limbs and face, hypotonia, and developmental delayJessica X Chong, Margaret J McMillin, Kathryn M Shively, et al.
Genome Biology|March 21, 2014
Decoding the massive genome of loblolly pine using haploid DNA and novel assembly strategiesDavid B Neale, Jill L Wegrzyn, Kristian A Stevens, et al.
Journal of Clinical Microbiology|October 27, 2021
Performance Characteristics of the Abbott BinaxNOW SARS-CoV-2 Antigen Test in Comparison to Real-Time Reverse Transcriptase PCR and Viral Culture in Community Testing Sites during November 2020Olivia Almendares, Jessica L Prince-Guerra, Leisha D Nolen, et al.
American Journal of Medical Genetics. Part A|July 16, 2026
Heterozygous RNF13 Truncating Variants Are Associated With Developmental and Epileptic EncephalopathyDonald R Latner, Susan M Hiatt, Candice R Finnila, et al.
MMWR. Morbidity and Mortality Weekly Report|January 21, 2021
Evaluation of Abbott BinaxNOW Rapid Antigen Test for SARS-CoV-2 Infection at Two Community-Based Testing Sites - Pima County, Arizona, November 3-17, 2020Jessica L Prince-Guerra, Olivia Almendares, Leisha D Nolen, et al.
American Journal of Human Genetics|June 30, 2015
Recurrent Mutations in the Basic Domain of TWIST2 Cause Ablepharon Macrostomia and Barber-Say SyndromesShannon Marchegiani, Taylor Davis, Federico Tessadori, et al.
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