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The Journal of Clinical Endocrinology and Metabolism|March 31, 2005
Detection of Turner syndrome using high-throughput quantitative genotypingHaiying Meng, Karl Hager, Scott A Rivkees, et al.
Leukemia Research Reports|February 2, 2026
Leukocytosis and a JAK2 mutation: The importance of expertise in somatic variant interpretationChristian J Puzo, Karl Hager, Michal Rose, et al.
The Journal of Clinical Endocrinology and Metabolism|December 24, 2010
A highly sensitive, high-throughput assay for the detection of Turner syndromeScott A Rivkees, Karl Hager, Seiyu Hosono, et al.
International Journal of Pediatric Endocrinology|April 25, 2012
Molecular diagnostic testing for Klinefelter syndrome and other male sex chromosome aneuploidiesKarl Hager, Kori Jennings, Seiyu Hosono, et al.
Human Genetics|September 1, 2005
TDT-association analysis of EKN1 and dyslexia in a Colorado twin cohortHaiying Meng, Karl Hager, Matthew Held, et al.
Frontiers in Immunology|December 5, 2019
Norovirus Changes Susceptibility to Type 1 Diabetes by Altering Intestinal Microbiota and Immune Cell FunctionsJames A Pearson, Ningwen Tai, Dilrukshi K Ekanayake-Alper, et al.
Neuroimage|July 4, 2012
Variants in the DYX2 locus are associated with altered brain activation in reading-related brain regions in subjects with reading disabilityNatalie Cope, John D Eicher, Haiying Meng, et al.
Leukemia & Lymphoma|May 5, 2020
Clinical outcomes and characteristics of patients with TP53-mutated acute myeloid leukemia or myelodysplastic syndromes: a single center experienceJan Philipp Bewersdorf, Rory M Shallis, Lohith Gowda, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 10, 2005
DCDC2 is associated with reading disability and modulates neuronal development in the brainHaiying Meng, Shelley D Smith, Karl Hager, et al.
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