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Plos One|March 13, 2008
Association analysis of the FTO gene with obesity in children of Caucasian and African ancestry reveals a common tagging SNPStruan F A Grant, Mingyao Li, Jonathan P Bradfield, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 3, 2024
Secondary ACMG and non-ACMG genetic findings in a multiethnic cohort of 16,713 pediatric participantsAmir Hossein Saeidian, Michael E March, Leila Youssefian, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|October 11, 2013
Functional maturation of the executive system during adolescenceTheodore D Satterthwaite, Daniel H Wolf, Guray Erus, et al.
Human Molecular Genetics|January 4, 2015
Mutation in mitochondrial ribosomal protein S7 (MRPS7) causes congenital sensorineural deafness, progressive hepatic and renal failure and lactic acidemiaMinal J Menezes, Yiran Guo, Jianguo Zhang, et al.
Nature Communications|January 9, 2021
Lossless integration of multiple electronic health records for identifying pleiotropy using summary statisticsRuowang Li, Rui Duan, Xinyuan Zhang, et al.
Molecular Genetics and Metabolism|March 14, 2020
Homozygous splice-variants in human ARV1 cause GPI-anchor synthesis deficiencyMariska Davids, Minal Menezes, Yiran Guo, et al.
JCO Precision Oncology|August 7, 2025
Implementation of DPYD and UGT1A1 Testing in Patients With GI Cancer: A Prospective, Nonrandomized Clinical TrialSony Tuteja, Mari Angelica S Cayabyab, Glenda Hoffecker, et al.
Plos One|July 22, 2015
Application of Whole Exome Sequencing in Six Families with an Initial Diagnosis of Autosomal Dominant Retinitis Pigmentosa: Lessons LearnedBerta Almoguera, Jiankang Li, Patricia Fernandez-San Jose, et al.
The Journal of Thoracic and Cardiovascular Surgery|December 26, 2015
Burden of potentially pathologic copy number variants is higher in children with isolated congenital heart disease and significantly impairs covariate-adjusted transplant-free survivalDaniel Seung Kim, Jerry H Kim, Amber A Burt, et al.
Human Molecular Genetics|June 19, 2019
Cross-disorder analysis of schizophrenia and 19 immune-mediated diseases identifies shared genetic riskJennie G Pouget, , Buhm Han, et al.
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