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Nature|February 9, 2023
Polygenic architecture of rare coding variation across 394,783 exomesDaniel J Weiner, Ajay Nadig, Karthik A Jagadeesh, et al.
Genome Research|May 30, 2023
Discordant calls across genotype discovery approaches elucidate variants with systematic errorsElizabeth G Atkinson, Mykyta Artomov, Alexander A Loboda, et al.
Epilepsia|February 16, 2022
Potential role of regulatory DNA variants in modifying the risk of severe cutaneous reactions induced by aromatic anti-seizure medicationsKerry A Mullan, Alison Anderson, Yi-Wu Shi, et al.
Psychological Medicine|December 12, 2023
Dynamic structure-function coupling across three major psychiatric disordersZhe Zhang, Wei Wei, Sujie Wang, et al.
Genome Research|June 3, 2018
Base-specific mutational intolerance near splice sites clarifies the role of nonessential splice nucleotidesSidi Zhang, Kaitlin E Samocha, Manuel A Rivas, et al.
Behavior Genetics|January 31, 2016
Tspyl2 Loss-of-Function Causes Neurodevelopmental Brain and Behavior Abnormalities in MiceQi Li, Siu Yuen Chan, Kwun K Wong, et al.
European Heart Journal|July 8, 2008
Epidermal fatty-acid-binding protein: a new circulating biomarker associated with cardio-metabolic risk factors and carotid atherosclerosisDennis C Y Yeung, Yu Wang, Aimin Xu, et al.
Plos One|June 10, 2010
Haplotype analysis reveals a possible founder effect of RET mutation R114H for Hirschsprung's disease in the Chinese populationBelinda K Cornes, Clara S Tang, Thomas Y Y Leon, et al.
Nucleic Acids Research|May 9, 2017
mTCTScan: a comprehensive platform for annotation and prioritization of mutations affecting drug sensitivity in cancersMulin Jun Li, Hongcheng Yao, Dandan Huang, et al.
Circulation|March 29, 2007
Circulating adipocyte-fatty acid binding protein levels predict the development of the metabolic syndrome: a 5-year prospective studyAimin Xu, Annette W K Tso, Bernard M Y Cheung, et al.
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