Associated Papers
Shared genetic architecture of hernias: A genome-wide association study with multivariable meta-analysis of multiple hernia phenotypes.
Ahmed WU et al.
Plos One, 2022
36584111 (PubMed )
Supplement: pone.0272261.s016.pdf
Deleterious variants in genes regulating mammalian reproduction in Neanderthals, Denisovans and extant humans.
Greer C et al.
Human Reproduction (oxford, England), 2021
33417716 (PubMed )
Supplement: deaa347_supplementary_data.zip › Suppl_Table_SV_Neand_Shared_Extinct_Revised.pdf
Dissecting Mechanisms of Melanoma Resistance to BRAF and MEK Inhibitors Revealed Genetic and Non-Genetic Patient- and Drug-Specific Alterations and Remarkable Phenotypic Plasticity.
Hartman ML et al.
Cells, 2020
31936151 (PubMed )
Supplement: cells-09-00142-s001.pdf
Whole-exome sequencing reveals novel genetic variants associated with diverse phenotypes of melanoma cells.
Hartman ML et al.
Molecular Carcinogenesis, 2019
Dual-specificity phosphatase 6 genetic variants associated with risk of lung squamous cell carcinoma in Han Chinese.
Wang TL et al.
Journal of Cancer Research and Therapeutics, 2018
Protein tyrosine phosphatase variants in human hereditary disorders and disease susceptibilities.
Hendriks WJ et al.
Biochimica Et Biophysica Acta, 2013
The genetic association of DUSP6 with bipolar disorder and its effect on ERK activity.
Kim SH et al.
Progress in Neuro-psychopharmacology & Biological Psychiatry, 2012
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