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Human Genomics|July 2, 2014
Ranking non-synonymous single nucleotide polymorphisms based on disease conceptsHashem A Shihab, Julian Gough, Matthew Mort, et al.Human Genomics|July 1, 2020
Novel biallelic loss-of-function variants in CEP290 cause Joubert syndrome in two siblingsXiang Wang, Zhu Zhang, Xueguang Zhang, et al.Human Genomics|April 18, 2015
Evaluation of copy number variation and gene expression in neurofibromatosis type-1-associated malignant peripheral nerve sheath tumoursLaura E Thomas, Jincy Winston, Ellie Rad, et al.Human Genomics|May 18, 2023
Genetic mutations in HER2-positive breast cancer: possible association with response to trastuzumab therapyNermine H Zakaria, Doaa Hashad, Marwa H Saied, et al.Human Genomics|November 20, 2012
6th Golden Helix Pharmacogenomics Day: pharmacogenomics and individualized therapyMaja Stojiljkovic, Amira Fazlagic, Lidija Dokmanovic-Krivokapic, et al.Human Genomics|November 20, 2012
Collaborative software for traditional and translational researchAri E Berman, William K Barnett, Sean D MooneyHuman Genomics|November 20, 2012
An emerging role for microRNAs in NF1 tumorigenesisAshni Sedani, David N Cooper, Meena UpadhyayaHuman Genomics|July 10, 2020
Human genetics and genomics meetings going virtual: practical lessons learned from two international meetings in early 2020Alistair R R Forrest, Gabriela M Repetto, Juergen K V ReichardtHuman Genomics|November 11, 2022
Placing human gene families into their evolutionary contextAlex Dornburg, Rittika Mallik, Zheng Wang, et al.Human Genomics|February 21, 2023
Neurofibromatosis-Noonan syndrome and growth deficiency in an Iranian girl due to a pathogenic variant in NF1 geneSetila Dalili, Seyyedeh Azade Hoseini Nouri, Reza Bayat, et al.Pageof 111