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Human Genomics|December 19, 2012
CXCL5 polymorphisms are associated with variable blood pressure in cardiovascular disease-free adultsAmber L Beitelshees, Christina L Aquilante, Hooman Allayee, et al.Human Genomics|December 4, 2012
16th Carbonyl Metabolism Meeting: from enzymology to genomicsEdmund MaserHuman Genomics|November 1, 2013
Update of the human and mouse SERPIN gene superfamilyClaire Heit, Brian C Jackson, Monica McAndrews, et al.Human Genomics|December 14, 2011
In-silico human genomics with GeneCardsGil Stelzer, Irina Dalah, Tsippi Iny Stein, et al.Human Genomics|October 22, 2013
CER1 gene variations associated with bone mineral density, bone markers, and early menopause in postmenopausal womenTheodora Koromila, Panagiotis Georgoulias, Zoe Dailiana, et al.Human Genomics|July 29, 2015
Epigenetic inheritance and the missing heritabilityMarco Trerotola, Valeria Relli, Pasquale Simeone, et al.Human Genomics|August 31, 2017
Falling giants and the rise of gene editing: ethics, private interests and the public goodBenjamin Capps, Ruth Chadwick, Yann Joly, et al.Human Genomics|November 8, 2017
Identification of a novel genetic locus underlying tremor and dystoniaDorota Monies, Hussam Abou Al-Shaar, Ewa A Goljan, et al.Human Genomics|November 11, 2017
Single nucleotide polymorphisms in the angiogenic and lymphangiogenic pathways are associated with lymphedema caused by Wuchereria bancroftiLinda Batsa Debrah, Anna Albers, Alexander Yaw Debrah, et al.Human Genomics|October 25, 2017
Whole transcriptome analysis of human erythropoietic cells during ontogenesis suggests a role of VEGFA gene as modulator of fetal hemoglobin and pharmacogenomic biomarker of treatment response to hydroxyurea in β-type hemoglobinopathy patientsVasiliki Chondrou, Petros Kolovos, Argyro Sgourou, et al.Pageof 112