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Identification of functional DNA variants in the constitutive promoter region of MDM2
Marie-Eve Lalonde, Manon Ouimet, Mathieu Larivière, Ekaterini A Kritikou, Daniel Sinnett Human Genomics 2012, 6:15 (1 September 2012)
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Patterns of gene expression in microarrays and expressed sequence tags from normal and cataractous lenses
Konstantinos Sousounis, Panagiotis A Tsonis Human Genomics 2012, 6:14 (1 September 2012)
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Genetic mechanisms and age-related macular degeneration: common variants, rare variants, copy number variations, epigenetics, and mitochondrial genetics
Melissa M Liu, Chi-Chao Chan, Jingsheng Tuo Human Genomics 2012, 6:13 (31 August 2012)
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Genotype-phenotype associations in neurofibromatosis type 1 (NF1): an increased risk of tumor complications in patients with NF1 splice-site mutations?
Adila Alkindy, Nadia Chuzhanova, Usha Kini, David N Cooper, Meena Upadhyaya Human Genomics 2012, 6:12 (13 August 2012)
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CXCL5 polymorphisms are associated with variable blood pressure in cardiovascular disease-free adults
Amber L Beitelshees, Christina L Aquilante, Hooman Allayee, Taimour Y Langaee, Gregory J Welder, Richard S Schofield, Issam Zineh Human Genomics 2012, 6:9 (2 August 2012)
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Local sequence determinants of two in-frame triplet deletion/duplication hotspots in the RHD/RHCE genes
Jian-Min Chen, David N Cooper, Claude Férec Human Genomics 2012, 6:8 (2 August 2012)
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‘Sifting the significance from the data’ - the impact of high-throughput genomic technologies on human genetics and health care
Angus J Clarke, David N Cooper, Michael Krawczak, Chris Tyler-Smith, Helen M Wallace, Andrew O M Wilkie, Frances Raymond, Ruth Chadwick, Nick Craddock, Ros John, John Gallacher, Mathias Chiano Human Genomics 2012, 6:11 (2 August 2012)
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Conservation of the three-dimensional structure in non-homologous or unrelated proteins
Konstantinos Sousounis, Carl E Haney, Jin Cao, Bharath Sunchu, Panagiotis A Tsonis Human Genomics 2012, 6:10 (2 August 2012)
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GWIDD: a comprehensive resource for genome-wide structural modeling of protein-protein interactions
Petras J Kundrotas, Zhengwei Zhu, Ilya A Vakser Human Genomics 2012, 6:7 (11 July 2012)
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The human protein disulfide isomerase gene family
James J Galligan, Dennis R Petersen Human Genomics 2012, 6:6 (5 July 2012)
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SNPTrackTM : an integrated bioinformatics system for genetic association studies
Joshua Xu, Reagan Kelly, Guangxu Zhou, Steven A Turner, Don Ding, Stephen C Harris, Huixiao Hong, Hong Fang, Weida Tong Human Genomics 2012, 6:5 (5 July 2012)
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Gene family matters: expanding the HGNC resource
Louise C Daugherty, Ruth L Seal, Mathew W Wright, Elspeth A Bruford Human Genomics 2012, 6:4 (5 July 2012)
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Mitochondrial and nuclear genomics and the emergence of personalized medicine
Ryan L Parr, Luis H Martin Human Genomics 2012, 6:3 (5 July 2012)
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Estimating ancestral proportions in a multi-ethnic US sample: implications for studies of admixed populations
Orna Levran, Olaoluwakitan Awolesi, Pei-Hong Shen, Miriam Adelson, Mary Kreek Human Genomics 2012, 6:2 (5 July 2012)
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A new home for Human Genomics
Vasilis Vasiliou, Daniel W Nebert Human Genomics 2012, 6:1 (5 July 2012)
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In-silico human genomics with GeneCards
Gil Stelzer, Irina Dalah, Tsippi Stein, Yigeal Satanower, Naomi Rosen, Noam Nativ, Danit Oz-Levi, Tsviya Olender, Frida Belinky, Iris Bahir, Hagit Krug, Paul Perco, Bernd Mayer, Eugene Kolker, Marilyn Safran, Doron Lancet Human Genomics 2011, 5:709-717 (1 October 2011)
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Overview of biological database mapping services for interoperation between different 'omics' datasets
Shweta S Chavan, John D Shaughnessy, Ricky D Edmondson Human Genomics 2011, 5:703-708 (1 October 2011)
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Update of the human secretoglobin (SCGB) gene superfamily and an example of 'evolutionary bloom' of androgen-binding protein genes within the mouse Scgb gene superfamily
Brian C Jackson, David C Thompson, Mathew W Wright, Monica McAndrews, Alfred Bernard, Daniel W Nebert, Vasilis Vasiliou Human Genomics 2011, 5:691-702 (1 October 2011)
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Neurofibromatosis type 1-associated tumours: Their somatic mutational spectrum and pathogenesis
Sebastian Spyk, Nick Thomas, David N Cooper, Meena Upadhyaya Human Genomics 2011, 5:623-690 (1 October 2011)
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Human genetics and genomics a decade after the release of the draft sequence of the human genome
Nasheen Naidoo, Yudi Pawitan, Richie Soong, David N Cooper, Chee-Seng Ku Human Genomics 2011, 5:577-622 (1 October 2011)
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The role of ALDH2 and ADH1B polymorphism in alcohol consumption and stroke in Han Chinese
Chung-Tay Yao, Chun-An Cheng, Hsu-Kun Wang, Shao-Wen Chiu, Yi-Chyan Chen, Ming-Fang Wang, Shih-Jiun Yin, Giia-Sheun Peng Human Genomics 2011, 5:569-576 (1 October 2011)
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Systems biology-based analysis implicates a novel role for vitamin D metabolism in the pathogenesis of age-related macular degeneration
Margaux A Morrison, Alexandra C Silveira, Nancy Huynh, Gyungah Jun, Silvia E Smith, Fani Zacharaki, Hajime Sato, Stephanie Loomis, Michael T Andreoli, Scott M Adams, Monte J Radeke, Austin S Jelcick, Yang Yuan, Aristoteles N Tsiloulis, Dimitrios Z Chatzoulis, Giuliana Silvestri, Maria G Kotoula, Evangelia E Tsironi, Bruce W Hollis, Rui Chen, Neena B Haider, Joan W Miller, Lindsay A Farrer, Gregory S Hageman, Ivana K Kim, Debra A Schaumberg, Margaret M DeAngelis Human Genomics 2011, 5:538-568 (1 October 2011)
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Role of CYP2E1 genotypes in susceptibility to colorectal cancer in the Kashmiri population
A Sameer, Saniya Nissar, Qurteeba Qadri, Shafia Alam, Shahid Baba, Mushtaq A Siddiqi Human Genomics 2011, 5:530-537 (1 October 2011)
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Research Highlights
Robert I Scheinman Human Genomics 2011, 5:522-529 (1 October 2011)
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Visionary genomics
J Petrash, Philip A Ruzycki, Gregory J Zablocki Human Genomics 2011, 5:519-521 (1 October 2011)
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