Submissions from 2010
Rare ATGL Haplotypes Are Associated with Increased Plasma Triglyceride Concentrations in the Greenland Inuit, Christopher T. Johansen, Zane R. Gallinger, Jian Wang, Matthew R. Ban, T. Kue Young, Peter Bjerregaard, and Robert A. Hegele
Translating Genomic Analyses into Improved Management of Coronary Artery Disease, Christopher T. Johansen, Matthew B. Lanktree, and Robert A. Hegele
Excess of Rare Variants in Genes Identified by Genome-wide Association Study of Hypertriglyceridemia, Christopher T. Johansen, Jian Wang, Matthew B. Lanktree, Henian Cao, Adam D. McIntyre, Matthew R. Ban, Rebecca A. Martins, Brooke A. Kennedy, Reina G. Hassell, Maartje E. Visser, Stephen M. Schwartz, Benjamin F. Voight, Roberto Elosua, Veikko Salomaa, Christopher J. O'Donnell, Geesje M. Dallinga-Thie, Sonia S. Anand, Salim Yusuf, Murray W. Huff, Sekar Kathiresan, and Robert A. Hegele
In Vivo Detection of PARACEST Agents with Relaxation Correction, Craig K. Jones, Alex X. Li, Mojmír Suchý, Robert H. E. Hudson, Ravi S. Menon, and Robert Bartha
Loops Govern SH2 Domain Specificity by Controlling Access to Binding Pockets, Tomonori Kaneko, Haiming Huang, Bing Zhao, Lei Li, Huadong Liu, Courtney K. Voss, Chenggang Wu, Martin R. Schiller, and Shawn Shun-Cheng Li
Mammalian Numb-interacting Protein 1/Dual Oxidase Maturation Factor 1 Directs Neuronal Fate in Stem Cells, Karen A. M. Kennedy, Elena A. Ostrakhovitch, Shelley D. E. Sandiford, Thamara Dayarathna, Xiaojun Xie, Elaine Y. L. Waese, Wing Y. Chang, Qingping Feng, Ilona S. Skerjanc, William L. Stanford, and Shawn S. C. Li
ATRX Partners with Cohesin and MeCP2 and Contributes to Developmental Silencing of Imprinted Genes in the Brain, Kristin D. Kernohan, Yan Jiang, Deanna C. Tremblay, Anne C. Bonvissuto, James H. Eubanks, Mellissa R. W. Mann, and Nathalie G. Bérubé
A Unified Genetic, Computational and Experimental Framework Identifies Functionally Relevant Residues of the Homing Endonuclease I-BmoI, Benjamin P. Kleinstiver, Andrew D. Fernandes, Gregory B. Gloor, and David R. Edgell
Laminar Flow Effects During Laser-Induced Oxidative Labeling for Protein Structural Studies by Mass Spectrometry, Lars Konermann, Bradley B. Stocks, and Tomasz Czarny
Mass Spectrometry Combined with Oxidative Labeling for Exploring Protein Structure and Folding, Lars Konermann, Bradley B. Stocks, Yan Pan, and Xin Tong
Toenail Selenium Status and DNA Repair Capacity among Female BRCA1 Mutation Carriers, Joanne Kotsopoulos, Zhou Chen, Katherine A. Vallis, Aletta Poll, Parviz Ghadirian, Greg Kennedy, Peter Ainsworth, and Steven A. Narod
APOC1 T45S Polymorphism Is Associated with Reduced Obesity Indices and Lower Plasma Concentrations of Leptin and Apolipoprotein C-I in Aboriginal Canadians, Piya Lahiry, Henian Cao, Matthew R. Ban, Rebecca L. Pollex, Mary Mamakeesick, Bernard Zinman, Stewart B. Harris, Anthony J. G. Hanley, Murray W. Huff, Philip W. Connelly, and Robert A. Hegele
Kinase Mutations in Human Disease: Interpreting Genotype-phenotype Relationships, Piya Lahiry, Ali Torkamani, Nicholas J. Schork, and Robert A. Hegele
Comprehensive Analysis of Genomic Variation in the LPA Locus and Its Relationship to Plasma Lipoprotein(a) in South Asians, Chinese, and European Caucasians, Matthew B. Lanktree, Sonia S. Anand, Salim Yusuf, Robert A. Hegele, and SHARE Investigators
Advances in Genomic Analysis of Stroke: What Have We Learned and Where Are We Headed?, Matthew B. Lanktree, Martin Dichgans, and Robert A. Hegele
Phenomics: Expanding the Role of Clinical Evaluation in Genomic Studies, Matthew B. Lanktree, Reina G. Hassell, Piya Lahiry, and Robert A. Hegele
Extremes of Unexplained Variation as a Phenotype: An Efficient Approach for Genome-Wide Association Studies of Cardiovascular Disease, Matthew B. Lanktree, Robert A. Hegele, Nicholas J. Schork, and J. David Spence
Genetic Variation in Hyaluronan Metabolism Loci Is Associated with Plasma Plasminogen Activator Inhibitor-1 Concentration, Matthew B. Lanktree, Christopher T. Johansen, Sonia S. Anand, A. Darlene Davis, Ruby Miller, Salim Yusuf, Robert A. Hegele, SHARE, and SHARE-AP Investigators
A Translational View of the Genetics of Lipodystrophy and Ectopic Fat Deposition, Matthew B. Lanktree, Christopher T. Johansen, Tisha R. Joy, and Robert A. Hegele
Association of Apolipoprotein B with Incident Type 2 Diabetes in an Aboriginal Canadian Population, Sylvia H. Ley, Stewart B. Harris, Philip W. Connelly, Mary Mamakeesick, Joel Gittelsohn, Thomas M. Wolever, Robert A. Hegele, Bernard Zinman, and Anthony J. Hanley
Assessing the Association of the HNF1A G319S Variant with C-reactive Protein in Aboriginal Canadians: A Population-based Epidemiological Study, Sylvia H. Ley, Robert A. Hegele, Philip W. Connelly, Stewart B. Harris, Mary Mamakeesick, Henian Cao, Joel Gittelsohn, Ravi Retnakaran, Bernard Zinman, and Anthony J. Hanley
Nerve Growth Factor Activation of the TrkA Receptor Induces Cell Death, by Macropinocytosis, in Medulloblastoma Daoy Cells, Chunhui Li, James I. S. Macdonald, Todd Hryciw, and Susan O. Meakin
Systematic Identification of Methyllysine-Driven Interactions for Histone and Nonhistone Targets, Huadong Liu, Marek Galka, Aimee Iberg, Zezhou Wang, Lei Li, Courtney Voss, Xinfeng Jiang, Gilles Lajoie, Zhiping Huang, Mark T. Bedford, and Shawn S. C. Li
Temtamy Preaxial Brachydactyly Syndrome Is Caused by Loss-of-Function Mutations in Chondroitin Synthase 1, a Potential Target of BMP Signaling, Yun Li, Kathrin Laue, Samia Temtamy, Mona Aglan, L. Damla Kotan, Gökhan Yigit, Husniye Canan, Barbara Pawlik, Gudrun Nürnberg, Emma L. Wakeling, Oliver W. Quarrell, Ingelore Baessmann, Matthew B. Lanktree, Mustafa Yilmaz, Robert A. Hegele, Khalda Amr, Klaus W. May, Peter Nürnberg, A. Kemal Topaloglu, Matthias Hammerschmidt, and Bernd Wollnik
Independent Mechanisms of Stimulation of Polynucleotide Kinase/Phosphatase by Phosphorylated and Non-phosphorylated XRCC1, Meiling Lu, Rajam S. Mani, Feridoun Karimi-Busheri, Mesfin Fanta, Hailin Wang, David W. Litchfeld, and Michael Weinfeld