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2013 (6) 2012 (2) 2011 (3) 2010 (1) 2009 (3) 2008 (1)

2013

    Whole-Exome Sequencing of 2,000 Danish Individuals and the Role of Rare Coding Variants in Type 2 Diabetes
    Lohmueller KE, Sparsø T, Li Q, Andersson E, Korneliussen T, Albrechtsen A, Banasik K, Grarup N, Hallgrimsdottir I, Kiil K, Kilpeläinen TO, Krarup NT, Pers TH, Sanchez G, Hu Y, DeGiorgio M, Jørgensen T, Sandbæk A, Lauritzen T, Brunak S, Kristiansen K, Li Y, Hansen T, Wang J, Nielsen R, Pedersen O
    Am J Hum Genet. 2013 - AJHG, 2013
    AJHG
    Integrative Annotation of Variants from 1092 Humans: Application to Cancer Genomics
    Khurana E, Fu Y, Colonna V, Mu XJ, Kang HM, Lappalainen T, Sboner A, Lochovsky L, Chen J, Harmanci A, Das J, Abyzov A, Balasubramanian S, Beal K, Chakravarty D, Challis D, Chen Y, Clarke D, Clarke L, Cunningham F, Evani US, Flicek P, Fragoza R, Garrison E, Gibbs R, Gümü? ZH, Herrero J, Kitabayashi N, Kong Y, Lage K, Liluashvili V, Lipkin SM, MacArthur DG, Marth G, Muzny D, Pers TH, Ritchie GRS, Rosenfeld JA, Sisu C, Wei X, Wilson M, Xue Y, Yu F, Dermitzakis ET, Yu H, Rubin MA, Tyler-Smith C, Gerstein M
    Science, 2013
    Relevant URL
    Concordance of gene expression in human protein complexes reveals tissue specificity and pathology
    Börnigen D, Pers TH, Thorrez L, Huttenhower C, Moreau Y, Brunak S
    Nucleic Acids Res. 2013, 2013
    PubMed
    Relevant URL
    Meta-analysis of genome-wide association studies identifies ten loci influencing allergic sensitization
    Bønnelykke K, Matheson MC, Pers TH, Granell R, Strachan DP, Alves AC, Linneberg A, Curtin JA, Warrington NM, Standl M, Kerkhof M, Jonsdottir I, Bukvic BK, Kaakinen M, Sleimann P, Thorleifsson G, Thorsteinsdottir U, Schramm K, Baltic S, Kreiner-Møller E, Simpson A, St Pourcain B, Coin L, Hui J, Walters EH, Gupta R, et al
    Nature Genetics (2013), 2013
    Relevant URL
    MetaRanker 2.0: a web server for prioritization of genetic variation data
    Pers TH, Dworzynski P, Thomas C, Lage K, Brunak S
    Nucleic Acids Research, 2013
    Relevant URL
    Mutations in FGF17, IL17RD, DUSP6, SPRY4, and FLRT3 Are Identified in Individuals with Congenital Hypogonadotropic Hypogonadism.
    Miraoui H, Dwyer A, Sykiotis GP, Plummer L, Chung W, Feng B, Beenken A, Clarke J, Pers TH, Dworzynski P, Keefe K, Niedziela M, Raivio T, Crowley Jr WF, Seminara SB, Quinton R, Hughes VA, Kumanov P, Young J, Yialamas MA, Hall JE, Van Vliet G, Chanoine JP, Rubenstein J, Mohammadi M, Tsai PS, Sidis Y, Lage K, Pitteloud N
    Am J Hum Genet., 2013
    PubMed
    Relevant URL

2012

    Novel Microcephalic Primordial Dwarfism Disorder Associated with Variants in the Centrosomal Protein Ninein
    Dauber A, LaFranchi SH, Maliga Z, Lui JC, Moon JE, McDeed C, Henke K, Zonana J, Kingman GA, Pers TH, Baron J, Rosenfeld RG, Hirschhorn JN, Harris MP, Hwa V
    The Journal of Clinical Endocrinology & Metabolism August 29, 2012 jc.2012-2150, 2012
    A genome-wide association study of men with symptoms of testicular dysgenesis syndrome and its network biology interpretation.
    Dalgaard MD, Weinhold N, Edsgärd D, Silver JD, Pers TH, Nielsen JE, Jørgensen N, Juul A, Gerds TA, Giwercman A, Giwercman YL, Cohn-Cedermark G, Virtanen HE, Toppari J, Daugaard G, Jensen TS, Brunak S, Rajpert-De Meyts E, Skakkebæk NE, Leffers H, Gupta R
    Journal of Medical Genetics, 2012
    Relevant URL

2011

    A distinct adipose tissue gene expression response to caloric restriction predicts 6-mo weight maintenance in obese subjects
    Mutch DM, Pers TH, Temanni MR, Pelloux V, Marquez-Quiñones A, Holst C, Martinez JA, Babalis D, van Baak MA, Hanjieva-Darlenska T, Walker CG, Astrup A, Saris WHM, Langin D, Viguerie N, Zucker JD, Clément K, on behalf of the DiOGenes Project
    American Journal of Clinical Nutrition, 2011
    Relevant URL
    Protein Interaction-Based Genome-Wide Analysis of Incident Coronary Heart Disease
    Jensen MK, Pers TH, Dworzynski P, Girman CJ, Brunak S, Rimm EB
    Circulation Cardiovascular Genetics, 2011
    PubMed
    Relevant URL
    Meta-analysis of heterogeneous data sources for genome-scale identification of risk genes in complex phenotypes
    Pers TH, Hansen NT, Lage K, Koefoed P, Dworzynski P, Miller ML, Flint TJ, Mellerup E, Dam H, Andreassen OA, Djurovic S, Melle I, Børglum AD, Werge T, Purcell S, Ferreira MA, Kouskoumvekaki I, Workman CT, Hansen T, Mors O, Brunak S
    Genet Epidemiol, April 11, 2011
    PubMed

2010

    Metabolic network topology reveals transcriptional regulatory signatures of type 2 diabetes
    Zelezniak A, Pers TH, Soares S, Patti ME, Patil KR
    PLoS Comput Biol, 2010
    PubMed

2009

    The validation and assessment of machine learning: a game of prediction from high-dimensional data
    Pers TH, Albrechtsen A, Holst C, Sørensen TI, Gerds TA
    PLoS One;4(8):e6287, 2009
    PubMed
    Macrophages and Adipocytes in Human Obesity: Adipose Tissue Gene Expression and Insulin Sensitivity during Calorie Restriction and Weight Stabilization
    Capel F, Klimcáková E, Viguerie N, Roussel B, Vítková M, Kováciková M, Polák J, Kovácová Z, Galitzky J, Maoret JJ, Hanácek J, Pers TH, Bouloumié A, Stich V, Langin D
    Diabetes (in press), 2009
    PubMed
    Fatness-associated FTO gene variant increases mortality independent of fatness--in cohorts of Danish men
    Zimmermann E, Kring SI, Berentzen TL, Holst C, Pers TH, Hansen T, Pedersen O, Sørensen TI, Jess T
    PLoS ONE. 2009;4(2):e4428, 2009
    PubMed

2008

    Prediction of fat oxidation capacity using 1H-NMR and LC-MS lipid metabolomic data
    Pers TH, Martin FP, Verdich C, Holst C, Johansen JV, Astrup A, Polak J, Martinez JA, Rezzi S, Blaak EE, Saris WHM, Kochhar S, Macdonald IA, Sørensen TIA, Ramadan Z
    Chemometrics and Intelligent Laboratory Systems 93, 34–42, 2008

2013 (6) 2012 (2) 2011 (3) 2010 (1) 2009 (3) 2008 (1)