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Items: 22


De novo repeat interruptions are associated with reduced somatic instability and mild or absent clinical features in myotonic dystrophy type 1.

Cumming SA, Hamilton MJ, Robb Y, Gregory H, McWilliam C, Cooper A, Adam B, McGhie J, Hamilton G, Herzyk P, Tschannen MR, Worthey E, Petty R, Ballantyne B; Scottish Myotonic Dystrophy Consortium, Warner J, Farrugia ME, Longman C, Monckton DG.

Eur J Hum Genet. 2018 Nov;26(11):1635-1647. doi: 10.1038/s41431-018-0156-9. Epub 2018 Jul 2.


Improving Process Quality by Means of Accurate and Traceable Calibration of Flow Devices with Process-oriented Liquids.

Bissig H, Tschannen M, de Huu M.

Chimia (Aarau). 2018 Mar 30;72(3):124-129. doi: 10.2533/chimia.2018.124.


Clinical heterogeneity of mitochondrial NAD kinase deficiency caused by a NADK2 start loss variant.

Pomerantz DJ, Ferdinandusse S, Cogan J, Cooper DN, Reimschisel T, Robertson A, Bican A, McGregor T, Gauthier J, Millington DS, Andrae JLW, Tschannen MR, Helbling DC, Demos WM, Denis S, Wanders RJA, Newman JN, Hamid R, Phillips JA 3rd; Collaborators of UDN.

Am J Med Genet A. 2018 Mar;176(3):692-698. doi: 10.1002/ajmg.a.38602. Epub 2018 Feb 1. Review.


Genetic Fine-Mapping and Identification of Candidate Genes and Variants for Adiposity Traits in Outbred Rats.

Keele GR, Prokop JW, He H, Holl K, Littrell J, Deal A, Francic S, Cui L, Gatti DM, Broman KW, Tschannen M, Tsaih SW, Zagloul M, Kim Y, Baur B, Fox J, Robinson M, Levy S, Flister MJ, Mott R, Valdar W, Solberg Woods LC.

Obesity (Silver Spring). 2018 Jan;26(1):213-222. doi: 10.1002/oby.22075. Epub 2017 Nov 28.


Plasma exosomal miRNAs-based prognosis in metastatic kidney cancer.

Du M, Giridhar KV, Tian Y, Tschannen MR, Zhu J, Huang CC, Kilari D, Kohli M, Wang L.

Oncotarget. 2017 Jul 22;8(38):63703-63714. doi: 10.18632/oncotarget.19476. eCollection 2017 Sep 8.


Thaumatin and gum arabic allergy in chewing gum factory workers.

Tschannen MP, Glück U, Bircher AJ, Heijnen I, Pletscher C.

Am J Ind Med. 2017 Jul;60(7):664-669. doi: 10.1002/ajim.22729. Epub 2017 May 24.


Regression forest-based automatic estimation of the articular margin plane for shoulder prosthesis planning.

Tschannen M, Vlachopoulos L, Gerber C, Székely G, Fürnstahl P.

Med Image Anal. 2016 Jul;31:88-97. doi: 10.1016/ Epub 2016 Mar 3.


Plasma genetic and genomic abnormalities predict treatment response and clinical outcome in advanced prostate cancer.

Xia S, Kohli M, Du M, Dittmar RL, Lee A, Nandy D, Yuan T, Guo Y, Wang Y, Tschannen MR, Worthey E, Jacob H, See W, Kilari D, Wang X, Hovey RL, Huang CC, Wang L.

Oncotarget. 2015 Jun 30;6(18):16411-21.


Identification of a novel gene for diabetic traits in rats, mice, and humans.

Tsaih SW, Holl K, Jia S, Kaldunski M, Tschannen M, He H, Andrae JW, Li SH, Stoddard A, Wiederhold A, Parrington J, Ruas da Silva M, Galione A, Meigs J; Meta-Analyses of Glucose and Insulin-Related Traits Consortium (MAGIC) Investigators, Hoffmann RG, Simpson P, Jacob H, Hessner M, Solberg Woods LC.

Genetics. 2014 Sep;198(1):17-29. doi: 10.1534/genetics.114.162982.


Prostate cancer risk locus at 8q24 as a regulatory hub by physical interactions with multiple genomic loci across the genome.

Du M, Yuan T, Schilter KF, Dittmar RL, Mackinnon A, Huang X, Tschannen M, Worthey E, Jacob H, Xia S, Gao J, Tillmans L, Lu Y, Liu P, Thibodeau SN, Wang L.

Hum Mol Genet. 2015 Jan 1;24(1):154-66. doi: 10.1093/hmg/ddu426. Epub 2014 Aug 22.


A learning-based approach for fast and robust vessel tracking in long ultrasound sequences.

De Luca V, Tschannen M, Székely G, Tanner C.

Med Image Comput Comput Assist Interv. 2013;16(Pt 1):518-25.


IreB, a Ser/Thr kinase substrate, influences antimicrobial resistance in Enterococcus faecalis.

Hall CL, Tschannen M, Worthey EA, Kristich CJ.

Antimicrob Agents Chemother. 2013 Dec;57(12):6179-86. doi: 10.1128/AAC.01472-13. Epub 2013 Sep 30.


Genome sequencing reveals loci under artificial selection that underlie disease phenotypes in the laboratory rat.

Atanur SS, Diaz AG, Maratou K, Sarkis A, Rotival M, Game L, Tschannen MR, Kaisaki PJ, Otto GW, Ma MC, Keane TM, Hummel O, Saar K, Chen W, Guryev V, Gopalakrishnan K, Garrett MR, Joe B, Citterio L, Bianchi G, McBride M, Dominiczak A, Adams DJ, Serikawa T, Flicek P, Cuppen E, Hubner N, Petretto E, Gauguier D, Kwitek A, Jacob H, Aitman TJ.

Cell. 2013 Aug 1;154(3):691-703. doi: 10.1016/j.cell.2013.06.040. Epub 2013 Jul 25.


Genomics in clinical practice: lessons from the front lines.

Jacob HJ, Abrams K, Bick DP, Brodie K, Dimmock DP, Farrell M, Geurts J, Harris J, Helbling D, Joers BJ, Kliegman R, Kowalski G, Lazar J, Margolis DA, North P, Northup J, Roquemore-Goins A, Scharer G, Shimoyama M, Strong K, Taylor B, Tsaih SW, Tschannen MR, Veith RL, Wendt-Andrae J, Wilk B, Worthey EA.

Sci Transl Med. 2013 Jul 17;5(194):194cm5. doi: 10.1126/scitranslmed.3006468.


Characterization of human plasma-derived exosomal RNAs by deep sequencing.

Huang X, Yuan T, Tschannen M, Sun Z, Jacob H, Du M, Liang M, Dittmar RL, Liu Y, Liang M, Kohli M, Thibodeau SN, Boardman L, Wang L.

BMC Genomics. 2013 May 10;14:319. doi: 10.1186/1471-2164-14-319.


Identification of somatic mutations in non-small cell lung carcinomas using whole-exome sequencing.

Liu P, Morrison C, Wang L, Xiong D, Vedell P, Cui P, Hua X, Ding F, Lu Y, James M, Ebben JD, Xu H, Adjei AA, Head K, Andrae JW, Tschannen MR, Jacob H, Pan J, Zhang Q, Van den Bergh F, Xiao H, Lo KC, Patel J, Richmond T, Watt MA, Albert T, Selzer R, Anderson M, Wang J, Wang Y, Starnes S, Yang P, You M.

Carcinogenesis. 2012 Jul;33(7):1270-6. doi: 10.1093/carcin/bgs148. Epub 2012 Apr 17.


Making a definitive diagnosis: successful clinical application of whole exome sequencing in a child with intractable inflammatory bowel disease.

Worthey EA, Mayer AN, Syverson GD, Helbling D, Bonacci BB, Decker B, Serpe JM, Dasu T, Tschannen MR, Veith RL, Basehore MJ, Broeckel U, Tomita-Mitchell A, Arca MJ, Casper JT, Margolis DA, Bick DP, Hessner MJ, Routes JM, Verbsky JW, Jacob HJ, Dimmock DP.

Genet Med. 2011 Mar;13(3):255-62. doi: 10.1097/GIM.0b013e3182088158.


Fine-mapping a locus for glucose tolerance using heterogeneous stock rats.

Solberg Woods LC, Holl K, Tschannen M, Valdar W.

Physiol Genomics. 2010 Mar 3;41(1):102-8. doi: 10.1152/physiolgenomics.00178.2009. Epub 2010 Jan 12.


Genetically hypertensive Brown Norway congenic rat strains suggest intermediate traits underlying genetic hypertension.

Bilusić M, Moreno C, Barreto NE, Tschannen MR, Harris EL, Porteous WK, Thompson CM, Grigor MR, Weder A, Boerwinkle E, Hunt SC, Curb JD, Jacob HJ, Kwitek AE.

Croat Med J. 2008 Oct;49(5):586-99.


Effects of chromosome 17 on features of the metabolic syndrome in the Lyon hypertensive rat.

Gilibert S, Kwitek AE, Hubner N, Tschannen M, Jacob HJ, Sassard J, Bataillard A.

Physiol Genomics. 2008 Apr 22;33(2):212-7. doi: 10.1152/physiolgenomics.00262.2007. Epub 2008 Feb 19.


Mapping the genetic determinants of hypertension, metabolic diseases, and related phenotypes in the lyon hypertensive rat.

Bilusic M, Bataillard A, Tschannen MR, Gao L, Barreto NE, Vincent M, Wang T, Jacob HJ, Sassard J, Kwitek AE.

Hypertension. 2004 Nov;44(5):695-701. Epub 2004 Sep 27.


Utilization of a labeled tracking oligonucleotide for visualization and quality control of spotted 70-mer arrays.

Hessner MJ, Singh VK, Wang X, Khan S, Tschannen MR, Zahrt TC.

BMC Genomics. 2004 Feb 9;5(1):12.

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