Format
Sort by
Items per page

Send to

Choose Destination

Search results

Items: 32

1.

Disease pattern in Danish patients with Peutz-Jeghers syndrome.

Jelsig AM, Qvist N, Sunde L, Brusgaard K, Hansen T, Wikman FP, Nielsen CB, Nielsen IK, Gerdes AM, Bojesen A, Ousager LB.

Int J Colorectal Dis. 2016 May;31(5):997-1004. doi: 10.1007/s00384-016-2560-3. Epub 2016 Mar 15.

PMID:
26979979
2.

A Novel Locus Harbouring a Functional CD164 Nonsense Mutation Identified in a Large Danish Family with Nonsyndromic Hearing Impairment.

Nyegaard M, Rendtorff ND, Nielsen MS, Corydon TJ, Demontis D, Starnawska A, Hedemand A, Buniello A, Niola F, Overgaard MT, Leal SM, Ahmad W, Wikman FP, Petersen KB, Crüger DG, Oostrik J, Kremer H, Tommerup N, Frödin M, Steel KP, Tranebjærg L, Børglum AD.

PLoS Genet. 2015 Jul 21;11(7):e1005386. doi: 10.1371/journal.pgen.1005386. eCollection 2015 Jul.

3.

[Juvenile polyposis syndrome and hereditary haemorrhagic telangiectasia syndrome in a patient a with SMAD4 mutation].

Jelsig AM, Tørring PM, Wikman F, Mortensen MB, Qvist N, Ousager LB.

Ugeskr Laeger. 2014 Oct 27;176(44). pii: V06130392. Danish.

PMID:
25354002
4.

Functional examination of MLH1, MSH2, and MSH6 intronic mutations identified in Danish colorectal cancer patients.

Petersen SM, Dandanell M, Rasmussen LJ, Gerdes AM, Krogh LN, Bernstein I, Okkels H, Wikman F, Nielsen FC, Hansen TV.

BMC Med Genet. 2013 Oct 3;14:103. doi: 10.1186/1471-2350-14-103.

5.

Biomedical informatics as support to individual healthcare in hereditary colon cancer: the Danish HNPCC system.

Bernstein IT, Lindorff-Larsen K, Timshel S, Brandt CA, Dinesen B, Fenger M, Gerdes AM, Iversen LH, Madsen MR, Okkels H, Sunde L, Rahr HB, Wikman FP, Rossing N.

Hum Mutat. 2011 May;32(5):551-6. doi: 10.1002/humu.21435. Epub 2011 Feb 22.

PMID:
21520332
6.

Frequent genomic loss at chr16p13.2 is associated with poor prognosis in colorectal cancer.

Andersen CL, Lamy P, Thorsen K, Kjeldsen E, Wikman F, Villesen P, Øster B, Laurberg S, Ørntoft TF.

Int J Cancer. 2011 Oct 15;129(8):1848-58. doi: 10.1002/ijc.25841. Epub 2011 Mar 11.

7.

Leiden Open Variation Database of the MUTYH gene.

Out AA, Tops CM, Nielsen M, Weiss MM, van Minderhout IJ, Fokkema IF, Buisine MP, Claes K, Colas C, Fodde R, Fostira F, Franken PF, Gaustadnes M, Heinimann K, Hodgson SV, Hogervorst FB, Holinski-Feder E, Lagerstedt-Robinson K, Olschwang S, van den Ouweland AM, Redeker EJ, Scott RJ, Vankeirsbilck B, Grønlund RV, Wijnen JT, Wikman FP, Aretz S, Sampson JR, Devilee P, den Dunnen JT, Hes FJ.

Hum Mutat. 2010 Nov;31(11):1205-15. doi: 10.1002/humu.21343.

PMID:
20725929
8.

Functional characterization of rare missense mutations in MLH1 and MSH2 identified in Danish colorectal cancer patients.

Christensen LL, Kariola R, Korhonen MK, Wikman FP, Sunde L, Gerdes AM, Okkels H, Brandt CA, Bernstein I, Hansen TV, Hagemann-Madsen R, Andersen CL, Nyström M, Ørntoft TF.

Fam Cancer. 2009;8(4):489-500. doi: 10.1007/s10689-009-9274-4. Epub 2009 Aug 21.

PMID:
19697156
9.

Major contribution from recurrent alterations and MSH6 mutations in the Danish Lynch syndrome population.

Nilbert M, Wikman FP, Hansen TV, Krarup HB, Orntoft TF, Nielsen FC, Sunde L, Gerdes AM, Cruger D, Timshel S, Bisgaard ML, Bernstein I, Okkels H.

Fam Cancer. 2009;8(1):75-83. doi: 10.1007/s10689-008-9199-3. Epub 2008 Jun 20.

PMID:
18566915
10.

The association between genetic variants in hMLH1 and hMSH2 and the development of sporadic colorectal cancer in the Danish population.

Christensen LL, Madsen BE, Wikman FP, Wiuf C, Koed K, Tjønneland A, Olsen A, Syvänen AC, Andersen CL, Orntoft TF.

BMC Med Genet. 2008 Jun 11;9:52. doi: 10.1186/1471-2350-9-52.

11.

BRCA1 and BRCA2 mutations in Danish families with hereditary breast and/or ovarian cancer.

Thomassen M, Hansen TV, Borg A, Lianee HT, Wikman F, Pedersen IS, Bisgaard ML, Nielsen FC, Kruse TA, Gerdes AM.

Acta Oncol. 2008;47(4):772-7. doi: 10.1080/02841860802004974.

PMID:
18465347
12.

A genome-wide linkage search for bipolar disorder susceptibility loci in a large and complex pedigree from the eastern part of Cuba.

Marcheco-Teruel B, Flint TJ, Wikman FP, Torralbas M, González L, Blanco L, Tan Q, Ewald H, Orntoft T, Kruse TA, Børglum AD, Mors O.

Am J Med Genet B Neuropsychiatr Genet. 2006 Dec 5;141B(8):833-43.

PMID:
16917938
13.

Genotyping and annotation of Affymetrix SNP arrays.

Lamy P, Andersen CL, Wikman FP, Wiuf C.

Nucleic Acids Res. 2006;34(14):e100. Epub 2006 Aug 9.

14.

Gene expression signatures for colorectal cancer microsatellite status and HNPCC.

Kruhøffer M, Jensen JL, Laiho P, Dyrskjøt L, Salovaara R, Arango D, Birkenkamp-Demtroder K, Sørensen FB, Christensen LL, Buhl L, Mecklin JP, Järvinen H, Thykjaer T, Wikman FP, Bech-Knudsen F, Juhola M, Nupponen NN, Laurberg S, Andersen CL, Aaltonen LA, Ørntoft TF.

Br J Cancer. 2005 Jun 20;92(12):2240-8.

15.

Presymptomatic diagnosis using a deletion of a single codon in families with hereditary non-polyposis colorectal cancer.

Ripa RS, Katballe N, Wikman FP, Jäger AC, Bernstein I, Orntoft T, Schwartz M, Nielsen FC, Bisgaard ML.

Mutat Res. 2005 Feb 15;570(1):89-96.

PMID:
15680406
16.

High-density single nucleotide polymorphism array defines novel stage and location-dependent allelic imbalances in human bladder tumors.

Koed K, Wiuf C, Christensen LL, Wikman FP, Zieger K, Møller K, von der Maase H, Orntoft TF.

Cancer Res. 2005 Jan 1;65(1):34-45.

17.

A genome-wide search for risk genes using homozygosity mapping and microarrays with 1,494 single-nucleotide polymorphisms in 22 eastern Cuban families with bipolar disorder.

Ewald H, Wikman FP, Teruel BM, Buttenschön HN, Torralba M, Als TD, El Daoud A, Flint TJ, Jorgensen TH, Blanco L, Kruse TA, Orntoft TF, Mors O.

Am J Med Genet B Neuropsychiatr Genet. 2005 Feb 5;133B(1):25-30.

PMID:
15558715
18.

EXO1 variants occur commonly in normal population: evidence against a role in hereditary nonpolyposis colorectal cancer.

Jagmohan-Changur S, Poikonen T, Vilkki S, Launonen V, Wikman F, Orntoft TF, Møller P, Vasen H, Tops C, Kolodner RD, Mecklin JP, Järvinen H, Bevan S, Houlston RS, Aaltonen LA, Fodde R, Wijnen J, Karhu A.

Cancer Res. 2003 Jan 1;63(1):154-8.

19.

Antibody-based screening for hereditary nonpolyposis colorectal carcinoma compared with microsatellite analysis and sequencing.

Christensen M, Katballe N, Wikman F, Primdahl H, Sørensen FB, Laurberg S, Ørntoft TF.

Cancer. 2002 Dec 1;95(11):2422-30.

20.

Neural network predicts sequence of TP53 gene based on DNA chip.

Spicker JS, Wikman F, Lu ML, Cordon-Cardo C, Workman C, ØRntoft TF, Brunak S, Knudsen S.

Bioinformatics. 2002 Aug;18(8):1133-4.

PMID:
12176837
21.

Allelic imbalances in human bladder cancer: genome-wide detection with high-density single-nucleotide polymorphism arrays.

Primdahl H, Wikman FP, von der Maase H, Zhou XG, Wolf H, Orntoft TF.

J Natl Cancer Inst. 2002 Feb 6;94(3):216-23.

PMID:
11830611
22.

Impact of alterations affecting the p53 pathway in bladder cancer on clinical outcome, assessed by conventional and array-based methods.

Lu ML, Wikman F, Orntoft TF, Charytonowicz E, Rabbani F, Zhang Z, Dalbagni G, Pohar KS, Yu G, Cordon-Cardo C.

Clin Cancer Res. 2002 Jan;8(1):171-9.

23.

Frequency of hereditary non-polyposis colorectal cancer in Danish colorectal cancer patients.

Katballe N, Christensen M, Wikman FP, Ørntoft TF, Laurberg S.

Gut. 2002 Jan;50(1):43-51.

24.

Patient accuracy of reporting on hereditary non-polyposis colorectal cancer-related malignancy in family members.

Katballe N, Juul S, Christensen M, Ørntoft TF, Wikman FP, Laurberg S.

Br J Surg. 2001 Sep;88(9):1228-33.

PMID:
11531872
25.

Role of chance in familial aggregation of colorectal cancer.

Katballe N, Bentzen SM, Christensen M, Wikman FP, Ørntoft T, Laurberg S.

Br J Cancer. 2001 Apr 20;84(8):1084-6.

26.

Evaluation of the performance of a p53 sequencing microarray chip using 140 previously sequenced bladder tumor samples.

Wikman FP, Lu ML, Thykjaer T, Olesen SH, Andersen LD, Cordon-Cardo C, Orntoft TF.

Clin Chem. 2000 Oct;46(10):1555-61.

27.
28.
29.

Crosslinking of elongation factor Tu to tRNA(Phe) by trans-diamminedichloroplatinum (II). Characterization of two crosslinking sites in the tRNA.

Wikman FP, Romby P, Metz MH, Reinbolt J, Clark BF, Ebel JP, Ehresmann C, Ehresmann B.

Nucleic Acids Res. 1987 Jul 24;15(14):5787-801.

30.

Interaction between initiator Met-tRNAfMet and elongation factor EF-Tu from E. coli.

Hansen PK, Wikman F, Clark BF, Hershey JW, Uffe Petersen H.

Biochimie. 1986 May;68(5):697-703.

PMID:
2425855
31.

Different conformations of tRNA in the ribosomal P-site and A-site.

Jørgensen T, Siboska GE, Wikman FP, Clark BF.

Eur J Biochem. 1985 Nov 15;153(1):203-9.

32.

The site of interaction of aminoacyl-tRNA with elongation factor Tu.

Wikman FP, Siboska GE, Petersen HU, Clark BF.

EMBO J. 1982;1(9):1095-100.

Supplemental Content

Loading ...
Support Center