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Items: 31

1.

Search for Early Pancreatic Cancer Blood Biomarkers in Five European Prospective Population Biobanks Using Metabolomics.

Fest J, Vijfhuizen LS, Goeman JJ, Veth O, Joensuu A, Perola M, Männistö S, Ness-Jensen E, Hveem K, Haller T, Tonisson N, Mikkel K, Metspalu A, van Duijn CM, Ikram A, Stricker BH, Ruiter R, van Eijck CHJ, van Ommen GB, ʼt Hoen PAC.

Endocrinology. 2019 Jul 1;160(7):1731-1742. doi: 10.1210/en.2019-00165.

2.

Role of Academic Biobanks in Public-Private Partnerships in the European Biobanking and BioMolecular Resources Research Infrastructure Community.

Hämäläinen I, Törnwall O, Simell B, Zatloukal K, Perola M, van Ommen GB.

Biopreserv Biobank. 2019;17(1):46-51. doi: 10.1089/bio.2018.0024. Epub 2018 Nov 30.

PMID:
30499696
3.

Enhancing Reuse of Data and Biological Material in Medical Research: From FAIR to FAIR-Health.

Holub P, Kohlmayer F, Prasser F, Mayrhofer MT, Schlünder I, Martin GM, Casati S, Koumakis L, Wutte A, Kozera Ł, Strapagiel D, Anton G, Zanetti G, Sezerman OU, Mendy M, Valík D, Lavitrano M, Dagher G, Zatloukal K, van Ommen GB, Litton JE.

Biopreserv Biobank. 2018 Apr;16(2):97-105. doi: 10.1089/bio.2017.0110. Epub 2018 Jan 23. Review.

4.

Effect of post-mortem delay on N-terminal huntingtin protein fragments in human control and Huntington disease brain lysates.

Schut MH, Patassini S, Kim EH, Bullock J, Waldvogel HJ, Faull RLM, Pepers BA, den Dunnen JT, van Ommen GB, van Roon-Mom WMC.

PLoS One. 2017 Jun 1;12(6):e0178556. doi: 10.1371/journal.pone.0178556. eCollection 2017.

5.

Huntington's disease blood and brain show a common gene expression pattern and share an immune signature with Alzheimer's disease.

Hensman Moss DJ, Flower MD, Lo KK, Miller JR, van Ommen GB, 't Hoen PA, Stone TC, Guinee A, Langbehn DR, Jones L, Plagnol V, van Roon-Mom WM, Holmans P, Tabrizi SJ.

Sci Rep. 2017 Mar 21;7:44849. doi: 10.1038/srep44849.

6.

25 years of the EJHG!

van Ommen GB.

Eur J Hum Genet. 2016 Jan;25(1):1. doi: 10.1038/ejhg.2016.167. No abstract available.

7.

A high-quality human reference panel reveals the complexity and distribution of genomic structural variants.

Hehir-Kwa JY, Marschall T, Kloosterman WP, Francioli LC, Baaijens JA, Dijkstra LJ, Abdellaoui A, Koval V, Thung DT, Wardenaar R, Renkens I, Coe BP, Deelen P, de Ligt J, Lameijer EW, van Dijk F, Hormozdiari F; Genome of the Netherlands Consortium, Uitterlinden AG, van Duijn CM, Eichler EE, de Bakker PI, Swertz MA, Wijmenga C, van Ommen GB, Slagboom PE, Boomsma DI, Schönhuth A, Ye K, Guryev V.

Nat Commun. 2016 Oct 6;7:12989. doi: 10.1038/ncomms12989.

8.

Akkermansia muciniphila and Helicobacter typhlonius modulate intestinal tumor development in mice.

Dingemanse C, Belzer C, van Hijum SA, Günthel M, Salvatori D, den Dunnen JT, Kuijper EJ, Devilee P, de Vos WM, van Ommen GB, Robanus-Maandag EC.

Carcinogenesis. 2015 Nov;36(11):1388-96. doi: 10.1093/carcin/bgv120. Epub 2015 Aug 29.

PMID:
26320104
9.

Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels.

Draisma HHM, Pool R, Kobl M, Jansen R, Petersen AK, Vaarhorst AAM, Yet I, Haller T, Demirkan A, Esko T, Zhu G, Böhringer S, Beekman M, van Klinken JB, Römisch-Margl W, Prehn C, Adamski J, de Craen AJM, van Leeuwen EM, Amin N, Dharuri H, Westra HJ, Franke L, de Geus EJC, Hottenga JJ, Willemsen G, Henders AK, Montgomery GW, Nyholt DR, Whitfield JB, Penninx BW, Spector TD, Metspalu A, Slagboom PE, van Dijk KW, 't Hoen PAC, Strauch K, Martin NG, van Ommen GB, Illig T, Bell JT, Mangino M, Suhre K, McCarthy MI, Gieger C, Isaacs A, van Duijn CM, Boomsma DI.

Nat Commun. 2015 Jun 12;6:7208. doi: 10.1038/ncomms8208.

10.

Characteristics of de novo structural changes in the human genome.

Kloosterman WP, Francioli LC, Hormozdiari F, Marschall T, Hehir-Kwa JY, Abdellaoui A, Lameijer EW, Moed MH, Koval V, Renkens I, van Roosmalen MJ, Arp P, Karssen LC, Coe BP, Handsaker RE, Suchiman ED, Cuppen E, Thung DT, McVey M, Wendl MC; Genome of Netherlands Consortium, Uitterlinden A, van Duijn CM, Swertz MA, Wijmenga C, van Ommen GB, Slagboom PE, Boomsma DI, Schönhuth A, Eichler EE, de Bakker PI, Ye K, Guryev V.

Genome Res. 2015 Jun;25(6):792-801. doi: 10.1101/gr.185041.114. Epub 2015 Apr 16.

11.

Huntington's disease biomarker progression profile identified by transcriptome sequencing in peripheral blood.

Mastrokolias A, Ariyurek Y, Goeman JJ, van Duijn E, Roos RA, van der Mast RC, van Ommen GB, den Dunnen JT, 't Hoen PA, van Roon-Mom WM.

Eur J Hum Genet. 2015 Oct;23(10):1349-56. doi: 10.1038/ejhg.2014.281. Epub 2015 Jan 28.

12.

The dystrophin gene and cognitive function in the general population.

Vojinovic D, Adams HH, van der Lee SJ, Ibrahim-Verbaas CA, Brouwer R, van den Hout MC, Oole E, van Rooij J, Uitterlinden A, Hofman A, van IJcken WF, Aartsma-Rus A, van Ommen GB, Ikram MA, van Duijn CM, Amin N.

Eur J Hum Genet. 2015 Jun;23(6):837-43. doi: 10.1038/ejhg.2014.183. Epub 2014 Sep 17.

13.

EJHG to follow variation nomenclature and stimulate data reporting.

van Ommen GB.

Eur J Hum Genet. 2013 May;21(5):479. doi: 10.1038/ejhg.2013.54. No abstract available.

14.

Increased sensitivity of next generation sequencing-based expression profiling after globin reduction in human blood RNA.

Mastrokolias A, den Dunnen JT, van Ommen GB, 't Hoen PA, van Roon-Mom WM.

BMC Genomics. 2012 Jan 18;13:28. doi: 10.1186/1471-2164-13-28.

15.

Comprehensive gene-expression survey identifies wif1 as a modulator of cardiomyocyte differentiation.

Buermans HP, van Wijk B, Hulsker MA, Smit NC, den Dunnen JT, van Ommen GB, Moorman AF, van den Hoff MJ, 't Hoen PA.

PLoS One. 2010 Dec 13;5(12):e15504. doi: 10.1371/journal.pone.0015504.

16.

Calpain 3 is a rapid-action, unidirectional proteolytic switch central to muscle remodeling.

de Morrée A, Lutje Hulsik D, Impagliazzo A, van Haagen HH, de Galan P, van Remoortere A, 't Hoen PA, van Ommen GB, Frants RR, van der Maarel SM.

PLoS One. 2010 Aug 4;5(8):e11940. doi: 10.1371/journal.pone.0011940.

17.

Mutant huntingtin activates Nrf2-responsive genes and impairs dopamine synthesis in a PC12 model of Huntington's disease.

van Roon-Mom WM, Pepers BA, 't Hoen PA, Verwijmeren CA, den Dunnen JT, Dorsman JC, van Ommen GB.

BMC Mol Biol. 2008 Oct 9;9:84. doi: 10.1186/1471-2199-9-84.

18.

Recreational genomics? Dreams and fears on genetic susceptibility screening.

van Ommen GB, Cornel MC.

Eur J Hum Genet. 2008 Apr;16(4):403-4. doi: 10.1038/ejhg.2008.32. No abstract available.

19.

A common reference for cDNA microarray hybridizations.

Sterrenburg E, Turk R, Boer JM, van Ommen GB, den Dunnen JT.

Nucleic Acids Res. 2002 Nov 1;30(21):e116.

20.

Expression profiling in stably regenerating skeletal muscle of dystrophin-deficient mdx mice.

Boer JM, de Meijer EJ, Mank EM, van Ommen GB, den Dunnen JT.

Neuromuscul Disord. 2002 Oct;12 Suppl 1:S118-24.

PMID:
12206806
21.

Fish mapping of 250 cosmid and 26 YAC clones to chromosome 4 with special emphasis on the FSHD region at 4q35.

Wijmenga C, Dauwerse HG, Padberg GW, Meyer N, Murray JC, Mills K, van Ommen GB, Hofker MH, Frants RR.

Muscle Nerve Suppl. 1995;(2):S14-8.

PMID:
23573581
22.

Fish mapping of 250 cosmid and 26 YAC clones to chromosome 4 with special emphasis on the FSHD region at 4q35.

Wijmenga C, Dauwerse HG, Padberg GW, Meyer N, Murray JC, Mills K, van Ommen GB, Hofker MH, Frants RR.

Muscle Nerve Suppl. 1995;2:S14-8.

PMID:
7739620
23.

Subcellular localization of the bcl-2 protein in malignant and normal lymphoid cells.

de Jong D, Prins FA, Mason DY, Reed JC, van Ommen GB, Kluin PM.

Cancer Res. 1994 Jan 1;54(1):256-60.

24.

Defining the proximal border of the Huntington disease candidate region by multipoint recombination analyses.

Skraastad MI, de Rooij KE, de Koning Gans PA, Verwest A, Vegter-van der Vlis M, Bakker E, den Dunnen JT, van Ommen GB.

Genomics. 1993 Jun;16(3):599-604.

PMID:
8325632
25.

Subcellular localization of bcl-2 protein.

de Jong D, Prins F, van Krieken HH, Mason DY, van Ommen GB, Kluin PM.

Curr Top Microbiol Immunol. 1992;182:287-92. No abstract available.

PMID:
1490366
26.

Mapping of facioscapulohumeral muscular dystrophy gene to chromosome 4q35-qter by multipoint linkage analysis and in situ hybridization.

Wijmenga C, Padberg GW, Moerer P, Wiegant J, Liem L, Brouwer OF, Milner EC, Weber JL, van Ommen GB, Sandkuyl LA, et al.

Genomics. 1991 Apr;9(4):570-5.

PMID:
2037288
27.

Report of the committee on the genetic constitution of chromosome 4.

Murray JC, van Ommen GB.

Cytogenet Cell Genet. 1990;55(1-4):97-110. Review. No abstract available.

PMID:
2073850
28.

Cosmid vector pCpG and plasmid vector pKNUN1, and their use for cloning DNA sequences adjacent to sites for rare cutting restriction endonucleases.

Dauwerse HG, van Ommen GB, Breuning MH, Pearson PL.

Nucleic Acids Res. 1989 May 11;17(9):3603. No abstract available.

29.

A polymorphic locus at Xq27-28 detected by the probe U6.2 [DXS304].

Dahl N, Hammarström-Heeroma K, van Ommen GB, Pettersson U.

Nucleic Acids Res. 1989 Apr 11;17(7):2884. No abstract available.

30.
31.

Merging autosomal dominance and recessivity.

Van Ommen GB.

Am J Hum Genet. 1987 Oct;41(4):689-91. No abstract available.

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