Zobrazeno 1 - 10 of 154 pro vyhledávání: '"Verkerk, M. A."'
1
Akademický článek
Where families and healthcare meet
Autor: Verkerk, M A, Lindemann, Hilde, McLaughlin, Janice, Scully, Jackie Leach, Kihlbom, Ulrik, Nelson, Jamie, Chin, Jacqueline
Publikováno v: Journal of Medical Ethics, 2015 Feb 01. 41(2), 183-185.
Externí odkaz: https://www.jstor.org/stable/43316792
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2
Akademický článek
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3
Akademický článek
Reflective Professionalism: Interpreting CanMEDS' "Professionalism"
Autor: Verkerk, M. A., de Bree, M. J., Mourits, M. J. E.
Publikováno v: Journal of Medical Ethics, 2007 Nov 01. 33(11), 663-666.
Externí odkaz: https://www.jstor.org/stable/27719978
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4
Occupational exposure to gases/fumes and mineral dust affect DNA methylation levels of genes regulating expression
Autor: Plaat, D. van der, Vonk, J.M., Terzikhan, N., Jong, K. de, Vries, M. de, Bastide-van Gemert, S. la, Diemen, C.C. van, Lahousse, L., Brusselle, G., Nedeljkovic, I., Amin, N., Kromhout, H., Vermeulen, R.C.H., Postma, D.S., Duijn, C.M. van, Boezen, H.M., Heijmans, B.T., Hoen, P.A.C.T., Meurs, J. van, Isaacs, A., Jansen, R., Franke, L., Boomsma, D.I., Pool, R., Dongen, J. van, Hottenga, J.J., Greevenbroek, M.M.J. van, Stehouwer, C.D.A., Kallen, C.J.H. van der, Schalkwijk, C.G., Wijmenga, C., Zhernakova, S., Tigchelaar, E.E., Slagboom, P.E., Beekman, M., Deelen, J., Heemst, D. van, Veldink, J.H., Berg, L.H. van den, Hofman, B.A., Uitterlinden, A.G., Jhamai, P.M., Verbiest, M., Suchiman, H.E.D., Verkerk, M., Breggen, R. van der, Rooij, J. van, Lakenberg, N., Mei, H., Iterson, M. van, Galen, M. van, Bot, J., Zhernakova, D.V., Hof, P.V., Deelen, P., Nooren, I., Moed, M., Vermaat, M., Luijk, R., Bonder, M.J., Dijk, F. van, Arindrarto, W., Kielbasa, S.M., Swertz, M.A., Zwet, E.W. van, Hoen, P.B. 't, BIOS Consortium
Publikováno v: Human Molecular Genetics, 28(15), 2477. Oxford University Press
Human Molecular Genetics, 28(15), 2477-2485. Oxford University Press
Human Molecular Genetics
BIOS Consortium, Boomsma, D, Pool, R, van Dongen, J & Hottenga, J J 2019, ' Occupational exposure to gases/fumes and mineral dust affect DNA methylation levels of genes regulating expression ', Human molecular genetics, vol. 28, no. 15, pp. 2477-2485 . https://doi.org/10.1093/hmg/ddz067
Human Molecular Genetics, 28(15), 2477-2485
HUMAN MOLECULAR GENETICS
Human molecular genetics, 28(15), 2477-2485. Oxford University Press
Many workers are daily exposed to occupational agents like gases/fumes, mineral dust or biological dust, which could induce adverse health effects. Epigenetic mechanisms, such as DNA methylation, have been suggested to play a role. We therefore aimed
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f0fcc6f6bac2bc4b27048a8dd8450bd4
https://cris.maastrichtuniversity.nl/en/publications/6a1f41cf-27f5-46f8-9d70-91af32912200
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5
Skewed X-inactivation is common in the general female population
Autor: Shvetsova, E, Sofronova, A, Monajemi, R, Gagalova, K, Draisma, HHM, White, SJ, Santen, GWE, Lopes, SMCDS, Heijmans, BT, Van Meurs, J, Jansen, R, Franke, L, Kielbasa, SM, Den Dunnen, JT, 't Hoen, PAC, Boomsma, DI, Pool, R, Van Dongen, J, Hottenga, JJ, Van Greevenbroek, MMJ, Da Stehouwer, C, Van der Kallen, CJH, Schalkwijk, CG, Wijmenga, C, Zhernakova, S, Tigchelaar, EF, Slagboom, PE, Beekman, M, Deelen, J, Van Heemst, D, Veldink, JH, Van den Berg, LH, Van Duijn, CM, Hofman, BA, Uitterlinden, AG, Jhamai, PM, Verbiest, M, Suchiman, HED, Verkerk, M, Van der Breggen, R, Van Rooij, J, Lakenberg, N, Mei, H, Bot, J, Zhernakova, DV, 't Hof, PV, Deelen, P, Nooren, I, Moed, M, Vermaat, M, Luijk, R, Bonder, MJ, Van Iterson, M, Van Dijk, F, Van Galen, M, Arindrarto, W, Swertz, MA, Van Zwet, EW, Isaacs, A, Francioli, LC, Menelaou, A, Pulit, SL, Palamara, PF, Elbers, CC, Neerincx, PB, Ye, K, Guryev, V, Kloosterman, WP, Abdellaoui, A, Van Leeuwen, EM, Van Oven, M, Li, M, Laros, JF, Karssen, LC, Kanterakis, A, Amin, N, Lameijer, EW, Kattenberg, M, Dijkstra, M, Byelas, H, Van Setten, J, Van Schaik, BD, Nijman, IJ, Renkens, I, Marschall, T, Schonhuth, A, Hehir-Kwa, JY, Handsaker, RE, Polak, P, Sohail, M, Vuzman, D, Hormozdiari, F, Van Enckevort, D, Koval, V, Moed, MH, Van der Velde, KJ, Rivadeneira, F, Estrada, K, Medina-Gomez, C, McCarroll, SA, De Craen, AJ, Suchiman, HE, Oostra, B, Willemsen, G, Platteel, M, Pitts, SJ, Potluri, S, Sundar, P, Cox, DR, Sunyaev, SR, Stoneking, M, De Knijff, P, Kayser, M, Li, Q, Li, Y, Du, Y, Chen, R, Cao, H, Li, N, Cao, S, Wang, J, Bovenberg, JA, Pe'er, I, Van Ommen, GJ, De Bakker, PI
Publikováno v: European Journal of Human Genetics
European Journal of Human Genetics, 27(3), 455-465. Nature Publishing Group
European journal of human genetics, 27(3), 455-465. Nature Publishing Group
European Journal of Human Genetics, 27(3), 455-465
European Journal of Human Genetics, 27, 455-465
European Journal of Human Genetics, 27(3), 455. Nature Publishing Group
European Journal of Human Genetics, 27, 3, pp. 455-465
Shvetsova, E, 't Hoen, P A C, Boomsma, D I, Pool, R, van Dongen, J, Hottenga, J J, Willemsen, G & BIOS Consortium 2019, ' Skewed X-inactivation is common in the general female population ', European Journal of Human Genetics, vol. 27, no. 3, pp. 455-465 . https://doi.org/10.1038/s41431-018-0291-3
Shvetsova, E, Sofronova, A, Monajemi, R, Gagalova, K, Draisma, H H M, White, S J, Santen, G W E, Chuva de Sousa Lopes, S M, Heijmans, B T, van Meurs, J, Jansen, R, Franke, L, Kiełbasa, S M, den Dunnen, J T, ‘t Hoen, P A C & BIOS Consortium 2019, ' Skewed X-inactivation is common in the general female population ', European Journal of Human Genetics, vol. 27, no. 3, pp. 455-465 . https://doi.org/10.1038/s41431-018-0291-3
X-inactivation is a well-established dosage compensation mechanism ensuring that X-chromosomal genes are expressed at comparable levels in males and females. Skewed X-inactivation is often explained by negative selection of one of the alleles. We dem
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5d16e7db74a66781c04e9903128640a4
https://doi.org/10.1038/s41431-018-0291-3
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6
Mendelian randomization integrating GWAS and eQTL data reveals genetic determinants of complex and clinical traits
Autor: Porcu, E., Rueger, S., Lepik, K., Agbessi, M., Ahsan, H., Alves, I., Andiappan, A., Arindrarto, W., Awadalla, P., Battle, A., Beutner, F., Bonder, M.J., Boomsma, D., Christiansen, M., Claringbould, A., Deelen, P., Esko, T., Fave, M.J., Franke, L., Frayling, T., Gharib, S.A., Gibson, G., Heijmans, B.T., Hemani, G., Jansen, R., Kahonen, M., Kalnapenkis, A., Kasela, S., Kettunen, J., Kim, Y., Kirsten, H., Kovacs, P., Krohn, K., Kronberg-Guzman, J., Kukushkina, V., Lee, B., Lehtimaki, T., Loeffler, M., Marigorta, U.M., Mei, H.L., Milani, L., Montgomery, G.W., Muller-Nurasyid, M., Nauck, M., Nivard, M., Penninx, B., Perola, M., Pervjakova, N., Pierce, B.L., Powell, J., Prokisch, H., Psaty, B.M., Raitakari, O.T., Ripatti, S., Rotzschke, O., Saha, A., Scholz, M., Schramm, K., Seppala, I., Slagboom, E.P., Stehouwer, C.D.A., Stumvoll, M., Sullivan, P., Hoen, P.A.C. 't, Teumer, A., Thiery, J., Tong, L., Tonjes, A., Dongen, J. van, Iterson, M. van, Meurs, J. van, Veldink, J.H., Verlouw, J., Visscher, P.M., Volker, U., Vosa, U., Westra, H.J., Wijmenga, C., Yaghootkar, H., Yang, J., Zeng, B., Zhang, F.T., Beekman, M., Boomsma, D.I., Bot, J., Deelen, J., Hofman, B.A., Hottenga, J.J., Isaacs, A., Jhamai, P.M., Kielbasa, S.M., Lakenberg, N., Luijk, R., Mei, H., Moed, M., Nooren, I., Pool, R., Schalkwijk, C.G., Slagboom, P.E., Suchiman, H.E.D., Swertz, M.A., Tigchelaar, E.F., Uitterlinden, A.G., Berg, L.H. van den, Breggen, R. van der, Kallen, C.J.H. van der, Dijk, F. van, Duijn, C.M. van, Galen, M. van, Greevenbroek, M.M.J. van, Heemst, D. van, Rooij, J. van, Van't Hof, P., Zwet, E.W. van, Vermaat, M., Verbiest, M., Verkerk, M., Zhernakova, D.V., Zhernakova, S., Santoni, F.A., Reymond, A., Kutalik, Z., eQTLGen Consortium, BIOS Consortium
Publikováno v: Porcu, E, Rüeger, S, Lepik, K, eQTLGen Consortium, BIOS Consortium, Santoni, F, Reymond, A & Kutalik, Z 2019, ' Mendelian randomization integrating GWAS and eQTL data reveals genetic determinants of complex and clinical traits ', Nature Communications, vol. 10, no. 1, 3300 . https://doi.org/10.1038/s41467-019-10936-0
Nature Communications, Vol 10, Iss 1, Pp 1-12 (2019)
Nature Communications
Nature Communications, 10:3300. Nature Publishing Group
eQTLGen Consortium & BIOS Consortium 2019, ' Mendelian randomization integrating GWAS and eQTL data reveals genetic determinants of complex and clinical traits ', Nature Communications, vol. 10, no. 1, 3300 . https://doi.org/10.1038/s41467-019-10936-0
Nat. Commun. 10:3300 (2019)
Nature Communications, 10(1):3300. Nature Publishing Group
Nature Communications, 10(1):3300. Nature Publishing Group UK
Nature communications, vol. 10, no. 1, pp. 3300
Nature Communications, 10
Porcu, E, Kutalik, Z, eQTLGen Consortium, BIOS Consortium, Boomsma, D I, Nivard, M G, Hottenga, J J, Pool, R & van Dongen, J 2019, ' Mendelian randomization integrating GWAS and eQTL data reveals genetic determinants of complex and clinical traits ', Nature Communications, vol. 10, no. 1, 3300 . https://doi.org/10.1038/s41467-019-10936-0
Genome-wide association studies (GWAS) have identified thousands of variants associated with complex traits, but their biological interpretation often remains unclear. Most of these variants overlap with expression QTLs, indicating their potential in
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9eef251064cec97623fab5b0fca75810
http://www.scopus.com/inward/record.url?scp=85069729041&partnerID=8YFLogxK
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8
Religieuze geletterdheid is het doel, religiewetenschap het middel: Gedachten vanuit de nieuwe, educatieve opleiding Religie en Levensbeschouwing in Leiden
Autor: Verkerk, M., Davidsen, M.A.
Publikováno v: Narthex, 20(1), 52-54
Religie speelt een grote rol in de wereld. Haar invloed is overal merkbaar, van de individuele vraag naar zingeving tot geopolitieke kwesties, van kleine gemeenschappen tot wereldwijde instituten. We vinden het belangrijk dat mensen de rol van religi
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::8239b6707bbff6d62a292615642f0b29
https://hdl.handle.net/1887/135543
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9
A characterization of cis- and trans-heritability of RNA-Seq-based gene expression
Autor: Ouwens, K.G., Jansen, R., Nivard, M.G., Dongen, J. van, Frieser, M.J., Hottenga, J.J., Arindrarto, W., Claringbould, A., Iterson, M. van, Mei, H.L., Franke, L., Heijmans, B.T., Hoen, P.A.C. 't, Meurs, J. van, Brooks, A.I., Penninx, B.W.J.H., Boomsma, D.I., Isaacs, A., Pool, R., Greevenbroek, M.M.J. van, Stehouwer, C.D.A., Kallen, C.J.H. van der, Schalkwijk, C.G., Wijmenga, C., Zhernakova, S., Tigchelaar, E.F., Slagboom, P.E., Beekman, M., Deelen, J., Heemst, D. van, Veldink, J.H., Berg, L.H. van den, Duijn, C.M. van, Hofman, B.A., Uitterlinden, A.G., Jhamai, P.M., Verbiest, M., Suchiman, H.E.D., Verkerk, M., Breggen, R. van der, Rooij, J. van, Lakenberg, N., Galen, M. van, Bot, J., Zhernakova, D.V., van't Hof, P., Deelen, P., Nooren, I., Moed, M., Vermaat, M., Luijk, R., Bonder, M.J., Dijk, F. van, Kielbasa, S.M., Swertz, M.A., Zwet, E.W. van, Hoen, P.B. 't, BIOS Consortium
Publikováno v: Ouwens, K G, Jansen, R, Nivard, M G, van Dongen, J, Frieser, M J, Hottenga, J-J, Arindrarto, W, Claringbould, A, van Iterson, M, Mei, H, Franke, L, Heijmans, B T, A. C. ’t Hoen, P, van Meurs, J, Brooks, A I, Boomsma, D I, Penninx, B W J H & BIOS Consortium 2020, ' A characterization of cis-and trans-heritability of RNA-Seq-based gene expression ', European Journal of Human Genetics, vol. 28, no. 2, pp. 253-263 . https://doi.org/10.1038/s41431-019-0511-5
European Journal of Human Genetics, 28(2), 253-263. Nature Publishing Group
Ouwens, K G, Jansen, R, Nivard, M G, van Dongen, J, Hottenga, J-J, Penninx, B W J H, Boomsma, D I & BIOS Consortium 2020, ' A characterization of cis-and trans-heritability of RNA-Seq-based gene expression ', European Journal of Human Genetics, vol. 28, no. 2, pp. 253-263 . https://doi.org/10.1038/s41431-019-0511-5
European Journal of Human Genetics, 28, 253-263
Eur J Hum Genet
European Journal of Human Genetics, 28, 2, pp. 253-263
European Journal of Human Genetics, 28(2), 253-263. NATURE PUBLISHING GROUP
Insights into individual differences in gene expression and its heritability (h2) can help in understanding pathways from DNA to phenotype. We estimated the heritability of gene expression of 52,844 genes measured in whole blood in the largest twin R
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b724edc5b8ecf280bc310da19b2529ee
https://research.vumc.nl/en/publications/029df33c-d648-47cb-b258-60c60eed93d1
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10
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