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المؤلفون: Hassan, S.M., Vossen, R.H.A.M., Chessa, R., den Dunnen, J.T., Bakker, E., Giordano, P.C., Harteveld, C.L.

المصدر: In Blood Cells, Molecules and Diseases September 2014 53(3):133-137

المؤلفون: Nadarajah, V.D., van Putten, M., Chaouch, A., Garrood, P., Straub, V., Lochmüller, H., Ginjaar, H.B., Aartsma-Rus, A.M., van Ommen, G.J.B., den Dunnen, J.T., ’t Hoen, P.A.C.

المصدر: In Neuromuscular Disorders August 2011 21(8):569-578

المؤلفون: den Dunnen, J.T., Taschner, P.E.M.

المصدر: In Molecular Diagnostics Edition: Third Edition. 2017:13-22

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المؤلفون: Thompson, B.A., Spurdle, A.B., Plazzer, J.P., Greenblatt, M.S., Akagi, K., Al-Mulla, F., Bapat, B.V., Bernstein, I.T., Capellá, G.M., Den Dunnen, J.T., Du Sart, D., Fabre, A.J., Farrell, M.P., Farrington, S.M., Frayling, I.M., Frébourg, T.H., Goldgar, D.E.J., Heinen, C.D., Holinski-Feder, E., Kohonen-Corish, M.R.J., Robinson, K.L., Leung, S.Y., Martins, A., Möller, P., Morak, M., Nyström, M., Peltomäki, P.T., Pineda, M., Qi, M., Ramesar, R., Rasmussen, L.J., Royer-Pokora, B., Scott, R.J., Sijmons, R.H., Tavtigian, S.V.S.V., Tops, C.M.J., Weber, T.K., Wijnen, J.T.H., Woods, M.O., Macrae, F.A., Genuardi, M., Castillejo, A., Sexton, A.C., Chan, A.K.W., Viel, A.G.M., Blanco, A.M., French, A.J., Laner, A., Wagner, A., Van Den Ouweland, A.M.W., Mensenkamp, A.R., Payá, A., Betz, B., Redeker, B.J.W., Smith, B.G., Espenschied, C.R., Cummings, C., Engel, C., Fornes, C., Valenzuela, C., Alenda, C., Buchanan, D.D., Barana, D., Konstantinova, D.V., Cairns, D., Glaser, E., Silva, F., Lalloo, F.I., Crucianelli, F., Hogervorst, F.B.L., Casey, G.R., Tomlinson, I.P.M., Blanco, I.B.S.I., Villar, I.L., García-Planells, J., Bigler, J., Shia, J., Martínez-López, J.J., Gille, J.J.P., Hopper, J.L., Potter, J.D., Soto, J.L., Kantelinen, J., Ellis, K., Mann, K., Varesco, L., Zhang, L., Marchand, L.L., Marafie, M.J., Nordling, Margareta, 1962, Tibiletti, M.G., Kahan, M.A., Ligtenberg, M.J.L., Clendenning, M., Jenkins, M.A., Speevak, M.D., Digweed, M., Kloor, M., Hitchins, M.P., Myers, M., Aronson, M.D., Valentin, M.D., Kutsche, M., Parsons, M.T., Walsh, M.D., Kansikas, M., Zahary, M.N., Pedroni, M., Heider, N., Poplawski, N.K., Rahner, N., Lindor, N.M., Sala, P., Nan, P., Propping, P., Newcomb, P., Sarin, R., Haile, R.W.C., Hofstra, R.M.W., Ward, R.L., Tricarico, R., Bacares, R., Young, S., Chialina, S.G., Kovalenko, S.P., Gunawardena, S.R., Moreno, S., Ho, S., Yuen, S.T., Thibodeau, S.N., Gallinger, S.S., Burnett, T.S., Teitsch, T., Chan, T.L., Smyrk, T.C., Cranston, T., Psofaki, V., Steinke-Lange, V., Barberá, V.M.

المصدر: Nature Genetics. 46(2):107-115

مصطلحات موضوعية: Medical Genetics, Medicinsk genetik

URL الوصول: https://gup.ub.gu.se/publication/213001

المؤلفون: White, S.J. Laros, J.F.J. Bakker, E. Cambon-Thomsen, A. Eden, M. Leonard, S. Lochmüller, H. Matthijs, G. Mattocks, C. Patton, S. Payne, K. Scheffer, H. Souche, E. Thomassen, E. Thompson, R. Traeger-Synodinos, J. Van Vooren, S. Janssen, B. den Dunnen, J.T.

URL الوصول: https://explore.openaire.eu/search/publication?articleId=od______2127::412acd61d64e24aeda3636ebbfab989d
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3086999

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المؤلفون: Francioli, L.C., Polak, P.P., Koren, A., Menelaou, A., Chun, S., Renkens, I., van Duijn, C.M., Swertz, M.A., Wijmenga, C., van Ommen, G.J., Slagboom, P.E., Boomsma, D.I., Ye, K., Guryev, V., Arndt, P.F., Kloosterman, W.P., Bakker, P.I.W., Sunyaev, S.R., Dijk, F., Neerincx, P.B.T., Pulit, S.L., Deelen, P., Elbers, C.C., Palamara, P.F., Pe'er, I., Abdellaoui, A., van Oven, M., Vermaat, M., Li, M., Laros, J.F.J., Stoneking, M., de Knijff, P., Kayser, M., Veldink, J.H., Van den Berg, L.H., Byelas, H., den Dunnen, J.T., Dijkstra, M., Amin, N., van der Velde, K.J., Hottenga, J.J., van Setten, J., van Leeuwen, E.M., Kanterakis, A., Kattenberg, V.M., Karssen, L.C., van Schaik, B.D.C., Bot, J., Nijman, I.J., van Enckevort, D., Mei, H., Koval, V., Estrada, K., Medina-Gomez, C., Lameijer, E.W., Moed, M.H., Hehir-Kwa, J.Y., Handsaker, R.E., McCarroll, S.A., Vuzman, D., Sohail, M., Hormozdiari, F., Marschall, T., Schönhuth, A., Beekman, M., de Craen, A.J., Suchiman, H.E.D., Hofman, A., Oostra, B., Isaacs, A., Rivadeneira, F., Uitterlinden, A.G., Willemsen, G., Platteel, M., Pitts, S.J., Potluri, S., Sundar, P., Cox, D.R., Li, Q., Li, Y., Du, Y., Chen, R., Cao, H., Li, N., Cao, S., Wang, J., Bovenberg, J.A., Brandsma, M.

المساهمون: Groningen Institute for Gastro Intestinal Genetics and Immunology (3GI), Stem Cell Aging Leukemia and Lymphoma (SALL), Groningen Research Institute for Asthma and COPD (GRIAC), Biological Psychology, Culture, Organization and Management, Neuroscience Campus Amsterdam - Neurobiology of Mental Health, Epidemiology, Pharmacy

المصدر: Nature Genetics, 47(7), 822-826.e3. Nature Publishing Group
Nature Genetics
Nature Genetics, 47(7), 822-826. Nature Publishing Group
Nature genetics
Nature Genetics, 47(7), 822-+. Nature Publishing Group
Nature Genetics, 47(7), 822
Francioli, L C, Polak, P P, Koren, A, Menelaou, A, Chun, S, Renkens, I, van Duijn, C M, Swertz, M A, Wijmenga, C, van Ommen, G J, Slagboom, P E, Boomsma, D I, Ye, K, Guryev, V, Arndt, P F, Kloosterman, W P, Bakker, P I W, Sunyaev, S R, Dijk, F, Neerincx, P B T, Pulit, S L, Deelen, P, Elbers, C C, Palamara, P F, Pe'er, I, Abdellaoui, A, van Oven, M, Vermaat, M, Li, M, Laros, J F J, Stoneking, M, de Knijff, P, Kayser, M, Veldink, J H, Van den Berg, L H, Byelas, H, den Dunnen, J T, Dijkstra, M, Amin, N, van der Velde, K J, Hottenga, J J, van Setten, J, van Leeuwen, E M, Kanterakis, A, Kattenberg, V M, Karssen, L C, van Schaik, B D C, Bot, J, Nijman, I J, van Enckevort, D, Mei, H, Koval, V, Estrada, K, Medina-Gomez, C, Lameijer, E W, Moed, M H, Hehir-Kwa, J Y, Handsaker, R E, McCarroll, S A, Vuzman, D, Sohail, M, Hormozdiari, F, Marschall, T, Schönhuth, A, Beekman, M, de Craen, A J, Suchiman, H E D, Hofman, A, Oostra, B, Isaacs, A, Rivadeneira, F, Uitterlinden, A G, Willemsen, G, Platteel, M, Pitts, S J, Potluri, S, Sundar, P, Cox, D R, Li, Q, Li, Y, Du, Y, Chen, R, Cao, H, Li, N, Cao, S, Wang, J, Bovenberg, J A & Brandsma, M 2015, ' Genome-wide patterns and properties of de novo mutations in humans ', Nature Genetics, vol. 47, no. 7, pp. 822-826 . https://doi.org/10.1038/ng.3292

مصطلحات موضوعية: Male, Netherlands Twin Register (NTR), Mutation rate, Population genetics, Twin Study, DISEASE, Nucleotide diversity, 0302 clinical medicine, Mutation Rate, ELEMENTS, Non-U.S. Gov't, POPULATION, Genetics, 0303 health sciences, education.field_of_study, Research Support, Non-U.S. Gov't, SUBSTITUTION, Mutation (genetic algorithm), Female, Pan troglodytes, Population, DNA-SEQUENCING DATA, Mutagenesis (molecular biology technique), Biology, Research Support, Article, Paternal Age, N.I.H, Evolution, Molecular, 03 medical and health sciences, Germline mutation, SDG 3 - Good Health and Well-being, Research Support, N.I.H., Extramural, Journal Article, Animals, Humans, education, Germ-Line Mutation, 030304 developmental biology, Models, Genetic, Genome, Human, Extramural, FRAMEWORK, POLYMORPHISM, RECOMBINATION RATES, RESOLUTION, RADIATION, Human genome, 030217 neurology & neurosurgery

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URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bcffa53d5a79b0ce9e9a5a500dbe44cb
https://research.rug.nl/en/publications/eb8bb667-af9e-4a22-b523-97671a070699

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