المؤلفون: Kalman, LV, Agundez, JAG, Appell, ML, Black, JL, Bell, GC, Boukouvala, S, Bruckner, C, Bruford, E, Caudle, K, Coulthard, SA, Daly, AK, Del Tredici, AL, den Dunnen, JT, Drozda, K, Everts, RE, Flockhart, D, Freimuth, RR, Gaedigk, A, Hachad, H, Hartshorne, T, Ingelman-Sundberg, M, Klein, TE, Lauschke, VM, Maglott, DR, McLeod, HL, McMillin, GA, Meyer, UA, Muller, DJ, Nickerson, DA, Oetting, WS, Pacanowski, M, Pratt, VM, Relling, MV, Roberts, A, Rubinstein, WS, Sangkuhl, K, Schwab, M, Scott, SA, Sim, SC, Thirumaran, RK, Toji, LH, Tyndale, RF, van Schaik, RHN, Whirl-Carrillo, M, Yeo, KTJ, Zanger, UM

المصدر: Clinical pharmacology and therapeutics. 99(2):172-185

مصطلحات موضوعية: Medicin och hälsovetenskap

الوصول الحر: http://kipublications.ki.se/Default.aspx?queryparsed=id:132892333Test

المؤلفون: Out, AA, Tops, CMJ, Nielsen, M, Weiss, MM, van Minderhout, IJHM, Fokkema, IFAC, Buisine, MP, Claes, K, Colas, C, Fodde, R, Fostira, F, Franken, PF, Gaustadnes, M, Heinimann, K, Hodgson, SV, Hogervorst, FBL, Holinski-Feder, E, Lagerstedt-Robinson, K, Olschwang, S, van den Ouweland, AMW, Redeker, EJW, Scott, RJ, Vankeirsbilck, B, Gronlund, RV, Wijnen, JT, Wikman, FP, Aretz, S, Sampson, JR, Devilee, P, den Dunnen, JT, Hes, FJ

المصدر: Human mutation. 31(11):1205-1215

مصطلحات موضوعية: Medicin och hälsovetenskap

الوصول الحر: http://kipublications.ki.se/Default.aspx?queryparsed=id:121523340Test

المؤلفون: Kohonen-Corish, MRJ, Al-Aama, JY, Auerbach, AD, Axton, M, Barash, CI, Bernstein, I, Beroud, C, Burn, J, Cunningham, F, Cutting, GR, den Dunnen, JT, Greenblatt, MS, Kaput, J, Katz, M, Lindblom, A, Macrae, F, Maglott, D, Moslein, G, Povey, S, Ramesar, R, Richards, S, Seminara, D, Sobrido, MJ, Tavtigian, S, Taylor, G, Vihinen, M, Winship, I, Cotton, RGH

المصدر: Human mutation. 31(12):1374-1381

مصطلحات موضوعية: Medicin och hälsovetenskap

الوصول الحر: http://kipublications.ki.se/Default.aspx?queryparsed=id:121937048Test

المؤلفون: Bruder, CEG, Piotrowski, A, Gijsbers, AACJ, Andersson, R, Erickson, S, de Stahl, TD, Menzel, U, Sandgren, J, von Tell, D, Poplawski, A, Crowley, M, Crasto, C, Partridge, EC, Tiwari, H, Allison, DB, Komorowski, J, van Ommen, GJB, Boomsma, DI, Pedersen, NL, den Dunnen, JT, Wirdefeldt, K, Dumanski, JP

المصدر: American journal of human genetics. 82(3):763-771

مصطلحات موضوعية: Medicin och hälsovetenskap

الوصول الحر: http://kipublications.ki.se/Default.aspx?queryparsed=id:116704812Test

المؤلفون: Boycott, K. M., Rath, A., Chong, J. X., Hartley, T., Alkuraya, F. S., Baynam, G., Brookes, Anthony J., Brudno, M., Carracedo, A., den Dunnen, JT, Dyke, S. O. M., Estivill, X., Goldblatt, J., Gonthier, C., Groft, SC, Gut, I., Hamosh, A., Hieter, P., Höhn, S., Hurles, M. E., Kaufmann, P., Knoppers, B. M., Krischer, J. P., Macek, M., Matthijs, G., Olry, A., Parker, S., Paschall, J., Philippakis, A .A., Rehm, H. L., Robinson, P. N., Sham, P-C., Stefanov, R., Taruscio, D., Unni, D., Vanstone, M. R., Zhang, F., Brunner, H., Bamshad, M. J., Lochmüller, H.

مصطلحات موضوعية: IRDiRC, Matchmaker Exchange, disease modeling, gene discovery, genome sequencing, ontologies, rare diseases, solving the unsolved, transcriptome sequencing, Databases, Factual, Exome, Genome, Human, Humans, International Cooperation

العلاقة: https://www.ncbi.nlm.nih.gov/pubmed/28475856Test; American Journal of Human Genetics, 2017, 100 (5), pp. 695-705; https://www.sciencedirect.com/science/article/pii/S0002929717301477?via%3DihubTest; http://hdl.handle.net/2381/42090Test; S0002-9297(17)30147-7

الإتاحة: https://doi.org/10.1016/j.ajhg.2017.04.003Test
https://www.sciencedirect.com/science/article/pii/S0002929717301477?via%3DihubTest
http://hdl.handle.net/2381/42090Test

المؤلفون: 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

المصدر: 465 ; 455

مصطلحات موضوعية: Science & Technology, Life Sciences & Biomedicine, Biochemistry & Molecular Biology, Genetics & Heredity, DUCHENNE MUSCULAR-DYSTROPHY, CHROMOSOME-INACTIVATION, DMD LOCUS, EXPRESSION, PATTERNS, TRANSLOCATION, ADRENOLEUKODYSTROPHY, CARRIERS, CONSEQUENCES, VARIABILITY, Calcium-Binding Proteins, Female, Humans, Intracellular Signaling Peptides and Proteins, Male, Membrane Glycoproteins, Netherlands, Polymorphism, Single Nucleotide, Population, Receptors, Cytoplasmic and Nuclear, Peptide, Septins, X Chromosome Inactivation, BIOS consortium

العلاقة: European Journal of Human Genetics; http://hdl.handle.net/10044/1/75694Test

الإتاحة: https://doi.org/10.1038/s41431-018-0291-3Test
http://hdl.handle.net/10044/1/75694Test

المؤلفون: Oliveira, J, Gruber, A, Cardoso, M, Taipa, R, Fineza, I, Gonçalves, A, Laner, A, Winder, TL, Schroeder, J, Rath, J, Oliveira, ME, Vieira, E, Sousa, AP, Vieira, JP, Lourenço, T, Almendra, L, Negrão, L, Santos, M, Melo-Pires, M, Coelho, T, den Dunnen, JT, Santos, R, Sousa, M

مصطلحات موضوعية: Alleles, Biomarkers, Brain, Computational Biology, Databases, Nucleic Acid, Gene Frequency, Genetic Variation, Genotype, Humans, Immunohistochemistry, Laminin, Magnetic Resonance Imaging, Muscular Dystrophies, Genetic Association Studies, Mutation, Phenotype, HDE GEN, HDE NEU PED

العلاقة: Hum Mutat . 2018 Oct;39(10):1314-1337; http://hdl.handle.net/10400.17/3495Test

الإتاحة: https://doi.org/10.1002/humu.23599Test
http://hdl.handle.net/10400.17/3495Test

المؤلفون: Thompson, BA, Spurdle, AB, Plazzer, JP, Greenblatt, MS, Akagi, K, Al-Mulla, F, Bapat, B, Bernstein, I, Capella, G, den Dunnen, JT, du Sart, D, Fabre, A, Farrell, MP, Farrington, SM, Frayling, IM, Frebourg, T, Goldgar, DE, Heinen, CD, Holinski-Feder, E, Kohonen-Corish, M, Robinson, KL, Leung, SY, Martins, A, Moller, P, Morak, M, Nystrom, M, Peltomaki, P, Pineda, M, Qi, M, Ramesar, R, Rasmussen, LJ, Royer-Pokora, B, Scott, RJ, Sijmons, R, Tavtigian, SV, Tops, CM, Weber, T, Wijnen, J, Woods, MO, Macrae, F, Genuardi, M

المصدر: Nature genetics. 46(2):107

مصطلحات موضوعية: Medicin och hälsovetenskap

الوصول الحر: http://kipublications.ki.se/Default.aspx?queryparsed=id:128358261Test

المؤلفون: Leigh, S, Futema, M, Whittall, R, Taylor-Beadling, A, Williams, M, den Dunnen, JT, Humphries, SE

المصدر: Journal of Medical Genetics , 54 (4) pp. 217-223. (2017)

وصف الملف: text

العلاقة: https://discovery.ucl.ac.uk/id/eprint/1529012/1/Leigh_UCL_low-density_lipoprotein.pdfTest; https://discovery.ucl.ac.uk/id/eprint/1529012/7/Leigh_UCL_low-density_lipoprotein_S1.pdfTest; https://discovery.ucl.ac.uk/id/eprint/1529012/8/Leigh_UCL_low-density_lipoprotein_S2.pdfTest; https://discovery.ucl.ac.uk/id/eprint/1529012/9/Leigh_UCL_low-density_lipoprotein_S3.pdfTest; https://discovery.ucl.ac.uk/id/eprint/1529012Test/

الإتاحة: https://discovery.ucl.ac.uk/id/eprint/1529012/1/Leigh_UCL_low-density_lipoprotein.pdfTest
https://discovery.ucl.ac.uk/id/eprint/1529012/7/Leigh_UCL_low-density_lipoprotein_S1.pdfTest
https://discovery.ucl.ac.uk/id/eprint/1529012/8/Leigh_UCL_low-density_lipoprotein_S2.pdfTest
https://discovery.ucl.ac.uk/id/eprint/1529012/9/Leigh_UCL_low-density_lipoprotein_S3.pdfTest
https://discovery.ucl.ac.uk/id/eprint/1529012Test/

المؤلفون: Kohonen-Corish, MRJ, Macrae, F, Genuardi, M, Aretz, S, Bapat, B, Bernstein, IT, Burn, J, Cotton, RGH, den Dunnen, JT, Frebourg, T, Greenblatt, MS, Hofstra, R, Holinski-Feder, E, Lappalainen, I, Lindblom, A, Maglott, D, Moller, P, Morreau, H, Moslein, G, Sijmons, R, Spurdle, AB, Tavtigian, S, Tops, CMJ, Weber, TK, de Wind, N, Woods, MO

المصدر: Human mutation. 32(4):491-494

مصطلحات موضوعية: Medicin och hälsovetenskap

الوصول الحر: http://kipublications.ki.se/Default.aspx?queryparsed=id:122228159Test