Human Genetics

Search results

  • A severe connatal form of Pelizaeus Merzbacher disease in a Czech boy caused by a novel mutation (725C>A, Ala242Glu) at the 'jimpy(msd) codon' in the PLP gene.

    Seeman, P., Paderova, K., Benes, V. & Sistermans, E. A., 1 Jan 2002, In: Internation Journal of Molecular Medicine. 9, 2, p. 125-129 5 p.

    Research output: Contribution to journal › Article › Academic › peer-review

    11 Citations (Scopus)

  • A short history of the first 3 years of the Community Genetics Network and its newsletter

    ten Kate, L. P. & Plourde, A., 2011, In: Journal of Community Genetics. 2, 3, p. 111-115

    Research output: Contribution to journal › Article › Academic › peer-review

    Open Access
    3 Citations (Scopus)

  • A simple method for co-segregation analysis to evaluate the pathogenicity of unclassified variants; BRCA1 and BRCA2 as an example

    Mohammadi, L., Vreeswijk, M. P., Oldenburg, R., van den Ouweland, A., Oosterwijk, J. C., van der Hout, A. H., Hoogerbrugge, N., Ligtenberg, M., Ausems, M. G., van der Luijt, R. B., Dommering, C. J., Gille, J. J., Verhoef, S., Hogervorst, F. B., van Os, T. A., García, E. G., Blok, M. J., Wijnen, J. T., Helmer, Q., Devilee, P., & 5 othersvan Asperen, C. J., van Houwelingen, H. C., van Vreeswijk, M., Blok, M. M. & Wijnen, J. G., 2009, In: BMC Cancer. 9, p. 211 211.

    Research output: Contribution to journal › Article › Academic › peer-review

    Open Access
    62 Citations (Scopus)

  • A Single-Cell Model for Synaptic Transmission and Plasticity in Human iPSC-Derived Neurons

    Meijer, M., Rehbach, K., Brunner, J. W., Classen, J. A., Lammertse, H. C. A., van Linge, L. A., Schut, D., Krutenko, T., Hebisch, M., Cornelisse, L. N., Sullivan, P. F., Peitz, M., Toonen, R. F., Brüstle, O. & Verhage, M., 14 May 2019, In: Cell reports. 27, 7, p. 2199-2211.e6

    Research output: Contribution to journal › Article › Academic › peer-review

    Open Access
    59 Citations (Scopus)

  • A SNX3-dependent retromer pathway mediates retrograde transport of the Wnt sorting receptor Wntless and is required for Wnt secretion

    Harterink, M., Port, F., Lorenowicz, M. J., McGough, I. J., Silhankova, M., Betist, M. C., Van Weering, J. R. T., Van Heesbeen, R. G. H. P., Middelkoop, T. C., Basler, K., Cullen, P. J. & Korswagen, H. C., 1 Aug 2011, In: Nature cell biology. 13, 8, p. 914-923 10 p.

    Research output: Contribution to journal › Article › Academic › peer-review

    262 Citations (Scopus)

  • A solution to dependency: using multilevel analysis to accommodate nested data

    Aarts, E., Verhage, M., Veenvliet, J. V., Dolan, C. V. & van der Sluis, S., 2014, In: Nature neuroscience. 17, 4, p. 491-496 6 p.

    Research output: Contribution to journal › Article › Academic › peer-review

    390 Citations (Scopus)

  • A Specific IFIH1 Gain-of-Function Mutation Causes Singleton-Merten Syndrome

    Rutsch, F., Macdougall, M., Lu, C., Buers, I., Mamaeva, O., Nitschke, Y., Rice, G. I., Erlandsen, H., Kehl, H. G., Thiele, H., Nürnberg, P., Höhne, W., Crow, Y. J., Feigenbaum, A. & Hennekam, R. C., 2015, In: American journal of human genetics. 96, 2, p. 275-282

    Research output: Contribution to journal › Article › Academic › peer-review

    163 Citations (Scopus)

  • A specific mutation in TBL1XR1 causes Pierpont syndrome

    Heinen, C. A., Jongejan, A., Watson, P. J., Redeker, B., Boelen, A., Boudzovitch-Surovtseva, O., Forzano, F., Hordijk, R., Kelley, R., Olney, A. H., Pierpont, M. E., Schaefer, G. B., Stewart, F., van Trotsenburg, A. S. P., Fliers, E., Schwabe, J. W. R. & Hennekam, R. C., 2016, In: Journal of medical genetics. 53, 5, p. 330-337

    Research output: Contribution to journal › Article › Academic › peer-review

    55 Citations (Scopus)

  • A spectrum of routing strategies for brain networks

    Avena-Koenigsberger, A., Yan, X., Kolchinsky, A., van den Heuvel, M. P., Hagmann, P. & Sporns, O., 8 Mar 2019, In: PLoS computational biology. 15, 3, p. 1-24 24 p., e1006833.

    Research output: Contribution to journal › Article › Academic › peer-review

    Open Access
    57 Citations (Scopus)

  • A Spotlight on Bridging Microscale and Macroscale Human Brain Architecture

    van den Heuvel, M. P. & Yeo, B. T. T., 22 Mar 2017, In: Neuron. 93, 6, p. 1248-1251 4 p.

    Research output: Contribution to journal › Short survey › Academic › peer-review

    Open Access
    35 Citations (Scopus)

  • Assembly defects of human tRNA splicing endonuclease contribute to impaired pre-tRNA processing in pontocerebellar hypoplasia

    Sekulovski, S., Devant, P., Panizza, S., Gogakos, T., Pitiriciu, A., Heitmeier, K., Ramsay, E. P., Barth, M., Schmidt, C., Tuschl, T., Baas, F., Weitzer, S., Martinez, J. & Trowitzsch, S., 1 Dec 2021, In: Nature communications. 12, 1, 5610.

    Research output: Contribution to journal › Article › Academic › peer-review

    Open Access
    21 Citations (Scopus)

  • Assessing associations between the AURKA-HMMR-TPX2-TUBG1 functional module and breast cancer risk in BRCA1/2 mutation carriers

    AUTHOR GROUP, Aittomaki, K., Jonson, L., Ejlertsen, B., de la Hoya, M., Caldees, T., Dunning, A. M., Oliver, C., Fineberg, E., Cook, M., Peock, S., McCann, E., Murray, A., Jacobs, C., Pichert, G., Lalloo, F., Chu, C., Dorkins, H., Paterson, J., Ong, K. R., & 33 othersTeixeira, M. R., Hogervorst, F. B. L., van der Hout, A. H., Seynaeve, C., van der Luijt, R. B., Ligtenberg, M. J. L., Devilee, P., Wijnen, J. T., Rookus, M. A., Blok, M. J., van den Ouweland, A. M. W., Rodriguez, G. C., Phillips, K. A. A., Piedmonte, M., Nerenstone, S. R., Bae-Jump, V. L., O'Malley, D. M., Ratner, E. S., Schmutzler, R. K., Wappenschmidt, B., Rhiem, K., Engel, C., Meindl, A., Ditsch, N., Arnold, N., Plendl, H. J., Niederacher, D., Sutter, C., Wang-Gohrke, S., Steinemann, D., Preisler-Adams, S., Antoniou, A. C. & Pujana, M. A., 2015, In: PLOS ONE. 10, 4, p. e0120020 e0120020.

    Research output: Contribution to journal › Article › Academic › peer-review

    32 Citations (Scopus)

  • Assessing educational priorities in genetics for general practitioners and specialists in five countries: factor structure of the Genetic-Educational Priorities (Gen-EP) scale

    Calefato, J. M., Nippert, I., Harris, H. J., Kristoffersson, U., Schmidtke, J., ten Kate, L. P., Anionwu, E., Benjamin, C. M., Challen, K., Plass, A. M. C., Harris, R. & Julian-Reynier, C., 2008, In: Genetics in medicine. 10, 2, p. 99-106

    Research output: Contribution to journal › Article › Academic › peer-review

    24 Citations (Scopus)

  • Assessing the landscape of STXBP1-related disorders in 534 individuals

    Xian, J., Parthasarathy, S., Ruggiero, S. M., Balagura, G., Fitch, E., Helbig, K., Gan, J., Ganesan, S., Kaufman, M. C., Ellis, C. A., Lewis-Smith, D., Galer, P., Cunningham, K., O'Brien, M., Cosico, M., Baker, K., Darling, A., Veiga de Goes, F., El Achkar, C. M., Doering, J. H., & 34 othersFuria, F., García-Cazorla, Á., Gardella, E., Geertjens, L., Klein, C., Kolesnik-Taylor, A., Lammertse, H., Lee, J., Mackie, A., Misra-Isrie, M., Olson, H., Sexton, E., Sheidley, B., Smith, L., Sotero, L., Stamberger, H., Syrbe, S., Thalwitzer, K. M., van Berkel, A., van Haelst, M., Yuskaitis, C., Weckhuysen, S., Prosser, B., Son Rigby, C., Demarest, S., Pierce, S., Zhang, Y., Møller, R. S., Bruining, H., Poduri, A., Zara, F., Verhage, M., Striano, P. & Helbig, I., 1 May 2022, In: Brain : a journal of neurology. 145, 5, p. 1668-1683 16 p.

    Research output: Contribution to journal › Article › Academic › peer-review

    Open Access
    36 Citations (Scopus)

  • Assessment of a new trauma workflow concept implementing a sliding CT scanner in the trauma room: the effect on workup times

    Fung Kon Jin, P. H. P., Goslings, J. C., Ponsen, K. J., van Kuijk, C., Hoogerwerf, N. & Luitse, J. S., 2008, In: Journal of trauma. 64, 5, p. 1320-1326

    Research output: Contribution to journal › Article › Academic › peer-review

    62 Citations (Scopus)

  • Assessment of Cancer Predisposition Syndromes in a National Cohort of Children With a Neoplasm

    Bakhuizen, J. J., Hopman, S. M. J., Bosscha, M. I., Dommering, C. J., van den Heuvel-Eibrink, M. M., Hol, J. A., Kester, L. A., Koudijs, M. J., Langenberg, K. P. S., Loeffen, J. L. C., van der Lugt, J., Moll, A. C., van Noesel, M. M., Smetsers, S. E., de Vos-Kerkhof, E., Merks, J. H. M., Kuiper, R. P. & Jongmans, M. C. J., 3 Feb 2023, In: JAMA network open. 6, 2, p. e2254157 e2254157.

    Research output: Contribution to journal › Article › Academic › peer-review

    Open Access
    9 Citations (Scopus)

  • Assessment of pharmacogenetic tests: Presenting measures of clinical validity and potential population impact in association studies

    Tonk, E. C. M., Gurwitz, D., Maitland-Van Der Zee, A. H. & Janssens, A. C. J. W., 1 Jul 2017, In: pharmacogenomics journal. 17, 4, p. 386-392 7 p.

    Research output: Contribution to journal › Article › Academic › peer-review

    40 Citations (Scopus)

  • Assessment of practical applicability and clinical relevance of a commonly used LDL-C polygenic score in patients with severe hypercholesterolemia

    Tromp, T. R., Cupido, A. J., Reeskamp, L. F., Stroes, E. S. G., Hovingh, G. K., Defesche, J. C., Schmidt, A. F. & Zuurbier, L., Jan 2022, In: Atherosclerosis. 340, p. 61-67 7 p.

    Research output: Contribution to journal › Article › Academic › peer-review

    Open Access
    7 Citations (Scopus)

  • Assessment of system dysfunction in the brain through MRI-based connectomics

    Filippi, M., van den Heuvel, M. P., Fornito, A., He, Y., Hulshoff Pol, H. E., Agosta, F., Comi, G. & Rocca, M. A., 1 Dec 2013, In: The Lancet Neurology. 12, 12, p. 1189-1199 11 p.

    Research output: Contribution to journal › Review article › Academic › peer-review

    176 Citations (Scopus)

  • Assisted reproductive technology and intrauterine inseminations in Europe, 2005: results generated from European registers by ESHRE

    Nyboe Andersen, A. N., Goossens, V. J., Bhattacharya, S., Ferraretti, A. P., Kupka, M. S., Lambalk, C. B., de Mouzon, J. & Nygren, K. G., 2009, In: Human Reproduction. 24, 6, p. 1267-1287

    Research output: Contribution to journal › Article › Academic › peer-review

    258 Citations (Scopus)

  • Assisted reproductive technology in Europe, 2006: results generated from European registers by ESHRE

    de Mouzon, J., Goossens, V., Bhattacharya, S., Castilla, J. A., Ferraretti, A. P., Korsak, V., Kupka, M., Lambalk, C. B., Nygren, K. G. & Nyboe Andersen, A. N., 2010, In: Human Reproduction. 25, 8, p. 1851-1862

    Research output: Contribution to journal › Article › Academic › peer-review

    340 Citations (Scopus)

  • Associated Genetics and Connectomic Circuitry in Schizophrenia and Bipolar Disorder

    Wei, Y., de Lange, S. C., Savage, J. E., Tissink, E., Qi, T., Repple, J., Gruber, M., Kircher, T., Dannlowski, U., Posthuma, D. & van den Heuvel, M. P., 15 Jul 2023, In: Biological Psychiatry. 94, 2, p. 174-183 10 p.

    Research output: Contribution to journal › Article › Academic › peer-review

    Open Access
    4 Citations (Scopus)

  • Associated Microscale Spine Density and Macroscale Connectivity Disruptions in Schizophrenia

    van den Heuvel, M. P., Scholtens, L. H., de Reus, M. A. & Kahn, R. S., 15 Aug 2016, In: Biological Psychiatry. 80, 4, p. 293-301 9 p.

    Research output: Contribution to journal › Article › Academic › peer-review

    53 Citations (Scopus)

  • Association analysis identifies 65 new breast cancer risk loci

    NBCS Collaborators, ABCTB Investigators, kConFab/AOCS Investigators, Bogdanova, N. V., Bojesen, S. E., Bonanni, B., Børresen-Dale, A-L., Brand, J. S., Brauch, H., Brennan, P., Brenner, H., Brinton, L., Broberg, P., Brock, I. W., Broeks, A., Brooks-Wilson, A., Brucker, S. Y., Brüning, T., Burwinkel, B., Butterbach, K., & 292 othersCai, Q., Cai, H., Caldés, T., Canzian, F., Carracedo, A., Carter, B. D., Castelao, J. E., Chan, T. L., David Cheng, T-Y., Seng Chia, K., Choi, J-Y., Christiansen, H., Clarke, C. L., Collée, M., Conroy, D. M., Cordina-Duverger, E., Cornelissen, S., Cox, D. G., Cox, A., Cross, S. S., Cunningham, J. M., Czene, K., Daly, M. B., Devilee, P., Doheny, K. F., Dörk, T., Dos-Santos-Silva, I., Dumont, M., Durcan, L., Dwek, M., Eccles, D. M., Ekici, A. B., Eliassen, A. H., Ellberg, C., Elvira, M., Engel, C., Eriksson, M., Fasching, P. A., Figueroa, J., Flesch-Janys, D., Fletcher, O., Flyger, H., Fritschi, L., Gaborieau, V., Gabrielson, M., Gago-Dominguez, M., Gao, Y-T., Gapstur, S. M., García-Sáenz, J. A., Gaudet, M. M., Georgoulias, V., Giles, G. G., Glendon, G., Goldberg, M. S., Goldgar, D. E., González-Neira, A., Grenaker Alnæs, G. I., Grip, M., Gronwald, J., Grundy, A., Guénel, P., Haeberle, L., Hahnen, E., Haiman, C. A., Håkansson, N., Hamann, U., Hamel, N., Hankinson, S., Harrington, P., Hart, S. N., Hartikainen, J. M., Hartman, M., Hein, A., Heyworth, J., Hicks, B., Hillemanns, P., Ho, D. N., Hollestelle, A., Hoover, R. N., Hopper, J. L., Hou, M-F., Hsiung, C-N., Huang, G., Humphreys, K., Ishiguro, J., Ito, H., Iwasaki, M., Iwata, H., Jakubowska, A., Janni, W., John, E. M., Johnson, N., Jones, K., Jones, M., Jukkola-Vuorinen, A., Kaaks, R., Kabisch, M., Kaczmarek, K., Kang, D., Kasuga, Y., Kerin, M. J., Khan, S., Khusnutdinova, E., Kiiski, J. I., Kim, S-W., Knight, J. A., Kosma, V-M., Kristensen, V. N., Krüger, U., Kwong, A., Lambrechts, D., Le Marchand, L., Lee, E., Lee, M. H., Lee, J. W., Neng Lee, C., Lejbkowicz, F., Li, J., Lilyquist, J., Lindblom, A., Lissowska, J., Lo, W-Y., Loibl, S., Long, J., Lophatananon, A., Lubinski, J., Luccarini, C., Lux, M. P., Ma, E. S. K., MacInnis, R. J., Maishman, T., Makalic, E., Malone, K. E., Kostovska, I. M., Mannermaa, A., Manoukian, S., Manson, J. E., Margolin, S., Mariapun, S., Martinez, M. E., Matsuo, K., Mavroudis, D., McKay, J., McLean, C., Meindl, A., Menéndez, P., Menon, U., Meyer, J., Miao, H., Miller, N., Taib, N. A. M., Muir, K., Mulligan, A. M., Mulot, C., Neuhausen, S. L., Nevanlinna, H., Neven, P., Nielsen, S. F., Noh, D-Y., Nordestgaard, B. G., Norman, A., Olopade, O. I., Olson, J. E., Olsson, H., Olswold, C., Orr, N., Pankratz, V. S., Park, S. K., Park-Simon, T-W., Lloyd, R., Perez, J. I. A., Peterlongo, P., Peto, J., Phillips, K-A., Pinchev, M., Plaseska-Karanfilska, D., Prentice, R., Presneau, N., Prokofyeva, D., Pugh, E., Pylkäs, K., Rack, B., Radice, P., Rahman, N., Rennert, G., Rennert, H. S., Rhenius, V., Romero, A., Romm, J., Ruddy, K. J., Rüdiger, T., Rudolph, A., Ruebner, M., Rutgers, E. J. T., Saloustros, E., Sandler, D. P., Sangrajrang, S., Sawyer, E. J., Schmidt, D. F., Schmutzler, R. K., Schneeweiss, A., Schoemaker, M. J., Schumacher, F., Schürmann, P., Scott, R. J., Scott, C., Seal, S., Seynaeve, C., Shah, M., Sharma, P., Shen, C-Y., Sheng, G., Sherman, M. E., Shrubsole, M. J., Shu, X-O., Smeets, A., Sohn, C., Southey, M. C., Spinelli, J. J., Stegmaier, C., Stewart-Brown, S., Stone, J., Stram, D. O., Surowy, H., Swerdlow, A., Tamimi, R., Taylor, J. A., Tengström, M., teo, S. H., Beth Terry, M., Tessier, D. C., Thanasitthichai, S., Thöne, K., Tollenaar, R. A. E. M., Tomlinson, I., Tong, L., Torres, D., Truong, T., Tseng, C-C., Tsugane, S., Ulmer, H-U., Ursin, G., Untch, M., Vachon, C., van Asperen, C. J., van den Berg, D., van den Ouweland, A. M. W., van der Kolk, L., van der Luijt, R. B., Vincent, D., Vollenweider, J., Wang-Gohrke, S., Weinberg, C. R., Wendt, C., Whittemore, A. S., Wildiers, H., Willett, W., Winqvist, R., Wolk, A., Wu, A. H., Xia, L., Yamaji, T., Yang, X. R., Har Yip, C., Yoo, K-Y., Yu, J-C., Zheng, W., Zheng, Y., Zhu, B., Ziogas, A., Ziv, E., Lakhani, S. R., Antoniou, A. C., Droit, A., Andrulis, I. L., Amos, C. I., Couch, F. J., Pharoah, P. D. P., Chang-Claude, J., Hall, P., Hunter, D. J., Milne, R. L., García-Closas, M., Schmidt, M. K., Chanock, S. J., Dunning, A. M., Edwards, S. L., Bader, G. D., Chenevix-Trench, G., Simard, J., Kraft, P. & Easton, D. F., 2 Nov 2017, In: NATURE. 551, 7678, p. 92-94 3 p.

    Research output: Contribution to journal › Article › Academic › peer-review

    852 Citations (Scopus)

  • Association between Adult Height and Risk of Colorectal, Lung, and Prostate Cancer: Results from Meta-analyses of Prospective Studies and Mendelian Randomization Analyses

    Khankari, N. K., Shu, X. O., Wen, W., Kraft, P., Lindström, S., Peters, U., Schildkraut, J., Schumacher, F., Bofetta, P., Risch, A., Bickeböller, H., Amos, C. I., Easton, D., Eeles, R. A., Gruber, S. B., Haiman, C. A., Hunter, D. J., Chanock, S. J., Pierce, B. L., Zheng, W., & 94 othersBlalock, K., Campbell, P. T., Casey, G., Conti, D. V., Edlund, C. K., Figueiredo, J., James Gauderman, W., Gong, J., Green, R. C., Harju, J. F., Harrison, T. A., Jacobs, E. J., Jenkins, M. A., Jiao, S., Li, L., Lin, Y., Manion, F. J., Moreno, V., Mukherjee, B., Raskin, L., Schumacher, F. R., Seminara, D., Severi, G., Stenzel, S. L., Thomas, D. C., Hopper, J. L., Southey, M. C., Makalic, E., Schmidt, D. F., Fletcher, O., Peto, J., Gibson, L., dos Santos Silva, I., Ahsan, H., Whittemore, A., Waisfisz, Q., Meijers-Heijboer, H., Adank, M., van der Luijt, R. B., Uitterlinden, A. G., Hofman, A., Meindl, A., Schmutzler, R. K., Müller-Myhsok, B., Lichtner, P., Nevanlinna, H., Muranen, T. A., Aittomäki, K., Blomqvist, C., Chang-Claude, J., Hein, R., Dahmen, N., Beckman, L., Crisponi, L., Hall, P., Czene, K., Irwanto, A., Liu, J., Easton, D. F., Turnbull, C., Rahman, N., Eeles, R., Kote-Jarai, Z., Muir, K., Giles, G., Neal, D., Donovan, J. L., Hamdy, F. C., Wiklund, F., Gronberg, H., Haiman, C., Schumacher, F., Travis, R., Riboli, E., Hunter, D., Gapstur, S., Berndt, S., Chanock, S., Han, Y., Su, L., Wei, Y., Hung, R. J., Brhane, Y., McLaughlin, J., Brennan, P., McKay, J. D., Rosenberger, A., Houlston, R. S., Caporaso, N., Teresa Landi, M., Heinrich, J., Wu, X., Ye, Y. & Christiani, D. C., 1 Sept 2016, In: PLoS medicine. 13, 9, e1002118.

    Research output: Contribution to journal › Article › Academic › peer-review

    63 Citations (Scopus)

  • Association between C677T polymorphism of methylene tetrahydrofolate reductase and congenital heart disease: Meta-analysis of 7697 cases and 13 125 controls

    Mamasoula, C., Prentice, R. R., Pierscionek, T., Pangilinan, F., Mills, J. L., Druschel, C., Pass, K., Russell, M. W., Hall, D., Töpf, A., Brown, D. L., Zelenika, D., Bentham, J., Cosgrove, C., Bhattacharya, S., Riveron, J. G., Setchfield, K., Brook, J. D., Bu'Lock, F. A., Thornborough, C., & 22 othersRahman, T. J., Doza, J. P., Tan, H. L., O'Sullivan, J., Stuart, A. G., Blue, G., Winlaw, D., Postma, A. V., Mulder, B. J. M., Zwinderman, A. H., Van Engelen, K., Moorman, A. F. M., Rauch, A., Gewillig, M., Breckpot, J., Devriendt, K., Lathrop, G. M., Farrall, M., Goodship, J. A., Cordell, H. J., Brody, L. C. & Keavney, B. D., Aug 2013, In: Circulation: Cardiovascular Genetics. 6, 4, p. 347-353 7 p.

    Research output: Contribution to journal › Article › Academic › peer-review

    Open Access
    31 Citations (Scopus)

  • Association between low fetal fraction in cell-free DNA screening and fetal chromosomal aberrations: A systematic review and meta-analysis

    Becking, E. C., Schuit, E., van Baar de Knegt, S. M. E., Sistermans, E. A., Henneman, L., Bekker, M. N. & Scheffer, P. G., Jun 2023, In: Prenatal diagnosis. 43, 7, p. 838-853 16 p.

    Research output: Contribution to journal › Review article › Academic › peer-review

    Open Access
    4 Citations (Scopus)

  • Association between low fetal fraction in cell-free DNA testing and adverse pregnancy outcome: A systematic review: A systematic review

    Scheffer, P. G., Wirjosoekarto, S. A. M., Becking, E. C., Weiss, M. M., Bax, C. J., Oepkes, D., Sistermans, E. A., Henneman, L. & Bekker, M. N., Sept 2021, In: Prenatal diagnosis. 41, 10, p. 1287-1295 9 p.

    Research output: Contribution to journal › Review article › Academic › peer-review

    Open Access
    17 Citations (Scopus)

  • Association between ovulation stimulation, in vitro fertilisation, and neural tube defects?

    Cornel, M. C., ten Kate, L. P. & te Meerman, G. J., 1 Jan 1990, In: Teratology. 42, 3, p. 201-203 3 p.

    Research output: Contribution to journal › Letter › Academic › peer-review

    11 Citations (Scopus)

  • Association between the CHEK2*1100delC germ line mutation and estrogen receptor status

    de Bock, G. H., Mourits, M. J. E., Schutte, M., Krol-Warmerdam, E. M. M., Seynaeve, C., Blom, J., Brekelmans, C. T. M., Meijers-Heijboer, H., van Asperen, C. J., Cornelisse, C. J., Devilee, P., Tollenaar, R. A. E. M. & Klijn, J. G. M., 2006, In: International journal of gynecological cancer. 16, Suppl. 2, p. 552-555

    Research output: Contribution to journal › Article › Academic › peer-review

    16 Citations (Scopus)

  • Association of breast cancer risk in BRCA1 and BRCA2 mutation carriers with genetic variants showing differential allelic expression: identification of a modifier of breast cancer risk at locus 11q22.3

    EMBRACE, GEMO Study Collaborators, HEBON, KConFab Investigators, Foretova, L., Fostira, F., Foulkes, W. D., Fountzilas, G., Friedman, E., Frost, D., Ganschow, P., Ganz, P. A., Garber, J., Gayther, S. A., Gerdes, A-M., Glendon, G., Godwin, A. K., Goldgar, D. E., Greene, M. H., Gronwald, J., & 102 othersHahnen, E., Hamann, U., Hansen, T. V. O., Hart, S., Hays, J. L., Hogervorst, F. B. L., Hulick, P. J., Imyanitov, E. N., Isaacs, C., Izatt, L., Jakubowska, A., James, P., Janavicius, R., Jensen, U. B., John, E. M., Joseph, V., Just, W., Kaczmarek, K., Karlan, B. Y., Kets, C. M., Kirk, J., Kriege, M., Laitman, Y., Laurent, M., Lazaro, C., Leslie, G., Lester, J., Lesueur, F., Liljegren, A., Loman, N., Loud, J. T., Manoukian, S., Mariani, M., Mazoyer, S., McGuffog, L., Meindl, A., Miller, A., Montagna, M., Mulligan, A. M., Nathanson, K. L., Neuhausen, S. L., Nevanlinna, H., Nussbaum, R. L., Olah, E., Olopade, O. I., Ong, K-R., Osorio, A., Papi, L., Park, S. K., Pedersen, I. S., Peissel, B., Segura, P. P., Peterlongo, P., Phelan, C. M., Radice, P., Rantala, J., Rappaport-Fuerhauser, C., Rennert, G., Richardson, A., Robson, M., Rodriguez, G. C., Rookus, M. A., Schmutzler, R. K., Sevenet, N., Shah, P. D., Singer, C. F., Slavin, T. P., Snape, K., Sokolowska, J., Sønderstrup, I. M. H., Southey, M., Spurdle, A. B., Stadler, Z., Stoppa-Lyonnet, D., Sukiennicki, G., Sutter, C., Tan, Y., tea, M-K., Teixeira, M. R., Teulé, A., teo, S-H., Terry, M. B., Thomassen, M., Tihomirova, L., Tischkowitz, M., Tognazzo, S., Toland, A. E., Tung, N., van den Ouweland, A. M. W., van der Luijt, R. B., van Rensburg, E. J., Varon-Mateeva, R., Wappenschmidt, B., Wijnen, J. T., Rebbeck, T., Chenevix-Trench, G., Offit, K., Couch, F. J., Nord, S., Easton, D. F., Antoniou, A. C. & Simard, J., 1 Jan 2017, In: Breast cancer research and treatment. 161, 1, p. 117-134 18 p.

    Research output: Contribution to journal › Article › Academic › peer-review

    19 Citations (Scopus)

  • Association of Chromosomal Instability, Microsatellite Instability and CPG Island Methylator Phenotype with Postcolonoscopy Colorectal Cancer in a Population Based Study

    Bogie, R. M. M., le Clercq, C. M. C., Voorham, Q. J. M., Cordes, M., Sie, D., Rausch, C., van den Broek, E., de Vries, S. D. J., van Grieken, N. C. T., Riedl, R. G., Sastrowijoto, P., van Engeland, M., Ylstra, B., Meijer, G. A., Masclee, A. A. M., Carvalho, B. & Sanduleanu, S., Sept 2018, In: Journal of pathology. 246, p. S31-S31

    Research output: Contribution to journal › Meeting Abstract › Academic

  • Association of Cognitive Function Trajectories in Centenarians With Postmortem Neuropathology, Physical Health, and Other Risk Factors for Cognitive Decline

    Beker, N., Ganz, A., Hulsman, M., Klausch, T., Schmand, B. A., Scheltens, P., Sikkes, S. A. M. & Holstege, H., 15 Jan 2021, In: JAMA network open. 4, 1, p. e2031654 e2031654.

    Research output: Contribution to journal › Article › Academic › peer-review

    Open Access
    29 Citations (Scopus)

  • Association of Genetic Risk for Schizophrenia and Bipolar Disorder With Infant Neuromotor Development

    Serdarevic, F., Jansen, P. R., Ghassabian, A., White, T., Jaddoe, V. W. V., Posthuma, D. & Tiemeier, H., 1 Jan 2018, In: JAMA Psychiatry. 75, 1, p. 96-98 3 p.

    Research output: Contribution to journal › Article › Academic › peer-review

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    15 Citations (Scopus)

  • Association of genetic susceptibility variants for type 2 diabetes with breast cancer risk in women of European ancestry

    Zhao, Z., Wen, W., Michailidou, K., Bolla, M. K., Wang, Q., Zhang, B., Long, J., Shu, X-O., Schmidt, M. K., Milne, R. L., Garcia-Closas, M., Chang-Claude, J., Lindstrom, S., Bojesen, S. E., Ahsan, H., Aittomaki, K., Andrulis, I. L., Anton-Culver, H., Arndt, V., Beckmann, M. W., & 98 othersBeeghly-Fadiel, A., Benitez, J., Blomqvist, C., Bogdanova, N. V., Borresen-Dale, A-L., Brand, J., Brauch, H., Brenner, H., Burwinkel, B., Cai, Q., Casey, G., Chenevix-Trench, G., Couch, F. J., Cox, A., Cross, S. S., Czene, K., Doerk, T., Dumont, M., Fasching, P. A., Figueroa, J., Flesch-Janys, D., Fletcher, O., Flyger, H., Fostira, F., Gammon, M., Giles, G. G., Guenel, P., Haiman, C. A., Hamann, U., Harrington, P., Hartman, M., Hooning, M. J., Hopper, J. L., Jakubowska, A., Jasmine, F., John, E. M., Johnson, N., Kabisch, M., Khan, S., Kibriya, M., Knight, J. A., Kosma, V-M., Kriege, M., Kristensen, V., Le Marchand, L., Lee, E., Li, J., Lindblom, A., Lophatananon, A., Luben, R., Lubinski, J., Malone, K. E., Mannermaa, A., Manoukian, S., Margolin, S., Marme, F., McLean, C., Meijers-Heijboer, H., Meindl, A., Miao, H., Muir, K., Neuhausen, S. L., Nevanlinna, H., Neven, P., Olson, J. E., Perkins, B., Peterlongo, P., Phillips, K-A., Pylkas, K., Rudolph, A., Santella, R., Sawyer, E. J., Schmutzler, R. K., Schoemaker, M., Shah, M., Shrubsole, M., Southey, M. C., Swerdlow, A. J., Toland, A. E., Tomlinson, I., Torres, D., Therese Truong, T., Ursin, G., Van Der Luijt, R. B., Verhoef, S., Wang-Gohrke, S., Whittemore, A. S., Winqvist, R., Zamora, M. P., Zhao, H., Dunning, A. M., Simard, J., Hall, P., Kraft, P., Pharoah, P., Hunter, D., Easton, D. F. & Zheng, W., May 2016, In: CCC. Cancer Causes and Control. 27, 5, p. 679-693

    Research output: Contribution to journal › Article › Academic › peer-review

    20 Citations (Scopus)

  • Association of Genomic Domains in BRCA1 and BRCA2 with Prostate Cancer Risk and Aggressiveness

    Patel, V. L., Busch, E. L., Friebel, T. M., Cronin, A., Leslie, G., McGuffog, L., Adlard, J., Agata, S., Agnarsson, B. A., Ahmed, M., Aittomäki, K., Alducci, E., Andrulis, I. L., Arason, A., Arnold, N., Artioli, G., Arver, B., Auber, B., Azzollini, J., Balmaña, J., & 244 othersBarkardottir, R. B., Barnes, D. R., Barroso, A., Barrowdale, D., Belotti, M., Benitez, J., Bertelsen, B., Blok, M. J., Bodrogi, I., Bonadona, V., Bonanni, B., Bondavalli, D., Boonen, S. E., Borde, J., Borg, A., Bradbury, A. R., Brady, A., Brewer, C., Brunet, J., Buecher, B., Buys, S. S., Cabezas-Camarero, S., Caldés, T., Caliebe, A., Caligo, M. A., Calvello, M., Campbell, I. G., Carnevali, I., Carrasco, E., Chan, T. L., Chu, A. T. W., Chung, W. K., Claes, K. B. M., Collaborators, G. S., Collaborators, E., Cook, J., Cortesi, L., Couch, F. J., Daly, M. B., Damante, G., Darder, E., Davidson, R., de la Hoya, M., Puppa, L. D., Dennis, J., Díez, O., Ding, Y. C., Ditsch, N., Domchek, S. M., Donaldson, A., Dworniczak, B., Easton, D. F., Eccles, D. M., Eeles, R. A., Ehrencrona, H., Ejlertsen, B., Engel, C., Evans, D. G., Faivre, L., Faust, U., Feliubadaló, L., Foretova, L., Fostira, F., Fountzilas, G., Frost, D., García-Barberán, V., Garre, P., Gauthier-Villars, M., Géczi, L., Gehrig, A., Gerdes, A. M., Gesta, P., Giannini, G., Glendon, G., Godwin, A. K., Radice, P., Greene, M. H., Gutierrez-Barrera, A. M., Hahnen, E., Hamann, U., Hauke, J., Herold, N., Hogervorst, F. B. L., Honisch, E., Hopper, J. L., Hulick, P. J., Investigators, KC. F., Investigators, H., Izatt, L., Jager, A., James, P., Janavicius, R., Jensen, U. B., Jensen, T. D., Johannsson, O. T., John, E. M., Joseph, V., Kang, E., Kast, K., Kiiski, J. I., Kim, S. W., Kim, Z., Ko, K. P., Konstantopoulou, I., Kramer, G., Krogh, L., Kruse, T. A., Kwong, A., Larsen, M., Lasset, C., Lautrup, C., Lazaro, C., Lee, J., Lee, J. W., Lee, M. H., Lemke, J., Lesueur, F., Liljegren, A., Lindblom, A., Llovet, P., Lopez-Fernández, A., Lopez-Perolio, I., Lorca, V., Loud, J. T., Ma, E. S. K., Mai, P. L., Manoukian, S., Mari, V., Martin, L., Matricardi, L., Mebirouk, N., Medici, V., Meijers-Heijboer, H. E. J., Meindl, A., Mensenkamp, A. R., Miller, C., Gomes, D. M., Montagna, M., Mooij, T. M., Moserle, L., Mouret-Fourme, E., Mulligan, A. M., Nathanson, K. L., Navratilova, M., Nevanlinna, H., Niederacher, D., Nielsen, F. C. C., Nikitina-Zake, L., Offit, K., Olah, E., Olopade, O. I., Ong, K. R., Osorio, A., Ott, C. E., Palli, D., Park, S. K., Parsons, M. T., Pedersen, I. S., Peissel, B., Peixoto, A., Pérez-Segura, P., Peterlongo, P., Petersen, A. H., Porteous, M. E., Pujana, M. A., Radice, P., Ramser, J., Rantala, J., Rashid, M. U., Rhiem, K., Rizzolo, P., Robson, M. E., Rookus, M. A., Rossing, C. M., Ruddy, K. J., Santos, C., Saule, C., Scarpitta, R., Schmutzler, R. K., Schuster, H., Senter, L., Seynaeve, C. M., Shah, P. D., Sharma, P., Shin, V. Y., Silvestri, V., Simard, J., Singer, C. F., Skytte, A. B., Snape, K., Solano, A. R., Soucy, P., Southey, M. C., Spurdle, A. B., Steele, L., Steinemann, D., Stoppa-Lyonnet, D., Stradella, A., Sunde, L., Sutter, C., Tan, Y. Y., Teixeira, M. R., Teo, S. H., Thomassen, M., Tibiletti, M. G., Tischkowitz, M., Tognazzo, S., Toland, A. E., Tommasi, S., Torres, D., Toss, A., Trainer, A. H., Tung, N., van Asperen, C. J., van der Baan, F. H., van der Kolk, L. E., van der Luijt, R. B., van Hest, L. P., Varesco, L., Varon-Mateeva, R., Viel, A., Vierstrate, J., Villa, R., von Wachenfeldt, A., Wagner, P., Wang-Gohrke, S., Wappenschmidt, B., Weitzel, J. N., Wieme, G., Yadav, S., Yannoukakos, D., Yoon, S. Y., Zanzottera, C., Zorn, K. K., D'Amico, A. V., Freedman, M. L., Pomerantz, M. M., Chenevix-Trench, G., Antoniou, A. C., Neuhausen, S. L., Ottini, L., Nielsen, H. R., Rebbeck, T. R. & Goldgar, D. E., 1 Feb 2020, In: Cancer research. 80, 3, p. 624-638 15 p.

    Research output: Contribution to journal › Article › Academic › peer-review

    36 Citations (Scopus)

  • Association of low-frequency and rare coding variants with information processing speed

    Bressler, J., Davies, G., Smith, A. V., Saba, Y., Bis, J. C., Jian, X., Hayward, C., Yanek, L., Smith, J. A., Mirza, S. S., Wang, R., Adams, H. H. H., Becker, D., Boerwinkle, E., Campbell, A., Cox, S. R., Eiriksdottir, G., Fawns-Ritchie, C., Gottesman, R. F., Grove, M. L., & 35 othersGuo, X., Hofer, E., Kardia, S. L. R., Knol, M. J., Koini, M., Lopez, O. L., Marioni, R. E., Nyquist, P., Pattie, A., Polasek, O., Porteous, D. J., Rudan, I., Satizabal, C. L., Schmidt, H., Schmidt, R., Sidney, S., Simino, J., Smith, B. H., Turner, S. T., van der Lee, S. J., Ware, E. B., Whitmer, R. A., Yaffe, K., Yang, Q., Zhao, W., Gudnason, V., Launer, L. J., Fitzpatrick, A. L., Psaty, B. M., Fornage, M., Arfan Ikram, M., van Duijn, C. M., Seshadri, S., Mosley, T. H. & Deary, I. J., 1 Dec 2021, In: Translational Psychiatry. 11, 1, 613.

    Research output: Contribution to journal › Article › Academic › peer-review

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    1 Citation (Scopus)

  • Association of MGMT and BIN1 genes with Alzheimer's disease risk across sex and APOE ε4 status

    EADB, GR@ACE, Degesco, EADI, GERAD, DemGene, 2 Dec 2023, (E-pub ahead of print) In: Alzheimer's & dementia : the journal of the Alzheimer's Association.

    Research output: Contribution to journal › Letter › Academic › peer-review

    Open Access

  • Association of mitochondrial variants and haplogroups identified by whole exome sequencing with Alzheimer's disease

    Alzheimer's Disease Sequencing Project, 2021, (Accepted/In press) In: Alzheimer's and Dementia.

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    Open Access
    8 Citations (Scopus)

  • Association of PHB 1630 C > T and MTHFR 677 C > T polymorphisms with breast and ovarian cancer risk in BRCA1/2 mutation carriers: results from a multicenter study

    AUTHOR GROUP, Nelen, M. R., van den Ouweland, A. M. W., Seynaeve, C., van der Luijt, R. B., Devilee, P., Easton, D. F., Peock, S., Frost, D., Platte, R., Ellis, S. D., Fineberg, E., Evans, D. G., Lalloo, F., Eeles, R., Jacobs, C., Adlard, J., Davidson, R., Eccles, D., Cole, T., & 31 othersCook, J., Godwin, A., Bove, B., Stoppa-Lyonnet, D., Caux-Moncoutier, V., Belotti, M., Tirapo, C., Mazoyer, S., Barjhoux, L., Boutry-Kryza, N., Pujol, P., Coupier, I., Peyrat, J. P., Vennin, P., Muller, D., Fricker, J. P., Venat-Bouvet, L., Johannsson, O., Isaacs, C., Schmutzler, R., Wappenschmidt, B., Meindl, A., Arnold, N., Varon-Mateeva, R., Niederacher, D., Sutter, C., Deissler, H., Preisler-Adams, S., Simard, J., Soucy, P. & Durocher, F., 2012, In: British journal of cancer. 106, 12, p. 2016-2024

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    23 Citations (Scopus)

  • Association of polygenic score for major depression with response to lithium in patients with bipolar disorder

    Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium, Jun 2021, In: Molecular psychiatry. 26, 6, p. 2457-2470 14 p.

    Research output: Contribution to journal › Article › Academic › peer-review

    Open Access
    38 Citations (Scopus)

  • Association of rare MSH6 variants with familial breast cancer

    Wasielewski, M., Riaz, M., Vermeulen, J., van den Ouweland, A., Labrijn-Marks, I., Olmer, R., van der Spaa, L., Klijn, J. G. M., Meijers-Heijboer, H., Dooijes, D. & Schutte, M., 2010, In: Breast cancer research and treatment. 123, 2, p. 315-320

    Research output: Contribution to journal › Article › Academic › peer-review

    Open Access
    11 Citations (Scopus)

  • Association of TNF-α serum levels and TNFA promoter polymorphisms with risk of myocardial infarction

    Bennet, A. M., van Maarle, M. C., Hallqvist, J., Morgenstern, R., Frostegård, J., Wiman, B., Prince, J. A. & de Faire, U., Aug 2006, In: Atherosclerosis. 187, 2, p. 408-414 7 p.

    Research output: Contribution to journal › Article › Academic › peer-review

    84 Citations (Scopus)

  • Association of Variants in the SPTLC1 Gene with Juvenile Amyotrophic Lateral Sclerosis

    Johnson, J. O., Chia, R., Miller, D. E., Li, R., Kumaran, R., Abramzon, Y., Alahmady, N., Renton, A. E., Topp, S. D., Gibbs, J. R., Cookson, M. R., Sabir, M. S., Dalgard, C. L., Troakes, C., Jones, A. R., Shatunov, A., Iacoangeli, A., Al Khleifat, A., Ticozzi, N., Silani, V., & 278 othersGellera, C., Blair, I. P., Dobson-Stone, C., Kwok, J. B., Bonkowski, E. S., Palvadeau, R., Tienari, P. J., Morrison, K. E., Shaw, P. J., Al-Chalabi, A., Brown, R. H., Calvo, A., Mora, G., Al-Saif, H., Gotkine, M., Leigh, F., Chang, I. J., Perlman, S. J., Glass, I., Scott, A. I., Shaw, C. E., Basak, A. N., Landers, J. E., Chiò, A., Crawford, T. O., Smith, B. N., Traynor, B. J., Smith, B. N., Ticozzi, N., Fallini, C., Gkazi, A. S., Topp, S. D., Scotter, E. L., Kenna, K. P., Keagle, P., Tiloca, C., Vance, C., Troakes, C., Colombrita, C., King, A., Pensato, V., Castellotti, B., Baas, F., ten Asbroek, A. L. M. A., McKenna-Yasek, D., McLaughlin, R. L., Polak, M., Asress, S., Esteban-Pérez, J., Stevic, Z., D'Alfonso, S., Mazzini, L., Comi, G. P., del Bo, R., Ceroni, M., Gagliardi, S., Querin, G., Bertolin, C., van Rheenen, W., Rademakers, R., van Blitterswijk, M., Lauria, G., Duga, S., Corti, S., Cereda, C., Corrado, L., Sorarù, G., Williams, K. L., Nicholson, G. A., Blair, I. P., Leblond-Manry, C., Rouleau, G. A., Hardiman, O., Morrison, K. E., Veldink, J. H., van den Berg, L. H., Al-Chalabi, A., Pall, H., Shaw, P. J., Turner, M. R., Talbot, K., Taroni, F., García-Redondo, A., Wu, Z., Glass, J. D., Gellera, C., Ratti, A., Brown, R. H., Silani, V., Shaw, C. E., Landers, J. E., Dalgard, C. L., Adeleye, A., Soltis, A. R., Alba, C., Viollet, C., Bacikova, D., Hupalo, D. N., Sukumar, G., Pollard, H. B., Wilkerson, M. D., Martinez, E. M., Abramzon, Y., Ahmed, S., Arepalli, S., Baloh, R. H., Bowser, R., Brady, C. B., Brice, A., Broach, J., Campbell, R. H., Camu, W., Chia, R., Cooper-Knock, J., Ding, J., Drepper, C., Drory, V. E., Dunckley, T. L., Eicher, J. D., England, B. K., Faghri, F., Feldman, E., Floeter, M. K., Fratta, P., Geiger, J. T., Gerhard, G., Gibbs, J. R., Gibson, S. B., Glass, J. D., Hardy, J., Harms, M. B., Heiman-Patterson, T. D., Hernandez, D. G., Jansson, L., Kirby, J., Kowall, N. W., Laaksovirta, H., Landeck, N., Landi, F., le Ber, I., Lumbroso, S., Macgowan, D. J. L., Maragakis, N. J., Mora, G., Mouzat, K., Murphy, N. A., Myllykangas, L., Nalls, M. A., Orrell, R. W., Ostrow, L. W., Pamphlett, R., Pickering-Brown, S., Pioro, E. P., Pletnikova, O., Pliner, H. A., Pulst, S. M., Ravits, J. M., Renton, A. E., Rivera, A., Robberecht, W., Rogaeva, E., Rollinson, S., Rothstein, J. D., Scholz, S. W., Sendtner, M., Shaw, P. J., Sidle, K. C., Simmons, Z., Singleton, A. B., Smith, N., Stone, D. J., Tienari, P. J., Troncoso, J. C., Valori, M., van Damme, P., van Deerlin, V. M., van den Bosch, L., Zinman, L., Landers, J. E., Chiò, A., Traynor, B. J., Angelocola, S. M., Ausiello, F. P., Barberis, M., Bartolomei, I., Battistini, S., Bersano, E., Bisogni, G., Borghero, G., Brunetti, M., Cabona, C., Calvo, A., Canale, F., Canosa, A., Cantisani, T. A., Capasso, M., Caponnetto, C., Cardinali, P., Carrera, P., Casale, F., Chiò, A., Colletti, T., Conforti, F. L., Conte, A., Conti, E., Corbo, M., Cuccu, S., Dalla Bella, E., D'Errico, E., Demarco, G., Dubbioso, R., Ferrarese, C., Ferraro, P. M., Filippi, M., Fini, N., Floris, G., Fuda, G., Gallone, S., Gianferrari, G., Giannini, F., Grassano, M., Greco, L., Iazzolino, B., Introna, A., la Bella, V., Lattante, S., Lauria, G., Liguori, R., Logroscino, G., Logullo, F. O., Lunetta, C., Mandich, P., Mandrioli, J., Manera, U., Manganelli, F., Marangi, G., Marinou, K., Marrosu, M. G., Martinelli, I., Messina, S., Moglia, C., Mora, G., Mosca, L., Murru, M. R., Origone, P., Passaniti, C., Petrelli, C., Petrucci, A., Pozzi, S., Pugliatti, M., Quattrini, A., Ricci, C., Riolo, G., Riva, N., Russo, M., Sabatelli, M., Salamone, P., Salivetto, M., Salvi, F., Santarelli, M., Sbaiz, L., Sideri, R., Simone, I., Simonini, C., Spataro, R., Tanel, R., Tedeschi, G., Ticca, A., Torriello, A., Tranquilli, S., Tremolizzo, L., Trojsi, F., Vasta, R., Vacchiano, V., Vita, G., Volanti, P., Zollino, M. & Zucchi, E., Oct 2021, In: JAMA Neurology. 78, 10, p. 1236-1248 13 p.

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    43 Citations (Scopus)

  • Association of whole-genome and NETRIN1 signaling pathway–derived polygenic risk scores for Major Depressive Disorder and white matter microstructure in the UK Biobank

    Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium & 23andMe Research Team, 1 Jan 2019, In: Biological Psychiatry: Cognitive Neuroscience and Neuroimaging. 4, 1, p. 91-100 10 p.

    Research output: Contribution to journal › Article › Academic › peer-review

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    17 Citations (Scopus)

  • Associations between epigenome-wide DNA methylation and height-related traits among Sub-Saharan Africans: The RODAM study

    Swart, G., Meeks, K., Chilunga, F., Venema, A., Agyemang, C., van der Linden, E. & Henneman, P., 4 Oct 2023, In: Journal of developmental origins of health and disease. 14, 5, p. 658-669

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  • Associations of autozygosity with a broad range of human phenotypes

    Clark, D. W., Okada, Y., Moore, K. H. S., Mason, D., Pirastu, N., Gandin, I., Mattsson, H., Barnes, C. L. K., Lin, K., Zhao, J. H., Deelen, P., Rohde, R., Schurmann, C., Guo, X., Giulianini, F., Zhang, W., Medina-Gomez, C., Karlsson, R., Bao, Y., Bartz, T. M., & 416 othersBaumbach, C., Biino, G., Bixley, M. J., Brumat, M., Chai, J-F., Corre, T., Cousminer, D. L., Dekker, A. M., Eccles, D. A., van Eijk, K. R., Fuchsberger, C., Gao, H., Germain, M., Gordon, S. D., de Haan, H. G., Harris, S. E., Hofer, E., Huerta-Chagoya, A., Igartua, C., Jansen, I. E., Jia, Y., Kacprowski, T., Karlsson, T., Kleber, M. E., Li, S. A., Li-Gao, R., Mahajan, A., Matsuda, K., Meidtner, K., Meng, W., Montasser, M. E., van der Most, P. J., Munz, M., Nutile, T., Palviainen, T., Prasad, G., Prasad, R. B., Priyanka, T. D. S., Rizzi, F., Salvi, E., Sapkota, B. R., Shriner, D., Skotte, L., Smart, M. C., Smith, A. V., van der Spek, A., Spracklen, C. N., Strawbridge, R. J., Tajuddin, S. 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    Research output: Contribution to journal › Article › Academic › peer-review

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    54 Citations (Scopus)

  • Associations of Brain Pathology Cognitive and Physical Markers With Age in Cognitively Normal Individuals Aged 60-102 Years

    Legdeur, N., Tijms, B. M., Konijnenberg, E., den Braber, A., ten Kate, M., Sudre, C. H., Tomassen, J., Badissi, M., Yaqub, M., Barkhof, F., van Berckel, B. N., Boomsma, D. I., Scheltens, P., Holstege, H., Maier, A. B. & Visser, P. J., 5 Jun 2020, In: The Journals of Gerontology. Series A, Biological Sciences and Medical Sciences. 75, 9, p. 1609-1617 9 p.

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    6 Citations (Scopus)

  • Associations of common breast cancer susceptibility alleles with risk of breast cancer subtypes in BRCA1 and BRCA2 mutation carriers

    AUTHOR GROUP, 2014, In: Breast Cancer Research. 16, 6, p. 3416

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    43 Citations (Scopus)

  • Associations of height, body mass index, and weight gain with breast cancer risk in carriers of a pathogenic variant in BRCA1 or BRCA2: the BRCA1 and BRCA2 Cohort Consortium

    EMBRACE Collaborators, Kast, K., John, E. M., Hopper, J. L., Andrieu, N., Noguès, C., Mouret-Fourme, E., Lasset, C., Fricker, J-P., Berthet, P., Mari, V. R., Salle, L., Schmidt, M. K., Ausems, M. G. E. M., Garcia, E. B. G., van de Beek, I., Wevers, M. R., Evans, D. G., Tischkowitz, M., Lalloo, F., & 31 othersCook, J., Izatt, L., Tripathi, V., Snape, K., Musgrave, H., Sharif, S., Murray, J., Colonna, S. V., Andrulis, I. L., Daly, M. B., Southey, M. C., de la Hoya, M., Osorio, A., Foretova, L., Berkova, D., Gerdes, A-M., Olah, E., Jakubowska, A., Singer, C. F., Tan, Y., Augustinsson, A., Rantala, J., Simard, J., Schmutzler, R. K., Milne, R. L., Phillips, K-A., Terry, M. B., Goldgar, D., van Leeuwen, F. E., Mooij, T. M. & Antoniou, A. C., 1 Dec 2023, In: Breast Cancer Research. 25, 1, 72.

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    Open Access