09 Laboratory specialisms

Research Output 1979 2020

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Erratum
2020

Author Correction: A global overview of pleiotropy and genetic architecture in complex traits (Nature Genetics, (2019), 51, 9, (1339-1348), 10.1038/s41588-019-0481-0)

Watanabe, K., Stringer, S., Frei, O., Mirkov, M. U., de Leeuw, C., Polderman, T. J. C., van der Sluis, S., Andreassen, O. A., Neale, B. M. & Posthuma, D., 1 Jan 2020, In : Nature Genetics.

Research output: Contribution to journalErratumAcademicpeer-review

Open Access

Erratum to “HPV16 whole genome minority variants in persistent infections from young Dutch women” [J. Clin. Virol. 119 (2019) 24–30](S1386653219301726)(10.1016/j.jcv.2019.08.003)

Lagström, S., van der Weele, P., Rounge, T. B., Christiansen, I. K., King, A. J. & Ambur, O. H., 1 Jan 2020, In : Journal of Clinical Virology. 104286.

Research output: Contribution to journalErratumAcademicpeer-review

Open Access
2019

Author Correction: GBA and APOE ε4 associate with sporadic dementia with Lewy bodies in European genome wide association study (Scientific Reports, (2019), 9, 1, (7013), 10.1038/s41598-019-43458-2)

Rongve, A., Witoelar, A., Ruiz, A., Athanasiu, L., Abdelnour, C., Clarimon, J., Heilmann-Heimbach, S., Hernández, I., Moreno-Grau, S., de Rojas, I., Morenas-Rodríguez, E., Fladby, T., Sando, S. B., Bråthen, G., Blanc, F., Bousiges, O., Lemstra, A. W., van Steenoven, I., Londos, E., Almdahl, I. S. & 20 othersPålhaugen, L., Eriksen, J. A., Djurovic, S., Stordal, E., Saltvedt, I., Ulstein, I. D., Bettella, F., Desikan, R. S., Idland, A-V., Toft, M., Pihlstrøm, L., Snaedal, J., Tárraga, L., Boada, M., Lleó, A., Stefánsson, H., Stefánsson, K. R., Ramírez, A., Aarsland, D. & Andreassen, O. A., 1 Dec 2019, In : Scientific Reports. 9, 1, 15168.

Research output: Contribution to journalErratumAcademicpeer-review

Open Access

Author Correction: GWAS of lifetime cannabis use reveals new risk loci, genetic overlap with psychiatric traits, and a causal effect of schizophrenia liability (Nature Neuroscience, (2018), 21, 9, (1161-1170), 10.1038/s41593-018-0206-1)

Pasman, J. A., Verweij, K. J. H., Gerring, Z., Stringer, S., Sanchez-Roige, S., Treur, J. L., Abdellaoui, A., Nivard, M. G., Baselmans, B. M. L., Ong, J-S., Ip, H. F., van der Zee, M. D., Bartels, M., Day, F. R., Fontanillas, P., Elson, S. L., de Wit, H., Davis, L. K., MacKillop, J., Derringer, J. L. & 31 othersBranje, S. J. T., Hartman, C. A., Heath, A. C., van Lier, P. A. C., Madden, P. A. F., Mägi, R., Meeus, W., Montgomery, G. W., Oldehinkel, A. J., Pausova, Z., Ramos-Quiroga, J. A., Paus, T., Ribases, M., Kaprio, J., Boks, M. P. M., Bell, J. T., Spector, T. D., Gelernter, J., Boomsma, D. I., Martin, N. G., MacGregor, S., Perry, J. R. B., Palmer, A. A., Posthuma, D., Munafò, M. R., Gillespie, N. A., Derks, E. M., Vink, J. M., the 23andMe Research Team, The Substance Use Disorders Working Group of the Psychiatric Genomics Consortium & International Cannabis Consortium, 1 Jul 2019, In : Nature Neuroscience. 22, 7, p. 1196 1 p.

Research output: Contribution to journalErratumAcademicpeer-review

Author Correction: TGF-β induces miR-100 and miR-125b but blocks let-7a through LIN28B controlling PDAC progression (Nature Communications, (2018), 9, 1, (1845), 10.1038/s41467-018-03962-x)

Ottaviani, S., Stebbing, J., Frampton, A. E., Zagorac, S., Krell, J., de Giorgio, A., Trabulo, S. M., Nguyen, V. T. M., Magnani, L., Feng, H., Giovannetti, E., Funel, N., Gress, T. M., Jiao, L. R., Lombardo, Y., Lemoine, N. R., Heeschen, C. & Castellano, L., 1 Dec 2019, In : Nature Communications. 10, 1, 3738.

Research output: Contribution to journalErratumAcademicpeer-review

Open Access

Correction: The Gen-Equip Project: evaluation and impact of genetics e-learning resources for primary care in six European languages (Genetics in Medicine, (2019), 21, 3, (718-726), 10.1038/s41436-018-0132-3)

Jackson, L., O’Connor, A., Paneque, M., Curtisova, V., Lunt, P. W., Pourova, R. K., MacekJr, M., Stefansdottir, V., Turchetti, D., Campos, M., Henneman, L., Godino, L., Skirton, H. & Cornel, M. C., 1 Jul 2019, In : Genetics in Medicine. 21, 7, p. 1669-1669 1 p.

Research output: Contribution to journalErratumAcademicpeer-review

Open Access

Correction: Genome-wide analysis reveals extensive genetic overlap between schizophrenia, bipolar disorder, and intelligence (Molecular Psychiatry, (2019), 10.1038/s41380-018-0332-x)

Smeland, O. B., Bahrami, S., Frei, O., Shadrin, A., O’Connell, K., Savage, J., Watanabe, K., Krull, F., Bettella, F., Steen, N. E., Ueland, T., Posthuma, D., Djurovic, S., Dale, A. M. & Andreassen, O. A., 2019, In : Molecular Psychiatry.

Research output: Contribution to journalErratumAcademicpeer-review

Open Access

Correction: The ARID1B spectrum in 143 patients: from nonsyndromic intellectual disability to Coffin–Siris syndrome (Genetics in Medicine, (2019), 21, 6, (1295-1307), 10.1038/s41436-018-0330-z)

van der Sluijs, P. J., Jansen, S., Vergano, S. A., Adachi-Fukuda, M., Alanay, Y., AlKindy, A., Baban, A., Bayat, A., Beck-Wödl, S., Berry, K., Bijlsma, E. K., Bok, L. A., Brouwer, A. F. J., van der Burgt, I., Campeau, P. M., Canham, N., Chrzanowska, K., Chu, Y. W. Y., Chung, B. H. Y., Dahan, K. & 85 othersde Rademaeker, M., Destree, A., Dudding-Byth, T., Earl, R., Elcioglu, N., Elias, E. R., Fagerberg, C., Gardham, A., Gener, B., Gerkes, E. H., Grasshoff, U., van Haeringen, A., Heitink, K. R., Herkert, J. C., den Hollander, N. S., Horn, D., Hunt, D., Kant, S. G., Kato, M., Kayserili, H. L., Kersseboom, R., Kilic, E., Krajewska-Walasek, M., Lammers, K., Laulund, L. W., Lederer, D., Lees, M., López-González, V., Maas, S., Mancini, G. M. S., Marcelis, C., Martinez, F., Maystadt, I., McGuire, M., McKee, S., Mehta, S., Metcalfe, K., Milunsky, J., Mizuno, S., Moeschler, J. B., Netzer, C., Ockeloen, C. W., Oehl-Jaschkowitz, B., Okamoto, N., Olminkhof, S. N. M., Orellana, C., Pasquier, L., Pottinger, C., Riehmer, V., Robertson, S. P., Roifman, M., Rooryck, C., Ropers, F. G., Rosello, M., Ruivenkamp, C. A. L., Sagiroglu, M. S., Sallevelt, S. C. E. H., Calvo, A. S., Simsek-Kiper, P. O., Soares, G., Solaeche, L., Sonmez, F. M., Splitt, M., Steenbeek, D., Stegmann, A. P. A., Stumpel, C. T. R. M., Tanabe, S., Uctepe, E., Utine, G. E., Veenstra-Knol, H. E., Venkateswaran, S., Vilain, C., Vincent-Delorme, C., Vulto-van Silfhout, A. T., Wheeler, P., Wilson, G. N., Wilson, L. C., Wollnik, B., Kosho, T., Wieczorek, D., Eichler, E., Pfundt, R., de Vries, B. B. A., Clayton-Smith, J. & Santen, G. W. E., 1 Sep 2019, In : Genetics in Medicine. 21, 9, p. 2160-2161

Research output: Contribution to journalErratumAcademicpeer-review

Open Access

Corrigendum to “An improved conjugate vaccine technology; induction of antibody responses to the tumor vasculature” (Vaccine (2018) 36(21) (3054–3060), (S0264410X1830433X), (10.1016/j.vaccine.2018.03.064))

Huijbers, E. J. M., van Beijnum, J. R., Lê, C. T., Langman, S., Nowak-Sliwinska, P., Mayo, K. H. & Griffioen, A. W., 9 Jul 2019, In : Vaccine. 37, 30, p. 4231-4232 2 p.

Research output: Contribution to journalErratumAcademicpeer-review

Open Access

Erratum: Cancer risks for PMS2-associated lynch syndrome (Journal of Clinical Oncology (2018) DOI: 10.1200/JCO.2018.78.4777)

van Hest, L., 1 Jan 2019, In : Journal of Clinical Oncology. 37, 9, p. 761

Research output: Contribution to journalErratumAcademicpeer-review

Erratum: De Novo Mutations Affecting the Catalytic Cα Subunit of PP2A, PPP2CA, Cause Syndromic Intellectual Disability Resembling Other PP2A-Related Neurodevelopmental Disorders (The American Journal of Human Genetics (2019) 104(1) (139–156), (S0002929718304531) (10.1016/j.ajhg.2018.12.002))

Reynhout, S., Jansen, S., Haesen, D., van Belle, S., de Munnik, S. A., Bongers, E. M. H. F., Schieving, J. H., Marcelis, C., Amiel, J., Rio, M., Mclaughlin, H., Ladda, R., Sell, S., Kriek, M., Peeters-Scholte, C. M. P. C. D., Terhal, P. A., van Gassen, K. L., Verbeek, N., Henry, S., Schwoerer, J. S. & 17 othersMalik, S., Revencu, N., Ferreira, C. R., Macnamara, E., Braakman, H. M. H., Brimble, E., Ruzhnikov, M. R. Z., Wagner, M., Harrer, P., Wieczorek, D., Kuechler, A., Tziperman, B., Barel, O., de Vries, B. B. A., Gordon, C. T., Janssens, V. & Vissers, L. E. L. M., 7 Feb 2019, In : American journal of human genetics. 104, 2, p. 357

Research output: Contribution to journalErratumAcademicpeer-review

Open Access

Erratum: Evolutionary expansion of connectivity between multimodal association areas in the human brain compared with chimpanzees(PNAS (2019) 116:14(7101-7106) DOI: 10.1073/pnas.1818512116)

Ardesch, D. J., Scholtens, L. H., Li, L., Preuss, T. M., Rilling, J. K. & van den Heuvel, M. P., 7 May 2019, In : Proceedings of the National Academy of Sciences of the United States of America. 116, 19, p. 9680 1 p.

Research output: Contribution to journalErratumAcademicpeer-review

Open Access

Publisher Correction: Gene expression imputation across multiple brain regions provides insights into schizophrenia risk (Nature Genetics, (2019), 51, 4, (659-674), 10.1038/s41588-019-0364-4)

Huckins, L. M., Dobbyn, A., Ruderfer, D. M., Hoffman, G., Wang, W., Pardiñas, A. F., Rajagopal, V. M., Als, T. D., t. Nguyen, H., Girdhar, K., Boocock, J., Roussos, P., Fromer, M., Kramer, R., Domenici, E., Gamazon, E. R., Purcell, S., CommonMind Consortium, The Schizophrenia Working Group of the Psychiatric Genomics Consortium, iPSYCH-GEMS Schizophrenia Working Group & 12 othersDemontis, D., Børglum, A. D., Walters, J. T. R., C. O’Donovan, M., Sullivan, P., Owen, M. J., Devlin, B., Sieberts, S. K., Cox, N. J., Im, H. K., Sklar, P. & Stahl, E. A., 1 Jun 2019, In : Nature Genetics. 51, 6, p. 1068 1 p.

Research output: Contribution to journalErratumAcademicpeer-review

Open Access
2018

Correction: Quantifying exosome secretion from single cells reveals a modulatory role for GPCR signaling

Verweij, F. J., Bebelman, M. P., Jimenez, C. R., Garcia-Vallejo, J. J., Janssen, H., Neefjes, J., Knol, J. C., de Goeij-de Haas, R., Piersma, S. R., Baglio, S. R., Verhage, M., Middeldorp, J. M., Zomer, A., van Rheenen, J., Coppolino, M. G., Hurbain, I., Raposo, G., Smit, M. J., Toonen, R. F. G., van Niel, G. & 1 othersPegtel, D. M., 5 Mar 2018, In : Journal of Cell Biology. 217, 3, p. 1157

Research output: Contribution to journalErratumAcademicpeer-review

Corrigendum: Fucosylated Antigens in Cancer: An Alliance Toward Tumor Progression, Metastasis, and Resistance to Chemotherapy

Blanas, A., Sahasrabudhe, N. M., Rodríguez, E., van Kooyk, Y. & van Vliet, S. J., 2018, In : Frontiers in Oncology. 8, MAY, 150.

Research output: Contribution to journalErratumAcademicpeer-review

Open Access

Erratum: Correction: A collaborative translational research framework for evaluating and implementing the appropriate use of human genome sequencing to improve health (PLoS medicine (2018) 15 8 (e1002631))

Khoury, M. J., Feero, W. G., Chambers, D. A., Brody, L. C., Aziz, N., Green, R. C., Janssens, A. C. J. W., Murray, M. F., Rodriguez, L. L., Rutter, J. L., Schully, S. D., Winn, D. M. & Mensah, G. A., 2018, In : PLoS Medicine. 15, 8, p. e1002650

Research output: Contribution to journalErratumAcademicpeer-review

Open Access

Erratum to: Majority of human traits do not show evidence for sex-specific genetic and environmental effects (Scientific Reports, (2017), 7, 1, (8688), 10.1038/s41598-017-09249-3)

Stringer, S., Polderman, T. J. C. & Posthuma, D., 2018, In : Scientific Reports. 8, 1, 18060.

Research output: Contribution to journalErratumAcademicpeer-review

Open Access

Erratum to: Telomerecat: A ploidy-agnostic method for estimating telomere length from whole genome sequencing data (Scientific Reports, (2018), 8, 1, (1300), 10.1038/s41598-017-14403-y)

NIHR BioResource - Rare Diseases, 2018, In : Scientific Reports. 8, 1, 13376.

Research output: Contribution to journalErratumAcademicpeer-review

Open Access

Genetic influences on eight psychiatric disorders based on family data of 4 408 646 full and half-siblings, and genetic data of 333 748 cases and controls - CORRIGENDUM

Pettersson, E., Lichtenstein, P., Larsson, H., Song, J., Agrawal, A., Børglum, A. D., Bulik, C. M., Daly, M. J., Davis, L. K., Demontis, D., Edenberg, H. J., Grove, J., Gelernter, J., Neale, B. M., Pardiñas, A. F., Stahl, E., Walters, J. T. R., Walters, R., Sullivan, P. F., Posthuma, D. & 1 othersPolderman, T. J. C., 2018, In : Psychological Medicine.

Research output: Contribution to journalErratumAcademicpeer-review

2011

Erratum: Fetal cardiac function between 11 and 35 weeks gestation and nuchal translucency thickness (Ultrasound Obstet Gynecol (2011) 37 (48-56) DOI: 10.1002/uog.8807)

Clur, S. A. B., Oude Rengerink, K., Mol, B. W. J., Ottenkamp, J. & Bilardo, C. M., 2011, In : Ultrasound in Obstetrics and Gynecology. 38, 4, p. 486

Research output: Contribution to journalErratumAcademicpeer-review

2009

Multi-contrast, isotropic, single-slab 3D MR imaging in multiple sclerosis

Moraal, B., Roosendaal, S. D., Pouwels, P. J. W., Vrenken, H., Van Schijndel, R. A., Meier, D. S., Guttmann, C. R. G., Geurts, J. J. G. & Barkhof, F., 27 Nov 2009, In : Neuroradiology Journal. 22, SUPPL. 1, p. 33-42 10 p.

Research output: Contribution to journalErratumAcademicpeer-review