GROW - Reproductive and Perinatal Medicine

Research output

Research output per year 2007 2014 2015 2016 2017 2018 2019 2020 2021 2022 2023 2024

• 1666 Article
• 179 (Systematic) Review article
• 140 Doctoral Thesis
• 64 Comment/Letter to the editor
• 173 More
  • 61 Editorial
  • 45 Chapter
  • 36 Erratum / corrigendum / retractions
  • 10 Conference Abstract/Poster in journal
  • 5 Abstract
  • 3 Book
  • 2 Report
  • 2 Farewell speech
  • 2 Inaugural speech
  • 2 Paper
  • 2 Preprint
  • 1 Book editing
  • 1 Conference article in proceeding
  • 1 Conference article in journal

Research output per year

Research output per year

Search results

• A Recurrent De Novo PACS2 Heterozygous Missense Variant Causes Neonatal-Onset Developmental Epileptic Encephalopathy, Facial Dysmorphism, and Cerebellar Dysgenesis (vol 102, pg 995, 2018)

  DDD Study, C4RCD Res Grp & Thauvin-Robinet, C., 4 Oct 2018, In: American Journal of Human Genetics. 103, 4, p. 631-631 1 p.

  Research output: Contribution to journal › Erratum / corrigendum / retractions › Academic

  Open Access

• Author Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language

  Blok, L. S., Rousseau, J., Twist, J., Ehresmann, S., Takaku, M., Venselaar, H., Rodan, L. H., Nowak, C. B., Douglas, J., Swoboda, K. J., Steeves, M. A., Sahai, I., Stumpel, C. T. R. M., Stegmann, A. P. A., Wheeler, P., Willing, M., Fiala, E., Kochhar, A., Gibson, W. T., Cohen, A. S. A., & 33 othersAgbahovbe, R., Innes, A. M., Au, P. Y. B., Rankin, J., Anderson, I. J., Skinner, S. A., Louie, R. J., Warren, H. E., Afenjar, A., Keren, B., Nava, C., Buratti, J., Isapof, A., Rodriguez, D., Lewandowski, R., Propst, J., van Essen, T., Choi, M., Lee, S., Chae, J. H., Price, S., Schnur, R. E., Douglas, G., Wentzensen, I. M., Zweier, C., Reis, A., Bialer, M. G., Moore, C., Koopmans, M., Brilstra, E. H., DDD Study, Fisher, S. E. & Campeau, P. M., 15 Feb 2019, In: Nature Communications. 10, p. 1-4 4 p., 883.

  Research output: Contribution to journal › Erratum / corrigendum / retractions › Academic

  Open Access

• Author Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language

  Snijders Blok, L., Rousseau, J., Twist, J., Ehresmann, S., Takaku, M., Venselaar, H., Rodan, L. H., Nowak, C. B., Douglas, J., Swoboda, K. J., Steeves, M. A., Sahai, I., Stumpel, C. T. R. M., Stegmann, A. P. A., Wheeler, P., Willing, M., Fiala, E., Kochhar, A., Gibson, W. T., Cohen, A. S. A., & 33 othersAgbahovbe, R., Innes, A. M., Au, P. Y. B., Rankin, J., Anderson, I. J., Skinner, S. A., Louie, R. J., Warren, H. E., Afenjar, A., Keren, B., Nava, C., Buratti, J., Isapof, A., Rodriguez, D., Lewandowski, R., Propst, J., van Essen, T., Choi, M., Lee, S., Chae, J. H., Price, S., Schnur, R. E., Douglas, G., Wentzensen, I. M., Zweier, C., Reis, A., Bialer, M. G., Moore, C., Jansen, S., Brunner, H. G., DDD Study, Fisher, S. E. & Campeau, P. M., 2 May 2019, In: Nature Communications. 10, 4 p., 2079.

  Research output: Contribution to journal › Erratum / corrigendum / retractions › Academic

  Open Access

• Consensus on Recording Deep Endometriosis Surgery: the CORDES statement

  Vanhie, A., Meuleman, C., Tomassetti, C., Timmerman, D., D'Hoore, A., Wolthuis, A., Van Cleynenbreugel, B., Dancet, E., Van den Broeck, U., Tsaltas, J., Renner, S. P., Ebert, A. D., Carmona, F., Abbott, J., Stepniewska, A., Taylor, H., Saridogan, E., Mueller, M., Keckstein, J., Pluchino, N., & 9 othersJanik, G., Zupi, E., Minelli, L., Cooper, M., Dunselman, G., Koh, C., Abrao, M. S., Chapron, C. & D'Hooghe, T., 1 Nov 2016, In: Human Reproduction. 31, 11, p. 2660-2660 1 p.

  Research output: Contribution to journal › Erratum / corrigendum / retractions › Academic

  Open Access

• Correction: The use of polygenic risk scores in pre-implantation genetic testing: an unproven, unethical practice

  Forzano, F., Antonova, O., Clarke, A., de Wert, G., Hentze, S., Jamshidi, Y., Moreau, Y., Perola, M., Prokopenko, I., Read, A., Reymond, A., Stefansdottir, V., van El, C., Genuardi, M. & Executive Committee of the European Society of Human Genetics, May 2022, In: European Journal of Human Genetics. 30, 5, p. 628-628 1 p., 628.

  Research output: Contribution to journal › Erratum / corrigendum / retractions › Academic

  Open Access

• Correction: The use of polygenic risk scores in pre-implantation genetic testing: an unproven, unethical practice

  Forzano, F., Antonova, O., Clarke, A., de Wert, G., Hentze, S., Jamshidi, Y., Moreau, Y., Perola, M., Prokopenko, I., Read, A., Reymond, A., Stefansdottir, V., van El, C., Genuardi, M. & Executive Committee of the European Society of Human Genetics, Nov 2022, In: European Journal of Human Genetics. 30, 11, p. 1306-1306 1 p.

  Research output: Contribution to journal › Erratum / corrigendum / retractions › Academic

  Open Access

• Correction: Exome sequencing of Pakistani consanguineous families identifies 30 novel candidate genes for recessive intellectual disability

  Riazuddin, S., Hussain, M., Razzaq, A., Iqbal, Z., Shahzad, M., Polla, D. L., Song, Y., van Beusekom, E., Khan, A. A., Tomas-Roca, L., Rashid, M., Zahoor, M. Y., Wissink-Lindhout, W. M., Basra, M. A. R., Ansar, M., Agha, Z., van Heeswijk, K., Rasheed, F., Van de Vorst, M., Veltman, J. A., & 15 othersGilissen, C., Akram, J., Kleefstra, T., Assir, M. Z., Grozeva, D., Carss, K., Raymond, F. L., O'Connor, T. D., Riazuddin, S. A., Khan, S. N., Ahmed, Z. M., de Brouwer, A. P. M., van Bokhoven, H., UK10K, U. K. . . K. & UK10K, 1 Nov 2020, In: Molecular Psychiatry. 25, 11, p. 3101-3102 2 p.

  Research output: Contribution to journal › Erratum / corrigendum / retractions › Academic

  Open Access

• Correction: Long-read trio sequencing of individuals with unsolved intellectual disability

  Pauper, M., Kucuk, E., Wenger, A. M., Chakraborty, S., Baybayan, P., Kwint, M., van der Sanden, B., Nelen, M. R., Derks, R., Brunner, H. G., Hoischen, A., Vissers, L. E. L. M. & Gilissen, C., Apr 2021, In: European Journal of Human Genetics. 29, 4, p. 720-720 1 p.

  Research output: Contribution to journal › Erratum / corrigendum / retractions › Academic

  Open Access

• Correction: Meta-analysis and multidisciplinary consensus statement: exome sequencing is a first-tier clinical diagnostic test for individuals with neurodevelopmental disorders

  Srivastava, S., Love-Nichols, J. A., Dies, K. A., Ledbetter, D. H., Martin, C. L., Chung, W. K., Firth, H. V., Frazier, T., Hansen, R. L., Prock, L., Brunner, H., Hoang, N., Scherer, S. W., Sahin, M., Miller, D. T. & NDD Exome Scoping Review Work Group, Oct 2020, In: Genetics in Medicine. 22, 10, p. 1731-1732 2 p.

  Research output: Contribution to journal › Erratum / corrigendum / retractions › Academic

  Open Access

• Correction: Solving unsolved rare neurological diseases—a Solve-RD viewpoint

  Schüle, R., Timmann, D., Erasmus, C. E., Reichbauer, J., Wayand, M., Baets, J., Balicza, P., Chinnery, P., Dürr, A., Haack, T., Hengel, H., Horvath, R., Houlden, H., Kamsteeg, E. J., Kamsteeg, C., Lohmann, K., Macaya, A., Marcé-Grau, A., Maver, A., Molnar, J., & 25 othersMünchau, A., Peterlin, B., Riess, O., Schöls, L., Stevanin, G., Synofzik, M., Timmerman, V., van de Warrenburg, B., van Os, N., Vandrovcova, J., Wilke, C., Bevot, A., Zuchner, S., Beltran, S., Laurie, S., Matalonga, L., Graessner, H., Zurek, B., Ellwanger, K., Ossowski, S., Demidov, G., Sturm, M., Brunner, H., Solve-RD-DITF-RND & SOLVE-RD Consortium, 1 Sept 2021, In: European Journal of Human Genetics. 29, 9, p. 1462-1465 4 p.

  Research output: Contribution to journal › Erratum / corrigendum / retractions › Academic

  Open Access

• Correction: The ARID1B spectrum in 143 patients: from nonsyndromic intellectual disability to Coffin–Siris syndrome: from nonsyndromic intellectual disability to Coffin-Siris syndrome (vol 21, pg 1295, 2019)

  van der Sluijs, P. J., Jansen, S., Vergano, S. A., Adachi-Fukuda, M., Alanay, Y., AlKindy, A., Baban, A., Bayat, A., Beck-Woedl, 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., Kersseboom, R., Kilic, E., Krajewska-Walasek, M., Lammers, K., Laulund, L. W., Lederer, D., Lees, M., Lopez-Gonzalez, 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., Sept 2019, In: Genetics in Medicine. 21, 9, p. 2160-2161 2 p.

  Research output: Contribution to journal › Erratum / corrigendum / retractions › Academic

  Open Access

• Correction:The effectiveness of immediate versus delayed tubal flushing with oil-based contrast in women with unexplained infertility (H2Oil-timing study): study protocol of a randomized controlled trial

  Kamphuis, D., Rosielle, K., van Welie, N., Roest, I., van Dongen, A. J. C. M., Brinkhuis, E. A., Bourdrez, P., Mozes, A., Verhoeve, H. R., van der Ham, D. P., Vrouenraets, F. P. J. M., Risseeuw, J. J., van de Laar, T., Janse, F., Hartog, J. E. D., de Hundt, M., Hooker, A. B., Huppelschoten, A. G., Pieterse, Q. D., Bongers, M. Y., & 8 othersStoker, J., Koks, C. A. M., Lambalk, C. B., Hemingway, A., Li, W., Mol, B. W. J., Dreyer, K. & Mijatovic, V., 10 Aug 2023, In: BMC Women's Health. 23, 1, 2 p., 424.

  Research output: Contribution to journal › Erratum / corrigendum / retractions › Academic

  Open Access

• Correction Missense variants in ANKRD11 cause KBG syndrome by impairment of stability or transcriptional activity of the encoded protein

  de Boer, E., Ockeloen, C. W., Kampen, R. A., Hampstead, J. E., Dingemans, A. J. M., Rots, D., Lütje, L., Ashraf, T., Baker, R., Barat-Houari, M., Angle, B., Chatron, N., Denommé-Pichon, A-S., Devinsky, O., Dubourg, C., Elmslie, F., Elloumi, H. Z., Faivre, L., Fitzgerald-Butt, S., Geneviève, D., & 30 othersGoos, J. A. C., Helm, B. M., Kini, U., Lasa-Aranzasti, A., Lesca, G., Lynch, S. A., Mathijssen, I. M. J., McGowan, R., Monaghan, K. G., Odent, S., Pfundt, R., Putoux, A., van Reeuwijk, J., Santen, G. W. E., Sasaki, E., Sorlin, A., van der Spek, P. J., Stegmann, A. P. A., Swagemakers, S. M. A., Valenzuela, I., Viora-Dupont, E., Vitobello, A., Ware, S. M., Wéber, M., Gilissen, C., Low, K. J., Fisher, S. E., Vissers, L. E. L. M., Wong, M. M. K. & Kleefstra, T., Nov 2023, In: Genetics in Medicine. 25, 11, 3 p., 100962.

  Research output: Contribution to journal › Erratum / corrigendum / retractions › Academic

  Open Access

• Correction to: Preferred prenatal counselling at the limits of viability: a survey among Dutch perinatal professionals

  Geurtzen, R., Van Heijst, A., Hermens, R., Scheepers, H., Woiski, M., Draaisma, J. & Hogeveen, M., 19 Feb 2018, In: BMC Pregnancy and Childbirth. 18, 1 p., 54.

  Research output: Contribution to journal › Erratum / corrigendum / retractions › Academic

  Open Access

• Correction to: Classical galactosemia: neuropsychological and psychosocial functioning beyond intellectual abilities (vol 15, 42, 2020)

  Welsink-Karssies, M. M., Oostrom, K. J., Hermans, M. E., Hollak, C. E. M., Janssen, M. C. H., Langendonk, J. G., Oussoren, E., Rubio Gozalbo, M. E., de Vries, M., Geurtsen, G. J. & Bosch, A. M., 7 Sept 2020, In: Orphanet Journal of Rare Diseases. 15, 1, 4 p., 238.

  Research output: Contribution to journal › Erratum / corrigendum / retractions › Academic

  Open Access

• Correction to: Group A streptococcal disease in paediatric inpatients: a European perspective

  Boeddha, N. P., Atkins, L., de Groot, R., Driessen, G., Hazelzet, J., Zenz, W., Carrol, E. D., Anderson, S. T., Martinon-Torres, F., Agyeman, P. K. A., Galassini, R., Herberg, J., Levin, M., Schlapbach, L. J. & Emonts, M., Feb 2023, In: European Journal of Pediatrics. 182, 2, p. 707-707 1 p.

  Research output: Contribution to journal › Erratum / corrigendum / retractions › Academic

  Open Access

• Correction to: Non-extensitivity and criticality of atomic hydropathicity around a voltage-gated sodium channel's pore: a modeling study

  Xenakis, M. N., Kapetis, D., Yang, Y., Heijman, J., Waxman, S. G., Lauria, G., Faber, C. G., Smeets, H. J., Lindsey, P. J. & Westra, R. L., Dec 2022, In: Journal of Biological Physics. 48, 4, p. 477-478 2 p.

  Research output: Contribution to journal › Erratum / corrigendum / retractions › Academic

  Open Access

• Correction to: Reply to Letter by Tellier et al., 'Scientific refutation of ESHG statement on embryo selection'

  Forzano, F., Antonova, O., Clarke, A., de Wert, G., Hentze, S., Jamshidi, Y., Moreau, Y., Perola, M., Prokopenko, I., Read, A., Reymond, A., Stefansdottir, V., van El, C., Genuardi, M. & Executive Committee of the European Society of Human Genetics, Mar 2023, In: European Journal of Human Genetics. 31, 3, p. 368-368 1 p.

  Research output: Contribution to journal › Erratum / corrigendum / retractions › Academic

  Open Access

• Correction to: Solve-RD: systematic pan-European data sharing and collaborative analysis to solve rare diseases

  Zurek, B., Ellwanger, K., Vissers, L. E. L. M., Schüle, R., Synofzik, M., Töpf, A., de Voer, R. M., Laurie, S., Matalonga, L., Gilissen, C., Ossowski, S., 't Hoen, P. A. C., Vitobello, A., Schulze-Hentrich, J. M., Riess, O., Brunner, H. G., Brookes, A. J., Rath, A., Bonne, G., Gumus, G., & 10 othersVerloes, A., Hoogerbrugge, N., Evangelista, T., Harmuth, T., Swertz, M., Spalding, D., Hoischen, A., Beltran, S., Graessner, H. & SOLVE-RD Consortium, Sept 2021, In: European Journal of Human Genetics. 29, 9, p. 1459-1461 3 p.

  Research output: Contribution to journal › Erratum / corrigendum / retractions › Academic

  Open Access

• Correction to: Solving patients with rare diseases through programmatic reanalysis of genome-phenome data

  Matalonga, L., Hernández-Ferrer, C., Piscia, D., Cohen, E., Cuesta, I., Danis, D., Denommé-Pichon, A. S., Duffourd, Y., Gilissen, C., Johari, M., Laurie, S., Li, S., Nelson, I., Peters, S., Paramonov, I., Prasanth, S., Robinson, P., Sablauskas, K., Savarese, M., Steyaert, W., & 36 othersvan der Velde, J. K., Vitobello, A., Schüle, R., Synofzik, M., Töpf, A., Vissers, L. E. L. M., de Voer, R., Aretz, S., Capella, G., de Voer, R. M., Evans, G., Pelaez, J. G., Holinski-Feder, E., Hoogerbrugge, N., Laner, A., Oliveira, C., Rump, A., Schröck, E., Sommer, A. K., Steinke-Lange, V., Paske, I. T., Tischkowitz, M., Valle, L., Banka, S., Benetti, E., Casari, G., Ciolfi, A., Clayton-Smith, J., Dallapiccola, B., Solve RD DITF-euroNMD, Solve RD DITF GENTURIS, Solve-RD DITF-ITHACA, Solve-RD-DITF-RND, Solve RD SNV Indel Working Group, SOLVE-RD Consortium & Brunner, H., 1 Sept 2021, In: European Journal of Human Genetics. 29, 9, p. 1466-1469 4 p.

  Research output: Contribution to journal › Erratum / corrigendum / retractions › Academic

  Open Access

• Corrigendum: Chorioamnionitis Is a Risk Factor for Intraventricular Hemorrhage in Preterm Infants: A Systematic Review and Meta-Analysis

  Villamor-Martinez, E., Fumagalli, M., Rahim, O. M., Passera, S., Cavallaro, G., Degraeuwe, P., Mosca, F. & Villamor, E., 15 Feb 2019, In: Frontiers in physiology. 10, 8 p., 102.

  Research output: Contribution to journal › Erratum / corrigendum / retractions › Academic

  Open Access

• Corrigendum: Chronic Intra-Uterine Ureaplasma parvum Infection Induces Injury of the Enteric Nervous System in Ovine Fetuses

  Heymans, C., de Lange, I. H., Huetten, M. C., Lenaerts, K., de Ruijter, N. J. E., Kessels, L. C. G. A., Rademakers, G., Melotte, V., Boesmans, W., Saito, M., Usuda, H., Stock, S. J., Spiller, O. B., Beeton, M. L., Payne, M. S., Kramer, B. W., Newnham, J. P., Jobe, A. H., Kemp, M. W., van Gemert, W. G., & 1 othersWolfs, T. G. A. M., 15 Apr 2020, In: Frontiers in Immunology. 11, 2 p., 672.

  Research output: Contribution to journal › Erratum / corrigendum / retractions › Academic

  Open Access

• Corrigendum: Diet associations in endometriosis

  Brouns, F., Van Haaps, A., Keszthelyi, D., Venema, K., Bongers, M., Maas, J. & Mijatovic, V., 1 Jan 2023, In: Frontiers in nutrition. 10, 1 p., 1295983.

  Research output: Contribution to journal › Erratum / corrigendum / retractions › Academic

  Open Access

• Corrigendum: Platelet Counts and Patent Ductus Arteriosus in Preterm Infants: An Updated Systematic Review and Meta-Analysis

  Gonzalez-Luis, G., Ghirardello, S., Bas-Suarez, P., Cavallaro, G., Mosca, F., Clyman, R. I. & Villamor, E., 19 May 2021, In: Frontiers in pediatrics. 9, 1 p., 694606.

  Research output: Contribution to journal › Erratum / corrigendum / retractions › Academic

  Open Access

• Corrigendum. The vaginal microbiome as a predictor for outcome of in vitro fertilization with or without intracytoplasmic sperm injection: a prospective study

  Koedooder, R., Singer, M., Schoenmakers, S., Savelkoul, P. H. M., Morre, S. A., de Jonge, J. D., Poort, L., Cuypers, W. J. S. S., Beckers, N. G. M., Broekmans, F. J. M., Cohlen, B. J., den Hartog, J. E., Fleischer, K., Lambalk, C. B., Smeenk, J. M. J. S., Budding, A. E. & Laven, J. S. E., Oct 2019, In: Human Reproduction. 34, 10, p. 2091-2092 2 p.

  Research output: Contribution to journal › Erratum / corrigendum / retractions › Academic

• Corrigendum to: The ethics of preconception expanded carrier screening in patients seeking assisted reproduction

  de Wert, G., van der Hout, S., Goddijn, M., Vassena, R., Frith, L., Vermeulen, N., Eichenlaub-Ritter, U. & ESHRE Ethics Committee, 2021, In: Human reproduction open. 2021, 2, 1 p., 014.

  Research output: Contribution to journal › Erratum / corrigendum / retractions › Academic

  Open Access

• Corrigendum to "Cognitive flexibility in autism spectrum disorder: Explaining the inconsistencies?" [Research in Autism Spectrum Disorders, 5, (2011) 1390-1401] DOI

  Van Eylen, L., Boets, B., Steyaert, J., Evers, K., Wagemans, J. & Noens, I., 1 Jan 2016, In: Research in Developmental Disabilities. 48, p. 94

  Research output: Contribution to journal › Erratum / corrigendum / retractions › Academic

• Corrigendum to “Cognitive flexibility in autism spectrum disorder: Explaining the inconsistencies?” [Res. Autism Spectr. Disord. 5 (2011) 1390–1401]

  Van Eylen, L., Boets, B., Steyaert, J., Evers, K., Wagemans, J. & Noens, I., Mar 2016, In: Research in Autism Spectrum Disorders. 23, p. 245-245

  Research output: Contribution to journal › Erratum / corrigendum / retractions › Academic

• De Novo Missense Mutations in DHX30 Impair Global Translation and Cause a Neurodevelopmental Disorder (vol 101, pg 716, 2017)

  DDD Study & C4RCD Res Grp, 4 Jan 2018, In: American Journal of Human Genetics. 102, 1, p. 196-196 1 p.

  Research output: Contribution to journal › Erratum / corrigendum / retractions › Academic

  Open Access

• Effectiveness of lifestyle intervention in subgroups of obese infertile women: a subgroup analysis of a RCT

  van Oers, A. M., Groen, H., Mutsaerts, M. A. Q., Burggraaff, J. M., Kuchenbecker, W. K. H., Perquin, D. A. M., Koks, C. A. M., van Golde, R., Kaaijk, E. M., Schierbeek, J. M., Oosterhuis, G. J. E., Broekmans, F. J., Vogel, N. E. A., Land, J. A., Mol, B. W. J., Hoek, A. & LIFEstyle Study Grp, 1 Feb 2017, In: Human Reproduction. 32, 2, p. 482-482 1 p.

  Research output: Contribution to journal › Erratum / corrigendum / retractions › Academic

  Open Access

• Erratum to: ALG6‐CDG: a recognizable phenotype with epilepsy, proximal muscle weakness, ataxia and behavioral and limb anomalies

  Morava, E., Tiemes, V., Thiel, C., Seta, N., de Lonlay, P., de Klerk, H., Mulder, M., Rubio-Gozalbo, E., Visser, G., van Hasselt, P., Horovitz, D. D. G., Moura de Souza, C. F., Schwartz, I. V. D., Green, A., Al-Owain, M., Uziel, G., Sigaudy, S., Chabrol, B., van Spronsen, F-J., Steinert, M., & 11 othersKomini, E., Wurm, D., Bevot, A., Ayadi, A., Huijben, K., Dercksen, M., Witters, P., Jaeken, J., Matthijs, G., Lefeber, D. J. & Wevers, R. A., Sept 2016, In: Journal of Inherited Metabolic Disease. 39, 5, p. 759-759

  Research output: Contribution to journal › Erratum / corrigendum / retractions › Academic

• Erratum to Parent-of-origin-specific signatures of de novo mutations (Nature Genetics, (2016), 48, 8, (935-939), 10.1038/ng.3597)

  Goldmann, J. M., Wong, W. S. W., Pinelli, M., Farrah, T., Bodian, D., Stittrich, A. B., Glusman, G., Vissers, L. E. L. M., Hoischen, A., Roach, J. C., Vockley, J. G., Veltman, J. A., Solomon, B. D., Gilissen, C. & Niederhuber, J. E., 1 Nov 2018, In: Nature Genetics. 50, 11, p. 1615

  Research output: Contribution to journal › Erratum / corrigendum / retractions › Academic

  Open Access

• Erratum to “Corrigendum to ‘Cognitive flexibility in autism spectrum disorder: Explaining the inconsistencies?’ [Res. Autism Spectr. Disord. 5 (2011) 1390–1401]”

  Van Eylen, L., Boets, B., Steyaert, J., Evers, K., Wagemans, J. & Noens, I., Jan 2016, In: Research in Developmental Disabilities. 48, p. R1

  Research output: Contribution to journal › Erratum / corrigendum / retractions › Academic

• Increased blood pressure and impaired endothelial function after accelerated growth in IVF/ICSI children

  Zandstra, H., van Montfoort, A. P. A., Dumoulin, J. C. M., Zimmermann, L. J. I. & Touwslager, R. N. H., 7 Feb 2020, In: Human reproduction open. 2020, 1, 1 p., hoaa004.

  Research output: Contribution to journal › Erratum / corrigendum / retractions › Academic

  Open Access

• Leigh syndrome caused by mutations in MTFMT is associated with a better prognosis

  Hayhurst, H., de Coo, I. F. M., Piekutowska-Abramczuk, D., Alston, C. L., Sharma, S., Thompson, K., Rius, R., He, L., Hopton, S., Ploski, R., Ciara, E., Lake, N. J., Compton, A. G., Delatycki, M. B., Verrips, A., Bonnen, P. E., Jones, S. A., Morris, A. A., Shakespeare, D., Christodoulou, J., & 9 othersWesol-Kucharska, D., Rokicki, D., Smeets, H. J. M., Pronicka, E., Thorburn, D. R., Gorman, G. S., McFarland, R., Taylor, R. W. & Ng, Y. S., Apr 2019, In: Annals of Clinical and Translational Neurology. 6, 4, p. 821-821 1 p.

  Research output: Contribution to journal › Erratum / corrigendum / retractions › Academic

  Open Access

• Recovery 3 and 12 months after hysterectomy: epidemiology and predictors of chronic pain, physical functioning, and global surgical recovery: Erratum (vol 95, e3980, 2017)

  Theunissen, M., Peters, M. L., Schepers, J., Maas, J. W. M., Tournois, F., van Suijlekom, H. A., Gramke, H-F. & Marcus, M. A. E., May 2017, In: Medicine. 96, 20, e6957.

  Research output: Contribution to journal › Erratum / corrigendum / retractions › Academic

  Open Access