Research output per year
Research output per year
Personal profile
Research interests
genome diagnostics i.p. epigenetics of disease
PubMed database Mannens M M A M, Mannens H M A M, Mannens M, Mannens M A, Mannens M A M, Mannens M M, Mannens M A M M, Mannens M M A
Specialisation
Genome diagnostics i.p. epigenetics of disease
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Collaborations and top research areas from the last five years
Recent external collaboration on country/territory level. Dive into details by clicking on the dots or
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Mutations in CCBE1 cause generalized lymph vessel dysplasia in humans
Alders, M., Hogan, B. M., Gjini, E., Salehi, F., Al-Gazali, L., Hennekam, E. A., Holmberg, E. E., Mannens, M. M. A. M., Mulder, M. F., Offerhaus, G. J. A., Prescott, T. E., Schroor, E. J., Verheij, J. B. G. M., Witte, M., Zwijnenburg, P. J., Vikkula, M., Schulte-Merker, S. & Hennekam, R. C., 2009, In: Nature genetics. 41, 12, p. 1272-1274 3 p.Research output: Contribution to journal › Article › Academic › peer-review
254 Citations (Scopus) -
Mutations in ZBTB20 cause Primrose syndrome
Cordeddu, V., Redeker, B., Stellacci, E., Jongejan, A., Fragale, A., Bradley, T. E. J., Anselmi, M., Ciolfi, A., Cecchetti, S., Muto, V., Bernardini, L., Azage, M., Carvalho, D. R., Espay, A. J., Male, A., Molin, A.-M., Posmyk, R., Battisti, C., Casertano, A. & Melis, D. & 7 others, , 2014, In: Nature genetics. 46, 8, p. 815-817Research output: Contribution to journal › Article › Academic › peer-review
80 Citations (Scopus) -
Yield of molecular and clinical testing for arrhythmia syndromes: report of 15 years' experience
Hofman, N., Tan, H. L., Alders, M., Kolder, I., de Haij, S., Mannens, M. M. A. M., Lombardi, M. P., Lekanne Deprez, R. H., van Langen, I. & Wilde, A. A. M., 2013, In: Circulation. 128, 14, p. 1513-1521Research output: Contribution to journal › Article › Academic › peer-review
126 Citations (Scopus) -
Expanding spectrum of human RYR2-related disease: new electrocardiographic, structural, and genetic features
Bhuiyan, Z. A., van den Berg, M. P., van Tintelen, J. P., Bink-Boelkens, M. T. E., Wiesfeld, A. C. P., Alders, M., Postma, A. V., van Langen, I., Mannens, M. M. A. M. & Wilde, A. A. M., 2007, In: Circulation. 116, 14, p. 1569-1576Research output: Contribution to journal › Article › Academic › peer-review
209 Citations (Scopus) -
Hypomethylation of the H19 gene causes not only Silver-Russell syndrome (SRS) but also isolated asymmetry or an SRS-like phenotype
Bliek, J., Terhal, P., van den Bogaard, M.-J., Maas, S., Hamel, B., Salieb-Beugelaar, G., Simon, M., Letteboer, T., van der Smagt, J., Kroes, H. & Mannens, M., 2006, In: American journal of human genetics. 78, 4, p. 604-614Research output: Contribution to journal › Article › Academic › peer-review
178 Citations (Scopus)
Press/Media
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Epigenetica laat ons trauma’s door kindermishandeling beter begrijpen
01/12/2021
1 item of Media coverage
Press/Media: Press / Media
Datasets
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Additional file 4: of The idiopathic preterm delivery methylation profile in umbilical cord blood DNA
Fernando, F. (Contributor), Keijser, R. (Creator), Henneman, P. (Creator), van der Kevie-Kersemaekers, A.-M. F. (Contributor), Mannens, M. M. A. M. (Creator), van der Post, J. A. M. (Contributor), Afink, G. B. (Creator) & Ris-Stalpers, C. (Creator), Figshare, 2015
DOI: 10.6084/m9.figshare.c.3622160_d3, https://springernature.figshare.com/articles/dataset/Additional_file_4_of_The_idiopathic_preterm_delivery_methylation_profile_in_umbilical_cord_blood_DNA/4397096
Dataset
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MOESM5 of A genome-wide DNA methylation signature for SETD1B-related syndrome
Krzyzewska, I. M. (Contributor), Maas, S. M. (Contributor), Henneman, P. (Contributor), Lip, K. V. D. (Contributor), Venema, A. (Contributor), Baranano, K. (Contributor), Chassevent, A. (Contributor), Aref-Eshghi, E. (Contributor), Fukuda, T. (Contributor), Ikeda, H. (Contributor), Jacquemont, M. (Contributor), Kim, H.-G. (Contributor), Labalme, A. (Contributor), Lewis, S. M. E. (Contributor), Lesca, G. (Contributor), Madrigal, I. (Contributor), Mahida, S. (Contributor), Matsumoto, N. (Contributor), Rabionet, R. (Contributor), Rajcan-Separovic, E. (Contributor), Qiao, Y. (Contributor), Sadikovic, B. (Contributor), Saitsu, H. (Contributor), Sweetser, D. A. (Contributor), Alders, M. (Contributor) & Mannens, M. M. A. M. (Contributor), Figshare, 2019
DOI: 10.6084/m9.figshare.10252100.v1, https://springernature.figshare.com/articles/MOESM5_of_A_genome-wide_DNA_methylation_signature_for_SETD1B-related_syndrome/10252100/1
Dataset
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MOESM4 of A genome-wide DNA methylation signature for SETD1B-related syndrome
Krzyzewska, I. M. (Contributor), Maas, S. M. (Contributor), Henneman, P. (Contributor), Lip, K. V. D. (Contributor), Venema, A. (Contributor), Baranano, K. (Contributor), Chassevent, A. (Contributor), Aref-Eshghi, E. (Contributor), Fukuda, T. (Contributor), Ikeda, H. (Contributor), Jacquemont, M. (Contributor), Kim, H.-G. (Contributor), Labalme, A. (Contributor), Lewis, S. M. E. (Contributor), Lesca, G. (Contributor), Madrigal, I. (Contributor), Mahida, S. (Contributor), Matsumoto, N. (Contributor), Rabionet, R. (Contributor), Rajcan-Separovic, E. (Contributor), Qiao, Y. (Contributor), Sadikovic, B. (Contributor), Saitsu, H. (Contributor), Sweetser, D. A. (Contributor), Alders, M. (Contributor) & Mannens, M. M. A. M. (Contributor), Figshare, 2019
DOI: 10.6084/m9.figshare.10252091, https://springernature.figshare.com/articles/MOESM4_of_A_genome-wide_DNA_methylation_signature_for_SETD1B-related_syndrome/10252091
Dataset
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Additional file 9: of Genome-wide methylation profiling of Beckwith-Wiedemann syndrome patients without molecular confirmation after routine diagnostics
Krzyzewska, I. M. (Contributor), Alders, M. (Contributor), Maas, S. M. (Contributor), Bliek, J. (Contributor), Venema, A. (Contributor), Henneman, P. (Contributor), Rezwan, F. I. (Contributor), Lip, K. V. D. (Contributor), Mul, A. N. (Contributor), Mackay, D. J. G. (Contributor) & Mannens, M. M. A. M. (Contributor), Figshare, 2019
DOI: 10.6084/m9.figshare.7878926, https://springernature.figshare.com/articles/Additional_file_9_of_Genome-wide_methylation_profiling_of_Beckwith-Wiedemann_syndrome_patients_without_molecular_confirmation_after_routine_diagnostics/7878926
Dataset
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Additional file 3: of Genome-wide methylation profiling of Beckwith-Wiedemann syndrome patients without molecular confirmation after routine diagnostics
Krzyzewska, I. M. (Contributor), Alders, M. (Contributor), Maas, S. M. (Contributor), Bliek, J. (Contributor), Venema, A. (Contributor), Henneman, P. (Contributor), Rezwan, F. I. (Contributor), Lip, K. V. D. (Contributor), Mul, A. N. (Contributor), Mackay, D. J. G. (Contributor) & Mannens, M. M. A. M. (Contributor), Figshare, 2019
DOI: 10.6084/m9.figshare.7878887, https://springernature.figshare.com/articles/Additional_file_3_of_Genome-wide_methylation_profiling_of_Beckwith-Wiedemann_syndrome_patients_without_molecular_confirmation_after_routine_diagnostics/7878887
Dataset