Jet Bliek

4.9k total citations
37 papers, 2.3k citations indexed

About

Jet Bliek is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Jet Bliek has authored 37 papers receiving a total of 2.3k indexed citations (citations by other indexed papers that have themselves been cited), including 33 papers in Molecular Biology, 28 papers in Genetics and 19 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Jet Bliek's work include Genetic Syndromes and Imprinting (27 papers), Epigenetics and DNA Methylation (26 papers) and Prenatal Screening and Diagnostics (18 papers). Jet Bliek is often cited by papers focused on Genetic Syndromes and Imprinting (27 papers), Epigenetics and DNA Methylation (26 papers) and Prenatal Screening and Diagnostics (18 papers). Jet Bliek collaborates with scholars based in Netherlands, United Kingdom and United States. Jet Bliek's co-authors include Marcel M. A. M. Mannens, Mariëlle Alders, A. Westerveld, Johannes M. F. G. Aerts, Anneke Strijland, Rolf G. Boot, G. Herma Renkema, Marri Verhoek, Eamonn R. Maher and Rosalyn Slater and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and The American Journal of Human Genetics.

In The Last Decade

Jet Bliek

35 papers receiving 2.2k citations

Peers

Countries citing papers authored by Jet Bliek

Since Specialization

Citations

This map shows the geographic impact of Jet Bliek's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Jet Bliek with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Jet Bliek more than expected).

Fields of papers citing papers by Jet Bliek

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Jet Bliek. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Jet Bliek. The network helps show where Jet Bliek may publish in the future.

Co-authorship network of co-authors of Jet Bliek

This figure shows the co-authorship network connecting the top 25 collaborators of Jet Bliek. A scholar is included among the top collaborators of Jet Bliek based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Jet Bliek. Jet Bliek is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Further Introduction of DNA Methylation (DNAm) Arrays in Regular Diagnostics 2022 ·Frontiers in Genetics ·Marcel M. A. M. Mannens, Maria Lombardi, Mariëlle Alders, Peter Henneman, Jet Bliek	9
2	Transcription alterations of KCNQ1 associated with imprinted methylation defects in the Beckwith–Wiedemann locus 2019 ·Genetics in Medicine ·(unknown), Angela Sparago, Andrea Freschi, (unknown), Saskia M. Maas, Suzanna G.M. Frints, Mariëlle Alders, Laura Pignata, Monica Franzese, Claudia Angelini, Diana Carli, Alessandro Mussa, (unknown), Fulvio Gabbarini, (unknown), Giovanni Battista Ferrero, Jet Bliek, Charles A. Williams, Andrea Riccio, Flavia Cerrato	32
3	Multiple tumors due to mosaic genome‐wide paternal uniparental disomy 2019 ·Pediatric Blood & Cancer ·(unknown), Jet Bliek, Carel J.M. van Noesel, Laura J. C. M. van Zutven, Jan C. Oosterwijk, Saskia Hopman, Johannes H. M. Merks, Raoul C. M. Hennekam	10
4	Phenotype, cancer risk, and surveillance in Beckwith–Wiedemann syndrome depending on molecular genetic subgroups 2016 ·American Journal of Medical Genetics Part A ·Saskia M. Maas, Fleur Vansenne, D.J. Kadouch, Abdulla Ibrahim, Jet Bliek, Saskia Hopman, Marcel M. A. M. Mannens, Johannes H. M. Merks, Eamonn R. Maher, Raoul C. M. Hennekam	124
5	Methylation analysis in tongue tissue of BWS patients identifies the (EPI)genetic cause in 3 patients with normal methylation levels in blood 2014 ·European Journal of Medical Genetics ·Mariëlle Alders, Saskia M. Maas, D.J. Kadouch, K. Lip, Jet Bliek, Chantal M.A.M. van der Horst, Marcel M. A. M. Mannens	20
6	Epigenotype–phenotype correlations in Silver–Russell syndrome 2010 ·Journal of Medical Genetics ·Emma Wakeling, (unknown), Mariëlle Alders, Jet Bliek, Elizabeth Forsythe, Sudhesh Kumar, Derek Lim, Fiona MacDonald, Deborah Mackay, Eamonn R. Maher, Gudrun E. Moore, (unknown), (unknown), Trine Tangeraas, (unknown), Mieke M. van Haelst, (unknown), I. Karen Temple, J. M. Cobben	120
7	Monozygotic twins discordant for vascular malformations and dysregulated growth 2009 ·European Journal of Medical Genetics ·Charlène E.U. Oduber, Jet Bliek, Chantal M.A.M. van der Horst, Maurice A. M. Van Steensel, Raoul C. M. Hennekam	4
8	Phenotypic discordance upon paternal or maternal transmission of duplications of the 11p15 imprinted regions 2009 ·European Journal of Medical Genetics ·Jet Bliek, Simone Snijder, Saskia M. Maas, Abeltje M. Polstra, K. Lip, Mariëlle Alders, Alida C. Knegt, Marcel M. A. M. Mannens	49
9	Determination of KCNQ1OT1 and H19 methylation levels in BWS and SRS patients using methylation-sensitive high-resolution melting analysis 2008 ·European Journal of Human Genetics ·Mariëlle Alders, Jet Bliek, (unknown), (unknown), Marcel M. A. M. Mannens	35
10	Epigenotype, Phenotype, and Tumors in Patients with Isolated Hemihyperplasia 2008 ·The Journal of Pediatrics ·Jet Bliek, Saskia M. Maas, Mariel Alders, Johannes H. M. Merks, Marcel M. A. M. Mannens	23
11	Hypomethylation of the H19 Gene Causes Not Only Silver-Russell Syndrome (SRS) but Also Isolated Asymmetry or an SRS-Like Phenotype 2006 ·The American Journal of Human Genetics ·Jet Bliek, Pauline Terhal, (unknown), Saskia M. Maas, Ben C.J. Hamel, Georgette B. Salieb–Beugelaar, Marleen Simon, Tom G.W. Letteboer, Jasper van der Smagt, (unknown), Marcel M. A. M. Mannens	151
12	Increased tumour risk for BWS patients correlates with aberrant H19 and not KCNQ1OT1 methylation: occurrence of KCNQ1OT1 hypomethylation in familial cases of BWS 2001 ·Human Molecular Genetics ·Jet Bliek	127
13	Disruption of a Novel Imprinted Zinc-Finger Gene, ZNF215, in Beckwith-Wiedemann Syndrome 2000 ·The American Journal of Human Genetics ·Mariëlle Alders, Andy Ryan, Matt Hodges, Jet Bliek, Andrew P. Feinberg, (unknown), A. Westerveld, P.F.R. Little, Marcel M. A. M. Mannens	40
14	A Dominant Negative Isoform of the Long QT Syndrome 1 Gene Product 1998 ·Journal of Biological Chemistry ·Sophie Demolombe, Isabelle Baró, Yann Péréon, Jet Bliek, Raha Mohammad-Panah, H. Pollard, (unknown), M. Mannens, Arthur A.M. Wilde, Jacques Barhanin, Flavien Charpentier, Denis Escande	69
15	The Human Chitotriosidase Gene 1998 ·Journal of Biological Chemistry ·Rolf G. Boot, G. Herma Renkema, Marri Verhoek, Anneke Strijland, Jet Bliek, (unknown), Marcel M. A. M. Mannens, Johannes M. F. G. Aerts	345
16	The Human Achaete-Scute Homologue 2 (ASCL2, HASH2) Maps to Chromosome 11p15.5, Close to IGF2 and is Expressed in Extravillus Trophoblasts 1997 ·Human Molecular Genetics ·Mariëlle Alders, Matt Hodges, Anna‐Katerina Hadjantonakis, (unknown), (unknown), Jet Bliek, (unknown), A. Westerveld, François Guillemot, Cees B.M. Oudejans, Peter Little, M. Mannens	69
17	An Integrated Physical Map of 210 Markers Assigned to the Short Arm of Human Chromosome 11 1994 ·Genomics ·E. Redeker, J.M.N. Hoovers, Mariëlle Alders, (unknown), Alasdair Ivens, Simon G. Gregory, Linda M. Kalikin, Jet Bliek, L. de Galan, (unknown), Jenny A. Visser, Robbert van der Voort, Andrew P. Feinberg, Peter Little, A. Westerveld, M. Mannens	23
18	High-resolution localization of 69 potential human zinc finger protein genes: A number are clustered 1992 ·Genomics ·J.M.N. Hoovers, M. Mannens, Rosalind M. John, Jet Bliek, Veronica van Heyningen, David J. Porteous, N. J. Leschot, A. Westerveld, Peter Little	114
19	The distal region of 11p13 and associated genetic diseases 1991 ·Genomics ·M. Mannens, J.M.N. Hoovers, E. M. Bleeker‐Wagemakers, E. Redeker, Jet Bliek, (unknown), G F Saunders, Bryan R.G. Williams, (unknown), Claudine Junien, Daniel A. Haber, Frank Speleman, Christa Heyting, Rosalyn Slater, N. J. Leschot, A. Westerveld	19
20	Autosomal dominant aniridia linked to the chromosome 11p13 markers catalase and D11S151 in a large Dutch family 1989 ·Cytogenetic and Genome Research ·M. Mannens, E. M. Bleeker‐Wagemakers, Jet Bliek, J.M.N. Hoovers, Ingrid A.M. Mandjes, Simon Tol, R.R. Frants, Christa Heyting, A. Westerveld, Rosalyn Slater	27

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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