K. Lip

440 total citations
6 papers, 221 citations indexed

About

K. Lip is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, K. Lip has authored 6 papers receiving a total of 221 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Molecular Biology, 4 papers in Genetics and 3 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in K. Lip's work include Genetic Syndromes and Imprinting (4 papers), Epigenetics and DNA Methylation (4 papers) and Prenatal Screening and Diagnostics (3 papers). K. Lip is often cited by papers focused on Genetic Syndromes and Imprinting (4 papers), Epigenetics and DNA Methylation (4 papers) and Prenatal Screening and Diagnostics (3 papers). K. Lip collaborates with scholars based in Netherlands and United Kingdom. K. Lip's co-authors include Mariëlle Alders, Marcel M. A. M. Mannens, Jet Bliek, Saskia M. Maas, Deborah Mackay, Alice S. Brooks, J. Peter van Tintelen, Alida C. Knegt, N. J. Leschot and Narayanswami Sreeram and has published in prestigious journals such as Circulation, European Journal of Human Genetics and Clinical Epigenetics.

In The Last Decade

K. Lip

6 papers receiving 205 citations

Peers

Countries citing papers authored by K. Lip

Since Specialization

Citations

This map shows the geographic impact of K. Lip'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 K. Lip with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites K. Lip more than expected).

Fields of papers citing papers by K. Lip

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by K. Lip. 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 K. Lip. The network helps show where K. Lip may publish in the future.

Co-authorship network of co-authors of K. Lip

This figure shows the co-authorship network connecting the top 25 collaborators of K. Lip. A scholar is included among the top collaborators of K. Lip 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 K. Lip. K. Lip is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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6 of 6 papers shown

#	Work	Indexed citations
1	Genome-wide methylation profiling of Beckwith-Wiedemann syndrome patients without molecular confirmation after routine diagnostics 2019 ·Clinical Epigenetics ·(unknown), Mariëlle Alders, Saskia M. Maas, Jet Bliek, (unknown), Peter Henneman, Faisal I. Rezwan, K. Lip, Adri N. Mul, Deborah Mackay, Marcel M. A. M. Mannens	18
2	Genetic susceptibility for cow’s milk allergy in Dutch children: the start of the allergic march? 2015 ·Clinical and Translational Allergy ·Peter Henneman, (unknown), Andrea Venema, (unknown), K. Lip, Raoul C. M. Hennekam, Marcel M. A. M. Mannens, A. B. Sprikkelman	11
3	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
4	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
5	Lessons from BWS twins: complex maternal and paternal hypomethylation and a common source of haematopoietic stem cells 2009 ·European Journal of Human Genetics ·Jet Bliek, Mariëlle Alders, Saskia M. Maas, Roelof‐Jan Oostra, Deborah Mackay, K. Lip, (unknown), Alice S. Brooks, (unknown), A. Westerveld, N. J. Leschot, Marcel M. A. M. Mannens	74
6	Homozygous Premature Truncation of the HERG Protein 1999 ·Circulation ·Theo M. Hoorntje, Mariëlle Alders, J. Peter van Tintelen, K. Lip, Narayanswami Sreeram, Allard C. van der Wal, M. Mannens, Arthur A.M. Wilde	49

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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