Peter Henneman

Publication Activity (10 Years)

Years Active: 2018-2024
Publications (10 Years): 17

Top Topics

Dna Methylation

Allergic Rhinitis

Top Venues

The journal of pathology. Clinical research

European heart journal open

This page only lists publications with an associated author ORCID identifier.

Publications

Fredrik Landfors, Peter Henneman, Elin Chorell, Stefan K Nilsson, Sander Kersten
Drug-target Mendelian randomization analysis supports lowering plasma ANGPTL3, ANGPTL4, and APOC3 levels as strategies for reducing cardiovascular disease risk. European heart journal open 4 (3) (2024)
Fredrik Landfors, Peter Henneman, Elin Chorell, Stefan K Nilsson, Sander Kersten
Drug-target Mendelian randomization analysis supports lowering plasma ANGPTL3, ANGPTL4, and APOC3 levels as strategies for reducing cardiovascular disease risk. European heart journal open 4 (3) (2024)
David Efwm van Toledo, Arne Gc Bleijenberg, Andrea Venema, Mireille J de Wit, Susanne van Eeden, Gerrit A Meijer, Beatrice Carvalho, Evelien Dekker, Peter Henneman, Joep Eg IJspeert, Carel J M van Noesel
Aberrant PRDM2 methylation as an early event in serrated lesions destined to evolve into microsatellite-instable colorectal cancers. The journal of pathology. Clinical research 10 (2) (2024)
Camilla Sarli, Liselot van der Laan, Jack Reilly, Slavica Trajkova, Diana Carli, Alfredo Brusco, Michael A Levy, Raissa Relator, Jennifer Kerkhof, Haley McConkey, Matthew L Tedder, Cindy D Skinner, Mariëlle Alders, Peter Henneman, Raoul C M Hennekam, Claudia Ciaccio, Stefano D'Arrigo, Antonio Vitobello, Laurence Olivier-Faivre, Sacha Weber, Aline Vincent-Devulder, Laurence Perrin, Alexia Bourgois, Toshiyuki Yamamoto, Kay Metcalfe, Marcella Zollino, Usha Kini, Daniela Oliveira, Sergio B Sousa, Denise Williams, Gerarda Cappuccio, Bekim Sadikovic, Nicola Brunetti-Pierri
Blepharophimosis with intellectual disability and Helsmoortel-Van Der Aa Syndrome share episignature and phenotype. American journal of medical genetics. Part C, Seminars in medical genetics (2024)
Fredrik Landfors, Peter Henneman, Elin Chorell, Stefan K Nilsson, Sander Kersten
Drug-target Mendelian randomization analysis supports lowering plasma ANGPTL3, ANGPTL4, and APOC3 levels as strategies for reducing cardiovascular disease risk. European heart journal open 4 (3) (2024)
David Efwm van Toledo, Arne Gc Bleijenberg, Andrea Venema, Mireille J de Wit, Susanne van Eeden, Gerrit A Meijer, Beatrice Carvalho, Evelien Dekker, Peter Henneman, Joep Eg IJspeert, Carel J M van Noesel
Aberrant PRDM2 methylation as an early event in serrated lesions destined to evolve into microsatellite-instable colorectal cancers. The journal of pathology. Clinical research 10 (2) (2024)
David Efwm van Toledo, Arne Gc Bleijenberg, Andrea Venema, Mireille J de Wit, Susanne van Eeden, Gerrit A Meijer, Beatrice Carvalho, Evelien Dekker, Peter Henneman, Joep Eg IJspeert, Carel J M van Noesel
Aberrant PRDM2 methylation as an early event in serrated lesions destined to evolve into microsatellite-instable colorectal cancers. The journal of pathology. Clinical research 10 (2) (2024)
Liselot van der Laan, Kathleen Rooney, Tessa Ma Trooster, Marcel M A M Mannens, Bekim Sadikovic, Peter Henneman
DNA methylation episignatures: insight into copy number variation. Epigenomics (2022)
Liselot van der Laan, Kathleen Rooney, Tessa Ma Trooster, Marcel M A M Mannens, Bekim Sadikovic, Peter Henneman
DNA methylation episignatures: insight into copy number variation. Epigenomics 14 (21) (2022)
Liselot van der Laan, Kathleen Rooney, Tessa Ma Trooster, Marcel M A M Mannens, Bekim Sadikovic, Peter Henneman
DNA methylation episignatures: insight into copy number variation. Epigenomics (2022)
Liselot van der Laan, Kathleen Rooney, Tessa Ma Trooster, Marcel M A M Mannens, Bekim Sadikovic, Peter Henneman
DNA methylation episignatures: insight into copy number variation. Epigenomics 14 (21) (2022)
Liselot van der Laan, Kathleen Rooney, Tessa Ma Trooster, Marcel M A M Mannens, Bekim Sadikovic, Peter Henneman
DNA methylation episignatures: insight into copy number variation. Epigenomics 14 (21) (2022)
Peter Henneman, Adri N Mul, Andrew Y F Li Yim, Izabela M Krzyzewska, Mariëlle Alders, Adelia Adelia, Mark R Mizee, Marcel M A M Mannens
Prenatal NeuN+ neurons of Down syndrome display aberrant integrative DNA methylation and gene expression profiles. Epigenomics 14 (7) (2022)
Liselot van der Laan, Kathleen Rooney, Tessa Ma Trooster, Marcel M A M Mannens, Bekim Sadikovic, Peter Henneman
DNA methylation episignatures: insight into copy number variation. Epigenomics 14 (21) (2022)
Felix Patience Chilunga, Peter Henneman, Andrea Venema, Karlijn Ac Meeks, Juan Ramón González-García, Carlos Ruiz-Arenas, Ana Requena Méndez, Erik Beune, Joachim Spranger, Liam Smeeth, Bahendeka Silver, Ellis Owusu-Dabo, Kerstin Klipstein-Grobusch, Adebowale A Adeyemo, Marcel M A M Mannens, Charles Agyemang
DNA methylation as the link between migration and the major noncommunicable diseases: the RODAM study. Epigenomics 13 (9) (2021)
Philip R Jansen, Nicole C M Petrus, Andrea Venema, Danielle Posthuma, Marcel M A M Mannens, Aline B Sprikkelman, Peter Henneman
Higher Polygenetic Predisposition for Asthma in Cow's Milk Allergic Children. Nutrients 10 (11) (2018)
Peter Henneman, Arjan Bouman, Adri Mul, Lia Knegt, Anne-Marie van der Kevie-Kersemaekers, Nitash Zwaveling-Soonawala, Hanne E J Meijers-Heijboer, A S Paul van Trotsenburg, Marcel M Mannens
Widespread domain-like perturbations of DNA methylation in whole blood of Down syndrome neonates. PloS one 13 (3) (2018)