Liselot van der Laan

Publication Activity (10 Years)

Years Active: 2022-2024
Publications (10 Years): 20

Top Topics

Dna Methylation

Spectrum Disorder

Top Venues

European journal of human genetics : EJHG

International journal of molecular sciences

American journal of medical genetics. Part C, Seminars in medical genetics

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

Publications

Amarens Hoogenboom, Farah A Falix, Liselot van der Laan, Jennifer Kerkhof, Mariëlle Alders, Bekim Sadikovic, Mieke M van Haelst
Novel PUF60 variant suggesting an interaction between Verheij and Cornelia de Lange syndrome: phenotype description and review of the literature. European journal of human genetics : EJHG 32 (4) (2024)
Stefano Giuseppe Caraffi, Liselot van der Laan, Kathleen Rooney, Slavica Trajkova, Roberta Zuntini, Raissa Relator, Sadegheh Haghshenas, Michael A Levy, Chiara Baldo, Giorgia Mandrile, Carolyn Lauzon, Duccio Maria Cordelli, Ivan Ivanovski, Anna Fetta, Elena Sukarova-Angelovska, Alfredo Brusco, Lisa Pavinato, Verdiana Pullano, Marcella Zollino, Haley McConkey, Tartaglia Marco, Giovanni Battista Ferrero, Bekim Sadikovic, Livia Garavelli
Identification of the DNA methylation signature of Mowat-Wilson syndrome. European journal of human genetics : EJHG 32 (6) (2024)
Amarens Hoogenboom, Farah A Falix, Liselot van der Laan, Jennifer Kerkhof, Mariëlle Alders, Bekim Sadikovic, Mieke M van Haelst
Novel PUF60 variant suggesting an interaction between Verheij and Cornelia de Lange syndrome: phenotype description and review of the literature. European journal of human genetics : EJHG (2024)
Stefano Giuseppe Caraffi, Liselot van der Laan, Kathleen Rooney, Slavica Trajkova, Roberta Zuntini, Raissa Relator, Sadegheh Haghshenas, Michael A Levy, Chiara Baldo, Giorgia Mandrile, Carolyn Lauzon, Duccio Maria Cordelli, Ivan Ivanovski, Anna Fetta, Elena Sukarova-Angelovska, Alfredo Brusco, Lisa Pavinato, Verdiana Pullano, Marcella Zollino, Haley McConkey, Tartaglia Marco, Giovanni Battista Ferrero, Bekim Sadikovic, Livia Garavelli
Identification of the DNA methylation signature of Mowat-Wilson syndrome. European journal of human genetics : EJHG 32 (6) (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)
Amarens Hoogenboom, Farah A Falix, Liselot van der Laan, Jennifer Kerkhof, Mariëlle Alders, Bekim Sadikovic, Mieke M van Haelst
Novel PUF60 variant suggesting an interaction between Verheij and Cornelia de Lange syndrome: phenotype description and review of the literature. European journal of human genetics : EJHG 32 (4) (2024)
Stefano Giuseppe Caraffi, Liselot van der Laan, Kathleen Rooney, Slavica Trajkova, Roberta Zuntini, Raissa Relator, Sadegheh Haghshenas, Michael A Levy, Chiara Baldo, Giorgia Mandrile, Carolyn Lauzon, Duccio Maria Cordelli, Ivan Ivanovski, Anna Fetta, Elena Sukarova-Angelovska, Alfredo Brusco, Lisa Pavinato, Verdiana Pullano, Marcella Zollino, Haley McConkey, Tartaglia Marco, Giovanni Battista Ferrero, Bekim Sadikovic, Livia Garavelli
Identification of the DNA methylation signature of Mowat-Wilson syndrome. European journal of human genetics : EJHG 32 (6) (2024)
Stefano Giuseppe Caraffi, Liselot van der Laan, Kathleen Rooney, Slavica Trajkova, Roberta Zuntini, Raissa Relator, Sadegheh Haghshenas, Michael A Levy, Chiara Baldo, Giorgia Mandrile, Carolyn Lauzon, Duccio Maria Cordelli, Ivan Ivanovski, Anna Fetta, Elena Sukarova-Angelovska, Alfredo Brusco, Lisa Pavinato, Verdiana Pullano, Marcella Zollino, Haley McConkey, Tartaglia Marco, Giovanni Battista Ferrero, Bekim Sadikovic, Livia Garavelli
Identification of the DNA methylation signature of Mowat-Wilson syndrome. European journal of human genetics : EJHG (2024)
Amarens Hoogenboom, Farah A Falix, Liselot van der Laan, Jennifer Kerkhof, Mariëlle Alders, Bekim Sadikovic, Mieke M van Haelst
Novel PUF60 variant suggesting an interaction between Verheij and Cornelia de Lange syndrome: phenotype description and review of the literature. European journal of human genetics : EJHG 32 (4) (2024)
Niels Vos, Lotte Kleinendorst, Liselot van der Laan, Jorrit van Uhm, Philip R Jansen, Agnies M van Eeghen, Saskia M Maas, Marcel M A M Mannens, Mieke M van Haelst
Evaluation of 100 Dutch cases with 16p11.2 deletion and duplication syndromes; from clinical manifestations towards personalized treatment options. European journal of human genetics : EJHG (2024)
Liselot van der Laan, Kathleen Rooney, Sadegheh Haghshenas, Ananília Silva, Haley McConkey, Raissa Relator, Michael A Levy, Irene Valenzuela, Laura Trujillano, Amaia Lasa-Aranzasti, Berta Campos, Neus Castells, Eline A Verberne, Saskia Maas, Mariëlle Alders, Marcel M A M Mannens, Mieke M van Haelst, Bekim Sadikovic, Peter Henneman
Functional Insight into and Refinement of the Genomic Boundaries of the JARID2 -Neurodevelopmental Disorder Episignature. International journal of molecular sciences 24 (18) (2023)
Izabela M Krzyzewska, Peter Lauffer, Adri N Mul, Liselot van der Laan, Andrew Y F Li Yim, Jan Maarten Cobben, Jacek Niklinski, Monika A Chomczyk, Smigiel Robert, Marcel M A M Mannens, Peter Henneman
Expression Quantitative Trait Methylation Analysis Identifies Whole Blood Molecular Footprint in Fetal Alcohol Spectrum Disorder (FASD). International journal of molecular sciences 24 (7) (2023)
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)
Eline A Verberne, Liselot van der Laan, Sadegheh Haghshenas, Kathleen Rooney, Michael A Levy, Mariëlle Alders, Saskia M Maas, Sandra Jansen, Agne Lieden, Britt-Marie Anderlid, Louise Rafael-Croes, Philippe M Campeau, Ayeshah Chaudhry, David A Koolen, Rolph Pfundt, Anna C E Hurst, Frederic Tran-Mau-Them, Ange-Line Bruel, Laetitia Lambert, Bertrand Isidor, Marcel M A M Mannens, Bekim Sadikovic, Peter Henneman, Mieke M van Haelst
DNA Methylation Signature for JARID2 -Neurodevelopmental Syndrome. International journal of molecular sciences 23 (14) (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, Mariëlle Alders, Raissa Relator, Haley McConkey, Jennifer Kerkhof, Michael A Levy, Peter Lauffer, Mio Aerden, Miel Theunis, Eric Legius, Matthew L Tedder, Lisenka E L M Vissers, Saskia Koene, Claudia Ruivenkamp, Mariette J V Hoffer, Dagmar Wieczorek, Nuria C Bramswig, Theresia Herget, Vanesa López González, Fernando Santos-Simarro, Pernille Mathiesen Torring, Anne Sophie Denommé-Pichon, Bertrand Isidor, Boris Keren, Sophie Julia, Elise Schaefer, Christine Francannet, Pierre-Yves Maillard, Mala Misra-Isrie, Hilde Van Esch, Marcel M A M Mannens, Bekim Sadikovic, Mieke M van Haelst, Peter Henneman
Episignature Mapping of TRIP12 Provides Functional Insight into Clark-Baraitser Syndrome. International journal of molecular sciences 23 (22) (2022)