All papers authored by Alex V. Postma
Refreshing results…
Lieve E. van der Maarel 
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Alex V. Postma ,
Vincent M. Christoffels
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Alex V. Postma ,
Vincent M. Christoffels
Genetics of sinoatrial node function and heart rate disorders
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Irma van de Beek ,
Iris E. Glykofridis,
Michael W. T. Tanck ,
Monique N. H. Luijten,
Theo M. Starink,
Jesper A. Balk,
Paul C. Johannesma,
Eric Hennekam,
Maurice J. B. van den Hoff,
Quinn D. Gunst,
Johan J. P. Gille,
Abeltje M. Polstra,
Pieter E. Postmus,
Maurice A. M. van Steensel,
Alex V. Postma
and 4 other authors
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Iris E. Glykofridis,
Michael W. T. Tanck ,
Monique N. H. Luijten,
Theo M. Starink,
Jesper A. Balk,
Paul C. Johannesma,
Eric Hennekam,
Maurice J. B. van den Hoff,
Quinn D. Gunst,
Johan J. P. Gille,
Abeltje M. Polstra,
Pieter E. Postmus,
Maurice A. M. van Steensel,
Alex V. Postma
and 4 other authors
Familial multiple discoid fibromas is linked to a locus on chromosome 5 including the FNIP1 gene
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Alex V. Postma ,
Christina K. Rapp ,
Katrin Knoflach,
Alexander E. Volk,
Johannes R. Lemke ,
Maximilian Ackermann ,
Nicolas Regamey,
Philipp Latzin,
Lucas Celant ,
Samara M. A. Jansen,
Harm J. Bogaard ,
Aho Ilgun,
Mariëlle Alders,
Karin Y. van Spaendonck-Zwarts,
Danny Jonigk
and 5 other authors
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Christina K. Rapp ,
Katrin Knoflach,
Alexander E. Volk,
Johannes R. Lemke ,
Maximilian Ackermann ,
Nicolas Regamey,
Philipp Latzin,
Lucas Celant ,
Samara M. A. Jansen,
Harm J. Bogaard ,
Aho Ilgun,
Mariëlle Alders,
Karin Y. van Spaendonck-Zwarts,
Danny Jonigk
and 5 other authors
Biallelic variants in the calpain regulatory subunit CAPNS1 cause pulmonary arterial hypertension
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2022
Irma van de Beek,
Iris E. Glykofridis ,
Jan C. Oosterwijk,
Peter C. van den Akker,
Gilles F. H. Diercks,
Maria C. Bolling,
Quinten Waisfisz,
Arjen R. Mensenkamp,
Jesper A. Balk,
Rob Zwart,
Alex V. Postma ,
Hanne E. J. Meijers-Heijboer,
R. Jeroen A. van Moorselaar,
Rob M. F. Wolthuis,
Arjan C. Houweling
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Jan C. Oosterwijk,
Peter C. van den Akker,
Gilles F. H. Diercks,
Maria C. Bolling,
Quinten Waisfisz,
Arjen R. Mensenkamp,
Jesper A. Balk,
Rob Zwart,
Alex V. Postma ,
Hanne E. J. Meijers-Heijboer,
R. Jeroen A. van Moorselaar,
Rob M. F. Wolthuis,
Arjan C. Houweling
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Stijntje Hibender,
Siyu Li,
Alex V. Postma ,
Myrthe E. Hoogeland,
Denise Klaver,
Richard B. Pouw,
Hans W. Niessen,
Antoine Hg Driessen,
David R. Koolbergen,
Carlie Jm de Vries,
Marieke Jh Baars,
Arjan C. Houweling,
Paul A. Krijnen,
Vivian de Waard
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Myrthe E. Hoogeland,
Denise Klaver,
Richard B. Pouw,
Hans W. Niessen,
Antoine Hg Driessen,
David R. Koolbergen,
Carlie Jm de Vries,
Marieke Jh Baars,
Arjan C. Houweling,
Paul A. Krijnen,
Vivian de Waard
No prominent role for complement C1-esterase inhibitor in Marfan syndrome mice
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Antoinette F. van Ouwerkerk,
Fernanda M. Bosada,
Karel van Duijvenboden,
Arjan C. Houweling ,
Koen T. Scholman,
Vincent Wakker ,
Cornelis P. Allaart ,
Jae-Sun Uhm ,
Inge B. Mathijssen,
Ton Baartscheer,
Alex V. Postma ,
Phil Barnett,
Arie O. Verkerk ,
Bastiaan J. Boukens,
Vincent M. Christoffels
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Koen T. Scholman,
Vincent Wakker ,
Cornelis P. Allaart ,
Jae-Sun Uhm ,
Inge B. Mathijssen,
Ton Baartscheer,
Alex V. Postma ,
Phil Barnett,
Arie O. Verkerk ,
Bastiaan J. Boukens,
Vincent M. Christoffels
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Doris Škorić Milosavljević,
Fernanda M. Bosada,
J. H. Van Weerd,
Rafik Tadros,
Odilia I. Woudstra,
Jan Hendrik van Weerd,
Fleur V. Y. Tjong,
Federico Tessadori,
Heather J. Cordell,
A. J. Agopian,
Gillian M. Blue,
Daniela Q. C. M. Barge-Schaapveld,
Marc Gewillig,
Christoph Preuss,
Elisabeth M. Lodder
and 79 other authors
Common Genetic Variants Contribute to Risk of Transposition of the Great Arteries
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Doris Škorić-Milosavljević,
Najim Lahrouchi,
Fernanda M. Bosada,
Gregor Dombrowsky,
Simon G. Williams,
Robert Lesurf,
Fleur V. Y. Tjong,
Roddy Walsh,
Ihssane El Bouchikhi,
Jeroen Breckpot,
Enrique Audain,
Aho Ilgun,
Leander Beekman,
Ilham Ratbi,
Alanna Strong
and 40 other authors
Rare variants in KDR, encoding VEGF Receptor 2, are associated with tetralogy of Fallot
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Enrique Audain,
Anna Wilsdon,
Jeroen Breckpot,
Jose M. G. Izarzugaza,
Tomas W. Fitzgerald,
Anne-Karin Kahlert,
Alejandro Sifrim,
Florian Wünnemann,
Yasset Perez-Riverol,
Hashim Abdul-Khaliq,
Mads Bak,
Anne S. Bassett,
D. Woodrow Benson,
Felix Berger,
Ingo Daehnert
and 35 other authors
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Enrique Audain ,
Woodrow D. Benson,
Felix Berger ,
Anna Wilsdon ,
Ingo Daehnert ,
J. W. Belmont,
Jeroen Breckpot,
Koenraad Devriendt ,
D. W. Benson,
Jose M. G. Izarzugaza,
Sven Dittrich ,
Piers Ef Daubeney ,
Tomas W. Fitzgerald ,
Vidu Garg ,
Karl Hackmann
and 37 other authors
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,
Woodrow D. Benson,
Felix Berger ,
Anna Wilsdon ,
Ingo Daehnert ,
J. W. Belmont,
Jeroen Breckpot,
Koenraad Devriendt ,
D. W. Benson,
Jose M. G. Izarzugaza,
Sven Dittrich ,
Piers Ef Daubeney ,
Tomas W. Fitzgerald ,
Vidu Garg ,
Karl Hackmann
and 37 other authors
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Lynne Rumping ,
Marja W. Wessels,
Alex V. Postma ,
Joost van Schuppen,
Marjon A. van Slegtenhorst,
Jasper J. Saris,
J. Peter van Tintelen,
Stephen P. Robertson ,
Mariëlle Alders,
Saskia M. Maas,
Ronald H. Lekanne Deprez
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Marja W. Wessels,
Alex V. Postma ,
Joost van Schuppen,
Marjon A. van Slegtenhorst,
Jasper J. Saris,
J. Peter van Tintelen,
Stephen P. Robertson ,
Mariëlle Alders,
Saskia M. Maas,
Ronald H. Lekanne Deprez
Terminal osseous dysplasia with pigmentary defects and cardiomyopathy caused by a novel FLNA variant
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Najim Lahrouchi ,
Alex V. Postma ,
Christian M. Salazar,
Fleur Tjong,
Lenka Piherová ,
Dominic Zimmerman,
Elisabeth M. Lodder,
Asaf Ta-Shma ,
Zeev Perles,
Aho Ilgun,
Quinn Gunst,
Mariam Hababa,
Doris Škorić-Milosavljević,
Viktor Stránecký ,
Viktor Tomek
and 41 other authors
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,
Alex V. Postma ,
Christian M. Salazar,
Fleur Tjong,
Lenka Piherová ,
Dominic Zimmerman,
Elisabeth M. Lodder,
Asaf Ta-Shma ,
Zeev Perles,
Aho Ilgun,
Quinn Gunst,
Mariam Hababa,
Doris Škorić-Milosavljević,
Viktor Stránecký ,
Viktor Tomek
and 41 other authors
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2020
Eva S. van Walree ,
van Walree Es,
Gregor Dombrowsky,
Iris E. Jansen,
Maša Umićević Mirkov,
Maša Umićević Mirkov,
Jansen Ie,
Rob Zwart,
Allard C. van der Wal,
Mirkov Mu,
Aho Ilgun,
Sally-Ann B. Clur,
Dongchuan Guo,
Ahmed S. Amin,
Jeanne E. Savage
and 20 other authors
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van Walree Es,
Gregor Dombrowsky,
Iris E. Jansen,
Maša Umićević Mirkov,
Maša Umićević Mirkov,
Jansen Ie,
Rob Zwart,
Allard C. van der Wal,
Mirkov Mu,
Aho Ilgun,
Sally-Ann B. Clur,
Dongchuan Guo,
Ahmed S. Amin,
Jeanne E. Savage
and 20 other authors
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Eline A. Verberne ,
Sonja Faries,
Marcel M. A. M. Mannens,
Mieke M. van Haelst,
Alex V. Postma ,
Mieke M. Haelst
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Sonja Faries,
Marcel M. A. M. Mannens,
Mieke M. van Haelst,
Alex V. Postma ,
Mieke M. Haelst
Expanding the phenotype of biallelic RNPC3 variants associated with growth hormone deficiency
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2019
Arjan C. Houweling,
Glenda M. Beaman ,
Alex V. Postma ,
T. Blair Gainous ,
Klaske D. Lichtenbelt ,
Francesco Brancati ,
Filipa M. Lopes,
Ingeborg van der Made,
Abeltje M. Polstra,
Michael L. Robinson ,
Kevin D. Wright,
Jamie M. Ellingford,
Ashley R. Jackson ,
Eline Overwater,
Rita Genesio
and 10 other authors
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Alex V. Postma ,
T. Blair Gainous ,
Klaske D. Lichtenbelt ,
Francesco Brancati ,
Filipa M. Lopes,
Ingeborg van der Made,
Abeltje M. Polstra,
Michael L. Robinson ,
Kevin D. Wright,
Jamie M. Ellingford,
Ashley R. Jackson ,
Eline Overwater,
Rita Genesio
and 10 other authors
Loss-of-function variants in myocardin cause congenital megabladder in humans and mice
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Doris Škorić‐Milosavljević ,
Fleur V. Y. Tjong,
Julien Barc,
Ad P. C. M. Backx,
Sally‐Ann B. Clur,
Karin Spaendonck‐Zwarts,
Karin van Spaendonck‐Zwarts,
Roelof‐Jan Oostra,
Najim Lahrouchi,
Leander Beekman,
Regina Bökenkamp,
Daniela Q. C. M. Barge‐Schaapveld,
Barbara J. Mulder,
Elisabeth M. Lodder,
Connie R. Bezzina
and 1 other authors
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,
Fleur V. Y. Tjong,
Julien Barc,
Ad P. C. M. Backx,
Sally‐Ann B. Clur,
Karin Spaendonck‐Zwarts,
Karin van Spaendonck‐Zwarts,
Roelof‐Jan Oostra,
Najim Lahrouchi,
Leander Beekman,
Regina Bökenkamp,
Daniela Q. C. M. Barge‐Schaapveld,
Barbara J. Mulder,
Elisabeth M. Lodder,
Connie R. Bezzina
and 1 other authors
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Jan Maarten Cobben,
Izabela M. Krzyzewska ,
Andrea Venema,
Adri N. Mul,
Abeltje Polstra,
Alex V. Postma ,
Robert Smigiel,
Karolina Pesz,
Jacek Niklinski,
Monika A. Chomczyk,
Peter Henneman,
Marcel Mam Mannens
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Andrea Venema,
Adri N. Mul,
Abeltje Polstra,
Alex V. Postma ,
Robert Smigiel,
Karolina Pesz,
Jacek Niklinski,
Monika A. Chomczyk,
Peter Henneman,
Marcel Mam Mannens
DNA methylation abundantly associates with fetal alcohol spectrum disorder and its subphenotypes
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