Eric A Haan (Eric Haan)

Publication Activity (10 Years)

Years Active: 2017-2022
Publications (10 Years): 13

Top Topics

Aortic Aneurysm

Prefrontal Cortex

Intellectual Disability

Top Venues

Circulation. Genomic and precision medicine

American journal of medical genetics. Part A

Science advances

Nature neuroscience

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

Publications

Edgar T Hoorntje, Charlotte Burns, Luisa Marsili, Ben Corden, Victoria N Parikh, Gerard J Te Meerman, Belinda Gray, Ahmet Adiyaman, Richard Douglas Bagnall, Daniela Q C M Barge-Schaapveld, Maarten P van den Berg, Marianne Bootsma, Laurens P Bosman, Gemma Correnti, Johan Duflou, Ruben N Eppinga, Diane Fatkin, Michael Fietz, Eric A Haan, Jan D H Jongbloed, Arnaud D Hauer, Lien Lam, Freyja H M van Lint, Amrit S Lota, Carlo L Marcelis, Hugh J McCarthy, Anneke M van Mil, Rogier A Oldenburg, Nicholas Pachter, R Nils Planken, Nicolette Chun, Christopher Semsarian, Jasper J van der Smagt, Tina Thompson, Jitendra Vohra, Paul G A Volders, Jaap I van Waning, Nicola Whiffin, Arthur van den Wijngaard, Ahmad S Amin, Arthur A M Wilde, Gijs van Woerden, Laura Yeates, Dominica Zentner, Euan A Ashley, Matthew T Wheeler, James Simon Ware, van J Peter Tintelen, Jodie Ingles
Variant Location Is a Novel Risk Factor for Individuals With Arrhythmogenic Cardiomyopathy Due to a Desmoplakin ( DSP ) Truncating Variant. Circulation. Genomic and precision medicine 16 (1) (2022)
Edgar T Hoorntje, Charlotte Burns, Luisa Marsili, Ben Corden, Victoria N Parikh, Gerard J Te Meerman, Belinda Gray, Ahmet Adiyaman, Richard Douglas Bagnall, Daniela Q C M Barge-Schaapveld, Maarten P van den Berg, Marianne Bootsma, Laurens P Bosman, Gemma Correnti, Johan Duflou, Ruben N Eppinga, Diane Fatkin, Michael Fietz, Eric A Haan, Jan D H Jongbloed, Arnaud D Hauer, Lien Lam, Freyja H M van Lint, Amrit S Lota, Carlo L Marcelis, Hugh J McCarthy, Anneke M van Mil, Rogier A Oldenburg, Nicholas Pachter, R Nils Planken, Nicolette Chun, Christopher Semsarian, Jasper J van der Smagt, Tina Thompson, Jitendra Vohra, Paul G A Volders, Jaap I van Waning, Nicola Whiffin, Arthur van den Wijngaard, Ahmad S Amin, Arthur A M Wilde, Gijs van Woerden, Laura Yeates, Dominica Zentner, Euan A Ashley, Matthew T Wheeler, James Simon Ware, van J Peter Tintelen, Jodie Ingles
Variant Location Is a Novel Risk Factor for Individuals With Arrhythmogenic Cardiomyopathy Due to a Desmoplakin ( DSP ) Truncating Variant. Circulation. Genomic and precision medicine 16 (1) (2022)
Edgar T Hoorntje, Charlotte Burns, Luisa Marsili, Ben Corden, Victoria N Parikh, Gerard J Te Meerman, Belinda Gray, Ahmet Adiyaman, Richard Douglas Bagnall, Daniela Q C M Barge-Schaapveld, Maarten P van den Berg, Marianne Bootsma, Laurens P Bosman, Gemma Correnti, Johan Duflou, Ruben N Eppinga, Diane Fatkin, Michael Fietz, Eric A Haan, Jan D H Jongbloed, Arnaud D Hauer, Lien Lam, Freyja H M van Lint, Amrit S Lota, Carlo L Marcelis, Hugh J McCarthy, Anneke M van Mil, Rogier A Oldenburg, Nicholas Pachter, R Nils Planken, Nicolette Chun, Christopher Semsarian, Jasper J van der Smagt, Tina Thompson, Jitendra Vohra, Paul G A Volders, Jaap I van Waning, Nicola Whiffin, Arthur van den Wijngaard, Ahmad S Amin, Arthur A M Wilde, Gijs van Woerden, Laura Yeates, Dominica Zentner, Euan A Ashley, Matthew T Wheeler, James Simon Ware, van J Peter Tintelen, Jodie Ingles
Variant Location Is a Novel Risk Factor for Individuals With Arrhythmogenic Cardiomyopathy Due to a Desmoplakin ( DSP ) Truncating Variant. Circulation. Genomic and precision medicine 16 (1) (2022)
Edgar T Hoorntje, Charlotte Burns, Luisa Marsili, Ben Corden, Victoria N Parikh, Gerard J Te Meerman, Belinda Gray, Ahmet Adiyaman, Richard Douglas Bagnall, Daniela Q C M Barge-Schaapveld, Maarten P van den Berg, Marianne Bootsma, Laurens P Bosman, Gemma Correnti, Johan Duflou, Ruben N Eppinga, Diane Fatkin, Michael Fietz, Eric A Haan, Jan D H Jongbloed, Arnaud D Hauer, Lien Lam, Freyja H M van Lint, Amrit S Lota, Carlo L Marcelis, Hugh J McCarthy, Anneke M van Mil, Rogier A Oldenburg, Nicholas Pachter, R Nils Planken, Nicolette Chun, Christopher Semsarian, Jasper J van der Smagt, Tina Thompson, Jitendra Vohra, Paul G A Volders, Jaap I van Waning, Nicola Whiffin, Arthur van den Wijngaard, Ahmad S Amin, Arthur A M Wilde, Gijs van Woerden, Laura Yeates, Dominica Zentner, Euan A Ashley, Matthew T Wheeler, James Simon Ware, van J Peter Tintelen, Jodie Ingles
Variant Location Is a Novel Risk Factor for Individuals With Arrhythmogenic Cardiomyopathy Due to a Desmoplakin ( DSP ) Truncating Variant. Circulation. Genomic and precision medicine 16 (1) (2022)
Edgar T Hoorntje, Charlotte Burns, Luisa Marsili, Ben Corden, Victoria N Parikh, Gerard J Te Meerman, Belinda Gray, Ahmet Adiyaman, Richard Douglas Bagnall, Daniela Q C M Barge-Schaapveld, Maarten P van den Berg, Marianne Bootsma, Laurens P Bosman, Gemma Correnti, Johan Duflou, Ruben N Eppinga, Diane Fatkin, Michael Fietz, Eric A Haan, Jan D H Jongbloed, Arnaud D Hauer, Lien Lam, Freyja H M van Lint, Amrit S Lota, Carlo L Marcelis, Hugh J McCarthy, Anneke M van Mil, Rogier A Oldenburg, Nicholas Pachter, R Nils Planken, Nicolette Chun, Christopher Semsarian, Jasper J van der Smagt, Tina Thompson, Jitendra Vohra, Paul G A Volders, Jaap I van Waning, Nicola Whiffin, Arthur van den Wijngaard, Ahmad S Amin, Arthur A M Wilde, Gijs van Woerden, Laura Yeates, Dominica Zentner, Euan A Ashley, Matthew T Wheeler, James Simon Ware, van J Peter Tintelen, Jodie Ingles
Variant Location Is a Novel Risk Factor for Individuals With Arrhythmogenic Cardiomyopathy Due to a Desmoplakin ( DSP ) Truncating Variant. Circulation. Genomic and precision medicine 16 (1) (2022)
Edgar T Hoorntje, Charlotte Burns, Luisa Marsili, Ben Corden, Victoria N Parikh, Gerard J Te Meerman, Belinda Gray, Ahmet Adiyaman, Richard Douglas Bagnall, Daniela Q C M Barge-Schaapveld, Maarten P van den Berg, Marianne Bootsma, Laurens P Bosman, Gemma Correnti, Johan Duflou, Ruben N Eppinga, Diane Fatkin, Michael Fietz, Eric A Haan, Jan D H Jongbloed, Arnaud D Hauer, Lien Lam, Freyja H M van Lint, Amrit S Lota, Carlo L Marcelis, Hugh J McCarthy, Anneke M van Mil, Rogier A Oldenburg, Nicholas Pachter, R Nils Planken, Nicolette Chun, Christopher Semsarian, Jasper J van der Smagt, Tina Thompson, Jitendra Vohra, Paul G A Volders, Jaap I van Waning, Nicola Whiffin, Arthur van den Wijngaard, Ahmad S Amin, Arthur A M Wilde, Gijs van Woerden, Laura Yeates, Dominica Zentner, Euan A Ashley, Matthew T Wheeler, James Simon Ware, van J Peter Tintelen, Jodie Ingles
Variant Location Is a Novel Risk Factor for Individuals With Arrhythmogenic Cardiomyopathy Due to a Desmoplakin ( DSP ) Truncating Variant. Circulation. Genomic and precision medicine 16 (1) (2022)
Edgar T Hoorntje, Charlotte Burns, Luisa Marsili, Ben Corden, Victoria N Parikh, Gerard J Te Meerman, Belinda Gray, Ahmet Adiyaman, Richard Douglas Bagnall, Daniela Q C M Barge-Schaapveld, Maarten P van den Berg, Marianne Bootsma, Laurens P Bosman, Gemma Correnti, Johan Duflou, Ruben N Eppinga, Diane Fatkin, Michael Fietz, Eric A Haan, Jan D H Jongbloed, Arnaud D Hauer, Lien Lam, Freyja H M van Lint, Amrit S Lota, Carlo L Marcelis, Hugh J McCarthy, Anneke M van Mil, Rogier A Oldenburg, Nicholas Pachter, R Nils Planken, Nicolette Chun, Christopher Semsarian, Jasper J van der Smagt, Tina Thompson, Jitendra Vohra, Paul G A Volders, Jaap I van Waning, Nicola Whiffin, Arthur van den Wijngaard, Ahmad S Amin, Arthur A M Wilde, Gijs van Woerden, Laura Yeates, Dominica Zentner, Euan A Ashley, Matthew T Wheeler, James Simon Ware, van J Peter Tintelen, Jodie Ingles
Variant Location Is a Novel Risk Factor for Individuals With Arrhythmogenic Cardiomyopathy Due to a Desmoplakin ( DSP ) Truncating Variant. Circulation. Genomic and precision medicine (2022)
Edgar T Hoorntje, Charlotte Burns, Luisa Marsili, Ben Corden, Victoria N Parikh, Gerard J Te Meerman, Belinda Gray, Ahmet Adiyaman, Richard Douglas Bagnall, Daniela Q C M Barge-Schaapveld, Maarten P van den Berg, Marianne Bootsma, Laurens P Bosman, Gemma Correnti, Johan Duflou, Ruben N Eppinga, Diane Fatkin, Michael Fietz, Eric A Haan, Jan D H Jongbloed, Arnaud D Hauer, Lien Lam, Freyja H M van Lint, Amrit S Lota, Carlo L Marcelis, Hugh J McCarthy, Anneke M van Mil, Rogier A Oldenburg, Nicholas Pachter, R Nils Planken, Nicolette Chun, Christopher Semsarian, Jasper J van der Smagt, Tina Thompson, Jitendra Vohra, Paul G A Volders, Jaap I van Waning, Nicola Whiffin, Arthur van den Wijngaard, Ahmad S Amin, Arthur A M Wilde, Gijs van Woerden, Laura Yeates, Dominica Zentner, Euan A Ashley, Matthew T Wheeler, James Simon Ware, van J Peter Tintelen, Jodie Ingles
Variant Location Is a Novel Risk Factor for Individuals With Arrhythmogenic Cardiomyopathy Due to a Desmoplakin ( DSP ) Truncating Variant. Circulation. Genomic and precision medicine 16 (1) (2022)
Edgar T Hoorntje, Charlotte Burns, Luisa Marsili, Ben Corden, Victoria N Parikh, Gerard J Te Meerman, Belinda Gray, Ahmet Adiyaman, Richard Douglas Bagnall, Daniela Q C M Barge-Schaapveld, Maarten P van den Berg, Marianne Bootsma, Laurens P Bosman, Gemma Correnti, Johan Duflou, Ruben N Eppinga, Diane Fatkin, Michael Fietz, Eric A Haan, Jan D H Jongbloed, Arnaud D Hauer, Lien Lam, Freyja H M van Lint, Amrit S Lota, Carlo L Marcelis, Hugh J McCarthy, Anneke M van Mil, Rogier A Oldenburg, Nicholas Pachter, R Nils Planken, Nicolette Chun, Christopher Semsarian, Jasper J van der Smagt, Tina Thompson, Jitendra Vohra, Paul G A Volders, Jaap I van Waning, Nicola Whiffin, Arthur van den Wijngaard, Ahmad S Amin, Arthur A M Wilde, Gijs van Woerden, Laura Yeates, Dominica Zentner, Euan A Ashley, Matthew T Wheeler, James Simon Ware, van J Peter Tintelen, Jodie Ingles
Variant Location Is a Novel Risk Factor for Individuals With Arrhythmogenic Cardiomyopathy Due to a Desmoplakin ( DSP ) Truncating Variant. Circulation. Genomic and precision medicine (2022)
Eric A Haan, Francois H Chamalaun, Steven A J Chamuleau, Leonard F Arnolda, John P Slavotinek, Nadia C Wise, Dimuth N Gunawardane, Ulrike Schwarze, Peter H Byers, Genevieve M Gabb
Marfan syndrome resulting from a rare pathogenic FBN1 variant, ascertained through a proband with IgG4-related arteriopathy. American journal of medical genetics. Part A 185 (7) (2021)
Hui Guo, Ying Li, Lu Shen, Tianyun Wang, Xiangbin Jia, Lijuan Liu, Tao Xu, Mengzhu Ou, Kendra Hoekzema, Huidan Wu, Madelyn A Gillentine, Cenying Liu, Hailun Ni, Pengwei Peng, Rongjuan Zhao, Yu Zhang, Chanika Phornphutkul, Alexander P A Stegmann, Carlos E Prada, Robert J Hopkin, Joseph T Shieh, Kirsty McWalter, Kristin G Monaghan, Peter M van Hasselt, Koen van Gassen, Ting Bai, Min Long, Lin Han, Yingting Quan, Meilin Chen, Yaowen Zhang, Kuokuo Li, Qiumeng Zhang, Jieqiong Tan, Tengfei Zhu, Yaning Liu, Nan Pang, Jing Peng, Daryl A Scott, Seema R Lalani, Mahshid S Azamian, Grazia M S Mancini, Darius J Adams, Malin Kvarnung, Anna Lindstrand, Ann Nordgren, Jonathan Pevsner, Ikeoluwa A Osei-Owusu, Corrado Romano, Giuseppe Calabrese, Ornella Galesi, Jozef Gecz, Eric A Haan, Judith Ranells, Melissa Racobaldo, Magnus Nordenskjold, Suneeta Madan-Khetarpal, Jessica Sebastian, Susie Ball, Xiaobing Zou, Jingping Zhao, Zhengmao Hu, Fan Xia, Pengfei Liu, Jill Anne Rosenfeld, Bert B A de Vries, Raphael A Bernier, Zhi-Qing David Xu, Honghui Li, Wei Xie, Robert B Hufnagel, Evan E Eichler, Kun Xia
Disruptive variants of CSDE1 associate with autism and interfere with neuronal development and synaptic transmission. Science advances 5 (9) (2019)
Suzanna G M Frints, Aysegul Ozanturk, Germán Rodríguez Criado, Ute Grasshoff, Bas de Hoon, Michael Field, Sylvie Manouvrier-Hanu, Scott E Hickey, Molka Kammoun, Karen W Gripp, Claudia Bauer, Christopher Schroeder, Annick Toutain, Theresa Mihalic Mosher, Benjamin J Kelly, Peter White, Andreas Dufke, Eveline Rentmeester, Sungjin Moon, Daniel C Koboldt, Kees E P van Roozendaal, Hao Hu, Stefan A Haas, Hans-Hilger Ropers, Lucinda Murray, Eric A Haan, Marie Shaw, Renee Carroll, Kathryn Friend, Jan Liebelt, Lynne Hobson, Marjan De Rademaeker, Joep Geraedts, Jean-Pierre Fryns, Joris Vermeesch, Martine Raynaud, Olaf Riess, Joost Gribnau, Nicholas Katsanis, Koen Devriendt, Peter Bauer, Jozef Gecz, Christelle Golzio, Cristina Gontan, Vera M Kalscheuer
Pathogenic variants in E3 ubiquitin ligase RLIM/RNF12 lead to a syndromic X-linked intellectual disability and behavior disorder. Molecular psychiatry 24 (11) (2018)
Madeleine R Geisheker, Gabriel Heymann, Tianyun Wang, Bradley P Coe, Tychele N Turner, Holly A F Stessman, Kendra Hoekzema, Malin Kvarnung, Marie Shaw, Kathryn Friend, Jan Liebelt, Christopher Barnett, Elizabeth M Thompson, Eric A Haan, Hui Guo, Britt-Marie Anderlid, Ann Nordgren, Anna Lindstrand, Geert Vandeweyer, Antonino Alberti, Emanuela Avola, Mirella Vinci, Stefania Giusto, Tiziano Pramparo, Karen Pierce, Srinivasa Nalabolu, Jacob J Michaelson, Zdenek Sedlacek, Gijs W E Santen, Hilde Peeters, Hakon Hakonarson, Eric Courchesne, Corrado Romano, R Frank Kooy, Raphael A Bernier, Magnus Nordenskjöld, Jozef Gecz, Kun Xia, Larry S Zweifel, Evan E Eichler
Hotspots of missense mutation identify neurodevelopmental disorder genes and functional domains. Nature neuroscience 20 (8) (2017)