Correction to: Rare variants in KDR, encoding VEGF Receptor 2, are associated with tetralogy of Fallot

Škorić-Milosavljević, Doris; Lahrouchi, Najim; Bosada, Fernanda M.; Dombrowsky, Gregor; Williams, Simon G.; Lesurf, Robert; Tjong, Fleur V. Y.; Walsh, Roddy; El Bouchikhi, Ihssane; Breckpot, Jeroen; Audain, Enrique; Ilgun, Aho; Beekman, Leander; Ratbi, Ilham; Strong, Alanna; Muenke, Maximilian; Heide, Solveig; Muir, Alison M.; Hababa, Mariam; Cross, Laura; Zhou, Dihong; Pastinen, Tomi; Zackai, Elaine; Atmani, Samir; Ouldim, Karim; Adadi, Najlae; Steindl, Katharina; Rauch, Anita; Brook, David; Wilsdon, Anna; Kuipers, Irene; Blom, Nico A.; Mulder, Barbara J.; Mefford, Heather C.; Keren, Boris; Joset, Pascal; Kruszka, Paul; Thiffault, Isabelle; Sheppard, Sarah E.; Roberts, Amy; Lodder, Elisabeth M.; Keavney, Bernard D.; Clur, Sally-Ann B.; Mital, Seema; Hitz, Marc-Philip; Christoffels, Vincent M.; Postma, Alex V.; Bezzina, Connie R.

doi:10.1038/s41436-021-01279-7

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Published: 14 September 2021

Correction to: Rare variants in KDR, encoding VEGF Receptor 2, are associated with tetralogy of Fallot

Doris Škorić-Milosavljević¹^na1,
Najim Lahrouchi¹^na1,
Fernanda M. Bosada²,
Gregor Dombrowsky³,
Simon G. Williams⁴,
Robert Lesurf⁵,
Fleur V. Y. Tjong¹,
Roddy Walsh¹,
Ihssane El Bouchikhi⁶,
Jeroen Breckpot⁷,
Enrique Audain³,
Aho Ilgun²,
Leander Beekman¹,
Ilham Ratbi^8,9,
Alanna Strong^10,11,
Maximilian Muenke¹²,
Solveig Heide¹³,
Alison M. Muir¹⁴,
Mariam Hababa¹,
Laura Cross¹⁵,
Dihong Zhou¹⁵,
Tomi Pastinen¹⁶,
German Competence Network for Congenital Heart Defects,
Elaine Zackai¹⁰,
Samir Atmani^17,18,
Karim Ouldim¹⁹,
Najlae Adadi^8,9,
Katharina Steindl²⁰,
Anita Rauch²⁰,
David Brook²¹,
Anna Wilsdon²¹,
Irene Kuipers²²,
Nico A. Blom^22,23,
Barbara J. Mulder¹,
Heather C. Mefford¹⁴,
Boris Keren¹³,
Pascal Joset²⁰,
Paul Kruszka¹²,
Isabelle Thiffault¹⁶,
Sarah E. Sheppard¹⁰,
Amy Roberts²⁴,
Elisabeth M. Lodder^1,25,
Bernard D. Keavney^4,26,
Sally-Ann B. Clur²²,
Seema Mital^27,28,
Marc-Philip Hitz^3,29,30,
Vincent M. Christoffels²,
Alex V. Postma^2,25^na1 &
…
Connie R. Bezzina¹^na1

Genetics in Medicine volume 23, page 2013 (2021)Cite this article

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The Original Article was published on 10 June 2021

Correction to: Genetics in Medicine 2021; https://doi.org/10.1038/s41436-021-01212-y; published online 10 June 2021

Due to a processing error the author’s Doris Škorić-Milosavljević, Najim Lahrouchi, Alex V. Postma, Connie R. Bezzina were assigned to affiliation 38. However, affiliation 38 does not exist.

In addition, the affiliations of Najim Lahrouchi, Elisabeth M. Lodder, and Connie R. Bezzina should be number 1 instead of number 2. The correct affiliation is Department of Clinical and Experimental Cardiology, Amsterdam University Medical Center, Amsterdam, The Netherlands.

The original article has been corrected.

Author information

These authors contributed equally: Doris Škorić-Milosavljević, Najim Lahrouchi, Fernanda M. Bosada, Alex V. Postma, Connie R. Bezzina.

Authors and Affiliations

Department of Clinical and Experimental Cardiology, Amsterdam University Medical Center, Amsterdam, The Netherlands
Doris Škorić-Milosavljević, Najim Lahrouchi, Fleur V. Y. Tjong, Roddy Walsh, Leander Beekman, Mariam Hababa, Barbara J. Mulder, Elisabeth M. Lodder & Connie R. Bezzina
Department of Medical Biology, Amsterdam University Medical Center, Amsterdam, The Netherlands
Fernanda M. Bosada, Aho Ilgun, Vincent M. Christoffels & Alex V. Postma
Department of Congenital Heart Disease and Pediatric Cardiology, Universitätsklinikum Schleswig-Holstein Kiel, Kiel, Germany
Gregor Dombrowsky, Enrique Audain & Marc-Philip Hitz
Division of Cardiovascular Sciences, School of Medical Sciences, Faculty of Biology, Medicine and Health, The University of Manchester, Manchester, UK
Simon G. Williams & Bernard D. Keavney
Genetics and Genome Biology Program, The Hospital for Sick Children, Toronto, ON, Canada
Robert Lesurf
Laboratory of Medical Genetics and Oncogenetics, HASSAN II University Hospital, Fez, Morocco
Ihssane El Bouchikhi
Center for Human Genetics Leuven and Catholic University Leuven, Leuven, Belgium
Jeroen Breckpot
Centre de Recherche en Génomique des Pathologies Humaines (GENOPATH), Faculté de Médecine et de Pharmacie, Mohammed V University of Rabat, Rabat, Morocco
Ilham Ratbi & Najlae Adadi
Département de génétique médicale, Institut National d’Hygiène, Rabat, Morocco
Ilham Ratbi & Najlae Adadi
Division of Human Genetics, Children’s Hospital of Philadelphia, Philadelphia, PA, USA
Alanna Strong, Elaine Zackai & Sarah E. Sheppard
Center for Applied Genomics, Children’s Hospital of Philadelphia, Philadelphia, PA, USA
Alanna Strong
Medical Genetics Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, MD, USA
Maximilian Muenke & Paul Kruszka
Département de génétique, Hôpital Pitié-Salpêtrière, APHP Sorbonne Université, Paris, France
Solveig Heide & Boris Keren
Department of Pediatrics, Division of Genetic Medicine, University of Washington, Seattle, WA, USA
Alison M. Muir & Heather C. Mefford
Division of Clinical Genetics, Children’s Mercy Hospital, Kansas City, MO, USA
Laura Cross & Dihong Zhou
Center for Pediatric Genomic Medicine, Children’s Mercy Hospital and School of Medicine, University of Missouri–Kansas City, Kansas City, MO, USA
Tomi Pastinen & Isabelle Thiffault
HASSAN II University Hospital, Fez, Morocco
Samir Atmani
University of Sidi Mohammed Ben Abdellah, Fez, Morocco
Samir Atmani
Faculty of Medicine and Pharmacy, Medical Genetics and Oncogenetics Unit, Sidi Mohamed Ben Abdellah University, Fez, Morocco
Karim Ouldim
Institute of Medical Genetics, University of Zurich, Zurich, Switzerland
Katharina Steindl, Anita Rauch & Pascal Joset
University of Nottingham, Queen’s Medical Centre, Nottingham, UK
David Brook & Anna Wilsdon
Department of Pediatric Cardiology, Amsterdam University Medical Center, Amsterdam, The Netherlands
Irene Kuipers, Nico A. Blom & Sally-Ann B. Clur
Department of Pediatric Cardiology, Leiden University Medical Center, Leiden, The Netherlands
Nico A. Blom
Department of Cardiology, Boston Children’s Hospital, and Department of Pediatrics, Harvard Medical School, Boston, MA, USA
Amy Roberts
Department of Clinical Genetics, Amsterdam University Medical Center, Amsterdam, The Netherlands
Elisabeth M. Lodder & Alex V. Postma
Manchester University NHS Foundation Trust, Manchester Academic Health Science Centre, Manchester, UK
Bernard D. Keavney
The Hospital for Sick Children, Toronto, ON, Canada
Seema Mital
University of Toronto, Toronto, ON, Canada
Seema Mital
DZHK (German Centre for Cardiovascular Research) Partner Site, Kiel, Germany
Marc-Philip Hitz
Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, Cambridge, UK
Marc-Philip Hitz
Universitätsklinikum Schleswig-Holstein Kiel, Kiel, Germany
Marc-Phillip Hitz
Universitätsklinikum des Saarlandes, Homburg, Germany
Hashim Abdul-Khaliq
Deutsches Herzzentrum Berlin, Berlin, Germany
Felix Berger
Herzzentrum Leipzig, Leipzig, Germany
Ingo Dähnert
Friedrich-Alexander-Universität Erlangen-Nürnberg, Erlangen, Germany
Sven Dittrich
Universitätsklinikum Schleswig-Holstein, Kiel, Germany
Anselm Uebing
Universitäts-Herzzentrum Freiburg Bad Krozingen, Freiburg, Germany
Brigitte Stiller

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Doris Škorić-Milosavljević
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Najim Lahrouchi
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Fernanda M. Bosada
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Gregor Dombrowsky
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Simon G. Williams
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Robert Lesurf
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Roddy Walsh
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Ihssane El Bouchikhi
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Jeroen Breckpot
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Enrique Audain
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Aho Ilgun
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Samir Atmani
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Paul Kruszka
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Amy Roberts
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Bernard D. Keavney
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Sally-Ann B. Clur
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Seema Mital
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Vincent M. Christoffels
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Alex V. Postma
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Connie R. Bezzina
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Consortia

German Competence Network for Congenital Heart Defects

Marc-Phillip Hitz
, Hashim Abdul-Khaliq
, Felix Berger
, Ingo Dähnert
, Sven Dittrich
, Anselm Uebing
& Brigitte Stiller

Corresponding authors

Correspondence to Alex V. Postma or Connie R. Bezzina.

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Škorić-Milosavljević, D., Lahrouchi, N., Bosada, F.M. et al. Correction to: Rare variants in KDR, encoding VEGF Receptor 2, are associated with tetralogy of Fallot. Genet Med 23, 2013 (2021). https://doi.org/10.1038/s41436-021-01279-7

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Published: 14 September 2021
Issue Date: October 2021
DOI: https://doi.org/10.1038/s41436-021-01279-7

Correction to: Rare variants in KDR, encoding VEGF Receptor 2, are associated with tetralogy of Fallot

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