Filomeen Haerynck

Primary Immunodeficiency Research Lab, Center for Primary Immunodeficiency Ghent, Jeffrey Modell Diagnosis and Research Center, Ghent University Hospital, Ghent, Belgium; Department of Pediatrics, Division of Pediatric Pulmonology, Infectious Diseases and Immunology, Ghent University Hospital, Ghent, Belgium. Electronic address:

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August 2020

Correction: Dominant-negative mutations in human IL6ST underlie hyper-IgE syndrome.

Authors:

Vivien Béziat Simon J Tavernier Yin-Huai Chen Cindy S Ma Marie Materna Arian Laurence Jens Staal Dominik Aschenbrenner Lisa Roels Lisa Worley Kathleen Claes Lisa Gartner Lisa A Kohn Marieke De Bruyne Klaus Schmitz-Abe Louis-Marie Charbonnier Sevgi Keles Justine Nammour Natasha Vladikine Majistor Raj Luxman Maglorius Renkilaraj Yoann Seeleuthner Mélanie Migaud Jérémie Rosain Mohamed Jeljeli Bertrand Boisson Eva Van Braeckel Jill A Rosenfeld Hongzheng Dai Lindsay C Burrage David R Murdock Bart N Lambrecht Véronique Avettand-Fenoel Tiphanie P Vogel Undiagnosed Diseases Network Charles R Esther Sule Haskologlu Figen Dogu Peter Ciznar David Boutboul Marie Ouachée-Chardin Jean Amourette Marie-Noëlle Lebras Clément Gauvain Colas Tcherakian Aydan Ikinciogullari Rudi Beyaert Laurent Abel Joshua D Milner Bodo Grimbacher Louis-Jean Couderc Manish J Butte Alexandra F Freeman Émilie Catherinot Claire Fieschi Talal A Chatila Stuart G Tangye Holm H Uhlig Filomeen Haerynck Jean-Laurent Casanova Anne Puel

J Exp Med 2020 Jun;217(7)

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June 2020

Blood-based test for diagnosis and functional subtyping of familial Mediterranean fever.

Ann Rheum Dis 2020 07 20;79(7):960-968. Epub 2020 Apr 20.

VIB Center for Inflammation Research, Zwijnaarde, Belgium

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July 2020

EuroFlow Standardized Approach to Diagnostic Immunopheneotyping of Severe PID in Newborns and Young Children.

Front Immunol 2020 19;11:371. Epub 2020 Mar 19.

Laboratory for Immunology, Department of Pediatrics, Leiden University Medical Center (LUMC), Leiden, Netherlands.

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March 2020

Dominant-negative mutations in human IL6ST underlie hyper-IgE syndrome.

Authors:

Vivien Béziat Simon J Tavernier Yin-Huai Chen Cindy S Ma Marie Materna Arian Laurence Jens Staal Dominik Aschenbrenner Lisa Roels Lisa Worley Kathleen Claes Lisa Gartner Lisa A Kohn Marieke De Bruyne Klaus Schmitz-Abe Louis-Marie Charbonnier Sevgi Keles Justine Nammour Natasha Vladikine Majistor Raj Luxman Maglorius Renkilaraj Yoann Seeleuthner Mélanie Migaud Jérémie Rosain Mohamed Jeljeli Bertrand Boisson Eva Van Braeckel Jill A Rosenfeld Hongzheng Dai Lindsay C Burrage David R Murdock Bart N Lambrecht Véronique Avettand-Fenoel Tiphanie P Vogel Charles R Esther Sule Haskologlu Figen Dogu Peter Ciznar David Boutboul Marie Ouachée-Chardin Jean Amourette Marie-Noëlle Lebras Clément Gauvain Colas Tcherakian Aydan Ikinciogullari Rudi Beyaert Laurent Abel Joshua D Milner Bodo Grimbacher Louis-Jean Couderc Manish J Butte Alexandra F Freeman Émilie Catherinot Claire Fieschi Talal A Chatila Stuart G Tangye Holm H Uhlig Filomeen Haerynck Jean-Laurent Casanova Anne Puel

J Exp Med 2020 Jun;217(6)

Laboratory of Human Genetics of Infectious Diseases, Necker Branch, Institut National de la Santé et de la Recherche Médicale (INSERM) U1163, Paris, France.

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June 2020

Long-term outcome of LRBA deficiency in 76 patients after various treatment modalities as evaluated by the immune deficiency and dysregulation activity (IDDA) score.

Authors:

Victoria Katharina Tesch Hassan Abolhassani Bella Shadur Joachim Zobel Yuliya Mareika Svetlana Sharapova Elif Karakoc-Aydiner Jacques G Rivière Marina Garcia-Prat Nicolette Moes Filomeen Haerynck Luis I Gonzales-Granado Juan Luis Santos Pérez Anna Mukhina Anna Shcherbina Asghar Aghamohammadi Lennart Hammarström Figen Dogu Sule Haskologlu Aydan I İkincioğulları Sevgi Köstel Bal Safa Baris Sara Sebnem Kilic Neslihan Edeer Karaca Necil Kutukculer Hermann Girschick Antonios Kolios Sevgi Keles Vedat Uygun Polina Stepensky Austen Worth Joris M van Montfrans Anke M J Peters Isabelle Meyts Mehdi Adeli Antonio Marzollo Nurcicek Padem Amer M Khojah Zahra Chavoshzadeh Magdalena Avbelj Stefanija Shahrzad Bakhtiar Benoit Florkin Marie Meeths Laura Gamez Bodo Grimbacher Mikko R J Seppänen Arjan Lankester Andrew R Gennery Markus G Seidel

J Allergy Clin Immunol 2020 May 27;145(5):1452-1463. Epub 2019 Dec 27.

Research Unit for Pediatric Hematology and Immunology, Medical University Graz, Graz, Austria; Division of Pediatric Hemato-Oncology, Department of Pediatrics and Adolescent Medicine, Medical University Graz, Graz, Austria. Electronic address:

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May 2020

GATA2 deficiency and haematopoietic stem cell transplantation: challenges for the clinical practitioner.

Authors:

Delfien J Bogaert Genevieve Laureys Leslie Naesens Dominiek Mazure Marieke De Bruyne Amy P Hsu Victoria Bordon Erik Wouters Simon J Tavernier Bart N Lambrecht Elfride De Baere Filomeen Haerynck Tessa Kerre

Br J Haematol 2020 03 11;188(5):768-773. Epub 2019 Nov 11.

Primary Immunodeficiency Research Lab, Center for Primary Immunodeficiency Ghent, Jeffrey Modell Diagnosis and Research Center, Ghent University Hospital, Ghent, Belgium.

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March 2020

A Computational Pipeline for the Diagnosis of CVID Patients.

Authors:

Annelies Emmaneel Delfien J Bogaert Sofie Van Gassen Simon J Tavernier Melissa Dullaers Filomeen Haerynck Yvan Saeys

Front Immunol 2019 30;10:2009. Epub 2019 Aug 30.

Department of Applied Mathematics, Computer Science and Statistics, Ghent University, Ghent, Belgium.

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September 2020

Homozygous gain-of-function mutation in siblings with a syndromic form of recurrent respiratory papillomatosis.

Proc Natl Acad Sci U S A 2019 09 4;116(38):19055-19063. Epub 2019 Sep 4.

St. Giles Laboratory of Human Genetics of Infectious Diseases, Rockefeller Branch, The Rockefeller University, New York, NY, 10065;

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September 2019

X-linked agammaglobulinemia (XLA):Phenotype, diagnosis, and therapeutic challenges around the world.

Authors:

Zeinab A El-Sayed Irina Abramova Juan Carlos Aldave Waleed Al-Herz Liliana Bezrodnik Rachida Boukari Ahmed Aziz Bousfiha Caterina Cancrini Antonio Condino-Neto Ghassan Dbaibo Beata Derfalvi Figen Dogu J David M Edgar Brian Eley Rasha Hasan El-Owaidy Sara Elva Espinosa-Padilla Nermeen Galal Filomeen Haerynck Rima Hanna-Wakim Elham Hossny Aydan Ikinciogullari Ebtihal Kamal Hirokazu Kanegane Nadia Kechout Yu Lung Lau Tomohiro Morio Viviana Moschese Joao Farela Neves Monia Ouederni Roberto Paganelli Kenneth Paris Claudio Pignata Alessandro Plebani Farah Naz Qamar Sonia Qureshi Nita Radhakrishnan Nima Rezaei Nelson Rosario John Routes Berta Sanchez Anna Sediva Mikko Rj Seppanen Edith Gonzalez Serrano Anna Shcherbina Surjit Singh Sangeetha Siniah Guiseppe Spadaro Mimi Tang Ana Maria Vinet Alla Volokha Kathleen E Sullivan

World Allergy Organ J 2019 22;12(3):100018. Epub 2019 Mar 22.

Division of Allergy Immunology, Department of Pediatrics, The Children's Hospital of Philadelphia, Philadelphia, PA, USA.

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March 2019

Defects in memory B-cell and plasma cell subsets expressing different immunoglobulin-subclasses in patients with CVID and immunoglobulin subclass deficiencies.

J Allergy Clin Immunol 2019 09 28;144(3):809-824. Epub 2019 Feb 28.

Department of Medicine, Cancer Research Centre (IBMCC, USAL-CSIC), Cytometry Service (NUCLEUS), University of Salamanca (USAL), Institute of Biomedical Research of Salamanca (IBSAL), Salamanca, Spain; Biomedical Research Networking Centre Consortium of Oncology (CIBERONC), number CB16/12/00400, Instituto de Salud Carlos III, Madrid, Spain. Electronic address:

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September 2019

Genes at the Crossroad of Primary Immunodeficiencies and Cancer.

Authors:

Charlotte Derpoorter Victoria Bordon Geneviève Laureys Filomeen Haerynck Tim Lammens

Front Immunol 2018 1;9:2544. Epub 2018 Nov 1.

Pediatric Hematology-Oncology and Stem Cell Transplantation, Ghent University Hospital, Ghent, Belgium.

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September 2019

A Founder Mutation Disrupts NF-κB Signaling by Inhibiting BCL10 and MALT1 Recruitment and Signalosome Formation.

Front Immunol 2018 31;9:2366. Epub 2018 Oct 31.

Primary Immunodeficiency Research Lab, Department of Pulmonary Medicine, Centre for Primary Immunodeficiencies, Jeffrey Modell Diagnosis and Research Centre, Ghent University Hospital, Ghent, Belgium.

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October 2019

A novel LPS-responsive beige-like anchor protein (LRBA) mutation presents with normal cytotoxic T lymphocyte-associated protein 4 (CTLA-4) and overactive T17 immunity.

Authors:

Marieke De Bruyne Delfien J Bogaert Koen Venken Lien Van den Bossche Carolien Bonroy Lisa Roels Simon J Tavernier Els van de Vijver Ann Driessen Marielle van Gijn Laura Gámez-Diaz Dirk Elewaut Bodo Grimbacher Filomeen Haerynck Nicolette Moes Melissa Dullaers

J Allergy Clin Immunol 2018 12 5;142(6):1968-1971. Epub 2018 Sep 5.

Clinical Immunology Research Lab, Department of Pulmonary Medicine, Ghent University Hospital, Ghent, Belgium; Center for Primary Immunodeficiency, Jeffrey Modell Diagnosis and Research Centre, Ghent University Hospital, Ghent, Belgium; Laboratory of Immunoregulation, VIB-UGent Inflammation Research Center, Ghent, Belgium; Department of Internal Medicine, Ghent University, Ghent, Belgium.

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December 2018

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