Publications by authors named "Iris H I M Hollink"

20Publications

Parents' Perspectives and Societal Acceptance of Implementation of Newborn Screening for SCID in the Netherlands.

Authors:
Maartje Blom Robbert G M Bredius Marleen E Jansen Gert Weijman Evelien A Kemper Clementien L Vermont Iris H I M Hollink Willem A Dik Joris M van Montfrans Mariëlle E van Gijn Stefanie S Henriet Koen J van Aerde Wouter Koole Arjan C Lankester Eugènie H B M Dekkers Peter C J I Schielen Martine C de Vries Lidewij Henneman Mirjam van der Burg

J Clin Immunol 2020 Oct 18. Epub 2020 Oct 18.

Department of Pediatrics, Laboratory for Pediatric Immunology, Willem-Alexander Children's Hospital, Leiden University Medical Center, Albinusdreef 2, 2333 ZA, Leiden, The Netherlands.

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October 2020

National external quality assessment for next-generation sequencing-based diagnostics of primary immunodeficiencies.

Authors:
Kim Elsink Manon M H Huibers Iris H I M Hollink Lars T van der Veken Robert F Ernst Annet Simons Evelien Zonneveld-Huijssoon Annemieke H van der Hout Kristin M Abbott Alexander Hoischen Marc Pieterse Taco W Kuijpers Joris M van Montfrans Mariëlle E van Gijn

Eur J Hum Genet 2021 Jan 30;29(1):20-28. Epub 2020 Jul 30.

Department of Genetics, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.

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January 2021

TRIDENT-2: National Implementation of Genome-wide Non-invasive Prenatal Testing as a First-Tier Screening Test in the Netherlands.

Authors:
Karuna R M van der Meij Erik A Sistermans Merryn V E Macville Servi J C Stevens Caroline J Bax Mireille N Bekker Caterina M Bilardo Elles M J Boon Marjan Boter Karin E M Diderich Christine E M de Die-Smulders Leonie K Duin Brigitte H W Faas Ilse Feenstra Monique C Haak Mariëtte J V Hoffer Nicolette S den Hollander Iris H I M Hollink Fernanda S Jehee Maarten F C M Knapen Angelique J A Kooper Irene M van Langen Klaske D Lichtenbelt Ingeborg H Linskens Merel C van Maarle Dick Oepkes Mijntje J Pieters G Heleen Schuring-Blom Esther Sikkel Birgit Sikkema-Raddatz Dominique F C M Smeets Malgorzata I Srebniak Ron F Suijkerbuijk Gita M Tan-Sindhunata A Jeanine E M van der Ven Shama L van Zelderen-Bhola Lidewij Henneman Robert-Jan H Galjaard Diane Van Opstal Marjan M Weiss

Am J Hum Genet 2019 12 7;105(6):1091-1101. Epub 2019 Nov 7.

Department of Clinical Genetics, Amsterdam UMC, Vrije Universiteit Amsterdam, 1081HV Amsterdam, the Netherlands.

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December 2019

ALPK1 missense pathogenic variant in five families leads to ROSAH syndrome, an ocular multisystem autosomal dominant disorder.

Authors:
Lloyd B Williams Asif Javed Amin Sabri Denise J Morgan Chad D Huff John R Grigg Xiu Ting Heng Alexis J Khng Iris H I M Hollink Margaux A Morrison Leah A Owen Katherine Anderson Krista Kinard Rebecca Greenlees Danica Novacic H Nida Sen Wadih M Zein George M Rodgers Albert T Vitale Neena B Haider Axel M Hillmer Pauline C Ng Shankaracharya Anson Cheng Linda Zheng Mark C Gillies Marjon van Slegtenhorst P Martin van Hagen Tom O A R Missotten Gary L Farley Michael Polo James Malatack Julie Curtin Frank Martin Susan Arbuckle Stephen I Alexander Megan Chircop Sonia Davila Kathleen B Digre Robyn V Jamieson Margaret M DeAngelis

Genet Med 2019 09 10;21(9):2103-2115. Epub 2019 Apr 10.

Department of Ophthalmology and Visual Sciences, John A Moran Eye Center, University of Utah School of Medicine, Salt Lake City, UT, USA.

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September 2019

Two novel cases expanding the phenotype of SETD2-related overgrowth syndrome.

Authors:
Maartje C van Rij Iris H I M Hollink Paulien Anna Terhal Sarina G Kant Claudia Ruivenkamp Arie van Haeringen J Anneke Kievit Martine J van Belzen

Am J Med Genet A 2018 05;176(5):1212-1215

Department of Clinical Genetics, Leiden University Medical Centre, Leiden, The Netherlands.

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May 2018

Correction: Broadening the phenotypic spectrum of pathogenic LARP7 variants: two cases with intellectual disability, variable growth retardation and distinct facial features.

Authors:
Iris H I M Hollink Majid Alfadhel Anwar S Al-Wakeel Farough Ababneh Rolph Pfundt Stella A de Man Rami Abou Jamra Arndt Rolfs Aida M Bertoli-Avella Ingrid M B H van de Laar

J Hum Genet 2018 04 8;63(4):539. Epub 2018 Mar 8.

Department of Clinical Genetics, Erasmus Medical Center, Rotterdam, The Netherlands.

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April 2018

A novel tissue-based ß-catenin gene and immunohistochemical analysis to exclude familial adenomatous polyposis among children with hepatoblastoma tumors.

Authors:
Hendrikus J Dubbink Iris H I M Hollink Carolina Avenca Valente Wenhui Wang Pengyu Liu Michail Doukas Max M van Noesel Winand N M Dinjens Anja Wagner Ron Smits

Pediatr Blood Cancer 2018 06 15;65(6):e26991. Epub 2018 Feb 15.

Gastroenterology and Hepatology, Erasmus MC Cancer Institute, University Medical Center, Rotterdam, The Netherlands.

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June 2018

Acute myeloid leukaemia in a case with Tatton-Brown-Rahman syndrome: the peculiar R882 mutation.

Authors:
Iris H I M Hollink Ans M W van den Ouweland H Berna Beverloo Susan T C J M Arentsen-Peters C Michel Zwaan Anja Wagner

J Med Genet 2017 12 21;54(12):805-808. Epub 2017 Apr 21.

Department of Clinical Genetics, Erasmus Medical Center, Rotterdam, The Netherlands.

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December 2017

Broadening the phenotypic spectrum of pathogenic LARP7 variants: two cases with intellectual disability, variable growth retardation and distinct facial features.

Authors:
Iris H I M Hollink Majid Alfadhel Anwar S Al-Wakeel Farough Ababneh Rolph Pfundt Stella A de Man Rami Abou Jamra Arndt Rolfs Aida M Bertoli-Avella Ingrid M B H van de Laar

J Hum Genet 2016 Mar 26;61(3):229-33. Epub 2015 Nov 26.

Department of Clinical Genetics, Erasmus Medical Center, Rotterdam, The Netherlands.

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March 2016

High GATA2 expression is a poor prognostic marker in pediatric acute myeloid leukemia.

Authors:
Maaike Luesink Iris H I M Hollink Vincent H J van der Velden Ruth H J N Knops Jan B M Boezeman Valérie de Haas Jan Trka Andre Baruchel Dirk Reinhardt Bert A van der Reijden Marry M van den Heuvel-Eibrink C Michel Zwaan Joop H Jansen

Blood 2012 Sep 11;120(10):2064-75. Epub 2012 Jul 11.

Department of Laboratory Medicine, Laboratory of Hematology, Radboud University Nijmegen Medical Centre and Nijmegen Centre for Molecular Life Sciences, Nijmegen, The Netherlands.

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September 2012

High frequency of copy number alterations in myeloid leukaemia of Down syndrome.

Authors:
Marjolein Blink Marry M van den Heuvel-Eibrink Anna M Aalbers Brian V Balgobind Iris H I M Hollink Jules P P Meijerink Vincent H J van der Velden Berna H Beverloo Valerie de Haas Henrik Hasle Dirk Reinhardt Jan-Henning Klusmann Rob Pieters Rodrigo T Calado Christian M Zwaan

Br J Haematol 2012 Sep 7;158(6):800-3. Epub 2012 Jul 7.

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September 2012

NUP98/NSD1 characterizes a novel poor prognostic group in acute myeloid leukemia with a distinct HOX gene expression pattern.

Authors:
Iris H I M Hollink Marry M van den Heuvel-Eibrink Susan T C J M Arentsen-Peters Marta Pratcorona Saman Abbas Jenny E Kuipers Janneke F van Galen H Berna Beverloo Edwin Sonneveld Gert-Jan J L Kaspers Jan Trka Andre Baruchel Martin Zimmermann Ursula Creutzig Dirk Reinhardt Rob Pieters Peter J M Valk C Michel Zwaan

Blood 2011 Sep 2;118(13):3645-56. Epub 2011 Aug 2.

Pediatric Oncology/Hematology, Erasmus MC-Sophia Children's Hospital, Rotterdam, The Netherlands.

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September 2011

Integrative analysis of type-I and type-II aberrations underscores the genetic heterogeneity of pediatric acute myeloid leukemia.

Authors:
Brian V Balgobind Iris H I M Hollink Susan T C J M Arentsen-Peters Martin Zimmermann Jochen Harbott H Berna Beverloo Anne R M von Bergh Jacqueline Cloos Gertjan J L Kaspers Valerie de Haas Zuzana Zemanova Jan Stary Jean-Michel Cayuela Andre Baruchel Ursula Creutzig Dirk Reinhardt Rob Pieters C Michel Zwaan Marry M van den Heuvel-Eibrink

Haematologica 2011 Oct 26;96(10):1478-87. Epub 2011 Jul 26.

Department of Pediatric Oncology/Hematology, Erasmus MC-Sophia Children's Hospital, Rotterdam, The Netherlands.

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October 2011

Characterization of CEBPA mutations and promoter hypermethylation in pediatric acute myeloid leukemia.

Authors:
Iris H I M Hollink Marry M van den Heuvel-Eibrink Susan T C J M Arentsen-Peters Martin Zimmermann Justine K Peeters Peter J M Valk Brian V Balgobind Edwin Sonneveld Gertjan J L Kaspers Eveline S J M de Bont Jan Trka Andre Baruchel Ursula Creutzig Rob Pieters Dirk Reinhardt C Michel Zwaan

Haematologica 2011 Mar 6;96(3):384-92. Epub 2010 Dec 6.

Pediatric Oncology/Hematology, Erasmus MC-Sophia Children's Hospital, Rotterdam, the Netherlands.

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March 2011

Evaluation of gene expression signatures predictive of cytogenetic and molecular subtypes of pediatric acute myeloid leukemia.

Authors:
Brian V Balgobind Marry M Van den Heuvel-Eibrink Renee X De Menezes Dirk Reinhardt Iris H I M Hollink Susan T J C M Arentsen-Peters Elisabeth R van Wering Gertjan J L Kaspers Jacqueline Cloos Evelien S J M de Bont Jean-Michel Cayuela Andre Baruchel Claus Meyer Rolf Marschalek Jan Trka Jan Stary H Berna Beverloo Rob Pieters C Michel Zwaan Monique L den Boer

Haematologica 2011 Feb 22;96(2):221-30. Epub 2010 Oct 22.

Erasmus MC-Sophia Children's Hospital, Department of Pediatric Oncology and Hematology, Room Sp2456, PO Box 2060, 3000 CB Rotterdam, Netherlands.

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February 2011

No prognostic impact of the WT1 gene single nucleotide polymorphism rs16754 in pediatric acute myeloid leukemia.

Authors:
Iris H I M Hollink Marry M van den Heuvel-Eibrink Martin Zimmermann Brian V Balgobind Susan T C J M Arentsen-Peters Marielle Alders Andre Willasch Gert-Jan J L Kaspers Jan Trka Andre Baruchel Ursula Creutzig Rob Pieters Dirk Reinhardt C Michel Zwaan

J Clin Oncol 2010 Oct 19;28(28):e523-6; author reply e527-e528. Epub 2010 Jul 19.

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October 2010

High-frequency type I/II mutational shifts between diagnosis and relapse are associated with outcome in pediatric AML: implications for personalized medicine.

Authors:
Costa Bachas Gerrit Jan Schuurhuis Iris H I M Hollink Zinia J Kwidama Bianca F Goemans C Michel Zwaan Marry M van den Heuvel-Eibrink Eveline S J M de Bont Dirk Reinhardt Ursula Creutzig Valerie de Haas Yehuda G Assaraf Gertjan J L Kaspers Jacqueline Cloos

Blood 2010 Oct 30;116(15):2752-8. Epub 2010 Jun 30.

Department of Pediatric Oncology/Hematology,VU University Medical Center, Amsterdam, The Netherlands.

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October 2010

Low frequency of MLL-partial tandem duplications in paediatric acute myeloid leukaemia using MLPA as a novel DNA screenings technique.

Authors:
Brian V Balgobind Iris H I M Hollink Dirk Reinhardt Elisabeth R van Wering Siebold S N de Graaf Andre Baruchel Jan Stary H Berna Beverloo Georgine E de Greef Rob Pieters C Michel Zwaan Marry M van den Heuvel-Eibrink

Eur J Cancer 2010 Jul 16;46(10):1892-9. Epub 2010 Mar 16.

Paediatric Oncology/Haematology, Erasmus MC/Sophia Children's Hospital, Rotterdam, The Netherlands.

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July 2010

CEBPA resembles Roman god Janus.

Authors:
Iris H I M Hollink Marry M van den Heuvel-Eibrink Christian Michel Zwaan

Blood 2009 Jun;113(26):6501-2

Erasmus MC-Sophia Children's Hospital.

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June 2009

Clinical relevance of Wilms tumor 1 gene mutations in childhood acute myeloid leukemia.

Authors:
Iris H I M Hollink Marry M van den Heuvel-Eibrink Martin Zimmermann Brian V Balgobind Susan T C J M Arentsen-Peters Marielle Alders Andre Willasch Gertjan J L Kaspers Jan Trka Andre Baruchel Siebold S N de Graaf Ursula Creutzig Rob Pieters Dirk Reinhardt C Michel Zwaan

Blood 2009 Jun 26;113(23):5951-60. Epub 2009 Jan 26.

Department of Pediatric Oncology/Hematology, Erasmus MC-Sophia Children's Hospital, Rotterdam, The Netherlands.

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June 2009