Works by Veldhuisen, Barbera

Results: 22

Genes homologous to the autosomal dominant polycystic kidney disease genes (PKD1 and PKD2).

Published in:

European Journal of Human Genetics, 1999, v. 7, n. 8, p. 860, doi. 10.1038/sj.ejhg.5200383

By:

Veldhuisen, Barbera;
Spruit, Lia;
Dauwerse, Hans G;
Breuning, Martijn H;
Peters, Dorien JM

Publication type:

Article

Age and Latent Cytomegalovirus Infection Do Not Affect the Magnitude of De Novo SARS‐CoV‐2‐Specific CD8<sup>+</sup> T Cell Responses.

Published in:

European Journal of Immunology, 2025, v. 55, n. 3, p. 1, doi. 10.1002/eji.202451565

By:

van den Dijssel, Jet;
Konijn, Veronique A. L.;
Duurland, Mariël C;
de Jongh, Rivka;
Koets, Lianne;
Veldhuisen, Barbera;
Raaphorst, Hilde;
Turksma, Annelies W.;
Freen‐van Heeren, Julian J.;
Steenhuis, Maurice;
Rispens, Theo;
van der Schoot, C Ellen;
van Ham, S. Marieke;
van Lier, Rene A. W.;
van Gisbergen, Klaas P. J. M.;
ten Brinke, Anja;
van de Sandt, Carolien E.

Publication type:

Article

Performance evaluation study of ID CORE XT, a high throughput blood group genotyping platform.

Published in:

Blood Transfusion (17232007), 2018, v. 16, n. 2, p. 193, doi. 10.2450/2016.0146-16

By:

López, Mónica;
Apraiz, Izaskun;
Rubia, Montserrat;
Piedrabuena, Mercedes;
Azkarate, Maria;
Veldhuisen, Barbera;
Vesga, Miguel Á.;
van Der Schoot, Ellen;
Puente, Fernando;
Tejedor, Diego

Publication type:

Article

Will Genotyping Replace Serology in Future Routine Blood Grouping? – Opinion 5.

Published in:

Transfusion Medicine & Hemotherapy, 2009, v. 36, n. 3, p. 234, doi. 10.1159/000214840

By:

Ellen van der Schoot;
Barbera Veldhuisen;
Masja De Haas

Publication type:

Article

Location of mutations within the PKD2 gene influences clinical outcome.

Published in:

Kidney International, 2000, v. 57, n. 4, p. 1444, doi. 10.1046/j.1523-1755.2000.00989.x

By:

Hateboer, Nick;
Veldhuisen, Barbera;
Peters, Dorien;
Breuning, Martijn H.;
San-Millán, José L.;
Bogdanova, Nadja;
Coto, Eliecer;
Dijk, Marjan A.V.;
Afzal, Ali R.;
Jeffery, Steve;
Saggar-Malik, Anand K.;
Torra, Roser;
Dimitrakov, Dimitar;
Martinez, Isabel;
De Castro, Saturnino Sanz;
Krawczak, Michael;
Ravine, David

Publication type:

Article

Identification of a novel single-nucleotide mutation in SMIM1 gene that results in low Vel antigen expression.

Published in:

2019

By:

Rijst, Marea V.E.;
Voorn, Lesley;
Veldhuisen, Barbera;
Jongerius, John M.;
Akker, Emile;
Schoot, C. Ellen;
van der Rijst, Marea V E;
van den Akker, Emile;
van der Schoot, C Ellen

Publication type:

journal article

Frequency and characterization of RHD variants in serologically D- Surinamese pregnant women and D- newborns.

Published in:

2019

By:

Zonneveld, Rens;
Kanhai, Humphrey H.H.;
Javadi, Ahmad;
Veldhuisen, Barbera;
Brand, Anneke;
Zijlmans, Wilco C.W.R.;
Schoot, C. Ellen;
Schonewille, Henk;
van der Schoot, C Ellen;
Rhesus in Surinamese Neonates (RheSuN) Study Group

Publication type:

journal article

Development of a recombinant anti-Vel immunoglobulin M to identify Vel-negative donors.

Published in:

2019

By:

van der Rijst, Marea V.E.;
Lissenberg‐Thunnissen, Suzanne N.;
Ligthart, Peter C.;
Visser, Remco;
Jongerius, John M.;
Voorn, Lesley;
Veldhuisen, Barbera;
Vidarsson, Gestur;
van den Akker, Emile;
van der Schoot, C. Ellen;
Lissenberg-Thunnissen, Suzanne N

Publication type:

journal article

Validation of the multiplex ligation-dependent probe amplification assay and its application on the distribution study of the major alleles of 17 blood group systems in Chinese donors from Guangzhou.

Published in:

2017

By:

Ji, Yanli;
Wen, Jizhi;
Veldhuisen, Barbera;
Haer‐Wigman, Lonneke;
Wang, Zhen;
Lodén‐van Straaten, Martin;
Wei, Ling;
Luo, Guangping;
Fu, Yongshui;
van der Schoot, C. Ellen

Publication type:

journal article

Identification of a novel frequent RHCE*ce308T variant allele in Chinese D- individuals, resulting in a C+c- phenotype.

Published in:

2016

By:

Stegmann, Tamara C.;
Ji, Yanli;
Bijman, Renate;
Wang, Zhen;
Wen, Jizhi;
Wei, Ling;
Veldhuisen, Barbera;
Haer‐Wigman, Lonneke;
Lighthart, Peter;
Lodén‐van Straaten, Martin;
Luo, Guangping;
van der Schoot, C. Ellen

Publication type:

journal article

Fetal RHD genotyping after bone marrow transplantation.

Published in:

2016

By:

Thurik, Florentine F.;
Page‐Christiaens, Godelieve C.M.L.;
Ait Soussan, Aicha;
Ligthart, Peter C.;
Cheroutre, Goedele M.A.F.;
Bossers, Bernadette;
Veldhuisen, Barbera;
van der Schoot, C. Ellen;
de Haas, Masja

Publication type:

Case Study

Novel alleles at the Kell blood group locus that lead to Kell variant phenotype in the Dutch population.

Published in:

Transfusion, 2015, v. 55, n. 2, p. 413, doi. 10.1111/trf.12838

By:

Ji, Yanli;
Veldhuisen, Barbera;
Ligthart, Peter;
Haer‐Wigman, Lonneke;
Jongerius, John;
Boujnan, Mohamed;
Ait Soussan, Aicha;
Luo, Guangping;
Fu, Yongshui;
Schoot, C. Ellen;
Haas, Masja

Publication type:

Article

Noninvasive prenatal blood group and HPA-1a genotyping: the current European experience.

Published in:

Transfusion, 2013, v. 53, n. 11pt2, p. 2834, doi. 10.1111/trf.12411

By:

Schoot, C. Ellen;
Thurik, Florentine F.;
Veldhuisen, Barbera;
Haas, Masja

Publication type:

Article

Comprehensive genotyping for 18 blood group systems using a multiplex ligation-dependent probe amplification assay shows a high degree of accuracy.

Published in:

Transfusion, 2013, v. 53, n. 11pt2, p. 2899, doi. 10.1111/trf.12410

By:

Haer‐Wigman, Lonneke;
Ji, Yanli;
Lodén, Martin;
Haas, Masja;
Schoot, C. Ellen;
Veldhuisen, Barbera

Publication type:

Article

RHD and RHCE variant and zygosity genotyping via multiplex ligation-dependent probe amplification.

Published in:

Transfusion, 2013, v. 53, n. 7, p. 1559, doi. 10.1111/j.1537-2995.2012.03919.x

By:

Haer‐Wigman, Lonneke;
Veldhuisen, Barbera;
Jonkers, Remco;
Lodén, Martin;
Madgett, Tracey E.;
Avent, Neil D.;
Haas, Masja;
Schoot, C. Ellen

Publication type:

Article

Molecular analysis of the York antigen of the Knops blood group system.

Published in:

Transfusion, 2011, v. 51, n. 7, p. 1389, doi. 10.1111/j.1537-2995.2010.02999.x

By:

Veldhuisen, Barbera;
Ligthart, Peter C.;
Vidarsson, Gestur;
Roels, Ingrid;
Folman, Claudia C.;
van der Schoot, C. Ellen;
de Haas, Masja

Publication type:

Article

Performance evaluation study of ID RHD XT, a new genotyping assay for the detection of high‐prevalence RhD negative and weak D types.

Published in:

Vox Sanguinis, 2018, v. 113, n. 7, p. 694, doi. 10.1111/vox.12701

By:

Molano, Araitz;
Apraiz, Izaskun;
España, Patricia;
Azkarate, Maria;
Vesga, Miguel Ángel;
Rubia, Montserrat;
Piedrabuena, Mercedes;
Puente, Fernando;
Veldhuisen, Barbera;
Schoot, Ellen;
Tejedor, Diego;
López, Mónica

Publication type:

Article

Rh‐null phenotype and stomatocytosis.

Published in:

British Journal of Haematology, 2021, v. 194, n. 5, p. 803, doi. 10.1111/bjh.17486

By:

Göttgens, Eva‐Leonne;
Ligthart, Peter C.;
Veldhuisen, Barbera;
Veldthuis, Martijn;
de Haas, Masja;
van Gammeren, Adriaan J.

Publication type:

Article

Frequency and characterization of known and novel RHD variant alleles in 37 782 Dutch D-negative pregnant women.

Published in:

British Journal of Haematology, 2016, v. 173, n. 3, p. 469, doi. 10.1111/bjh.13960

By:

Stegmann, Tamara C.;
Veldhuisen, Barbera;
Bijman, Renate;
Thurik, Florentine F.;
Bossers, Bernadette;
Cheroutre, Goedele;
Jonkers, Remco;
Ligthart, Peter;
Haas, Masja;
Haer‐Wigman, Lonneke;
Schoot, C. Ellen

Publication type:

Article

PIGG defines the Emm blood group system.

Published in:

Scientific Reports, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41598-021-98090-w

By:

Lane, William J.;
Aeschlimann, Judith;
Vege, Sunitha;
Lomas-Francis, Christine;
Burgos, Anna;
Mah, Helen H.;
Halls, Justin B. L.;
Baeck, Peter;
Ligthart, Peter C.;
Veldhuisen, Barbera;
Shah, Ripal J.;
Joshi, Sanmukh R.;
Westhoff, Connie M.

Publication type:

Article

Novel variants in Krueppel like factor 1 that cause persistence of fetal hemoglobin in In(Lu) individuals.

Published in:

Scientific Reports, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41598-021-97149-y

By:

Eernstman, Jesse;
Veldhuisen, Barbera;
Ligthart, Peter;
von Lindern, Marieke;
van der Schoot, C. Ellen;
van den Akker, Emile

Publication type:

Article

Prevalence of RhD status and clinical application of non-invasive prenatal determination of fetal RHD in maternal plasma: a 5 year experience in Cyprus.

Published in:

BMC Research Notes, 2016, v. 9, p. 1, doi. 10.1186/s13104-016-2002-x

By:

Papasavva, Thessalia;
Martin, Pete;
Legler, Tobias J.;
Liasides, Marios;
Anastasiou, George;
Christofides, Agathoklis;
Christodoulou, Tasos;
Demetriou, Sotos;
Kerimis, Prokopis;
Kontos, Charis;
Leontiades, George;
Papapetrou, Demetris;
Patroclos, Telis;
Phylaktou, Marios;
Zottis, Nikos;
Karitzie, Eleni;
Pavlou, Eleni;
Kountouris, Petros;
Veldhuisen, Barbera;
van der Schoot, Ellen

Publication type:

Article