Works by Veldhuisen, Barbera

Results: 21

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
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
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
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
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
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
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
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
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
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