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Servi JC Stevens
Servi JC Stevens
Clinical Laboratory Geneticist, Dept. of Clinical Genetics, Maastricht University Medical Center
Verified email at mumc.nl
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Cited by
Cited by
Year
Meta-analysis of 2,104 trios provides support for 10 new genes for intellectual disability
SH Lelieveld, MRF Reijnders, R Pfundt, HG Yntema, EJ Kamsteeg, ...
Nature neuroscience 19 (9), 1194-1196, 2016
4612016
Frequent monitoring of Epstein-Barr virus DNA load in unfractionated whole blood is essential for early detection of posttransplant lymphoproliferative disease in high-risk …
SJC Stevens, EAM Verschuuren, I Pronk, W van der Bij, MC Harmsen, ...
Blood, The Journal of the American Society of Hematology 97 (5), 1165-1171, 2001
3282001
TRIDENT-2: national implementation of genome-wide non-invasive prenatal testing as a first-tier screening test in the Netherlands
KRM van der Meij, EA Sistermans, MVE Macville, SJC Stevens, CJ Bax, ...
The American Journal of Human Genetics 105 (6), 1091-1101, 2019
2742019
Detection of clinically relevant copy-number variants by exome sequencing in a large cohort of genetic disorders
R Pfundt, M Del Rosario, LELM Vissers, MP Kwint, IM Janssen, ...
Genetics in Medicine 19 (6), 667-675, 2017
1822017
Toward standardization of Epstein-Barr virus DNA load monitoring: unfractionated whole blood as preferred clinical specimen
SJC Stevens, I Pronk, JM Middeldorp
Journal of Clinical Microbiology 39 (4), 1211-1216, 2001
1722001
Genome-wide karyomapping accurately identifies the inheritance of single-gene defects in human preimplantation embryos in vitro
SA Natesan, AJ Bladon, S Coskun, W Qubbaj, R Prates, S Munne, ...
Genetics in Medicine 16 (11), 838-845, 2014
1702014
Disruption of POGZ is associated with intellectual disability and autism spectrum disorders
HAF Stessman, MH Willemsen, M Fenckova, O Penn, A Hoischen, ...
The American Journal of Human Genetics 98 (3), 541-552, 2016
1662016
Treatment of posttransplant lymphoproliferative disease with rituximab: the remission, the relapse, and the complication
EAM Verschuuren, SJC Stevens, GW van Imhoff, JM Middeldorp, ...
Transplantation 73 (1), 100-104, 2002
1602002
Monitoring of Epstein-Barr virus DNA load in peripheral blood by quantitative competitive PCR
SJC Stevens, MBHJ Vervoort, AJC van den Brule, PL Meenhorst, ...
Journal of clinical microbiology 37 (9), 2852-2857, 1999
1511999
A phase I trial of epstein-barr virus gp350 vaccine for children with chronic kidney disease awaiting transplantation
L Rees, EJ Tizard, AJ Morgan, WD Cubitt, S Finerty, TA Oyewole-Eletu, ...
Transplantation 88 (8), 1025-1029, 2009
1472009
Noninvasive diagnosis of nasopharyngeal carcinoma: nasopharyngeal brushings reveal high Epstein‐Barr virus DNA load and carcinoma‐specific viral BARF1 mRNA
SJC Stevens, SAWM Verkuijlen, B Hariwiyanto, Harijadi, DK Paramita, ...
International journal of cancer 119 (3), 608-614, 2006
1412006
Role of Epstein-Barr virus DNA load monitoring in prevention and early detection of post-transplant lymphoproliferative disease
SJC Stevens, EAM Verschuuren, SAWM Verkuijlen, AJC Van Den Brule, ...
Leukemia & lymphoma 43 (4), 831-840, 2002
1222002
Diagnostic value of measuring Epstein-Barr virus (EBV) DNA load and carcinoma-specific viral mRNA in relation to anti-EBV immunoglobulin A (IgA) and IgG antibody levels in …
SJC Stevens, SAWM Verkuijlen, B Hariwiyanto, Harijadi, J Fachiroh, ...
Journal of clinical microbiology 43 (7), 3066-3073, 2005
1132005
High Epstein–Barr virus (EBV) DNA loads in HIV-infected patients: correlation with antiretroviral therapy and quantitative EBV serology
SJC Stevens, BSN Blank, PHM Smits, PL Meenhorst, JM Middeldorp
Aids 16 (7), 993-1001, 2002
1072002
De novo mutations in SON disrupt RNA splicing of genes essential for brain development and metabolism, causing an intellectual-disability syndrome
JH Kim, DN Shinde, MRF Reijnders, NS Hauser, RL Belmonte, GR Wilson, ...
The American Journal of Human Genetics 99 (3), 711-719, 2016
982016
Molecular fine-specificity analysis of antibody responses to human cytomegalovirus and design of novel synthetic-peptide-based serodiagnostic assays
AE Greijer, JMG van de Crommert, SJC Stevens, JM Middeldorp
Journal of clinical microbiology 37 (1), 179-188, 1999
961999
Phenotypic spectrum associated with PTCHD1 deletions and truncating mutations includes intellectual disability and autism spectrum disorder
A Chaudhry, A Noor, B Degagne, K Baker, LA Bok, AF Brady, D Chitayat, ...
Clinical genetics 88 (3), 224-233, 2015
892015
Epstein-Barr virus DNA load in nasopharyngeal brushings and whole blood in nasopharyngeal carcinoma patients before and after treatment
M Adham, AE Greijer, SAWM Verkuijlen, H Juwana, S Fleig, L Rachmadi, ...
Clinical Cancer Research 19 (8), 2175-2186, 2013
802013
MYT1L is a candidate gene for intellectual disability in patients with 2p25.3 (2pter) deletions
SJC Stevens, CMA van Ravenswaaij‐Arts, JWH Janssen, ...
American Journal of Medical Genetics Part A 155 (11), 2739-2745, 2011
752011
PURA syndrome: clinical delineation and genotype-phenotype study in 32 individuals with review of published literature
MRF Reijnders, R Janowski, M Alvi, JE Self, TJ Van Essen, M Vreeburg, ...
Journal of medical genetics 55 (2), 104-113, 2018
712018
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