Daphne Huigh
Overview
Explore the profile of Daphne Huigh including associated specialties, affiliations and a list of published articles.
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Articles
5
Citations
30
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0
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Recent Articles
1.
Kuiper R, Wright V, Habgood-Coote D, Shimizu C, Huigh D, Tremoulet A, et al.
Pediatr Res
. 2022 Jun;
93(3):559-569.
PMID: 35732822
Background: Kawasaki disease (KD) is a systemic vasculitis that mainly affects children under 5 years of age. Up to 30% of patients develop coronary artery abnormalities, which are reduced with...
2.
van Beers E, Huigh D, Bosman L, de Best L, Kuiper R, Spaan M, et al.
J Mol Diagn
. 2020 Nov;
23(1):120-129.
PMID: 33152501
Multiple myeloma (MM) is an incurable plasma cell cancer with a large variability in survival. Patients with MM classified as high risk by the SKY92 gene expression classifier are at...
3.
Ten Kate C, Brouwer R, van Bever Y, Martens V, Brands T, van Beelen N, et al.
Birth Defects Res
. 2020 Apr;
112(9):670-687.
PMID: 32298054
Background: Patients born with esophageal atresia (EA) have a higher incidence of infantile hypertrophic pyloric stenosis (IHPS), suggestive of a relationship. A shared etiology makes sense from a developmental perspective...
4.
Verkerk A, Zeidler S, Breedveld G, Overbeek L, Huigh D, Koster L, et al.
Eur J Hum Genet
. 2018 Jan;
26(4):552-560.
PMID: 29374277
Intellectual disability (ID) comprises a large group of heterogeneous disorders, often without a known molecular cause. X-linked ID accounts for 5-10% of male ID cases. We investigated a large, three-generation...
5.
Florisson J, Verkerk A, Huigh D, Hoogeboom A, Swagemakers S, Kremer A, et al.
Am J Med Genet A
. 2013 Aug;
161A(10):2626-33.
PMID: 23949913
We describe a family that segregated an autosomal dominant form of craniosynostosis characterized by variable expression and limited extra-cranial features. Linkage analysis and genome sequencing were performed to identify the...