I Celine Hanson
Overview
Explore the profile of I Celine Hanson including associated specialties, affiliations and a list of published articles.
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Articles
26
Citations
1389
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0
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Recent Articles
1.
Martinez C, Aguayo-Hiraldo P, Chaimowitz N, Forbes L, Rider N, Nicholas S, et al.
Blood Adv
. 2022 Dec;
7(9):1823-1830.
PMID: 36453638
There is no consensus on the best donor for children with nonmalignant disorders and immune deficiencies in the absence of a matched related donor (MRD). We evaluated the 2-year overall...
2.
Squire J, Vazquez S, Chan A, Smith M, Chellapandian D, Vose L, et al.
Front Immunol
. 2020 Dec;
11:581475.
PMID: 33362767
Chronic granulomatous disease (CGD) is a primary immune deficiency due to defects in phagocyte respiratory burst leading to severe and life-threatening infections. Patients with CGD also suffer from disorders of...
3.
Chaimowitz N, Ebenezer S, Hanson I, Anderson M, Forbes L
N Engl J Med
. 2020 Oct;
383(15):1494-1496.
PMID: 33027576
No abstract available.
4.
Kuhny M, Forbes L, Cakan E, Vega-Loza A, Kostiuk V, Dinesh R, et al.
J Clin Invest
. 2020 Jun;
130(8):4411-4422.
PMID: 32484799
Patients with common variable immunodeficiency associated with autoimmune cytopenia (CVID+AIC) generate few isotype-switched B cells with severely decreased frequencies of somatic hypermutations (SHMs), but their underlying molecular defects remain poorly...
5.
Bucciol G, Nicholas S, Calvo P, Cant A, Edgar J, Espanol T, et al.
J Allergy Clin Immunol
. 2019 Jan;
143(5):1952-1956.e6.
PMID: 30682461
No abstract available.
6.
Ngwube A, Hanson I, Orange J, Rider N, Seeborg F, Shearer W, et al.
Biol Blood Marrow Transplant
. 2017 Dec;
24(3):537-541.
PMID: 29196075
Wiskott-Aldrich syndrome (WAS) is a rare X-linked disorder characterized by a triad of immunodeficiency, eczema, and thrombocytopenia. Currently, hematopoietic stem cell transplantation (HSCT) is the most reliable curative treatment with...
7.
Chinn I, Sanders R, Stray-Pedersen A, Coban-Akdemir Z, Kim V, Dadi H, et al.
Front Immunol
. 2017 Jun;
8:576.
PMID: 28603521
With the advent of high-throughput genomic sequencing techniques, novel genetic etiologies are being uncovered for previously unexplained Mendelian phenotypes, and the underlying genetic architecture of disease is being unraveled. Although...
8.
Stray-Pedersen A, Sorte H, Samarakoon P, Gambin T, Chinn I, Coban Akdemir Z, et al.
J Allergy Clin Immunol
. 2016 Sep;
139(1):232-245.
PMID: 27577878
Background: Primary immunodeficiency diseases (PIDDs) are clinically and genetically heterogeneous disorders thus far associated with mutations in more than 300 genes. The clinical phenotypes derived from distinct genotypes can overlap....
9.
de Ravin S, Wu X, Moir S, Anaya-OBrien S, Kwatemaa N, Littel P, et al.
Sci Transl Med
. 2016 Apr;
8(335):335ra57.
PMID: 27099176
X-linked severe combined immunodeficiency (SCID-X1) is a profound deficiency of T, B, and natural killer (NK) cell immunity caused by mutations inIL2RGencoding the common chain (γc) of several interleukin receptors....
10.
Naik S, Nicholas S, Martinez C, Leen A, Hanley P, Gottschalk S, et al.
J Allergy Clin Immunol
. 2016 Feb;
137(5):1498-1505.e1.
PMID: 26920464
Background: Viral infections are a leading fatal complication for patients with primary immunodeficiencies (PIDs) who require hematopoietic stem cell transplantation (HSCT). Use of virus-specific T lymphocytes (VSTs) has been successful...