Noemi B A Roy
Overview
Explore the profile of Noemi B A Roy including associated specialties, affiliations and a list of published articles.
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Articles
28
Citations
678
Followers
0
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Recent Articles
1.
Scott C, Dale-Harris I, Armitage A, Preston A, Stanworth S, James T, et al.
Haematologica
. 2024 Oct;
110(3):739-743.
PMID: 39363869
No abstract available.
2.
Crocker J, Moore L, Ogden M, Crowe S, Khan M, Schoemaker C, et al.
Health Expect
. 2024 Jun;
27(3):e14096.
PMID: 38895996
Introduction: James Lind Alliance (JLA) Priority Setting Partnerships (PSPs) produce 'Top 10' lists of health and care research priorities through a structured, shared decision-making process with patients or service users,...
3.
Gok V, Leblebisatan G, Gurlek Gokcebay D, Guler S, Dogan M, Bozdogan S, et al.
Br J Haematol
. 2024 May;
205(1):236-242.
PMID: 38811201
Pyruvate kinase (PK) is a key enzyme of anaerobic glycolysis. The genetic heterogeneity of PK deficiency (PKD) is high, and over 400 unique variants have been identified. Twenty-nine patients who...
4.
Martell D, Merens H, Caulier A, Fiorini C, Ulirsch J, Ietswaart R, et al.
Dev Cell
. 2023 Aug;
58(20):2112-2127.e4.
PMID: 37586368
Controlled release of promoter-proximal paused RNA polymerase II (RNA Pol II) is crucial for gene regulation. However, studying RNA Pol II pausing is challenging, as pause-release factors are almost all...
5.
Bain B, Daniel Y, Henthorn J, De la Salle B, Hogan A, Roy N, et al.
Br J Haematol
. 2023 Jun;
201(6):1047-1065.
PMID: 37271570
Antenatal screening/testing of pregnant women should be carried out according to the guidelines of the National Health Service (NHS) Sickle Cell and Thalassaemia Screening Programme. Newborn screening and, when necessary,...
6.
Iskander D, Roy N, Payne E, Drasar E, Hennessy K, Harrington Y, et al.
Blood Rev
. 2023 Jun;
61:101097.
PMID: 37263874
Diamond-Blackfan anemia (DBA) is a rare bone marrow failure syndrome, usually caused by loss-of function variants in genes encoding ribosomal proteins. The hallmarks of DBA are anemia, congenital anomalies and...
7.
Badat M, Ejaz A, Hua P, Rice S, Zhang W, Hentges L, et al.
Nat Commun
. 2023 Apr;
14(1):2238.
PMID: 37076455
Haemoglobin E (HbE) β-thalassaemia causes approximately 50% of all severe thalassaemia worldwide; equating to around 30,000 births per year. HbE β-thalassaemia is due to a point mutation in codon 26...
8.
Roy N, Da Costa L, Russo R, Bianchi P, Manu-Pereira M, Fermo E, et al.
Hemasphere
. 2022 Jun;
6(6):e739.
PMID: 35686139
No abstract available.
9.
Roy N, Da Costa L, Russo R, Bianchi P, Manu-Pereira M, Fermo E, et al.
Br J Haematol
. 2022 Jun;
198(3):459-477.
PMID: 35661144
No abstract available.
10.
Scott C, Bartolovic K, Clark S, Waithe D, Hill Q, Okoli S, et al.
Br J Haematol
. 2022 Apr;
198(1):e10-e14.
PMID: 35417566
No abstract available.