The DOI matches its Crossref record; 70 of the 70 references it cites were found in a registry or an index.
Hydrops Fetalis Caused by α-Thalassemia: An Emerging Health Care Problem
Abstract
HYDROPS FETALIS is a serious disorder, usually indicative of an ominous prognosis for the affected fetus. There are many causes, including both hereditary and acquired diseases.[1-3][1] In southeast Asia, α-thalassemia is the most common cause of fetal hydrops, accounting for 60% to 90% of the
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Survival in Medically Treated Patients with Homozygous β-Thalassemia
Olivieri, N. F., Nathan, D. G., MacMillan, J. H., Wayne, A. S., Liu, P. P., McGee, A., Martin, M., Koren, G., & Cohen, A. R. (1994) · New England Journal of Medicine · doi:10.1056/nejm199409013310903 · Cited by 852
Brittenham, G. M., Griffith, P. M., Nienhuis, A. W., McLaren, C. E., Young, N. S., Tucker, E. E., Allen, C. J., Farrell, D. E., & Harris, J. W. (1994) · New England Journal of Medicine · doi:10.1056/nejm199409013310902 · Cited by 829
The Molecular Basis of Blood Diseases.
(1987) · Annals of Internal Medicine · doi:10.7326/0003-4819-107-6-950_3 · Cited by 632
A review of the molecular genetics of the human alpha-globin gene cluster
Higgs, D., Vickers, M., Wilkie, A., Pretorius, I., Jarman, A., & Weatherall, D. (1989) · Blood · doi:10.1182/blood.v73.5.1081.1081 · Cited by 507
A major positive regulatory region located far upstream of the human alpha-globin gene locus.
Higgs, D. R., Wood, W. G., Jarman, A. P., Sharpe, J., Lida, J., Pretorius, I. M., & Ayyub, H. (1990) · Genes & Development · doi:10.1101/gad.4.9.1588 · Cited by 336
Hemoglobinopathies in Southeast Asia
Fucharoen, S., & Winichagoon, P. (1987) · Hemoglobin · doi:10.3109/03630268709036587 · Cited by 301
Cheung, M.-C., Goldberg, J. D., & Kan, Y. W. (1996) · Nature Genetics · doi:10.1038/ng1196-264 · Cited by 251
Taylor, J. M., Dozy, A. M., Kan, Y. W., VARMUS, H. E., Lie‐Injo, L. E., Ganesan, J., & Todd, D. (1974) · Nature · doi:10.1038/251392a0 · Cited by 229
Peschle, C., Mavilio, F., Carè, A., Migliaccio, G., Migliaccio, A. R., Salvo, G., Samoggia, P., Petti, S., Guerriero, R., Marinucci, M., et al. (1985) · Nature · doi:10.1038/313235a0 · Cited by 227
α-Globin gene organisation in blacks precludes the severe form of α-thalassaemia
DOZY, A. M., KAN, Y. W., EMBURY, S. H., MENTZER, W. C., WANG, W. C., LUBIN, B., DAVIS, J. R., & KOENIG, H. M. (1979) · Nature · doi:10.1038/280605a0 · Cited by 222
Cited by
Global epidemiology of haemoglobin disorders and derived service indicators
Modell, B. (2008) · Bulletin of the World Health Organization · doi:10.2471/blt.06.036673 · Cited by 1,924
Harteveld, C. L., & Higgs, D. R. (2010) · Orphanet Journal of Rare Diseases · doi:10.1186/1750-1172-5-13 · Cited by 508
Hardison, R. C., Chui, D. H. K., Giardine, B., Riemer, C., Patrinos, G. P., Anagnou, N., Miller, W., & Wajcman, H. (2002) · Human Mutation · doi:10.1002/humu.10044 · Cited by 439
Self-citationIonizable lipid nanoparticles for in utero mRNA delivery
Riley, R. S., Kashyap, M. V., Billingsley, M. M., White, B., Alameh, M.-G., Bose, S. K., Zoltick, P. W., Li, H., Zhang, R., Cheng, A. Y., et al. (2021) · Science Advances · doi:10.1126/sciadv.aba1028 · Cited by 222
TUNGWIWAT, W., FUCHAROEN, S., FUCHAROEN, G., RATANASIRI, T., & SANCHAISURIYA, K. (2006) · Annals of the New York Academy of Sciences · doi:10.1196/annals.1368.013 · Cited by 47
Metadata
- Authors
- Chui, D. H. K., & Waye, J. S.
- Venue
- Blood
- Publisher
- American Society of Hematology
- Published
- 1998-04-01
- Volume
- 91
- Issue
- 7
- Pages
- 2213-2222
- ISSN
- 0006-4971 (ISSN-L)
- 1528-0020
- OpenAlex
- W1559307951
- Cited by
- 270
- References
- 70
- FWCI
- 7.45
- Type
- journal article
- Language
- en
- Open access
- closed
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review
How to cite
Cite CoChat for the checks on this page, and the paper for its own findings.
- This page
- CoChat. (2026). Citation check: Hydrops Fetalis Caused by α-Thalassemia: An Emerging Health Care Problem. https://app.cochat.ai/papers/10.1182/blood.v91.7.2213
- The paper
- Chui, D. H. K., & Waye, J. S. (1998). Hydrops Fetalis Caused by α-Thalassemia: An Emerging Health Care Problem. Blood. https://doi.org/10.1182/blood.v91.7.2213
Data sources
Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.