{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,10]],"date-time":"2026-09-10T11:12:55Z","timestamp":1789038775953,"version":"build-2803163510"},"reference-count":33,"publisher":"Elsevier BV","license":[{"start":{"date-parts":[[2013,9,1]],"date-time":"2013-09-01T00:00:00Z","timestamp":1377993600000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"}],"funder":[{"name":"Sciences and Technology Research Project of Chongqing","award":["CSTC2011AC5200"],"award-info":[{"award-number":["CSTC2011AC5200"]}]}],"content-domain":{"domain":["elsevier.com","sciencedirect.com"],"crossmark-restriction":true},"short-container-title":["Clinica Chimica Acta"],"published-print":{"date-parts":[[2013,9]]},"DOI":"10.1016\/j.cca.2013.05.004","type":"journal-article","created":{"date-parts":[[2013,5,13]],"date-time":"2013-05-13T18:32:35Z","timestamp":1368469955000},"page":"131-135","update-policy":"https:\/\/doi.org\/10.1016\/elsevier_cm_policy","source":"Crossref","is-referenced-by-count":10,"special_numbering":"C","title":["Determination of optimal cutoff value to accurately identify glucose-6-phosphate dehydrogenase-deficient heterozygous female neonates"],"prefix":"10.1016","volume":"424","author":[{"given":"Jing-Kun","family":"Miao","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Qi-Xiong","family":"Chen","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Li-Ming","family":"Bao","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Yi","family":"Huang","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Juan","family":"Zhang","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Ke-Xing","family":"Wan","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Jing","family":"Yi","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Shi-Yi","family":"Wang","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Lin","family":"Zou","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Ting-Yu","family":"Li","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"78","reference":[{"key":"10.1016\/j.cca.2013.05.004_bb0005","doi-asserted-by":"crossref","first-page":"64","DOI":"10.1016\/S0140-6736(08)60073-2","article-title":"Glucose-6-phosphate dehydrogenase deficiency","volume":"371","author":"Cappellini","year":"2008","journal-title":"Lancet"},{"key":"10.1016\/j.cca.2013.05.004_bb0010","doi-asserted-by":"crossref","first-page":"121","DOI":"10.1053\/siny.2002.0099","article-title":"Glucose-6-phosphate dehydrogenase deficiency: a potential source of severe neonatal hyperbilirubinaemia and kernicterus","volume":"7","author":"Kaplan","year":"2002","journal-title":"Semin Neonatol"},{"key":"10.1016\/j.cca.2013.05.004_bb0015","doi-asserted-by":"crossref","first-page":"191","DOI":"10.1016\/j.jpeds.2012.02.018","article-title":"Glucose-6-phosphate dehydrogenase deficiency and borderline deficiency: association with neonatal hyperbilirubinemia","volume":"161","author":"Riskin","year":"2012","journal-title":"J Pediatr"},{"key":"10.1016\/j.cca.2013.05.004_bb0020","doi-asserted-by":"crossref","first-page":"155","DOI":"10.1053\/j.semperi.2011.02.010","article-title":"Neonatal screening for glucose-6-phosphate dehydrogenase deficiency: biochemical versus genetic technologies","volume":"35","author":"Kaplan","year":"2011","journal-title":"Semin Perinatol"},{"key":"10.1016\/j.cca.2013.05.004_bb0025","doi-asserted-by":"crossref","first-page":"255","DOI":"10.1023\/B:EJEP.0000020445.48298.3f","article-title":"Neonatal screening for glucose-6-phosphate dehydrogenase deficiency fails to detect heterozygote females","volume":"19","author":"Zaffanello","year":"2004","journal-title":"Eur J Epidemiol"},{"key":"10.1016\/j.cca.2013.05.004_bb0030","doi-asserted-by":"crossref","first-page":"1003","DOI":"10.1369\/jhc.2009.953828","article-title":"Glucose-6-phosphate dehydrogenase deficiency and malaria: cytochemical detection of heterozygous G6PD deficiency in women","volume":"57","author":"Peters","year":"2009","journal-title":"J Histochem Cytochem"},{"key":"10.1016\/j.cca.2013.05.004_bb0035","doi-asserted-by":"crossref","first-page":"46","DOI":"10.1136\/jms.7.1.46","article-title":"Glucose-6-phosphate dehydrogenase deficiency neonatal screening: preliminary evidence that a high percentage of partially deficient female neonates are missed during routine screening","volume":"7","author":"Reclos","year":"2000","journal-title":"J Med Screen"},{"key":"10.1016\/j.cca.2013.05.004_bb0040","doi-asserted-by":"crossref","first-page":"553","DOI":"10.1182\/blood.V28.4.553.553","article-title":"A series of new screening procedures for pyruvate kinase deficiency, glucose-6-phosphate dehydrogenase deficiency and glutathione reductase deficiency","volume":"28","author":"Beutler","year":"1966","journal-title":"Blood"},{"key":"10.1016\/j.cca.2013.05.004_bb0045","doi-asserted-by":"crossref","first-page":"816","DOI":"10.1182\/blood.V32.5.816.816","article-title":"Special modifications of the fluorescent screening method for glucose-6-phosphate dehydrogenase deficiency","volume":"32","author":"Beutler","year":"1968","journal-title":"Blood"},{"key":"10.1016\/j.cca.2013.05.004_bb0050","doi-asserted-by":"crossref","first-page":"561","DOI":"10.1093\/clinchem\/39.4.561","article-title":"Receiver-operating characteristic (ROC) plots: a fundamental evaluation tool in clinical medicine","volume":"39","author":"Zweig","year":"1993","journal-title":"Clin Chem"},{"key":"10.1016\/j.cca.2013.05.004_bb0055","first-page":"S140","article-title":"Using the fluorescence spot test for neonatal screening of G6PD deficiency","volume":"34","author":"Jiang","year":"2003","journal-title":"Southeast Asian J Trop Med Public Health"},{"key":"10.1016\/j.cca.2013.05.004_bb0060","doi-asserted-by":"crossref","first-page":"133","DOI":"10.1159\/000022860","article-title":"Detection of the most common G6PD gene mutations in Chinese using amplification refractory mutation system","volume":"49","author":"Du","year":"1999","journal-title":"Hum Hered"},{"key":"10.1016\/j.cca.2013.05.004_bb0065","doi-asserted-by":"crossref","first-page":"405","DOI":"10.1002\/ajh.20126","article-title":"Rapid detection of common Chinese glucose-6-phosphate dehydrogenase (G6PD) mutations by microarray-based assay","volume":"76","author":"Bang-Ce","year":"2004","journal-title":"Am J Hematol"},{"key":"10.1016\/j.cca.2013.05.004_bb0070","doi-asserted-by":"crossref","first-page":"463","DOI":"10.1007\/s00439-005-0126-5","article-title":"Structure and function of glucose-6-phosphate dehydrogenase-deficient variants in Chinese population","volume":"119","author":"Jiang","year":"2006","journal-title":"Hum Genet"},{"key":"10.1016\/j.cca.2013.05.004_bb0075","doi-asserted-by":"crossref","first-page":"465","DOI":"10.1111\/j.1365-2141.1979.tb03774.x","article-title":"International committee for standardization in haematology: recommended screening test for glucose-6-phosphate dehydrogenase (G6PD) deficiency","volume":"43","author":"Beutler","year":"1979","journal-title":"Br J Haematol"},{"key":"10.1016\/j.cca.2013.05.004_bb0080","first-page":"1321","article-title":"Incidence and complete molecular characterization of glucose-6-phosphate dehydrogenase deficiency in the Guangxi Zhuang autonomous region of southern China: description of four novel mutations","volume":"91","author":"Yan","year":"2006","journal-title":"Haematologica"},{"key":"10.1016\/j.cca.2013.05.004_bb0085","first-page":"749","article-title":"The theory of reference values Part 5. Statistical treatment of collected reference values. Determination of reference limits","volume":"21","author":"Solberg","year":"1983","journal-title":"J Clin Chem Clin Biochem"},{"key":"10.1016\/j.cca.2013.05.004_bb0090","doi-asserted-by":"crossref","first-page":"9","DOI":"10.1073\/pnas.48.1.9","article-title":"The normal human females as a mosaic of X-chromosome activity: studies using for G6PD deficiency as a marker","volume":"48","author":"Beutler","year":"1962","journal-title":"Proc Natl Acad Sci U S A"},{"key":"10.1016\/j.cca.2013.05.004_bb0095","doi-asserted-by":"crossref","first-page":"16","DOI":"10.1182\/blood-2007-04-077412","article-title":"Glucose-6-phosphate dehydrogenase deficiency: a historical perspective","volume":"111","author":"Beutler","year":"2008","journal-title":"Blood"},{"key":"10.1016\/j.cca.2013.05.004_bb0100","doi-asserted-by":"crossref","first-page":"7","DOI":"10.1016\/0092-8674(90)90231-3","article-title":"Human red cell glucose-6-phosphate dehydrogenase: all active enzyme has sequence predicted by the X chromosome-encoded cDNA","volume":"62","author":"Beutler","year":"1990","journal-title":"Cell"},{"key":"10.1016\/j.cca.2013.05.004_bb0105","doi-asserted-by":"crossref","first-page":"9","DOI":"10.1016\/0092-8674(90)90232-4","article-title":"Human red cell glucose-6-phosphate dehydrogenase is encoded only on the X chromosome","volume":"62","author":"Mason","year":"1990","journal-title":"Cell"},{"key":"10.1016\/j.cca.2013.05.004_bb0110","doi-asserted-by":"crossref","first-page":"68","DOI":"10.1542\/peds.104.1.68","article-title":"Neonatal hyperbilirubinemia in glucose-6-phosphate dehydrogenase deficient heterozygote","volume":"104","author":"Kaplan","year":"1999","journal-title":"Pediatrics"},{"key":"10.1016\/j.cca.2013.05.004_bb0115","doi-asserted-by":"crossref","first-page":"137","DOI":"10.1067\/mpd.2001.115312","article-title":"Acute haemolysis and severe neonatal hyper -bilirubinemia in glucose-6-phosphate dehydrogenase deficient heterozygote","volume":"139","author":"Kaplan","year":"2001","journal-title":"J Pediatr"},{"key":"10.1016\/j.cca.2013.05.004_bb0120","doi-asserted-by":"crossref","first-page":"S46","DOI":"10.1038\/jp.2008.216","article-title":"The need for neonatal glucose-6-phosphate dehydrogenase screening: a global perspective","volume":"29","author":"Kaplan","year":"2009","journal-title":"J Perinatol"},{"key":"10.1016\/j.cca.2013.05.004_bb0125","first-page":"405","article-title":"Semiquantitative screening test for G6PD deficiency detects severe deficiency but misses a substantial proportion of partially-deficient females","volume":"34","author":"Ainoon","year":"2003","journal-title":"Southeast Asian J Trop Med Public Health"},{"key":"10.1016\/j.cca.2013.05.004_bb0175","doi-asserted-by":"crossref","first-page":"197","DOI":"10.1016\/j.jpeds.2012.02.045","article-title":"Quantitative neonatal glucose-6-phosphate dehydrogenase screening: distribution, reference values, and classification by phenotype","volume":"161","author":"Algur","year":"2012","journal-title":"J Pediatr"},{"issue":"86","key":"10.1016\/j.cca.2013.05.004_bb0140","doi-asserted-by":"crossref","first-page":"212","DOI":"10.1016\/j.ymgme.2005.05.008","article-title":"Alternative DNA-based newborn screening for glucose-6-phosphate dehydrogenase deficiency","volume":"2005","author":"Lin","year":"2005","journal-title":"Mol Genet Metab"},{"key":"10.1016\/j.cca.2013.05.004_bb0145","doi-asserted-by":"crossref","first-page":"179","DOI":"10.1016\/j.jpeds.2012.04.001","article-title":"Screening for glucose-6-phosphate dehydrogenase deficiency in newborns \u2014 practical considerations","volume":"161","author":"Watchko","year":"2012","journal-title":"J Pediatr"},{"key":"10.1016\/j.cca.2013.05.004_bb0150","doi-asserted-by":"crossref","first-page":"27","DOI":"10.1002\/iub.137","article-title":"Glucose-6-phosphate dehydrogenase laboratory assay: how, when, and why?","volume":"61","author":"Minucci","year":"2009","journal-title":"IUBMB Life"},{"key":"10.1016\/j.cca.2013.05.004_bb0155","first-page":"62","article-title":"Comparison of detection of glucose-6-phosphate dehydrogenase deficiency using fluorescent spot test, enzyme assay and molecular method for prediction of severe neonatal hyperbilirubinaemia","volume":"50","author":"Wang","year":"2009","journal-title":"Singapore Med J"},{"key":"10.1016\/j.cca.2013.05.004_bb0160","doi-asserted-by":"crossref","first-page":"969","DOI":"10.1007\/s12098-010-0150-x","article-title":"Preliminary report on neonatal screening for congenital hypothyroidism, congenital adrenal hyperplasia and glucose-6-phosphate dehydrogenase deficiency: a Chandigarh experience","volume":"77","author":"Kaur","year":"2010","journal-title":"Indian J Pediatr"},{"key":"10.1016\/j.cca.2013.05.004_bb0165","doi-asserted-by":"crossref","first-page":"1093","DOI":"10.1182\/blood.V91.3.1093","article-title":"UGT1 promoter polymorphism accounts for increased neonatal appearance of hereditary spherocytosis","volume":"91","author":"Iolascon","year":"1998","journal-title":"Blood"},{"key":"10.1016\/j.cca.2013.05.004_bb0170","doi-asserted-by":"crossref","first-page":"148","DOI":"10.1016\/S0168-8278(01)00056-3","article-title":"Heterozygosity for a polymorphism in the promoter region of the UGT1A1 gene","volume":"35","author":"Kaplan","year":"2001","journal-title":"J Hepatol"}],"container-title":["Clinica Chimica Acta"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0009898113001988?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0009898113001988?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2020,7,26]],"date-time":"2020-07-26T17:43:53Z","timestamp":1595785433000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S0009898113001988"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2013,9]]},"references-count":33,"alternative-id":["S0009898113001988"],"URL":"https:\/\/doi.org\/10.1016\/j.cca.2013.05.004","relation":{},"ISSN":["0009-8981"],"issn-type":[{"value":"0009-8981","type":"print"}],"subject":[],"published":{"date-parts":[[2013,9]]},"assertion":[{"value":"Elsevier","name":"publisher","label":"This article is maintained by"},{"value":"Determination of optimal cutoff value to accurately identify glucose-6-phosphate dehydrogenase-deficient heterozygous female neonates","name":"articletitle","label":"Article Title"},{"value":"Clinica Chimica Acta","name":"journaltitle","label":"Journal Title"},{"value":"https:\/\/doi.org\/10.1016\/j.cca.2013.05.004","name":"articlelink","label":"CrossRef DOI link to publisher maintained version"},{"value":"article","name":"content_type","label":"Content Type"},{"value":"Copyright \u00a9 2013 Elsevier B.V. All rights reserved.","name":"copyright","label":"Copyright"}]}}