G. Fucharoen

发表

Interaction of hemoglobin Grey Lynn (Vientiane) with a non-deletional α+-thalassemia in an adult Thai proband

Kritsada Singha, G. Fucharoen, S. Fucharoen, 2014, Biochemia medica.

Thalassemia and hemoglobinopathies rather than iron deficiency are major causes of pregnancy-related anemia in northeast Thailand.

F. Schelp, P. Sanchaisuriya, G. Fucharoen, 2006, Blood cells, molecules & diseases.

Molecular basis of β-thalassemia in Thailand: analysis of β-thalassemia mutations using the polymerase chain reaction

Y. Fukumaki, V. Suvatte, V. Tanphaichitr, 1989, Human Genetics.

Routine screening for α-thalassaemia using an immunochromatographic strip assay for haemoglobin Bart's

G. Fucharoen, S. Fucharoen, Patcharawadee Prayalaw, 2014, Journal of medical screening.

Variability of hemoglobin F expression in hemoglobin EE disease: hematological and molecular analysis.

G. Fucharoen, S. Fucharoen, K. Sanchaisuriya, 2014, Blood cells, molecules & diseases.

A spurious haemoglobin A1c result associated with double heterozygote for haemoglobin Raleigh (β1[NA1]Val → Ala) and α +-thalassaemia

Kritsada Singha, G. Fucharoen, S. Fucharoen, 2012, Annals of clinical biochemistry.

Genetic origin of α0-thalassemia (SEA deletion) in Southeast Asian populations and application to accurate prenatal diagnosis of Hb Bart’s hydrops fetalis syndrome

Xiangmin Xu, G. Fucharoen, S. Fucharoen, 2017, Journal of Human Genetics.

Two Independent Genetic Origins of β+- Thalassemia Due to -31 A to G Mutation in Thai and Japanese Populations

G. Fucharoen, S. Fucharoen, Supawadee Yamsri, 2015 .

No Evidence for Role of Common Anion Exchanger 1 Mutations on the Severity Difference in HB E-β-Thalassemia Disease in Northeast Thailand

G. Fucharoen, S. Fucharoen, K. Sanchaisuriya, 2013 .

A single nucleotide deletion in codon 123 of the β‐globin gene causes an inclusion body β‐thalassaemia trait: a novel elongated globin chain βMakabe

K. Miyazono, Y. Fukumaki, F. Takaku, 1990 .

Double heterozygosity of the β‐malay and a novel β‐thalassemia gene in a thai patient

Y. Fukumaki, G. Fucharoen, S. Fucharoen, 1991 .

Effect of health education on severe thalassemia prevention and control in communities in Cambodia

P. Sanchaisuriya, G. Fucharoen, S. Fucharoen, 2018, Archives of Public Health.

alpha/beta-Globin mRNA ratio determination by multiplex quantitative real-time reverse transcription-polymerase chain reaction as an indicator of globin gene function.

P. Wilairat, G. Fucharoen, S. Fucharoen, 2007, Clinical biochemistry.

H63D Mutation of the Hemochromatosis Gene and Serum Ferritin Levels in Thai Thalassemia Carriers

S. Wiangnon, P. Sanchaisuriya, G. Fucharoen, 2007, Acta Haematologica.

Hemoglobin Lepore EF Bart’s disease: a molecular, hematological, and diagnostic aspects

G. Fucharoen, S. Fucharoen, A. Jetsrisuparb, 2011, Annals of Hematology.

Accuracy of fetal gender detection using a conventional nested PCR assay of maternal plasma in daily practice

G. Fucharoen, S. Fucharoen, K. Sanchaisuriya, 2008, The Australian & New Zealand journal of obstetrics & gynaecology.

Non-invasive fetal sex determination using a conventional nested PCR analysis of fetal DNA in maternal plasma.

G. Fucharoen, S. Fucharoen, K. Sanchaisuriya, 2003, Clinica chimica acta; international journal of clinical chemistry.

Elevations of Thrombotic Biomarkers in Hemoglobin H Disease

G. Fucharoen, S. Fucharoen, A. Jetsrisuparb, 2018, Acta Haematologica.

The Correlation Between Ineffective Erythropoiesis Biomarkers and Development of Extramedullary Hematopoiesis in Patients with Thalassemia

G. Fucharoen, S. Fucharoen, N. Teawtrakul, 2022, Mediterranean journal of hematology and infectious diseases.

Molecular Understanding of Non-Transfusion-Dependent Thalassemia Associated with Hemoglobin E-β-Thalassemia in Northeast Thailand

G. Fucharoen, S. Fucharoen, K. Sanchaisuriya, 2016, Acta Haematologica.

Phenotype and Genotype in a Cohort of 312 Adult Patients with Nontransfusion-Dependent Thalassemia in Northeast Thailand

G. Fucharoen, S. Fucharoen, A. Jetsrisuparb, 2015, Acta Haematologica.

Molecular Characterization of a β-Thalassemia Intermedia Patient Presenting Inferior Vena Cava Thrombosis: Interaction of the β-Globin Erythroid Krüppel-Like Factor Binding Site Mutation with Hb E and α+-Thalassemia

G. Fucharoen, S. Fucharoen, N. Teawtrakul, 2014, Hemoglobin.

Molecular, hematological and clinical aspects of thalassemia major and thalassemia intermedia associated with Hb E-beta-thalassemia in Northeast Thailand.

S. Wiangnon, G. Fucharoen, S. Fucharoen, 2009, Blood cells, molecules & diseases.

δ-Hemoglobinopathies in Thailand: screening, molecular basis, genotype-phenotype interaction, and implication for prevention and control of thalassemia

Kritsada Singha, G. Fucharoen, S. Fucharoen, 2021, Annals of Hematology.

β‐Hemoglobinopathies in the Lao People's Democratic Republic: Molecular diagnostics and implication for a prevention and control program

Kritsada Singha, G. Fucharoen, S. Fucharoen, 2020, International journal of laboratory hematology.

Molecular characterisation of haemoglobin E-Udon Thani (HBB:c.[79G>A;92+7A>G]): a novel form of Hb E-β-thalassaemia syndrome

Kritsada Singha, G. Fucharoen, S. Fucharoen, 2019, Journal of Clinical Pathology.

Prevalence of Thalassemia among Newborns: A Re-visited after 20 Years of a Prevention and Control Program in Northeast Thailand

G. Fucharoen, S. Fucharoen, Kanda Sornkayasit, 2018, Mediterranean journal of hematology and infectious diseases.

EE score: an index for simple differentiation of homozygous hemoglobin E and hemoglobin E-β0-thalassemia

Kritsada Singha, G. Fucharoen, S. Fucharoen, 2018, Clinical chemistry and laboratory medicine.

A proficiency testing program of hemoglobin analysis in prevention and control of severe hemoglobinopathies in Thailand

G. Fucharoen, S. Fucharoen, Rossarin Karnpean, 2012, Clinical chemistry and laboratory medicine.

MOLECULAR CHARACTERIZATION OF Hb D-PUNJAB [β121(GH4)Glu→Gln] IN THAILAND

G. Fucharoen, S. Fucharoen, K. Sanchaisuriya, 2002, Hemoglobin.

Hemoglobin profiles and hematologic features of thalassemic newborns: application to screening of alpha-thalassemia 1 and hemoglobin E.

P. Sanchaisuriya, G. Fucharoen, S. Fucharoen, 2008, Archives of pathology & laboratory medicine.

Prenatal and post-natal screening of β-thalassemia and hemoglobin E genes in Thailand using denaturing high performance liquid chromatography

G. Fucharoen, S. Fucharoen, N. Siriratmanawong, 2013, Molecular Biology Reports.

Anemia, iron deficiency and iron deficiency anemia among female university students in Khon Kaen Province: relationship to menstruation

P. Sanchaisuriya, G. Fucharoen, S. Fucharoen, 2015 .

Burden of Anemia in Relation to Thalassemia and Iron Deficiency among Vietnamese Pregnant Women

P. Hoa, F. Schelp, P. Sanchaisuriya, 2013, Acta Haematologica.

Hemoglobins F, A2, and E levels in Laotian children aged 6‐23 months with Hb E disorders: Effect of age, sex, and thalassemia types

S. Hess, S. Kounnavong, G. Fucharoen, 2020, International journal of laboratory hematology.

Frequency Distribution and Haplotypic Heterogeneity of βE-Globin Gene among Eight Minority Groups of Northeast Thailand

G. Fucharoen, S. Fucharoen, K. Sanchaisuriya, 2002, Human Heredity.

Molecular characterization of hemoglobin C in Thailand

G. Fucharoen, S. Fucharoen, K. Sanchaisuriya, 2001, American journal of hematology.

A large cohort of β(+)-thalassemia in Thailand: molecular, hematological and diagnostic considerations.

Kritsada Singha, G. Fucharoen, S. Fucharoen, 2015, Blood cells, molecules & diseases.

Genotype and phenotype characterizations in a large cohort of β-thalassemia heterozygote with different forms of α-thalassemia in northeast Thailand.

G. Fucharoen, S. Fucharoen, K. Sanchaisuriya, 2011, Blood cells, molecules & diseases.

Molecular and hematological profiles of hemoglobin EE disease with different forms of α-thalassemia

G. Fucharoen, S. Fucharoen, K. Sanchaisuriya, 2006, Annals of Hematology.

Prevention of severe thalassemia in northeast Thailand: 16 years of experience at a single university center

G. Fucharoen, S. Fucharoen, K. Sanchaisuriya, 2010, Prenatal diagnosis.

Thalassemia and hemoglobinopathies in pregnant women attended antenatal care service at Yala Hospital

G. Fucharoen, S. Fucharoen, K. Sanchaisuriya, 2014 .

Micromapping of Thalassemia and Hemoglobinopathies in Diferent Regions of Northeast Thailand and Vientaine, Laos People's Democratic Republic

F. Schelp, P. Sanchaisuriya, G. Fucharoen, 2012, Hemoglobin.

Compound Heterozygous Hb Tak/Hb E Causes Secondary Erythrocytosis in a Thai Family

G. Fucharoen, N. Teawtrakul, C. Sirijirachai, 2010, Hemoglobin.

Diagnostic value of fetal hemoglobin Bart’s for evaluation of fetal α-thalassemia syndromes: application to prenatal characterization of fetal anemia caused by undiagnosed α-hemoglobinopathy

Kritsada Singha, G. Fucharoen, S. Fucharoen, 2022, Orphanet Journal of Rare Diseases.

Molecular Analysis of Non-Transfusion Dependent Thalassemia Associated with Hemoglobin E-β-Thalassemia Disease without α-Thalassemia

G. Fucharoen, S. Fucharoen, K. Sanchaisuriya, 2019, Mediterranean journal of hematology and infectious diseases.

Nine known and five novel mutations in the erythroid transcription factor KLF1 gene and phenotypic expression of fetal hemoglobin in hemoglobin E disorder.

Xiangmin Xu, G. Fucharoen, S. Fucharoen, 2016, Blood cells, molecules & diseases.

Krüppel-like factor 1 mutations and expression of hemoglobins F and A2 in homozygous hemoglobin E syndrome

G. Fucharoen, S. Fucharoen, K. Sanchaisuriya, 2015, Annals of Hematology.

Molecular analysis of haemoglobin E in Southeast Asian populations

G. Fucharoen, S. Fucharoen, K. Sanchaisuriya, 2017, Annals of human biology.

Molecular characterization and origins of Hb Constant Spring and Hb Paksé in Southeast Asian populations

G. Fucharoen, S. Fucharoen, K. Sanchaisuriya, 2007, Annals of Hematology.

Development of Severe Anemia During Fever Episodes in Patients With Hemoglobin E Trait and Hemoglobin H Disease Combinations

S. Wiangnon, G. Fucharoen, S. Fucharoen, 2006, Journal of pediatric hematology/oncology.

A New Indicator Derived From Reticulocyte Hemoglobin Content for Screening Iron Deficiency in an Area Prevalent for Thalassemia.

P. Sanchaisuriya, G. Fucharoen, S. Fucharoen, 2020, Laboratory medicine.

FLT3-ITD Mutations in Acute Myeloid Leukemia Patients in Northeast Thailand.

S. Wiangnon, Su-on Chainansamit, G. Fucharoen, 2016, Asian Pacific journal of cancer prevention : APJCP.

Anemia, iron deficiency, and thalassemia among the Thai population inhabiting at the Thailand-Lao PDR-Cambodia triangle

G. Fucharoen, S. Fucharoen, S. Singsanan, 2022, Scientific Reports.

Factors associated with anaemia and iron deficiency among women of reproductive age in Northeast Thailand: a cross-sectional study

F. Ahmed, P. Sanchaisuriya, G. Fucharoen, 2020, BMC public health.

Molecular and hematological characteristics of a novel form of α-globin gene triplication: the hemoglobin St.Luke's-Thailand [α95(G2)Pro→Arg] or Hb St. Luke's [A2] HBA2.

Kritsada Singha, G. Fucharoen, S. Fucharoen, 2013, Clinical biochemistry.

BCL11A is a major HbF quantitative trait locus in three different populations with beta-hemoglobinopathies.

P. Sebastiani, L. Farrer, B. Vardarajan, 2008, Blood cells, molecules & diseases.

Molecular Characteristics of Hb New York [β113(G15)Val→Glu, HBB: c.341T>A] in Thailand

Kritsada Singha, G. Fucharoen, S. Fucharoen, 2018, Hemoglobin.

PILOT SCREENING PROGRAM FOR THALASSEMIA IN A COUNTRY WITH LIMITED RESOURCES: A COLLABORATION MODEL BETWEEN CLOSE NEIGHBORING COUNTRIES.

F. Schelp, P. Sanchaisuriya, G. Fucharoen, 2016, The Southeast Asian journal of tropical medicine and public health.

Thalassemia and erythroid transcription factor KLF1 mutations associated with borderline hemoglobin A2 in the Thai population

G. Fucharoen, S. Fucharoen, K. Sanchaisuriya, 2020, Archives of medical science : AMS.

Dominant β-thalassaemia with unusually high Hb A2 and Hb F caused by βCD121(−G) (HBB:c.364delG) in exon 3 of β-globin gene

Kritsada Singha, G. Fucharoen, S. Fucharoen, 2019, Journal of Clinical Pathology.

Novel interactions of two α-Hb variants with SEA deletion α0-thalassemia: hematological and molecular analyses

Kritsada Singha, G. Fucharoen, S. Fucharoen, 2018, Hematology.

Hemoglobin variants in Thailand: Data from a referral center at Khon Kaen University in 2015

G. Fucharoen, S. Fucharoen, 2016 .

Known and new hemoglobin A2 variants in Thailand and implication for β-thalassemia screening.

G. Fucharoen, S. Fucharoen, S. Panyasai, 2015, Clinica chimica acta; international journal of clinical chemistry.

A Large Cohort of Hemoglobin Variants in Thailand: Molecular Epidemiological Study and Diagnostic Consideration

Kritsada Singha, G. Fucharoen, S. Fucharoen, 2014, PloS one.

Rapid molecular characterization of Hb Queens and Hb Siam: two variants easily misidentified as sickle Hb.

G. Fucharoen, S. Fucharoen, K. Sanchaisuriya, 2007, Clinical biochemistry.

A reliable screening protocol for thalassemia and hemoglobinopathies in pregnancy: an alternative approach to electronic blood cell counting.

F. Schelp, P. Sanchaisuriya, G. Fucharoen, 2005, American journal of clinical pathology.

A simplified screening strategy for thalassaemia and haemoglobin E in rural communities in south-east Asia.

G. Fucharoen, S. Fucharoen, K. Sanchaisuriya, 2004, Bulletin of the World Health Organization.

The Diverse Molecular Basis and Hematological Features of Hb H and AEBart’s Diseases in Northeast Thailand

S. Wiangnon, G. Fucharoen, S. Fucharoen, 2004, Acta Haematologica.

Hb Paksé [(α2) CODON 142 (TA A→TA T OR Term→Tyr)] IN THAI PATIENTS WITH EABart's DISEASE AND Hb H DISEASE

G. Fucharoen, S. Fucharoen, K. Sanchaisuriya, 2002, Hemoglobin.

Simultaneous PCR detection of β – thalassemia and α – thalassemia 1 (SEA type) in prenatal diagnosis of complex thalassemia syndrome

G. Fucharoen, S. Fucharoen, K. Sanchaisuriya, 2001 .

Genetic and non-genetic factors affecting hemoglobin A2 expression in a large cohort of Thai individuals: implication for population screening for thalassemia.

Kritsada Singha, G. Fucharoen, S. Fucharoen, 2021, American journal of translational research.

Molecular analysis of a Thai β-thalassaemia heterozygote with normal haemoglobin A2 level: implication for population screening

G. Fucharoen, S. Fucharoen, K. Sanchaisuriya, 2002, Annals of clinical biochemistry.

Thalassemia Screening Using Different Automated Blood Cell Counters: Consideration of Appropriate Cutoff Values.

P. Sanchaisuriya, G. Fucharoen, S. Fucharoen, 2016, Clinical laboratory.

Phenotypic expression of hemoglobins A₂, E and F in various hemoglobin E related disorders.

G. Fucharoen, S. Fucharoen, K. Sanchaisuriya, 2012, Blood cells, molecules & diseases.

Thalassemia and hemoglobinopathies in pregnant Lao women: carrier screening, prevalence and molecular basis

G. Fucharoen, S. Fucharoen, K. Sanchaisuriya, 2008, Annals of Hematology.

Coexistence of Southeast Asian ovalocytosis and β‐thalassemia: A molecular and hematological analysis

G. Fucharoen, S. Fucharoen, K. Sanchaisuriya, 2007, American journal of hematology.

A Simplified Screening for α-Thalassemia 1 (SEA Type) Using a Combination of a Modified Osmotic Fragility Test and a Direct PCR on Whole Blood Cell Lysates

G. Fucharoen, S. Fucharoen, K. Sanchaisuriya, 2002, Acta Haematologica.

Thalassemia and iron deficiency in a group of northeast Thai school children: relationship to the occurrence of anemia

F. Schelp, P. Sanchaisuriya, G. Fucharoen, 2010, European Journal of Pediatrics.

Association of Hb Q‐Thailand with homozygous Hb E and heterozygous Hb Constant Spring in pregnancy

P. Sanchaisuriya, G. Fucharoen, S. Fucharoen, 2005, European journal of haematology.

Application of maternal plasma DNA analysis for noninvasive prenatal diagnosis of Hb E-beta-thalassemia.

G. Fucharoen, S. Fucharoen, K. Sanchaisuriya, 2007, Translational research : the journal of laboratory and clinical medicine.

Compound heterozygote states for Hb C/Hb Malay and Hb C/Hb E in pregnancy: a molecular and hematological analysis.

G. Fucharoen, S. Fucharoen, K. Sanchaisuriya, 2005, Blood cells, molecules & diseases.

Flow cytometric determination of zeta globin chian in red blood cells

G. Fucharoen, S. Fucharoen, N. Sae-Ung, 2012 .

Multiplex allele-specific PCR assay for differential diagnosis of Hb S, Hb D-Punjab and Hb Tak.

G. Fucharoen, S. Fucharoen, K. Sanchaisuriya, 2004, Clinica chimica acta; international journal of clinical chemistry.

Thalassemia and hemoglobinopathies in Southeast Asian newborns: diagnostic assessment using capillary electrophoresis system.

G. Fucharoen, S. Fucharoen, P. Komwilaisak, 2011, Clinical biochemistry.

Genetic heterogeneity of hemoglobin AEBart's disease: a large cohort data from a single referral center in northeast Thailand.

G. Fucharoen, S. Fucharoen, A. Chaibunruang, 2014, Blood cells, molecules & diseases.

Analysis of fetal blood using capillary electrophoresis system: a simple method for prenatal diagnosis of severe thalassemia diseases

G. Fucharoen, S. Fucharoen, K. Sanchaisuriya, 2009, European journal of haematology.

Three-base deletion in exon 3 of the beta-globin gene produced a novel variant (beta gunma) with a thalassemia-like phenotype [letter]

S. Fucharoen, Y. Fukumaki, Ken Yamamoto, 1990 .

Molecular and hematological characterization of hemoglobin Hope/hemoglobin E and hemoglobin Hope/alpha-thalassemia 2 in Thai patients.

G. Fucharoen, S. Fucharoen, K. Sanchaisuriya, 2004, Laboratory hematology : official publication of the International Society for Laboratory Hematology.

Thalassemia and iron deficiency among pregnant women attending antenatal care service at Khao Wong Hospital, Kalasin province

P. Sanchaisuriya, G. Fucharoen, S. Fucharoen, 2010 .

Three major lineages of Asian Y chromosomes: implications for the peopling of east and southeast Asia

K. Tokunaga, S. Horai, M. Matsuo, 2001, Human Genetics.

Hemoglobin EE disease in young Laotian children: Hematologic features and the contributions of genetic variations to Hb F expression

S. Kounnavong, G. Fucharoen, S. Fucharoen, 2023, International journal of laboratory hematology.

α0-thalassemia in affected fetuses with hemoglobin E-β0-thalassemia disease in a high-risk population in Thailand.

G. Fucharoen, S. Fucharoen, K. Sanchaisuriya, 2022, American journal of translational research.

Interactions of hemoglobin Lepore (deltabeta hybrid hemoglobin) with various hemoglobinopathies: A molecular and hematological characteristics and differential diagnosis.

G. Fucharoen, S. Fucharoen, K. Sanchaisuriya, 2010, Blood cells, molecules & diseases.

Molecular characteristics of α+-thalassemia (3.7 kb deletion) in Southeast Asia: Molecular subtypes, haplotypic heterogeneity, multiple founder effects and laboratory diagnostics.

Kritsada Singha, G. Fucharoen, S. Fucharoen, 2019, Clinical biochemistry.

Molecular Heterogeneity of Thalassemia among Pregnant Laotian Women

F. Schelp, P. Sanchaisuriya, G. Fucharoen, 2015, Acta Haematologica.

α⁰-Thalassemia and Related Disorders in Northeast Thailand: A Molecular and Hematological Characterization

G. Fucharoen, S. Fucharoen, K. Sanchaisuriya, 2006, Acta Haematologica.

Interaction of hemoglobin E and several forms of alpha-thalassemia in Cambodian families.

G. Fucharoen, S. Fucharoen, K. Sanchaisuriya, 2003, Haematologica.

Molecular basis and hematologic characterization of δβ-thalassemia and hereditary persistence of fetal hemoglobin in Thailand

G. Fucharoen, S. Fucharoen, K. Sanchaisuriya, 2004 .

Erythrocyte indices in a large cohort of β‐thalassemia carrier: Implication for population screening in an area with high prevalence and heterogeneity of thalassemia

Kritsada Singha, G. Fucharoen, S. Fucharoen, 2019, International journal of laboratory hematology.

Fetal Red Blood Cell Parameters in Thalassemia and Hemoglobinopathies

G. Fucharoen, S. Fucharoen, T. Ratanasiri, 2013, Fetal Diagnosis and Therapy.

Molecular and hematological studies in a large cohort of α(0)-thalassemia in northeast Thailand: data from a single referral center.

G. Fucharoen, S. Fucharoen, K. Sanchaisuriya, 2013, Blood cells, molecules & diseases.

Accurate Prenatal Diagnosis of Hb Bart’s Hydrops Fetalis in Daily Practice with a Double-Check PCR System

G. Fucharoen, S. Fucharoen, K. Sanchaisuriya, 2009, Acta Haematologica.

Mitochondrial DNA polymorphisms in Thailand

S. Horai, G. Fucharoen, S. Fucharoen, 2001, Journal of Human Genetics.

Eight-base deletion in exon 3 of the beta-globin gene produced a novel variant (beta khon kaen) with an inclusion body beta-thalassemia trait.

Y. Fukumaki, S. Fuchareon, G. Fucharoen, 1991, Blood.

Improvement of alpha(0)-thalassemia screening using combined osmotic fragility, dichlorophenolindophenol and Hb H inclusion tests.

G. Fucharoen, S. Fucharoen, K. Sanchaisuriya, 2010, Clinical laboratory.

Incidence of Hb Constant Spring and Hb Paksé in Khon Kaen province: Examination using capillary electrophoresis and DNA analysis

G. Fucharoen, S. Fucharoen, Kanda Sornkayasit, 2012 .

Screening of (–SEA) α-thalassaemia using an immunochromatographic strip assay for the ζ-globin chain in a population with a high prevalence and heterogeneity of haemoglobinopathies

G. Fucharoen, S. Fucharoen, K. Sanchaisuriya, 2016, Journal of Clinical Pathology.

Prenatal Diagnosis of Hb Bart’s Hydrops Fetalis Caused by a Genetic Compound Heterozygosity for Two Different αo-Thalassemia Determinants

G. Fucharoen, S. Fucharoen, N. Siriratmanawong, 2007, Fetal Diagnosis and Therapy.

Response to Dr. Dong-Zhi Li

G. Fucharoen, S. Fucharoen, K. Sanchaisuriya, 2009, Acta Haematologica.

Selection of couple at risk of having fetus with hemoglobin Bart’s hydrops fetalis: 6 years of experience at Suratthani hospital

G. Fucharoen, S. Fucharoen, N. Sae-Ung, 2014 .

Thalassemia and Hemoglobinopathies in an Ethnic Minority Group in Northern Vietnam

Dung Nguyen Tien, F. Schelp, P. Sanchaisuriya, 2019, Hemoglobin.

Prenatal diagnosis of thalassemia using capillary electrophoresis system experience from northeast Thailand

G. Fucharoen, S. Fucharoen, 2011 .

Thalassemia intermedia associated with the Hb Constant Spring EE Bart's disease in pregnancy: a molecular and hematological analysis.

G. Fucharoen, S. Fucharoen, K. Sanchaisuriya, 2007, Blood cells, molecules & diseases.

Complex interaction of Hb Hekinan [α27(B8) Glu–Asp] and Hb E [β26(B8) Glu–Lys] with a deletional α‐thalassemia 1 in a Thai family

G. Fucharoen, S. Fucharoen, K. Sanchaisuriya, 2003, European journal of haematology.

Molecular and hematological characterization of HPFH‐6/Indian deletion–inversion Gγ(Aγδβ)0‐thalassemia and Gγ(Aγδβ)0‐thalassemia/HbE in Thai patients

G. Fucharoen, S. Fucharoen, K. Sanchaisuriya, 2002 .

Molecular Characterization of Thalassemia intermedia Associated with HPFH-6/β-Thalassemia and HPFH-6/Hb E in Thai Patients

G. Fucharoen, S. Fucharoen, K. Sanchaisuriya, 2002, Acta Haematologica.

Molecular characterization of (δβ)°/β°‐thalassemia and (δβ)°‐thalassemia/hemoglobin E in Thai patients

G. Fucharoen, S. Fucharoen, K. Sanchaisuriya, 2001 .

Simple non-radioactive method for detecting haemoglobin Constant Spring gene

Y. Fukumaki, G. Fucharoen, S. Fucharoen, 1990, The Lancet.

α/β Globin mRNA of β-thalassemia genes with premature termination

G. Fucharoen, S. Fucharoen, K. Sanchaisuriya, 2010 .

Three-base deletion in exon 3 of the beta-globin gene produced a novel variant (beta gunma) with a thalassemia-like phenotype.

S. Fucharoen, Y. Fukumaki, G. Fucharoen, 1990, Blood.

Phosphatidylserine-exposed red blood cells and ineffective erythropoiesis biomarkers in patients with thalassemia.

G. Fucharoen, S. Fucharoen, N. Teawtrakul, 2022, American journal of translational research.

Atypical hemoglobin H disease in a Thai patient resulting from a combination of α‐thalassemia 1 and hemoglobin Constant Spring with hemoglobin J Bangkok heterozygosity

G. Fucharoen, S. Fucharoen, K. Sanchaisuriya, 2001, European journal of haematology.

Southeast Asian Ovalocytosis and Hemoglobinopathies in Newborns: Prevalence, Molecular, and Hematological Analyses.

G. Fucharoen, S. Fucharoen, Supawadee Yamsri, 2020, Journal of pediatric hematology/oncology.

Molecular basis of Hb H and AEBart’s diseases in the Lao People’s Democratic Republic

Kritsada Singha, G. Fucharoen, S. Fucharoen, 2020, International journal of laboratory hematology.

Hb H Disease with Various β Hemoglobinopathies: Molecular, Hematological and Diagnostic Aspects

G. Fucharoen, S. Fucharoen, 2012, Hemoglobin.

Hemoglobin Q-Thailand related disorders: origin, molecular, hematological and diagnostic aspects.

G. Fucharoen, S. Fucharoen, K. Sanchaisuriya, 2010, Blood cells, molecules & diseases.

Generation of a single‐tube quality control material for hemoglobin and DNA analyses of hemoglobinopathies

G. Fucharoen, S. Fucharoen, K. Sanchaisuriya, 2021, International journal of laboratory hematology.

A novel SNP rs11759328 on Rho GTPase-activating protein 18 gene is associated with the expression of Hb F in hemoglobin E-related disorders

G. Fucharoen, S. Fucharoen, Supawadee Yamsri, 2019, Annals of Hematology.

Differentiation of homozygous hemoglobin E and hemoglobin E‐β0‐thalassemia in children

Kritsada Singha, G. Fucharoen, S. Fucharoen, 2019, International journal of laboratory hematology.

Prenatal and post-natal screening of β-thalassemia and hemoglobin E genes in Thailand using denaturing high performance liquid chromatography

G. Fucharoen, S. Fucharoen, N. Siriratmanawong, 2013, Molecular Biology Reports.

Anemia, Iron Deficiency and Thalassemia among Adolescents in Northeast Thailand: Results from Two Independent Surveys

G. Fucharoen, S. Fucharoen, Anupong Pansuwan, 2011, Acta Haematologica.

Effects of heparin on thalassemia genes analysis by PCR

G. Fucharoen, S. Fucharoen, K. Singha, 2010 .

Hb Bart’s and Hb E in cord blood : analysis using two automated Hb analyzers

P. Sanchaisuriya, G. Fucharoen, S. Fucharoen, 2010 .

Effect of the maternal betaE-globin gene on hematologic responses to iron supplementation during pregnancy.

E. Dietz, F. Schelp, P. Sanchaisuriya, 2007, The American journal of clinical nutrition.

Thalassemia Intermedia Associated with Complex Interaction of Hb Beijing [α16(A14)Lys→Asn] and Hb E [β26(B8)Glu→Lys] with a Deletional α-Thalassemia-1 in a Thai Family

G. Fucharoen, S. Fucharoen, K. Sanchaisuriya, 2005 .

Prenatal detection of fetal hemoglobin E gene from maternal plasma

G. Fucharoen, S. Fucharoen, K. Sanchaisuriya, 2003, Prenatal diagnosis.

Triple Heterozygosity of a Hemoglobin Variant: Hemoglobin Pyrgos With Other Hemoglobinopathies

S. Wiangnon, G. Fucharoen, S. Fucharoen, 2002, International journal of hematology.

Results from 8 years of the proficiency testing program for diagnosis of hemoglobinopathies under the prevention and control program of thalassemia in Thailand

G. Fucharoen, S. Fucharoen, Supawadee Yamsri, 2021, International journal of laboratory hematology.

A Newly Modified Hemoglobin H Inclusion Test as a Secondary Screening for α⁰-Thalassemia in Southeast Asian Populations

G. Fucharoen, S. Fucharoen, A. Chaibunruang, 2013, Acta Haematologica.

Development and Application of a Real‐Time Quantitative PCR for Prenatal Detection of Fetal α0‐Thalassemia from Maternal Plasma

G. Fucharoen, S. Fucharoen, K. Sanchaisuriya, 2006 .

Molecular basis of a high Hb A2/Hb Fβ-thalassemia trait: a retrospective analysis, genotype-phenotype interaction, diagnostic implication, and identification of a novel interaction with α-globin gene triplication

Kritsada Singha, G. Fucharoen, S. Fucharoen, 2023, PeerJ.

A novel (A)γδβ(0)-thalassemia caused by DNA deletion-inversion-insertion of the β-globin gene cluster and five olfactory receptor genes: Genetic interactions, hematological phenotypes and molecular characterization.

Kritsada Singha, G. Fucharoen, S. Fucharoen, 2015, Clinical biochemistry.

Genetic origin and interaction of the Filipino β⁰-thalassemia with Hb E and α-thalassemia in a Thai family.

G. Fucharoen, S. Fucharoen, K. Sanchaisuriya, 2012, Translational research : the journal of laboratory and clinical medicine.

Molecular basis and hematologic characterization of deltabeta-thalassemia and hereditary persistence of fetal hemoglobin in Thailand.

G. Fucharoen, S. Fucharoen, K. Sanchaisuriya, 2004, Haematologica.

Secondary Erythrocytosis Caused by Hemoglobin Tak/(δβ)⁰-Thalassemia Syndrome

G. Fucharoen, S. Fucharoen, S. Singsanan, 2010, Acta Haematologica.

Frequency of unnecessary prenatal diagnosis of hemoglobinopathies: A large retrospective analysis and implication to improvement of the control program

Kritsada Singha, G. Fucharoen, S. Fucharoen, 2023, PloS one.

Five Hemoglobin Variants in a Double Heterozygote for α- and β-Globin Chain Defects

Kritsada Singha, G. Fucharoen, S. Fucharoen, 2013, Acta Haematologica.

Hemoglobin Variants in Northern Thailand: Prevalence, Heterogeneity and Molecular Characteristics.

G. Fucharoen, S. Fucharoen, S. Panyasai, 2016, Genetic Testing and Molecular Biomarkers.

Clinical Course of Homozygous Hemoglobin Constant Spring in Pediatric Patients

G. Fucharoen, R. Komwilaisak, Junya Jirapradittha, 2018, Journal of pediatric hematology/oncology.

Complex Interaction of Hb E [β26(B8)Glu→Lys], Hb Korle-Bu [β73(E17)Asp→Asn] and a Deletional α-thalassemia-1 in Pregnancy

G. Fucharoen, S. Fucharoen, S. Singsanan, 2009, Hemoglobin.

Compound heterozygote state for GγAγ(δβ)°‐thalassemia and hereditary persistence of fetal hemoglobin

G. Fucharoen, S. Fucharoen, K. Sanchaisuriya, 2005 .

Hemoglobin Constant Spring among Southeast Asian Populations: Haplotypic Heterogeneities and Phylogenetic Analysis

G. Fucharoen, S. Fucharoen, K. Sanchaisuriya, 2015, PloS one.

Molecular Survey of Hemoglobinopathies in Myanmar Workers in Northeast Thailand Revealed an Unexpectedly High Prevalence of α+-Thalassemia

Kritsada Singha, G. Fucharoen, S. Fucharoen, 2019, Hemoglobin.

Thalassemia and hemoglobinopathies in an ethnic minority group in Central Vietnam: implications to health burden and relationship between two ethnic minority groups

P. Sanchaisuriya, G. Fucharoen, S. Fucharoen, 2017, Journal of Community Genetics.

Thalassemia and Hemoglobinopathies in Thua Thien Hue Province, Central Vietnam

F. Schelp, P. Sanchaisuriya, G. Fucharoen, 2013, Hemoglobin.

Molecular basis of non-deletional HPFH in Thailand and identification of two novel mutations at the binding sites of CCAAT and GATA-1 transcription factors

Kritsada Singha, G. Fucharoen, S. Fucharoen, 2023, Scientific reports.

Molecular and haematological characterisation of haemolytic anaemia associated with biallelic KLF1 mutations: a case series

Kritsada Singha, G. Fucharoen, S. Fucharoen, 2023, Journal of clinical pathology.

mtDNA polymorphism in East Asian Populations, with special reference to the peopling of Japan.

S. Horai, K. Hayasaka, K. Park, 1996, American journal of human genetics.

Association of Hb Thailand [α56(E5)Lys→Thr] and Hb Phnom Penh [α117(GH5)-Ile-α118(H1)] with α0-Thalassemia: Molecular and Hematological Features and Differential Diagnosis

Kritsada Singha, G. Fucharoen, S. Fucharoen, 2013, Hemoglobin.

High resolution melting analytical platform for rapid prenatal and postnatal diagnosis of β-thalassemia common among Southeast Asian population.

G. Fucharoen, S. Fucharoen, Thanet Prajantasen, 2015, Clinica chimica acta; international journal of clinical chemistry.

Molecular basis of beta thalassemia in the south of thailand

Y. Fukumaki, G. Fucharoen, S. Fucharoen, 1992, American journal of hematology.

Presentation of Compound Heterozygous Hemoglobin Constant Spring and Hemoglobin Pakse in Neonates

G. Fucharoen, Junya Jirapradittha, P. Kiatchoosakun, 2019, Journal of pediatric hematology/oncology.

Interaction of hemoglobin E and several forms of alpha-thalassemia in Cambodian families.

J. Garcia-conde, A. Schmitt-Graeff, R. Paroni, 2003, Haematologica.

Co‐inheritance of α0‐thalassemia elevates Hb A2 level in homozygous Hb E: Diagnostic implications

S. Fucharoen, Kritsada Singha, G. Fucharoen, 2017, International journal of laboratory hematology.