Citations (32)
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Jinia Saha, Amrita Panja & Kaustav Nayek. (2021) The Prevalence of HBB Mutations among the Transfusion-Dependent and Non Transfusion-Dependent Hb E/β-Thalassemia Children in a Tertiary Center of West Bengal, India . Hemoglobin 45:3, pages 157-162.
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Roshan B. Colah, Anita H. Nadkarni, Ajit C. Gorakshakar, Pratibha M. Sawant, Pallavi R. Mehta, Manju S. Gorivale, Priya Hariharan, Dipika Mohanty & Kanjaksha Ghosh. (2021) The Changing Trends in Prenatal Diagnosis of Hemoglobinopathies in India: The Quest of a Single Center to Reduce the Burden of Disease over Three Decades. Hemoglobin 45:2, pages 112-118.
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Aditya N. Jha, Hrishikesh Mishra, Henu K. Verma, Isha Pandey & Bhaskar V.K.S. Lakkakula. (2018) Compound Heterozygosity of β-Thalassemia and the Sickle Cell Hemoglobin in Various Populations of Chhattisgarh State, India. Hemoglobin 42:2, pages 84-90.
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Sandra S. Lazarte, María E. Mónaco, Ana C. Haro, Cecilia L. Jiménez, Myriam E. Ledesma Achem & Blanca A. Issé. (2014) Molecular Characterization and Phenotypical Study of β-Thalassemia in Tucumán, Argentina. Hemoglobin 38:6, pages 394-401.
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Ashwin P. Patel, Rupesh B. Patel, Saumyaa A. Patel, Salil N. Vaniawala, Dipika S. Patel, Naina S. Shrivastava, Narmadeshwar P. Sharma, Jayendrasinh V. Zala, Prakash H. Parmar & Madhuben R. Naik. (2014) β-Thalassemia Mutations in Western India: Outcome of Prenatal Diagnosis in a Hemoglobinopathies Project. Hemoglobin 38:5, pages 329-334.
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Sudhansu Sekhar Nishank, Manoranjan Ranjit, Shantanu K. Kar & Guru Prasad Chhotray. (2009) Molecular variants and clinical importance of β-thalassaemia traits found in the state of Orissa, India. Hematology 14:5, pages 290-296.
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Anita Nadkarni, Ajit Gorakshakar, Reema Surve, Pratibha Sawant, Supriya Phanasgaonkar, Sona Nair, Kanjaksha Ghosh & Roshan B. Colah. (2009) Hematological and Molecular Analysis of Novel and Rare β-Thalassemia Mutations in the Indian Population. Hemoglobin 33:1, pages 59-65.
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Guru Prasad Chhotray, Bisnu Prasad Dash & Manoranjan Ranjit. (2004) Spectrum of Hemoglobinopathies in Orissa, India. Hemoglobin 28:2, pages 117-122.
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Ajit C. Gorakshakar, Supriya P. Phanasgaonkar, Anita H. Nadkarni, Roshan B. Colah & Dipika Mohanty. (2004) Detection of Rare β‐Thalassemia Mutations by Denaturing Gradient Gel Electrophoresis Among Indians. Hemoglobin 28:1, pages 15-24.
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Articles from other publishers (23)
Shouriyo Ghosh, Sila Chakrabarti & Maitreyee Bhattacharyya. (2020) Prenatal Screening and Diagnosis of ß-Thalassemia in India: Is ARMS-PCR Enough?. Indian Journal of Hematology and Blood Transfusion 37:3, pages 448-452.
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Tapasree Basu, Sourav Panja, Anil Khushalrao Shendge, Abhishek Das & Nripendranath Mandal. (2018) A natural antioxidant, tannic acid mitigates iron-overload induced hepatotoxicity in Swiss albino mice through ROS regulation. Environmental Toxicology 33:5, pages 603-618.
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Saurav Banerjee, Rabindra Kumar Singh, Ramesh Kumar Shrivastava & Sunil Kumar Mahto. (2016) STUDY OF HAEMOGLOBINOPATHIES IN PATIENTS OF ANAEMIA USING HIGH PERFORMANCE LIQUID CHROMATOGRAPHY (HPLC) IN RIMS (A PREMIER INSTITUTE OF JHARKHAND). Journal of Evolution of Medical and Dental Sciences 5:46, pages 2929-2933.
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Rinkle Mohapatra, Prashant Warang, Kanjaksha Ghosh & Roshan Colah. (2016) Hemoglobinopathy screening by osmotic fragility test based on flow cytometer or naked eye. Cytometry Part B: Clinical Cytometry 90:3, pages 279-284.
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SantoshKumar Mondal & Saikat Mandal. (2016) Prevalence of thalassemia and hemoglobinopathy in eastern India: A 10-year high-performance liquid chromatography study of 119,336 cases. Asian Journal of Transfusion Science 10:1, pages 105.
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Suman K. Maji, Prakas K. Mandal, Rajkumar Bera & Tuphan K. Dolai. (2014) The Prevalence and Characterization of β-Thalassemia Trait by Using High-Performance Liquid Chromatography among the Rural Population in West Bengal, India. Thalassemia Reports 4:1, pages 2188.
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Dipal S. Bhukhanvala, Khushnooma Italia, Pratibha Sawant, Roshan Colah, Kanjaksha Ghosh & Snehalata C. Gupte. (2013) Molecular characterization of β-thalassemia in four communities in South Gujarat—codon 30 (G → A) a predominant mutation in the Kachhiya Patel community. Annals of Hematology 92:11, pages 1473-1476.
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Nongthombam AchoubiMohammad AsgharKallur Nava SaraswathyBenrithung Murry. (2012) Prevalence of β-Thalassemia and Hemoglobin E in Two Migrant Populations of Manipur, North East India. Genetic Testing and Molecular Biomarkers 16:10, pages 1195-1200.
Crossref
Crossref
Sandeep B. Satpute, Mangesh P. Bankar & Abdulrahaman A. Momin. (2012) The Prevalence Of β-Thalassemia Mutations in South Western Maharashtra. Indian Journal of Clinical Biochemistry 27:4, pages 389-393.
Crossref
Crossref
Ali Reza Rezaee, Mohammad Mehdi Banoei, Elham Khalili & Massoud Houshmand. (2012) Beta-Thalassemia in Iran: New Insight into the Role of Genetic Admixture and Migration. The Scientific World Journal 2012, pages 1-7.
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Roshan Colah, Ajit Gorakshakar, Supriya Phanasgaonkar, Edna D’Souza, Anita Nadkarni, Reema Surve, Pratibha Sawant, Dilip Master, Ramesh Patel, Kanjaksha Ghosh & Dipika Mohanty. (2010) Epidemiology of β-thalassaemia in Western India: mapping the frequencies and mutations in sub-regions of Maharashtra and Gujarat. British Journal of Haematology 149:5, pages 739-747.
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Antonio Amato, Maria Pia Cappabianca, Alessia Colosimo, Maria Perri, Paola Grisanti, Ivo Zaghis, Donatella Ponzini & Maria Lerone. (2010) Current Genetic Epidemiology of -Thalassemias and Structural Hemoglobin Variants in the Lazio Region (Central Italy) Following Recent Migration Movements. Advances in Hematology 2010, pages 1-5.
Crossref
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S. Sinha, M. L. Black, S. Agarwal, R. Colah, R. Das, K. Ryan, M. Bellgard & A. H. Bittles. (2010) Profiling β-thalassaemia mutations in India at state and regional levels: implications for genetic education, screening and counselling programmes. The HUGO Journal 3:1-4, pages 51-62.
Crossref
Crossref
Roshan Colah, Ajit Gorakshakar, Anita Nadkarni, Supriya Phanasgaonkar, Reema Surve, Pratibha Sawant, Dipika Mohanty & Kanjaksha Ghosh. (2009) Regional heterogeneity of β-thalassemia mutations in the multi ethnic Indian population. Blood Cells, Molecules, and Diseases 42:3, pages 241-246.
Crossref
Crossref
Parag M. Tamhankar, Sarita Agarwal, Vandana Arya, Ravindra Kumar, U. R. Gupta & S. S. Agarwal. (2009) Prevention of homozygous beta thalassemia by premarital screening and prenatal diagnosis in India. Prenatal Diagnosis 29:1, pages 83-88.
Crossref
Crossref
R. Colah, A. Nadkarni, A. Gorakshakar, S. Phanasgaonkar, P. Sawant, R. Surve, D. Mohanty & K. Ghosh. (2008) Hb Showa Yakushiji [β 110 (G12) Leu→Pro] in 3 families from Western India: First report on homozygous Hb Showa Yakushiji. Blood Cells, Molecules, and Diseases 41:2, pages 166-168.
Crossref
Crossref
J. J. Sheth, F. J. Sheth, Pooja Pandya, Rashi Priya, Sejal Davla, Chitra Thakur & Vaz Flavin. (2008) β-Thalassemia mutations in western India. The Indian Journal of Pediatrics 75:6, pages 567-570.
Crossref
Crossref
Partha Chakrabarti, Ramkrishna Gupta, Ashutosh Mishra, Madhukar Rai, Vijay Pratap Singh & Debabrata Dash. (2005) Spectrum of β-thalassemia mutations in North Indian states: A β-thalassemia trait with two mutations in cis. Clinical Biochemistry 38:6, pages 576-578.
Crossref
Crossref
Aditi Bandyopadhyay, Sanmay Bandyopadhyay, Jayasri Basak, Bama Charan Mondal, Anjali Angelika Sarkar, Sunipa Majumdar, Mani Kanchan Das, Sharmila Chandra, Ashis Mukhopadhyay, Mamtaj Sanghamita, Kusagradhi Ghosh & Uma B. Dasgupta. (2004) Profile of β‐thalassemia in eastern India and its prenatal diagnosis. Prenatal Diagnosis 24:12, pages 992-996.
Crossref
Crossref
A. NADKARNI, T. SAKAGUCHI, A. GORAKSHAKAR, S. PHANASGAONKAR, R. KIYAMA, R. COLAH & D. MOHANTY. (2004) An interplay of alleviating mutations in the clinical phenotype of beta-thalassaemia intermedia. Clinical and Laboratory Haematology 26:6, pages 419-422.
Crossref
Crossref
Ishwar C. Verma. 2004. Genetic Disorders of the Indian Subcontinent. Genetic Disorders of the Indian Subcontinent
501
518
.
Anju Gupta, Yukio Hattori, Usha R. Gupta, Swati Sarwai, Nitu Nigam, Pragya Singhal & Sarita Agarwal. (2003) Molecular Genetic Testing of β-Thalassemia Patients of Indian Origin and a Novel 8-bp Deletion Mutation at Codons 36/37/38/39. Genetic Testing 7:2, pages 163-168.
Crossref
Crossref
I. C. Verma, Renu Saxena, Meena Lall, Sunita Bijarnia & Rajesh Sharma. (2003) Genetic counseling and prenatal diagnosis in India — experience at Sir Ganga Ram Hospital. The Indian Journal of Pediatrics 70:4, pages 293-297.
Crossref
Crossref