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Roshan Colah

bhabha atomic research center (barc)

36H指数
243论文数
5.0K被引数
收录论文 32
发表时间
Casting light on the national mission to eliminate sickle cell disease in India
err2024-10-19
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errOAAI
errPiel, Frederic B.; Colah, Roshan; Jain, Dipty L.
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Defining global strategies to improve outcomes in sickle cell disease: a Lancet Haematology Commission
err2023-08-01
err41
errOAAI
errPiel, Frederic B.; Rees, David C.; DeBaun, Michael R.; Nnodu, Obiageli; Ranque, Brigitte; Thompson, Alexis A.; Ware, Russell E.; Abboud, Miguel R.; Abraham, Allistair; Ambrose, Emmanuela E.; Andemariam, Biree; Colah, Roshan; Colombatti, Raffaella; Conran, Nicola; Costa, Fernando F.; Cronin, Robert M.; de Montalembert, Mariane; Elion, Jacques; Esrick, Erica; Greenway, Anthea L.; Idris, Ibrahim M.; Issom, David-Zacharie; Jain, Dipty; Jordan, Lori C.; Kaplan, Zane S.; King, Allison A.; Lloyd-Puryear, Michele; Oppong, Samuel A.; Sharma, Akshay; Sung, Lillian; Tshilolo, Leon; Wilkie, Diana J.; Ohene-Frempong, Kwaku
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Significance of borderline HbA2 levels in β thalassemia carrier screening
err2022-03-30
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errOAAI
errColaco, Stacy; Colah, Roshan; Nadkarni, Anita
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Newborn Screening for Sickle Cell Disease Among Tribal Populations in the States of Gujarat and Madhya Pradesh in India: Evaluation and Outcome Over 6 Years
err2022-02-15
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errOAAI
errThaker, Pallavi; Colah, Roshan B.; Patel, Jignisha; Raicha, Bhavesh; Mistry, Abhishek; Mehta, Vishal; Italia, Yazdi; Desai, Shrey; Dave, Kapilkumar; Shanmugam, Rajasubramaniam; Ghosh, Kanjaksha; Mukherjee, Malay B.
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Editorial: Frontiers in Hemoglobinopathies: New Insights and Methods
err2021-03-19
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errOAAI
errRisoluti, Roberta; Colah, Roshan; Materazzi, Stefano
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Genotypic-phenotypic heterogeneity of δβ-thalassemia and hereditary persistence of fetal hemoglobin (HPFH) in India
err2020-06-10
err6
PREAI
errHariharan, Priya; Kishnani, Pooja; Sawant, Pratibha; Gorivale, Manju; Mehta, Pallavi; Kargutkar, Neha; Colah, Roshan; Nadkarni, Anita
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Differential role of Kruppel like factor 1 (KLF1) gene in red blood cell disorders
err2019-12-01
err19
errOAAI
errHariharan, Priya; Colah, Roshan; Ghosh, Kanjaksha; Nadkarni, Anita
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The spatial epidemiology of sickle-cell anaemia in India
err2018-12-06
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errOAAI
errHockham, Carinna; Bhatt, Samir; Colah, Roshan; Mukherjee, Malay B.; Penman, Bridget S.; Gupta, Sunetra; Piel, Frederic B.
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Can hydroxyurea serve as a free radical scavenger and reduce iron overload in β-thalassemia patients?
err2016-07-27
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PREAI
errItalia, Khushnooma; Chandrakala, S.; Ghosh, Kanjaksha; Colah, Roshan
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Influence of single nucleotide polymorphisms in the BCL11A and HBS1L-MYB gene on the HbF levels and clinical severity of sickle cell anaemia patients
err2016-04-20
err7
PREAI
errUpadhye, Dipti; Jain, Dipty; Trivedi, Yogesh; Nadkarni, Anita; Ghosh, Kanjaksha; Colah, Roshan
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Correlation between 'H' blood group antigen and Plasmodium falciparum invasion
err2016-04-12
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PREAI
errPathak, Vrushali; Colah, Roshan; Ghosh, Kanjaksha
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Diverse phenotypes and transfusion requirements due to interaction of β-thalassemias with triplicated α-globin genes
err2015-08-29
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PREAI
errMehta, Pallavi R.; Upadhye, Dipti S.; Sawant, Pratibha M.; Gorivale, Manju S.; Nadkarni, Anita H.; Shanmukhaiah, Chandrakala; Ghosh, Kanjaksha; Colah, Roshan B.
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Do UGT1A1 and HMOX1 gene promoter polymorphisms increase the risk of hyperbilirubinemia and gallstones in patients with hereditary spherocytosis?
err2014-06-20
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PREAI
errWarang, Prashant; Devendra, Rati; D'Silva, Selma; Chiddarwar, Ashish; Kedar, Prabhakar; Ghosh, Kanjaksha; Colah, Roshan; Mukherjee, Malay B.
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Sickle cell disease in India
err2014-05-01
err49
PREAI
errColah, Roshan; Mukherjee, Malay; Ghosh, Kanjaksha
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Clinical and hematological presentation among Indian patients with common hemoglobin variants
err2014-04-01
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PREAI
errItalia, Khushnooma; Upadhye, Dipti; Dabke, Pooja; Kangane, Harshada; Colaco, Stacy; Sawant, Pratibha; Nadkarni, Anita; Gorakshakar, Ajit; Jain, Dipty; Italia, Yazdi; Ghosh, Kanjaksha; Colah, Roshan
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Molecular characterization of β-thalassemia in four communities in South Gujarat-codon 30 (G →aEuroparts per thousandA) a predominant mutation in the Kachhiya Patel community
err2013-05-11
err8
PREAI
errBhukhanvala, Dipal S.; Italia, Khushnooma; Sawant, Pratibha; Colah, Roshan; Ghosh, Kanjaksha; Gupte, Snehalata C.
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