Dr Roshan B. Colah

vidwan id: 12033

Female

Scientist F,
Institute of immunodhaemetology (indian counsil of medical research)

7003396083

Publications

Total Articles 197

Books 0

Proceedings 0

Publications

Scopus

Citations 79

h-index 5

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Citations 79

h-index 4

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Bio

Hemoglobinopathies, Enzymopathies, Molecular Genetics

Personal Details

Female
Scientist F , Institute of immunodhaemetology (indian counsil of medical research)
Mumbai, Maharashtra, India

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Scientist F — – Present

Institute of immunodhaemetology (indian counsil of medical research)

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Organisations (1+)

Dr Umair Ahmed Bargir

Scientist C

Dr Babu Rao Vundinti

Scientist F

Co-Authors (5)

Dr Jagadish Mahanta

Regional Medical Research Centre ICMR

Dr Kanjaksha Ghosh

Institute of immunodhaemetology (indian counsil of medical research)

Prof Mitali Mukerji

Indian Institute of Technology Jodhpur

Prof Partha Pratim Majumder

National Institute Of Biomedical Genomics

Dr Selma Dsilva

Advanced Centre for Treatment, Research and Education in Cancer

Scholarly Work

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Scholarly Publications

Molecular characterization of β-thalassemia in four communities in South Gujarat - Codon 30 (G → A) a predominant mutation in the Kachhiya Patel community

Open Access

ARTICLE

Annals of Hematology. Year: 2013. Volume: 92 , Pages: 1473-1476 .

Authors: Bhukhanvala, Dipal S.;Italia, Khushnooma;Sawant, Pratibha;Colah, Roshan;Ghosh, Kanjaksha;Gupte, Snehalata C.

10.1007/s00277-013-1777-2

Effect of cis acting potential regulators in the ß globin gene cluster on the production of HbF in thalassemia patients

Open Access

ARTICLE

Mediterranean Journal of Hematology and Infectious Diseases. Year: 2013. Volume: 5 , Pages: 1533-1539 .

Authors: Dabke, Pooja;Colah, Roshan;Ghosh, Kanjaksha;Nadkarni, Anita

10.4084/MJHID.2013.012

Antenatal screening for identification of couples for prenatal diagnosis of severe hemoglobinopathies in Surat, South Gujarat

Open Access

ARTICLE

Year: 2013. Volume: 63 , Pages: 123-127 .

Authors: Bhukhanvala, Dipal S.;Sorathiya, Smita M.;Sawant, Pratibha;Colah, Roshan;Ghosh, Kanjaksha;Gupte, Snehalata C.

10.1007/s13224-012-0271-4

New missense homozygous mutation (Q270Ter) in the pyrimidine 5′ nucleotidase type I-related gene in two Indian families with hereditary non-spherocytic hemolytic anemia

Open Access

ARTICLE

Annals of Hematology. Year: 2013. Volume: 92 , Pages: 715-717 .

Authors: Warang, Prashant;Kedar, Prabhakar;Kar, Rakhee;Ghosh, Kanjaksha;Colah, Roshan

10.1007/s00277-012-1616-x

Variable presentation of HB H disease due to homozygosity for the rare polyadenylation signal a TIndian (AATAAA>AATA-) mutation in four Indian families

Open Access

ARTICLE

Hemoglobin. Year: 2013. Volume: 37 , Pages: 277-284 .

Authors: Nair, S.B., Nadkarni, A.H., Ghosh, K., Colah, R.B.

10.3109/03630269.2013.774284

The Fc receptor polymorphisms and expression of neutrophil activation markers in patients with sickle cell disease from western India

Open Access

ARTICLE

BioMed Research International. Year: 2013. Volume: 2013 , Pages: 381-393 .

Authors: Kangne, Harshada K.;Jijina, Farah F.;Italia, Yazdi M.;Jain, Dipti L.;Nadkarni, Anita H.;Gupta, Maya;Pradhan, Vandana;Mukesh, Rati D.;Ghosh, Kanjaksha K.;Colah, Roshan B.

10.1155/2013/457656

Hydroxyurea could be a good clinically relevant iron chelator

Open Access

ARTICLE

PLoS ONE. Year: 2013. Volume: 8 , Pages: 101-119 .

Authors: Italia, Khushnooma;Colah, Roshan;Ghosh, Kanjaksha

10.1371/journal.pone.0082928

UDP-glucuronosyltransferase 1A1 (UGT1A1) gene haplotypes and their effect on serum bilirubin concentration in healthy Indian adults

Open Access

Article

Year: 2013. Volume: 513 , Issue: 1 , Pages: 36-39 .

Authors: D'Silva S.;Colah R.;Ghosh K.;Mukherjee M.

10.1016/j.gene.2012.10.081

Dr Roshan B. Colah

Publications

Publications

Scopus

CrossRef

Google Scholar

Professional Recognition

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Community & Membership

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Bio

Personal Details

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Related Profiles

Experts (0)

Organisations (1+)

Co-Authors (5)

Scholarly Work

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Scholarly Publications

Molecular characterization of β-thalassemia in four communities in South Gujarat - Codon 30 (G → A) a predominant mutation in the Kachhiya Patel community

Effect of cis acting potential regulators in the ß globin gene cluster on the production of HbF in thalassemia patients

Antenatal screening for identification of couples for prenatal diagnosis of severe hemoglobinopathies in Surat, South Gujarat

New missense homozygous mutation (Q270Ter) in the pyrimidine 5′ nucleotidase type I-related gene in two Indian families with hereditary non-spherocytic hemolytic anemia

Variable presentation of HB H disease due to homozygosity for the rare polyadenylation signal a TIndian (AATAAA&gt;AATA-) mutation in four Indian families

The Fc receptor polymorphisms and expression of neutrophil activation markers in patients with sickle cell disease from western India

Hydroxyurea could be a good clinically relevant iron chelator

UDP-glucuronosyltransferase 1A1 (UGT1A1) gene haplotypes and their effect on serum bilirubin concentration in healthy Indian adults

Variable presentation of HB H disease due to homozygosity for the rare polyadenylation signal a TIndian (AATAAA>AATA-) mutation in four Indian families