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Dr Roshan B. Colah

vidwan id: 12033
Female

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

Publications

Total Articles 197
Books 0
Proceedings 0

Publications

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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+)

Co-Authors (5)

Jagadish

Dr Jagadish Mahanta

Regional Medical Research Centre ICMR

Kanjaksha

Dr Kanjaksha Ghosh

Institute of immunodhaemetology (indian counsil of medical research)

Mitali

Prof Mitali Mukerji

Indian Institute of Technology Jodhpur

Partha Pratim

Prof Partha Pratim Majumder

National Institute Of Biomedical Genomics

Selma

Dr Selma Dsilva

Advanced Centre for Treatment, Research and Education in Cancer

Scholarly Work

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Scholarly Publications

Iron deficiency anaemia in sickle cell disorders in India

Open Access
ARTICLE
Authors: Mohanty, Dipika;Mukherjee, M. B.;Colah, R. B.;Wadia, M.;Ghosh, K.;Chottray, G. P.;Jain, D.;Italia, Y.;Ashokan, K.;Kaul, R.;Shukla, D. K.;Muthuswamy, V.

Hb Showa Yakushiji [β 110 (G12) Leu → Pro] in 3 families from Western India: First report on homozygous Hb Showa Yakushiji

Open Access
ARTICLE
Authors: Colah, R.;Nadkarni, A.;Gorakshakar, A.;Phanasgaonkar, S.;Sawant, P.;Surve, R.;Mohanty, D.;Ghosh, K.

Evaluation of the use of monoclonal antibodies and nested PCR for noninvasive prenatal diagnosis of hemoglobinopathies in India

Open Access
ARTICLE
Authors: D'Souza, Edna;Sawant, Pratibha M.;Nadkarni, Anita H.;Gorakshakar, Ajit;Mohanty, Dipika;Ghosh, Kanjaksha;Colah, Roshan B.

Prevalence and molecular characterization of α-thalassemia syndromes among Indians

Open Access
ARTICLE
Authors: Nadkarni, Anita;Phanasgaonkar, Supriya;Colah, Roshan;Mohanty, Dipika;Ghosh, Kanjaksha

A novel G143D mutation in the NADH-cytochrome b5 reductase gene in an Indian patient with type I recessive hereditary methemoglobinemia

Open Access
ARTICLE

Frequency of partial D in Western India

Open Access
ARTICLE
Authors: Kulkarni, S.;Colah, R.;Gorakshakar, A.;Gupte, S.;Vasantha, K.;Mohanty, D.;Ghosh, K.

A novel R198H mutation in the glucose-6-phosphate dehydrogenase gene in the tribal groups of the Nilgiris in Southern India

Open Access
ARTICLE
Authors: Chalvam, R.;Kedar, P. S.;Colah, R. B.;Ghosh, K.;Mukherjee, M. B.

Molecular characterization of δβ-thalassemia and hereditary persistence of fetal hemoglobin in the Indian population

Open Access
ARTICLE
Authors: Nadkarni, Anita;Wadia, Marukh;Gorakshakar, Ajit;Kiyama, Ryoiti;Colah, Roshan B.;Mohanty, Dipika