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

CrossRef

Citations 79

h-index 4

Google Scholar

Loading Scholar statistics...

Professional Recognition

No Data Found

There is currently nothing to display here.

Community & Membership

No Data Found

There is currently nothing to display here.

No Data Found

There is currently nothing to display here.

Bio

Hemoglobinopathies, Enzymopathies, Molecular Genetics

Personal Details

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

No Data Found

There is currently nothing to display here.

Scientist F — – Present

Institute of immunodhaemetology (indian counsil of medical research)

Related Profiles

Experts (0)

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

No Data Found

There is currently nothing to display here.

No Data Found

There is currently nothing to display here.

No Data Found

There is currently nothing to display here.

Scholarly Publications

Production of Murine Monoclonal Antibody to Fetal Hemoglobin

Open Access

ARTICLE

Hemoglobin. Year: 2003. Volume: 27 , Pages: 229-234 .

Authors: Iyer, Yegneshwar S.;Patwardhan, Manisha;Pujari, Vaishali;Shinde, Gayatri;Keertikar, Paritosh;Kulkarni, Swati;Colah, Roshan B.;Mohanty, Dipika

10.1081/HEM-120026047

Co-existence of the codon 16 (-C) (β0) and codon 10 (C→A) (β+) mutations on the same β-globin gene

Open Access

ARTICLE

Hemoglobin. Year: 2003. Volume: 27 , Pages: 133-135 .

Authors: Colah, R.B., Nadkarni, A., Pawar, A., Gorakshakar, A., Phanasgaonkar, S., Mohanty, D.

10.1081/HEM-120021549

Molecular characterization of G6PD Insuli - A novel 989 CGC → CAC (330 Arg → His) mutation in the Indian population

Open Access

ARTICLE

Blood Cells, Molecules, and Diseases. Year: 2003. Volume: 30 , Pages: 246-247 .

Authors: Sukumar, S.;Mukherjee, M. B.;Colah, R. B.;Mohanty, D.

10.1016/S1079-9796(03)00018-4

G6PD deficiency and malaria in India [1]

Open Access

ARTICLE

AMERICAN JOURNAL OF HEMATOLOGY. Year: 2003. Volume: 72 , Pages: 150-151 .

Authors: Mohanty, D.;Sukumar, S.;Mukherjee, M. B.;Colah, R. B.

10.1002/ajh.10276

Congenital methemoglobinemia due to NADH-methemo-globin reductase deficiency in three Indian families

Open Access

ARTICLE

Year: 2002. Volume: 32 , Pages: 543-549 .

Authors: Kedar, Prabhakar S.;Colah, Roshan B.;Ghosh, Kanjaksha;Mohanty, Dipika

Genetic disorders in haematological practice in India

Open Access

ARTICLE

Year: 2002. Volume: 5 , Pages: 197-200 .

Authors: Mohanty, D.;Colah, R. B.;Gorakshakar, A. C.;Nadkarni, A. H.;Phanasgaonkar, S. P.;Shetty, S.;Ghosh, K.;Mukherjee, M. B.

10.1159/000066336

Chronic persistent hemolysis in an infant: Can we afford to forget malaria as a cause? [1]

Open Access

ARTICLE

Year: 2002. Volume: 3 , Pages: 114-115 .

Authors: Kedar, Prabhakar S.;Ghosh, Kanjaksha;Colah, Roshan B.;Mohanty, Dipika

10.1038/sj.thj.6200155

A novel β0-thalassemia mutation at codon 55 (-A) and a rare 17 bp deletion at codons 126-131 in the Indian population

Open Access

ARTICLE

Hemoglobin. Year: 2002. Volume: 26 , Pages: 41-47 .

Authors: Nadkarni, A., Sakaguchi, T., Takaku, H., Gorakshakar, A., Phanasgaonkar, S., Colah, R.B., Mohanty, D., Kiyama, R.

10.1081/HEM-120002939

Showing 153 to 160 of 197 results