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

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Professional Recognition

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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)

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

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Scholarly Publications

Congenital methemoglobinemia caused by Hb-MRatnagiri (β-63CAT→TAT, His→Tyr) in an Indian family

Open Access

ARTICLE

AMERICAN JOURNAL OF HEMATOLOGY. Year: 2005. Volume: 79 , Pages: 168-170 .

Authors: Kedar, P.S., Nadkarni, A.H., Phanasgoankar, S., Madkaikar, M., Ghosh, K., Gorakshakar, A.C., Colah, R.B., Mohanty, D.

10.1002/ajh.20368

Three novel polymorphisms in the β globin gene

Open Access

ARTICLE

AMERICAN JOURNAL OF HEMATOLOGY. Year: 2005. Volume: 80 , Pages: 161-163 .

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

10.1002/ajh.20453

Two distinct Indian G6PD variants G6PD Jamnagar and G6PD Rohini caused by the same 949 G→A mutation

Open Access

ARTICLE

Blood Cells, Molecules, and Diseases. Year: 2005. Volume: 35 , Pages: 193-195 .

Authors: Sukumar, Sridevi;Mukherjee, Malay B.;Colah, Roshan B.;Mohanty, Dipika

10.1016/j.bcmd.2005.03.001

Hemoglobin sickle D Punjab - A case report

Open Access

ARTICLE

Year: 2005. Volume: 11 , Pages: 154-155 .

Authors: Mukherjee, M. B.;Surve, R. R.;Gangakhedkar, R. R.;Mohanty, D.;Colah, R. B.

Detection of two rare β-thalassemia mutations [-90 (C → T) and CD 26 (C → T)] among Indians

Open Access

ARTICLE

Year: 2005. Volume: 11 , Pages: 76-79 .

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

Prenatal diagnosis of sickle syndromes in India: Dilemmas in counselling

Open Access

ARTICLE

PRENATAL DIAGNOSIS. Year: 2005. Volume: 25 , Pages: 345-349 .

Authors: Colah, Roshan;Surve, Reema;Nadkarni, Anita;Gorakshakar, Ajit;Phanasgaonkar, Supriya;Satoskar, Poornima;Mohanty, Dipika

10.1002/pd.1131

Prenatal diagnosis in a family at risk for β-thalassemia and hemophilia A: An uncommon association

Open Access

ARTICLE

Hemoglobin. Year: 2004. Volume: 28 , Pages: 343-346 .

Authors: Colah, Roshan B.;Shetty, Shrimati D.;Surve, Reema R.;Phanasgaonkar, Supriya P.;Nadkarni, Anita H.;Gorakshakar, Ajit C.;Ghosh, Kanjaksha;Parekh, Sunil J.;Mohanty, Dipika

10.1081/HEM-200037719

Masking of the clinical severity of severe haemophilia A in a patient with β-thalassemia major - Its implications in prenatal diagnosis [3]

Open Access

ARTICLE

PRENATAL DIAGNOSIS. Year: 2004. Volume: 24 , Pages: 925-926 .

Authors: Colah, Roshan;Shetty, Shrimati;Nadkarni, Anita;Ghosh, Kanjaksha;Mohanty, Dipika

10.1002/pd.979

Showing 137 to 144 of 197 results