Ministry of Education
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Dr Roshan B. Colah

vidwan id: 12033
Female

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

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Publications

Total Articles 197
Books 0
Proceedings 0

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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+)

Umair Ahmed

Dr Umair Ahmed Bargir

Scientist C

Babu Rao

Dr Babu Rao Vundinti

Scientist F

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

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.
DOI 10.1007/s13224-012-0271-4

Hereditary non-spherocytic hemolytic anemia and severe glucose phosphate isomerase deficiency in an Indian patient homozygous for the L487F mutation in the human GPI gene

Open Access
ARTICLE
International Journal of Hematology. Year: 2012. Volume: 96 , Pages: 263-267 .
Authors: Warang, Prashant;Kedar, Prabhakar;Ghosh, Kanjaksha;Colah, Roshan B.
DOI 10.1007/s12185-012-1122-x

Prenatal diagnosis of HbE-Lepore and Hb Lepore-β-thalassemia: The importance of accurate genotyping of the couple at risk

Open Access
ARTICLE
PRENATAL DIAGNOSIS. Year: 2012. Volume: 32 , Pages: 703-707 .
Authors: Italia, Khushnooma;Sheth, Jayesh;Sawant, Pratibha;Nadkarni, Anita;Ghosh, Kanjaksha;Colah, Roshan
DOI 10.1002/pd.3884

Variable haematological and clinical presentation of β-thalassaemia carriers and homozygotes with the Poly A (T→C) mutation in the Indian population

Open Access
ARTICLE
EUROPEAN JOURNAL OF HAEMATOLOGY. Year: 2012. Volume: 89 , Pages: 160-164 .
Authors: Italia, Khushnooma;Sawant, Pratibha;Surve, Reema;Wadia, Marukh;Nadkarni, Anita;Ghosh, Kanjaksha;Colah, Roshan
DOI 10.1111/j.1600-0609.2012.01810

Newborn screening shows a high incidence of sickle cell anemia in central India

Open Access
ARTICLE
Hemoglobin. Year: 2012. Volume: 36 , Pages: 316-322 .
Authors: Jain, Dipty L.;Sarathi, Vijaya;Upadhye, Dipty;Gulhane, Rohini;Nadkarni, Anita H.;Ghosh, Kanjaksha;Colah, Roshan B.
DOI 10.3109/03630269.2012.691434

First case of Hb Fontainebleau with sickle haemoglobin and other non-deletional α gene variants identified in neonates during newborn screening for sickle cell disorders

Open Access
ARTICLE
Year: 2012. Volume: 65 , Pages: 654-659 .
Authors: Upadhye, Dipti S.;Jain, Dipty;Nair, Sona B.;Nadkarni, Anita H.;Ghosh, Kanjaksha;Colah, Roshan B.
DOI 10.1136/jclinpath-2011-200642

G71R mutation of the UGT1A1 gene is not associated with neonatal hyperbilirubinemia in India

Open Access
Letter
Year: 2012. Volume: 25 , Issue: 9 , Pages: 1833-1834 .
Authors: D'Silva S.;Colah R.;Ghosh K.;Mukherjee M.
DOI 10.3109/14767058.2011.644362
4 5

Recessive congenital methemoglobinemia due to NADH-cytochrome b5 reductase deficiency associated with recurrent early pregnancy loss (REPL) in an Indian family

Open Access
ARTICLE
Annals of Hematology. Year: 2012. Volume: 91 , Pages: 1985-1986 .
Authors: Kedar, Prabhakar;Warang, Prashant;Ghosh, Kanjaksha;Colah, Roshan
DOI 10.1007/s00277-012-1513-3