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Roshan Colah

This is a preview profile on BiomedExperts - the first literature-based scientific social network. It brings the right researchers together and allows them to collaborate online. Collexis and Dell provide the BiomedExperts network of +1.5 Million pre-calculated profiles free of charge to researchers worldwide.

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Geographic Areas

India

Disorders

Chemicals & Drugs

Procedures

Physiology

Living Beings

Heterozygote

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Co-Publications
Name
53
Mohanty, Dipika
35
Ghosh, Kanjaksha
30
Gorakshakar, Ajit
27
Nadkarni, Anita
17
Surve, Reema
16
Phanasgaonkar, Dr. Supriya
14
Mukherjee, Malay
10
Kedar, Prabhakar
7
Pawar, Aruna
5
Wadia, Mahrukh
4
Shetty, Shrimati
4
Tamankar, AA
4
Kiyama, Ryoiti
4
Gangakhedkar, Raman
3
Krishnamoorthy, Rajagopal

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Publications

TOP 3
Chalvam Rati; Colah Roshan B; Mohanty Dipika; Ghosh Kanjaksha; Mukherjee Malay B
Molecular heterogeneity of glucose-6-phosphate dehydrogenase deficiency among the tribals in Western India.
Italia Khushnooma Y; Jijina Farah J; Merchant Rashid; Panjwani Sangeeta; Nadkarni Anita H; Sawant Pratibha M; Nair Sona B; Ghosh Kanjaksha; Colah Roshan B
Response to hydroxyurea in beta thalassemia major and intermedia: experience in western India.
Colah Roshan; Gorakshakar Ajit; Nadkarni Anita; Phanasgaonkar Supriya; Surve Reema; Sawant Pratibha; Mohanty Dipika; Ghosh Kanjaksha
Regional heterogeneity of beta-thalassemia mutations in the multi ethnic Indian population.

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All Publications

2009: Chalvam Rati; Colah Roshan B; Mohanty Dipika; Ghosh Kanjaksha; Mukherjee Malay B
Molecular heterogeneity of glucose-6-phosphate dehydrogenase deficiency among the tribals in Western India.
Blood cells, molecules & diseases 2009;43(2):156-7.
2009: Italia Khushnooma Y; Jijina Farah J; Merchant Rashid; Panjwani Sangeeta; Nadkarni Anita H; Sawant Pratibha M; Nair Sona B; Ghosh Kanjaksha; Colah Roshan B
Response to hydroxyurea in beta thalassemia major and intermedia: experience in western India.
Clinica chimica acta; international journal of clinical chemistry 2009;407(1-2):10-5.
2009: Colah Roshan; Gorakshakar Ajit; Nadkarni Anita; Phanasgaonkar Supriya; Surve Reema; Sawant Pratibha; Mohanty Dipika; Ghosh Kanjaksha
Regional heterogeneity of beta-thalassemia mutations in the multi ethnic Indian population.
Blood cells, molecules & diseases 2009;42(3):241-6.
2009: Colah Roshan B
Evaluation of chromatographic & electrophoretic methods for diagnosis of the beta-thalassaemias.
The Indian journal of medical research 2009;129(3):221-2.
2009: Italia Khushnooma; Jain Dipty; Gattani Sushma; Jijina Farah; Nadkarni Anita; Sawant Pratibha; Nair Sona; Mohanty Dipika; Ghosh Kanjaksha; Colah Roshan
Hydroxyurea in sickle cell disease--a study of clinico-pharmacological efficacy in the Indian haplotype.
Blood cells, molecules & diseases 2009;42(1):25-31.
2009: Nadkarni Anita; Gorakshakar Ajit; Surve Reema; Sawant Pratibha; Phanasgaonkar Supriya; Nair Sona; Ghosh Kanjaksha; Colah Roshan B
Hematological and molecular analysis of novel and rare beta-thalassemia mutations in the Indian population.
Hemoglobin 2009;33(1):59-65.
2008: D'Souza Edna; Sawant Pratibha M; Nadkarni Anita H; Gorakshakar Ajit; Mohanty Dipika; Ghosh Kanjaksha; Colah Roshan B
Evaluation of the use of monoclonal antibodies and nested PCR for noninvasive prenatal diagnosis of hemoglobinopathies in India.
American journal of clinical pathology 2008;130(2):202-9.
2008: Nadkarni Anita; Phanasgaonkar Supriya; Colah Roshan; Mohanty Dipika; Ghosh Kanjaksha
Prevalence and molecular characterization of alpha-thalassemia syndromes among Indians.
Genetic testing 2008;12(2):177-80.
2008: Colah Roshan; Surve Reema; Wadia Marukh; Solanki Prakash; Mayekar Pramod; Thomas Mariamma; Gorakshakar Ajit; Dastur Adi; Mohanty Dipika
Carrier screening for beta-thalassemia during pregnancy in India: a 7-year evaluation.
Genetic testing 2008;12(2):181-5.
2008: Kedar Prabhakar S; Warang Prashant; Nadkarni Anita H; Colah Roshan B; Ghosh Kanjaksha
A novel G143D mutation in the NADH-cytochrome b5 reductase gene in an Indian patient with type I recessive hereditary methemoglobinemia.
Blood cells, molecules & diseases 2008;40(3):323-7.
2008: Nadkarni Anita; Wadia Marukh; Gorakshakar Ajit; Kiyama Ryoiti; Colah Roshan B; Mohanty Dipika
Molecular characterization of delta beta-thalassemia and hereditary persistence of fetal hemoglobin in the Indian population.
Hemoglobin 2008;32(5):425-33.
2008: Chalvam R; Kedar P S; Colah R B; Ghosh K; Mukherjee M B
A novel R198H mutation in the glucose-6-phosphate dehydrogenase gene in the tribal groups of the Nilgiris in Southern India.
Journal of human genetics 2008;53(2):181-4.
2007: Italia K Y; Colah R; Mohanty D
Evaluation of F cells in sickle cell disorders by flow cytometry -- comparison with the Kleihauer-Betke's slide method.
International journal of laboratory hematology 2007;29(6):409-14.
2007: Gorakshakar Ajit C; Das Manoj K; Phanasgaokar Supriya P; Nadkarni Anita H; Colah Roshan B; Mohanty Dipika
Origin of the codon 47 (+A) beta-thalassaemia mutation among the Nicobarese of the Andaman and Nicobar islands in India.
British journal of haematology 2007;139(2):345-6.
2007: Nadkarni A; Surve R; Colah R; Ghosh K; Holay M; Dani A; Shrikhande A; Bharti V; Suryawanshi S
Thalassemia intermedia due to homozygosity for an Asian Indian (Agammadeltabeta) degrees deletional inversion.
Clinica chimica acta; international journal of clinical chemistry 2007;385(1-2):81-3.
2007: Colah R B; Surve R; Sawant P; D'Souza E; Italia K; Phanasgaonkar S; Nadkarni A H; Gorakshakar A C
HPLC studies in hemoglobinopathies.
Indian journal of pediatrics 2007;74(7):657-62.
2007: Kulkarni S S; Gorakshakar A C; Colah R B; Gupte S C; Mohanty D
Usefulness of prenatal detection of RhD typing by molecular analysis in Indians.
Journal of postgraduate medicine 2007;53(2):149.
2007: Chalvam R; Mukherjee M B; Colah R B; Mohanty D; Ghosh K
G6PD Namoru (208 T--> C) is the major polymorphic variant in the tribal populations in southern India.
British journal of haematology 2007;136(3):512-3.
2007: Gupta Neerja; Bianchi Paola; Fermo Elisa; Kabra Madhulika; Warang Prashant; Kedar Prabhakar; Gupta Nomeeta; Colah Roshan
Prenatal diagnosis for a novel homozygous mutation in PKLR gene in an Indian family.
Prenatal diagnosis 2007;27(2):117-8.
2007: Phanasgaonkar S; Colah R; Ghosh K; Mohanty D; Gupte S
Hb Q(India) and its interaction with beta-thalassaemia: a study of 64 cases from India.
British journal of biomedical science 2007;64(4):160-3.
2007: Kedar P S; Nampoothiri S; Sreedhar S; Ghosh K; Shimizu K; Kanno H; Colah R B
First-trimester prenatal diagnosis of pyruvate kinase deficiency in an Indian family with the pyruvate kinase-Amish mutation.
Genetics and molecular research : GMR 2007;6(2):470-5.
2007: Colah Roshan; Thomas Mariamma; Mayekar Pramod
Assessing the impact of screening and counselling high school children for beta-thalassaemia in India.
Journal of medical screening 2007;14(3):158.
2007: D'Souza Edna; Kulkarni Swati; Colah Roshan B; Mohanty Dipika
An improved flow cytometric approach for isolation of fetal cells from maternal blood for non invasive prenatal diagnosis of hemoglobinopathies.
Hemoglobin 2007;31(1):39-48.
2006: Kedar Prabhakar S; Warang Prashant; Colah Roshan B; Mohanty Dipika
Red cell pyruvate kinase deficiency in neonatal jaundice cases in India.
Indian journal of pediatrics 2006;73(11):985-8.
2006: Babu Rao V; Colah Roshan B
Chromosomal instability in bone marrow failure syndromes.
The Indian journal of medical research 2006;124(1):11-2.
2005: Nadkarni A; Sakaguchi T; Gorakshakar A; Phanasgaonkar S; Colah R; Mohanty D; Kiyama R
Three novel polymorphisms in the beta globin gene.
American journal of hematology 2005;80(2):161-3.
2005: Sukumar Sridevi; Mukherjee Malay B; Colah Roshan B; Mohanty Dipika
Two distinct Indian G6PD variants G6PD Jamnagar and G6PD Rohini caused by the same 949 G-->A mutation.
Blood cells, molecules & diseases 2005;35(2):193-5.
2005: Kedar Prabhakar S; Nadkarni Anita H; Phanasgoankar Supriya; Madkaikar Manisha; Ghosh Kanjaksha; Gorakshakar Ajit C; Colah Roshan B; Mohanty Dipika
Congenital methemoglobinemia caused by Hb-MRatnagiri (beta-63CAT-->TAT, His-->Tyr) in an Indian family.
American journal of hematology 2005;79(2):168-70.
2005: Colah Roshan; Surve Reema; Nadkarni Anita; Gorakshakar Ajit; Phanasgaonkar Supriya; Satoskar Poornima; Mohanty Dipika
Prenatal diagnosis of sickle syndromes in India: dilemmas in counselling.
Prenatal diagnosis 2005;25(5):345-9.
2004: Nadkarni A; Sakaguchi T; Gorakshakar A; Phanasgaonkar S; Kiyama R; Colah R; Mohanty D
An interplay of alleviating mutations in the clinical phenotype of beta-thalassaemia intermedia.
Clinical and laboratory haematology 2004;26(6):419-22.
2004: Colah Roshan; Shetty Shrimati; Nadkarni Anita; Ghosh Kanjaksha; Mohanty Dipika
Masking of the clinical severity of severe haemophilia A in a patient with beta-thalassemia major--its implications in prenatal diagnosis.
Prenatal diagnosis 2004;24(11):925-6.
2004: Colah Roshan; Nadkarni Anita; Gorakshakar Ajit; Phanasgaonkar Supriya; Surve Reema; Subramaniam P G; Bondge Nagnath; Pujari Kamala; Ghosh Kanjaksha; Mohanty Dipika
Impact of beta globin gene mutations on the clinical phenotype of beta thalassemia in India.
Blood cells, molecules & diseases 2004;33(2):153-7.
2004: Sukumar Sridevi; Mukherjee Malay B; Colah Roshan B; Mohanty Dipika
Molecular basis of G6PD deficiency in India.
Blood cells, molecules & diseases 2004;33(2):141-5.
2004: Mohanty Dipika; Mukherjee Malay B; Colah Roshan B
Glucose-6-phosphate dehydrogenase deficiency in India.
Indian journal of pediatrics 2004;71(6):525-9.
2004: Kedar Prabhakar S; Colah Roshan B; Ghosh Kanjaksha; Mohanty Dipika
Hereditary spherocytosis in association with severe G6PD deficiency: report of an unusual case.
Clinica chimica acta; international journal of clinical chemistry 2004;344(1-2):221-4.
2004: Mukherjee Malay B; Surve Reema R; Gangakhedkar Raman R; Ghosh Kanjaksha; Colah Roshan B; Mohanty Dipika
Beta-globin gene cluster haplotypes linked to the betaS gene in western India.
Hemoglobin 2004;28(2):157-61.
2004: Gorakshakar Ajit C; Phanasgaonkar Supriya P; Nadkarni Anita H; Colah Roshan B; Mohanty Dipika
Detection of rare beta-thalassemia mutations by denaturing gradient gel electrophoresis among Indians.
Hemoglobin 2004;28(1):15-24.
2004: 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
Prenatal diagnosis in a family at risk for beta-thalassemia and hemophilia A: an uncommon association.
Hemoglobin 2004;28(4):343-6.
2003: Kedar P S; Colah R B; Kulkarni S; Ghosh K; Mohanty D
Experience with eosin-5'-maleimide as a diagnostic tool for red cell membrane cytoskeleton disorders.
Clinical and laboratory haematology 2003;25(6):373-6.
2003: Iyer Yegneshwar S; Patwardhan Manisha; Pujari Vaishali; Shinde Gayatri; Keertikar Paritosh; Kulkarni Swati; Colah Roshan B; Mohanty Dipika
Production of murine monoclonal antibody to fetal hemoglobin.
Hemoglobin 2003;27(4):229-34.
2003: Colah Roshan B; Nadkarni Anita; Pawar Aruna; Gorakshakar Ajit; Phanasgaonkar Supriya; Mohanty Dipika
Co-existence of the codon 16 (-C) (beta(o)) and codon 10 (C --> A) (beta+) mutations on the same beta-globin gene.
Hemoglobin 2003;27(2):133-5.
2003: Sukumar S; Mukherjee M B; Colah R B; Mohanty D
Molecular characterization of G6PD Insuli--a novel 989 CGC --> CAC (330 Arg --> His) mutation in the Indian population.
Blood cells, molecules & diseases 2003;30(3):246-7.
2003: Mohanty D; Sukumar S; Mukherjee M B; Colah R B
G6PD deficiency and malaria in India.
American journal of hematology 2003;72(2):150-1.
2002: Sukumar Sridevi; Colah Roshan; Mohanty Dipika
G6PD gene mutations in India producing drug-induced haemolytic anaemia.
British journal of haematology 2002;116(3):671-2.
2002: Nadkarni Anita; Sakaguchi Takehisa; Takaku Hiroshi; Gorakshakar Ajit; Phanasgaonkar Supriya; Colah Roshan B; Mohanty Dipika; Kiyama Ryoiti
A novel beta0-thalassemia mutation at codon 55 (-A) and a rare 17 bp deletion at codons 126-131 in the Indian population.
Hemoglobin 2002;26(1):41-7.
2002: Wadia Mahrukh R; Phanasgaokar Supriya P; Nadkarni Anita H; Surve Reema R; Gorakshakar Ajit C; Colah Roshan B; Mohanty Dipika
Usefulness of automated chromatography for rapid fetal blood analysis for second trimester prenatal diagnosis of beta-thalassemia.
Prenatal diagnosis 2002;22(2):153-7.
2002: Mohanty D; Colah R B; Gorakshakar A C; Nadkarni A H; Phanasgaonkar S P; Shetty S; Ghosh K; Mukherjee M B
Genetic disorders in haematological practice in India.
Community genetics 2002;5(3):197-200.
2002: Kedar Prabhakar S; Colah Roshan B; Ghosh Kanjaksha; Mohanty Dipika
Congenital methemoglobinemia due to NADH-methemoglobin reductase deficiency in three Indian families.
Haematologia 2002;32(4):543-9.
2002: Kedar Prabhakar S; Ghosh Kanjaksha; Colah Roshan B; Mohanty Dipika
Chronic persistent hemolysis in an infant: can we afford to forget malaria as a cause?
The hematology journal : the official journal of the European Haematology Association / EHA 2002;3(2):114-5.
2001: Murhekar K M; Murhekar M V; Mukherjee M B; Gorakshakar A C; Surve R; Wadia M; Phanasgaonkar S; Shridevi S; Colah R B; Mohanty D
Red cell genetic abnormalities, beta-globin gene haplotypes, and APOB polymorphism in the Great Andamanese, a primitive Negrito tribe of Andaman and Nicobar Islands, India.
Human biology; an international record of research 2001;73(5):739-44.
2001: Nadkarni A; Gorakshakar A C; Lu C Y; Krishnamoorthy R; Ghosh K; Colah R; Mohanty D
Molecular pathogenesis and clinical variability of beta-thalassemia syndromes among Indians.
American journal of hematology 2001;68(2):75-80.
2001: Colah R; Wadia M; Surve R; Nadkarni A; Phanasgaonkar S; Gorakshakar A; Mohanty D; Promé D; Wajcman H
Hb D-Agri [beta9(A6)Ser --> Tyr;beta121(GH4)Glu --> Gln]: a new Indian hemoglobin variant with two amino acid substitutions in the same beta chain.
Hemoglobin 2001;25(3):317-21.
2001: Mukherjee M B; Surve R R; Gorakshakar A C; Gangakhedkar R R; Colah R B; Mohanty D
Symptomatic presentation of a sickle cell heterozygote: an evaluation of genetic factors.
American journal of hematology 2001;66(4):307-8.
2001: Colah R; Gorakshakar A; Surve R; Wadia M; Ghosh K; Mohanty D
Feasibility of antenatal screening of beta-thalassemia in Mumbai, India.
Acta haematologica 2001;105(4):252.
2000: Pawar A R; Lu C Y; Besmond C; Gorakshakar A C; Colah R B; Mohanty D; Krishnamoorthy R
A simple approach to the characterization of three common Indian beta-thalassemia mutations by artificially created restriction sites.
Hemoglobin 2000;24(4):311-8.
2000: Gorakshakar A C; Ghosh K; Colah R B; Mohanty D
Beta-thalassemia gene flow from India to Mauritius.
American journal of hematology 2000;65(3):263-4.
2000: Ghosh K; Mukherjee M B; Surve R R; Shankarkumar U; Kate S L; Nagtilak S B; Colah R B; Tamankar A A; Mohanty D
Splenomegaly in school children in a remote tribal area of Dhole district, Maharashtra.
Indian journal of malariology 2000;37(3-4):68-73.
2000: Surve R R; Mukherjee M B; Kate S L; Nagtilak S B; Wadia M; Tamankar A A; Ghosh K; Colah R B; Mohanty D
Detection of the beta s gene: an evaluation of the solubility test against automated chromatography and haemoglobin electrophoresis.
British journal of biomedical science 2000;57(4):292-4.
2000: Mukherjee M B; Surve R R; Ghosh K; Colah R B; Mohanty D
Clinical diversity of sickle cell disease in western india - influence of genetic factors.
Acta haematologica 2000;103(2):122-3.
1999: Nadkarni A; Ghosh K; Gorakshakar A; Colah R; Mohanty D
Variable clinical severity of Hb E beta-thalassemia among Indians.
The Journal of the Association of Physicians of India 1999;47(10):966-8.
1999: Gorakshakar A C; Pawar A R; Nadkarni A H; Lu C Y; Mohanty D; Krishnamoorthy R; Besmond C; Colah R B
Potential of denaturing gradient gel electrophoresis for scanning of beta-thalassemia mutations in India.
American journal of hematology 1999;61(2):120-5.
1998: Mukherjee M B; Surve R; Tamankar A; Colah R; Mohanty D
Trimodal distribution of HbS levels in sickle heterozygotes--an useful predictor of the alpha-genotype for population screening.
The Indian journal of medical research 1998;108():285-90.
1998: Colah R; Mohanty D
Beta-thalassemias: expression, molecular mechanisms and mutations in Indians.
Indian journal of pediatrics 1998;65(6):815-23.
1998: Desai S N; Colah R B; Mohanty D
Comparison of FPLC with cellulose acetate electrophoresis for the diagnosis of beta-thalassaemia trait.
The Indian journal of medical research 1998;108():145-8.
1998: Shetty S; Colah R; Gorakshakar A; Bhide A; Ghosh K; Pathare A; Jijina F; Mohanty D
Prenatal diagnosis of haemophilia: a preliminary report.
The National medical journal of India 1998;11(5):218-9.
1998: Mukherjee M B; Surve R; Tamankar A; Gangakhedkar R R; Ghosh K; Lu C Y; Krishnamoorthy R; Colah R; Mohanty D
The influence of alpha-thalassaemia on the haematological & clinical expression of sickle cell disease in western India.
The Indian journal of medical research 1998;107():178-81.
1997: Gorakshakar A C; Lulla C P; Nadkarni A H; Pawar A R; Desai S N; Colah R B; Mohanty D
Prenatal diagnosis of beta-thalassemia among Indians using denaturing gradient gel electrophoresis.
Hemoglobin 1997;21(5):421-35.
1997: Nadkarni A H; Ghosh K; Mohanty D; Colah R
Hemoglobin E and pyrimidine 5' nucleotidase deficiency.
Blood 1997;90(4):1716.
1997: Desai S; Colah R; Gupte S; Mohanty D
Is cellulose acetate electrophoresis a suitable technique for detection of Hb Bart's at birth?
Human heredity 1997;47(4):181-4.
1997: Mukherjee M B; Lu C Y; Ducrocq R; Gangakhedkar R R; Colah R B; Kadam M D; Mohanty D; Nagel R L; Krishnamoorthy R
Effect of alpha-thalassemia on sickle-cell anemia linked to the Arab-Indian haplotype in India.
American journal of hematology 1997;55(2):104-9.
1997: Colah R B; Nadkarni A H; Mukherjee M B; Gorakshakar A C; Surve R; Mohanty D
Beta-thalassaemia heterozygotes with alpha-globin gene triplication.
British journal of haematology 1997;97(2):506-7.
1997: Pawar A R; Colah R B; Mohanty D
A novel beta+-thalassemia mutation (codon 10 GCC --> GCA) and a rare transcriptional mutation (-28A --> G) in Indians.
Blood 1997;89(10):3888-9.
1997: Shetty S; Ghosh K; Pathare A; Colah R; Badakare S; Mohanty D
Factor VIII and IX gene polymorphisms and carrier analysis in Indian population.
American journal of hematology 1997;54(4):271-5.
1997: Mukherjee M B; Colah R B; Ghosh K; Mohanty D; Krishnamoorthy R
Milder clinical course of sickle cell disease in patients with alpha thalassemia in the Indian subcontinent.
Blood 1997;89(2):732.
1996: Nadkarni A H; Gorakshakar A C; Mohanty D; Colah R B
Alpha genotyping in a heterogeneous Indian population.
American journal of hematology 1996;53(2):149-50.
1995: Nadkarni A; Pawar A; Mudera V C; Mohanty D; Colah R
Clinical heterogeneity of silent-gene b-thalassemia among Indians.
Annals of hematology 1995;70(1):61-4.
1994: Colah R B
Strategies for prevention of thalassemia and hemoglobinopathies.
The Journal of the Association of Physicians of India 1994;42(10):810-4.
1993: Shinde M T; Purandare M; Pawar A; Colah R; Apte S V
Assessment of transcervical chorion villus aspiration biopsy in early pregnancy.
The National medical journal of India 1993;6(1):14-6.
1992: Sayyed Z; Mukherjee M B; Mudera V C; Colah R; Gupte S
Characterization of G6PD Rohini--a new class III Indian variant.
The Indian journal of medical research 1992;96():96-100.

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