R. V. Shaji

发表

E2 sequence variations of HPV 16 among patients with cervical neoplasia seen in the Indian subcontinent.

G. Chandy, N. Sathish, G. Sridharan, 2004, Gynecologic oncology.

Distribution of the different genotypes of HCV among patients attending a tertiary care hospital in south India.

G. Chandy, B. Ramakrishna, G. Sridharan, 2003, Journal of clinical virology : the official publication of the Pan American Society for Clinical Virology.

Cytochrome P4501A1 and Glutathione S Transferase Gene Polymorphisms in Patients with Aplastic Anemia in India

B. George, M. Chandy, A. Srivastava, 2005, Acta Haematologica.

Treatment of children with newly diagnosed acute promyelocytic leukemia with arsenic trioxide: a single center experience

B. George, M. Chandy, V. Mathews, 2004, Leukemia.

Comparison of Molecular and Conventional Methods for Typing of Enteroviral Isolates

T. Cherian, N. Sathish, G. Sridharan, 2002, Journal of Clinical Microbiology.

Analysis of β globin mutations in the Indian population: presence of rare and novel mutations and region‐wise heterogeneity

B. George, M. Chandy, V. Mathews, 2008, Clinical genetics.

Interaction of Hemoglobin E with Other Abnormal Hemoglobins

M. Chandy, A. Srivastava, E. Edison, 2011, Acta Haematologica.

Hyperbilirubinemia in Homozygous HbE Disease Is Associated with the UGT1A1 Gene Polymorphism

M. Chandy, A. Srivastava, E. Edison, 2005, Hemoglobin.

HCV genotype 4--an emerging threat as a cause of chronic liver disease in Indian (south) patients.

B. Ramakrishna, G. Sridharan, P. Abraham, 2004, Journal of clinical virology : the official publication of the Pan American Society for Clinical Virology.

An outbreak of echovirus meningitis in children.

T. Cherian, N. Sathish, G. Sridharan, 2004, Indian pediatrics.

Polymorphism in factor VII gene modifies phenotype of severe haemophilia

B. George, K. Lakshmi, A. Viswabandya, 2009, Haemophilia : the official journal of the World Federation of Hemophilia.

Identification of factor VIII gene mutations in 101 patients with haemophilia A: mutation analysis by inversion screening and multiplex PCR and CSGE and molecular modelling of 10 novel missense substitutions

M. Chandy, G. Jayandharan, A. Srivastava, 2005, Haemophilia : the official journal of the World Federation of Hemophilia.

Six novel mutations including triple heterozygosity for Phe31Ser, 514delT and 516T→G factor X gene mutations are responsible for congenital factor X deficiency in patients of Nepali and Indian origin

B. George, A. Viswabandya, M. Chandy, 2005, Journal of thrombosis and haemostasis : JTH.

Argatroban inhibits staphylothrombin

F. Rosendaal, M. Chandy, G. Jayandharan, 2003, Journal of thrombosis and haemostasis : JTH.

HPV DNA in plasma of patients with cervical carcinoma.

G. Chandy, N. Sathish, G. Sridharan, 2004, Journal of clinical virology : the official publication of the Pan American Society for Clinical Virology.

High Frequency of the 1896 Precore Mutation in Patients and Blood Donors with Hepatitis B Virus Infection from the Indian Subcontinent

P. Vivekanandan, G. Chandy, G. Sridharan, 2012, Molecular Diagnosis.

Compound Heterozygosity for Hb E and Hb Lepore-Hollandia in India; First Report and Potential Diagnostic Pitfalls

M. Chandy, A. Srivastava, E. Edison, 2005, Hemoglobin.

Hb Lepore in the Indian Population

M. Chandy, A. Srivastava, R. Krishnamoorthy, 2003, Hemoglobin.

Rapid Detection of β-Globin Gene Mutations and Polymorphisms by Temporal Temperature Gradient Gel Electrophoresis

M. Chandy, A. Srivastava, E. Edison, 2003 .

Hb Showa-Yakushiji [β110(G12)Leu→Pro] in Four Unrelated Patients from West Bengal

M. Chandy, A. Srivastava, E. Edison, 2005, Hemoglobin.

Prenatal diagnosis of beta-thalassaemia mutations using the reverse dot blot technique.

M. Mathai, A. Srivastava, V. Srivastava, 1996, The National medical journal of India.

A NOVEL β-THALASSEMIA MUTATION IN AN ASIAN INDIAN

M. Chandy, A. Srivastava, R. Krishnamoorthy, 2002 .

Determination of the breakpoint and molecular diagnosis of a common α‐thalassaemia‐1 deletion in the Indian population

M. Chandy, A. Srivastava, S. Baidya, 2003, British journal of haematology.

Novel missense mutations in two patients with factor XI deficiency (Val271Leu and Tyr351Ser) and one patient with combined factor XI and factor IX deficiency (Phe349Val)

M. Chandy, G. Jayandharan, A. Srivastava, 2005, Journal of thrombosis and haemostasis : JTH.

A single tube multiplex PCR method to detect the common alpha+ thalassemia alleles.

M. Chandy, A. Srivastava, R. Krishnamoorthy, 2000, Blood.

Molecular genetics of hereditary prothrombin deficiency in Indian patients: identification of a novel Ala362→Thr (Prothrombin Vellore 1) mutation

A. Viswabandya, M. Chandy, G. Jayandharan, 2005, Journal of thrombosis and haemostasis : JTH.

Thalassemia β0 due to an identical frameshift mutation, codon 15 (−T) in both parents

D. Bandyopadhyay, B. Gajra, Madhusnata De, 2004, American journal of hematology.

HIV-2 subtype circulating in India (south).

M. Jesudason, S. Ramalingam, G. Sridharan, 2003, Journal of acquired immune deficiency syndromes.

Investigation of persistent hypochromic microcytosis unmasks hemoglobin Evanston [α 14 (A12) Try → Arg] in a patient of cyclic thrombocytopenia preceding Takayasu's disease

G. Garewal, J. Ahluwalia, R. Das, 2005, Hematology.

Molecular characterization of factor IX gene mutations in 53 patients with haemophilia B in India

M. Chandy, G. Jayandharan, S. Nair, 2005, Thrombosis and Haemostasis.

Rapid detection of beta-globin gene mutations and polymorphisms by temporal temperature gradient gel electrophoresis.

M. Chandy, A. Srivastava, E. Edison, 2003, Clinical Chemistry.