PubRank

R V Shaji

Author PubWeight™ 21.67‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Treatment of children with newly diagnosed acute promyelocytic leukemia with arsenic trioxide: a single center experience. Leukemia 2004 1.76
2 Distribution of the different genotypes of HCV among patients attending a tertiary care hospital in south India. J Clin Virol 2003 1.21
3 Amelioration of dextran sulfate colitis by butyrate: role of heat shock protein 70 and NF-kappaB. Am J Physiol Gastrointest Liver Physiol 2003 1.09
4 Comparison of molecular and conventional methods for typing of enteroviral isolates. J Clin Microbiol 2002 1.07
5 Genotype phenotype correlation in Wilson's disease within families--a report on four south Indian families. World J Gastroenterol 2008 1.06
6 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. Haemophilia 2005 1.05
7 Analysis of beta globin mutations in the Indian population: presence of rare and novel mutations and region-wise heterogeneity. Clin Genet 2008 1.02
8 HPV DNA in plasma of patients with cervical carcinoma. J Clin Virol 2004 0.92
9 ATP7B mutations in families in a predominantly Southern Indian cohort of Wilson's disease patients. Indian J Gastroenterol 2007 0.87
10 Fludarabine-based conditioning for allogeneic stem cell transplantation for multiply transfused patients with Fanconi's anemia. Bone Marrow Transplant 2005 0.86
11 Molecular genetics of hereditary prothrombin deficiency in Indian patients: identification of a novel Ala362 --> Thr (Prothrombin Vellore 1) mutation. J Thromb Haemost 2005 0.86
12 E2 sequence variations of HPV 16 among patients with cervical neoplasia seen in the Indian subcontinent. Gynecol Oncol 2004 0.85
13 Thalassemia beta0 due to an identical frameshift mutation, codon 15 (-T) in both parents. Am J Hematol 2004 0.84
14 Central nervous system relapse in a patient with acute promyelocytic leukaemia treated with arsenic tri-oxide. Br J Haematol 2001 0.84
15 Carbonyl reductase 1 expression influences daunorubicin metabolism in acute myeloid leukemia. Eur J Clin Pharmacol 2012 0.81
16 HCV genotype 4--an emerging threat as a cause of chronic liver disease in Indian (south) patients. J Clin Virol 2004 0.81
17 Developing an algorithm of informative markers for evaluation of chimerism after allogeneic bone marrow transplantation. Bone Marrow Transplant 2006 0.81
18 Cytochrome P4501A1 and glutathione S transferase gene polymorphisms in patients with aplastic anemia in India. Acta Haematol 2005 0.80
19 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. J Thromb Haemost 2005 0.80
20 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). J Thromb Haemost 2005 0.79
21 Polymorphism in factor VII gene modifies phenotype of severe haemophilia. Haemophilia 2009 0.77
22 Prenatal diagnosis of beta-thalassaemia mutations using the reverse dot blot technique. Natl Med J India 1997 0.77
23 A single tube multiplex PCR method to detect the common alpha+ thalassemia alleles. Blood 2000 0.77
24 Identification of factor IX gene defects using a multiplex PCR and CSGE strategy-a first report. J Thromb Haemost 2003 0.76
25 Informativeness of linkage analysis for genetic diagnosis of haemophilia A in India. Haemophilia 2004 0.76
26 Molecular remission with arsenic trioxide in patients with newly diagnosed acute promyelocytic leukemia. Haematologica 2004 0.75
27 Investigation of persistent hypochromic microcytosis unmasks hemoglobin Evanston [alpha 14 (A12) Try--> Arg] in a patient of cyclic thrombocytopenia preceding Takayasu's disease. Hematology 2005 0.75
28 Gene symbol: ATP7B. Disease: Wilson disease. Hum Genet 2006 0.75
29 A novel β-globin gene mutation HBB.c.22 G>C produces a hemoglobin variant (Hb Vellore) mimicking HbS in HPLC. Int J Lab Hematol 2012 0.75
30 Gene symbol: ATP7B. Disease: Wilson disease. Hum Genet 2006 0.75
31 Gene symbol: ATP7B. Disease: Wilson disease. Hum Genet 2006 0.75
32 Transvaginal chorionic villus sampling-an alternative approach. Aust N Z J Obstet Gynaecol 1999 0.75
33 Gene symbol: ATP7B. Disease: Wilson's disease. Hum Genet 2004 0.75
34 An outbreak of echovirus meningitis in children. Indian Pediatr 2004 0.75
35 Novel digestion patterns with hepatitis B virus strains from the Indian subcontinent detected using restriction fragment length polymorphism. Indian J Med Microbiol 2008 0.75
36 A novel δ-globin gene mutation (HBD: c.323G>A) masking the diagnosis of β-thalassemia: a first report from India. Int J Hematol 2012 0.75
37 Gene symbol: ATP7B. Disease: Wilson disease. Hum Genet 2006 0.75