Published in Indian J Med Res on January 01, 1979
An interesting prenatal diagnosis: double aneuploidy. Case Rep Obstet Gynecol (2013) 0.75
Schizophrenia is associated with elevated amphetamine-induced synaptic dopamine concentrations: evidence from a novel positron emission tomography method. Proc Natl Acad Sci U S A (1997) 3.00
Converging evidence for a pseudoautosomal cytokine receptor gene locus in schizophrenia. Mol Psychiatry (2007) 2.70
Brain-derived neurotrophic factor val66met polymorphism and volume of the hippocampal formation. Mol Psychiatry (2005) 2.29
Fine mapping of ZNF804A and genome-wide significant evidence for its involvement in schizophrenia and bipolar disorder. Mol Psychiatry (2010) 2.21
Apolipoprotein E epsilon 4 and clinical phenotype in schizophrenia. Lancet (1997) 2.02
Clozapine and risperidone in chronic schizophrenia: effects on symptoms, parkinsonian side effects, and neuroendocrine response. Am J Psychiatry (1999) 1.79
Assessment of newborn baby's temperature by human touch: a potentially useful primary care strategy. Indian Pediatr (1992) 1.69
Association of ketamine-induced psychosis with focal activation of the prefrontal cortex in healthy volunteers. Am J Psychiatry (1997) 1.64
Comparison of ketamine-induced thought disorder in healthy volunteers and thought disorder in schizophrenia. Am J Psychiatry (1999) 1.63
Pressure dynamics of various irrigation techniques commonly used in the emergency department. Ann Emerg Med (1994) 1.60
Impaired attention as an endophenotype for molecular genetic studies of schizophrenia. Am J Med Genet (2001) 1.51
Recommendations for locus-specific databases and their curation. Hum Mutat (2008) 1.49
Thrombocytopenic purpura following DPT vaccination. Pediatr Hematol Oncol (1994) 1.41
Effects of ketamine on thought disorder, working memory, and semantic memory in healthy volunteers. Biol Psychiatry (1998) 1.38
Dengue haemorrhagic fever in children in Delhi. Bull World Health Organ (1992) 1.37
Split-hand and split-foot deformity inherited as an autosomal recessive trait. Clin Genet (1976) 1.36
Thesis during MD: must or bust? Indian J Pediatr (2007) 1.36
Perinatal mortality-incidence and effect of various maternal factors, Part I. Indian J Pediatr (1982) 1.28
Nephrotic syndrome in indian children. Arch Dis Child (1975) 1.25
SCA12 is a rare locus for autosomal dominant cerebellar ataxia: a study of an Indian family. Ann Neurol (2001) 1.20
Paraganglioma of the pancreas: literature review and case report. Dig Dis Sci (2000) 1.18
Development of immune response during typhoid fever in man. Clin Exp Immunol (1977) 1.17
Relationship of undernutrition to diarrhoea in infants and children. Indian J Med Res (1970) 1.14
The global distribution of length polymorphisms of the promoters of the glucuronosyltransferase 1 gene (UGT1A1): hematologic and evolutionary implications. Blood Cells Mol Dis (2003) 1.14
Down's syndrome and related abnormalities in an area of high background radiation in coastal Kerala. Nature (1976) 1.11
Sugar intolerance in malnourished infants and children. Br Med J (1968) 1.10
Carisoprodol abuse: a report from India. Acta Psychiatr Scand (1993) 1.10
Major factors in diarrhoea related mortality among rural children. Indian J Med Res (1986) 1.10
Is the spectrum of mutations in Indian patients with cystic fibrosis different? Am J Med Genet (2000) 1.08
Cannabis and cognitive functions: a prospective study. Drug Alcohol Depend (1988) 1.04
Mechanism of peripheral noradrenergic stimulation by clozapine. Neuropsychopharmacology (1999) 1.04
High frequency of neural-tube defects in North India. Lancet (1978) 1.04
Genetic counseling in acrocallosal syndrome. Indian J Pediatr (2003) 1.03
Bacterial meningitis in India: an IJP survey. Indian J Pediatr (1992) 1.02
A gene for recessive nonsyndromic sensorineural deafness (DFNB18) maps to the chromosomal region 11p14-p15.1 containing the Usher syndrome type 1C gene. Genomics (1998) 1.02
Spectrum of respiratory distress syndrome in the newborn in North India: a prospective study. Indian J Pediatr (1981) 1.01
A clinical and cytogenetic study of Turner syndrome. Indian Pediatr (1995) 1.01
Intralesional immunotherapy with killed Mycobacterium w vaccine for the treatment of ano-genital warts: an open label pilot study. J Eur Acad Dermatol Venereol (2008) 1.01
Coeliac disease in North Indian children. Br Med J (1966) 1.00
GWA study data mining and independent replication identify cardiomyopathy-associated 5 (CMYA5) as a risk gene for schizophrenia. Mol Psychiatry (2010) 1.00
Effects of NMDA antagonism on striatal dopamine release in healthy subjects: application of a novel PET approach. Synapse (1998) 0.99
BCG and Mantoux intradermal tests in the diagnosis of tuberculosis. Indian Pediatr (1974) 0.99
Spectrum of severe skeletal dysplasias in North India. Indian J Pediatr (2007) 0.99
Study of physical growth of Indian children in Delhi. Indian J Pediatr (1968) 0.98
A profile of pyogenic meningitis in children. J Indian Med Assoc (1991) 0.96
Sickle cell trait & disease among tribal communities in Orissa, Madhya Pradesh & Kerala. Indian J Med Res (1997) 0.96
Small bowel changes in iron-deficiency anaemia of childhood. Arch Dis Child (1968) 0.95
Intracranial tuberculoma. Evaluation and treatment. Clin Pediatr (Phila) (1988) 0.94
Utility of family studies in diagnosing abnormal hemoglobins/thalassemic states. Indian J Pediatr (2009) 0.92
Study of serum copper and copper oxidase in patients with Indian childhood cirrhosis. Indian J Med Res (1971) 0.92
Efficacy of mung bean (lentil) and pop rice based rehydration solutions in comparison with the standard glucose electrolyte solution. J Pediatr Gastroenterol Nutr (1988) 0.91
Guidelines for optimal medical care of persons with Down syndrome. International League of Societies for Persons with Mental Handicap (ILSMH). Acta Paediatr (1995) 0.91
An epidemiologic approach to Indian childhood cirrhosis. Indian Pediatr (1973) 0.91
The liver in siblings of patients with Indian childhood cirrhosis: a light and electron microscopic study. Gut (1981) 0.90
Rhizomelic chondrodysplasia punctata type 1: report of mutations in 3 children from India. J Appl Genet (2010) 0.90
Primary immunodeficiency states in Indian children. Indian J Med Res (1976) 0.89
Mixed gonadal dysgenesis and dysgenetic male pseudohermaphroditism--a critical analysis. Indian J Pediatr (1992) 0.89
Chemotaxis, random mobility, and mobilization of polymorphonuclear leucocytes in malnutrition. J Clin Pathol (1976) 0.89
An outbreak of diarrhea due to citrobacter freundii in a neonatal special care nursery. Indian J Pediatr (1981) 0.88
Hepatitis-associated antigen and depressed cellular immunity in Indian childhood cirrhosis. Am J Dis Child (1972) 0.88
Development and assessment of a screening test for detecting childhood disabilities. Indian J Pediatr (2000) 0.88
Spectrum of EEG abnormalities during clozapine treatment. Electroencephalogr Clin Neurophysiol (1994) 0.88
Molecular analysis of Huntington's disease and linked polymorphisms in the Indian population. Acta Neurol Scand (2003) 0.87
Malaria and ABO blood groups. Indian J Malariol (1992) 0.87
In vitro lymphoblastoid transformation in the presence of tuberculin as a diagnostic aid in tuberculous meningoencephalitis. Am Rev Respir Dis (1974) 0.86
The relation between dopamine D2 receptor density and personality: preliminary evidence from the NEO personality inventory-revised. Neuropsychiatry Neuropsychol Behav Neurol (2000) 0.86
Familial pancreatitis. (A case report). Indian Pediatr (1971) 0.85
An autosomal recessive form of lethal chondrodystrophy with severe thoracic narrowing, rhizoacromelic type of micromelia, polydacytly and genital anomalies. Birth Defects Orig Artic Ser (1975) 0.85
Menkes' Kinky Hair disease: new considerations. Indian Pediatr (1996) 0.85
Trichohepatoenteric syndrome: founder mutation in asian indians. Mol Syndromol (2012) 0.85
Cyclophosphamide therapy in the management of nephrotic syndrome. Indian Pediatr (1974) 0.85
Molecular characterization of mutations in Indian children with congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiency. J Pediatr Endocrinol Metab (2001) 0.85
Individual variation in D2 dopamine receptor occupancy in clozapine-treated patients. Am J Psychiatry (1996) 0.84
Mutation studies in X-linked myotubular myopathy in three Indian families. Indian J Pediatr (2010) 0.84
Interaction of malarial infection and glucose-6-phosphate dehydrogenase deficiency in Muria gonds of district Bastar, central India. Trop Geogr Med (1992) 0.84
Microphthalmos and anterior segment dysgenesis in a family. Ophthalmic Paediatr Genet (1991) 0.84
Evaluation of patients with bundle branch block and "unexplained" syncope: a study based on comprehensive electrophysiologic testing and ajmaline stress. Pacing Clin Electrophysiol (1988) 0.83
The role of DMSA scans in evaluation of the correlation between urinary tract infection, vesicoureteric reflux, and renal scarring. Pediatr Surg Int (2002) 0.83
Neurocognitive phenomics: examining the genetic basis of cognitive abilities. Psychol Med (2012) 0.83
Effect of acute metabolic stress on pituitary-adrenal axis activation in patients with schizophrenia. Am J Psychiatry (1998) 0.83
Multi drug resistant Salmonella typhi infection: clinical profile and therapy. Indian Pediatr (1991) 0.83
Jarcho-Levin syndrome. Indian Pediatr (1994) 0.83
Biotinidase deficiency--a treatable entity. Indian J Pediatr (2000) 0.83
Helping parents to face perinatal loss. Indian J Pediatr (1991) 0.83
Effect of transcendental meditation on the performance of some cognitive psychological tests. Indian J Med Res (1982) 0.83
Serum immunoglobulins in the newborn. Indian J Pediatr (1970) 0.82
Neurofibromatosis I with unusual hypopigmentation masquerading as leprosy. J Assoc Physicians India (2004) 0.82
Conduction velocity of motor nerves in children suffering from protein-calorie malnutrition and marasmus. Electromyogr Clin Neurophysiol (1977) 0.82
Blood lead levels of children with pica and surma use. Indian J Pediatr (1992) 0.82
Genetic association study between antipsychotic-induced weight gain and the melanocortin-4 receptor gene. Pharmacogenomics J (2012) 0.82
Are there ethnic differences in deletions in the dystrophin gene? Am J Med Genet (1997) 0.82
Campylobacter jejuni as a cause of childhood diarrhoea in a north Indian community. J Diarrhoeal Dis Res (1983) 0.82
Prevalence of fragile X(A) syndrome in mentally retarded children at a genetics referral centre in Delhi, India. Indian J Med Res (1998) 0.82
Factor VIII gene polymorphisms in the Asian Indian population. Haemophilia (2000) 0.82
Lactose and milk intolerance in recurrent abdominal pain of childhood. Indian J Pediatr (1982) 0.81
Pulmonary function studies in normal children. Indian Pediatr (1975) 0.81