PubRank

Ranajit Chakraborty

Author PubWeight™ 105.14‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Integrative annotation of 21,037 human genes validated by full-length cDNA clones. PLoS Biol 2004 7.17
2 Distribution of recombination crossovers and the origin of haplotype blocks: the interplay of population history, recombination, and mutation. Am J Hum Genet 2002 4.29
3 Genetic evidence supports demic diffusion of Han culture. Nature 2004 2.92
4 The H-Invitational Database (H-InvDB), a comprehensive annotation resource for human genes and transcripts. Nucleic Acids Res 2007 2.07
5 Y-chromosome evidence of southern origin of the East Asian-specific haplogroup O3-M122. Am J Hum Genet 2005 1.86
6 Association of apolipoprotein E4 and haplotypes of the apolipoprotein E gene with lobar intracerebral hemorrhage. Stroke 2005 1.65
7 Admixture in Hispanics: distribution of ancestral population contributions in the Continental United States. Hum Biol 2003 1.64
8 Assessment of optimal size and composition of the U.S. National Registry of hematopoietic stem cell donors. Transplantation 2004 1.59
9 Analyses of genetic structure of Tibeto-Burman populations reveals sex-biased admixture in southern Tibeto-Burmans. Am J Hum Genet 2004 1.57
10 Population genetic analyses of the NGM STR loci. Int J Legal Med 2010 1.50
11 Interpreting Y chromosome STR haplotype mixture. Leg Med (Tokyo) 2010 1.47
12 V75R576 IL-4 receptor alpha is associated with allergic asthma and enhanced IL-4 receptor function. J Immunol 2002 1.40
13 Examining population stratification via individual ancestry estimates versus self-reported race. Cancer Epidemiol Biomarkers Prev 2005 1.33
14 Genetic analysis and attribution of microbial forensics evidence. Crit Rev Microbiol 2005 1.31
15 Genome-wide structural and evolutionary analysis of the P450 monooxygenase genes (P450ome) in the white rot fungus Phanerochaete chrysosporium: evidence for gene duplications and extensive gene clustering. BMC Genomics 2005 1.27
16 Haplotype and linkage disequilibrium architecture for human cancer-associated genes. Genome Res 2002 1.26
17 Mutation rates at Y chromosome short tandem repeats in Texas populations. Forensic Sci Int Genet 2009 1.26
18 Association of Phosphodiesterase 4D with ischemic stroke: a population-based case-control study. Stroke 2005 1.25
19 Comparisons of familial DNA database searching strategies. J Forensic Sci 2011 1.25
20 Randomly distributed crossovers may generate block-like patterns of linkage disequilibrium: an act of genetic drift. Hum Genet 2003 1.23
21 DNA identification by pedigree likelihood ratio accommodating population substructure and mutations. Investig Genet 2010 1.20
22 Evidence for a major gene influence on persistent developmental stuttering. Hum Biol 2004 1.15
23 Forensics and mitochondrial DNA: applications, debates, and foundations. Annu Rev Genomics Hum Genet 2003 1.15
24 A Ser49Cys variant in the ataxia telangiectasia, mutated, gene that is more common in patients with breast carcinoma compared with population controls. Cancer 2004 1.11
25 Genome-wide association of serum uric acid concentration: replication of sequence variants in an island population of the Adriatic coast of Croatia. Ann Hum Genet 2012 1.08
26 Genetic structure of Hmong-Mien speaking populations in East Asia as revealed by mtDNA lineages. Mol Biol Evol 2004 1.07
27 Effect of surgical weight loss on sleep architecture in adolescents with severe obesity. Obes Surg 2008 1.07
28 Choosing relatives for DNA identification of missing persons. J Forensic Sci 2010 1.07
29 Diisocyanate asthma and gene-environment interactions with IL4RA, CD-14, and IL-13 genes. Ann Allergy Asthma Immunol 2006 1.06
30 Association of ApoE genetic variants with obstructive sleep apnea in children. Sleep Med 2007 1.06
31 Mutation rate variation at human dinucleotide microsatellites. Genetics 2005 1.06
32 Texas population substructure and its impact on estimating the rarity of Y STR haplotypes from DNA evidence*. J Forensic Sci 2009 1.06
33 Toward a system of microbial forensics: from sample collection to interpretation of evidence. Appl Environ Microbiol 2005 1.05
34 Unequal contributions of male and female gene pools from parental populations in the African descendants of the city of Melo, Uruguay. Am J Phys Anthropol 2002 1.01
35 Common SNPs in FTO gene are associated with obesity related anthropometric traits in an island population from the eastern Adriatic coast of Croatia. PLoS One 2010 1.01
36 Temporal-spatial activation of apoptosis and epithelial injury in murine experimental biliary atresia. Hepatology 2008 1.01
37 Whole-genome amplification: relative efficiencies of the current methods. Leg Med (Tokyo) 2005 1.00
38 Staging of biliary atresia at diagnosis by molecular profiling of the liver. Genome Med 2010 0.99
39 Distribution and effects of nonsense polymorphisms in human genes. PLoS One 2008 0.99
40 Analysis of human CYP1A1 and CYP1A2 genes and their shared bidirectional promoter in eight world populations. Hum Mutat 2010 0.98
41 Use of prior odds for missing persons identifications. Investig Genet 2011 0.98
42 Uncertainties in estimating health risks associated with exposure to ionising radiation. J Radiol Prot 2013 0.98
43 Genomewide scan for gout in taiwanese aborigines reveals linkage to chromosome 4q25. Am J Hum Genet 2004 0.97
44 Association of ALOX5AP with ischemic stroke: a population-based case-control study. Hum Genet 2007 0.97
45 Twelve short tandem repeat loci Y chromosome haplotypes: genetic analysis on populations residing in North America. Forensic Sci Int 2005 0.97
46 Quality sample collection, handling, and preservation for an effective microbial forensics program. Appl Environ Microbiol 2006 0.96
47 Concept, measurement and use of acculturation in health and disease risk studies. Coll Antropol 2010 0.95
48 Incidence of cystic fibrosis in five different states of Brazil as determined by screening of p.F508del, mutation at the CFTR gene in newborns and patients. J Cyst Fibros 2007 0.95
49 Statistical power of association using the extreme discordant phenotype design. Pharmacogenet Genomics 2006 0.92
50 Genotypic interaction between DRD4 and DAT1 loci is a high risk factor for attention-deficit/hyperactivity disorder in Chilean families. Am J Med Genet B Neuropsychiatr Genet 2006 0.92
51 Genetic and environmental risk factors for childhood eczema development and allergic sensitization in the CCAAPS cohort. J Invest Dermatol 2009 0.92
52 Genome-wide association study for regions of systemic sclerosis susceptibility in a Choctaw Indian population with high disease prevalence. Arthritis Rheum 2003 0.91
53 Criteria for validation of methods in microbial forensics. Appl Environ Microbiol 2008 0.91
54 p53 codon 72 polymorphism and risk of cervical cancer. Biol Res 2003 0.90
55 Genetic admixture in three Mexican Mestizo populations based on D1S80 and HLA-DQA1 loci. Am J Hum Biol 2002 0.90
56 Population studies on three Native Alaska population groups using STR loci. Forensic Sci Int 2002 0.90
57 Finding missing heritability in less significant Loci and allelic heterogeneity: genetic variation in human height. PLoS One 2012 0.89
58 Complex SNP-based haplotypes in three human helicases: implications for cancer association studies. Genome Res 2002 0.89
59 Replication of genetic variants from genome-wide association studies with metabolic traits in an island population of the Adriatic coast of Croatia. Eur J Hum Genet 2010 0.88
60 Microbial forensics: the next forensic challenge. Int J Legal Med 2005 0.88
61 Genetic susceptibility to obstructive sleep apnea in the obese child. Sleep Med 2007 0.87
62 A shared Y-chromosomal heritage between Muslims and Hindus in India. Hum Genet 2006 0.87
63 Patients of African ancestry with hemophagocytic lymphohistiocytosis share a common haplotype of PRF1 with a 50delT mutation. J Pediatr 2006 0.87
64 Haplotype block: a new type of forensic DNA markers. Int J Legal Med 2009 0.85
65 Re: Leptin and leptin receptor gene polymorphisms in obstructive sleep apnea syndrome. Chest 2008 0.85
66 Phylogenetic construction of 17 bacterial phyla by new method and carefully selected orthologs. Gene 2008 0.83
67 Accelerated evolution of the pituitary adenylate cyclase-activating polypeptide precursor gene during human origin. Genetics 2005 0.83
68 HLA class II haplotypes in Mexican systemic lupus erythematosus patients. Hum Immunol 2004 0.83
69 Utility of the Y-STR typing systems Y-PLEX 6 and Y-PLEX 5 in forensic casework and 11 Y-STR haplotype database for three major population groups in the United States. J Forensic Sci 2004 0.82
70 Prevalence of metabolic syndrome in the interior of Croatia: the Baranja region. Coll Antropol 2008 0.82
71 The effects of Asian population substructure on Y STR forensic analyses. Leg Med (Tokyo) 2008 0.82
72 Influence of polymorphisms at loci encoding DNA repair proteins on cancer susceptibility and G2 chromosomal radiosensitivity. Environ Mol Mutagen 2007 0.82
73 Genetic epidemiology of intracerebral hemorrhage. J Stroke Cerebrovasc Dis 2007 0.80
74 Rank-based genome-wide analysis reveals the association of ryanodine receptor-2 gene variants with childhood asthma among human populations. Hum Genomics 2013 0.80
75 Extent of height variability explained by known height-associated genetic variants in an isolated population of the Adriatic coast of Croatia. PLoS One 2011 0.80
76 Global genetic variation at nine short tandem repeat loci and implications on forensic genetics. Eur J Hum Genet 2003 0.80
77 Addressing the use of phylogenetics for identification of sequences in error in the SWGDAM mitochondrial DNA database. J Forensic Sci 2004 0.80
78 US forensic Y-chromosome short tandem repeats database. Leg Med (Tokyo) 2010 0.80
79 Automated analysis of sequence polymorphism in STR alleles by PCR and direct electrospray ionization mass spectrometry. Forensic Sci Int Genet 2012 0.79
80 A prioritization analysis of disease association by data-mining of functional annotation of human genes. Genomics 2011 0.79
81 Informativeness of the CODIS STR loci for admixture analysis. J Forensic Sci 2005 0.79
82 Genetic signatures of pre-expansion bottleneck in the Choctaw population of Oklahoma. Am J Phys Anthropol 2004 0.78
83 Prediction of protein-destabilizing polymorphisms by manual curation with protein structure. PLoS One 2012 0.78
84 Subarachnoid hemorrhage: tests of association with apolipoprotein E and elastin genes. BMC Med Genet 2007 0.78
85 Further remarks on: "Paternity analysis in special fatherless cases without direct testing of alleged father" [FSI 146S (2004) S159-S161] and remarks on it [FSI 163 (2006) 158-160]. Forensic Sci Int 2007 0.78
86 Maximum likelihood estimates of admixture in Northeastern Mexico using 13 short tandem repeat loci. Am J Hum Biol 2002 0.78
87 Response to: Use of prior odds for missing persons identifications - authors' reply. Investig Genet 2012 0.78
88 Linkage disequilibria and haplotype structure of four SNPs of the interleukin 1 gene cluster in seven Asian Indian populations. Hum Biol 2006 0.78
89 Modeling metabolic syndrome through structural equations of metabolic traits, comorbid diseases, and GWAS variants. Obesity (Silver Spring) 2013 0.77
90 Directional mating and a rapid male population expansion in a hybrid Uruguayan population. Am J Hum Biol 2005 0.77
91 Genetic variation at nine short tandem repeat loci among islanders of the eastern Adriatic coast of Croatia. Hum Biol 2005 0.77
92 Admixture effects in the traditional linkage analysis of admixed families. Ethn Dis 2002 0.77
93 Genetic variation and population structure of interleukin genes among seven ethnic populations from Karnataka, India. J Genet 2007 0.77
94 Examination of the possible role of biologically relevant genes around FBN1 in systemic sclerosis in the Choctaw population. Arthritis Rheum 2003 0.76
95 Y-STR loci diversity in native Alaskan populations. Int J Legal Med 2011 0.76
96 Comments on "Interpreting Y chromosome STR haplotype mixture". Leg Med (Tokyo) 2010 0.75
97 Non-homogeneous infinite sites model under demographic change: mathematical description and asymptotic behavior of pairwise distributions. Math Biosci 2002 0.75
98 Sensitivity and specificity of body mass index as a definition of the obesity component of metabolic syndrome. Coll Antropol 2007 0.75
99 Partial matches in heterogeneous offender databases do not call into question the validity of random match probability calculations. Int J Legal Med 2008 0.75
100 Metabolic syndrome in an island population of the eastern Adriatic coast of Croatia. Coll Antropol 2008 0.75
101 Pedigree likelihood ratio for lineage markers. Int J Legal Med 2010 0.75