Ranajit Chakraborty | Academic Influence

Ranajit Chakraborty's AcademicInfluence.com Rankings

Ranajit Chakraborty

Biology

#2897

World Rank

#4524

Historical Rank

Genetics

#218

World Rank

#264

Historical Rank

biology Degrees

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Biology

Ranajit Chakraborty's Degrees

PhD Biological Sciences University of Calcutta
Masters Zoology University of Calcutta
Bachelors Zoology University of Calcutta

Why Is Ranajit Chakraborty Influential?

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According to Wikipedia, Ranajit Chakraborty was a human and population geneticist. At the time of his death, he was Director of the Center for Computational Genomics at the Institute of Applied Genetics and Professor in the Department of Forensic and Investigative Genetics at the University of North Texas Health Science Center in Fort Worth, Texas. His scientific contributions include studies in human genetics, population genetics, genetic epidemiology, statistical genetics, and forensic genetics.

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Ranajit Chakraborty's Published Works

Number of citations in a given year to any of this author's works

Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author

Published Works

THE BOTTLENECK EFFECT AND GENETIC VARIABILITY IN POPULATIONS (1975) (3311)
Genetic variation at five trimeric and tetrameric tandem repeat loci in four human population groups. (1992) (1479)
An adoption study of human obesity. (1986) (1256)
Analysis of the VNTR locus D1S80 by the PCR followed by high-resolution PAGE. (1991) (963)
A genome–wide search for human non–insulin–dependent (type 2) diabetes genes reveals a major susceptibility locus on chromosome 2 (1996) (608)
Kin selection, social structure, gene flow, and the evolution of chimpanzees. (1994) (547)
Distribution of recombination crossovers and the origin of haplotype blocks: the interplay of population history, recombination, and mutation. (2002) (463)
Evaluation of 13 short tandem repeat loci for use in personal identification applications. (1994) (459)
Relative mutation rates at di-, tri-, and tetranucleotide microsatellite loci. (1997) (438)
Y-Chromosome evidence for a northward migration of modern humans into Eastern Asia during the last Ice Age. (1999) (395)
BOTTLENECK EFFECTS ON AVERAGE HETEROZYGOSITY AND GENETIC DISTANCE WITH THE STEPWISE MUTATION MODEL (1977) (388)
Genetic evidence supports demic diffusion of Han culture (2004) (386)
Admixture as a tool for finding linked genes and detecting that difference from allelic association between loci. (1988) (385)
Integrative Annotation of 21,037 Human Genes Validated by Full-Length cDNA Clones (2004) (346)
VNTR allele frequency distributions under the stepwise mutation model: a computer simulation approach. (1993) (333)
Apparent heterozygote deficiencies observed in DNA typing data and their implications in forensic applications (1992) (325)
A novel measure of genetic distance for highly polymorphic tandem repeat loci. (1995) (312)
Forensics and mitochondrial DNA: applications, debates, and foundations. (2003) (264)
The use of measured genotype information in the analysis of quantitative phenotypes in man (1986) (248)
Development of a highly polymorphic STR marker for identity testing purposes at the human androgen receptor gene (HUMARA). (1998) (244)
DNA Fingerprinting: Approaches and Applications (1991) (236)
Signatures of population expansion in microsatellite repeat data. (1998) (232)
DNA Fingerprinting: State of the Science (1993) (231)
A unified approach to study hypervariable polymorphisms: statistical considerations of determining relatedness and population distances. (1993) (230)
Parentage analysis with genetic markers in natural populations. I. The expected proportion of offspring with unambiguous paternity. (1988) (226)
Caucasian genes in American blacks: new data. (1992) (226)
CODIS STR loci data from 41 sample populations. (2001) (224)
Y chromosome haplotypes reveal prehistorical migrations to the Himalayas (2009) (193)
Gene admixture in human populations: Models and predictions (1986) (193)
Statistical studies on protein polymorphism in natural populations. I. Distribution of single locus heterozygosity. (1977) (179)
Y-chromosome evidence of southern origin of the East Asian-specific haplogroup O3-M122. (2005) (176)
Analyses of genetic structure of Tibeto-Burman populations reveals sex-biased admixture in southern Tibeto-Burmans. (2004) (172)
Lack of correspondence between genetic and morphologic variability patterns in Atlantic herring (Clupea harengus) (1984) (168)
Population amalgamation and genetic variation: observations on artificially agglomerated tribal populations of Central and South America. (1988) (167)
Mitochondrial DNA polymorphisms in Chilean aboriginal populations: implications for the peopling of the southern cone of the continent. (2000) (166)
Population genetics of dinucleotide (dC-dA)n.(dG-dT)n polymorphisms in world populations. (1995) (165)
Estimation of genetic distance and coefficient of gene diversity from single-probe multilocus DNA fingerprinting data. (1994) (163)
Genetic variation in subdivided populations and conservation genetics (1986) (163)
Polynesian origins: insights from the Y chromosome. (2000) (162)
Determination of relatedness between individuals using DNA fingerprinting. (1993) (158)
Population genetics of hypervariable loci: analysis of PCR based VNTR polymorphism within a population. (1991) (157)
Inbreeding and risk of late onset complex disease (2003) (143)
Interpreting DNA evidence (2000) (142)
Relationship of prevalence of non‐insulin‐dependent diabetes mellitus to Amerindian admixture in the Mexican Americans of San Antonio, Texas (1986) (142)
Statistical Studies on Protein Polymorphism in Natural Populations. III. Distribution of Allele Frequencies and the Number of Alleles per Locus. (1980) (139)
The distribution of the number of heterozygous Loci in an individual in natural populations. (1981) (135)
V75R576 IL-4 Receptor α Is Associated with Allergic Asthma and Enhanced IL-4 Receptor Function1 (2002) (132)
Mitochondrial DNA polymorphism reveals hidden heterogeneity within some Asian populations. (1990) (123)
Estimation of nonpaternity in the Mexican population of Nuevo Leon: a validation study with blood group markers. (1999) (118)
Infinite allele model with varying mutation rate. (1976) (118)
Sample size requirements for addressing the population genetic issues of forensic use of DNA typing. (1992) (117)
Assessment of Optimal Size and Composition of the U.S. National Registry of Hematopoietic Stem Cell Donors (2004) (116)
Genetic structure of Hmong-Mien speaking populations in East Asia as revealed by mtDNA lineages. (2005) (116)
Paternity testing in the DNA era. (1994) (106)
Population structure, stepwise mutations, heterozygote deficiency and their implications in DNA forensics (1995) (105)
p53 codon 72 polymorphism and risk of cervical cancer. (2003) (105)
Genetic differentiation of quantitative characters between populations or species: I. Mutation and random genetic drift (1982) (105)
Problems in the assessment of relative risk of chronic disease among biological relatives of affected individuals. (1982) (96)
Exclusion of paternity: the current state of the art. (1974) (93)
Measures of variation at DNA repeat loci under a general stepwise mutation model. (1996) (93)
Haplotype and linkage disequilibrium architecture for human cancer-associated genes. (2002) (92)
Estimating the frequency of nonpaternity in Switzerland. (1994) (89)
Genome-wide association study for regions of systemic sclerosis susceptibility in a Choctaw Indian population with high disease prevalence. (2003) (85)
Characteristics of polymorphism at a VNTR locus 3' to the apolipoprotein B gene in five human populations. (1992) (85)
Conservation of human chromosome 13 polymorphic microsatellite (CA)n repeats in chimpanzees. (1994) (83)
A note on Nei's measure of gene diversity in a substructured population (1974) (83)
Examining Population Stratification via Individual Ancestry Estimates versus Self-Reported Race (2005) (82)
Intra‐ and inter‐population diversity at short tandem repeat loci in diverse populations of the world (1995) (82)
Genetic admixture in three mexican mestizo populations based on D1S80 and HLA‐DQA1 Loci (2002) (82)
A single polymorphic STR system in the human phenylalanine hydroxylase gene permits rapid prenatal diagnosis and carrier screening for phenylketonuria. (1993) (81)
Y-chromosome SNP haplotypes suggest evidence of gene flow among caste, tribe, and the migrant Siddi populations of Andhra Pradesh, South India (2001) (81)
D1S80 population data in African Americans, Caucasians, southeastern Hispanics, southwestern Hispanics, and Orientals. (1995) (80)
Dynamics of repeat polymorphisms under a forward-backward mutation model: within- and between-population variability at microsatellite loci. (1996) (79)
Genetic diversity and population history of the red panda (Ailurus fulgens) as inferred from mitochondrial DNA sequence variations. (2001) (78)
Microbial forensics: the next forensic challenge (2005) (78)
Association of Apolipoprotein E4 and Haplotypes of the Apolipoprotein E Gene With Lobar Intracerebral Hemorrhage (2005) (77)
V75R576 IL-4 receptor alpha is associated with allergic asthma and enhanced IL-4 receptor function. (2002) (75)
Twelve short tandem repeat loci Y chromosome haplotypes: genetic analysis on populations residing in North America. (2005) (74)
Association of Phosphodiesterase 4D with ischemic stroke: a population-based case-control study. (2006) (74)
Population genetic analyses of the NGM STR loci (2010) (73)
Distribution of three HIV-1 resistance-conferring polymorphisms (SDF1-3′A, CCR2-64I, and CCR5-Δ32) in global populations (2000) (73)
Mutation rates at Y chromosome short tandem repeats in Texas populations. (2009) (72)
Statistical Studies on Protein Polymorphism in Natural Populations II. Gene Differentiation between Populations. (1978) (72)
Heterozygote deficiency, population substructure and their implications in DNA fingerprinting (2004) (71)
The use of restriction fragment length polymorphisms in paternity analysis. (1986) (70)
Maximum likelihood estimates of admixture in northeastern Mexico using 13 short tandem repeat loci (2002) (70)
A power analysis of microsatellite-based statistics for inferring past population growth. (2000) (69)
Whole-genome amplification: relative efficiencies of the current methods. (2005) (69)
Genetic variation of the mitochondrial DNA genome in American Indians is at mutation-drift equilibrium. (1991) (68)
Testing the neutral mutation hypothesis by distribution of single locus heterozygosity (1976) (68)
Uncertainties in estimating health risks associated with exposure to ionising radiation (2013) (68)
Genomic diversity : applications in human population genetics (1999) (67)
Ionizing radiation and genetic risks. XIII. Summary and synthesis of papers VI to XII and estimates of genetic risks in the year 2000. (2000) (67)
The H-Invitational Database (H-InvDB), a comprehensive annotation resource for human genes and transcripts* (2007) (66)
Toward a System of Microbial Forensics: from Sample Collection to Interpretation of Evidence (2005) (66)
Detection of nonrandom association of alleles from the distribution of the number of heterozygous loci in a sample. (1984) (66)
Estimating minimum allele frequencies for DNA profile frequency estimates for PCR-based loci (2005) (65)
Unequal contributions of male and female gene pools from parental populations in the African descendants of the city of Melo, Uruguay. (2002) (65)
'Unique' alleles in admixed populations: a strategy for determining 'hereditary' population differences of disease frequencies. (1991) (63)
Dynamics of gene differentiation between incompletely isolated populations of unequal sizes. (1974) (63)
Nondetectability of restriction fragments and independence of DNA fragment sizes within and between loci in RFLP typing of DNA. (1994) (62)
Genomewide scan for gout in taiwanese aborigines reveals linkage to chromosome 4q25. (2004) (62)
Quality Sample Collection, Handling, and Preservation for an Effective Microbial Forensics Program (2006) (62)
Distribution of two HIV-1-resistant polymorphisms (SDF1-3'A and CCR2-64I) in East Asian and world populations and its implication in AIDS epidemiology. (1999) (61)
Cancer predisposition, radiosensitivity and the risk of radiation-induced cancers. I. Background. (1995) (61)
Genetic Analysis and Attribution of Microbial Forensics Evidence (2005) (60)
Estimation of race admixture--a new method. (1975) (59)
Diisocyanate asthma and gene-environment interactions with IL4RA, CD-14, and IL-13 genes. (2006) (57)
Statistical power of association using the extreme discordant phenotype design (2006) (56)
Source Attribution of a Forensic DNA Profile (2000) (56)
Dispersion of human Y chromosome haplotypes based on five microsatellites in global populations. (1996) (56)
Association of ALOX5AP with ischemic stroke: a population-based case-control study (2007) (56)
Global genetic variation at nine short tandem repeat loci and implications on forensic genetics (2003) (55)
Comparisons of Familial DNA Database Searching Strategies (2011) (55)
Frequencies of complex diseases in hybrid populations. (1986) (55)
Frequency of minisatellite repeat number changes at the MS205 locus in human sperm before and after cancer chemotherapy (2000) (54)
Segregation distortion of the CTG repeats at the myotonic dystrophy locus. (1996) (53)
Genome‐Wide Association of Serum Uric Acid Concentration: Replication of Sequence Variants in an Island Population of the Adriatic Coast of Croatia (2012) (53)
Choosing Relatives for DNA Identification of Missing Persons (2011) (52)
Randomly distributed crossovers may generate block-like patterns of linkage disequilibrium: an act of genetic drift (2003) (52)
The C677T polymorphism of the methylenetetrahydrofolate reductase gene in Mexican mestizo neural-tube defect parents, control mestizo and native populations. (2000) (52)
Relationship of mean and variance of genotypic values with heterozygosity per individual in a natural population. (1983) (52)
Evaluation of standard error and confidence interval of estimated multilocus genotype probabilities, and their implications in DNA forensics. (1993) (52)
Ethnicity determination by names among the Aymara of Chile and Bolivia. (1989) (51)
Dental morphology and population diversity. (1977) (50)
Estimation of time of divergence from phylogenetic studies. (1977) (50)
Distribution and evolution of CTG repeats at the myotonin protein kinase gene in human populations. (1996) (50)
Differences in the relative distribution of human gene diversity between electrophoretic and red and white cell antigen loci. (1983) (50)
Paternity exclusion by DNA markers: effects of paternal mutations. (1996) (50)
Non-invasive sampling and DNA amplification for paternity exclusion, community structure, and phylogeography in wild chimpanzees (1993) (49)
Rank-based genome-wide analysis reveals the association of Ryanodine receptor-2 gene variants with childhood asthma among human populations (2013) (48)
Resolving the etiology of atopic disorders by using genetic analysis of racial ancestry. (2016) (48)
Analysis of human CYP1A1 and CYP1A2 genes and their shared bidirectional promoter in eight world populations (2010) (47)
Genetic and environmental risk factors for childhood eczema development and allergic sensitization in the CCAAPS cohort. (2010) (47)
Population variation at the CODIS core short tandem repeat loci in Europeans. (2001) (47)
Allelic associations of two polymorphic microsatellites in intron 40 of the human von Willebrand factor gene. (1994) (47)
Elevated frequency of Tay-Sachs disease among Ashkenazic Jews unlikely by genetic drift alone. (1978) (45)
Cancer mortality in relatives of retinoblastoma patients. (1984) (45)
Haplotype block: a new type of forensic DNA markers (2009) (45)
Can molecular imprinting explain heterozygote deficiency and hybrid vigor? (1989) (44)
Ionizing radiation and genetic risks. VI. Chronic multifactorial diseases: a review of epidemiological and genetical aspects of coronary heart disease, essential hypertension and diabetes mellitus. (1999) (44)
A method to detect excess risk of disease in structured data: Cancer in relatives of retinoblastoma patients (1984) (44)
Texas Population Substructure and Its Impact on Estimating the Rarity of Y STR Haplotypes from DNA Evidence * (2009) (42)
Distribution and Effects of Nonsense Polymorphisms in Human Genes (2008) (42)
POLYMORPHIC DNA HAPLOTYPES AT THE PHENYLALANINE HYDROXYLASE LOCUS IN PRENATAL DIAGNOSIS OF PHENYLKETONURIA (1986) (40)
Biochemical heterozygosity and phenotypic variability of polygenic traits (1987) (40)
Application of a time-dependent coalescence process for inferring the history of population size changes from DNA sequence data. (1998) (39)
Criteria for Validation of Methods in Microbial Forensics (2008) (39)
Simultaneous estimation of all the parameters of a stepwise mutation model. (1998) (38)
Common SNPs in FTO Gene Are Associated with Obesity Related Anthropometric Traits in an Island Population from the Eastern Adriatic Coast of Croatia (2010) (38)
The St. Lawrence Island Eskimos: genetic variation and genetic distance. (1981) (37)
9 Measurement of genetic variation for evolutionary studies (1991) (37)
Statistical power of an exact test of Hardy-Weinberg proportions of genotypic data at a multiallelic locus. (1994) (37)
Subunit molecular weight and genetic variability of proteins in natural populations. (1978) (37)
Description and validation of a method for simultaneous estimation of effective population size and mutation rate from human population data. (1989) (36)
A collation of marker gene and dermatoglyphic diversity at various levels of population differentiation. (1977) (36)
7 Analysis of population structure: A comparative study of different estimators of wright's fixation indices (1991) (36)
Use of prior odds for missing persons identifications (2011) (36)
On consanguineous marriages and the genetic load (2004) (35)
Phylogeny of six Sciurus aberti subspecies based on nucleotide sequences of cytochrome b. (1995) (34)
Genetic structure of Pileolaria pseudomilitaris (Polychaeta: Spirorbidae). (1980) (34)
The exact numbers of possible microsatellite motifs. (1994) (34)
Genetic characterization of American and Western Samoans. (1994) (34)
Rate and directionality of mutations and effects of allele size constraints at anonymous, gene-associated, and disease-causing trinucleotide loci. (1999) (34)
Gene differentiation among the Dhangar caste-cluster of Maharashtra, India. (1978) (34)
Gene differentiation among ten endogamous groups of West Bengal, India. (1986) (33)
HLA class II haplotypes in Mexican systemic lupus erythematosus patients. (2004) (33)
Finding Missing Heritability in Less Significant Loci and Allelic Heterogeneity: Genetic Variation in Human Height (2012) (32)
The genetics of shovel shape in maxillary central incisors in man. (1976) (32)
Polymorphisms at VNTR loci suggest homogeneity of the white population of Utah. (1991) (32)
Mutation Rate Variation at Human Dinucleotide Microsatellites (2005) (31)
Characterization of 114 insertion/deletion (INDEL) polymorphisms, and selection for a global INDEL panel for human identification. (2014) (31)
Cancer predisposition, radiosensitivity and the risk of radiation-induced cancers. III. Effects of incomplete penetrance and dose-dependent radiosensitivity on cancer risks in populations. (1997) (31)
A bias-corrected estimate of heterozygosity for single-probe multilocus DNA fingerprints. (1993) (31)
Bioassay of Kinship in Populations of Middle Eastern Origin and Controls [and Comments and Replies] (1982) (30)
Phylogenetic construction of 17 bacterial phyla by new method and carefully selected orthologs. (2009) (30)
Haplotype Diversity in 11 Candidate Genes Across Four Populations (2005) (29)
The role of heredity and environment on dermatoglyphic traits. (1991) (29)
Selection of highly informative SNP markers for population affiliation of major US populations (2016) (29)
DNA identification by pedigree likelihood ratio accommodating population substructure and mutations (2010) (28)
Automated analysis of sequence polymorphism in STR alleles by PCR and direct electrospray ionization mass spectrometry. (2012) (28)
US forensic Y-chromosome short tandem repeats database. (2010) (28)
Signatures of natural selection on genetic variants affecting complex human traits☆ (2013) (28)
Genetic distance analysis of twenty-two South American Indian populations. (1975) (27)
Estimation of mutation rates from parentage exclusion data: applications to STR and VNTR loci. (1996) (27)
CORRELATIONS BETWEEN SOME MEASURES OF GENETIC DISTANCE (1976) (27)
Quantitative traits in relation to population structure: why and how are they used and what do they imply? (1990) (27)
Sex dimorphism in adult stature in four Chilean populations. (1978) (27)
Population Genetic Characteristics of the D1S80 locus in seven human populations (1994) (26)
Genetic distance and electrophoretic identity of proteins between taxa (1973) (26)
Association between genetic variation at the porphobilinogen deaminase gene and schizophrenia (1993) (26)
Accelerated Evolution of the Pituitary Adenylate Cyclase-Activating Polypeptide Precursor Gene During Human Origin (2005) (26)
Utility of Y-Chromosome Short Tandem Repeat Haplotypes in Forensic Applications. (2003) (25)
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. (2004) (25)
Allele sharing at six VNTR loci and genetic distances among three ethnically defined human populations (1992) (25)
Data entry errors in an on-line operation. (1981) (25)
Variation in allele frequencies among caste groups of the Dhangars of Maharashtra, India: an analysis with Wright's Fst statistic. (1977) (25)
The inheritance of pyloric stenosis explained by a multifactorial threshold model with sex dimorphism for liability (1986) (24)
A class of population genetic questions formulated as the generalized occupancy problem. (1993) (24)
Effects of the Ion PGM™ Hi-Q™ sequencing chemistry on sequence data quality (2016) (24)
Population studies on three Native Alaska population groups using STR loci. (2002) (24)
The effects of Asian population substructure on Y STR forensic analyses. (2009) (24)
Hidden genetic variability within electromorphs in finite populations. (1976) (23)
Heredity, stress and blood pressure, a family set method--V. Heritability estimates. (1977) (23)
An HIV-resistant allele is exceptionally frequent in New Guinean highlanders. (1998) (23)
Complex SNP-based haplotypes in three human helicases: implications for cancer association studies. (2002) (23)
A comparison of three methods for assessing Amerindian admixture in Mexican Americans. (1993) (23)
A note on the distribution of the number of exclusions to be expected in paternity testing. (1976) (22)
Directional mating and a rapid male population expansion in a hybrid Uruguayan population (2005) (22)
Addressing the use of phylogenetics for identification of sequences in error in the SWGDAM mitochondrial DNA database. (2004) (21)
Prevalence of metabolic syndrome and related metabolic traits in an island population of the Adriatic (2012) (21)
Relative risks of diseases in the presence of incomplete penetrance and sporadics. (1983) (21)
Informativeness of the CODIS STR loci for admixture analysis. (2005) (21)
Genetic profile of cosmopolitan populations: effects of hidden subdivision. (1990) (21)
Subarachnoid hemorrhage: tests of association with apolipoprotein E and elastin genes (2007) (21)
Intraclass and interclass correlations of allele sizes within and between loci in DNA typing data. (1993) (21)
Correlation of heterozygosity and the number of alleles in different frequency classes (1982) (20)
Interpreting Y chromosome STR haplotype mixture. (2010) (20)
Development and validation of a novel multiplexed DNA analysis system, InnoTyper® 21. (2017) (20)
Cancer predisposition, radiosensitivity and the risk of radiation-induced cancers. II. A Mendelian single-locus model of cancer predisposition and radiosensitivity for predicting cancer risks in populations. (1995) (20)
Replication of genetic variants from genome-wide association studies with metabolic traits in an island population of the Adriatic coast of Croatia (2011) (20)
Genetic variability in Chilean Indian populations and its association with geography, language, and culture. (1976) (19)
Hierarchical gene diversity analysis and its application to brown trout population data (2008) (19)
Comparison of five tandem repeat loci between humans and chimpanzees. (1992) (19)
Genetic distance analysis among nine endogamous population groups of Maharashtra, India (1979) (19)
Familial aggregation of cancer in Laredo, Texas: A generally low‐risk Mexican‐American population (1986) (19)
Modeling metabolic syndrome through structural equations of metabolic traits, comorbid diseases, and GWAS variants (2013) (19)
A shared Y-chromosomal heritage between Muslims and Hindus in India (2006) (19)
Linkage disequilibria among (CA)n polymorphisms in the human dystrophin gene and their implications in carrier detection and prenatal diagnosis in Duchenne and Becker muscular dystrophies. (1994) (19)
Blood group genetics of some caste groups of Southern 24 Parganas, West Bengal. (1975) (19)
Complex segregation analysis of facial clefting in Chile. (1997) (19)
Genetic structure of the populations migrating from San Luis Potosi and Zacatecas to Nuevo León in Mexico. (1991) (18)
Patterns of instability of expanded CAG repeats at the ERDA1 locus in general populations. (1999) (17)
Ionizing radiation and genetic risks. XII. The concept of "potential recoverability correction factor" (PRCF) and its use for predicting the risk of radiation-inducible genetic disease in human live births. (2000) (17)
Genetic and linguistic correlation of the Kra–Dai-speaking groups in Thailand (2015) (17)
Analysis of Genetic Structure of Populations: Meaning, Methods, and Implications (1993) (17)
Epidemiology of breast cancer in a Mexican-American population. (1985) (17)
An application of a general branching process in the study of the genetics of aging. (2001) (16)
Paternity exclusion and the paternity index for two linked loci. (1983) (16)
Population genetic study in ten endogamous groups of West Bengal, India. (1987) (16)
World population data for the HLA-DQA1, PM and D1S80 loci with least and most common profile frequencies for combinations of loci estimated following NRC II guidelines. (2000) (16)
Genetic variation at twentythree microsatellite loci in sixteen human populations (2008) (16)
Normal CAG repeat variation at the DRPLA locus in world populations. (1995) (15)
Forensic analysis of the mitochondrial coding region and association to disease (2005) (15)
Part IV: Genes and epidemiology in anthropological adaptation studies: Familial correlations in lung function in populations residing at different altitudes in Chile (1980) (15)
Cancer predisposition, radiosensitivity and the risk of radiation-induced cancers. IV. Prediction of risks in relatives of cancer-predisposed individuals. (1998) (15)
Genetic differentiation of quantitative characters between populations or species II: optimal selection in infinite populations (1987) (15)
Distribution of nucleotide differences between two randomly chosen cistrons in a population of variable size. (1977) (15)
Ionizing radiation and genetic risks. VIII. The concept of mutation component and its use in risk estimation for multifactorial diseases. (1998) (15)
A simple test for the aggregation of disease occurrence in genealogical data. (1981) (15)
Genetic studies among the Siddis of Karnataka, India: a migrant population from Africa. (1987) (15)
Heredity, stress and blood pressure, a family set method: epilogue. (1977) (15)
A semigroup representation and asymptotic behavior of certain statistics of the fisher-wright-moran coalescent (2001) (14)
Immunoglobulin (Gm and Km) allotypes in nine endogamous groups of West Bengal, India. (1987) (14)
Multiple alleles and estimation of genetic parameters: computational equations showing involvement of all alleles. (1992) (14)
Genetic epidemiology of intracerebral hemorrhage. (2005) (14)
Dermatoglyphic variation among South American tribal populations and its association with marker gene, linguistic, and geographic distances. (1979) (13)
Empirical relationship between the number of nucleotide substitutions and interspecific identity of amino acid sequences in some proteins (1976) (13)
Single-Locus and Multilocus Analysis of Genetic Differentiation of the Races of Man: A Critique (1978) (13)
A prioritization analysis of disease association by data-mining of functional annotation of human genes. (2012) (13)
Genetic components of variations of red cell glycolytic intermediates at two altitudes among the South American Aymara. (1983) (13)
Paternity evaluation in cases lacking a mother and nondetectable alleles (2005) (13)
Distribution of HIV-1 resistance-conferring polymorphic allelesSDF-1-3′A, CCR2-64I andCCR5-Δ32 in diverse populations of Andhra Pradesh, South India (2001) (13)
Population dynamics of DNA fingerprint patterns within and between populations. (1994) (13)
Analysis of allele distribution for six short tandem repeat loci in the French Canadian population of Québec. (1997) (12)
Genetic polymorphism and fertility parameters in the Aymara of Chile and Bolivia (1986) (12)
Statistical interpretation of DNA typing data. (1991) (12)
Detection of the inbreeding coefficient from ABO blood-group data. (1972) (12)
Examination of the possible role of biologically relevant genes around FBN1 in systemic sclerosis in the Choctaw population. (2003) (12)
Variations on dermal ridges in nine population groups of Maharashtra, India. I. Intra- and interpopulation diversity. (1980) (12)
Correlation of paternity index with probability of exclusion and efficiency criteria of genetic markers for paternity testing. (1982) (12)
Y-STR loci diversity in native Alaskan populations (2011) (12)
Prevalence of metabolic syndrome in the interior of Croatia: the Baranja region. (2008) (12)
Cultural, language and geographical correlates of genetic variability in Andean highland Indians (1976) (11)
HOW MUCH OF VARIABILITY IN APOLIPOPROTEIN AII CONCENTRATIONS IS EXPLAINED BY POLYMORPHISM ADJACENT TO APO-AII GENE? (1985) (11)
Selection pressure on human STR loci and its relevance in repeat expansion disease (2016) (11)
Distribution of ABO Blood Groups on the Indian Subcontinent: A Cluster-Analytic Approach [and Comments and Reply] (1982) (11)
Autosomal STR allele frequencies and Y-STR and mtDNA haplotypes in Chilean sample populations (2009) (11)
Neonatal Variables, Altitude of Residence and Aymara Ancestry in Northern Chile (2015) (11)
Empirical testing of a 23-AIMs panel of SNPs for ancestry evaluations in four major US populations (2016) (10)
HLA-DQB1, -DQA1, -DRB1 linkage disequilibrium and haplotype diversity in a Mestizo population from Guadalajara, Mexico. (2004) (10)
Ionizing radiation and genetic risks. V. Multifactorial diseases: a review of epidemiological and genetic aspects of congenital abnormalities in man and of models on maintenance of quantitative traits in populations. (1994) (10)
Dynamic balance of segregation distortion and selection maintains normal allele sizes at the myotonic dystrophy locus. (1998) (10)
Molecular evolution and phylogenetics, Masatoshi Nei and Sudhir Kumar. Oxford University Press, Oxford, England/New York, USA, 2000, xiv + 333 pages (hardback) $75; (paperback) $35.00 (2002) (10)
Diversity in palmar pattern ridge counts among 12 Iranian populations. (1986) (10)
Priniciples for Estimating the Rarity of Y-STR Haplotypes Derived from Forensic Evidence (2007) (10)
Reproductive History in Mothers of Children with Neural Tube Defects (2000) (10)
Mutations in names: implications for assessing identity by descent from historical records. (1983) (10)
Role of genomics in eliminating health disparities (2015) (10)
Phenotypic bioassay of five tribes of Orissa, India. (1973) (10)
Non-homogeneous infinite sites model under demographic change: mathematical description and asymptotic behavior of pairwise distributions. (2002) (10)
Use of odds of paternity computations in determining the reliability of single exclusions in paternity testing. (1981) (10)
Selective neutrality of surname, distribution in an immigrant indian community of Houston, Texas (1990) (10)
Association of Phosphodiesterase 4 D With Ischemic Stroke (2006) (10)
Estimation of the incidence of a rare genetic disease through a two-tier mutation survey. (1993) (9)
Impact of Cancer Predisposition and Radiosensitivity on the Population Risk of Radiation-Induced Cancers (2001) (9)
Some sampling properties of selectively neutral alleles:Effects of variability of mutation rates (1979) (9)
Partial matches in heterogeneous offender databases do not call into question the validity of random match probability calculations (2008) (9)
Mean and variance of the number of samples showing heterozygote excess or deficiency (1981) (9)
Evaluation of paternity-testing data from the joint distribution of paternity index and rate of exclusion. (2008) (9)
Relationship between heterozygosity and genetic distance in the three major races of man. (1984) (8)
Distribution of the number of heterozygous loci in the Kota population of Nilgiri hills of India and estimation of average heterozygosity. (1981) (8)
Statistical Weight of a DNA Match in Cold-Hit Cases (2009) (8)
Genetic signatures of pre-expansion bottleneck in the Choctaw population of Oklahoma. (2004) (8)
Genetic heterogeneity and population structure in eastern India: red cell enzyme variability in ten Assamese populations. (1989) (8)
Multistage risk models and the age pattern in familial polyposis coli. (1984) (8)
Statistical studies of protein polymorphism. (1981) (8)
Wherefore art thou Romio? Name frequency patterns and their use in automated genealogy assembly (1980) (8)
Part VI: Evaluation of relative risks from the correlation between relatives: A theoretical approach (1980) (8)
23 Selection biases of samples and their resolutions (2000) (7)
A test for the radomness of the occurrence of a disease trait in familial or other similar ordered sequences of epidemiological data. (1980) (7)
Nonrandom sampling in human genetics: Skewness and kurtosis (1987) (7)
Allocation Versus Variation: The Issue of Genetic Differences Between Human Racial Groups (1982) (7)
Extent of Height Variability Explained by Known Height-Associated Genetic Variants in an Isolated Population of the Adriatic Coast of Croatia (2011) (7)
Phylogeny of mitochondrial DNA clones in tassel‐eared squirrels Sciurus aberti (1994) (7)
The impact of population admixture on traditional linkage analysis. (2001) (7)
Paternity exclusion in primates: Two strategies (1979) (7)
Five tribes of Orissa, India: anthropometry and kinship. (1973) (7)
On allele frequency computation from DNA typing data (2005) (7)
A population genetic study in the Ochamchir region, Abkhazia, SSR. (1985) (7)
Pedigree likelihood ratio for lineage markers (2011) (7)
Metabolic syndrome in an island population of the eastern Adriatic coast of Croatia. (2008) (7)
Genetic variation and population structure of interleukin genes among seven ethnic populations from Karnataka, India (2007) (7)
Variations on dermal ridges in nine population groups of maharashtra, india. III. Asymmetry and interdigital diversity (1982) (7)
Twinning and neural tube defects: environmental factors. (1995) (7)
Adoption study of obesity. (1986) (6)
Clarification of Statistical Issues Related to the Operation of CODIS (2006) (6)
Global genetic variation of select opiate metabolism genes in self-reported healthy individuals (2017) (6)
Mutations in the BRCA1 gene: implications of inter-population differences for predicting the risk of radiation-induced breast cancers. (1998) (6)
Study of three hypervariable DNA loci (D1S7; D7S22 and D12S11) in three European populations. (1998) (6)
Genetic considerations for interpreting molecular microbial forensic evidence (2004) (6)
Variations in asymmetry and interdigital diversity for three ridge-count measures among the Dhangar caste-cluster of Maharashtra, India (1981) (6)
Low Dose Effect of Chronic Lead Exposure on Neuromotor Response Impairment in Children is Moderated by Genetic Polymorphisms (2008) (6)
Intratribal Genetic Differentiation as Assessed through Electrophoresis (1990) (6)
Estimation of mutation rates from the number of rare alleles in a sample. (1981) (6)
Electrophoretically silent alleles in a finite population (1976) (5)
Human genetics : a selection of insights (1979) (5)
Worldwide genetic diversity at the HLA‐DQA1 locus (1997) (5)
Differentiation of Hispanic biogeographic ancestry with 80 ancestry informative markers (2020) (5)
D1S80 allele frequencies in a Chinese population (1994) (5)
Human mating patterns (1989) (5)
Fixed cluster designs in human genetic studies: interpretations and usefulness. (1979) (5)
Genetic variation by birth cohorts in Mexican Americans of Starr County, Texas (1994) (5)
A comparative study of genetic variation at five VNTR loci in three ethnic groups of Houston, Texas. (1995) (4)
Ionizing radiation and genetic risks. VII. The concept of mutation component and its use in risk estimation for Mendelian diseases. (1998) (4)
Estimation of linkage disequilibrium from conditional haplotype data: Application to β‐globin gene cluster in American blacks (1986) (4)
Consanguinity and demography in some Chilean populations. (1975) (4)
Heterozygosity and genetic distance of proteins (1983) (4)
Genome mapping: A practical approach (1999) (4)
The generalized Wright's model and population structure with special reference to the ABO blood group system. (1974) (4)
Genetically-regulated transcriptomics & copy number variation of proctitis points to altered mitochondrial and DNA repair mechanisms in individuals of European ancestry (2020) (4)
Comments on "Interpreting Y chromosome STR haplotype mixture". (2011) (4)
Prediction of Protein-Destabilizing Polymorphisms by Manual Curation with Protein Structure (2012) (3)
Linkage Disequilibria and Haplotype Structure of Four SNPs of the Interleukin 1 Gene Cluster in Seven Asian Indian Populations (2006) (3)
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]. (2007) (3)
Admixture effects in the traditional linkage analysis of admixed families. (2002) (3)
Response to: DNA identification by pedigree likelihood ratio accommodating population substructure and mutations- authors' reply (2011) (3)
Distribution of repeat unit differences between alleles at tandem repeat microsatellite loci (1994) (3)
Trinucleotide Repeats, Genetic Instability and Variation in the Human Genome (1999) (3)
Response to: Use of prior odds for missing persons identifications - authors' reply (2012) (3)
Simulation results with stepwise mutation model and their interpretations (1977) (3)
Rank-based genome-wide analysis reveals the association of Ryanodine receptor-2 gene variants with childhood asthma among human populations (2013) (2)
Immunoglobulin (Gm and Km) allotypes in the Aymara of Chile and Bolivia. (1985) (2)
Detection of excess disease risk in family data: Response to Lubin and Bale (1987) (2)
Further considerations of difficulties of estimating familial risks from pedigree data. (1987) (2)
Inter- and Intra-Island Genetic Diversity in Adriatic Populations of Croatia: Implications for Studying Complex Diseases in Isolated Populations (2003) (2)
Statistical Issues Regarding the Use of Microsatellite Loci for Molecular Anthropological Studies (1999) (2)
Analysis of D1S80 VNTR Allele Polymorphism and Association with a Nearby Flanking Sequence Polymorphism in Two Spanish Populations (1996) (2)
Correction: Integrative Annotation of 21,037 Human Genes Validated by Full-Length cDNA Clones (2004) (2)
Heredity and risk of disease (1978) (2)
SAMPLING PROPERTIES OF ESTIMATORS OF NUCLEOTIDE DIVERSITY AT DISCOVERED SNP SITES (2003) (2)
Human Population Genetics: Drift and Migration (2001) (2)
Nonrandom sampling in genetic epidemiology: An implementation of the Hanis‐Chakraborty method for multifactorial analysis (1989) (2)
Confidence Bands for the Survival Function S(t/z) and the Relation with Decision Analysis: Theory (1991) (1)
Statistical Basis of Risk Calculations (2004) (1)
Is there a pattern of gene differentiation in the Indian populations (1978) (1)
Comments on ‘A note on the variance of the estimate of the fixation index F’ (2016) (1)
T-cell receptor genes in tassel-eared squirrels (Sciurus aberti). I. Genetic polymorphism and divergence in the Abert and Kaibab subspecies. (1990) (1)
Culture and genetic variability (reply) (1977) (1)
Kidney-Survival Analysis of IgA-Nephropathy Patients: A Case Study (1991) (1)
Effects of population bottlenecks on the allele frequency distribution. (1980) (1)
A test of allelic independence based on distributions of allele size differences at microsatellite loci. (1997) (1)
Reply to Baer. (1993) (1)
Hidden genetic variability within and between electromorphs in finite populations (1976) (1)
T-cell receptor genes in tassel-eared squirrels (Sciurus aberti) (1990) (1)
Letter to the Editor: comments on biostatistical power of sibling analysis by STR markers (2016) (1)
Human polymorphic genes world distributions. By Arun K. Roychoudhury and Masatoshi Nei. New York: Oxford University Press. 1988. ix ± 393 pp., figures, tables, references. $56.00 (cloth) (1989) (1)
Hardy–Weinberg Equilibrium† (2005) (1)
Population Genetics: Historical Aspects (2006) (1)
Single-Locus Genetic Association Analysis by Ordinal Tests☆ (2012) (1)
Parent-offspring correlation in an equilibrium population. (1970) (1)
Reply to Reed (1992) (1)
Multiple Testing of Hypotheses in Biomedical Research (2012) (1)
Letter to the editor (2005) (1)
Detection of inbreeding and efficiency of mating bioassay. (1974) (1)
Population Genetic Considerations in Statistical Interpretation of Microbial Forensic Data in Comparison with Human DNA Forensic Standard (2011) (1)
Correlation of DNA fragment sizes within loci in the presence of non-detectable alleles (1995) (1)
Comparing the "family set" approach to estimate heritability with other conventional estimators: a Monte Carlo simulation. (1980) (1)
Gene-Environment Interaction between CD14 -159C→T and Diesel Exhaust Particle (DEP) Exposure Underlying Aero Allergen Sensitization (2006) (0)
Symposium on variation in the human genome, held at the Ciba Foundation, London 13-15 June 1995 - Final discussion (1996) (0)
Contents Vol. 49, 2000 (2000) (0)
Mutation rates from rare variants of proteins in Indian tribes (1978) (0)
Stated race/ethnicity is not a definitive indicator of patrilineal ancestry in males of major US populations. (2015) (0)
Buchbesprechung – Book Review – Livre nouveau (1973) (0)
Mathematical Aspects of Genetic Equilibrium (1978) (0)
Tale of 12 , 000 Y Chromosomes African Origin of Modern Humans in East Asia : A (2007) (0)
Theoretical Population Genetics (1991) (0)
Drift variance of race admixture (1976) (0)
Subject Index, Vol. 25, 1975 (1975) (0)
Paternity calculations in a di-spermy case (2017) (0)
A Note on Counting Method of Estimation for MNSs Blood Group System (1971) (0)
Correlation Analyses Reveal a Substantial Influence of Allelic Gaps on the Investigation of Genetic Diversity of Modern Human Populations with Microsatellites (2008) (0)
DNA technology and forensic science. (1991) (0)
Subject Index Vol. 49, 2000 (2000) (0)
DNA FORENSICS: A POPULATION GENETIC AND BIOLOGICAL ANTHROPOLOGOCAL PERSPECTIVE (2011) (0)
Subject Index, Vol. 31, 1981 (1981) (0)
Nonparametric evaluations of familial aggregation (2007) (0)
Sequence Variations of Interleukin-1 receptor antagonist (IL-1Ra) gene in humans and non-human primates (2001) (0)
Function ReceptorAllergic Asthma and Enhanced IL-4 Is Associated with α V 75 R 576 IL-4 Receptor (2002) (0)
A Rooster Crow Does Not Cause the Sun To Rise (2001) (0)
Distribution of the number of exclusions in paternity testing (1976) (0)
Handbook of Statistics, Volume 28: Bioinformatics in Human Health and Heredity (2012) (0)
INOSA Guidelines in the era of precision medicine (2015) (0)
Familial Aggregation of Cancer in Laredo (1986) (0)
Subject Index Vol. 44, 1994 (1994) (0)
Microsatellite genetic variation in the Indian subcontinent (2003) (0)
On some theoretical studies on gene differentiation in natural populations. (1975) (0)
Transcriptomics & copy number variation of radiotoxicity points to altered mitochondrial and DNA repair mechanisms (2020) (0)
FIFTH INTERNATIONAL CONGRESS OF HUMAN GENETICS (1976) (0)
DNA profiling on trial (1994) (0)
Fu Y-X, Chakraborty R.. Simultaneous estimation of all the parameters of a stepwise mutation model. Genetics 150: 487-497 (1998) (0)
A Molecular Information Method to Estimate Population Admixture (2012) (0)
Introduction: Wither Bioinformatics in Human Health and Heredity (2012) (0)
Probabilistic approaches of DNA mixture interpretations: Advantages and limitations (2013) (0)
Genetically-regulated transcriptomics & copy number variation of proctitis points to altered mitochondrial and DNA repair mechanisms in individuals of European ancestry (2020) (0)
KinSelection, SocialStructure, Gene Flow,and the Evolutionof Chimpanzees (2016) (0)
MICROBIAL FORENSIC BIOCRIMES AND HIV (2003) (0)
Ward Boundary Mass Extinction Sudden Productivity Collapse Associated with the Triassic-Jurassic (2011) (0)
Heterozygosity and monomorphism reconsidered (1978) (0)
Paternity exclusion for relatives. (1978) (0)
Genetic Differentiation of Hispanic Populations Using Ancestry Informative Markers (2017) (0)
Estimation of Linkage in Presence of Incomplete Penetration for Both the Factors (1969) (0)
Evaluation ofStandard ErrorandConfidence Interval of Estimated Multilocus GenotypeProbabilities, andTheir Implications inDNA Forensics (1993) (0)
Bias of heritability estimates from twin data in presence of errors of zygosity determination (1990) (0)
Erratum (2012) (0)
Power of assaying inbreeding through sampling of phenotypes and mating types (1975) (0)
Population genetics and molecular evolution. Edited by Tomoko Ohta and Kenichi Aoki. Tokyo: Japan Scientific Societies Press and Springer‐Verlag. 1985. xvii + 503 pp., figures, tables, index. $53.50 (cloth) (1987) (0)
GENETIC STRUCTURE OF PZLEOLARZA PSEUDOMZLZTARZS (POLYCHAETA: SPIRORBIDAE) (1980) (0)
Heterogeneity within Some Asian Populations (2006) (0)
Letter to the editor (2008) (0)
Differentiation of Hispanic biogeographic ancestry with 80 ancestry informative markers (2020) (0)
Response to the Letter of G. Mezei and R. Kavet (2002) (0)
Bioinformatics in human health and heredity (2012) (0)
Relative Reduction in the Extent of Genetic Diversity at STR Loci in Adriatic Island Populations (2002) (0)
Population Genetics of the Human Angiotensin - 1 Converting Enzyme (ACE) Locus (2002) (0)
Gene Flow , and the Evolution of Chimpanzees (2014) (0)
Towards a Comprehensive Pharmacogenetic Profile for Predicting Opiate Metabolizer Phenotype (2017) (0)
Convergent issues in genetics and demography. Edited by J.A. Adams, A. Hermalin, D. Lam, and P.E. Smouse. xii + 361 pp. New York: Oxford University Press. 1990. $49.95 (cloth) (1992) (0)
Additional variance of serum lipid levels explained by incorporating less significant genetic variants and allelic heterogeneity (2012) (0)
Contents, Vol. 44, 1994 (1994) (0)
Selection pressure on human STR loci and its relevance in repeat expansion disease (2016) (0)
Effects of Inclusion of Relatives in DNA Databases: Empirical Observations from 13K SNPs in Hap-Map Population Data (2012) (0)
Effects of population bottlenecks upon the mean and variance of the number of alleles in a population. (1980) (0)
Current developments in anthropological genetics. Volume 2. Edited by M.H. Crawford and J.H. Mielke. New York: Academic Press. 1982. xvii + 525 pp., figures, tables, index. $59.50 (cloth) (1983) (0)
Current developments in anthropological genetics. Volume I. Edited by J. H. Mielke and M. H. Crawford. New York: Plenum Press. 1980. XIV + 436 pp., figures, tables, references, index. $ 45.00 (cloth) (1982) (0)

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