1.8(top 50%)
impact factor
3.4K(top 5%)
papers
110.1K(top 5%)
citations
125(top 5%)
h-index
1.8(top 50%)
impact factor
4.2K
all documents
113.8K
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211(top 5%)
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Top Articles

#TitleJournalYearCitations
1ON ESTIMATING THE RELATION BETWEEN BLOOD GROUP AND DISEASEAnnals of Human Genetics19552,680
2The inheritance of liability to certain diseases, estimated from the incidence among relativesAnnals of Human Genetics19651,490
3F‐statistics and analysis of gene diversity in subdivided populationsAnnals of Human Genetics19771,103
4THE ESTIMATION AND SIGNIFICANCE OF THE LOGARITHM OF A RATIO OF FREQUENCIESAnnals of Human Genetics1956924
5Monte Carlo tests for associations between disease and alleles at highly polymorphic lociAnnals of Human Genetics1995886
6Estimation of fixation indices and gene diversitiesAnnals of Human Genetics1983876
7Extension of covariance selection mathematicsAnnals of Human Genetics1972875
8The phylogeography of Y chromosome binary haplotypes and the origins of modern human populationsAnnals of Human Genetics2001665
9A cytogenetic study of 1000 spontaneous abortionsAnnals of Human Genetics1980650
10An extended transmission/disequilibrium test (TDT) for multi‐allele marker lociAnnals of Human Genetics1995625
11Haplotype relative risks: an easy reliable way to construct a proper control sample for risk calculationsAnnals of Human Genetics1987610
12Apolipoprotein E (APOE) allele distribution in the world. IsAPOE*4a ‘thrifty’ allele?Annals of Human Genetics1999578
13Characterization of a panel of highly variable minisatellites cloned from human DNAAnnals of Human Genetics1987544
14Extensions to multivariate normal models for pedigree analysisAnnals of Human Genetics1982502
15Adenosine deaminase polymorphism in manAnnals of Human Genetics1968469
16Esterase D: a new human polymorphismAnnals of Human Genetics1973425
17The recognition and estimation of cyclic trendsAnnals of Human Genetics1961424
18Genome‐Wide Association Study Confirms SNPs in SNCA and the MAPT Region as Common Risk Factors for Parkinson DiseaseAnnals of Human Genetics2010417
19A cytogenetic survey of 11,680 newborn infantsAnnals of Human Genetics1974414
20Extensions to pedigree analysis III. Variance components by the scoring methodAnnals of Human Genetics1976409
21The marker (X) syndrome: a cytogenetic and genetic analysisAnnals of Human Genetics1984384
22The use of multiple thresholds in determining the mode of transmission of semi‐continuous traits*Annals of Human Genetics1972376
23Human triploidy: relationship between parental origin of the additional haploid complement and development of partial hydatidiform moleAnnals of Human Genetics1982366
24Developmental changes and polymorphism in human alcohol dehydrogenaseAnnals of Human Genetics1971365
25Phylogeography of mitochondrial DNA in western EuropeAnnals of Human Genetics1998363
26Age Related Changes in 5‐methylcytosine Content in Human Peripheral Leukocytes and Placentas: an HPLC‐based StudyAnnals of Human Genetics2004362
27Fisher's ‘fundamental theorem’ made clearAnnals of Human Genetics1972335
28Tuberous Sclerosis: from Tubers to mTORAnnals of Human Genetics2003321
29THE ESTIMATION OF GENE FREQUENCIES IN A RANDOM‐MATING POPULATIONAnnals of Human Genetics1955305
30Testing for heterogeneity of recombination fraction values in Human GeneticsAnnals of Human Genetics1963304
31The use of measured genotype information in the analysis of quantitative phenotypes in manAnnals of Human Genetics1986302
32How selection shapes variation of the human major histocompatibility complex: a reviewAnnals of Human Genetics2001299
33The Phenotypic Consequences of CFTR MutationsAnnals of Human Genetics2003296
34Apparent heterozygote deficiencies observed in DNA typing data and their implications in forensic applicationsAnnals of Human Genetics1992294
35Apert's syndrome (a type of acrocephalosyndactyly)?observations on a British series of thirty-nine cases*Annals of Human Genetics1959274
36MONOZYGOTIC AND DIZYGOTIC TWIN DIAGNOSISAnnals of Human Genetics1955265
37A new algorithm for haplotype-based association analysis: the Stochastic-EM algorithmAnnals of Human Genetics2004258
38Two loci for Tuberous Sclerosis: one on 9q34 and one on 16p13Annals of Human Genetics1994256
39Inherited variations in human phosphohexose isomeraseAnnals of Human Genetics1968255
40The generalized sib pair IBD distribution: its use in the detection of linkageAnnals of Human Genetics1978247
41The estimation of pairwise relationshipsAnnals of Human Genetics1975244
42The inheritance of liability to diseases with variable age of onset, with particular reference to diabetes mellitusAnnals of Human Genetics1967239
43Standardized Subsets of the HGDP-CEPH Human Genome Diversity Cell Line Panel, Accounting for Atypical and Duplicated Samples and Pairs of Close RelativesAnnals of Human Genetics2006233
44Refined Geographic Distribution of the Oriental ALDH2*504Lys (nee 487Lys) VariantAnnals of Human Genetics2009232
45Racial admixture in north‐eastern BrazilAnnals of Human Genetics1965216
46Estimation of admixture and detection of linkage in admixed populations by a Bayesian approach: application to African-American populationsAnnals of Human Genetics2000216
47Further data on the adenosine deaminase (ADA) polymorphism and a report of a new phenotypeAnnals of Human Genetics1969214
48Signatures of Positive Selection in Genes Associated with Human Skin Pigmentation as Revealed from Analyses of Single Nucleotide PolymorphismsAnnals of Human Genetics2007212
49Chromosome deletion in a case of retinoblastomaAnnals of Human Genetics1963210
50Update and Analysis of the University College London Low Density Lipoprotein Receptor Familial Hypercholesterolemia DatabaseAnnals of Human Genetics2008210