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exaly
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Journals
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Annals of Human Genetics
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top-articles
Annals of Human Genetics
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
doc citations
211
(top 5%)
g
-index
Top Articles
#
Title
Journal
Year
Citations
1
ON ESTIMATING THE RELATION BETWEEN BLOOD GROUP AND DISEASE
Annals of Human Genetics
1955
2,680
2
The inheritance of liability to certain diseases, estimated from the incidence among relatives
Annals of Human Genetics
1965
1,490
3
F
‐statistics and analysis of gene diversity in subdivided populations
Annals of Human Genetics
1977
1,103
4
THE ESTIMATION AND SIGNIFICANCE OF THE LOGARITHM OF A RATIO OF FREQUENCIES
Annals of Human Genetics
1956
924
5
Monte Carlo tests for associations between disease and alleles at highly polymorphic loci
Annals of Human Genetics
1995
886
6
Estimation of fixation indices and gene diversities
Annals of Human Genetics
1983
876
7
Extension of covariance selection mathematics
Annals of Human Genetics
1972
875
8
The phylogeography of Y chromosome binary haplotypes and the origins of modern human populations
Annals of Human Genetics
2001
665
9
A cytogenetic study of 1000 spontaneous abortions
Annals of Human Genetics
1980
650
10
An extended transmission/disequilibrium test (TDT) for multi‐allele marker loci
Annals of Human Genetics
1995
625
11
Haplotype relative risks: an easy reliable way to construct a proper control sample for risk calculations
Annals of Human Genetics
1987
610
12
Apolipoprotein E (APOE) allele distribution in the world. IsAPOE*4a ‘thrifty’ allele?
Annals of Human Genetics
1999
578
13
Characterization of a panel of highly variable minisatellites cloned from human DNA
Annals of Human Genetics
1987
544
14
Extensions to multivariate normal models for pedigree analysis
Annals of Human Genetics
1982
502
15
Adenosine deaminase polymorphism in man
Annals of Human Genetics
1968
469
16
Esterase D: a new human polymorphism
Annals of Human Genetics
1973
425
17
The recognition and estimation of cyclic trends
Annals of Human Genetics
1961
424
18
Genome‐Wide Association Study Confirms SNPs in
SNCA
and the
MAPT
Region as Common Risk Factors for Parkinson Disease
Annals of Human Genetics
2010
417
19
A cytogenetic survey of 11,680 newborn infants
Annals of Human Genetics
1974
414
20
Extensions to pedigree analysis III. Variance components by the scoring method
Annals of Human Genetics
1976
409
21
The marker (X) syndrome: a cytogenetic and genetic analysis
Annals of Human Genetics
1984
384
22
The use of multiple thresholds in determining the mode of transmission of semi‐continuous traits*
Annals of Human Genetics
1972
376
23
Human triploidy: relationship between parental origin of the additional haploid complement and development of partial hydatidiform mole
Annals of Human Genetics
1982
366
24
Developmental changes and polymorphism in human alcohol dehydrogenase
Annals of Human Genetics
1971
365
25
Phylogeography of mitochondrial DNA in western Europe
Annals of Human Genetics
1998
363
26
Age Related Changes in 5‐methylcytosine Content in Human Peripheral Leukocytes and Placentas: an HPLC‐based Study
Annals of Human Genetics
2004
362
27
Fisher's ‘fundamental theorem’ made clear
Annals of Human Genetics
1972
335
28
Tuberous Sclerosis: from Tubers to mTOR
Annals of Human Genetics
2003
321
29
THE ESTIMATION OF GENE FREQUENCIES IN A RANDOM‐MATING POPULATION
Annals of Human Genetics
1955
305
30
Testing for heterogeneity of recombination fraction values in Human Genetics
Annals of Human Genetics
1963
304
31
The use of measured genotype information in the analysis of quantitative phenotypes in man
Annals of Human Genetics
1986
302
32
How selection shapes variation of the human major histocompatibility complex: a review
Annals of Human Genetics
2001
299
33
The Phenotypic Consequences of CFTR Mutations
Annals of Human Genetics
2003
296
34
Apparent heterozygote deficiencies observed in DNA typing data and their implications in forensic applications
Annals of Human Genetics
1992
294
35
Apert's syndrome (a type of acrocephalosyndactyly)?observations on a British series of thirty-nine cases*
Annals of Human Genetics
1959
274
36
MONOZYGOTIC AND DIZYGOTIC TWIN DIAGNOSIS
Annals of Human Genetics
1955
265
37
A new algorithm for haplotype-based association analysis: the Stochastic-EM algorithm
Annals of Human Genetics
2004
258
38
Two loci for Tuberous Sclerosis: one on 9q34 and one on 16p13
Annals of Human Genetics
1994
256
39
Inherited variations in human phosphohexose isomerase
Annals of Human Genetics
1968
255
40
The generalized sib pair IBD distribution: its use in the detection of linkage
Annals of Human Genetics
1978
247
41
The estimation of pairwise relationships
Annals of Human Genetics
1975
244
42
The inheritance of liability to diseases with variable age of onset, with particular reference to diabetes mellitus
Annals of Human Genetics
1967
239
43
Standardized Subsets of the HGDP-CEPH Human Genome Diversity Cell Line Panel, Accounting for Atypical and Duplicated Samples and Pairs of Close Relatives
Annals of Human Genetics
2006
233
44
Refined Geographic Distribution of the Oriental
ALDH2*504Lys
(nee
487Lys
) Variant
Annals of Human Genetics
2009
232
45
Racial admixture in north‐eastern Brazil
Annals of Human Genetics
1965
216
46
Estimation of admixture and detection of linkage in admixed populations by a Bayesian approach: application to African-American populations
Annals of Human Genetics
2000
216
47
Further data on the adenosine deaminase (ADA) polymorphism and a report of a new phenotype
Annals of Human Genetics
1969
214
48
Signatures of Positive Selection in Genes Associated with Human Skin Pigmentation as Revealed from Analyses of Single Nucleotide Polymorphisms
Annals of Human Genetics
2007
212
49
Chromosome deletion in a case of retinoblastoma
Annals of Human Genetics
1963
210
50
Update and Analysis of the University College London Low Density Lipoprotein Receptor Familial Hypercholesterolemia Database
Annals of Human Genetics
2008
210
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