Alec Jeffreys | Academic Influence

Alec Jeffreys's AcademicInfluence.com Rankings

Alec Jeffreys

Biology

#137

World Rank

#249

Historical Rank

Genetics

#25

World Rank

#43

Historical Rank

Molecular Biology

#156

World Rank

#160

Historical Rank

biology Degrees

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Biology

Alec Jeffreys's Degrees

PhD Genetics University of Oxford
Bachelors Biochemistry University of Oxford

Why Is Alec Jeffreys Influential?

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According to Wikipedia, Sir Alec John Jeffreys, is a British geneticist known for developing techniques for genetic fingerprinting and DNA profiling which are now used worldwide in forensic science to assist police detective work and to resolve paternity and immigration disputes. He is Professor of Genetics at the University of Leicester, and became an honorary freeman of the City of Leicester on 26 November 1992. In 1994, he was knighted for services to genetics.

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Alec Jeffreys'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

Hypervariable ‘minisatellite’ regions in human DNA (1985) (3577)
Individual-specific ‘fingerprints’ of human DNA (1985) (2041)
Forensic application of DNA ‘fingerprints’ (1985) (1004)
Intensely punctate meiotic recombination in the class II region of the major histocompatibility complex (2001) (856)
Spontaneous mutation rates to new length alleles at tandem-repetitive hypervariable loci in human DNA (1988) (767)
Chromosome 5 allele loss in human colorectal carcinomas (1987) (586)
Positive identification of an immigration test-case using human DNA fingerprints (1985) (546)
Complex gene conversion events in germline mutation at human minisatellites (1994) (544)
Characterization of a panel of highly variable minisatellites cloned from human DNA (1987) (521)
Amplification of human minisatellites by the polymerase chain reaction: towards DNA fingerprinting of single cells. (1988) (506)
A physical map of the DNA regions flanking the rabbit β-globin gene (1977) (479)
Repeat unit sequence variation in minisatellites: A novel source of DNA polymorphism for studying variation and mutation by single molecule analysis (1990) (463)
Minisatellite repeat coding as a digital approach to DNA typing (1991) (416)
Human minisatellite mutation rate after the Chernobyl accident (1996) (405)
Isolation of human simple repeat loci by hybridization selection. (1994) (395)
DNA fingerprints of dogs and cats. (2009) (393)
DNA sequence variants in the G γ-, A γ-, δ- and β-globin genes of man (1979) (339)
Where the crossovers are: recombination distributions in mammals (2004) (338)
The rabbit β-globin gene contains a large insert in the coding sequence (1977) (336)
Identification of the skeletal remains of a murder victim by DNA analysis (1991) (322)
Clustering of hypervariable minisatellites in the proterminal regions of human autosomes. (1988) (304)
DNA "fingerprints" and segregation analysis of multiple markers in human pedigrees. (1986) (298)
PRDM9 variation strongly influences recombination hot-spot activity and meiotic instability in humans (2010) (294)
Intense and highly localized gene conversion activity in human meiotic crossover hot spots (2004) (292)
The PiGMaP consortium linkage map of the pig (Sus scrofa) (1995) (282)
Deletion of genes on chromosome 1 in endocrine neoplasia (1987) (266)
Reciprocal crossover asymmetry and meiotic drive in a human recombination hot spot (2002) (250)
The frequency of uniparental disomy in Prader-Willi syndrome. Implications for molecular diagnosis. (1992) (245)
Cloning a selected fragment from a human DNA 'fingerprint': isolation of an extremely polymorphic minisatellite. (1986) (239)
Identification of the skeletal remains of Josef Mengele by DNA analysis. (1992) (237)
DNA Fingerprinting: State of the Science (1993) (231)
The retinoblastoma gene is frequently altered leading to loss of expression in primary breast tumours. (1989) (223)
High-resolution mapping of crossovers in human sperm defines a minisatellite-associated recombination hotspot. (1998) (223)
High resolution analysis of haplotype diversity and meiotic crossover in the human TAP2 recombination hotspot. (2000) (220)
Mouse DNA 'fingerprints': analysis of chromosome localization and germ-line stability of hypervariable loci in recombinant inbred strains. (1987) (217)
Characterization of a highly unstable mouse minisatellite locus: evidence for somatic mutation during early development. (1989) (192)
Human recombination hot spots hidden in regions of strong marker association (2005) (191)
Highly variable minisatellites and DNA fingerprints. (1987) (186)
Minisatellite diversity supports a recent African origin for modern humans (1996) (182)
Mouse minisatellite mutations induced by ionizing radiation (1993) (177)
The efficiency of multilocus DNA fingerprint probes for individualization and establishment of family relationships, determined from extensive casework. (1991) (174)
Stage specificity, dose response, and doubling dose for mouse minisatellite germ-line mutation induced by acute radiation. (1998) (172)
Further evidence for elevated human minisatellite mutation rate in Belarus eight years after the Chernobyl accident. (1997) (170)
Factors influencing recombination frequency and distribution in a human meiotic crossover hotspot. (2005) (161)
Unequal crossingover between homologous chromosomes is not the major mechanism involved in the generation of new alleles at VNTR loci. (1989) (155)
Systematic cloning of human minisatellites from ordered array charomid libraries. (1990) (154)
Linkage of adult α- and β-globin genes in X. laevis and gene duplication by tetraploidization (1980) (147)
Genome stability: Transgenerational mutation by radiation (2000) (141)
Detection of somatic changes in human cancer DNA by DNA fingerprint analysis. (1987) (138)
DNA fingerprints applied to gene introgression in breeding programs. (1990) (137)
Minisatellite mutation rate variation associated with a flanking DNA sequence polymorphism (1994) (135)
A somatic BRCA1 mutation in an ovarian tumour (1995) (132)
Repeat instability at human minisatellites arising from meiotic recombination (1998) (129)
Variants of the protein PRDM9 differentially regulate a set of human meiotic recombination hotspots highly active in African populations (2011) (125)
Recombination hotspots rather than population history dominate linkage disequilibrium in the MHC class II region. (2003) (119)
Mechanisms underlying telomere repeat turnover, revealed by hypervariable variant repeat distribution patterns in the human Xp/Yp telomere. (1995) (118)
A novel single molecule analysis of spontaneous and radiation-induced mutation at a mouse tandem repeat locus. (2002) (113)
Organization of the human myoglobin gene. (1984) (113)
Somatic mutation processes at a human minisatellite. (1997) (111)
Crossover clustering and rapid decay of linkage disequilibrium in the Xp/Yp pseudoautosomal gene SHOX (2002) (110)
Sequences flanking the repeat arrays of human minisatellites: association with tandem and dispersed repeat elements. (1989) (109)
A tetranucleotide repeat mouse minisatellite displaying substantial somatic instability during early preimplantation development. (1993) (108)
Meiotic recombination hot spots and human DNA diversity. (2004) (108)
USE OF MINISATELLITE DNA PROBES FOR DETERMINATION OF TWIN ZYGOSITY AT BIRTH (1985) (106)
Analysis of somatic mutations at human minisatellite loci in tumors and cell lines. (1989) (105)
Polymorphism in the activity of human crossover hotspots independent of local DNA sequence variation. (2006) (102)
Gestational and nongestational trophoblastic tumors distinguished by DNA analysis (1992) (100)
Allelic diversity at minisatellite MS205 (D16S309): evidence for polarized variability. (1993) (100)
Instability of long inverted repeats within mouse transgenes. (1996) (94)
Mutation rate heterogeneity and the generation of allele diversity at the human minisatellite MS205 (D16S309). (1996) (93)
Evolutionary transience of hypervariable minisatellites in man and the primates (1991) (91)
DNA fingerprints of poultry. (2009) (90)
Minisatellite instability and germline mutation (1999) (90)
The evolution of DNA sequences. (1986) (89)
Radiation-induced germline instability at minisatellite loci. (1998) (87)
Induction of minisatellite mutations in the mouse germline by low-dose chronic exposure to gamma-radiation and fission neutrons. (2000) (85)
Evolution of the β-globin gene cluster in man and the primates (1981) (81)
The seal myoglobin gene: an unusually long globin gene (1983) (80)
Processes of copy-number change in human DNA: the dynamics of {alpha}-globin gene deletion. (2006) (79)
Human telomeres that carry an integrated copy of human herpesvirus 6 are often short and unstable, facilitating release of the viral genome from the chromosome (2013) (79)
Influences of array size and homogeneity on minisatellite mutation (1998) (77)
Sperm cross-over activity in regions of the human genome showing extreme breakdown of marker association (2008) (75)
A novel unstable mouse VNTR family expanded from SINE B1 elements. (1998) (75)
High‐resolution sperm typing of meiotic recombination in the mouse MHC Eβ gene (2003) (74)
Highly polymorphic minisatellite sequences: allele frequencies and mutation rates for five locus-specific probes in a Caucasian population. (1990) (72)
Crossover breakpoint mapping identifies a subtelomeric hotspot for male meiotic recombination. (2000) (71)
A subterminal satellite located adjacent to telomeres in chimpanzees is absent from the human genome (1994) (70)
DNA fingerprinting of spontaneously hypertensive and Wistar-Kyoto rats: implications for hypertension research. (1989) (69)
APPLICATION OF DNA "FINGERPRINTS" TO PATERNITY DETERMINATIONS (1988) (68)
A comparison of vertebrate interferon gene families detected by hybridization with human interferon DNA. (1983) (67)
Spontaneous mutation at the hypervariable mouse minisatellite locus Ms6-hm: flanking DNA sequence and analysis of germline and early somatic mutation events (1991) (67)
Human minisatellites, repeat DNA instability and meiotic recombination (1999) (67)
Allelic recombination and de novo deletions in sperm in the human beta-globin gene region. (2006) (66)
Biology and applications of human minisatellite loci. (1992) (66)
A physical map of the DNA regions flanking the rabbit beta-globin gene. (1977) (64)
Digital DNA typing at a second hypervariable locus by minisatellite variant repeat mapping. (1993) (64)
Minisatellite mutation frequency in human sperm following radiotherapy. (2000) (64)
The rise and fall of a human recombination hot spot (2009) (64)
Hypervariable minisatellite DNA sequences in the Indian peafowl Pavo cristatus. (1991) (64)
Allele diversity and germline mutation at the insulin minisatellite. (2000) (63)
Extremely complex repeat shuffling during germline mutation at human minisatellite B6.7. (1999) (63)
Processes of de novo duplication of human α-globin genes (2007) (61)
Detection of a novel minisatellite-specific DNA-binding protein. (1990) (58)
Mutation processes at human minisatellites (1995) (57)
No correlation between germline mutation at repeat DNA and meiotic crossover in male mice exposed to X-rays or cisplatin. (2000) (56)
Influence of allele lineage on the role of the insulin minisatellite in susceptibility to type 1 diabetes. (2000) (56)
Localized breakdown in linkage disequilibrium does not always predict sperm crossover hot spots in the human MHC class II region. (2005) (55)
Big, bad minisatellites (1997) (54)
Isolation of telomere junction fragments by anchored polymerase chain reaction (1992) (53)
The 5' flanking region of human epsilon-globin gene. (1980) (52)
The primate ψβ1 gene: An ancient β-globin pseudogene (1984) (51)
Meiotic recombination and flanking marker exchange at the highly unstable human minisatellite CEB1 (D2S90). (2000) (51)
Isolation and sequence analysis of a hybrid δ-globin pseudogene from the brown lemur (1982) (51)
Transmission Distortion Affecting Human Noncrossover but Not Crossover Recombination: A Hidden Source of Meiotic Drive (2014) (51)
Species-wide distribution of highly polymorphic minisatellite markers suggests past and present genetic exchanges among house mouse subspecies (2007) (48)
Spontaneous and induced minisatellite instability (1997) (46)
A novel human DNA polymorphism resulting from transfer of DNA from chromosome 6 to chromosome 16. (1990) (46)
Use of minisatellite DNA probes for recognition and characterization of relapse after allogeneic bone marrow transplantation (1988) (46)
Somatic versus germline mutation processes at minisatellite CEB1 (D2S90) in humans and transgenic mice. (2000) (44)
Genetic fingerprinting (2005) (44)
Recombination regulator PRDM9 influences the instability of its own coding sequence in humans (2012) (44)
Human tandem repeat sequences in forensic DNA typing. (2005) (43)
Localisation of the Gγ-, Aγ-, δ- and β-globin genes on the short arm of human chromosome 11 (1979) (43)
EVOLUTION OF GLOBIN GENES (1981) (43)
Principles and recent advances in human DNA fingerprinting. (1991) (43)
Brief introduction to human DNA fingerprinting. (1993) (43)
DNA fingerprinting Dolly (1998) (42)
Processes of gene duplication (1982) (42)
Activation of the ALT pathway for telomere maintenance can affect other sequences in the human genome. (2005) (41)
Global haplotype diversity in the human insulin gene region. (2003) (41)
Myoglobin expression: early induction and subsequent modulation of myoglobin and myoglobin mRNA during myogenesis (1986) (40)
Highly variable minisatellites and DNA fingerprints. (1987) (38)
Isolation and characterization of mouse minisatellites. (1998) (38)
Comparative sequence analysis of human minisatellites showing meiotic repeat instability. (1999) (38)
Allele-specific MVR-PCR analysis at minisatellite D1S8. (1993) (37)
A major recombination hotspot in the XqYq pseudoautosomal region gives new insight into processing of human gene conversion events. (2012) (37)
The mouse myoglobin gene. Characterisation and sequence comparison with other mammalian myoglobin genes. (1986) (36)
Structural analysis of insulin minisatellite alleles reveals unusually large differences in diversity between Africans and non-Africans. (2002) (35)
Processes of copy-number change in human DNA : The dynamics of-globin gene deletion (2006) (34)
DNA enrichment by allele-specific hybridization (DEASH): a novel method for haplotyping and for detecting low-frequency base substitutional variants and recombinant DNA molecules. (2003) (34)
Minisatellite binding protein Msbp-1 is a sequence-specific single-stranded DNA-binding protein. (1991) (33)
Application of DNA fingerprinting probes to old world monkeys (1988) (32)
Analysis of meiotic recombination products from human sperm. (2009) (32)
Processes of de novo duplication of human alpha-globin genes. (2007) (31)
DNA variability and parentage testing in captive Waldrapp ibises (1994) (31)
IDENTIFICATION OF POST-TRANSPLANT CELL POPULATION BY DNA FINGERPRINT ANALYSIS (1986) (31)
Four-state MVR-PCR: increased discrimination of digital DNA typing by simultaneous analysis of two polymorphic sites within minisatellite variant repeats at D1S8. (1993) (31)
The use of minisatellite variant repeat-polymerase chain reaction (MVR-PCR) to determine the source of saliva on a used postage stamp. (1994) (30)
The rabbit beta-globin gene contains a large large insert in the coding sequence. (1977) (30)
Development of a flow-cytometric HLA-A locus mutation assay for human peripheral blood lymphocytes. (1992) (30)
Human minisatellite alleles detectable only after PCR amplification. (1992) (30)
Seventh international meeting on single nucleotide polymorphism and complex genome analysis: ‘ever bigger scans and an increasingly variable genome’ (2006) (29)
DNA sequence variants in the G gamma-, A gamma-, delta- and beta-globin genes of man. (1979) (28)
Use of vectorette and subvectorette PCR to isolate transgene flanking DNA. (1994) (27)
A hypervariable locus D16S309 located at the distal end of 16p. (1992) (27)
Two modes of germline instability at human minisatellite MS1 (locus D1S7): complex rearrangements and paradoxical hyperdeletion. (2003) (27)
DNA 'fingerprinting' of captive family groups of common marmosets (Callithrix jacchus). (1988) (26)
DNA typing: approaches and applications. (1993) (26)
Minisatellite variant repeat mapping: application to DNA typing and mutation analysis. (1993) (25)
Tandemly repeated transgenes of the human minisatellite MS32 (D1S8), with novel mouse gamma satellite integration. (1994) (25)
Analysis of proteins synthesized in mitochondria of cultured mammalian cells. An assessment of current approaches and problems in interpretation. (1976) (24)
Frequency of heterozygous complete hydatidiform moles, estimated by locus-specific minisatellite and Y chromosome-specific probes (1989) (24)
Increased Rate of Spontaneous Mitotic Recombination in T Lymphocytes from a Bloom's Syndrome Patient Using a Flow‐cytometric Assay at HLA‐A Locus (1994) (23)
Use of a hypervariable minisatellite DNA probe (33.15) for evaluating engraftment two or more years after bone marrow transplantation for aplastic anaemia (1988) (23)
DNA Fingerprinting of Free-Ranging Groups of Common Marmosets (Callithrix jacchus jacchus) in NE Brazil (1992) (23)
Minisatellite variant repeat (MVR) mapping: analysis of 'null' repeat units at D1S8. (1992) (23)
Rapid identification of donor and recipient cells after allogeneic bone marrow transplantation using specific genetic markers (1989) (23)
Hypervariable 'minisatellite' regions in human DNA. 1985. (1992) (22)
Length of uninterrupted repeats determines instability at the unstable mouse expanded simple tandem repeat family MMS10 derived from independent SINE B1 elements (2001) (22)
Nucleotide sequence analysis of the lemur beta-globin gene family: evidence for major rate fluctuations in globin polypeptide evolution. (1986) (22)
Distribution of tandem repeat polymorphism within minisatellite MS621 (D5S110) (1996) (21)
Cloning, Characterization and Evolution of Indian Peafowl Pavo cristatus Minisatellite Loci (1991) (21)
Minisatellite "isoallele" discrimination in pseudohomozygotes by single molecule PCR and variant repeat mapping. (1991) (20)
Human minisatellite MS32 (D1S8) displays somatic but not germline instability in transgenic mice. (1997) (20)
High resolution analysis of haplotype diversity and meiotic crossover in the human TAP 2 recombination hotspot (2000) (19)
Dynamics and processes of copy number instability in human γ-globin genes (2010) (17)
Palaemolecular biology: Raising the dead and buried (1984) (17)
Spontaneous and induced minisatellite instability in the human genome. (1997) (17)
DNA profiling reveals remarkably low genetic variability in a herd of SLA homozygous pigs. (1999) (16)
Variable germline and embryonic instability of the human minisatellite MS32 (D1S8) in transgenic mice. (1994) (16)
Differences in the mitochondrially synthesized subunits of human and mouse cytochrome c oxidase (1977) (16)
Mouse minisatellite mutations induced by ionizing radiation : Nature Genet., 5, 92–94 (1993) (16)
Detection of chromosomal 7 loss in myelodysplasia using an extremely polymorphic DNA probe. (1988) (15)
Isolation of human minisatellite loci detected by synthetic tandem repeat probes: direct comparison with cloned DNA fingerprinting probes. (1992) (14)
Abnormal segregation of alleles in CEPH pedigree DNAs arising from allele loss in lymphoblastoid DNA. (1993) (14)
Isolation and detailed characterization of human cell lines resistant to D-threo-chloramphenicol. (1976) (14)
Recent advances in minisatellite biology (1992) (13)
The application of minisatellite variant repeat mapping by PCR (MVR-PCR) in a paternity case showing false exclusion due to STR mutation. (2001) (13)
The human myoglobin gene: a third dispersed globin locus in the human genome. (1984) (12)
Chimaeric and constitutive DNA fingerprints in the common marmoset (Callithrix jacchus) (2007) (12)
"Major minisatellite loci" detected by minisatellite clones 33.6 and 33.15 correspond to the cognate loci D1S111 and D7S437. (1990) (12)
Effects of radiation on children (1996) (12)
Linkage analysis of British and Indian families with Von Recklinghausen neurofibromatosis. (1987) (11)
Monitoring spontaneous and induced human mutation by RAPD-PCR: a response to Weinberg et al. (2001) (2001) (11)
The zygosity determination of Japanese twins using a minisatellite core probe (1987) (11)
Localization of repetitive and unique DNA sequences neighbouring the rabbit beta-globin gene. (1980) (10)
L1 Hybridization Enrichment: A Method for Directly Accessing De Novo L1 Insertions in the Human Germline (2011) (10)
Differences in the products of mitochondrial protein synthesis in vivo in Human and mouse cells and their potential use as markers for the mitochondrial genome in human--mouse somatic cell hybrids. (1974) (10)
Application of human minisatellite probes to the development of informative DNA fingerprints and the isolation of locus-specific markers in animals. (1993) (9)
Minisatellites show rare and simple intra-allelic instability in the mouse germ line. (2002) (9)
Attempts to detect retrotransposition and de novo deletion of Alus and other dispersed repeats at specific loci in the human genome (2001) (9)
STS for minisatellite MS607 (D22S163). (1991) (8)
Evolutionary fate of an unstable human minisatellite deduced from sperm-mutation spectra of individual alleles. (2002) (8)
Distinguishing minisatellite mutation from non-paternity by MVR-PCR. (2000) (8)
Minisatellite isoalleles can be distinguished by single-stranded conformational polymorphism analysis in agarose gels. (1994) (8)
A pseudoautosomal minisatellite in the pig (2004) (7)
The potential contribution of MVR-PCR to paternity probabilities in a case lacking a mother. (1999) (7)
Are DNA profiles breed-specific? A pilot study in pigs. (2000) (7)
Sequence variation and evolution of nuclear DNA in man and the primates. (1981) (7)
DNA typing of the D1S8 (MS32) locus by rapid detection minisatellite variant repeat (MVR) mapping using polymerase chain reaction (PCR) assay. (1994) (7)
DNA fingerprint analysis in immigration test-cases (reply) (1986) (7)
Physical mapping of repetitive DNA sequences neighboring the rabbit beta-globin gene. (1978) (6)
GENETIC TYPING AND CONFIRMATION OF PARENTHOOD (1987) (6)
Principles and Recent Advances in DNA Fingerprinting (1991) (5)
Molecular cloning of seal myoglobin mRNA. (1982) (5)
[DNA typing and analysis of the D1S8 (MS 32) allele in the Japanese population by the minisatellite variant repeat (MVR) mapping by polymerase chain reaction (PCR) assay]. (1992) (5)
The man behind the DNA fingerprints: an interview with Professor Sir Alec Jeffreys (2013) (5)
Increased band sharing in DNA fingerprints of an inbred human population (1991) (5)
Angelman syndrome can result from uniparental paternal isodisomy (1990) (5)
Localisation of the G gamma-, A gamma-, delta- and beta-globin genes on the short arm of human chromosome 11. (1979) (4)
Human minisatellite loci composed of interspersed GGA-GGT triplet repeats (1995) (4)
Minisatellite MS32 Alleles Show Population Specificity Among Thai, Chinese, and Japanese (2009) (4)
A panel of VNTR markers in pigs (1996) (3)
Minisatellite mutation and recombination (1993) (3)
Detection of an MboI RFLP at the porcine clotting factor IX locus and verification of sex linkage. (1996) (3)
Proteins made in mitochondria of cultured animal cells. (1975) (3)
The primate psi beta 1 gene. An ancient beta-globin pseudogene. (1984) (3)
Minisatellite DNA profiles: rapid sample identification in linkage analysis. (1990) (2)
The Structure of the Rabbit β-Globin Gene (1978) (2)
A polymorphic minisatellite (pMS628) on chromosome 3 (D3S1084). (1991) (2)
Application of minisatellite DNA probes to linkage in MEN-2. (1987) (2)
Title : Processes of copy number change in human DNA : the dynamics of a-globin gene deletion (2007) (2)
A highly polymorphic minisatellite (pMS627) on chromosome 14 (D14S44). (1991) (2)
Molecular biology and human diversity: Digital DNA typing of human paternal lineages (1996) (2)
Evolution of the beta-globin gene cluster in man and the primates. (1981) (2)
Human Recombination Hotspots: Before and After the HapMap Project (2007) (2)
Isolation and sequence analysis of a hybrid delta-globin pseudogene from the brown lemur. (1982) (2)
Whither Cloning? (2000) (1)
1 DNA fingerprinting of spontaneously hypertensive and Wistar‐Kyoto rats: a method of analysing the genetic basis of hypertension in the spontaneously hypertensive rat (1988) (1)
Evaluation of fragmentation of specimen dna (1989) (1)
Allelic structures at hypervariable minisatellite B6.7 in Japanese show population specificity (2002) (1)
Radiation-induced mutations in mouse minisatellite DNA (1993) (1)
Amplifi ' cation of human niinisatellites by the polymerase chain reaction : towards DNA flgerprinting of single cells (1)
Theoretical analysis of (dA-dT) cluster distributions in DNA. (1977) (1)
Rapid genotyping of a pig minisatellite using long PCR. (1997) (1)
Two hypervariable minisatellites D19S192 (pMS207.2) and D19S193 (pMS301.2) located at the distal ends of 19p and 19q respectively. (1992) (1)
Radiation sensitivity in male mouse germ cells (1998) (0)
The structure of the rabbit beta-globin gene. (1978) (0)
A hypervariable minisatellite (pMS502) on chromosome 8 (D8S162). (1991) (0)
The Evolution of DNA Sequences. Proceedings of a Royal Society Discussion Meeting, March 13 and 14, 1985. (1988) (0)
cis- and trans- regulation controls of human meiotic recombination at a hotspot (2017) (0)
Germline mutation induction at tandem repeat DNA loci January 2002 (2009) (0)
Extreme variability in the Xp:Yp pseudoautosomal telomere revealed by telomere variant repeat mapping (1994) (0)
A method of assessing DNA fragmentation, polynucleotide probes and kits for its implementation (1989) (0)
Erratum: Intense and highly localized gene conversion activity in human meiotic crossover hot spots (2004) (0)
33.6 (D1S111) and pMLAJ1 (D1S61) identify the same VNTR on chromosome 1. (1991) (0)
Method for characterizing an analytical sample of genomic dna by extending nucleotide sequences, and diagnostic kits for carrying out said method (1989) (0)
Linkage analysis of the halothane sensitivity locus in pigs (2008) (0)
Pseudogenes (1984) (0)
Substitutional Variants and Recombinant DNA Molecules Method for Haplotyping and for Detecting Low-Frequency Base DNA Enrichment by Allele-Specific Hybridization ( DEASH ) : A Novel (2003) (0)
Trans- and cis-regulators of meiotic recombination control in humans (2017) (0)
presence detection method of a variable length locus in a DNA sequence, nucleotide sequence and its use (1989) (0)
Human mitochondrial genome can replicate in the Yarrowia lipolytica yeast (2016) (0)
Nucleic Acids Research (2009) (0)
Nucleic Acids Research The 5 ' flanking region of human eglobin gene (0)
Identification de sequences repetees simples en tandem (1994) (0)
A hypervariable minisatellite (pMS400) on chromosome 19 (D19S176). (1991) (0)
Processes of de novo duplication of human (cid:1) -globin genes (2007) (0)
Title : Sperm crossover activity in regions of the human genome showing extreme breakdown of marker association (2008) (0)
[News from allied medical fields. Medical genetics. DNA fingerprinting: procedures and applications]. (1993) (0)
A highly polymorphic minisatellite (pMS626) on chromosome 13 (D13S103). (1991) (0)
Report of the second international workshop on human chromosome 5 mapping: consensus genetic map. (1992) (0)
DNA in the Courtroom : The 21 st Century Begins (2007) (0)
Polynucleotide for determination of genomic characteristics (1992) (0)
STS for minisatellite 33.1 (D9S49): direct typing by PCR. (1991) (0)
DNA profiling. (1993) (0)
A method for the assessment of sample dna fragmentation and polynucleotide probes therefor (1989) (0)
Radiation-Induced Mutation at Mammalian Minisatellite Loci (1999) (0)
Alec John Jeffreys (1950–) (2018) (0)
Analysis of four polymorphic minisatellites suggests frequent genetic exchanges among House Mouse subspecies (2007) (0)
A hypervariable minisatellite locus D20S73 (pMS214.2) is located on 20q. (1992) (0)
The Evolution of the Genome (1982) (0)

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