Username

Password

Preview

Sign-in free and Explore the Exciting World of BiomedExperts:

Over 1.500.000 Profiles
More than 1.800 Organizations worldwide
State of the Art Network Visualizations

Manage your own Profile
Locate Experts in your Country/Region
Locate Experts in your 1. and 2. Level Network
Connect to Experts Worldwide

NetworkView

Trefor Jenkins

This is a preview profile on BiomedExperts - the first literature-based scientific social network. It brings the right researchers together and allows them to collaborate online. Collexis and Dell provide the BiomedExperts network of +1.5 Million pre-calculated profiles free of charge to researchers worldwide.

Research Profile (preview)

Living Beings

Geographic Areas

Physiology

Concepts & Ideas

Chemicals & Drugs

Genes & Molecular Sequences

Alleles

Anatomy

Sign-in to see full Profile

Sign-in to see all Coauthors

Publications

TOP 3
Jenkins T
The impact of HIV / AIDS on blood transfusion practice in South Africa: some ethical issues.
John Premila R; Makova Kateryna; Li Wen-Hsiung; Jenkins Trefor; Ramsay Michele
DNA polymorphism and selection at the melanocortin-1 receptor gene in normally pigmented southern African individuals.
Manga P; Kromberg J; Turner A; Jenkins T; Ramsay M
In Southern Africa, brown oculocutaneous albinism (BOCA) maps to the OCA2 locus on chromosome 15q: P-gene mutations identified.

Sign-in to see all Publications

Sign in free and see...

Visualized networks:

See your personal network in
sophisticated graphical views

GeoTargeted Searches:

Locate experts around the world
and connect with global collaborators

Research Profiles:

See the visualized research activity
of experts around the globe

Sign-in to see more

Geonetwork of Trefor Jenkins (preview)

Cities where this author has publications
Cities where co-authors of this author have publications

Flash Player Required

Sign-in to see more

All Publications

2007: Jenkins T
The impact of HIV / AIDS on blood transfusion practice in South Africa: some ethical issues.
South African medical journal = Suid-Afrikaanse tydskrif vir geneeskunde 2007;97(11 Pt 3):1206-10.
2003: John Premila R; Makova Kateryna; Li Wen-Hsiung; Jenkins Trefor; Ramsay Michele
DNA polymorphism and selection at the melanocortin-1 receptor gene in normally pigmented southern African individuals.
Annals of the New York Academy of Sciences 2003;994():299-306.
2001: Manga P; Kromberg J; Turner A; Jenkins T; Ramsay M
In Southern Africa, brown oculocutaneous albinism (BOCA) maps to the OCA2 locus on chromosome 15q: P-gene mutations identified.
American journal of human genetics 2001;68(3):782-7.
1999: Kromberg J G; Krause A; Spurdle A B; Temlett J A; Lucas M; Rodseth D; Stevens G; Jenkins T
Utilisation of predictive, prenatal and diagnostic testing for Huntington's disease in Johannesburg.
South African medical journal = Suid-Afrikaanse tydskrif vir geneeskunde 1999;89(7):774-8.
1999: Manga N; Jenkins T; Jackson H; Whittaker D A; Lane A B
The molecular basis of transferase galactosaemia in South African negroids.
Journal of inherited metabolic disease 1999;22(1):37-42.
1999: Padoa C; Goldman A; Jenkins T; Ramsay M
Cystic fibrosis carrier frequencies in populations of African origin.
Journal of medical genetics 1999;36(1):41-4.
1997: Manga P; Kromberg J G; Box N F; Sturm R A; Jenkins T; Ramsay M
Rufous oculocutaneous albinism in southern African Blacks is caused by mutations in the TYRP1 gene.
American journal of human genetics 1997;61(5):1095-101.
1997: Starfield M; Hennies H C; Jung M; Jenkins T; Wienker T; Hull P; Spurdle A; Küster W; Ramsay M; Reis A
Localization of the gene causing keratolytic winter erythema to chromosome 8p22-p23, and evidence for a founder effect in South African Afrikaans-speakers.
American journal of human genetics 1997;61(2):370-8.
1997: Jenkins T
The molecular basis of South African genetic porphyria established at last!
South African medical journal = Suid-Afrikaanse tydskrif vir geneeskunde 1997;87(6):733-5.
1997: Dangerfield B T; Manga P; Field S P; Hartman E; Jenkins T; Krause A
Feasibility of prenatal diagnosis and carrier detection in South African haemophilia A patients.
British journal of haematology 1997;97(3):558-60.
1997: Stevens G; Ramsay M; Jenkins T
Oculocutaneous albinism (OCA2) in sub-Saharan Africa: distribution of the common 2.7-kb P gene deletion mutation.
Human genetics 1997;99(4):523-7.
1996: Spurdle A B; Jenkins T
The origins of the Lemba "Black Jews" of southern Africa: evidence from p12F2 and other Y-chromosome markers.
American journal of human genetics 1996;59(5):1126-33.
1996: Goldman A; Krause A; Ramsay M; Jenkins T
Founder effect and prevalence of myotonic dystrophy in South Africans: molecular studies.
American journal of human genetics 1996;59(2):445-52.
1996: Hewitt R; Krause A; Goldman A; Campbell G; Jenkins T
Beta-globin haplotype analysis suggests that a major source of Malagasy ancestry is derived from Bantu-speaking Negroids.
American journal of human genetics 1996;58(6):1303-8.
1996: Goldman A; Ramsay M; Jenkins T
Ethnicity and myotonic dystrophy: a possible explanation for its absence in sub-Saharan Africa.
Annals of human genetics 1996;60(Pt 1):57-65.
1995: Goldman A; Ramsay M; Jenkins T
Molecular analysis of the CTG trinucleotide repeat in South African myotonic dystrophy families--implications for diagnosis and counselling.
South African medical journal = Suid-Afrikaanse tydskrif vir geneeskunde 1995;85(11):1161-4.
1995: Goldman A; Ramsay M; Jenkins T
New founder haplotypes at the myotonic dystrophy locus in southern Africa.
American journal of human genetics 1995;56(6):1373-8.
1995: Stevens G; van Beukering J; Jenkins T; Ramsay M
An intragenic deletion of the P gene is the common mutation causing tyrosinase-positive oculocutaneous albinism in southern African Negroids.
American journal of human genetics 1995;56(3):586-91.
1994: Goldman A; Jenkins T; Ramsay M
Analysis of 40 known cystic fibrosis mutations in South African patients.
Clinical genetics 1994;46(6):398-400.
1994: McLean G R; Jenkins T
HIV testing and informed consent--ethical considerations.
South African medical journal = Suid-Afrikaanse tydskrif vir geneeskunde 1994;84(10):669-74.
1994: Spurdle A B; Jenkins T
The Y-specific pDP31 rearrangement polymorphism in southern African populations.
Human heredity 1994;44(5):261-5.
1994: Spurdle A B; Krause A; Ramsay M; Jenkins T
The high frequency of the Hb B2 variant in the Herero population: a founder effect?
Hemoglobin 1994;18(4-5):317-23.
1994: Spurdle A B; Woodfield D G; Hammer M F; Jenkins T
The genetic affinity of Polynesians: evidence from Y chromosome polymorphisms.
Annals of human genetics 1994;58(Pt 3):251-63.
1994: Jenkins T
Hunter-gatherers in southern Africa.
South African medical journal = Suid-Afrikaanse tydskrif vir geneeskunde 1994;Suppl():10-2.
1994: Kedda M A; Stevens G; Manga P; Viljoen C; Jenkins T; Ramsay M
The tyrosinase-positive oculocutaneous albinism gene shows locus homogeneity on chromosome 15q11-q13 and evidence of multiple mutations in southern African negroids.
American journal of human genetics 1994;54(6):1078-84.
1994: Spurdle A B; Hammer M F; Jenkins T
The Y Alu polymorphism in southern African populations and its relationship to other Y-specific polymorphisms.
American journal of human genetics 1994;54(2):319-30.
1994: Goldman A; Ramsay M; Jenkins T
Absence of myotonic dystrophy in southern African Negroids is associated with a significantly lower number of CTG trinucleotide repeats.
Journal of medical genetics 1994;31(1):37-40.
1993: Soodyall H; Jenkins T
Mitochondrial DNA polymorphisms in Negroid populations from Namibia: new light on the origins of the Dama, Herero and Ambo.
Annals of human biology 1993;20(5):477-85.
1993: Colman M A; Stevens G; Ramsay M; Kwon B; Jenkins T
Exclusion of two candidate pigment loci, c and b, part of chromosome 11p, and 33 random polymorphic markers as the locus for tyrosinase-positive oculocutaneous albinism.
Human genetics 1993;90(5):556-60.
1993: Spurdle A B; Jenkins T
Complex polymorphisms are revealed by Y chromosome probe 49a with BglII, HindIII, PstI and SstI.
Annals of human genetics 1993;57(Pt 1):41-53.
1993: Stevens G; Ramsay M; Kluve-Beckerman B; Jenkins T
A new negroid-specific HindIII polymorphism in the serum amyloid A1 (SAA1) gene increases the usefulness of the SAA locus in linkage studies.
Genomics 1993;15(1):242-3.
1992: Ramsay M; Colman M A; Stevens G; Zwane E; Kromberg J; Farrall M; Jenkins T
The tyrosinase-positive oculocutaneous albinism locus maps to chromosome 15q11.2-q12.
American journal of human genetics 1992;51(4):879-84.
1992: Soodyall H; Jenkins T
Mitochondrial DNA polymorphisms in Khoisan populations from southern Africa.
Annals of human genetics 1992;56(Pt 4):315-24.
1992: Denter M; Ramsay M; Jenkins T
Cystic fibrosis. Part I. Frequency of the delta F508 mutation in South African families with cystic fibrosis.
South African medical journal = Suid-Afrikaanse tydskrif vir geneeskunde 1992;82(1):7-10.
1992: Denter M; Ramsay M; Jenkins T
Cystic fibrosis. Part II. New developments in cystic fibrosis--implications for carrier detection and genetic counselling.
South African medical journal = Suid-Afrikaanse tydskrif vir geneeskunde 1992;82(1):11-3.
1992: Spurdle A; Ramsay M; Jenkins T
The Y-associated XY275 low allele is not restricted to indigenous African peoples.
American journal of human genetics 1992;50(6):1301-7.
1992: Spurdle A; Jenkins T
The search for Y chromosome polymorphism is extended to negroids.
Human molecular genetics 1992;1(3):169-70.
1992: Kromberg J G; Christianson A L; Duthie-Nurse G; Zwane E; Jenkins T
Down syndrome in the black population.
South African medical journal = Suid-Afrikaanse tydskrif vir geneeskunde 1992;81(6):337.
1992: Spurdle A; Jenkins T
Y chromosome probe p49a detects complex PvuII haplotypes and many new TaqI haplotypes in southern African populations.
American journal of human genetics 1992;50(1):107-25.
1992: Spurdle A; Jenkins T
The inverted Y-chromosome polymorphism in the Gujarati Muslim Indian population of South Africa has a single origin.
Human heredity 1992;42(5):330-2.
1991: Colman M A; Segalo P; Ramsay M; Jenkins T
A third TaqI allele is detected by the probe pTD3-21 (D15S10) in southern African chromosomes.
Nucleic acids research 1991;19(18):5097.
1991: Morris D J; Heim R A; Verga V; Denter M; Dunn D S; Jenkins T
Study of 30 DNA markers in three southern African populations.
Gene geography : a computerized bulletin on human gene frequencies 1991;5(1-2):1-12.
1991: Spurdle A; Kromberg J; Rosendorff J; Jenkins T
Prenatal diagnosis for Huntington's disease: a molecular and psychological study.
Prenatal diagnosis 1991;11(3):177-185.
1991: Colman M A; Shibahara S; Kwon B; Jenkins T; Ramsay M
A two allele XbaI RFLP at the catalase 2 locus.
Nucleic acids research 1991;19(4):960.
1990: Jenkins T
Medical genetics in South Africa.
Journal of medical genetics 1990;27(12):760-79.
1990: Jenkins T; Heim R A; Dunn D S; Zwane E; Colman M A; Ramsay M; Kromberg J G
In quest of the tyrosinase-positive oculocutaneous albinism gene.
Ophthalmic paediatrics and genetics 1990;11(4):251-4.
1990: Kromberg J G; Castle D J; Zwane E M; Bothwell J; Kidson S; Bartel P; Phillips J I; Jenkins T
Red or rufous albinism in southern Africa.
Ophthalmic paediatrics and genetics 1990;11(3):229-35.
1990: Spurdle A B; Jenkins T
pDP1007, detects an X polymorphism with HindIII in negroids at the ZFX locus.
Nucleic acids research 1990;18(11):3430.
1990: Meyer T; Baynes R; Bothwell T; Jenkins T; Jooste P; Du Toit E; Martell R; Jacobs P
Phenotypic expression of the HLA linked iron-loading gene in males over the age of 40 years: a population study using serial serum ferritin estimations.
Journal of internal medicine 1990;227(6):397-406.
1990: Stevens G; Spurdle A B; Jenkins T
New TaqI allele detected by X-chromosome probe s21 (DXS17).
Nucleic acids research 1990;18(10):3113.
1989: Lombard E H; Kromberg J G; Thomson P D; Milner L S; van Biljon I; Jenkins T
Autosomal recessive polycystic kidney disease. Evidence for high frequency of the gene in the Afrikaans-speaking population.
South African medical journal = Suid-Afrikaanse tydskrif vir geneeskunde 1989;76(7):321-3.
1989: Kromberg J G; Bernstein R; Jacobson M J; Rosendorff J; Jenkins T
A decade of mid-trimester amniocentesis in Johannesburg. Prenatal diagnosis, problems and counselling.
South African medical journal = Suid-Afrikaanse tydskrif vir geneeskunde 1989;76(7):344-9.
1989: Dunn D S; Testa T; Morgan C; Bartleet S C; Jenkins T; Bartlett R G; Joffe M
The usefulness of various polymorphisms in paternity testing. Experience with three southern African populations.
South African medical journal = Suid-Afrikaanse tydskrif vir geneeskunde 1989;76(7):303-7.
1989: Morris D J; dos Santos M; Povey S; Willem P; Jenkins T
A new marker on chromosome 4q, D4S138, detects two RFLPs.
Nucleic acids research 1989;17(17):7123.
1989: Morris D J; dos Santos M; Ramsay M; Povey S; Jenkins T
An anonymous single copy probe, D3S153, detects an SstI RFLP.
Nucleic acids research 1989;17(17):7122.
1989: Morris D J; dos Santos M; Povey S; Ramsay M; Jenkins T
A new anonymous marker on chromosome 11, D11S347, detects two TaqI RFLPs.
Nucleic acids research 1989;17(17):7120.
1989: Morris D J; dos Santos M; Povey S; Ramsay M; Jenkins T
A new anonymous marker on chromosome 7, D7S420, identifies a PvuII RFLP.
Nucleic acids research 1989;17(17):7119.
1989: Morris D J; dos Santos M; Povey S; Ramsay M; Jenkins T
A new marker on chromosome 15, D15S74, detects three RFLPs.
Nucleic acids research 1989;17(17):7121.
1989: Kromberg J G; Castle D; Zwane E M; Jenkins T
Albinism and skin cancer in Southern Africa.
Clinical genetics 1989;36(1):43-52.
1989: Verga V; Dos Santos M; Marques I; Povey S; Ramsay M; Jenkins T
A high frequency two allele TaqI RFLP detected by an anonymous sequence VC61 [D2S65] on chromosome 2.
Nucleic acids research 1989;17(13):5424.
1989: Verga V; Dos Santos M; Marques I; Povey S; Ramsay M; Jenkins T
An arbitrary single copy human DNA sequence VC63 [D4S129] detects a TaqI RFLP on chromosome 4.
Nucleic acids research 1989;17(13):5423.
1989: Verga V; Dos Santos M; Marques I; Povey S; Ramsay M; Jenkins T
An arbitrary single copy sequence VC64 [D1S86] detects a moderate frequency TaqI RFLP on chromosome 1.
Nucleic acids research 1989;17(13):5422.
1989: Verga V; Dos Santos M; Marques I; Povey S; Ramsay M; Jenkins T
Detection of a 3 allele AvaII RFLP by a single copy anonymous DNA sequence VC75 [D7S404] localized to chromosome 7.
Nucleic acids research 1989;17(13):5421.
1989: Verga V; Dos Santos M; Marques I; Povey S; Ramsay M; Jenkins T
An arbitrary single copy DNA sequence VC85 [D1S85] detects a 500 bp insertion/deletion polymorphism on chromosome 1.
Nucleic acids research 1989;17(13):5420.
1989: Castle D J; Jenkins T; Shawinsky A A
The oculocerebral syndrome in association with generalised hypopigmentation. A case report.
South African medical journal = Suid-Afrikaanse tydskrif vir geneeskunde 1989;76(1):35-6.
1989: Verga V; Dos Santos M; Marques I; Povey S; Ramsay M; Jenkins T
A high frequency two allele TaqI RFLP detected by an anonymous sequence VC61 [D2S65] on chromosome 2.
Nucleic acids research 1989;17(10):4011.
1989: Verga V; Dos Santos M; Marques I; Povey S; Ramsay M; Jenkins T
An arbitrary single copy human DNA sequence VC63 [D4S129] detects a TaqI RFLP on chromosome 4]
Nucleic acids research 1989;17(10):4010.
1989: Verga V; Dos Santos M; Marques I; Povey S; Ramsay M; Jenkins T
An arbitrary single copy sequence VC64 [D1S86] detects a moderate frequency TaqI RFLP on chromosome 1]
Nucleic acids research 1989;17(10):4009.
1989: Verga V; Dos Santos M; Marques I; Povey S; Ramsay M; Jenkins T
Detection of a 3 allele AvaII RFLP by a single copy anonymous DNA sequence VC75 [D7S404] localized to chromosome 7.
Nucleic acids research 1989;17(10):4008.
1989: Verga V; Dos Santos M; Marques I; Povey S; Ramsay M; Jenkins T
An arbitrary single copy DNA sequence VC85 [D1S85] detects a 500 bp insertion/deletion polymorphism on chromosome 1.
Nucleic acids research 1989;17(10):4007.
1988: Krause A; Lane A B; Jenkins T
A new high activity plasma cholinesterase variant.
Journal of medical genetics 1988;25(10):677-81.
1988: Ramsay M; Jenkins T
Alpha-globin gene cluster haplotypes in the Kalahari San and southern African Bantu-speaking blacks.
American journal of human genetics 1988;43(4):527-33.
1988: Ramsay M; Bernstein R; Zwane E; Page D C; Jenkins T
XX true hermaphroditism in southern African blacks: an enigma of primary sexual differentiation.
American journal of human genetics 1988;43(1):4-13.
1988: Ramsay M; Reeders S T; Thomson P D; Milner L S; Lazarou L; Barratt T M; Yau A; Lehmann O J; Jenkins T
Mutations for the autosomal recessive and autosomal dominant forms of polycystic kidney disease are not allelic.
Human genetics 1988;79(1):73-5.
1988: Heim R A; Dunn D S; Candy S E; Zwane E; Kromberg J G; Jenkins T
The tyrosinase-positive oculocutaneous albinism locus is not linked to the beta-globin locus in man.
Human genetics 1988;79(1):89.
1988: Meyer T E; Baynes R D; Bothwell T H; Jenkins T; Ballot D; Jooste P L; Green A; Du Toit E; Jacobs P
Phenotypic expression of the HLA-linked iron-loading gene in the Afrikaner population of the western Cape.
South African medical journal = Suid-Afrikaanse tydskrif vir geneeskunde 1988;73(5):269-74.
1987: Ramsay M; Jenkins T
Globin gene-associated restriction-fragment-length polymorphisms in southern African peoples.
American journal of human genetics 1987;41(6):1132-44.
1987: Kromberg J G; Zwane E M; Jenkins T
The response of black mothers to the birth of an albino infant.
American journal of diseases of children (1960) 1987;141(8):911-6.
1987: Rosendorff J; Bernstein R; Macdougall L; Jenkins T
Fanconi anemia: another disease of unusually high prevalence in the Afrikaans population of South Africa.
American journal of medical genetics 1987;27(4):793-7.
1987: Nurse G T; Dunn D S; Rootman A J; Jenkins T
Sero-genetic studies on the Ambo of Namibia.
Gene geography : a computerized bulletin on human gene frequencies 1987;1(2):65-79.
1987: Kromberg J G; Zwane E; Castle D; Jenkins T
Albinism in South African blacks.
Lancet 1987;2(8555):388-9.
1987: Meyer T E; Ballot D; Bothwell T H; Green A; Derman D P; Baynes R D; Jenkins T; Jooste P L; du Toit E D; Jacobs P J
The HLA linked iron loading gene in an Afrikaner population.
Journal of medical genetics 1987;24(6):348-56.
1987: Ballot D; Meyer T E; Bothwell T H; Bezwoda W R; Green A; Baynes R D; Joffe M; Jenkins T
Idiopathic haemochromatosis. Family studies and results of a pilot prevalence survey.
South African medical journal = Suid-Afrikaanse tydskrif vir geneeskunde 1987;71(10):639-42.
1987: Jenkins T; Speirs J; Dunn D S; Nurse G T
Serogenetic and haematological studies on the Kgalagadi of Botswana.
Annals of human biology 1987;14(2):143-53.
1983: Jenkins T; Dunn D S; Gibney S F; Nurse G T
Serogenetic studies on the Daga of the interior of the mainland of Milne Bay Province, Papua New Guinea.
Annals of human biology 1983;10(4):357-64.
1981: Jenkins T; Gibney S F; Nurse G T; Penketh R J
Persistent high intestinal lactase activity in Papua New Guinea. Lactose absorption curves in two populations.
Annals of human biology 1981;8(5):447-51.

Sign-in to see more

Sign-in free and Explore the Exciting World of BiomedExperts:

NetworkView

Trefor Jenkins

Research Profile (preview)

Living Beings

Geographic Areas

Physiology

Concepts & Ideas

Chemicals & Drugs

Genes & Molecular Sequences

Anatomy

Disorders

Phenomena

Procedures

Network (preview)

Publications

Sign in free and see...

Visualized networks:

GeoTargeted Searches:

Research Profiles:

Geonetwork of Trefor Jenkins (preview)

All Publications