J. S. Wainscoat

发表

Missense glucokinase mutation in maturity–onset diabetes of the young and mutation screening in late–onset diabetes

R. C. Turner, G. I. Bell, J. I. Bell, 1992, Nature Genetics.

Presence of fetal DNA in maternal plasma and serum

I. Sargent, C. Redman, Y. Lo, 1997, The Lancet.

PRENATAL SEX DETERMINATION BY DNA AMPLIFICATION FROM MATERNAL PERIPHERAL BLOOD

K. Fleming, Y. Lo, J. Wainscoat, 1989, The Lancet.

Prenatal Determination of Fetal Rhesus D Status by DNA Amplification of Peripheral Blood of Rhesus‐Negative Mothers

K. Fleming, I. Mackenzie, P. Chamberlain, 1994, Annals of the New York Academy of Sciences.

Non-Invasive prenatal diagnosis

K. Fleming, Y. Lo, J. Wainscoat, 1994, The Lancet.

Prenatal sex determination from maternal peripheral blood using the polymerase chain reaction

K. Fleming, Y. Lo, P. Chamberlain, 2004, Human Genetics.

Direct haplotype determination by double ARMS: specificity, sensitivity and genetic applications

Alexander F. Markham, P. Patel, Y. M. Lo, 1991, Nucleic Acids Res..

Prenatal sex determination

K. Fleming, Y. Lo, P. Patel, 1990, The Lancet.

Multipoint linkage analysis of the short arm of chromosome 11 in non-insulin dependent diabetes including maturity onset diabetes of youth

S. O’Rahilly, R. Turner, A. Tybjaerg-hansen, 1992, Human Genetics.

Quantitation of circulating DNA in the serum of breast cancer patients by real-time PCR

A. Harris, Y. Lo, Cheng Han, 2004, British Journal of Cancer.

Linkage of type 2 diabetes to the glucokinase gene

A. Hattersley, M. Permutt, S. O’Rahilly, 1992, The Lancet.

Determination of RhD zygosity: comparison of a double amplification refractory mutation system approach and a multiplex real-time quantitative PCR approach.

R. Chiu, Y. Lo, B. Zee, 2001, Clinical chemistry.

Prenatal diagnosis of fetal RhD status by molecular analysis of maternal plasma.

N M Hjelm, C Fidler, I. Sargent, 1998, The New England journal of medicine.

Quantitative analysis of fetal DNA in maternal plasma and serum: implications for noninvasive prenatal diagnosis.

T K Lau, N M Hjelm, Y. Lo, 1998, American journal of human genetics.

Determination of Fetal RhD Status by Maternal Plasma DNA Analysis

I. Sargent, C. Redman, N. M. Hjelm, 2000, Annals of the New York Academy of Sciences.

Technical Optimization of RhD Zygosity Determination by Real‐Time Quantitative Polymerase Chain Reaction

R. Chiu, Melissa S. Murphy, C. Fidler, 2001, Annals of the New York Academy of Sciences.

Detection of Mammaglobin mRNA in the Plasma of Breast Cancer Patients

A. Harris, Y. Lo, S. Gal, 2001, Annals of the New York Academy of Sciences.

Analysis of the pro-opiomelanocortin gene in non-insulin dependent diabetic families.

S. O’Rahilly, R. Turner, P. Patel, 1989, Diabetes research (Edinburgh, Scotland).

Type 2 (non-insulin-dependent) diabetes mellitus new genetics for old nightmares

S. O’Rahilly, R. Turner, J. Wainscoat, 1988, Diabetologia.

Linkage Analysis of Maturity-Onset Diabetes of the Young With Microsatellite Polymorphisms: No Linkage to ADA or GLUT2 Genes in Two Families

A. Hattersley, J. Nerup, R. Turner, 1992, Diabetes.

Availability of Type II Diabetic Families for Detection of Diabetes Susceptibility Genes

J. Levy, A. Hattersley, R. Holman, 1993, Diabetes.

Distribution of Type II Diabetes in Nuclear Families

J. Levy, A. Hattersley, R. Turner, 1993, Diabetes.

Detection of Plasmodium falciparum DNA in Plasma

D. Roberts, S. Gal, C. Fidler, 2001, Annals of the New York Academy of Sciences.

An RFLP associated with insulinoma amyloid polypeptide locus (IAPP).

S. O’Rahilly, R. Turner, S. Mosselman, 1989, Nucleic acids research.

Two-way cell traffic between mother and fetus: biologic and clinical implications.

I. Sargent, B. Thilaganathan, Y. Lo, 1996, Blood.

Segregation analysis of NIDDM in Caucasian families

J. Levy, A. Hattersley, R. Turner, 1994, Diabetologia.

Microsatellite Polymorphisms at the Glucokinase Locus: a Population Association Study in Caucasian Type 2 Diabetic Subjects

A. Hattersley, M. Permutt, I. Stratton, 1993, Diabetic medicine : a journal of the British Diabetic Association.

Multiple restriction fragment length polymorphisms at the GLUT2 locus: GLUT2 haplotypes for genetic analysis of Type 2 (non-insulin-dependent) diabetes mellitus

R. Turner, G. Bell, P. Patel, 1991, Diabetologia.

Detection of susceptability alleles to insulin-dependent diabetes mellitus at the DQB1 locus by artificial PCR-RFLP

J. Bell, P. Patel, J. Wainscoat, 2004, Immunogenetics.

Analysis of the HepG2/erythrocyte glucose transporter locus in a family with Type 2 (non-insulin-dependent) diabetes and obesity

S. O’Rahilly, R. Turner, P. Patel, 1989, Diabetologia.

A NEW DNA POLYMORPHISM IN THE β‐GLOBIN GENE CLUSTER CAN BE USED FOR ANTENATAL DIAGNOSIS OF β‐THALASSAEMIA

J. Wainscoat, J. Old, J. S. Wainscoat, 1983 .

Linkage analysis of the human insulin receptor gene in Type 2 (non-insulin-dependent) diabetic families and a family with maturity onset diabetes of the young

S. O’Rahilly, R. Turner, R. Trembath, 1988, Diabetologia.

Analysis of complex genetic systems by ARMS-SSCP: application to HLA genotyping.

J. Bell, K. Fleming, Y. Lo, 1992, Nucleic acids research.

Dinucleotide repeat polymorphism at the human GLUT2 locus.

R. Turner, G. I. Bell, Y. Lo, 1991, Nucleic acids research.

Non-linkage of the islet amyloid polypeptide gene with Type 2 (non-insulin-dependent) diabetes mellitus

S. O’Rahilly, R. Turner, S. Mosselman, 1991, Diabetologia.