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Prediction of Preeclampsia – A Workshop Report

Placenta, 2008-03, Vol.29 (Suppl A), p.83-85

2008

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A novel exonic variant (221delT) in the LGALS13 gene encoding placental protein 13 (PP13) is associated with preterm labour in a low risk population

Journal of reproductive immunology, 2009-11, Vol.82 (2), p.166-173

2009

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Chromosomal assignment of the second locus for autosomal dominant cerebellar ataxia (SCA2) to chromosome 12q23-24.1

Nature genetics, 1993-07, Vol.4 (3), p.295-299

1993

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Spectrum of Mutations in the HFE Gene Implicated in Haemochromatosis and Porphyria

Human molecular genetics, 1999-08, Vol.8 (8), p.1517-1522

1999

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Improvement of Lyme Borreliosis Serodiagnosis by a Newly Developed Recombinant Immunoglobulin G (IgG) and IgM Line Immunoblot Assay and Addition of VlsE and DbpA Homologues

Journal of Clinical Microbiology, 2005-08, Vol.43 (8), p.3602-3609

2005

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Maternal and fetal single nucleotide polymorphisms in the epoxide hydrolase and gluthatione S-transferase P1 genes are not associated with pre-eclampsia in the Coloured population of the Western Cape, South Africa

Journal of obstetrics and gynaecology, 2004-11, Vol.24 (8), p.866-872

2004

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The Glu298Asp variant of the endothelial nitric oxide synthase gene is associated with an increased risk for abruptio placentae in pre-eclampsia

Journal of human genetics, 2005-09, Vol.50 (8), p.415-419

2005

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Collection of fetal cells in cervical secretions without ultrasound guidance

Journal of obstetrics and gynaecology, 2004-09, Vol.24 (6), p.662-663

2004

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Parallel assessment of circulatory fetal DNA and corticotropin-releasing hormone mRNA in early- and late-onset preeclampsia

Clinical chemistry (Baltimore, Md.), 2005-09, Vol.51 (9), p.1730-1733

2005

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Prenatal diagnosis of familial hypercholesterolemia: importance of DNA analysis in the high-risk South African population

Genetic counseling, 2001, Vol.12 (2), p.121

2001

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The SHB Adaptor Protein Maps to Human Chromosome 9

Genomics (San Diego, Calif.), 1994-12, Vol.24 (3), p.615-617

1994

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Circulatory nucleosome levels are significantly increased in early and late-onset preeclampsia

Prenatal diagnosis, 2005-08, Vol.25 (8), p.700-703

2005

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The Friedreich's ataxia gene encodes a novel phosphatidylinositol-4-phosphate 5-kinase

Nature genetics, 1996-10, Vol.14 (2), p.157-162

1996

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Combined heterozygosity for methylenetetrahydrofolate reductase (MTHFR) mutations C677T and A1298C is associated with abruptio placentae but not with intrauterine growth restriction

European journal of obstetrics & gynecology and reproductive biology, 2001-08, Vol.97 (2), p.174-177

2001

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Minimal Alteration in the Ratio of Circulatory Fetal DNA to Fetal Corticotropin-Releasing Hormone mRNA Level in Preeclampsia

Fetal diagnosis and therapy, 2006-01, Vol.21 (3), p.246-249

2006

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Physical evidence for the position of the Friedreich's ataxia locus FRDA proximal to D9S5

Cytogenetic and genome research, 1995-01, Vol.71 (3), p.214-216

1995

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Frataxin fracas

Nature genetics, 1997-04, Vol.15 (4), p.337-338

1997

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Maternal and fetal single nucleotide polymorphisms in the epoxide hydrolase and gluthatione S-transferase PI genes are not associated with pre-eclampsia in the Coloured population of the Western Cape; South Africa

Journal of obstetrics and gynaecology, 2004-11, Vol.24 (8), p.866

2004

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Heterogeneous distribution of two common MTHFR gene mutations in the diverse south African population correlates significantly with ethnic differences in cardiovascular disease risk

Atherosclerosis, 1999-05, Vol.144, p.137-137

1999

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Mutation −59c→t in Repeat 2 of the LDL Receptor Promoter: Reduction in Transcriptional Activity and Possible Allelic Interaction in a South African Family with Familial Hypercholesterolaemia

Human molecular genetics, 1999-10, Vol.8 (11), p.2025-2030

1999

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Analysis of two mutations in the mthfr gene associated with mild hyperhomocysteinaemia: Heterogeneous distribution in the South African population

South African medical journal, 2002-06, Vol.92 (6), p.464-467

2002

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Founder mutations in the LDL receptor gene contribute significantly to the familial hypercholesterolemia phenotype in the indigenous South African population of mixed ancestry

Clinical genetics, 1999-05, Vol.55 (5), p.340-345

1999

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Mutations in prothrombin and factor V genes do not contribute significantly to placental vasculopathy in a high-risk patient cohort in South Africa

South African medical journal, 2002-07, Vol.92 (7), p.526-527

2002

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Multiple sclerosis, porphyria-like symptoms, and a history of iron deficiency anemia in a family of Scottish descent

American journal of medical genetics, 1999-09, Vol.86 (2), p.194-196

1999

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Mutation -59c arrow right t in repeat 2 of the LDL receptor promoter: reduction in transcriptional activity and possible allelic interaction in a South African family with familial hypercholesterolaemia

Human molecular genetics, 1999-10, Vol.8 (11), p.2025-2030

1999

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Prediction of Preeclampsia – A Workshop Report

A novel exonic variant (221delT) in the LGALS13 gene encoding placental protein 13 (PP13) is associated with preterm labour in a low risk population

Chromosomal assignment of the second locus for autosomal dominant cerebellar ataxia (SCA2) to chromosome 12q23-24.1

Spectrum of Mutations in the HFE Gene Implicated in Haemochromatosis and Porphyria

Improvement of Lyme Borreliosis Serodiagnosis by a Newly Developed Recombinant Immunoglobulin G (IgG) and IgM Line Immunoblot Assay and Addition of VlsE and DbpA Homologues

Maternal and fetal single nucleotide polymorphisms in the epoxide hydrolase and gluthatione S-transferase P1 genes are not associated with pre-eclampsia in the Coloured population of the Western Cape, South Africa

The Glu298Asp variant of the endothelial nitric oxide synthase gene is associated with an increased risk for abruptio placentae in pre-eclampsia

Collection of fetal cells in cervical secretions without ultrasound guidance

Parallel assessment of circulatory fetal DNA and corticotropin-releasing hormone mRNA in early- and late-onset preeclampsia

Prenatal diagnosis of familial hypercholesterolemia: importance of DNA analysis in the high-risk South African population

The SHB Adaptor Protein Maps to Human Chromosome 9

Circulatory nucleosome levels are significantly increased in early and late-onset preeclampsia

The Friedreich's ataxia gene encodes a novel phosphatidylinositol-4-phosphate 5-kinase

Combined heterozygosity for methylenetetrahydrofolate reductase (MTHFR) mutations C677T and A1298C is associated with abruptio placentae but not with intrauterine growth restriction

Minimal Alteration in the Ratio of Circulatory Fetal DNA to Fetal Corticotropin-Releasing Hormone mRNA Level in Preeclampsia

Physical evidence for the position of the Friedreich's ataxia locus FRDA proximal to D9S5

Frataxin fracas

Maternal and fetal single nucleotide polymorphisms in the epoxide hydrolase and gluthatione S-transferase PI genes are not associated with pre-eclampsia in the Coloured population of the Western Cape; South Africa

Heterogeneous distribution of two common MTHFR gene mutations in the diverse south African population correlates significantly with ethnic differences in cardiovascular disease risk

Mutation −59c→t in Repeat 2 of the LDL Receptor Promoter: Reduction in Transcriptional Activity and Possible Allelic Interaction in a South African Family with Familial Hypercholesterolaemia

Analysis of two mutations in the mthfr gene associated with mild hyperhomocysteinaemia: Heterogeneous distribution in the South African population

Founder mutations in the LDL receptor gene contribute significantly to the familial hypercholesterolemia phenotype in the indigenous South African population of mixed ancestry

Mutations in prothrombin and factor V genes do not contribute significantly to placental vasculopathy in a high-risk patient cohort in South Africa

Multiple sclerosis, porphyria-like symptoms, and a history of iron deficiency anemia in a family of Scottish descent

Mutation -59c arrow right t in repeat 2 of the LDL receptor promoter: reduction in transcriptional activity and possible allelic interaction in a South African family with familial hypercholesterolaemia

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