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Glutathione S-transferase gene variations influence BU pharmacokinetics and outcome of hematopoietic SCT in pediatric patients

Bone marrow transplantation (Basingstoke), 2013-07, Vol.48 (7), p.939-946

2013

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Unique origin and specific ethnic distribution of the Friedreich ataxia GAA expansion

Neurology, 2000-06, Vol.54 (12), p.2322

2000

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Family study and segregation analysis of Tourette syndrome : Evidence for a mixed model of inheritance

American journal of human genetics, 1996-09, Vol.59 (3), p.684-693

1996

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Quantitative Founder-Effect Analysis of French Canadian Families Identifies Specific Loci Contributing to Metabolic Phenotypes of Hypertension

American journal of human genetics, 2005-05, Vol.76 (5), p.815-832

2005

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Incidence of dominant spinocerebellar and Friedreich triplet repeats among 361 ataxia families

Neurology, 1998-12, Vol.51 (6), p.1666

1998

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Linkage disequilibrium analysis in young populations : Pseudo-vitamin D-deficiency rickets and the founder effect in French Canadians

American journal of human genetics, 1996-09, Vol.59 (3), p.633-643

1996

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Polymorphisms in Genes Encoding Drugs and Xenobiotic Metabolizing Enzymes, DNA Repair Enzymes, and Response to Treatment of Childhood Acute Lymphoblastic Leukemia

Clinical cancer research, 2002-03, Vol.8 (3), p.802-810

2002

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Common genetic mechanisms in alcohol, drug, and mental disorder comorbidity

Drug and alcohol dependence, 1995-08, Vol.39 (2), p.129-138

1995

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A follow-up report of a genome search for affective disorder predisposition loci in the Old Order Amish

American journal of human genetics, 1996-12, Vol.59 (6), p.1343-1362

1996

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Pseudohypoparathyroidism 1b: Exclusion of parathyroid hormone and its receptors as candidate disease genes

The journal of clinical endocrinology and metabolism, 2000-06, Vol.85 (6), p.2239-2246

2000

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Evidence for a genetic aetiology in reading disability of twins

Nature (London), 1987-10, Vol.329 (6139), p.537-539

1987

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A nonpathogenic GAAGGA repeat in the Friedreich gene: implications for pathogenesis

Neurology, 1999-11, Vol.53 (8), p.1854

1999

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Central European Dobrava Hantavirus Isolate from a Striped Field Mouse (Apodemus agrarius)

Journal of Clinical Microbiology, 2005-06, Vol.43 (6), p.2756-2763

2005

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Twin closeness and co-twin risk for substance use disorders: assessing the impact of the equal environment assumption

Psychiatry research, 1997-05, Vol.70 (3), p.155-164

1997

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Family Outbreak of Alimentary Tick-Borne Encephalitis in Slovakia Associated with a Natural Focus of Infection

European journal of epidemiology, 1996-08, Vol.12 (4), p.373-375

1996

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Friedreich's ataxia: Point mutations and clinical presentation of compound heterozygotes

Annals of neurology, 1999-02, Vol.45 (2), p.200-206

1999

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Linkage Mapping by Simultaneous Screening of Multiple Polymorphic Loci Using Alu Oligonucleotide-Directed PCR

Proceedings of the National Academy of Sciences - PNAS, 1992-09, Vol.89 (18), p.8448-8451

1992

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First Molecular Identification of Human Dobrava Virus Infection in Central Europe

Journal of Clinical Microbiology, 2004-03, Vol.42 (3), p.1322-1325

2004

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Anatomy of a founder effect : myotonic dystrophy in northeastern quebec

Human genetics, 2005-07, Vol.117 (2-3), p.177-187

2005

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Unusual EEG pattern linked to chromosome 3p in a family with idiopathic generalized epilepsy

Neurology, 1998-08, Vol.51 (2), p.493

1998

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Genetics of Vitamin D 1α-Hydroxylase Deficiency in 17 Families

American journal of human genetics, 1998-12, Vol.63 (6), p.1694-1702

1998

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The Friedreich Ataxia GAA Triplet Repeat: Premutation and Normal Alleles

Human molecular genetics, 1997-08, Vol.6 (8), p.1261-1266

1997

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Quality control assessment for the serological diagnosis of tick borne encephalitis virus infections

Journal of clinical virology, 2007-03, Vol.38 (3), p.260-264

2007

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Quality control assessment for the PCR diagnosis of tick-borne encephalitis virus infections

Journal of clinical virology, 2007-01, Vol.38 (1), p.73-77

2007

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Linkage of bipolar affective disorders to markers on chromosome 11p is excluded in a second lateral extension of Amish Pedigree 110

Genomics (San Diego, Calif.), 1991-11, Vol.11 (3), p.730-736

1991

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Glutathione S-transferase gene variations influence BU pharmacokinetics and outcome of hematopoietic SCT in pediatric patients

Unique origin and specific ethnic distribution of the Friedreich ataxia GAA expansion

Family study and segregation analysis of Tourette syndrome : Evidence for a mixed model of inheritance

Quantitative Founder-Effect Analysis of French Canadian Families Identifies Specific Loci Contributing to Metabolic Phenotypes of Hypertension

Incidence of dominant spinocerebellar and Friedreich triplet repeats among 361 ataxia families

Linkage disequilibrium analysis in young populations : Pseudo-vitamin D-deficiency rickets and the founder effect in French Canadians

Polymorphisms in Genes Encoding Drugs and Xenobiotic Metabolizing Enzymes, DNA Repair Enzymes, and Response to Treatment of Childhood Acute Lymphoblastic Leukemia

Common genetic mechanisms in alcohol, drug, and mental disorder comorbidity

A follow-up report of a genome search for affective disorder predisposition loci in the Old Order Amish

Pseudohypoparathyroidism 1b: Exclusion of parathyroid hormone and its receptors as candidate disease genes

Evidence for a genetic aetiology in reading disability of twins

A nonpathogenic GAAGGA repeat in the Friedreich gene: implications for pathogenesis

Central European Dobrava Hantavirus Isolate from a Striped Field Mouse (Apodemus agrarius)

Twin closeness and co-twin risk for substance use disorders: assessing the impact of the equal environment assumption

Family Outbreak of Alimentary Tick-Borne Encephalitis in Slovakia Associated with a Natural Focus of Infection

Friedreich's ataxia: Point mutations and clinical presentation of compound heterozygotes

Linkage Mapping by Simultaneous Screening of Multiple Polymorphic Loci Using Alu Oligonucleotide-Directed PCR

First Molecular Identification of Human Dobrava Virus Infection in Central Europe

Anatomy of a founder effect : myotonic dystrophy in northeastern quebec

Unusual EEG pattern linked to chromosome 3p in a family with idiopathic generalized epilepsy

Genetics of Vitamin D 1α-Hydroxylase Deficiency in 17 Families

The Friedreich Ataxia GAA Triplet Repeat: Premutation and Normal Alleles

Quality control assessment for the serological diagnosis of tick borne encephalitis virus infections

Quality control assessment for the PCR diagnosis of tick-borne encephalitis virus infections

Linkage of bipolar affective disorders to markers on chromosome 11p is excluded in a second lateral extension of Amish Pedigree 110

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