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Linkage disequilibrium between the beta frequency of the human EEG and a GABAA receptor gene locus

Proceedings of the National Academy of Sciences - PNAS, 2002-03, Vol.99 (6), p.3729-3733

2002

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High frequency of gastrointestinal manifestations in myotonic dystrophy type 1 and type 2

Neurology, 2017-09, Vol.89 (13), p.1348

2017

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DNA Identifications after the 9/11 World Trade Center Attack

Science (American Association for the Advancement of Science), 2005-11, Vol.310 (5751), p.1122-1123

2005

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Differences in duration of Huntington’s disease based on age at onset

Journal of neurology, neurosurgery and psychiatry, 1999-01, Vol.66 (1), p.52-56

1999

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SNPing Away at Complex Diseases: Analysis of Single-Nucleotide Polymorphisms around APOE in Alzheimer Disease

American journal of human genetics, 2000-08, Vol.67 (2), p.383-394

2000

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Mutant prion proteins in Gerstmann-Sträussler-Scheinker disease with neurofibrillary tangles

Nature genetics, 1992-04, Vol.1 (1), p.68-71

1992

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Contribution of the LRP5 Gene to Normal Variation in Peak BMD in Women

Journal of bone and mineral research, 2005-01, Vol.20 (1), p.75-80

2005

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Contribution of the LRP5 Gene to Normal Variation in Peak BMD in Women

Journal of bone and mineral research, 2005-01, Vol.20 (1), p.75-80

2005

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Progression of symptoms in the early and middle stages of Huntington disease

Archives of neurology (Chicago), 2001-02, Vol.58 (2), p.273

2001

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Localization of the gene for familial primary pulmonary hypertension to chromosome 2q31-32

Nature genetics, 1997-03, Vol.15 (3), p.277-280

1997

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Genome Screen for Quantitative Trait Loci Underlying Normal Variation in Femoral Structure

Journal of bone and mineral research, 2001-06, Vol.16 (6), p.985-991

2001

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A genomic scan for habitual smoking in families of alcoholics: Common and specific genetic factors in substance dependence

American journal of medical genetics, 2004-01, Vol.124A (1), p.19-27

2004

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Confirmation of Linkage to Chromosome 1q for Peak Vertebral Bone Mineral Density in Premenopausal White Women

American journal of human genetics, 2004-02, Vol.74 (2), p.223-228

2004

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The complexity of complex diseases

American journal of human genetics, 2003-02, Vol.72 (2), p.229-232

Conneally, P Michael

2003

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The collaborative study on the genetics of alcoholism: Sample and clinical data

Genes, brain and behavior, 2023-10, Vol.22 (5), p.e12860

2023

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Sibling Pair Linkage and Association Studies between Peak Bone Mineral Density and the Gene Locus for the Osteoclast-Specific Subunit (OC116) of the Vacuolar Proton Pump on Chromosome 11p12-13

The journal of clinical endocrinology and metabolism, 2002-08, Vol.87 (8), p.3819-3824

2002

Volltextzugriff (PDF)

Sibling Pair Linkage and Association Studies between Peak Bone Mineral Density and the Gene Locus for the Osteoclast-Specific Subunit (OC116) of the Vacuolar Proton Pump on Chromosome 11p12-13

The journal of clinical endocrinology and metabolism, 2002-08, Vol.87 (8), p.3819-3824

2002

Volltextzugriff (PDF)

Venezuelan Kindreds Reveal That Genetic and Environmental Factors Modulate Huntington's Disease Age of Onset

Proceedings of the National Academy of Sciences - PNAS, 2004-03, Vol.101 (10), p.3498-3503

2004

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Evaluation of psychological symptoms among presymptomatic HD gene carriers as measured by selected MMPI scales

Journal of psychiatric research, 2002-11, Vol.36 (6), p.377-382

2002

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Heterozygous germline mutations in BMPR2 , encoding a TGF-β receptor, cause familial primary pulmonary hypertension

Nature genetics, 2000-09, Vol.26 (1), p.81-84

2000

Volltextzugriff (PDF)

Linkage disequilibrium between the beta frequency of the human EEG and a GABA A receptor gene locus

Proceedings of the National Academy of Sciences - PNAS, 2002-03, Vol.99 (6), p.3729-3733

2002

Volltextzugriff (PDF)

A polymorphic DNA marker genetically linked to Huntington's disease

Nature (London), 1983-11, Vol.306 (5940), p.234-238

1983

Volltextzugriff (PDF)

Genome-wide search for genes affecting the risk for alcohol dependence

American journal of medical genetics, 1998-05, Vol.81 (3), p.207-215

1998

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Epidemiology. DNA identifications after the 9/11 World Trade Center attack

Science (American Association for the Advancement of Science), 2005-11, Vol.310 (5751), p.1122-1123

2005

Volltextzugriff (PDF)

If you build a rare disease registry, will they enroll and will they use it? Methods and data from the National Registry of Myotonic Dystrophy (DM) and Facioscapulohumeral Muscular Dystrophy (FSHD)

Contemporary clinical trials, 2012-03, Vol.33 (2), p.302-311

2012

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Linkage disequilibrium between the beta frequency of the human EEG and a GABAA receptor gene locus

High frequency of gastrointestinal manifestations in myotonic dystrophy type 1 and type 2

DNA Identifications after the 9/11 World Trade Center Attack

Differences in duration of Huntington’s disease based on age at onset

SNPing Away at Complex Diseases: Analysis of Single-Nucleotide Polymorphisms around APOE in Alzheimer Disease

Mutant prion proteins in Gerstmann-Sträussler-Scheinker disease with neurofibrillary tangles

Contribution of the LRP5 Gene to Normal Variation in Peak BMD in Women

Contribution of the LRP5 Gene to Normal Variation in Peak BMD in Women

Progression of symptoms in the early and middle stages of Huntington disease

Localization of the gene for familial primary pulmonary hypertension to chromosome 2q31-32

Genome Screen for Quantitative Trait Loci Underlying Normal Variation in Femoral Structure

A genomic scan for habitual smoking in families of alcoholics: Common and specific genetic factors in substance dependence

Confirmation of Linkage to Chromosome 1q for Peak Vertebral Bone Mineral Density in Premenopausal White Women

The complexity of complex diseases

The collaborative study on the genetics of alcoholism: Sample and clinical data

Sibling Pair Linkage and Association Studies between Peak Bone Mineral Density and the Gene Locus for the Osteoclast-Specific Subunit (OC116) of the Vacuolar Proton Pump on Chromosome 11p12-13

Sibling Pair Linkage and Association Studies between Peak Bone Mineral Density and the Gene Locus for the Osteoclast-Specific Subunit (OC116) of the Vacuolar Proton Pump on Chromosome 11p12-13

Venezuelan Kindreds Reveal That Genetic and Environmental Factors Modulate Huntington's Disease Age of Onset

Evaluation of psychological symptoms among presymptomatic HD gene carriers as measured by selected MMPI scales

Heterozygous germline mutations in BMPR2 , encoding a TGF-β receptor, cause familial primary pulmonary hypertension

Linkage disequilibrium between the beta frequency of the human EEG and a GABA A receptor gene locus

A polymorphic DNA marker genetically linked to Huntington's disease

Genome-wide search for genes affecting the risk for alcohol dependence

Epidemiology. DNA identifications after the 9/11 World Trade Center attack

If you build a rare disease registry, will they enroll and will they use it? Methods and data from the National Registry of Myotonic Dystrophy (DM) and Facioscapulohumeral Muscular Dystrophy (FSHD)

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