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BMPR2 germline mutations in pulmonary hypertension associated with fenfluramine derivatives

The European respiratory journal, 2002-09, Vol.20 (3), p.518-523

2002

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Familial Primary Pulmonary Hypertension (Gene PPH1) Is Caused by Mutations in the Bone Morphogenetic Protein Receptor–II Gene

American journal of human genetics, 2000-09, Vol.67 (3), p.737-744

2000

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The Power to Detect Linkage in Complex Disease by Means of Simple LOD-Score Analyses

American journal of human genetics, 1998-09, Vol.63 (3), p.870-879

1998

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Direct Power Comparisons between Simple LOD Scores and NPL Scores for Linkage Analysis in Complex Diseases

American journal of human genetics, 1999-09, Vol.65 (3), p.847-857

1999

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Loss of information due to ambiguous haplotyping of SNPs

Nature genetics, 1999-04, Vol.21 (4), p.360-361

1999

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Mapping of familial primary pulmonary hypertension locus (PPH1) to chromosome 2q31-q32

Circulation (New York, N.Y.), 1997-06, Vol.95 (12), p.2603-2606

1997

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Panic disorder is associated with the serotonin transporter gene ( ) but not the promoter region (5-HTTLPR)

Molecular psychiatry, 2010-02, Vol.15 (2), p.166-176

2010

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Measurement of statistical evidence on an absolute scale following thermodynamic principles

Theory in biosciences = Theorie in den Biowissenschaften, 2013-09, Vol.132 (3), p.181-194

2013

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Fine mapping of PPH1, a gene for familial primary pulmonary hypertension, to a 3-cM region on chromosome 2q33

American journal of respiratory and critical care medicine, 2000-03, Vol.161 (3), p.1055-1059

2000

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Magnitude of type I error when single-locus linkage analysis is maximized over models : A simulation study

American journal of human genetics, 1997, Vol.60 (1), p.217-227

1997

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No association or linkage between polymorphisms in the genes encoding cholecystokinin and the cholecystokinin B receptor and panic disorder

Molecular psychiatry, 2001, Vol.6 (1), p.59-65

2001

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Results of a genome-wide genetic screen for panic disorder

American journal of medical genetics, 1998-03, Vol.81 (2), p.139-147

1998

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Potential panic disorder syndrome: Clinical and genetic linkage evidence

American journal of medical genetics, 2000-02, Vol.96 (1), p.24-35

2000

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Logistic regression model for analyzing extended haplotype data

Genetic epidemiology, 1998, Vol.15 (2), p.173-181

1998

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Linkage analysis versus association analysis : distinguishing between two models that explain disease-marker associations

American journal of human genetics, 1993-08, Vol.53 (2), p.367-384

HODGE, S. E

1993

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The problem of ascertainment for linkage analysis

American journal of human genetics, 1996-05, Vol.58 (5), p.1072-1084

1996

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Lack of genetic linkage or association between a functional serotonin transporter polymorphism and panic disorder

Psychiatric genetics, 1999-03, Vol.9 (1), p.1-6

1999

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The Essence of Single Ascertainment

Genetics (Austin), 1996-11, Vol.144 (3), p.1215-1223

1996

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Inherent intractability of the ascertainment problem for pedigree data : a general likelihood framework

American journal of human genetics, 1995, Vol.56 (1), p.33-43

1995

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No genetic linkage or association between a functional promoter polymorphism in the monoamine oxidase-A gene and panic disorder

Molecular psychiatry, 2000-09, Vol.5 (5), p.465-466

2000

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quantitative genetic basis of polyandry in the parasitoid wasp, Nasonia vitripennis

Heredity, 2007-02, Vol.98 (2), p.69-73

2007

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Genetic anticipation and imprinting in bipolar I illness

British journal of psychiatry, 1997-02, Vol.170 (2), p.162-166

1997

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Power, Mode of Inheritance, and Type I Error in Lod Scores and Affecteds-Only Methods: Reply to Kruglyak

American journal of human genetics, 1998-01, Vol.62 (1), p.202-204

1998

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Using Lod Scores to Detect Sex Differences in Male-Female Recombination Fractions

Human heredity, 2004-01, Vol.57 (2), p.100-108

2004

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Affecteds-only linkage methods are not a panacea

American journal of human genetics, 1996-04, Vol.58 (4), p.892-895

1996

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BMPR2 germline mutations in pulmonary hypertension associated with fenfluramine derivatives

Familial Primary Pulmonary Hypertension (Gene PPH1) Is Caused by Mutations in the Bone Morphogenetic Protein Receptor–II Gene

The Power to Detect Linkage in Complex Disease by Means of Simple LOD-Score Analyses

Direct Power Comparisons between Simple LOD Scores and NPL Scores for Linkage Analysis in Complex Diseases

Loss of information due to ambiguous haplotyping of SNPs

Mapping of familial primary pulmonary hypertension locus (PPH1) to chromosome 2q31-q32

Panic disorder is associated with the serotonin transporter gene ( ) but not the promoter region (5-HTTLPR)

Measurement of statistical evidence on an absolute scale following thermodynamic principles

Fine mapping of PPH1, a gene for familial primary pulmonary hypertension, to a 3-cM region on chromosome 2q33

Magnitude of type I error when single-locus linkage analysis is maximized over models : A simulation study

No association or linkage between polymorphisms in the genes encoding cholecystokinin and the cholecystokinin B receptor and panic disorder

Results of a genome-wide genetic screen for panic disorder

Potential panic disorder syndrome: Clinical and genetic linkage evidence

Logistic regression model for analyzing extended haplotype data

Linkage analysis versus association analysis : distinguishing between two models that explain disease-marker associations

The problem of ascertainment for linkage analysis

Lack of genetic linkage or association between a functional serotonin transporter polymorphism and panic disorder

The Essence of Single Ascertainment

Inherent intractability of the ascertainment problem for pedigree data : a general likelihood framework

No genetic linkage or association between a functional promoter polymorphism in the monoamine oxidase-A gene and panic disorder

quantitative genetic basis of polyandry in the parasitoid wasp, Nasonia vitripennis

Genetic anticipation and imprinting in bipolar I illness

Power, Mode of Inheritance, and Type I Error in Lod Scores and Affecteds-Only Methods: Reply to Kruglyak

Using Lod Scores to Detect Sex Differences in Male-Female Recombination Fractions

Affecteds-only linkage methods are not a panacea

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