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Uterine leiomyomata and decreased height: a common HMGA2 predisposition allele

Human genetics, 2009-04, Vol.125 (3), p.257-263

2009

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The impact of race as a risk factor for symptom severity and age at diagnosis of uterine leiomyomata among affected sisters

American journal of obstetrics and gynecology, 2008-02, Vol.198 (2), p.168.e1-168.e9

2008

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MDR1 Ala893 Polymorphism Is Associated with Inflammatory Bowel Disease

American journal of human genetics, 2003-12, Vol.73 (6), p.1282-1292

2003

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Polymorphisms in the Insulin-Degrading Enzyme Gene Are Associated With Type 2 Diabetes in Men From the NHLBI Framingham Heart Study

Diabetes (New York, N.Y.), 2003-06, Vol.52 (6), p.1562-1567

2003

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Involvement of fumarate hydratase in nonsyndromic uterine leiomyomas: Genetic linkage analysis and FISH studies

Genes chromosomes & cancer, 2004-11, Vol.41 (3), p.183-190

2004

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Variation and heritability of Hb F and F‐cells among β‐thalassemia heterozygotes in Hong Kong

American journal of hematology, 2008-06, Vol.83 (6), p.458-464

2008

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Functional annotation of a novel NFKB1 promoter polymorphism that increases risk for ulcerative colitis

Human molecular genetics, 2004-01, Vol.13 (1), p.35-45

2004

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Confirmation and Generalization of an Alcohol-Dependence Locus on Chromosome 10q

Neuropsychopharmacology (New York, N.Y.), 2010-05, Vol.35 (6), p.1325-1332

2010

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NOD2 CARD15 Genotype and Phenotype Differences between Ashkenazi and Sephardic Jews with Crohn's Disease

The American journal of gastroenterology, 2004-06, Vol.99 (6), p.1134-1140

2004

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A genome scan in 260 inflammatory bowel disease‐affected relative pairs

Inflammatory bowel diseases, 2004-01, Vol.10 (1), p.15-22

2004

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A genome scan in 260 inflammatory bowel disease‐affected relative pairs

Inflammatory bowel diseases, 2004-09, Vol.10 (5), p.513-520

2004

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The combined effect of paraoxonase promoter and coding region polymorphisms on the risk of arterial ischemic stroke among young adults

Archives of neurology (Chicago), 2004-03, Vol.61 (3), p.351

2004

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Identification of genetic loci for basal cell nevus syndrome and inflammatory bowel disease in a single large pedigree

Human genetics, 2006-08, Vol.120 (1), p.31-41

2006

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A genome-wide scan for loci linked to plasma levels of glucose and HbA1c in a community-based sample of Caucasian pedigrees: The Framingham Offspring Study

Diabetes (New York, N.Y.), 2002-03, Vol.51 (3), p.833-840

2002

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A Genome-Wide Scan for Loci Linked to Plasma Levels of Glucose and HbA1c in a Community-Based Sample of Caucasian Pedigrees

Diabetes (New York, N.Y.), 2002-03, Vol.51 (3), p.833-840

2002

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Parental sex effect in families with alcoholism

Genetic epidemiology, 1999, Vol.17 (S1), p.S409-S413

1999

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Genetic Susceptibility to Asthma — Bronchial Hyperresponsiveness Coinherited with a Major Gene for Atopy

The New England journal of medicine, 1995-10, Vol.333 (14), p.894-900

1995

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Genome-wide screen for heavy alcohol consumption

BMC genetics, 2003-12, Vol.4 Suppl 1 (S1), p.S106, Article S106

2003

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Empirically derived phenotypic subgroups - qualitative and quantitative trait analyses

BMC genetics, 2003-12, Vol.4 Suppl 1 (S1), p.S15, Article S15

2003

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Search for genetic factors predisposing to atherogenic dyslipidemia

BMC genetics, 2003-12, Vol.4 Suppl 1 (S1), p.S100, Article S100

2003

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Characterization of obstructive airway disease in family members of probands with asthma: An algorithm for the diagnosis of asthma

American journal of respiratory and critical care medicine, 1998-06, Vol.157 (6), p.1734-1742

1998

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Two-locus approach of segregation and linkage analysis in the study of complex traits

Genetic epidemiology, 1995, Vol.12 (6), p.825-830

1995

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A genome-wide scan for loci linked to plasma levels of glucose and HbA(1c) in a community-based sample of Caucasian pedigrees: The Framingham Offspring Study

Diabetes (New York, N.Y.), 2002-03, Vol.51 (3), p.833-840

2002

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Susceptibility Loci Regulating Total Serum IgE Levels, Bronchial Hyperresponsiveness, and Clinical Asthma Map to Chromosome 5q

Chest, 1997-06, Vol.111 (6), p.77S-78S

1997

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Complement Factor H Polymorphism and Age-Related Macular Degeneration

Science (American Association for the Advancement of Science), 2005-04, Vol.308 (5720), p.421-424

2005

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Uterine leiomyomata and decreased height: a common HMGA2 predisposition allele

The impact of race as a risk factor for symptom severity and age at diagnosis of uterine leiomyomata among affected sisters

MDR1 Ala893 Polymorphism Is Associated with Inflammatory Bowel Disease

Polymorphisms in the Insulin-Degrading Enzyme Gene Are Associated With Type 2 Diabetes in Men From the NHLBI Framingham Heart Study

Involvement of fumarate hydratase in nonsyndromic uterine leiomyomas: Genetic linkage analysis and FISH studies

Variation and heritability of Hb F and F‐cells among β‐thalassemia heterozygotes in Hong Kong

Functional annotation of a novel NFKB1 promoter polymorphism that increases risk for ulcerative colitis

Confirmation and Generalization of an Alcohol-Dependence Locus on Chromosome 10q

NOD2 CARD15 Genotype and Phenotype Differences between Ashkenazi and Sephardic Jews with Crohn's Disease

A genome scan in 260 inflammatory bowel disease‐affected relative pairs

A genome scan in 260 inflammatory bowel disease‐affected relative pairs

The combined effect of paraoxonase promoter and coding region polymorphisms on the risk of arterial ischemic stroke among young adults

Identification of genetic loci for basal cell nevus syndrome and inflammatory bowel disease in a single large pedigree

A genome-wide scan for loci linked to plasma levels of glucose and HbA1c in a community-based sample of Caucasian pedigrees: The Framingham Offspring Study

A Genome-Wide Scan for Loci Linked to Plasma Levels of Glucose and HbA1c in a Community-Based Sample of Caucasian Pedigrees

Parental sex effect in families with alcoholism

Genetic Susceptibility to Asthma — Bronchial Hyperresponsiveness Coinherited with a Major Gene for Atopy

Genome-wide screen for heavy alcohol consumption

Empirically derived phenotypic subgroups - qualitative and quantitative trait analyses

Search for genetic factors predisposing to atherogenic dyslipidemia

Characterization of obstructive airway disease in family members of probands with asthma: An algorithm for the diagnosis of asthma

Two-locus approach of segregation and linkage analysis in the study of complex traits

A genome-wide scan for loci linked to plasma levels of glucose and HbA(1c) in a community-based sample of Caucasian pedigrees: The Framingham Offspring Study

Susceptibility Loci Regulating Total Serum IgE Levels, Bronchial Hyperresponsiveness, and Clinical Asthma Map to Chromosome 5q

Complement Factor H Polymorphism and Age-Related Macular Degeneration

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