Lista de obras -

A Gene Map of the Human Genome

artículo científico publicado en 1996

A P3G generic access agreement for population genomic studies

artículo científico publicado en 2013

A common allele on chromosome 9 associated with coronary heart disease

artículo científico publicado en 2007

A genome scan for hypertension susceptibility loci in populations of Chinese and Japanese origins

artículo científico publicado en 2003

A genomewide admixture map for Latino populations

artículo científico publicado en 2007

A genomewide association study of skin pigmentation in a South Asian population

artículo científico publicado en 2007

A high-density association screen of 155 ion transport genes for involvement with common migraine

artículo científico publicado en 2008

A physical map of the human genome

artículo científico publicado en 2001

A polymorphism in the beta1 adrenergic receptor is associated with resting heart rate

artículo científico publicado en 2002

A second generation human haplotype map of over 3.1 million SNPs

artículo científico publicado en 2007

A sequence-based variation map of 8.27 million SNPs in inbred mouse strains

artículo científico publicado en 2007

Advice to governments: scientific give and take

Aging as accelerated accumulation of somatic variants: whole-genome sequencing of centenarian and middle-aged monozygotic twin pairs

artículo científico publicado en 2013

Allele-specific KRT1 expression is a complex trait

artículo científico publicado en 2006

Analysis of allelic differential expression in human white blood cells

artículo científico publicado en 2006

Application of pooled genotyping to scan candidate regions for association with HDL cholesterol levels

artículo científico publicado en 2004

Assessing the phenotypic effects in the general population of rare variants in genes for a dominant Mendelian form of diabetes

artículo científico publicado en 2013

B cell exchange across the blood-brain barrier in multiple sclerosis

artículo científico publicado en 2012

Cardiac Myosin Activation: A Potential Therapeutic Approach for Systolic Heart Failure ⬇️

artículo científico publicado el 18 de marzo de 2011

Clustering and heritability of insulin resistance in Chinese and Japanese hypertensive families: a Stanford-Asian Pacific Program in Hypertension and Insulin Resistance sibling study

artículo científico publicado en 2002

Comprehensive whole-genome and candidate gene analysis for response to statin therapy in the Treating to New Targets (TNT) cohort

artículo científico publicado en 2009

Effect of genome and environment on metabolic and inflammatory profiles

artículo científico publicado en 2015

Evaluation of the SNP tagging approach in an independent population sample—array-based SNP discovery in Sami

Fine mapping in 94 inbred mouse strains using a high-density haplotype resource

artículo científico publicado en 2010

From genomic databases to translation: a call to action

artículo científico publicado en 2011

Gender-specific gene expression in post-mortem human brain: localization to sex chromosomes

artículo científico publicado en 2004

Generation and annotation of the DNA sequences of human chromosomes 2 and 4

artículo científico publicado en 2005

Genetic variants in the MRPS30 region and postmenopausal breast cancer risk

artículo científico publicado en 2011

Genetic variants in the MRPS30 region and postmenopausal breast cancer risk

artículo científico publicado en 2012

Genetic variation in response to a typhoid vaccine ⬇️

artículo científico publicado el 12 de marzo de 2010

Genome-wide definitive haplotypes determined using a collection of complete hydatidiform moles

artículo científico publicado en 2005

Genome-wide detection and characterization of positive selection in human populations

artículo científico publicado en 2007

Genome-wide scan identifies variation in MLXIPL associated with plasma triglycerides

artículo científico publicado en 2008

Genomewide SNP variation reveals relationships among landraces and modern varieties of rice

scholarly article

Genomic DNA insertions and deletions occur frequently between humans and nonhuman primates

artículo científico publicado en 2003

High-throughput genotyping of single nucleotide polymorphisms using new biplex invader technology

artículo científico publicado en 2002

Identification of common variants in the SHBG gene affecting sex hormone-binding globulin levels and breast cancer risk in postmenopausal women

artículo científico publicado en 2008

In vitro human keratinocyte migration rates are associated with SNPs in the KRT1 interval

artículo científico publicado en 2007

Initial sequencing and analysis of the human genome

artículo científico publicado en 2001

Large-scale association analysis identifies new risk loci for coronary artery disease

artículo científico publicado en 2012

Loss-of-function mutations in SLC30A8 protect against type 2 diabetes

artículo científico publicado en 2014

Matching strategies for genetic association studies in structured populations

artículo científico publicado en 2004

Naive antibody gene-segment frequencies are heritable and unaltered by chronic lymphocyte ablation

artículo científico publicado en 2011

Noncoding sequences conserved in a limited number of mammals in the SIM2 interval are frequently functional

artículo científico publicado en 2004

Population-based study designs in molecular epidemiology

artículo científico

Precise determination of the diversity of a combinatorial antibody library gives insight into the human immunoglobulin repertoire

artículo científico publicado en 2009

Principles, organization, and operation of a DNA bank for clinical trials: a Department of Veterans Affairs cooperative study

artículo científico publicado en 2002

Revealing sequence variation patterns in rice with machine learning methods

scholarly article by Regina Bohnert et al published 2008 in BMC Bioinformatics

Segmental phylogenetic relationships of inbred mouse strains revealed by fine-scale analysis of sequence variation across 4.6 mb of mouse genome

artículo científico publicado en 2004

Single nucleotide polymorphisms in protein tyrosine phosphatase 1beta (PTPN1) are associated with essential hypertension and obesity

artículo científico publicado en 2004

Single nucleotide polymorphisms in protein tyrosine phosphatase 1β (PTPN1) are associated with essential hypertension and obesity

Structure of mouse kallikrein gene family suggests a role in specific processing of biologically active peptides

scientific journal article

Synthetic antibodies designed on natural sequence landscapes

artículo científico publicado en 2011

Title Page / Table of Contents

article

Toward a roadmap in global biobanking for health

artículo científico publicado en 2012

Uncompromised 10-year survival of oldest old carrying somatic mutations in DNMT3A and TET2.

artículo científico publicado en 2016

Variation in the FGFR2 gene and the effect of a low-fat dietary pattern on invasive breast cancer

artículo científico publicado en 2010

Variation in the FGFR2 gene and the effects of postmenopausal hormone therapy on invasive breast cancer

scientific article published on 27 October 2009

Lista de obras de

A Gene Map of the Human Genome

A P3G generic access agreement for population genomic studies

A common allele on chromosome 9 associated with coronary heart disease

A genome scan for hypertension susceptibility loci in populations of Chinese and Japanese origins

A genomewide admixture map for Latino populations

A genomewide association study of skin pigmentation in a South Asian population

A high-density association screen of 155 ion transport genes for involvement with common migraine

A physical map of the human genome

A polymorphism in the beta1 adrenergic receptor is associated with resting heart rate

A second generation human haplotype map of over 3.1 million SNPs

A sequence-based variation map of 8.27 million SNPs in inbred mouse strains

Advice to governments: scientific give and take

Aging as accelerated accumulation of somatic variants: whole-genome sequencing of centenarian and middle-aged monozygotic twin pairs

Allele-specific KRT1 expression is a complex trait

Analysis of allelic differential expression in human white blood cells

Application of pooled genotyping to scan candidate regions for association with HDL cholesterol levels

Assessing the phenotypic effects in the general population of rare variants in genes for a dominant Mendelian form of diabetes

B cell exchange across the blood-brain barrier in multiple sclerosis

Cardiac Myosin Activation: A Potential Therapeutic Approach for Systolic Heart Failure ⬇️

Clustering and heritability of insulin resistance in Chinese and Japanese hypertensive families: a Stanford-Asian Pacific Program in Hypertension and Insulin Resistance sibling study

Comprehensive whole-genome and candidate gene analysis for response to statin therapy in the Treating to New Targets (TNT) cohort

Effect of genome and environment on metabolic and inflammatory profiles

Evaluation of the SNP tagging approach in an independent population sample—array-based SNP discovery in Sami

Fine mapping in 94 inbred mouse strains using a high-density haplotype resource

From genomic databases to translation: a call to action

Gender-specific gene expression in post-mortem human brain: localization to sex chromosomes

Generation and annotation of the DNA sequences of human chromosomes 2 and 4

Genetic variants in the MRPS30 region and postmenopausal breast cancer risk

Genetic variants in the MRPS30 region and postmenopausal breast cancer risk

Genetic variation in response to a typhoid vaccine ⬇️

Genome-wide definitive haplotypes determined using a collection of complete hydatidiform moles

Genome-wide detection and characterization of positive selection in human populations

Genome-wide scan identifies variation in MLXIPL associated with plasma triglycerides

Genomewide SNP variation reveals relationships among landraces and modern varieties of rice

Genomic DNA insertions and deletions occur frequently between humans and nonhuman primates

High-throughput genotyping of single nucleotide polymorphisms using new biplex invader technology

Identification of common variants in the SHBG gene affecting sex hormone-binding globulin levels and breast cancer risk in postmenopausal women

In vitro human keratinocyte migration rates are associated with SNPs in the KRT1 interval

Initial sequencing and analysis of the human genome

Large-scale association analysis identifies new risk loci for coronary artery disease

Loss-of-function mutations in SLC30A8 protect against type 2 diabetes

Matching strategies for genetic association studies in structured populations

Naive antibody gene-segment frequencies are heritable and unaltered by chronic lymphocyte ablation

Noncoding sequences conserved in a limited number of mammals in the SIM2 interval are frequently functional

Population-based study designs in molecular epidemiology

Precise determination of the diversity of a combinatorial antibody library gives insight into the human immunoglobulin repertoire

Principles, organization, and operation of a DNA bank for clinical trials: a Department of Veterans Affairs cooperative study

Revealing sequence variation patterns in rice with machine learning methods

Segmental phylogenetic relationships of inbred mouse strains revealed by fine-scale analysis of sequence variation across 4.6 mb of mouse genome

Single nucleotide polymorphisms in protein tyrosine phosphatase 1beta (PTPN1) are associated with essential hypertension and obesity

Single nucleotide polymorphisms in protein tyrosine phosphatase 1β (PTPN1) are associated with essential hypertension and obesity

Structure of mouse kallikrein gene family suggests a role in specific processing of biologically active peptides

Synthetic antibodies designed on natural sequence landscapes

Title Page / Table of Contents

Toward a roadmap in global biobanking for health

Uncompromised 10-year survival of oldest old carrying somatic mutations in DNMT3A and TET2.

Variation in the FGFR2 gene and the effect of a low-fat dietary pattern on invasive breast cancer

Variation in the FGFR2 gene and the effects of postmenopausal hormone therapy on invasive breast cancer