Lista de obras - Eleanor Feingold - Dominio Público Uruguay

A Genome-wide Association Study of Nonsyndromic Cleft Palate Identifies an Etiologic Missense Variant in GRHL3.

artículo científico publicado en 2016

A Likelihood-Based Approach for Missing Genotype Data.

artículo científico publicado en 2010

A Pipeline for Classifying Relationships Using Dense SNP/SNV Data and Putative Pedigree Information

artículo científico publicado en 2015

A comparison of principal component analysis and factor analysis strategies for uncovering pleiotropic factors

artículo científico publicado en 2009

A hierarchical model for estimating significance levels of non-parametric linkage statistics for large pedigrees

article

A multi-ethnic genome-wide association study identifies novel loci for non-syndromic cleft lip with or without cleft palate on 2p24.2, 17q23 and 19q13.

scientific article published on 30 March 2016

A powerful and robust new linkage statistic for discordant sibling pairs

artículo científico publicado en 2004

A rare duplication on chromosome 16p11.2 is identified in patients with psychosis in Alzheimer's disease

artículo científico publicado en 2014

A survey of affected-sibship statistics for nonparametric linkage analysis

artículo científico publicado en 2001

A systematic genetic analysis and visualization of phenotypic heterogeneity among orofacial cleft GWAS signals

artículo científico publicado en 2019

A trisomic transmission disequilibrium test

artículo científico publicado en 2004

A variant of the glucocorticoid receptor gene is not associated with adrenal androgen excess in women with polycystic ovary syndrome

article

Age of onset in hereditary lymphedema

artículo científico publicado en 2003

Altered patterns of multiple recombinant events are associated with nondisjunction of chromosome 21.

scientific article published on 09 December 2011

An examination of the relationship between hotspots and recombination associated with chromosome 21 nondisjunction

artículo científico publicado en 2014

An excess of deleterious variants in VEGF-A pathway genes in Down-syndrome-associated atrioventricular septal defects

artículo científico publicado en 2012

Association between NEDD4L gene and sodium lithium countertransport

artículo científico publicado en 2010

Association between maternal age and meiotic recombination for trisomy 21.

artículo científico publicado en 2004

Association signals unveiled by a comprehensive gene set enrichment analysis of dental caries genome-wide association studies

artículo científico publicado en 2013

Association studies of low-frequency coding variants in nonsyndromic cleft lip with or without cleft palate.

artículo científico publicado en 2017

Association tests using kernel-based measures of multi-locus genotype similarity between individuals

artículo científico publicado en 2010

Caries Experience Differs between Females and Males across Age Groups in Northern Appalachia

artículo científico publicado en 2015

Characterization of susceptible chiasma configurations that increase the risk for maternal nondisjunction of chromosome 21

scientific article published on 01 September 1997

Clustering tooth surfaces into biologically informative caries outcomes.

artículo científico publicado en 2012

Comparison of allele-sharing statistics for general pedigrees

artículo científico publicado en 2000

Composite statistics for QTL mapping with moderately discordant sibling pairs

artículo científico publicado en 2000

Comprehensive literature review and statistical considerations for GWAS meta-analysis

artículo científico publicado en 2012

Comprehensive literature review and statistical considerations for microarray meta-analysis

artículo científico publicado en 2012

Connexin 47 mutations increase risk for secondary lymphedema following breast cancer treatment

artículo científico publicado en 2012

Decreased expression of miR-125b and miR-100 in oral cancer cells contributes to malignancy

artículo científico publicado en 2009

Demographic, socioeconomic, and behavioral factors affecting patterns of tooth decay in the permanent dentition: principal components and factor analyses

artículo científico publicado en 2012

Detectable clonal mosaicism from birth to old age and its relationship to cancer

artículo científico publicado en 2012

Effects of enamel matrix genes on dental caries are moderated by fluoride exposures

artículo científico publicado en 2014

Effects of smoking and genotype on the PSR index of periodontal disease in adults aged 18-49.

artículo científico publicado en 2012

Efficient Identification of Null-Allele Single Nucleotide Polymorphism Markers

artículo científico publicado en 2015

Efficient simulation of P values for linkage analysis

artículo científico publicado en 2004

Epidemiology of Down syndrome: new insight into the multidimensional interactions among genetic and environmental risk factors in the oocyte

artículo científico publicado en 2011

Etiology of Down syndrome: Evidence for consistent association among altered meiotic recombination, nondisjunction, and maternal age across populations

artículo científico publicado en 2009

Evaluation of disease burden and response to treatment in adults with type 1 Gaucher disease using a validated disease severity scoring system (DS3)

artículo científico publicado en 2015

Evidence for dysregulation of genome-wide recombination in oocytes with nondisjoined chromosomes 21.

scientific article published on 06 September 2013

FOOTER: a web tool for finding mammalian DNA regulatory regions using phylogenetic footprinting

artículo científico publicado en 2005

Footer: a quantitative comparative genomics method for efficient recognition of cis-regulatory elements

artículo científico publicado en 2005

GJC2 missense mutations cause human lymphedema

artículo científico publicado en 2010

GWAS of dental caries patterns in the permanent dentition

scientific journal article

Gender-specific association of ATP-binding cassette transporter 1 (ABCA1) polymorphisms with the risk of late-onset Alzheimer's disease

artículo científico publicado en 2006

Gene-dropping vs. empirical variance estimation for allele-sharing linkage statistics

artículo científico publicado en 2006

Genetic Association of MPPED2 and ACTN2 with Dental Caries.

artículo científico publicado en 2014

Genetic Determinants of Survival in Patientswith Alzheimer’s Disease.

artículo científico publicado en 2015

Genetic analysis of variation in human meiotic recombination

artículo científico publicado en 2009

Genetic association of ubiquilin with Alzheimer's disease and related quantitative measures.

artículo científico publicado en 2006

Genetic variation in fatty acid-binding protein-4 and peroxisome proliferator-activated receptor gamma interactively influence insulin sensitivity and body composition in males

artículo científico publicado en 2004

Genetic variation in uncoupling protein 3 is associated with dietary intake and body composition in females

artículo científico publicado en 2004

Genetics. Genetic control of hotspots

artículo científico publicado en 2010

Genome partitioning of genetic variation for complex traits using common SNPs

artículo científico publicado en 2011

Genome scans of facial features in East Africans and cross-population comparisons reveal novel associations

artículo científico publicado en 2021

Genome-Wide Association Study Reveals Multiple Loci Influencing Normal Human Facial Morphology

artículo científico publicado en 2016

Genome-Wide Association Study of Down Syndrome-Associated Atrioventricular Septal Defects.

artículo científico publicado en 2015

Genome-Wide Association Study of Meiotic Recombination Phenotypes.

artículo científico publicado en 2016

Genome-wide association analysis of age-at-onset in Alzheimer's disease

artículo científico publicado en 2011

Genome-wide association scan for childhood caries implicates novel genes

scientific journal article

Genome-wide association scan of dental caries in the permanent dentition

artículo científico publicado en 2012

Genome-wide association studies in dogs and humans identify ADAMTS20 as a risk variant for cleft lip and palate

artículo científico publicado en 2015

Genome-wide association studies of pit-and-fissure- and smooth-surface caries in permanent dentition

artículo científico publicado en 2013

Genome-wide association studies: prospects and challenges for oral health

artículo científico publicado en 2012

Genome-wide association study of Alzheimer's disease

artículo científico publicado en 2012

Genome-wide association study of facial morphology reveals novel associations with FREM1 and PARK2.

artículo científico publicado en 2017

Genome-wide association study of periodontal health measured by probing depth in adults ages 18-49 years

artículo científico publicado en 2014

Genome-wide association study of primary dentition pit-and-fissure and smooth surface caries

artículo científico publicado en 2014

Genome-wide copy-number variation study of psychosis in Alzheimer's disease.

artículo científico publicado en 2015

Genome-wide interaction studies identify sex-specific risk alleles for nonsyndromic orofacial clefts

artículo científico publicado en 2018

Genotype-phenotype correlations of pheochromocytoma in two large von Hippel-Lindau (VHL) type 2A kindreds with different missense mutations

Heritable patterns of tooth decay in the permanent dentition: principal components and factor analyses

artículo científico publicado en 2012

Host Genetics, Steatosis and Insulin Resistance among African Americans and Caucasian Americans with Hepatitis C Virus Genotype-1 Infection

artículo científico publicado en 2009

Identification of 16q21 as a modifier of nonsyndromic orofacial cleft phenotypes

artículo científico publicado en 2017

Identification of a New Susceptibility Locus for Systemic Lupus Erythematosus on Chromosome 12 in Individuals of European Ancestry

artículo científico publicado en 2015

Identifying Genetic Sources of Phenotypic Heterogeneity in Orofacial Clefts by Targeted Sequencing

artículo científico publicado en 2017

Increased expression of interferon-inducible genes in macaque lung tissues during simian immunodeficiency virus infection

artículo científico publicado en 2006

Investigation of factors associated with paternal nondisjunction of chromosome 21

Is there an interchromosomal effect in reciprocal translocation carriers? Sperm FISH studies

Letter to the Editor

Life factors affecting depression and burden in amyotrophic lateral sclerosis caregivers

artículo científico publicado en 2014

Linkage disequilibrium mapping in trisomic populations: analytical approaches and an application to congenital heart defects in Down syndrome

artículo científico publicado en 2004

Local high-capacity adenovirus-mediated mCTLA4Ig and mCD40Ig expression prolongs recombinant gene expression in skeletal muscle

artículo científico publicado en 2001

Long-term outcomes, branch-specific expressivity, and disease-related mortality in von Hippel-Lindau type 2A.

artículo científico publicado en 2011

Mass spectral determination of fasting tear glucose concentrations in nondiabetic volunteers

artículo científico publicado en 2007

Maternal Telomere Length and Risk of Down Syndrome: Epidemiological Impact of Smokeless Chewing Tobacco and Oral Contraceptive on Segregation of Chromosome 21.

artículo científico publicado en 2015

Multi-dimensional prioritization of dental caries candidate genes and its enriched dense network modules

artículo científico publicado en 2013

Multicolor fluorescence in situ hybridization analysis of the spermatozoa of a male heterozygous for a reciprocal translocation t(11;22)(q23;q11)

article

Multipoint estimation of genetic maps for human trisomies with one parent or other partial data

artículo científico publicado en 2000

New insights into human nondisjunction of chromosome 21 in oocytes

artículo científico publicado en 2008

No "bias" toward the null hypothesis in most conventional multipoint nonparametric linkage analyses

artículo científico publicado en 2004

No observed association for mitochondrial SNPs with preterm delivery and related outcomes

artículo científico publicado en 2012

Non-disjunction in human sperm: evidence for an effect of increasing paternal age.

artículo científico publicado en 1995

Peripheral blood mononuclear cell gene expression profiles predict poor outcome in idiopathic pulmonary fibrosis

artículo científico publicado en 2013

Polymorphic haplotypes ofCRELD1differentially predispose Down syndrome and euploids individuals to atrioventricular septal defect

artículo científico publicado en 2012

Pooling-based genome-wide association study implicates gamma-glutamyltransferase 1 (GGT1) gene in pancreatic carcinogenesis

artículo científico publicado en 2010

Predictors of dental care utilization in north-central Appalachia in the USA

artículo científico publicado en 2019

QTL mapping with discordant and concordant sibling pairs: new statistics and new design strategies

artículo científico publicado en 2005

Recent advances in human quantitative-trait-locus mapping: comparison of methods for discordant sibling pairs

artículo científico publicado en 2003

Recent advances in human quantitative-trait-locus mapping: comparison of methods for selected sibling pairs

artículo científico publicado en 2003

Referral to cancer genetic counseling: are there stages of readiness?

artículo científico publicado en 2006

Regionally Smoothed Meta-Analysis Methods for GWAS Datasets

artículo científico publicado en 2015

Regression-based quantitative-trait-locus mapping in the 21st century

scientific article published on August 2002

Regulatory conservation of protein coding and microRNA genes in vertebrates: lessons from the opossum genome

artículo científico publicado en 2007

Relationship of recombination patterns and maternal age among non-disjoined chromosomes 21.

artículo científico publicado en 2006

Replication of a genome-wide association study of birth weight in preterm neonates

artículo científico publicado en 2011

Robust score statistics for QTL linkage analysis

artículo científico publicado en 2008

Skeletal muscle fatigue, strength, and quality in the elderly: the Health ABC Study

artículo científico publicado en 2005

Smarter clustering methods for SNP genotype calling

artículo científico publicado en 2008

Statistics for nonparametric linkage analysis of X-linked traits in general pedigrees

artículo científico publicado en 2001

Systemic delivery of a high-capacity adenoviral vector expressing mouse CTLA4Ig improves skeletal muscle gene therapy

artículo científico publicado en 2002

Telomere length is associated with types of chromosome 21 nondisjunction: a new insight into the maternal age effect on Down syndrome birth.

artículo científico publicado en 2010

Testing for contributions of mitochondrial DNA mutations to complex diseases

artículo científico publicado en 1998

The C161-->T polymorphism in peroxisome proliferator-activated receptor gamma, but not P12A, is associated with insulin resistance in Hispanic and non-Hispanic white women: evidence for another functional variant in peroxisome proliferator-activated

artículo científico publicado en 2005

The Gene, Environment Association Studies consortium (GENEVA): maximizing the knowledge obtained from GWAS by collaboration across studies of multiple conditions

artículo científico publicado en 2010

The elusive goal of pedigree weights

artículo científico publicado en 2007

The origin of trisomy 22: evidence for acrocentric chromosome-specific patterns of nondisjunction

artículo científico publicado en 2007

Using family data as a verification standard to evaluate copy number variation calling strategies for genetic association studies

artículo científico publicado en 2012

Variation in folate pathway genes contributes to risk of congenital heart defects among individuals with Down syndrome

artículo científico publicado en 2010

Web-Based Identification of Evolutionary Conserved DNA cis -Regulatory Elements

What's the best statistic for a simple test of genetic association in a case-control study?

artículo científico publicado en 2010

Lista de obras de Eleanor Feingold

A Genome-wide Association Study of Nonsyndromic Cleft Palate Identifies an Etiologic Missense Variant in GRHL3.

A Likelihood-Based Approach for Missing Genotype Data.

A Pipeline for Classifying Relationships Using Dense SNP/SNV Data and Putative Pedigree Information

A comparison of principal component analysis and factor analysis strategies for uncovering pleiotropic factors

A hierarchical model for estimating significance levels of non-parametric linkage statistics for large pedigrees

A multi-ethnic genome-wide association study identifies novel loci for non-syndromic cleft lip with or without cleft palate on 2p24.2, 17q23 and 19q13.

A powerful and robust new linkage statistic for discordant sibling pairs

A rare duplication on chromosome 16p11.2 is identified in patients with psychosis in Alzheimer's disease

A survey of affected-sibship statistics for nonparametric linkage analysis

A systematic genetic analysis and visualization of phenotypic heterogeneity among orofacial cleft GWAS signals

A trisomic transmission disequilibrium test

A variant of the glucocorticoid receptor gene is not associated with adrenal androgen excess in women with polycystic ovary syndrome

Age of onset in hereditary lymphedema

Altered patterns of multiple recombinant events are associated with nondisjunction of chromosome 21.

An examination of the relationship between hotspots and recombination associated with chromosome 21 nondisjunction

An excess of deleterious variants in VEGF-A pathway genes in Down-syndrome-associated atrioventricular septal defects

Association between NEDD4L gene and sodium lithium countertransport

Association between maternal age and meiotic recombination for trisomy 21.

Association signals unveiled by a comprehensive gene set enrichment analysis of dental caries genome-wide association studies

Association studies of low-frequency coding variants in nonsyndromic cleft lip with or without cleft palate.

Association tests using kernel-based measures of multi-locus genotype similarity between individuals

Caries Experience Differs between Females and Males across Age Groups in Northern Appalachia

Characterization of susceptible chiasma configurations that increase the risk for maternal nondisjunction of chromosome 21

Clustering tooth surfaces into biologically informative caries outcomes.

Comparison of allele-sharing statistics for general pedigrees

Composite statistics for QTL mapping with moderately discordant sibling pairs

Comprehensive literature review and statistical considerations for GWAS meta-analysis

Comprehensive literature review and statistical considerations for microarray meta-analysis

Connexin 47 mutations increase risk for secondary lymphedema following breast cancer treatment

Decreased expression of miR-125b and miR-100 in oral cancer cells contributes to malignancy

Demographic, socioeconomic, and behavioral factors affecting patterns of tooth decay in the permanent dentition: principal components and factor analyses

Detectable clonal mosaicism from birth to old age and its relationship to cancer

Effects of enamel matrix genes on dental caries are moderated by fluoride exposures

Effects of smoking and genotype on the PSR index of periodontal disease in adults aged 18-49.

Efficient Identification of Null-Allele Single Nucleotide Polymorphism Markers

Efficient simulation of P values for linkage analysis

Epidemiology of Down syndrome: new insight into the multidimensional interactions among genetic and environmental risk factors in the oocyte

Etiology of Down syndrome: Evidence for consistent association among altered meiotic recombination, nondisjunction, and maternal age across populations

Evaluation of disease burden and response to treatment in adults with type 1 Gaucher disease using a validated disease severity scoring system (DS3)

Evidence for dysregulation of genome-wide recombination in oocytes with nondisjoined chromosomes 21.

FOOTER: a web tool for finding mammalian DNA regulatory regions using phylogenetic footprinting

Footer: a quantitative comparative genomics method for efficient recognition of cis-regulatory elements

GJC2 missense mutations cause human lymphedema

GWAS of dental caries patterns in the permanent dentition

Gender-specific association of ATP-binding cassette transporter 1 (ABCA1) polymorphisms with the risk of late-onset Alzheimer's disease

Gene-dropping vs. empirical variance estimation for allele-sharing linkage statistics

Genetic Association of MPPED2 and ACTN2 with Dental Caries.

Genetic Determinants of Survival in Patientswith Alzheimer’s Disease.

Genetic analysis of variation in human meiotic recombination

Genetic association of ubiquilin with Alzheimer's disease and related quantitative measures.

Genetic variation in fatty acid-binding protein-4 and peroxisome proliferator-activated receptor gamma interactively influence insulin sensitivity and body composition in males

Genetic variation in uncoupling protein 3 is associated with dietary intake and body composition in females

Genetics. Genetic control of hotspots

Genome partitioning of genetic variation for complex traits using common SNPs

Genome scans of facial features in East Africans and cross-population comparisons reveal novel associations

Genome-Wide Association Study Reveals Multiple Loci Influencing Normal Human Facial Morphology

Genome-Wide Association Study of Down Syndrome-Associated Atrioventricular Septal Defects.

Genome-Wide Association Study of Meiotic Recombination Phenotypes.

Genome-wide association analysis of age-at-onset in Alzheimer's disease

Genome-wide association scan for childhood caries implicates novel genes

Genome-wide association scan of dental caries in the permanent dentition

Genome-wide association studies in dogs and humans identify ADAMTS20 as a risk variant for cleft lip and palate

Genome-wide association studies of pit-and-fissure- and smooth-surface caries in permanent dentition

Genome-wide association studies: prospects and challenges for oral health

Genome-wide association study of Alzheimer's disease

Genome-wide association study of facial morphology reveals novel associations with FREM1 and PARK2.

Genome-wide association study of periodontal health measured by probing depth in adults ages 18-49 years

Genome-wide association study of primary dentition pit-and-fissure and smooth surface caries

Genome-wide copy-number variation study of psychosis in Alzheimer's disease.

Genome-wide interaction studies identify sex-specific risk alleles for nonsyndromic orofacial clefts

Genotype-phenotype correlations of pheochromocytoma in two large von Hippel-Lindau (VHL) type 2A kindreds with different missense mutations

Heritable patterns of tooth decay in the permanent dentition: principal components and factor analyses

Host Genetics, Steatosis and Insulin Resistance among African Americans and Caucasian Americans with Hepatitis C Virus Genotype-1 Infection

Identification of 16q21 as a modifier of nonsyndromic orofacial cleft phenotypes

Identification of a New Susceptibility Locus for Systemic Lupus Erythematosus on Chromosome 12 in Individuals of European Ancestry

Identifying Genetic Sources of Phenotypic Heterogeneity in Orofacial Clefts by Targeted Sequencing

Increased expression of interferon-inducible genes in macaque lung tissues during simian immunodeficiency virus infection

Investigation of factors associated with paternal nondisjunction of chromosome 21

Is there an interchromosomal effect in reciprocal translocation carriers? Sperm FISH studies