Eleanor Feingold

Eleanor Feingold's AcademicInfluence.com Rankings

Eleanor Feingold

Biology

#14332

World Rank

#18054

Historical Rank

Genetics

#1643

World Rank

#1751

Historical Rank

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Biology

Why Is Eleanor Feingold Influential?

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According to Wikipedia, Eleanor Feingold is an American statistical geneticist. She is a professor of human genetics and of biostatistics, and executive associate dean, in the University of Pittsburgh Graduate School of Public Health.

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Eleanor Feingold's Published Works

Number of citations in a given year to any of this author's works

Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author

Published Works

Genome-wide Association Studies (2012) (1122)
Genome partitioning of genetic variation for complex traits using common SNPs (2011) (869)
Detectable clonal mosaicism from birth to old age and its relationship to cancer (2012) (514)
Comprehensive literature review and statistical considerations for GWAS meta-analysis (2012) (355)
Comprehensive literature review and statistical considerations for microarray meta-analysis (2012) (313)
Gaussian models for genetic linkage analysis using complete high-resolution maps of identity by descent. (1993) (282)
Decreased expression of miR‐125b and miR‐100 in oral cancer cells contributes to malignancy (2009) (234)
Peripheral Blood Mononuclear Cell Gene Expression Profiles Predict Poor Outcome in Idiopathic Pulmonary Fibrosis (2013) (225)
Characterization of susceptible chiasma configurations that increase the risk for maternal nondisjunction of chromosome 21. (1997) (222)
Genome-wide association study of Alzheimer's disease (2012) (220)
Non-disjunction in human sperm: evidence for an effect of increasing paternal age. (1995) (192)
Familial transmission of the FMR1 CGG repeat. (1996) (185)
New Insights into Human Nondisjunction of Chromosome 21 in Oocytes (2008) (181)
Genetic Analysis of Variation in Human Meiotic Recombination (2009) (167)
The gene, environment association studies consortium (GENEVA): maximizing the knowledge obtained from GWAS by collaboration across studies of multiple conditions (2010) (161)
Genome-wide mapping of global-to-local genetic effects on human facial shape (2018) (157)
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. (2016) (154)
Association between maternal age and meiotic recombination for trisomy 21. (2005) (139)
GJC2 missense mutations cause human lymphedema. (2010) (135)
Molecular Anatomy of an Intracranial Aneurysm: Coordinated Expression of Genes Involved in Wound Healing and Tissue Remodeling (2001) (134)
Genome-Wide Association Study Reveals Multiple Loci Influencing Normal Human Facial Morphology (2016) (132)
Genome-wide Association Scan for Childhood Caries Implicates Novel Genes (2011) (115)
Genome-wide meta-analyses of nonsyndromic orofacial clefts identify novel associations between FOXE1 and all orofacial clefts, and TP63 and cleft lip with or without cleft palate (2017) (111)
A Genome-wide Association Study of Nonsyndromic Cleft Palate Identifies an Etiologic Missense Variant in GRHL3. (2016) (109)
An excess of deleterious variants in VEGF-A pathway genes in Down-syndrome-associated atrioventricular septal defects. (2012) (103)
Mass spectral determination of fasting tear glucose concentrations in nondiabetic volunteers. (2007) (102)
Connexin 47 Mutations Increase Risk for Secondary Lymphedema Following Breast Cancer Treatment (2012) (98)
Genome-wide association analysis of age-at-onset in Alzheimer's disease (2012) (93)
Etiology of Down syndrome: Evidence for consistent association among altered meiotic recombination, nondisjunction, and maternal age across populations (2009) (90)
Association tests using kernel‐based measures of multi‐locus genotype similarity between individuals (2009) (84)
Genome-Wide Association Studies in Dogs and Humans Identify ADAMTS20 as a Risk Variant for Cleft Lip and Palate (2015) (80)
Genome-wide association Scan of dental caries in the permanent dentition (2012) (78)
Variation in folate pathway genes contributes to risk of congenital heart defects among individuals with Down syndrome (2010) (76)
GWAS of Dental Caries Patterns in the Permanent Dentition (2013) (75)
Genetic variation in fatty acid-binding protein-4 and peroxisome proliferator-activated receptor gamma interactively influence insulin sensitivity and body composition in males. (2004) (74)
Is there an interchromosomal effect in reciprocal translocation carriers? Sperm FISH studies (2000) (72)
Gender-specific association of ATP-binding cassette transporter 1 (ABCA1) polymorphisms with the risk of late-onset Alzheimer's disease (2007) (72)
Regression-based quantitative-trait-locus mapping in the 21st century. (2002) (71)
Genome-wide association study of facial morphology reveals novel associations with FREM1 and PARK2 (2017) (68)
Sex ratio in normal and disomic sperm: evidence that the extra chromosome 21 preferentially segregates with the Y chromosome. (1996) (66)
Genetic association of ubiquilin with Alzheimer's disease and related quantitative measures (2006) (66)
Insights into the genetic architecture of the human face (2020) (58)
Genome-wide Association Studies of Pit-and-Fissure- and Smooth-surface Caries in Permanent Dentition (2013) (57)
Genome-Wide Association Study of Periodontal Health Measured by Probing Depth in Adults Ages 18−49 years (2013) (56)
Methods for linkage analysis of quantitative trait loci in humans. (2001) (53)
Telomere length is associated with types of chromosome 21 nondisjunction: a new insight into the maternal age effect on Down syndrome birth (2010) (47)
Referral to cancer genetic counseling: Are there stages of readiness? (2006) (46)
Novel genetic loci affecting facial shape variation in humans (2019) (46)
Caries Experience Differs between Females and Males across Age Groups in Northern Appalachia (2015) (45)
Multicolor fluorescence in situ hybridization analysis of the spermatozoa of a male heterozygous for a reciprocal translocation t(11;22)(q23;q11) (1999) (43)
Pooling-Based Genome-Wide Association Study Implicates Gamma-Glutamyltransferase 1 (GGT1) Gene in Pancreatic Carcinogenesis (2010) (43)
A survey of affected-sibship statistics for nonparametric linkage analysis. (2001) (42)
What's the best statistic for a simple test of genetic association in a case‐control study? (2009) (42)
Genome-wide variation in recombination in female meiosis: a risk factor for non-disjunction of chromosome 21. (2000) (42)
Variation in the FABP2 promoter alters transcriptional activity and is associated with body composition and plasma lipid levels (2003) (41)
Epidemiology of Down syndrome: new insight into the multidimensional interactions among genetic and environmental risk factors in the oocyte. (2011) (41)
Local high-capacity adenovirus-mediated mCTLA4Ig and mCD40Ig expression prolongs recombinant gene expression in skeletal muscle. (2001) (40)
Altered patterns of multiple recombinant events are associated with nondisjunction of chromosome 21 (2012) (40)
Genetic variation in uncoupling protein 3 is associated with dietary intake and body composition in females. (2004) (39)
Composite statistics for QTL mapping with moderately discordant sibling pairs. (2000) (39)
Life factors affecting depression and burden in amyotrophic lateral sclerosis caregivers (2014) (39)
Genome-wide association study of brain amyloid deposition as measured by Pittsburgh Compound-B (PiB)-PET imaging (2018) (35)
Genome scanning for segments shared identical by descent among distant relatives in isolated populations. (1997) (35)
Investigating the shared genetics of non-syndromic cleft lip/palate and facial morphology (2018) (34)
Footer: a quantitative comparative genomics method for efficient recognition of cis-regulatory elements. (2005) (34)
Relationship of recombination patterns and maternal age among non-disjoined chromosomes 21. (2006) (34)
Heritable patterns of tooth decay in the permanent dentition: principal components and factor analyses (2012) (34)
FOOTER: a web tool for finding mammalian DNA regulatory regions using phylogenetic footprinting (2005) (33)
Effects of enamel matrix genes on dental caries are moderated by fluoride exposures (2015) (33)
Regulatory conservation of protein coding and microRNA genes in vertebrates: lessons from the opossum genome (2007) (33)
Strategies for mapping heterogeneous recessive traits by allele-sharing methods. (1997) (33)
Investigation of factors associated with paternal nondisjunction of chromosome 21 (2009) (32)
Age of onset in hereditary lymphedema. (2003) (31)
Inherited genetic susceptibility of acute lymphoblastic leukemia in Down syndrome. (2019) (31)
Multiethnic GWAS Reveals Polygenic Architecture of Earlobe Attachment (2017) (31)
Genome-wide Enrichment of De Novo Coding Mutations in Orofacial Cleft Trios. (2020) (31)
Recent advances in human quantitative-trait-locus mapping: comparison of methods for discordant sibling pairs. (2003) (30)
Genome-Wide Association Study of Primary Dentition Pit-and-Fissure and Smooth Surface Caries (2014) (30)
Demographic, socioeconomic, and behavioral factors affecting patterns of tooth decay in the permanent dentition: principal components and factor analyses. (2013) (30)
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 receptor gamma. (2005) (30)
Association studies of low‐frequency coding variants in nonsyndromic cleft lip with or without cleft palate (2017) (28)
The origin of trisomy 22: Evidence for acrocentric chromosome‐specific patterns of nondisjunction (2007) (28)
Evaluation of disease burden and response to treatment in adults with type 1 gaucher disease using a validated disease severity scoring system (DS3) (2015) (27)
Replication of a genome-wide association study of birth weight in preterm neonates. (2012) (27)
Increased expression of interferon-inducible genes in macaque lung tissues during simian immunodeficiency virus infection. (2006) (27)
Inverted duplication pattern in anaphase bridges confirms the breakage-fusion-bridge (BFB) cycle model for 11q13 amplification (2007) (27)
Genetic Control of Hotspots (2010) (26)
No Observed Association for Mitochondrial SNPs with Preterm Delivery and Related Outcomes (2012) (26)
Associations Between Medical History, Cognition, and Behavior in Youth With Down Syndrome: A Report From the Down Syndrome Cognition Project. (2018) (26)
Identification of a New Susceptibility Locus for Systemic Lupus Erythematosus on Chromosome 12 in Individuals of European Ancestry (2016) (26)
Genome-Wide Microarray Expression Analysis of CD4+ T Cells from Nonobese Diabetic Congenic Mice Identifies Cd55 (Daf1) and Acadl as Candidate Genes for Type 1 Diabetes1 (2008) (26)
Clustering Tooth Surfaces into Biologically Informative Caries Outcomes (2013) (25)
Systemic delivery of a high-capacity adenoviral vector expressing mouse CTLA4Ig improves skeletal muscle gene therapy. (2002) (25)
A comparison of principal component analysis and factor analysis strategies for uncovering pleiotropic factors (2009) (25)
Multi-Dimensional Prioritization of Dental Caries Candidate Genes and Its Enriched Dense Network Modules (2013) (24)
Meiotic products of two reciprocal translocations studied by multicolor fluorescence in situ hybridization (1998) (24)
Smarter clustering methods for SNP genotype calling (2008) (24)
Estimating meiotic exchange patterns from recombination data: an application to humans. (1997) (24)
Identifying Genetic Sources of Phenotypic Heterogeneity in Orofacial Clefts by Targeted Sequencing. (2017) (23)
Evidence for dysregulation of genome-wide recombination in oocytes with nondisjoined chromosomes 21. (2014) (23)
A systematic genetic analysis and visualization of phenotypic heterogeneity among orofacial cleft GWAS signals (2018) (23)
SNPs Associated With Testosterone Levels Influence Human Facial Morphology (2018) (23)
Genetic Association of MPPED2 and ACTN2 with Dental Caries (2014) (23)
Linkage disequilibrium mapping in trisomic populations: Analytical approaches and an application to congenital heart defects in Down syndrome (2004) (23)
A candidate gene analysis and GWAS for genes associated with maternal nondisjunction of chromosome 21 (2019) (22)
A variant of the glucocorticoid receptor gene is not associated with adrenal androgen excess in women with polycystic ovary syndrome. (2000) (22)
Genome-Wide Association Study of Down Syndrome-Associated Atrioventricular Septal Defects (2015) (22)
Genome-wide copy-number variation study of psychosis in Alzheimer's disease (2015) (21)
Genotype–phenotype correlations of pheochromocytoma in two large von Hippel–Lindau (VHL) type 2A kindreds with different missense mutations (2011) (21)
A Preliminary Genome-Wide Association Study of Pain-Related Fear: Implications for Orofacial Pain (2017) (19)
Six NSCL/P Loci Show Associations With Normal-Range Craniofacial Variation (2018) (19)
Association of maternal CNVs in GSTT1/GSTT2 with smoking, preterm delivery, and low birth weight (2013) (18)
An Examination of the Relationship between Hotspots and Recombination Associated with Chromosome 21 Nondisjunction (2014) (18)
Methods for genetic linkage analysis using trisomies. (1995) (17)
A Rare Duplication on Chromosome 16p11.2 Is Identified in Patients with Psychosis in Alzheimer's Disease (2014) (17)
Limb development genes underlie variation in human fingerprint patterns (2022) (17)
Multipoint estimation of genetic maps for human trisomies with one parent or other partial data. (2000) (17)
FaceBase 3: analytical tools and FAIR resources for craniofacial and dental research (2020) (17)
Identification of 16q21 as a modifier of nonsyndromic orofacial cleft phenotypes (2017) (17)
Recent advances in human quantitative-trait-locus mapping: comparison of methods for selected sibling pairs. (2003) (16)
Markov processes for modeling and analyzing a new genetic mapping method (1993) (16)
Association of low‐frequency genetic variants in regulatory regions with nonsyndromic orofacial clefts (2019) (16)
Association Signals Unveiled by a Comprehensive Gene Set Enrichment Analysis of Dental Caries Genome-Wide Association Studies (2013) (15)
Estimating the Frequency Distribution of Crossovers during Meiosis from Recombination Data (2001) (15)
Efficient Simulation of P Values for Linkage Analysis (2004) (15)
Robust score statistics for QTL linkage analysis. (2008) (14)
The Association between SNPs and a Quantitative Trait: Power Calculation (2018) (14)
Genome-wide association study of facial morphology reveals novel associations with FREM 1 and PARK 2 (2017) (14)
Population-based genome-wide association study of cognitive decline in older adults free of dementia: identification of a novel locus for the attention domain (2019) (14)
Comparison of allele‐sharing statistics for general pedigrees (2000) (14)
Statistics for X‐chromosome associations (2018) (14)
Multiple signals at the extended 8p23 locus are associated with susceptibility to systemic lupus erythematosus (2017) (14)
Effects of Smoking and Genotype on the PSR Index of Periodontal Disease in Adults Aged 18–49 (2012) (13)
Predictors of dental care utilization in north-central Appalachia in the USA. (2019) (13)
Maternal Telomere Length and Risk of Down Syndrome: Epidemiological Impact of Smokeless Chewing Tobacco and Oral Contraceptive on Segregation of Chromosome 21 (2015) (13)
Whole genome sequencing of orofacial cleft trios from the Gabriella Miller Kids First Pediatric Research Consortium identifies a new locus on chromosome 21 (2019) (13)
Whole-Exome Sequencing Analysis of Alzheimer's Disease in Non-APOE*4 Carriers. (2020) (12)
Gene‐dropping vs. empirical variance estimation for allele‐sharing linkage statistics (2006) (12)
Allelic Interaction between CRELD1 and VEGFA in the Pathogenesis of Cardiac Atrioventricular Septal Defects (2014) (12)
An Empirical Bayesian Method for Differential Expression Studies Using One-Channel Microarray Data (2003) (11)
Identifying Genetic Sources of Phenotypic Heterogeneity in Orofacial Clefts by Targeted Sequencing. (2017) (11)
Using Family Data as a Verification Standard to Evaluate Copy Number Variation Calling Strategies for Genetic Association Studies (2012) (11)
Variants on chromosome 4q21 near PKD2 and SIBLINGs are associated with dental caries (2016) (11)
Apolipoprotein E-C1-C4-C2 gene cluster region and inter-individual variation in plasma lipoprotein levels: a comprehensive genetic association study in two ethnic groups (2019) (11)
Genetic Determinants of Survival in Patientswith Alzheimer’s Disease. (2015) (10)
Genome-Wide Association Study of Meiotic Recombination Phenotypes (2016) (10)
Mapping genetic variants for cranial vault shape in humans (2018) (10)
Genome‐wide interaction studies identify sex‐specific risk alleles for nonsyndromic orofacial clefts (2018) (10)
Genome scans of facial features in East Africans and cross-population comparisons reveal novel associations (2021) (10)
Polymorphic haplotypes of CRELD1 differentially predispose Down syndrome and euploids individuals to atrioventricular septal defect (2012) (10)
Variation in the Zinc Finger of PRDM9 is Associated with the Absence of Recombination along Nondisjoined Chromosomes 21 of Maternal Origin (2016) (10)
Combined association of Presenilin-1 and Apolipoprotein E polymorphisms with maternal meiosis II error in Down syndrome births (2017) (9)
Host Genetics, Steatosis and Insulin Resistance among African Americans and Caucasian Americans with Hepatitis C Virus Genotype-1 Infection (2009) (9)
Genome-Wide Association Study of Non-syndromic Orofacial Clefts in a Multiethnic Sample of Families and Controls Identifies Novel Regions (2020) (9)
Insights into the genetic architecture of the human face (2020) (9)
Pilot GWAS of caries in African-Americans shows genetic heterogeneity (2019) (9)
Genetic Association of MMP10, MMP14, and MMP16 with Dental Caries (2017) (8)
Investigating the GWAS-Implicated Loci for Rheumatoid Arthritis in the Pakistani Population (2020) (8)
No "bias" toward the null hypothesis in most conventional multipoint nonparametric linkage analyses. (2004) (8)
SNPs made routine (2004) (8)
A sequencing study of CTLA4 in Pakistani rheumatoid arthritis cases (2020) (7)
A trisomic transmission disequilibrium test (2004) (7)
Association between NEDD4L gene and sodium lithium countertransport. (2011) (7)
Statistical models for trisomic phenotypes. (1996) (7)
Regionally Smoothed Meta‐Analysis Methods for GWAS Datasets (2016) (7)
The PAX1 locus at 20p11 is a potential genetic modifier for bilateral cleft lip (2021) (6)
Testing for contributions of mitochondrial DNA mutations to complex diseases (1998) (6)
Novel caries loci in children and adults implicated by genome-wide analysis of families (2018) (6)
The elusive goal of pedigree weights (2007) (6)
A powerful and robust new linkage statistic for discordant sibling pairs. (2004) (6)
Statistics for nonparametric linkage analysis of X-linked traits in general pedigrees. (2002) (5)
Structural and Genomic Variation in Preterm Birth (2016) (5)
A Pipeline for Classifying Relationships Using Dense SNP/SNV Data and Putative Pedigree Information (2016) (5)
Assessment of genetic risk of type 2 diabetes among Pakistanis based on GWAS-implicated loci. (2021) (4)
FAT4 identified as a potential modifier of orofacial cleft laterality (2021) (4)
QTL mapping with discordant and concordant sibling pairs: new statistics and new design strategies (2005) (4)
Association of VPREB1 Gene Copy Number Variation and Rheumatoid Arthritis Susceptibility (2020) (4)
Exploration of shared genetic susceptibility loci between type 1 diabetes and rheumatoid arthritis in the Pakistani population (2019) (4)
Long-term outcomes, branch-specific expressivity, and disease-related mortality in von Hippel-Lindau type 2A (2011) (4)
Methods for Analyzing the Spatial Distribution of Chiasmata During Meiosis Based on Recombination Data (2002) (3)
GWAS reveals loci associated with velopharyngeal dysfunction (2018) (3)
Web-based identification of evolutionary conserved DNA cis-regulatory elements. (2007) (3)
Association Study of Coronary Artery Disease-Associated Genome-Wide Significant SNPs with Coronary Stenosis in Pakistani Population (2020) (3)
Analyses stratified by maternal age and recombination further characterize genes associated with maternal nondisjunction of chromosome 21 (2021) (3)
A Likelihood-Based Approach for Missing Genotype Data (2010) (3)
Is there an interchromosomal effect in reciprocal translocation carriers? Sperm FISH studies (2000) (3)
PRICKLE1 × FOCAD Interaction Revealed by Genome-Wide vQTL Analysis of Human Facial Traits (2021) (3)
Modeling a new genetic mapping method (1993) (3)
Genome Wide Interaction Studies Identify Sex-Specific Risk Alleles for Nonsyndromic Orofacial Clefts (2018) (2)
A hierarchical model for estimating significance levels of non‐parametric linkage statistics for large pedigrees (2007) (2)
Pancreatitis-associated PRSS1-PRSS2 haplotype alters T cell receptor beta (TRB) repertoire more strongly than PRSS1 expression. (2022) (2)
Impact of low-frequency coding variants on human facial shape (2020) (2)
Altered patterns of multiple recombinant events are associated with nondisjunction of chromosome 21 (2011) (2)
Effects of enamel matrix genes on dental caries are moderated by fluoride exposures (2014) (2)
Comparison of amyloid burden in individuals with Down syndrome versus autosomal dominant Alzheimer's disease: a cross-sectional study (2023) (2)
Genome-wide association Scan of dental caries in the permanent dentition (2012) (1)
Abstract 21122: Contribution of ABCA1 Genetic Variation to Plasma Lipid Levels in Non-Hispanic White Americans (2017) (1)
Association of Early Childhood Caries with Bitter Taste Receptors: A Meta-Analysis of Genome-Wide Association Studies and Transcriptome-Wide Association Study (2022) (1)
Information to Share (1996) (1)
Detecting Gene-Environment Interaction for Maternal Exposures Using Case-Parent Trios Ascertained Through a Case With Non-Syndromic Orofacial Cleft (2021) (1)
Genome-wide mapping of global-to-local genetic effects on human facial shape (2018) (1)
Treatment of Uninformative Families in Mean Allele Sharing Tests for Linkage (2006) (1)
Rare variants found in clinical gene panels illuminate the genetic and allelic architecture of orofacial clefting (2022) (1)
Genome-wide Interaction Study Implicates VGLL2 and Alcohol Exposure and PRL and Smoking in Orofacial Cleft Risk (2020) (1)
Meta-analysis identifies 48 SNPs with multiple independent effects on human facial features (2019) (1)
A simple allele sharing statistic for multiple locus systems (1999) (1)
Genome‐wide meta‐analysis of age‐related cognitive decline in population‐based older individuals (2021) (1)
Increased disomic homozygosity in the telomeric region of chromosome 21 among Down Syndrome individuals with duodenal atresia (1994) (1)
Genome-wide association study of multiethnic non-syndromic orofacial cleft families identifies novel loci specific to family and phenotypic subtypes (2021) (1)
Genome‐wide association study of multiethnic nonsyndromic orofacial cleft families identifies novel loci specific to family and phenotypic subtypes (2022) (1)
Gene Expression and Cardiometabolic Phenotypes of Vitamin D-Deficient Overweight and Obese Black Children (2019) (1)
Association of Fc Gamma Receptor 3B Gene Copy Number Variation with Rheumatoid Arthritis Susceptibility (2022) (0)
Letter to the Editor (2010) (0)
M.P.1.04 Comparison of disease-causing mutations in Duchenne muscular dystrophy from the Cooperative International Neuromuscular Research Group with two large DMD mutation databases (2009) (0)
Impact of low-frequency coding variants on human facial shape (2021) (0)
Investigation of the independent role of a rare APOE variant (L28P; APOE*4Pittsburgh) in late-onset Alzheimer disease (2022) (0)
292 A Genome-Wide Association Study of Spontaneous Preterm Delivery (2010) (0)
IAP Membership Application Form 2010 (2010) (0)
TARGETED SEQUENCING OF GWAS-IMPLICATED LOCI IN ALZHEIMER’S DISEASE (2017) (0)
Validation study of a DS3 severity score index for adult patients with type 1 Gaucher disease (GD1) (2014) (0)
Novel caries loci in children and adults implicated by genome-wide analysis of families (2018) (0)
Meta‐analysis of age‐related cognitive decline reveals a novel locus for the attention domain and implicates a COVID‐19 related gene for global cognitive function (2022) (0)
A novel method for systematic genetic analysis and visualization of phenotypic heterogeneity applied to orofacial clefts (2018) (0)
Genome‐wide association study of plasma apolipoprotein E levels and risk of dementia in older adults (2022) (0)
Category Smarter Clustering Methods for SNP Genotype Calling (2008) (0)
Coding de novo mutations identified by WGS reveal novel orofacial cleft genes (2020) (0)
Modular 3D dense surface analysis and GWAS reveal localized genetic effects on human facial morphology involving multiple novel loci (2017) (0)
Efficient Identification of Null-Allele Single Nucleotide Polymorphism Markers (2015) (0)
Statistical Models forTrisomic Phenotypes (1996) (0)
Genome-Wide Association Study of Incident Dementia in a Community-Based Sample of Older Subjects (2022) (0)
Structural and genomic variation in preterm birth (2017) (0)
GWAS reveals loci associated with velopharyngeal dysfunction (2018) (0)
A comprehensive association study of apolipoprotein E-C1-C4-C2 gene cluster variation with plasma lipoprotein traits. (2017) (0)
The PAX1 locus at 20p11 is a modifier for bilateral cleft lip only (2020) (0)
A whole‐genome‐sequencing study to identify genetic variants associated with Alzheimer’s disease progression (2022) (0)
Predictive Biomarkers and Personalized Medicine Connexin 47 Mutations Increase Risk for Secondary Lymphedema Following Breast Cancer Treatment (2012) (0)
Factors Associated with Specific Patterns of Tooth Decay 33 (2012) (0)
ASSOCIATION OF ALZHEIMER’S DISEASE GENETIC RISK VARIANTS WITH PATHOLOGY ENDOPHENOTYPES (2018) (0)
An association between melotic recombination and advancing maternal age for trisomy 21 (2003) (0)
Pilot GWAS of caries in African-Americans shows genetic heterogeneity (2019) (0)
Abstract B116: Comparison of African American (AA) and Caucasian patients with respect to radiotherapy (RT) delivery in National Surgical Adjuvant Breast & Bowel Project (NSABP) breast cancer treatment trials (2010) (0)
Whole genome sequencing of orofacial cleft trios from the Gabriella Miller Kids First Pediatric Research Consortium identifies a new locus on chromosome 21 (2019) (0)
Evaluation of Disease Burden and Response to Treatment in Adults with Type 1 Gaucher Disase Using a Validated DS3 Severity Score Index (2014) (0)
Heritable patterns of tooth decay in the permanent dentition: principal components and factor analyses (2012) (0)
Exploration of shared genetic susceptibility loci between type 1 diabetes and rheumatoid arthritis in the Pakistani population (2019) (0)
Biological Pathways of Long-Term Visit-to-Visit Blood Pressure Variability in the American Population: Cardiovascular Health Study and Women’s Health Initiatives (2020) (0)
Comparison of African American (AA) and White (W) Patients with Respect to Radiotherapy (RT) Delivery in National Surgical Adjuvant Breast and Bowel Project (NSABP) Breast Cancer Treatment Trials (2010) (0)
Genome-wide meta-analyses of nonsyndromic orofacial clefts identify novel associations between FOXE1 and all orofacial clefts, and TP63 and cleft lip with or without cleft palate (2017) (0)
Oral health and related risk indicators in north-central Appalachia differ by rurality. (2020) (0)
The haptoglobin 2-2 genotype is associated with cardiac autonomic neuropathy in type 1 diabetes: the RETRO HDLc study (2019) (0)
Genomic landscape of Down syndrome-associated acute lymphoblastic leukemia. (2023) (0)

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Other Resources About Eleanor Feingold

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What Schools Are Affiliated With Eleanor Feingold?

Eleanor Feingold is affiliated with the following schools:

Emory University
Stanford University
University of Pittsburgh