Terri H Beaty

发表

Inferring Disease Risk Genes from Sequencing Data in Multiplex Pedigrees Through Sharing of Rare Variants

Ingo Ruczinski, Alexandre Bureau, Ferdouse Begum, 2018, bioRxiv.

Integration of Molecular Interactome and Targeted Interaction Analysis to Identify a COPD Disease Network Module

Xiaobo Zhou, Maksim Kitsak, Edwin K Silverman, 2018, Scientific Reports.

Optimized distributed systems achieve significant performance improvement on sorted merging of massive VCF files

Ingo Ruczinski, Fusheng Wang, Jingjing Gao, 2018, GigaScience.

Multipoint linkage detection in the presence of heterogeneity.

Kung-Yee Liang, Terri H Beaty, Yen-Feng Chiu, 2002, Biostatistics.

Rapid Testing of SNPs and Gene–Environment Interactions in Case–Parent Trio Data Based on Exact Analytic Parameter Estimation

Holger Schwender, Ingo Ruczinski, Margaret A Taub, 2012, Biometrics.

Detecting Disease Variants in Case‐Parent Trio Studies Using the Bioconductor Software Package trio

Holger Schwender, Ingo Ruczinski, Qing Li, 2014, Genetic epidemiology.

Resequencing candidate genes implicates rare variants in asthma susceptibility.

Daniel Capurso, Terri H Beaty, Ryan D. Hernandez, 2012, American journal of human genetics.

Incorporating Genotype Uncertainties Into the Genotypic TDT for Main Effects and Gene‐Environment Interactions

Holger Schwender, Ingo Ruczinski, Thomas A Louis, 2012, Genetic epidemiology.

Genetic loci associated with chronic obstructive pulmonary disease overlap with loci for lung function and pulmonary fibrosis

Harry J de Koning, Edwin K Silverman, Matthijs Oudkerk, 2017, Nature Genetics.

Recombination rates in admixed individuals identified by ancestry-based inference

Ingo Ruczinski, John Novembre, Sharon L R Kardia, 2011, Nature Genetics.

Genetic control of gene expression at novel and established chronic obstructive pulmonary disease loci.

John Quackenbush, Christoph Lange, Weiliang Qiu, 2015, Human molecular genetics.

COPDGene® 2019: Redefining the Diagnosis of Chronic Obstructive Pulmonary Disease.

Nicola A Hanania, Jennifer G. Dy, Raúl San José Estépar, 2019, Chronic obstructive pulmonary diseases.

Identifying a Deletion Affecting Total Lung Capacity Among Subjects in the COPDGene Study Cohort

Ingo Ruczinski, Edwin K Silverman, Douglas Curran-Everett, 2016, Genetic epidemiology.

Identification of functional variants for cleft lip with or without cleft palate in or near PAX7, FGFR2, and NOG by targeted sequencing of GWAS loci.

Ingo Ruczinski, Qunyuan Zhang, Ferdouse Begum, 2015, American journal of human genetics.

A genome-wide association study of cleft lip with and without cleft palate identifies risk variants near MAFB and ABCA 4

Hong Wang, Holger Schwender, Ingo Ruczinski, 2010 .

GOLD 2011 disease severity classification in COPDGene: a prospective cohort study.

Edwin K Silverman, Douglas Curran-Everett, Terri H Beaty, 2013, The Lancet. Respiratory medicine.

A genome-wide association study of cleft lip with and without cleft palate identifies risk variants near MAFB and ABCA4

Holger Schwender, Ingo Ruczinski, Jacqueline B Hetmanski, 2010, Nature Genetics.

Genetic Association and Risk Scores in a Chronic Obstructive Pulmonary Disease Meta‐analysis of 16,707 Subjects

Edwin K Silverman, Terri H Beaty, Michael H Cho, 2017, American journal of respiratory cell and molecular biology.

Genome-wide interaction studies reveal sex-specific asthma risk alleles.

Weiliang Qiu, Terri H Beaty, Vincent J Carey, 2014, Human molecular genetics.

Integrated genome-wide association, coexpression network, and expression single nucleotide polymorphism analysis identifies novel pathway in allergic rhinitis

Weiliang Qiu, Eric E Schadt, Blanca E Himes, 2014, BMC Medical Genomics.

Epidemiology, genetics, and subtyping of preserved ratio impaired spirometry (PRISm) in COPDGene

Edwin K Silverman, Douglas Curran-Everett, Terri H Beaty, 2014, Respiratory Research.

Association between IRF6 and nonsyndromic cleft lip with or without cleft palate in four populations

Jacqueline B Hetmanski, Alan F Scott, Terri H Beaty, 2007, Genetics in Medicine.

Evidence for gene‐environment interaction in a genome wide study of nonsyndromic cleft palate

Holger Schwender, Ingo Ruczinski, Jacqueline B Hetmanski, 2011, Genetic epidemiology.

Genome-wide association study identiﬁes peanut allergy-speciﬁc loci and evidence of epigenetic mediation in US children

Kari Christine Nadeau, Xin Xu, Terri H Beaty, 2022 .

Genome-wide association identifies regulatory Loci associated with distinct local histogram emphysema patterns.

Raúl San José Estépar, Edwin K Silverman, Terri H Beaty, 2014, American journal of respiratory and critical care medicine.

Exome Sequencing Analysis in Severe, Early-Onset Chronic Obstructive Pulmonary Disease.

Michael Bamshad, Christoph Lange, Edwin K Silverman, 2016, American journal of respiratory and critical care medicine.

Whole exome association of rare deletions in multiplex oral cleft families

Ingo Ruczinski, Alexandre Bureau, Hasan Albacha-Hejazi, 2017, Genetic epidemiology.

Erratum: A genome-wide association study of cleft lip with and without cleft palate identifies risk variants near MAFB and ABCA4

Holger Schwender, Alan F Scott, Jeffrey C Murray, 2010, Nature Genetics.

The FaceBase Consortium: a comprehensive program to facilitate craniofacial research.

Harry Hochheiser, Axel Visel, Jeffrey C Murray, 2011, Developmental biology.

Whole exome sequencing analysis in severe chronic obstructive pulmonary disease

Michael Bamshad, Ingo Ruczinski, Christoph Lange, 2018, Human molecular genetics.

Characterization of large structural genetic mosaicism in human autosomes.

William Wheeler, Nan Hu, Peter Kraft, 2015, American journal of human genetics.

Genome-wide association studies identify CHRNA5/3 and HTR4 in the development of airflow obstruction.

Edwin K Silverman, Vilmundur Gudnason, Thomas Lumley, 2012, American journal of respiratory and critical care medicine.

A genome-wide study of de novo deletions identifies a candidate locus for non-syndromic isolated cleft lip/palate risk

Holger Schwender, Ingo Ruczinski, Alan F Scott, 2014, BMC Genetics.

Detecting Familial Aggregation.

Terri H Beaty, Adam C Naj, 2017, Methods in molecular biology.

Comparison of SNP tagging methods using empirical data: association study of 713 SNPs on chromosome 12q14.3–12q24.21 for asthma and total serum IgE in an African Caribbean population

Alan F Scott, Terri H Beaty, Rasika A Mathias, 2006, Genetic epidemiology.

Risk loci for chronic obstructive pulmonary disease: a genome-wide association study and meta-analysis.

Christoph Lange, Manuel Mattheisen, Edwin K Silverman, 2014, The Lancet. Respiratory medicine.

CT-based Visual Classification of Emphysema: Association with Mortality in the COPDGene Study

Edwin K Silverman, Hans-Ulrich Kauczor, Douglas Curran-Everett, 2018, Radiology.

Genome-wide association study identifies peanut allergy-specific loci and evidence of epigenetic mediation in US children

Kari Christine Nadeau, Xin Xu, Terri H Beaty, 2015 .

Variants of DENND1B associated with asthma in children.

Ingo Ruczinski, James Flory, Terri H Beaty, 2010, The New England journal of medicine.

Whole‐Genome Sequencing in Severe Chronic Obstructive Pulmonary Disease

Christoph Lange, Edwin K Silverman, Terri H Beaty, 2018, American journal of respiratory cell and molecular biology.

A Genome-Wide Association Study of Emphysema and Airway Quantitative Imaging Phenotypes.

Raúl San José Estépar, Edwin K Silverman, Terri H Beaty, 2015, American journal of respiratory and critical care medicine.

A colorectal cancer prediction model using traditional and genetic risk scores in Koreans

Terri H Beaty, Sun Ha Jee, Daeyoun Won, 2015, BMC Genetics.

A graphical assessment of p-values from sliding window haplotype tests of association to identify asthma susceptibility loci on chromosome 11q

Terri H Beaty, Rasika A Mathias, Alexander F Wilson, 2006, BMC Genetics.

African Ancestry is a Risk Factor for Asthma and High Total IgE Levels in African Admixed Populations

Ingo Ruczinski, Rachel Lewis, Candelaria Vergara, 2013, Genetic epidemiology.

Analytic power and sample size calculation for the genotypic transmission/disequilibrium test in case‐parent trio studies

Holger Schwender, Ingo Ruczinski, Margaret A Taub, 2014, Biometrical journal. Biometrische Zeitschrift.

Genome-wide association analyses for lung function and chronic obstructive pulmonary disease identify new loci and potential druggable targets

Christian Gieger, Ingo Ruczinski, H Lester Kirchner, 2017, Nature Genetics.