Citation Impact
Citing Papers
Developmental trajectories in 22q11.2 deletion syndrome
2015
Genotypic Diversity Within a Natural Coastal Bacterioplankton Population
2005 Science
Loss of the Mismatch Repair Protein MSH6 in Human Glioblastomas Is Associated with Tumor Progression during Temozolomide Treatment
2007
Regulatory T cells in autoimmune kidney diseases and transplantation
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High throughput ANI analysis of 90K prokaryotic genomes reveals clear species boundaries
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Comprehensive genomic characterization defines human glioblastoma genes and core pathways
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Transcriptional and epigenetic basis of Treg cell development and function: its genetic anomalies or variations in autoimmune diseases
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Tregopathies: Monogenic diseases resulting in regulatory T-cell deficiency
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Rare-Variant Association Testing for Sequencing Data with the Sequence Kernel Association Test
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DNA Sequencing versus Standard Prenatal Aneuploidy Screening
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A stabilizing reagent prevents cell-free DNA contamination by cellular DNA in plasma during blood sample storage and shipping as determined by digital PCR
2013
Mechanisms of hepatic stellate cell activation
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Molecular mechanisms of epithelial–mesenchymal transition
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Circulating cell free DNA: Preanalytical considerations
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The plastic in microplastics: A review
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Possible Influence of Glutathione S -Transferase GSTT1 Null Genotype on Age of Onset of Sporadic Colorectal Adenocarcinoma
2003
Assessment of Fetal Sex Chromosome Aneuploidy Using Directed Cell-Free DNA Analysis
2013
Immunoglobulin Isotype Switching Is Inhibited and Somatic Hypermutation Perturbed in UNG-Deficient Mice
2002 StandoutNobel
Human MutY Homolog, a DNA Glycosylase Involved in Base Excision Repair, Physically and Functionally Interacts with Mismatch Repair Proteins Human MutS Homolog 2/Human MutS Homolog 6
2002
Noninvasive prenatal testing for fetal trisomies in a routinely screened first-trimester population
2012
22q11.21 Deletion Syndromes: A Review of Proximal, Central, and Distal Deletions and Their Associated Features
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Cell-free DNA Analysis for Noninvasive Examination of Trisomy
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The genetics of exceptional human longevity
2002
The science, policy and practice of nature-based solutions: An interdisciplinary perspective
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Identification ofCaenorhabditis elegansGenes Regulating Longevity Using Enhanced RNAi-sensitive Strains
2007 StandoutNobel
Cancer genes and the pathways they control
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Dangerous hitchhikers? Evidence for potentially pathogenic Vibrio spp. on microplastic particles
2016
Environmental exposure to microplastics: An overview on possible human health effects
2019 Standout
Mutation–selection networks of cancer initiation: tumor suppressor genes and chromosomal instability
2003
Noninvasive prenatal detection and selective analysis of cell-free DNA obtained from maternal blood: evaluation for trisomy 21 and trisomy 18
2012
The preterm parturition syndrome
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Gestational mutations and carcinogenesis
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Liquid biopsies come of age: towards implementation of circulating tumour DNA
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Review on nanoparticles and nanostructured materials: history, sources, toxicity and regulations
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FAST-SeqS: A Simple and Efficient Method for the Detection of Aneuploidy by Massively Parallel Sequencing
2012
A gene expression atlas of the central nervous system based on bacterial artificial chromosomes
2003 StandoutNature
Single-Nucleotide Polymorphism–Based Noninvasive Prenatal Screening in a High-Risk and Low-Risk Cohort
2014
Base excision repair in a network of defence and tolerance
2001
EMT: 2016
2016 Standout
Non-Invasive Chromosomal Evaluation (NICE) Study: results of a multicenter prospective cohort study for detection of fetal trisomy 21 and trisomy 18
2012
Maternal Plasma Cell-Free Fetal and Maternal DNA at 11-13 Weeks' Gestation: Relation to Fetal and Maternal Characteristics and Pregnancy Outcomes
2013
From prenatal genomic diagnosis to fetal personalized medicine: progress and challenges
2012
Occurrence, genotoxicity, and carcinogenicity of regulated and emerging disinfection by-products in drinking water: A review and roadmap for research
2007 Standout
Increased susceptibility of HIF-1α heterozygous-null mice to cardiovascular malformations associated with maternal diabetes
2013 StandoutNobel
Lectin Domains of Polypeptide GalNAc Transferases Exhibit Glycopeptide Binding Specificity
2011 StandoutNobel
The merging of community ecology and phylogenetic biology
2009 Standout
Cancer as an evolutionary and ecological process
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Down syndrome
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22q11.2 deletion syndrome
2015 Standout
Metapopulation structure of Vibrionaceae among coastal marine invertebrates
2010
GATA4 loss in the septum transversum mesenchyme promotes liver fibrosis in mice
2014
A strategy to discover genes that carry multi-allelic or mono-allelic risk for common diseases: A cohort allelic sums test (CAST)
2006
Tumour heterogeneity and resistance to cancer therapies
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Marine viruses — major players in the global ecosystem
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Performance of Streck cfDNA Blood Collection Tubes for Liquid Biopsy Testing
2016
GSTM1, GSTT1, GSTP1, GSTA1 and colorectal cancer risk: A comprehensive meta-analysis
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The cancer genome
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Quadruplex DNA: sequence, topology and structure
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Multistage carcinogenesis and the incidence of human cancer
2003
Down Syndrome
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SNP‐based non‐invasive prenatal testing detects sex chromosome aneuploidies with high accuracy
2013
Patterns and mechanisms of genetic and phenotypic differentiation in marine microbes
2006
Mismatch Repair Deficiency Does Not Mediate Clinical Resistance to Temozolomide in Malignant Glioma
2008 StandoutNobel
Transparent Reporting of a multivariable prediction model for Individual Prognosis Or Diagnosis (TRIPOD): Explanation and Elaboration
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Regulatory T Cells and Human Disease
2020 StandoutNobel
Rare copy number variations in congenital heart disease patients identify unique genes in left-right patterning
2011
Microdeletions/duplications involving TBX1 gene in fetuses with conotruncal heart defects which are negative for 22q11.2 deletion on fluorescence in‐situ hybridization
2013
Shifting the genomic gold standard for the prokaryotic species definition
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Endocardial and Epicardial Epithelial to Mesenchymal Transitions in Heart Development and Disease
2012
Advances in the Understanding of the Genetic Determinants of Congenital Heart Disease and Their Impact on Clinical Outcomes
2018
Hypoxia-Inducible Factor 1 and Cardiovascular Disease
2013 StandoutNobel
Induction of Transitional Cell Hyperplasia in the Urinary Bladder and Aberrant Crypt Foci in the Colon of Rats Treated with Individual and a Mixture of Drinking Water Disinfection By-Products
2003
AnFgf8mouse mutant phenocopies human 22q11 deletion syndrome
2002 StandoutNobel
Oxidative DNA damage: mechanisms, mutation, and disease
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Hypermutation in human cancer genomes: footprints and mechanisms
2014
Repair and Genetic Consequences of Endogenous DNA Base Damage in Mammalian Cells
2004 StandoutNobel
The significance of information frameworks in integrated risk assessment and management
2007
Genetic dissection of Down syndrome-associated congenital heart defects using a new mouse mapping panel
2016
Genetic and environmental risk factors in congenital heart disease functionally converge in protein networks driving heart development
2012
Analysis of cell‐free DNA in maternal blood in screening for fetal aneuploidies: updated meta‐analysis
2015
Insights into the Genome of Large Sulfur Bacteria Revealed by Analysis of Single Filaments
2007
Preterm labor: One syndrome, many causes
2014 StandoutScience
Plastic and Human Health: A Micro Issue?
2017 Standout
Formation of magnetite by bacteria and its application
2008
Clinical experience of noninvasive prenatal testing with cell‐free DNA for fetal trisomies 21, 18, and 13, in a general screening population
2013
Life in the “Plastisphere”: Microbial Communities on Plastic Marine Debris
2013 Standout
The Bacterial Species Challenge: Making Sense of Genetic and Ecological Diversity
2009 Science
Phylogenetic Ecology of the Freshwater Actinobacteria acI Lineage
2007
High‐resolution analysis of copy number variants in adults with simple‐to‐moderate congenital heart disease
2013
Microplastics as an emerging threat to terrestrial ecosystems
2017 Standout
Gestational age and maternal weight effects on fetal cell‐free DNA in maternal plasma
2013
Neurodevelopmental Outcomes in Children With Congenital Heart Disease: Evaluation and Management
2012 Standout
Noninvasive prenatal testing of fetal aneuploidies by massively parallel sequencing in a prospective Chinese population
2013
Screening Newborn Blood Spots for 22q11.2 Deletion Syndrome Using Multiplex Droplet Digital PCR
2014
Works of Aoy Tomita‐Mitchell being referenced
Mutation, cell kinetics, and subpopulations at risk for colon cancer in the United States
1998
Population risk and physiological rate parameters for colon cancer. The union of an explicit model for carcinogenesis with the public health records of the United States
2000
Scanning the β‐globin gene for mutations in large populations by denaturing capillary and gel electrophoresis
2005
Influence of Temperature during Transportation on Cell-Free DNA Analysis
2012
Detection and frequency estimation of rare variants in pools of genomic DNA from large populations using mutational spectrometry
2005
Mismatch repair deficient human cells: spontaneous and MNNG-induced mutational spectra in the HPRT gene
2000
GATA4 sequence variants in patients with congenital heart disease
2007
Non-Invasive Prenatal Detection of Trisomy 21 Using Tandem Single Nucleotide Polymorphisms
2010
Spectrum of heart disease associated with murine and human GATA4 mutation
2007
Single nucleotide polymorphism spectra in newborns and centenarians: identification of genes coding for rise of mortal disease1Published in conjunction with A Wisconsin Gathering Honouring Waclaw Szybalski on the occasion of his 75th year and 20 years of Editorship-in-Chief of Gene, 10–11 August 1997, University of Wisconsin, Madison, WI, USA.1
1998
Use of Combination Chemotherapy for Treatment of Granulomatous and Lymphocytic Interstitial Lung Disease (GLILD) in Patients with Common Variable Immunodeficiency (CVID)
2012
Diversity and Dynamics of a North Atlantic Coastal Vibrio Community
2004
The mutational spectrum of the HPRT gene from human T cells in vivo shares a significant concordant set of hot spots with MNNG-treated human cells.
2003
Selective analysis of cell‐free DNA in maternal blood for evaluation of fetal trisomy
2012
Multiplexed quantitative real-time PCR to detect 22q11.2 deletion in patients with congenital heart disease
2010
Impact of MYH6 variants in hypoplastic left heart syndrome
2016
Chromosomal Imbalances in Patients with Congenital Cardiac Defects: A Meta-analysis Reveals Novel Potential Critical Regions Involved in Heart Development
2014