Citation Impact
Citing Papers
2010 ACCF/AHA/AATS/ACR/ASA/SCA/SCAI/SIR/STS/SVM Guidelines for the Diagnosis and Management of Patients With Thoracic Aortic Disease
2010 Standout
Triggering a Cell Shape Change by Exploiting Preexisting Actomyosin Contractions
2012 StandoutScienceNobel
The 22q11.2 Deletion Syndrome
2001
Epidemiology and causes of preterm birth
2008 Standout
Adults with genetic syndromes and cardiovascular abnormalities: clinical history and management
2008
A core gut microbiome in obese and lean twins
2008 StandoutNature
Global Cancer Statistics 2020: GLOBOCAN Estimates of Incidence and Mortality Worldwide for 36 Cancers in 185 Countries
2021 Standout
Expanding the scope of noninvasive prenatal testing: detection of fetal microdeletion syndromes
2014
Maternal Periodontitis and Prematurity. Part I: Obstetric Outcome of Prematurity and Growth Restriction
2001
Genetic contributions to preterm birth: Implications from epidemiological and genetic association studies
2008
Genetic and Environmental Factors in Relative Body Weight and Human Adiposity
1997
Evaluation of Two Putative Susceptibility Loci for Oral Clefts in the Danish Population
2001
A Randomized Trial of Prenatal versus Postnatal Repair of Myelomeningocele
2011 Standout
Prevalence of Obesity and Trends in the Distribution of Body Mass Index Among US Adults, 1999-2010
2012 Standout
National, regional, and worldwide estimates of preterm birth rates in the year 2010 with time trends since 1990 for selected countries: a systematic analysis and implications
2012 Standout
MSX1 mutation is associated with orofacial clefting and tooth agenesis in humans
2000
Role of Transforming Growth Factor β in Human Disease
2000 Standout
Influence of Metabolism on Epigenetics and Disease
2013 StandoutNobel
The genetics of folate metabolism and maternal risk of birth of a child with Down syndrome and associated congenital heart defects
2015
A polymorphism in the promoter region of TNF and bacterial vaginosis: preliminary evidence of gene-environment interaction in the etiology of spontaneous preterm birth
2004
Prevalence of Obesity and Trends in Body Mass Index Among US Children and Adolescents, 1999-2010
2012 Standout
Childhood obesity: public-health crisis, common sense cure
2002 Standout
Toward understanding the genetic basis of neural tube defects
2007
Identification of SATB2 as the cleft palate gene on 2q32-q33
2003
Application of transmission disequilibrium tests to nonsyndromic oral clefts: Including candidate genes and environmental exposures in the models
1997
Oral Clefts, Transforming Growth Factor Alpha Gene Variants, and Maternal Smoking: A Population-based Case-Control Study in Denmark, 1991-1994
1999
Neural-Tube Defects
1999 Standout
Chromosome 22q11.2 Deletion Syndrome (DiGeorge Syndrome/Velocardiofacial Syndrome)
2010
Association between the Transforming Growth Factor Alpha Gene and Nonsyndromic Oral Clefts: A HuGE Review
2006
Changes in the distribution of body mass index of adults and children in the US population
2000
The use of high‐dimensional biology (genomics, transcriptomics, proteomics, and metabolomics) to understand the preterm parturition syndrome
2006
Making or Breaking the Heart: From Lineage Determination to Morphogenesis
2006
Low maternal alcohol consumption during pregnancy and oral clefts in offspring: The Slone birth defects study
2003
Evidence for linkage of nonsyndromic cleft lip with or without cleft palate to a region on chromosome 2
2003
Mutation of PVRL1 is associated with sporadic, non-syndromic cleft lip/palate in northern Venezuela
2001
Association of MSX1 and TGFB3 with Nonsyndromic Clefting in Humans
1998
Spontaneous preterm birth, a clinical dilemma: Etiologic, pathophysiologic and genetic heterogeneities and racial disparity
2008
Impact of DEL22q11, trisomy 21, and other genetic syndromes on surgical outcome of conotruncal heart defects
2009
Prevalence and clinical manifestations of 22q11.2 microdeletion in adults with selected conotruncal anomalies
2005
Cleft lip and palate: understanding genetic and environmental influences
2011 Standout
22q11.2 Deletion syndrome is associated with increased perioperative events and more complicated postoperative course in infants undergoing infant operative correction of truncus arteriosus communis or interrupted aortic arch
2014
Cleft lip and palate
2009 Standout
A myocardial lineage derives from Tbx18 epicardial cells
2008 StandoutNature
Prenatal diagnosis of the 22q11.2 deletion syndrome
2001
Sulfur containing amino acids and human disease
2003
Deletion of chromosome 22q11.2 and outcome in patients with pulmonary atresia and ventricular septal defect
2003
The PRISMA statement for reporting systematic reviews and meta-analyses of studies that evaluate health care interventions: explanation and elaboration
2009 Standout
Extracardiac features predicting 22q11.2 Deletion Syndrome in adult congenital heart disease
2008
Nrk, an X-linked Protein Kinase in the Germinal Center Kinase Family, Is Required for Placental Development and Fetoplacental Induction of Labor
2011 StandoutNobel
Long term behavioural outcome after neonatal arterial switch operation for transposition of the great arteries
2002
Prenatal diagnosis of interruption of the aortic arch and its association with deletion of chromosome 22q11
2002
NEOPLASTIC DISEASE AND DELETION 22q11.2: A MULTICENTRIC STUDY AND REPORT OF TWO CASES
2003
Folate intake, markers of folate status and oral clefts: is the evidence converging?
2008
22q11 deletions in fetuses with malformations of the outflow tracts or interruption of the aortic arch: impact of additional ultrasound signs
2003
A gene expression atlas of the central nervous system based on bacterial artificial chromosomes
2003 StandoutNature
Genetic variation associated with preterm birth: A HuGE review
2005
Familial risk of oral clefts by morphological type and severity: population based cohort study of first degree relatives
2008
Polymorphisms in 1-Carbon Metabolism, Epigenetics and Folate-Related Pathologies
2011
The clinical, immunological, and molecular spectrum of chromosome 22q11.2 deletion syndrome and DiGeorge syndrome
2004
An obesity-associated gut microbiome with increased capacity for energy harvest
2006 StandoutNature
Molecular and Genetic Aspects of DiGeorge/Velocardiofacial Syndrome
2006
A review of airborne polycyclic aromatic hydrocarbons (PAHs) and their human health effects
2013 Standout
Transforming growth factor α locus and nonsyndromic cleft lip with or without cleft palate: A reappraisal
1997
Tetralogy of Fallot associated with chromosome 22q11.2 deletion in adolescents and young adults
2001
Maternal Smoking and Environmental Tobacco Smoke Exposure and the Risk of Orofacial Clefts
2007
Direct Reprogramming of Fibroblasts into Functional Cardiomyocytes by Defined Factors
2010 Standout
Complex Congenital Heart Disease in Unaffected Relatives of Adults With 22q11.2 Deletion Syndrome
2011
22q11.2 Deletion syndrome is associated with perioperative outcome in tetralogy of Fallot
2013
Periodontal diseases
2005 Standout
Down's syndrome
2003 Standout
Absent or hypoplastic thymus on ultrasound: a marker for deletion 22q11.2 in fetal cardiac defects
2002
Prevalence and Trends in Obesity Among US Adults, 1999-2000
2002 Standout
The Enigma of Spontaneous Preterm Birth
2010
Lectin Domains of Polypeptide GalNAc Transferases Exhibit Glycopeptide Binding Specificity
2011 StandoutNobel
The PRISMA statement for reporting systematic reviews and meta-analyses of studies that evaluate healthcare interventions: explanation and elaboration
2009 Standout
Cardiac defects and results of cardiac surgery in 22q11.2 deletion syndrome
2008
22q11.2 deletion syndrome
2015 Standout
Interaction between the ADH1C polymorphism and maternal alcohol intake in the risk of nonsyndromic oral clefts: An evaluation of the contribution of child and maternal genotypes
2004
Interactions between endothelial nitric oxide synthase and sex hormones in vascular protection in mice
2002 StandoutNobel
Identification of susceptibility loci for nonsyndromic cleft lip with or without cleft palate in a two stage genome scan of affected sib-pairs
2000
Genetic polymorphisms in methylenetetrahydrofolate reductase and methionine synthase, folate levels in red blood cells, and risk of neural tube defects
1999
Oral clefts and life style factors — A case-cohort study based on prospective Danish data
2007
Sec24b selectively sorts Vangl2 to regulate planar cell polarity during neural tube closure
2009 StandoutNobel
Genetics and development of neural tube defects
2009
Molecular Basis for G Protein Control of the Prokaryotic ATP Sulfurylase
2006 StandoutNobel
The PRISMA Statement for Reporting Systematic Reviews and Meta-Analyses of Studies That Evaluate Health Care Interventions: Explanation and Elaboration
2009 Standout
Folic acid–containing supplement consumption during pregnancy and risk for oral clefts: A meta‐analysis
2006
Quadruplex DNA: sequence, topology and structure
2006 Standout
Folate and Clefts of the Lip and Palate—A U.K.-Based Case-Control Study: Part I: Dietary and Supplemental Folate
2008
Outdoor air pollution and cancer: An overview of the current evidence and public health recommendations
2020
Down Syndrome
2020 Standout
2018 AHA/ACC Guideline for the Management of Adults With Congenital Heart Disease: A Report of the American College of Cardiology/American Heart Association Task Force on Clinical Practice Guidelines
2018
Cardiovascular Anomalies in Patients Diagnosed With a Chromosome 22q11 Deletion Beyond 6 Months of Age
2001
Genetic Assembly of the Heart: Implications for Congenital Heart Disease
2001
A Population-Based Study of the 22q11.2 Deletion: Phenotype, Incidence, and Contribution to Major Birth Defects in the Population
2003
Graphene Oxide: Preparation, Functionalization, and Electrochemical Applications
2012 Standout
Synthesis of Light-Emitting Conjugated Polymers for Applications in Electroluminescent Devices
2009 Standout
Host-Bacterial Mutualism in the Human Intestine
2005 StandoutScience
Directed and Systematic Differentiation of Cardiovascular Cells From Mouse Induced Pluripotent Stem Cells
2008 StandoutNobel
Rare copy number variations in congenital heart disease patients identify unique genes in left-right patterning
2011
22q11.2 Deletion Status and Disease Burden in Children and Adolescents With Tetralogy of Fallot
2015
Targeted disruption of semaphorin 3C leads to persistent truncus arteriosus and aortic arch interruption
2001
Interactions between endothelial nitric oxide synthase and sex hormones in vascular protection in mice
2002 StandoutNobel
Missense Mutations and Gene Interruption in PROSIT240 , a Novel TRAP240 -Like Gene, in Patients With Congenital Heart Defect (Transposition of the Great Arteries)
2003
Analysis of Cardiovascular Phenotype and Genotype-Phenotype Correlation in Individuals With a JAG1 Mutation and/or Alagille Syndrome
2002
ACC/AHA 2008 Guidelines for the Management of Adults With Congenital Heart Disease: Executive Summary
2008 Standout
AnFgf8mouse mutant phenocopies human 22q11 deletion syndrome
2002 StandoutNobel
Electrochemiluminescence (ECL)
2004 Standout
Multiplexed quantitative real-time PCR to detect 22q11.2 deletion in patients with congenital heart disease
2010
2020 ACC/AHA Guideline for the Management of Patients With Valvular Heart Disease: A Report of the American College of Cardiology/American Heart Association Joint Committee on Clinical Practice Guidelines
2020 Standout
Conditional Deletion of Focal Adhesion Kinase Leads to Defects in Ventricular Septation and Outflow Tract Alignment
2007 StandoutNobel
ECL—Electrochemical luminescence
2007
Superoxide Ion: Generation and Chemical Implications
2016 Standout
The PRISMA Statement for Reporting Systematic Reviews and Meta-Analyses of Studies That Evaluate Health Care Interventions: Explanation and Elaboration
2009 Standout
Electrogenerated Chemiluminescence and Its Biorelated Applications
2008 Standout
Preterm labor: One syndrome, many causes
2014 StandoutScience
Telephone follow-up, initiated by a hospital-based health professional, for postdischarge problems in patients discharged from hospital to home
2006
Lethal mitochondrial cardiomyopathy in a hypomorphic Med30 mouse mutant is ameliorated by ketogenic diet
2011 StandoutNobel
Perioperative Risk Factors in Patients with 22q11.2 Deletion Syndrome Requiring Surgery for Velopharyngeal Dysfunction
2014
Natural Androgens Inhibit Male Atherosclerosis
1999
Works of Laura E. Mitchell being referenced
Epidemiology of Ebstein anomaly: Prevalence and patterns in Texas, 1999–2005
2011
Retinoic Acid Receptor Alpha Gene Variants, Multivitamin Use, and Liver Intake as Risk Factors for Oral Clefts: A Population-based Case-Control Study in Denmark, 1991-1994
2003
An intervention to increase use and effectiveness of self-care measures for breast cancer chemotherapy patients
1999
Development and application of a quantitative, specific assay for Cryptosporidium parvum oocyst detection in high-turbidity environmental water samples.
2001
Cumulative ligand activity of NODAL mutations and modifiers are linked to human heart defects and holoprosencephaly
2009
Spina bifida
2004
Frequency of 22q11 deletions in patients with conotruncal defects
1998
Correlates of genetic risk for non‐syndromic cleft lip with or without cleft palate
1993
Assessment of adiposity in an Indian population: Familial correlations
1993
22q11.2 Deletions in Patients with Conotruncal Defects: Data from 1,610 Consecutive Cases
2013
Genetic influences on premature parturition in an Australian twin sample
2000
Epidemiology of neural tube defects
2005
Maternal Genetic Effects, Exerted by Genes Involved in Homocysteine Remethylation, Influence the Risk of Spina Bifida
2002
Relationship between case-control studies and the transmission/disequilibrium test
2000
The Reduced Folate Carrier (SLC19A1) c.80G>A Polymorphism is Associated with Red Cell Folate Concentrations Among Women
2009
Evaluation of potential modifiers of the cardiac phenotype in the 22q11.2 deletion syndrome
2008
Genetic Epidemiology of Birth Defects: Nonsyndromic Cleft Lip and Neural Tube Defects
1997
Mode of inheritance of nonsyndromic cleft lip with or without cleft palate: a reanalysis.
1992
Evaluation of Potential Modifiers of the Palatal Phenotype in the 22q11.2 Deletion Syndrome
2006
Traffic‐related air pollution and the incidence of childhood central nervous system tumors: Texas, 2001–2009
2015
Familial recurrence-pattern analysis of nonsyndromic isolated cleft palate--a Danish Registry study.
1996
Genetic effects on variation in red-blood-cell folate in adults: implications for the familial aggregation of neural tube defects.
1997
Guidelines for the Design and Analysis of Studies on Nonsyndromic Cleft Lip and Cleft Palate in Humans: Summary Report From a Workshop of the International Consortium for Oral Clefts Genetics
2002
Evaluation of Potential Modifiers of the Palatal Phenotype in the 22q11.2 Deletion Syndrome
2006
Evidence for an association between nonsyndromic cleft lip with or without cleft palate and a gene located on the long arm of chromosome 4.
1995
Maternal Occupational Exposure to Polycyclic Aromatic Hydrocarbons: Effects on Gastroschisis among Offspring in the National Birth Defects Prevention Study
2012
Evidence for an association between dehydroepiandrosterone sulfate and nonfatal, premature myocardial infarction in males.
1994
Commingling analysis of adiposity in an Indian population.
1994