Citation Impact
Citing Papers
2014 ESC Guidelines on diagnosis and management of hypertrophic cardiomyopathy
2014 Standout
Birth Outcomes Following West Nile Virus Infection of Pregnant Women in the United States: 2003-2004
2006
Comprehensive genomic characterization of head and neck squamous cell carcinomas
2015 StandoutNature
Association Between Pregnancy Intention and Reproductive-health Related Behaviors Before and After Pregnancy Recognition, National Birth Defects Prevention Study, 1997–2002
2009
Depression
2018 Standout
Reproductive hormone sensitivity and risk for depression across the female life cycle: a continuum of vulnerability?
2008
Acute kidney injury
2012 Standout
Growth Hormone Treatment of Non–Growth Hormone-Deficient Growth Disorders
2007
CHD7 Targets Active Gene Enhancer Elements to Modulate ES Cell-Specific Gene Expression
2010
Hepatocellular carcinoma
2018 Standout
Maternal fever during early pregnancy and the risk of oral clefts
2010
Cooperation between the transcription factors p63 and IRF6 is essential to prevent cleft palate in mice
2010
Epigenomic Annotation of Enhancers Predicts Transcriptional Regulators of Human Neural Crest
2012
Genomic distribution of CHD7 on chromatin tracks H3K4 methylation patterns
2009
Epithelial-Mesenchymal Transitions in Development and Disease
2009 Standout
Identification of microdeletions in candidate genes for cleft lip and/or palate
2009
Cloning of Rat Vitamin K-Dependent γ-Glutamyl Carboxylase and Developmentally Regulated Gene Expression in Postimplantation Embryos
1998
Molecular mechanisms of epithelial–mesenchymal transition
2014 Standout
Mutations in VKORC1 cause warfarin resistance and multiple coagulation factor deficiency type 2
2004 StandoutNature
Maternal Periconceptional Alcohol Consumption and Risk of Orofacial Clefts
2007
Childhood obesity: public-health crisis, common sense cure
2002 Standout
Multiplexed DNA Sequence Capture of Mitochondrial Genomes Using PCR Products
2010 StandoutNobel
Microdeletions within 22q11 associated with sporadic and familial DiGeorge syndrome
1991
Looking past the lump: genetic aspects of inguinal hernia in children
2009
Maternal and child undernutrition and overweight in low-income and middle-income countries
2013 Standout
A CGH study of 27 patients with CHARGE association
2002
Orofacial clefts in the National Birth Defects Prevention Study, 1997–2004
2009
Fibromuscular Dysplasia
2004 Standout
Super-Enhancers in the Control of Cell Identity and Disease
2013 Standout
Human piebaldism: relationship between phenotype and site of kit gene mutation
2010
Cleft lip and palate: understanding genetic and environmental influences
2011 Standout
Cleft lip and palate
2009 Standout
Association between prepregnancy body mass index and congenital heart defects
2009
CHARGE syndrome: an update
2007
Glypican-3: a novel serum and histochemical marker for hepatocellular carcinoma
2003
Hypertension and antihypertensive drugs in pregnancy and perinatal outcomes
2012
Myocarditis
2011 Standout
The genetics of isolated orofacial clefts: from genotypes to subphenotypes
2009
Language trees support the express-train sequence of Austronesian expansion
2000 Nature
A gene expression atlas of the central nervous system based on bacterial artificial chromosomes
2003 StandoutNature
Targeting the Raf-MEK-ERK mitogen-activated protein kinase cascade for the treatment of cancer
2007 Standout
Mutations in a new member of the chromodomain gene family cause CHARGE syndrome
2004 Standout
Depression in adolescence
2012 Standout
EMT: 2016
2016 Standout
Epigenetic variation during the adult lifespan: cross‐sectional and longitudinal data on monozygotic twin pairs
2012
Adolescent idiopathic scoliosis
2008 Standout
Single-Cell Transcriptomic Analysis of Primary and Metastatic Tumor Ecosystems in Head and Neck Cancer
2017 Standout
Maternal Smoking and Environmental Tobacco Smoke Exposure and the Risk of Orofacial Clefts
2007
The Human Obesity Gene Map: The 2001 Update
2002
Lupus nephritis: where are we now?
2010
Zika Virus and Birth Defects — Reviewing the Evidence for Causality
2016 Standout
The basics of epithelial-mesenchymal transition
2009 Standout
Vitamin K antagonists and pregnancy outcome
2006
The Hallmarks of Aging
2013 Standout
Maternal treatment with opioid analgesics and risk for birth defects
2011
Reconstructing Indian population history
2009 StandoutNature
22q11.2 deletion syndrome
2015 Standout
Spontaneous Dissection of the Carotid and Vertebral Arteries
2001 Standout
Moyamoya Disease and Moyamoya Syndrome
2009 Standout
Exclusion of PITX2 mutations as a major cause of CHARGE association
2002
Coarctation of the aorta: outcome of pregnancy
2001
Periconceptional Use of Opioids and the Risk of Neural Tube Defects
2013
Declines in Unintended Pregnancy in the United States, 2008–2011
2016 Standout
The PDGF-C regulatory region SNP rs28999109 decreases promoter transcriptional activity and is associated with CL/P
2008
Pre-eclampsia
2015 Standout
Principles of Cancer Therapy: Oncogene and Non-oncogene Addiction
2009 Standout
CHD7 cooperates with PBAF to control multipotent neural crest formation
2010 StandoutNature
Language-tree divergence times support the Anatolian theory of Indo-European origin
2003 StandoutNature
Epithelial-mesenchymal transitions: the importance of changing cell state in development and disease
2009
I787 provides signals for c-Kit receptor internalization and functionality that control mast cell survival and development
2010 StandoutNobel
Review: Problems associated with long-term treatment with selective serotonin reuptake inhibitors
2008
Origins and dispersals of Pacific peoples: Evidence from mtDNA phylogenies of the Pacific rat
2004
Radiocarbon and DNA evidence for a pre-Columbian introduction of Polynesian chickens to Chile
2007 Standout
Global Strategies to Reduce the Health Care Burden of Craniofacial Anomalies: Report of WHO Meetings on International Collaborative Research on Craniofacial Anomalies
2004
2011 ACCF/AHA Guideline for the Diagnosis and Treatment of Hypertrophic Cardiomyopathy
2011 Standout
Cardiovascular Malformations and Complications in Turner Syndrome
1998
MITOCHONDRIAL DNA AND HUMAN EVOLUTION
2005
Excavating Neandertal and Denisovan DNA from the genomes of Melanesian individuals
2016 StandoutScienceNobel
ACC/AHA 2008 Guidelines for the Management of Adults With Congenital Heart Disease: Executive Summary
2008 Standout
Language Phylogenies Reveal Expansion Pulses and Pauses in Pacific Settlement
2009 Science
CHARGE (Coloboma, Heart Defect, Atresia Choanae, Retarded Growth and Development, Genital Hypoplasia, Ear Anomalies/Deafness) Syndrome and Chromosome 22q11.2 Deletion Syndrome: A Comparison of Immunologic and Nonimmunologic Phenotypic Features
2009
CDC Guideline for Prescribing Opioids for Chronic Pain—United States, 2016
2016 Standout
Mapping the Origins and Expansion of the Indo-European Language Family
2012 StandoutScience
Cerebrovascular abnormalities in a population of children with neurofibromatosis type 1
2005
ACC/AHA 2006 Guidelines for the Management of Patients With Valvular Heart Disease
2006 Standout
Coexistence of fibromuscular dysplasia and cystic medial necrosis in a patient with Marfan's syndrome and bilateral carotid artery dissections.
1994
Mitochondrial DNA analysis reveals diverse histories of tribal populations from India
2003
Nf1 limits epicardial derivative expansion by regulating epithelial to mesenchymal transition and proliferation
2012
Development of heart valves requiresGata4expression in endothelial-derived cells
2006
2014 AHA/ACC/HRS Guideline for the Management of Patients With Atrial Fibrillation
2014 Standout
Conditional Deletion of Focal Adhesion Kinase Leads to Defects in Ventricular Septation and Outflow Tract Alignment
2007 StandoutNobel
Challenges Posed by Adults With Repaired Congenital Heart Disease
2001
Transcription factor genes Smad4 and Gata4 cooperatively regulate cardiac valve development
2011
CHARGE association in newborns: A registry-based study
1999
CHD7 Gene Polymorphisms Are Associated with Susceptibility to Idiopathic Scoliosis
2007
Competing Risks for Death and Cardiac Transplantation in Children With Dilated Cardiomyopathy
2011
Epithelial Plasticity: A Common Theme in Embryonic and Cancer Cells
2013 StandoutScience
Protein Glycoengineering Enabled by the Versatile Synthesis of Aminooxy Glycans and the Genetically Encoded Aldehyde Tag
2011 StandoutNobel
Progression of Aortic Dilatation and the Benefit of Long-Term β-Adrenergic Blockade in Marfan's Syndrome
1994
Diagnosing and Treating Depression During Pregnancy
2015
Losartan, an AT1 Antagonist, Prevents Aortic Aneurysm in a Mouse Model of Marfan Syndrome
2006 StandoutScience
Bantu expansion shows that habitat alters the route and pace of human dispersals
2015 Standout
Functions of Cell Surface Heparan Sulfate Proteoglycans
1999 Standout
2011 ACCF/AHA Guideline for the Diagnosis and Treatment of Hypertrophic Cardiomyopathy
2011
Works of Angela E. Lin being referenced
Adults with genetic syndromes and cardiovascular abnormalities: clinical history and management
2008
Five additional Costello syndrome patients with rhabdomyosarcoma: Proposal for a tumor screening protocol
2002
Clinical and molecular aspects of the Simpson-Golabi-Behmel syndrome
1998
Central nervous system malformations in the CHARGE association
1990
Seeking causes: Classifying and evaluating congenital heart defects in etiologic studies
2007
Guidelines for case classification for the national birth defects prevention study
2003
HRAS mutation analysis in Costello syndrome: Genotype and phenotype correlation
2005
Cardiovascular malformations and other cardiovascular abnormalities in neurofibromatosis 1
2000
Previously apparently undescribed syndrome: Shallow orbits, ptosis, coloboma, trigonocephaly, gyral malformations, and mental and growth retardation
1995
Maternal caffeine consumption and risk of cardiovascular malformations
2007
Interstitial and terminal deletions of the long arm of chromosome 4: Further delineation of phenotypes
1988
Toward a genetic etiology of CHARGE syndrome: I. A systematic scan for submicroscopic deletions
2003
TFAP2A Mutations Result in Branchio-Oculo-Facial Syndrome
2008
Further delineation of cardiac abnormalities in Costello syndrome
2002
Reviewing the evidence for mycophenolate mofetil as a new teratogen: Case report and review of the literature
2009
Spectrum of CHD7 Mutations in 110 Individuals with CHARGE Syndrome and Genotype-Phenotype Correlation
2006
Adults with Sotos syndrome: Review of 21 adults with molecularly confirmed NSD1 alterations, including a detailed case report of the oldest person
2011
Cardiovascular disease in neurofibromatosis 1: Report of the NF1 Cardiovascular Task Force
2002
Vitamin K deficiency embryopathy: A phenocopy of the warfarin embryopathy due to a disorder of embryonic vitamin K metabolism
1997
First-Trimester Use of Selective Serotonin-Reuptake Inhibitors and the Risk of Birth Defects
2008
The Pattern of Cardiovascular Malformation in the CHARGE Association
1987
Further Delineation of Aortic Dilation, Dissection, and Rupture in Patients With Turner Syndrome
1998
Upper limb malformations associated with congenital heart disease
1985
Clinical Approach to Genetic Cardiomyopathy in Children
1996
Congenital heart disease in supernumerary der(22), t(11;22) syndrome
1986
Genetic Disorders and Major Extracardiac Anomalies Associated With the Hypoplastic Left Heart Syndrome
1988
CHARGE Association: An Update and Review for the Primary Pediatrician
1998
Genetic aspects of atrioventricular septal defects
2000
First-Trimester Use of Selective Serotonin-Reuptake Inhibitors and the Risk of Birth Defects
2007
Diagnosis and management of infantile marfan syndrome.
1990
Aortic dilation, dissection, and rupture in patients with turner syndrome
1986