Citation Impact
Citing Papers
Chromosome Abnormalities and Genetic Counseling
2011
Teratoma Formation by Human Embryonic Stem Cells Is Site Dependent and Enhanced by the Presence of Matrigel
2008
Coordinated but physically separable interaction with H3K27-demethylase and H3K4-methyltransferase activities are required for T-box protein-mediated activation of developmental gene expression
2008
Etiologic yield of subspecialists' evaluation of young children with global developmental delay
2000
Transcription factors in bone: developmental and pathological aspects
2002
Truncated CBP protein leads to classical Rubinstein-Taybi syndrome phenotypes in mice: implications for a dominant-negative mechanism
1999
T-box genes in human disorders
2003
Arthrogryposis multiplexa congenita: an epidemiologic study of nearly 9 million births in 24 EUROCAT registers
2011
Brain development in rodents and humans: Identifying benchmarks of maturation and vulnerability to injury across species
2013 Standout
The Human Obesity Gene Map: The 2005 Update
2006
Histone methylation: a dynamic mark in health, disease and inheritance
2012 Standout
Jmjd3 and UTX Play a Demethylase-Independent Role in Chromatin Remodeling to Regulate T-Box Family Member-Dependent Gene Expression
2010
22q11.21 Deletion Syndromes: A Review of Proximal, Central, and Distal Deletions and Their Associated Features
2015 Standout
Mutation analysis and molecular genetics of epidermolysis bullosa
1999
Biological roles of glycans
2016 Standout
Super-Enhancers in the Control of Cell Identity and Disease
2013 Standout
Cancer stem cells in solid tumours: accumulating evidence and unresolved questions
2008 Standout
Cleft lip and palate: understanding genetic and environmental influences
2011 Standout
Cleft lip and palate
2009 Standout
A myocardial lineage derives from Tbx18 epicardial cells
2008 StandoutNature
Autoimmune Channelopathies and Related Neurological Disorders
2006
Spontaneous spinal cerebrospinal fluid leaks and minor skeletal features of Marfan syndrome: a microfibrillopathy
2002
The pathobiology of mucositis
2004 Standout
Antibodies to Kv1 potassium channel-complex proteins leucine-rich, glioma inactivated 1 protein and contactin-associated protein-2 in limbic encephalitis, Morvan’s syndrome and acquired neuromyotonia
2010 Standout
6-Alkynyl fucose is a bioorthogonal analog for O-fucosylation of epidermal growth factor-like repeats and thrombospondin Type-1 repeats by protein O-fucosyltransferases 1 and 2
2012
Neuroligin-1 Deletion Results in Impaired Spatial Memory and Increased Repetitive Behavior
2010 StandoutNobel
Selective inhibition of NF-κB blocks osteoclastogenesis and prevents inflammatory bone destruction in vivo
2004 Standout
Stochastic State Transitions Give Rise to Phenotypic Equilibrium in Populations of Cancer Cells
2011 Standout
N-methyl-d-aspartate antibody encephalitis: temporal progression of clinical and paraclinical observations in a predominantly non-paraneoplastic disorder of both sexes
2010 Standout
Zebrafish as a Model Vertebrate for Investigating Chemical Toxicity
2005 Standout
Spontaneous Spinal Cerebrospinal Fluid Leaks and Intracranial Hypotension
2006 Standout
A duplicated gene in the breakpoint regions of the 7q11.23 Williams- Beuren syndrome deletion encodes the initiator binding protein TFII-I and BAP-135, a phosphorylation target of BTK
1998
The Human Obesity Gene Map: The 2003 Update
2004
Impact of Informing Overweight Individuals about the Role of Genetics in Obesity: An Online Experimental Study
2013 Standout
Chemical Lectinology: Tools for Probing the Ligands and Dynamics of Mammalian Lectins In Vivo
2015 StandoutNobel
Chromosomal Abnormalities in a Series of Children with Autistic Disorder
1999
Mechanisms of Bone Metastasis
2004 Standout
Health Supervision for Children With Down Syndrome
2011 Standout
Integrins
2002 Standout
What Have We Learned from Glycosyltransferase Knockouts in Mice?
2016
Genetics of Food Intake Self-Regulation in Childhood: Literature Review and Research Opportunities
2013 Standout
The Human Obesity Gene Map: The 2004 Update
2005
Myasthenia gravis: subgroup classification and therapeutic strategies
2015 Standout
Tbx3, a transcriptional factor, involves in proliferation and osteogenic differentiation of human adipose stromal cells
2006
HAT activity is essential for CBP‐1‐dependent transcription and differentiation in Caenorhabditis elegans
2002 StandoutNobel
Pathophysiology of Human Visceral Obesity: An Update
2013 Standout
Theheartstringsmutation in zebrafish causes heart/fin Tbx5 deficiency syndrome
2002
Obesity and Cardiovascular Disease: Pathophysiology, Evaluation, and Effect of Weight Loss
2005 Standout
The coregulator exchange in transcriptional functions of nuclear receptors
2000 Standout
The Genetic Basis of the Pierre Robin Sequence
2006
T-box genes coordinate regional rates of proliferation and regional specification during cardiogenesis
2005
Anisomastia Associated with Interstitial Duplication of Chromosome 16, Mental Retardation, Obesity, Dysmorphic Facies, and Digital Anomalies: Molecular Mapping of a New Syndrome by Fluorescent in Situ Hybridization and Microsatellites to 16q13 (D16S419-D16S503)*
2000
Making Sense of the Epithelial Barrier: What Molecular Biology and Genetics Tell Us About the Functions of Oral Mucosal and Epidermal Tissues
2002
Differentiation of Effector CD4 T Cell Populations
2010 Standout
Chemical Glycoproteomics
2016 StandoutNobel
TBX3 Is Overexpressed in Breast Cancer and Represses p14ARF by Interacting with Histone Deacetylases
2008
Works of Robert Wallerstein being referenced
Fetal arthrogryposis and maternal serum antibodies
2006
The Spectrum of Mutations in TBX3: Genotype/Phenotype Relationship in Ulnar-Mammary Syndrome
1999
18q‐ Chromosomal Abnormality in a Phenotypically Normal 21/2‐year‐Old Male with Autism
1992
Outcome of prenatally diagnosed trisomy 6 mosaicism
2002
Novel ITGB4 Mutations in Lethal and Nonlethal Variants of Epidermolysis Bullosa with Pyloric Atresia: Missense versus Nonsense
1998
Mutation analysis of B3GALTL in Peters Plus syndrome
2008
Factors in decision making following genetic counseling for pre‐natal diagnosis of de novo chromosomal rearrangements
2006
Partial Trisomy 11q in a Female Infant with Robin Sequence and Congenital Heart Disease
1992
Submicroscopic deletions at 16p13.3 in Rubinstein-Taybi syndrome: frequency and clinical manifestations in a North American population.
1997
Lateral meningocele syndrome: Three new patients and review of the literature
1997
Long term follow‐up of developmental delay in a child with prenatally‐diagnosed trisomy 20 mosaicism
2005
Are Referrals to Developmental Pediatricians Appropriate?
1994