Standout Papers
Citation Impact
Citing Papers
Hypogonadotropic hypogonadism due to loss of function of the KiSS1-derived peptide receptor GPR54
2003 Standout
β-Catenin Controls Hair Follicle Morphogenesis and Stem Cell Differentiation in the Skin
2001 Standout
Pitx2promotes development of splanchnic mesoderm-derived branchiomeric muscle
2006
Chimerism of the Transplanted Heart
2002 Standout
Acromegaly
2006 Standout
Developmental neurotoxicity of industrial chemicals
2006 Standout
Pitx2, a Bicoid-Type Homeobox Gene, Is Involved in a Lefty-Signaling Pathway in Determination of Left-Right Asymmetry
1998
Cone-Rod Dystrophy Due to Mutations in a Novel Photoreceptor-Specific Homeobox Gene () Essential for Maintenance of the Photoreceptor
1997
Role of Transforming Growth Factor β in Human Disease
2000 Standout
Pitx2 determines left–right asymmetry of internal organs in vertebrates
1998 Nature
Role for ELOVL3 and Fatty Acid Chain Length in Development of Hair and Skin Function
2004 StandoutNobel
The dual role of thymidine phosphorylase in cancer development and chemotherapy
2009
Distribution, silencing potential and evolutionary impact of promoter DNA methylation in the human genome
2007 StandoutNobel
Axenfeld-Rieger syndrome resulting from mutation of the FKHL7 gene on chromosome 6p25
2000
Cushing's syndrome
2015 Standout
Retinopathy of prematurity
2013 Standout
High-Resolution Profiling of Histone Methylations in the Human Genome
2007 Standout
Pitx2 regulates lung asymmetry, cardiac positioning and pituitary and tooth morphogenesis
1999 Nature
Isolation of Endothelial Cells from Brain, Lung, and Kidney: Expression of the Multidrug Resistance P-Glycoprotein Isoforms
2001
A Bivalent Chromatin Structure Marks Key Developmental Genes in Embryonic Stem Cells
2006 Standout
Akt2-mediated phosphorylation of Pitx2 controls Ccnd1 mRNA decay during muscle cell differentiation
2009
The gene for achondroplasia maps to the telomeric region of chromosome 4p
1994
Tumor suppressor genes
1991 Standout
Crx, a Novel otx-like Homeobox Gene, Shows Photoreceptor-Specific Expression and Regulates Photoreceptor Differentiation
1997
Inflammation and insulin resistance
2006 Standout
A family of LIM domain-associated cofactors confer transcriptional synergism between LIM and Otx homeodomain proteins.
1997
Pitx2 promotes heart repair by activating the antioxidant response after cardiac injury
2016 Nature
Nobox is a homeobox-encoding gene preferentially expressed in primordial and growing oocytes
2002
Candidate genes for nonsyndromic cleft lip and palate and maternal cigarette smoking and alcohol consumption: Evaluation of genotype-environment interactions from a population-based case-control study of orofacial clefts
1999
Primary open-angle glaucoma
2004 Standout
The Transcription Factor Pitx2 Mediates Situs-Specific Morphogenesis in Response to Left-Right Asymmetric Signals
1998
PRDM16 controls a brown fat/skeletal muscle switch
2008 StandoutNature
Super-Enhancers in the Control of Cell Identity and Disease
2013 Standout
Association of MSX1 and TGFB3 with Nonsyndromic Clefting in Humans
1998
Cleft lip and palate
2009 Standout
The Mammalian Epigenome
2007 Standout
Sequential activation of transcription factors in lens induction
2000
Cig30 and Pitx3 Genes Are Arranged in a Partially Overlapping Tail-to-Tail Array Resulting in Complementary Transcripts
1999
Mutations in the p53 gene occur in diverse human tumour types
1989 StandoutNature
The forkhead transcription factor gene FKHL7 is responsible for glaucoma phenotypes which map to 6p25
1998
Apert syndrome results from localized mutations of FGFR2 and is allelic with Crouzon syndrome
1995 Standout
Nuclear exclusion of Smad2 is a mechanism leading to loss of competence
2002 StandoutNobel
A Review of the Microcirculation of Adipose Tissue: Anatomic, Metabolic, and Angiogenic Perspectives
1997
Differential Sensitivity of Children and Adults to Chemical Toxicity
2002
The pan-Pituitary Activator of Transcription, Ptx1 (Pituitary Homeobox 1), Acts in Synergy with SF-1 and Pit1 and Is an Upstream Regulator of the Lim-Homeodomain Gene Lim3/Lhx3
1998
Mutations in MTMR13, a New Pseudophosphatase Homologue of MTMR2 and Sbf1, in Two Families with an Autosomal Recessive Demyelinating Form of Charcot-Marie-Tooth Disease Associated with Early-Onset Glaucoma
2003
Human and murine PTX1/Ptx1 gene maps to the region for Treacher Collins Syndrome
1997
Active chromatin domains are defined by acetylation islands revealed by genome-wide mapping
2005
High-yield selection and extraction of two promoter-defined phenotypes of neural stem cells from the fetal human brain
2001 StandoutNobel
The immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome (IPEX) is caused by mutations of FOXP3
2001 StandoutNobel
A completely biological tissue-engineered human blood vessel
1998
Gene expression patterns of insulin-like growth factor 1, 2 (IGF-1, IGF-2) and insulin-like growth factor binding protein 3 (IGFBP-3) in human placenta from preterm deliveries: influence of additional factors
2011
Mutations in the human homologue of mouse dl cause autosomal recessive and dominant hypohidrotic ectodermal dysplasia
1999
Transcriptional control of precursor proliferation in the early phases of pituitary development
2004
Deletions and a translocation interrupt a cloned gene at the neurofibromatosis type 1 locus
1990 Standout
Mechanisms for pituitary tumorigenesis: the plastic pituitary
2003
p63 is essential for regenerative proliferation in limb, craniofacial and epithelial development
1999 StandoutNature
Protein Tyrosine Phosphatases in the Human Genome
2004 Standout
Cushing's syndrome
2006 Standout
The TNF and TNF Receptor Superfamilies
2001 Standout
Magnetic Nanoparticles: Synthesis, Protection, Functionalization, and Application
2007 Standout
Mutations of the Forkhead/Winged-Helix Gene, FKHL7, in Patients with Axenfeld-Rieger Anomaly
1998
Pitx2 Participates in the Late Phase of the Pathway Controlling Left-Right Asymmetry
1998
Myocilin Glaucoma
2002
Notch1 and Notch3 Instructively Restrict bFGF-Responsive Multipotent Neural Progenitor Cells to an Astroglial Fate
2001 StandoutNobel
Expression patterns of Brx1 (Rieg gene), Sonic hedgehog, Nkx2.2, Dlx1 and Arx during zona limitans intrathalamica and embryonic ventral lateral geniculate nuclear formation
1997
Angiopoietin/Tie2 Pathway Influences Smooth Muscle Hyperplasia in Idiopathic Pulmonary Hypertension
2006
Activity of the Caenorhabditis elegans UNC-86 POU transcription factor modulates olfactory sensitivity
2003 StandoutNobel
Use of magnetic techniques for the isolation of cells.
1999
Obesity and Cardiovascular Disease: Pathophysiology, Evaluation, and Effect of Weight Loss
2005 Standout
Molecular Basis of Combined Pituitary Hormone Deficiencies
2002
Gene Regulatory Networks and the Evolution of Animal Body Plans
2006 StandoutScience
Regulation of touch receptor differentiation by the Caenorhabditis elegans mec-3 and unc-86 genes
1998 StandoutNobel
Nurr1, an orphan nuclear receptor, is a transcriptional activator of endogenous tyrosine hydroxylase in neural progenitor cells derived from the adult brain
1999
Functional Arteries Grown in Vitro
1999 StandoutScience
Coordinated Transcriptional Regulation of theunc-25Glutamic Acid Decarboxylase and theunc-47GABA Vesicular Transporter by theCaenorhabditis elegansUNC-30 Homeodomain Protein
1999 StandoutNobel
Chromone: A Valid Scaffold in Medicinal Chemistry
2014 Standout
Genetics of Atrial Fibrillation
2010
Signalling interactions during facial development
1998
Biological Action of Leptin as an Angiogenic Factor
1998 StandoutScience
Functional tests of enhancer conservation between distantly related species
2003 StandoutNobel
TheC. elegansPOU-domain transcription factor UNC-86 regulates thetph-1tryptophan hydroxylase gene and neurite outgrowth in specific serotonergic neurons
2002 StandoutNobel
Conserved Function ofCaenorhabditis elegansUNC-30 and Mouse Pitx2 in Controlling GABAergic Neuron Differentiation
2001
The Molecular Pathogenesis of Corticotroph Tumors
1999
2014 AHA/ACC/HRS Guideline for the Management of Patients With Atrial Fibrillation
2014 Standout
Type 1 Neurofibromatosis Gene: Identification of a Large Transcript Disrupted in Three NF1 Patients
1990 StandoutScience
Endothelial Hypoxia-Inducible Factor-2α Is Required for the Maintenance of Airway Microvasculature
2019 StandoutNobel
Detection of bacteria in suspension by using a superconducting quantum interference device
2003 StandoutNobel
Reactive Oxygen Species (ROS)-Based Nanomedicine
2019 Standout
Mutations in mouse Aspm (abnormal spindle-like microcephaly associated) cause not only microcephaly but also major defects in the germline
2010 StandoutNobel
Ultrasensitive magnetic biosensor for homogeneous immunoassay
2000 StandoutNobel
Multipoint linkage analysis in neurofibromatosis type I: an international collaboration.
1989
Physical Mapping of a Translocation Breakpoint in Neurofibromatosis
1989 Science
Use of magnetic techniques for the isolation of cells
1999
The von Recklinghausen neurofibromatosis region on chromosome 17--genetic and physical maps come into focus.
1989
Diverse gap junctions modulate distinct mechanisms for fiber cell formation during lens development and cataractogenesis
2006 StandoutNobel
Works of J.C. Murray being referenced
Maternal and fetal variation in genes of cholesterol metabolism is associated with preterm delivery
2007
Cloning and characterization of a novel bicoid-related homeobox transcription factor gene, RIEG, involved in Rieger syndrome
1996 Standout
Platelet-derived endothelial cell growth factor expression and angiogenesis in cervical intraepithelial neoplasia and squamous cell carcinoma of the cervix
2000
Maternal alcohol use and risk of orofacial cleft birth defects
1996
Isolation and characterization of microvessel endothelial cells from human mammary adipose tissue
1993
Characterization of the human HOX 7 cDNA and identification of polymorphic markers
1992
Isolation of a New Homeobox Gene Belonging to the Pitx/Rieg Family: Expression During Lens Development and Mapping to the Aphakia Region on Mouse Chromosome 19
1997
Immunomagnetic purification of human microvessel endothelial cells using Dynabeads coated with monoclonal antibodies to PECAM-1.
1993
Linkage analysis of neurofibromatosis type I, using chromosome 17 DNA markers.
1989
Orofacial clefts, parental cigarette smoking, and transforming growth factor-alpha gene variants.
1996