Citation Impact
Citing Papers
Human Hypertension Caused by Mutations in WNK Kinases
2001 StandoutScience
The human olfactory receptor gene family
2004 StandoutNobel
Structures of the calcium-activated, non-selective cation channel TRPM4
2017 Nature
lincRNAs: Genomics, Evolution, and Mechanisms
2013 Standout
Structure of a mammalian ryanodine receptor
2014 StandoutNatureNobel
Multipotent Embryonic Isl1+ Progenitor Cells Lead to Cardiac, Smooth Muscle, and Endothelial Cell Diversification
2006
Notch signaling and inherited disease syndromes
2003
Ryanodine receptors and ventricular arrhythmias: Emerging trends in mutations, mechanisms and therapies
2006
Discoveries in structure and physiology of mechanically activated ion channels
2020 StandoutNatureNobel
Genetic Control of Heart Function and Aging in Drosophila
2007
A High-Resolution STS, EST, and Gene-Based Physical Map of the Hereditary Paraganglioma Region on Chromosome 11q23
1997
MALAT-1, a novel noncoding RNA, and thymosin β4 predict metastasis and survival in early-stage non-small cell lung cancer
2003 Standout
Voltage-Gated Sodium Channels: Mutations, Channelopathies and Targets
2011
A Murine Model of Holt-Oram Syndrome Defines Roles of the T-Box Transcription Factor Tbx5 in Cardiogenesis and Disease
2001
hERG potassium channels and cardiac arrhythmia
2006 Nature
Mutations in VKORC1 cause warfarin resistance and multiple coagulation factor deficiency type 2
2004 StandoutNature
Early cardiac hypertrophy in mice with impaired calmodulin regulation of cardiac muscle Ca2+ release channel
2007 StandoutNobel
DNA sequence of the translocation breakpoints in undifferentiated embryonal sarcoma arising in mesenchymal hamartoma of the liver harboring the t(11;19)(q11;q13.4) translocation
2007
Regulation of the cardiac voltage‐gated Na+ channel (H1) by the ubiquitin‐protein ligase Nedd4
2000
Ostia, the inflow tracts of the Drosophila heart, develop from a genetically distinct subset of cardial cells
2001
Identification of Cd36 (Fat) as an insulin-resistance gene causing defective fatty acid and glucose metabolism in hypertensive rats
1999
Development
2000
Functional Classification and Experimental Dissection of Long Noncoding RNAs
2018 Standout
Adult Cardiac Stem Cells Are Multipotent and Support Myocardial Regeneration
2003 Standout
Molecular basis of the Cd36 chromosomal deletion underlying SHR defects in insulin action and fatty acid metabolism
2002
Mouse models of SCN5A-related cardiac arrhythmias
2008
Immunogenicity of induced pluripotent stem cells
2011 StandoutNature
Making or Breaking the Heart: From Lineage Determination to Morphogenesis
2006
Super-Enhancers in the Control of Cell Identity and Disease
2013 Standout
Genetic Susceptibility for Human Familial Essential Hypertension in a Region of Homology with Blood Pressure Linkage on Rat Chromosome 10
1997 StandoutNobel
A genetic blueprint for cardiac development
2000 Nature
Chromosomes, 11q and cancer: a review
1999
Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias
1996
Repositioning the hereditary paraganglioma critical region on chromosome band 11q23
1999
A myocardial lineage derives from Tbx18 epicardial cells
2008 StandoutNature
CD36 is a sensor of diacylglycerides
2005 StandoutNatureNobel
An early Cenozoic perspective on greenhouse warming and carbon-cycle dynamics
2008 StandoutNature
Roles of JUMONJI in mouse embryonic development
2004
Genomic assignment of the warfarin resistance locus, Rw, in the rat
1999
EMT: 2016
2016 Standout
Hypoxia-inducible Factor (HIF) Asparagine Hydroxylase Is Identical to Factor Inhibiting HIF (FIH) and Is Related to the Cupin Structural Family
2002 StandoutNobel
Chromosome aberrations in B-cell chronic lymphocytic leukemia: reassessment based on molecular cytogenetic analysis
1999
A constitutively open potassium channel formed by KCNQ1 and KCNE3
2000 StandoutNature
Gata5 is required for the development of the heart and endoderm in zebrafish
1999
FKBP12.6 Deficiency and Defective Calcium Release Channel (Ryanodine Receptor) Function Linked to Exercise-Induced Sudden Cardiac Death
2003
Tbx5 associates with Nkx2-5 and synergistically promotes cardiomyocyte differentiation
2001
Genomic Aberrations and Survival in Chronic Lymphocytic Leukemia
2000 Standout
A novel mutation in the potassium channel gene KVLQT1 causes the Jervell and Lange-Nielsen cardioauditory syndrome
1997
GATA4 mutations cause human congenital heart defects and reveal an interaction with TBX5
2003 StandoutNature
Patterns of recurrence of congenital heart disease
2003
Asparagine and Aspartate Hydroxylation of the Cytoskeletal Ankyrin Family Is Catalyzed by Factor-inhibiting Hypoxia-inducible Factor
2010 StandoutNobel
Atherosclerosis
2000 StandoutNature
The Canonical Notch Signaling Pathway: Unfolding the Activation Mechanism
2009 Standout
Converging Pathways and Principles in Heart Development and Disease
2002
Increased susceptibility of HIF-1α heterozygous-null mice to cardiovascular malformations associated with maternal diabetes
2013 StandoutNobel
Intracardiac fluid forces are an essential epigenetic factor for embryonic cardiogenesis
2003 StandoutNature
Pathophysiological Mechanisms of Dominant and Recessive KvLQT1 K+ Channel Mutations Found in Inherited Cardiac Arrhythmias
1997
Organization and Evolution of Olfactory Receptor Genes on Human Chromosome 11
1998
Specific Role of the Truncated βIV-Spectrin Σ6 in Sodium Channel Clustering at Axon Initial Segments and Nodes of Ranvier
2006 StandoutNobel
Ataxia-Telangiectasia:Closer to Unraveling the Mystery
1995
The Polycomb complex PRC2 and its mark in life
2011 StandoutNature
Genetics of heart development
2000
A decade of discoveries in cardiac biology
2004
Master Transcription Factors and Mediator Establish Super-Enhancers at Key Cell Identity Genes
2013 Standout
Slowed conduction and ventricular tachycardia after targeted disruption of the cardiac sodium channel gene Scn5a
2002
Fibrosis, not cell size, delineates β-myosin heavy chain reexpression during cardiac hypertrophy and normal aging in vivo
2006 StandoutNobel
The kinase Grk2 regulates Nedd4/Nedd4-2-dependent control of epithelial Na + channels
2004 StandoutNobel
HIF-1α is required for development of the sympathetic nervous system
2019 StandoutNobel
Directed and Systematic Differentiation of Cardiovascular Cells From Mouse Induced Pluripotent Stem Cells
2008 StandoutNobel
Crystallographic insights into sodium-channel modulation by the β4 subunit
2013
Nonimmunoglobulin target loci of activation-induced cytidine deaminase (AID) share unique features with immunoglobulin genes
2012 StandoutNobel
Beyond methane: Towards a theory for the Paleocene–Eocene Thermal Maximum
2006
ACC/AHA 2008 Guidelines for the Management of Adults With Congenital Heart Disease
2008 Standout
Genomic circuits and the integrative biology of cardiac diseases
2000 Nature
Evidence for Linkage Between Essential Hypertension and a Putative Locus on Human Chromosome 17
1999
Extreme hydrops fetalis and cardiovascular abnormalities in mice lacking a functional Adrenomedullin gene
2001 StandoutNobel
Cardiac hypertrophy and sudden death in mice with a genetically clamped renin transgene
2004 StandoutNobel
The Evolution of Dinosaurs
1999 StandoutScience
Functional mapping of disease susceptibility loci using cell biology
2006 StandoutNobel
Brugada Syndrome: Report of the Second Consensus Conference
2005 Standout
ACC/AHA 2008 Guidelines for the Management of Adults With Congenital Heart Disease: Executive Summary
2008 Standout
Recent Stem Cell Advances: Induced Pluripotent Stem Cells for Disease Modeling and Stem Cell–Based Regeneration
2010 StandoutNobel
Tbx20 dose-dependently regulates transcription factor networks required for mouse heart and motoneuron development
2005
Mechanically activated piezo channels modulate outflow tract valve development through the Yap1 and Klf2-Notch signaling axis
2019
Spectrum of Mutations in Long-QT Syndrome Genes
2000
Jumonji, a Nuclear Protein That Is Necessary for Normal Heart Development
2000
Extensive 200-Million-Year-Old Continental Flood Basalts of the Central Atlantic Magmatic Province
1999 Science
Arabidopsis Transcription Factors: Genome-Wide Comparative Analysis Among Eukaryotes
2000 StandoutScience
Pharmacology of the Na v 1.1 domain IV voltage sensor reveals coupling between inactivation gating processes
2017 StandoutNobel
Transcription factor genes Smad4 and Gata4 cooperatively regulate cardiac valve development
2011
Genomic analysis of orthologous mouse and human olfactory receptor loci
2001 StandoutNobel
T-box genes coordinate regional rates of proliferation and regional specification during cardiogenesis
2005
Transcriptional Regulatory Elements in the Human Genome
2006
11q Deletions Identify a New Subset of B-Cell Chronic Lymphocytic Leukemia Characterized by Extensive Nodal Involvement and Inferior Prognosis
1997
Cloning of an Alpha-TFEB fusion in renal tumors harboring the t(6;11)(p21;q13) chromosome translocation
2003
Building the heart piece by piece: modularity of cis-elements regulating Nkx2-5 transcription
1999
Mutations in SDHD , a Mitochondrial Complex II Gene, in Hereditary Paraganglioma
2000 StandoutScience
Islet1 cardiovascular progenitors: a single source for heart lineages?
2007
Structural insights into TRPM8 inhibition and desensitization
2019 StandoutScienceNobel
GATA4 haploinsufficiency in patients with interstitial deletion of chromosome region 8p23.1 and congenital heart disease
1999
Hypermorphic mutation of the voltage-gated sodium channel encoding gene Scn10a causes a dramatic stimulus-dependent neurobehavioral phenotype
2011 StandoutNobel
Conservation of sequence and structure flanking the mouse and human β-globin loci: The β-globin genes are embedded within an array of odorant receptor genes
1999 StandoutNobel
Spectrin and Ankyrin-Based Pathways: Metazoan Inventions for Integrating Cells Into Tissues
2001
Fine mapping of an imprinted gene for familial nonchromaffin paragangliomas, on chromosome 11q23.
1997
Mouse Model of SCN5A -Linked Hereditary Lenegre’s Disease
2005
ATP-sensitive potassium channel (K ATP )–dependent regulation of cardiotropic viral infections
2011 StandoutNobel
Works of Jean‐Jacques Schott being referenced
TRPM4 non-selective cation channel variants in long QT syndrome
2017
Familial Deafness, Congenital Heart Defects, and Posterior Embryotoxon Caused by Cysteine Substitution in the First Epidermal-Growth-Factor–Like Domain of Jagged 1
2002
Unusual clinical presentation in a family with catecholaminergic polymorphic ventricular tachycardia due to a G14876A ryanodine receptor gene mutation
2005
A genetic linkage map of the rat derived from recombinant inbred strains
1996
Mapping of quantitative trait loci for blood pressure and cardiac mass in the rat by genome scanning of recombinant inbred strains.
1995
Cardiac conduction defects associate with mutations in SCN5A
1999
Molecular Genetics and Functional Anomalies in a Series of 248 Brugada Cases with 11 Mutations in the TRPM4 Channel
2013
Haploinsufficiency in combination with aging causes SCN5A-linked hereditary Lenègre disease
2003
Cardiac Expression of the Ventricle-Specific Homeobox Gene Irx4 Is Modulated by Nkx2-5 and dHand
2000
Ankyrin-B mutation causes type 4 long-QT cardiac arrhythmia and sudden cardiac death
2003 Nature
Sodium channel β1 subunit mutations associated with Brugada syndrome and cardiac conduction disease in humans
2008
A radiation hybrid map of 506 STS markers spanning human chromosome 11
1994
Genotype-phenotype relationship in Brugada syndrome: electrocardiographic features differentiate SCN5A-related patients from non–SCN5A-related patients
2002
Developmental basis for filamin-A-associated myxomatous mitral valve disease
2012
Loss of function and inhibitory effects of human CSX/NKX2.5 homeoprotein mutations associated with congenital heart disease
2000
Type of SCN5A mutation determines clinical severity and degree of conduction slowing in loss-of-function sodium channelopathies
2008
Novel Brugada SCN5A Mutation Leading to ST Segment Elevation in the Inferior or the Right Precordial Leads
2003
Ridge segmentation and the magnetic structure of the Southwest Indian Ridge (at 50°30′E, 55°30′E and 66°20′E): Implications for magmatic processes at ultraslow‐spreading centers
2004
Paleomagnetism and potassium-argon age of the Messejana dike (Portugal and Spain): angular limitation to the rotation of the Iberian Peninsula since the Middle Jurassic
1981
NovelSCN5AMutation Leading Either to Isolated Cardiac Conduction Defect or Brugada Syndrome in a Large French Family
2001
Mapping of a gene for long QT syndrome to chromosome 4q25-27.
1995
Congenital Heart Disease Caused by Mutations in the Transcription Factor NKX2-5
1998 Science