Citation Impact
Citing Papers
Human cerebral organoids recapitulate gene expression programs of fetal neocortex development
2015 StandoutNobel
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
Tumor-reactive CD4+ T cells develop cytotoxic activity and eradicate large established melanoma after transfer into lymphopenic hosts
2010 StandoutNobel
Human-specific gene ARHGAP11B promotes basal progenitor amplification and neocortex expansion
2015 StandoutScienceNobel
Plasma β-amyloid in Alzheimer’s disease and vascular disease
2016 StandoutNobel
Comprehensive molecular portraits of human breast tumours
2012 StandoutNature
Deficient long-term memory in mice with a targeted mutation of the cAMP-responsive element-binding protein
1994 Standout
Magnesium in the Central Nervous System
2011
Chemical and photochemical probing of DNA complexes
1990
Restricted and Regulated Overexpression Reveals Calcineurin as a Key Component in the Transition from Short-Term to Long-Term Memory
1998 StandoutNobel
Maternal Immune Activation Alters Fetal Brain Development through Interleukin-6
2007 Standout
Myasthenia Gravis
2016 Standout
Mutations in human cause limb and cardiac malformation in Holt-Oram syndrome
1997
NFAT dysregulation by increased dosage of DSCR1 and DYRK1A on chromosome 21
2006 StandoutNature
STED Microscopy with Optimized Labeling Density Reveals 9-Fold Arrangement of a Centriole Protein
2012 StandoutNobel
Role of platelet-derived growth factors in physiology and medicine
2008 Standout
Dual Detection of Fungal Infections in Drosophila via Recognition of Glucans and Sensing of Virulence Factors
2006 StandoutNobel
The molecular basis of human retinal and vitreoretinal diseases
2010 Standout
Transcriptional regulation of the MHC II gene DRA in untransformed human thyrocytes
2000
Do Mammalian Cells Really Need to Export and Import Heme?
2017
A Novel Transcription Factor, T-bet, Directs Th1 Lineage Commitment
2000 Standout
Arrestin Development: Emerging Roles for β-arrestins in Developmental Signaling Pathways
2009 StandoutNobel
Clinical Practice Guideline for Screening and Management of High Blood Pressure in Children and Adolescents
2017 Standout
NOX enzymes and the biology of reactive oxygen
2004 Standout
Maternal neuronal antibodies associated with autism and a language disorder
2003
Structurally Mapping Endogenous Heme in the CcmCDE Membrane Complex for Cytochrome c Biogenesis
2018 StandoutNobel
Prognosis and Decision Making in Severe Stroke
2005
The NOX Family of ROS-Generating NADPH Oxidases: Physiology and Pathophysiology
2007 Standout
A transition zone complex regulates mammalian ciliogenesis and ciliary membrane composition
2011
Cleft lip and palate: understanding genetic and environmental influences
2011 Standout
Non-viral vectors for gene-based therapy
2014 Standout
Aberrant splicing is a common mutational mechanism inMKS1, a key player in Meckel-Gruber syndrome
2007
Myosin binding protein C1: a novel gene for autosomal dominant distal arthrogryposis type 1
2010
Human Splicing Finder: an online bioinformatics tool to predict splicing signals
2009 Standout
Holt-Oram syndrome is caused by mutations in TBX5, a member of the Brachyury (T) gene family
1997 Standout
Stabilized plasmid–lipid particles containing PEG-diacylglycerols exhibit extended circulation lifetimes and tumor selective gene expression
2005
Heme transport and erythropoiesis
2013
Arthrogryposis: A Review and Update
2009
Unraveling the therapeutic potential of the Hedgehog pathway in cancer
2013 Standout
Evaluation of Factors Related to Late Recurrence - Later than 10 Years after the Initial Treatment - in Primary Breast Cancer
2013 Standout
Alzheimer's disease
2006 Standout
Links Between the Pathology of Alzheimer's Disease and Vascular Dementia
2004
Defining roles of specific reactive oxygen species (ROS) in cell biology and physiology
2022 Standout
GATA4 mutations cause human congenital heart defects and reveal an interaction with TBX5
2003 StandoutNature
Hypoxia-Induced Down-Regulation of Neprilysin by Histone Modification in Mouse Primary Cortical and Hippocampal Neurons
2011
Myasthenia gravis in pregnancy and birth: identifying risk factors, optimising care
2006
AKT/PKB Signaling: Navigating the Network
2017 Standout
The neuronal endopeptidase ECEL1 is associated with a distinct form of recessive distal arthrogryposis
2012
Heme in pathophysiology: a matter of scavenging, metabolism and trafficking across cell membranes
2014
Lectin Domains of Polypeptide GalNAc Transferases Exhibit Glycopeptide Binding Specificity
2011 StandoutNobel
Regulation of transcription and cell identity by POU domain proteins
1991 StandoutNobel
Limitations of oxygen delivery to cells in culture: An underappreciated problem in basic and translational research
2017
Antibodies to Neuronal Targets in Neurological and Psychiatric Diseases
2003
The nematophagous fungus Verticillium chlamydosporium produces a chymoelastase-like protease which hydrolyses host nematode proteins in situ
1994
Mutations in ECEL1 Cause Distal Arthrogryposis Type 5D
2012
Somatic Activation of AKT3 Causes Hemispheric Developmental Brain Malformations
2012
Centrioles, Centrosomes, and Cilia in Health and Disease
2009
Transcriptional regulation by CREB and its relatives
1993
Pre-eclampsia
2015 Standout
Neurovascular pathways to neurodegeneration in Alzheimer's disease and other disorders
2011 Standout
Efficacy and safety of angiotensin II receptor type 1 antagonists in children and adolescents
2009
Optimising sample collection for placental research
2013
The Unexpected Importance of the Primary Structure of the Hydrophobic Part of One-Component Ionizable Amphiphilic Janus Dendrimers in Targeted mRNA Delivery Activity
2022 StandoutNobel
Guidelines for the Early Management of Patients With Acute Ischemic Stroke
2013 Standout
Magnesium in Man: Implications for Health and Disease
2014 Standout
Rare copy number variations in congenital heart disease patients identify unique genes in left-right patterning
2011
Cystic diseases of the kidney: ciliary dysfunction and cystogenic mechanisms
2010
Stillbirths: Where? When? Why? How to make the data count?
2011 Standout
Diagnostic evaluation of intrauterine fetal deaths in Stockholm 1998–99
2002
Neural progenitors, neurogenesis and the evolution of the neocortex
2014
Oxidative Nucleobase Modifications Leading to Strand Scission
1998 Standout
ACC/AHA 2008 Guidelines for the Management of Adults With Congenital Heart Disease: Executive Summary
2008 Standout
Gain-of-function mutations in the mechanically activated ion channel PIEZO2 cause a subtype of Distal Arthrogryposis
2013 StandoutNobel
Cilia and Developmental Signaling
2007
Arthrogryposis multiplex congenita
1998
Transcription factor Oct-2A contains functionally redundant activating domains and works selectively from a promoter but not from a remote enhancer position in non-lymphoid (HeLa) cells.
1990
Protein synthesis in vesicular stomatitis virus-infected HeLa cells
1970
Clinical practice guidelines for support of the family in the patient-centered intensive care unit: American College of Critical Care Medicine Task Force 2004–2005
2007
Identification of the Vesicular Stomatitis Virus Large Protein as a Unique Viral Protein
1973 StandoutNobel
Cby1 promotes Ahi1 recruitment to a ring-shaped domain at the centriole–cilium interface and facilitates proper cilium formation and function
2014 StandoutNobel
A family of octamer-specific proteins present during mouse embryogenesis: evidence for germline-specific expression of an Oct factor.
1989
Part 8: Post–Cardiac Arrest Care
2015 Standout
Cleavage of amyloid precursor protein elicited by chronic cerebral hypoperfusion
2000
Targeted Delivery of mRNA with One-Component Ionizable Amphiphilic Janus Dendrimers
2021 StandoutNobel
An NAD(P)H oxidase regulates growth and transcription in melanoma cells
2002
Pluripotency and nuclear reprogramming
2008 StandoutNobel
Joubert Syndrome 2 (JBTS2) in Ashkenazi Jews Is Associated with a TMEM216 Mutation
2010
A single splice site mutation in human-specific ARHGAP11B causes basal progenitor amplification
2016 StandoutNobel
Multiple pterygium syndrome
1980
CREB: A Stimulus-Induced Transcription Factor Activated by A Diverse Array of Extracellular Signals
1999 Standout
Translation of Vesicular Stomatitis Messenger RNA by Extracts from Mammalian and Plant Cells
1974 StandoutNobel
The base of the cilium: roles for transition fibres and the transition zone in ciliary formation, maintenance and compartmentalization
2012
Works of P. Cox being referenced
Transcription and cancer
1991
An ATF/CREB binding motif is required for aberrant constitutive expression of the MHC class II DRα promoter and activation by SV4O T-antigen
1992
A distinct octamer-binding protein present in malignant melanoma cells
1988
Mutations in FLVCR2 Are Associated with Proliferative Vasculopathy and Hydranencephaly-Hydrocephaly Syndrome (Fowler Syndrome)
2010
Magnesium Sulfate Treatment after Transient Hypoxia-Ischemia in the Newborn Piglet Does Not Protect against Cerebral Damage
2000
BEST PRACTICE NO 178
2004
Placental angioarchitecture in monochorionic twin pregnancies: Relationship to fetal growth, fetofetal transfusion syndrome, and pregnancy outcome
2000
Mosaic trisomy 1q: The longest surviving case
2009
Intensive care management of paediatric organ donors and its effect on post-transplant organ function
1996
Mutations in the Embryonal Subunit of the Acetylcholine Receptor (CHRNG) Cause Lethal and Escobar Variants of Multiple Pterygium Syndrome
2006
The Meckel–Gruber Syndrome proteins MKS1 and meckelin interact and are required for primary cilium formation
2006
Prenatal findings in generalized amyoplasia
1995
The chemical composition of the egg shells of the potato cyst-nematode, Heterodera rostochiensis Woll
1967
Defective embryogenesis with angiotensin II receptor antagonists in pregnancy
2003
Statement of the 5th International Consensus Conference in Critical Care Challenges in end-of-life care in the ICU☆Brussels, Belgium, April 2003
2004
Asymptomatic maternal myasthenia as a cause of the Pena-Shokeir phenotype
2000
Expression of amyloid precursor protein (β‐APP) in the neonatal brain following hypoxic ischaemic injury
1998
Use of a New Buffer in the Culture of Animal Cells
1968
A translocation at 12q2 refines the interval containing the Holt-Oram syndrome 1 gene.
1996