Citation Impact
Citing Papers
Histone demethylase KDM6A directly senses oxygen to control chromatin and cell fate
2019 StandoutScienceNobel
Hypoxia-inducible transcription factor 2α promotes steatohepatitis through augmenting lipid accumulation, inflammation, and fibrosis
2011
Neuronal apoptosis linked to EglN3 prolyl hydroxylase and familial pheochromocytoma genes: Developmental culling and cancer
2005 StandoutNobel
HIF overexpression correlates with biallelic loss of fumarate hydratase in renal cancer: Novel role of fumarate in regulation of HIF stability
2005 StandoutNobel
Gene expression profiling predicts clinical outcome of breast cancer
2002 StandoutNature
Mechanical Properties of Adult Vertebral Cancellous Bone: Correlation With Collagen Intermolecular Cross‐Links
2002
A role for mitochondrial enzymes in inherited neoplasia and beyond
2003
Fibrosis in Systemic Sclerosis
2008
A High-Resolution STS, EST, and Gene-Based Physical Map of the Hereditary Paraganglioma Region on Chromosome 11q23
1997
IDH1andIDH2Mutations in Gliomas
2009 Standout
Psoriasis
2009 Standout
Integrative genomic analyses identify MITF as a lineage survival oncogene amplified in malignant melanoma
2005 StandoutNature
The R22X Mutation of the SDHD Gene in Hereditary Paraganglioma Abolishes the Enzymatic Activity of Complex II in the Mitochondrial Respiratory Chain and Activates the Hypoxia Pathway
2001
Expression of Angiogenic Growth Factors in Paragangliomas
2000
The pressure rises: update on the genetics of phaeochromocytoma
2002
Pathogenesis and therapy of psoriasis
2007 StandoutNature
Wound repair and regeneration
2008 StandoutNature
Cancer Metastasis: Building a Framework
2006 Standout
Phaeochromocytoma
2005 Standout
Genetic instabilities in human cancers
1998 StandoutNature
Effective Detection of Human Leukocyte Antigen Risk Alleles in Celiac Disease Using Tag Single Nucleotide Polymorphisms
2008
Genome-wide Detection of Allelic Imbalance Using Human SNPs and High-density DNA Arrays
2000
Familial paragangliomas: Linkage to chromosome 11q23 and clinical implications
1997
Hereditary paraganglioma targets diverse paraganglia: Table 1
2002
Genomic instability in Ip and human malignancies
1996
Founder Effect at PGL1 in Hereditary Head and Neck Paraganglioma Families from The Netherlands
1998
Tumor Metastasis: Molecular Insights and Evolving Paradigms
2011 Standout
Collagens, modifying enzymes and their mutations in humans, flies and worms
2003
Risks of cancer in BRCA1-mutation carriers
1994 Standout
17q21-q25 aberrations in breast cancer: combined allelotyping and CGH analysis reveals 5 regions of allelic imbalance among which two correspond to DNA amplification
1999
Systemic sclerosis
2017 Standout
Prevalence of SDHB, SDHC, and SDHD germline mutations in clinic patients with head and neck paragangliomas
2002
Oxygen sensing by HIF hydroxylases
2004 StandoutNobel
Detailed deletion analysis of sporadic breast tumors defines an interstitial region of allelic loss on l7q25
1996
Scleroderma
2009 Standout
Bone Quality — The Material and Structural Basis of Bone Strength and Fragility
2006 Standout
Characterization of RAC3, a Novel Member of the Rho Family
1997
Genomic organization and precise physical location of protein phosphatase 2A regulatory subunit A beta isoform gene on chromosome band 11q23
1998
Celiac Disease
2007 Standout
Mitochondria: In Sickness and in Health
2012 Standout
PLINK: A Tool Set for Whole-Genome Association and Population-Based Linkage Analyses
2007 Standout
Fumarate and Succinate Regulate Expression of Hypoxia-inducible Genes via TET Enzymes
2015 StandoutNobel
What a difference a hydroxyl makes: mutant IDH, (R)-2-hydroxyglutarate, and cancer
2013 StandoutNobel
Allelic Loss of Chromosome 18q and Prognosis in Colorectal Cancer
1994
Hypoxia and the extracellular matrix: drivers of tumour metastasis
2014 StandoutNobel
Chromosomes, 11q and cancer: a review
1999
Repositioning the hereditary paraganglioma critical region on chromosome band 11q23
1999
Getting under the skin: the immunogenetics of psoriasis
2005
Increased formation of pyridinoline cross-links due to higher telopeptide lysyl hydroxylase levels is a general fibrotic phenomenon
2004
SDH mutations in cancer
2011
A long noncoding RNA maintains active chromatin to coordinate homeotic gene expression
2011 StandoutNature
Genomic imprinting and environment in hereditary paraganglioma
2004
The fission yeast gene pmt1+encodes a DNA methyltransferase homologue
1995 StandoutNobel
Genetic alterations in breast cancer
1995
The role of collagen in bone strength
2005
Novel mutations and the emergence of a common mutation in theSDHD gene causing familial paraganglioma
2001
Distinct Clinical Features of Paraganglioma Syndromes Associated With <EMPH TYPE="ITAL">SDHB</EMPH> and <EMPH TYPE="ITAL">SDHD</EMPH> Gene Mutations
2004
Endothelin is a downstream mediator of profibrotic responses to transforming growth factor β in human lung fibroblasts
2007
Histology-Based Expression Profiling Yields Novel Prognostic Markers in Human Glioblastoma
2005
European Society for Pediatric Gastroenterology, Hepatology, and Nutrition Guidelines for the Diagnosis of Coeliac Disease
2011 Standout
Pheochromocytoma: The Expanding Genetic Differential Diagnosis
2003
Understanding the Intersections between Metabolism and Cancer Biology
2017 Standout
Paragangliomas of the head and neck region show complete loss of heterozygosity at 11 q22-q23 in chief cells and the flow-sorted dna aneuploid fraction
1998
Primary brain tumours in adults
2012 Standout
Parental imprinting of autosomal mammalian genes
1994
Asparagine and Aspartate Hydroxylation of the Cytoskeletal Ankyrin Family Is Catalyzed by Factor-inhibiting Hypoxia-inducible Factor
2010 StandoutNobel
Genome screening by searching for shared segments: mapping a gene for benign recurrent intrahepatic cholestasis
1994
Collagens and collagen-related diseases
2001
Mismatch Repair Deficiency in Phenotypically Normal Human Cells
1995 StandoutScienceNobel
Recent Developments in Myofibroblast Biology
2012
Platelet-Derived Growth Factor Receptor Association with Na+/H+ Exchanger Regulatory Factor Potentiates Receptor Activity
2000 StandoutNobel
Lysine Hydroxylation and Crosslinking of Collagen
2003
Gene Expression Signature of Fibroblast Serum Response Predicts Human Cancer Progression: Similarities between Tumors and Wounds
2004
Interleukin-4 Receptor α Signaling in Myeloid Cells Controls Collagen Fibril Assembly in Skin Repair
2015
Matrix Crosslinking Forces Tumor Progression by Enhancing Integrin Signaling
2009 Standout
Elevated formation of pyridinoline cross-links by profibrotic cytokines is associated with enhanced lysyl hydroxylase 2b levels
2004
Mutations in SDHC cause autosomal dominant paraganglioma, type 3
2000
Celiac Disease Genetics: Current Concepts and Practical Applications
2005
The kinesin KIF1Bβ acts downstream from EglN3 to induce apoptosis and is a potential 1p36 tumor suppressor
2008 StandoutNobel
Lysine post-translational modifications of collagen
2012
Understanding the molecular basis of celiac disease: What genetic studies reveal
2006
Regulation of hypoxia-inducible factor is preserved in the absence of a functioning mitochondrial respiratory chain
2001 StandoutNobel
Posttranslational hydroxylation of ankyrin repeats in IκB proteins by the hypoxia-inducible factor (HIF) asparaginyl hydroxylase, factor inhibiting HIF (FIH)
2006 StandoutNobel
Mitochondrial Reactive Oxygen Species (ROS) and ROS-Induced ROS Release
2014 Standout
Adaptive and Maladaptive Cardiorespiratory Responses to Continuous and Intermittent Hypoxia Mediated by Hypoxia-Inducible Factors 1 and 2
2012 StandoutNobel
ThreeC. elegansRac proteins and several alternative Rac regulators control axon guidance, cell migration and apoptotic cell phagocytosis
2001 StandoutNobel
Metabolic reprogramming and cancer progression
2020 StandoutScience
Hydroxylation of the eukaryotic ribosomal decoding center affects translational accuracy
2014 StandoutNobel
Molecular genetic analysis of oligodendroglial tumors shows preferential allelic deletions on 19q and 1p.
1994
Allelotyping of ductal carcinoma in situ of the breast: deletion of loci on 8p, 13q, 16q, 17p and 17q.
1995
Biochemical and mechanical properties of subchondral bone in osteoarthritis.
2004
Inflammation and metabolism in tissue repair and regeneration
2017 StandoutScience
THRA1 and D17S183 flank an interval of < 4 cM for the breast-ovarian cancer gene (BRCA1) on chromosome 17q21.
1993
The Complete Nucleotide Sequence of the Human Immunoglobulin Heavy Chain Variable Region Locus
1998 StandoutNobel
Osteoarthritis: an update with relevance for clinical practice
2011 Standout
Mutations in SDHD , a Mitochondrial Complex II Gene, in Hereditary Paraganglioma
2000 StandoutScience
Role ofVHLGene Mutation in Human Cancer
2004 StandoutNobel
Understanding the Warburg Effect: The Metabolic Requirements of Cell Proliferation
2009 StandoutScience
Treatment of erythropoietin deficiency in mice with systemically administered siRNA
2012 StandoutNobel
Chemical Glycoproteomics
2016 StandoutNobel
Fine mapping of an imprinted gene for familial nonchromaffin paragangliomas, on chromosome 11q23.
1997
Works of A. Bardoel being referenced
Further Localization of the Genefor Hereditary Paragangliomasand Evidence for Linkage inUnrelated Families
1994
A major non-HLA locus in celiac disease maps to chromosome 191 1This study is dedicated to the memory of Lodewijk Sandkuijl (1953–2002), who died shortly after its completion. He was an inspiration to us and was a world expert on biostatistics.
2003
PCR-based microsatellite polymorphisms in the detection of loss of heterozygosity in fresh and archival tumour tissue
1993
A gene subject to genomic imprinting and responsible for hereditary paragangliomas maps to chromosome 11q23-qter
1992
Allelotype of head and neck paragangliomas: Allelic imbalance is confined to the long arm of chromosome 11, the site of the predisposing locus PGL
1994
Defining the contribution of the HLA region to cis DQ2-positive coeliac disease patients
2004
Identification of PLOD2 as Telopeptide Lysyl Hydroxylase, an Important Enzyme in Fibrosis
2003
Defective collagen crosslinking in bone, but not in ligament or cartilage, in Bruck syndrome: Indications for a bone-specific telopeptide lysyl hydroxylase on chromosome 17
1999
Frequent somatic imbalance of marker alleles for chromosome 1 in human primary breast carcinoma.
1991
Linkage to markers for the chromosome region 17q12-q21 in 13 Dutch breast cancer kindreds.
1993
Allele loss patterns on chromosome 17q in 109 breast carcinomas indicate at least two distinct target regions.
1993