Citation Impact

Citing Papers

2015 American Thyroid Association Management Guidelines for Adult Patients with Thyroid Nodules and Differentiated Thyroid Cancer: The American Thyroid Association Guidelines Task Force on Thyroid Nodules and Differentiated Thyroid Cancer
2015 Standout
Multiple Sp1 sites efficiently drive transcription of the TATA-less promoter of the human glypican 3 (GPC3) gene
1998
Mutations in GPC3, a glypican gene, cause the Simpson-Golabi-Behmel overgrowth syndrome
1996
Glypican-3–Deficient Mice Exhibit Developmental Overgrowth and Some of the Abnormalities Typical of Simpson-Golabi-Behmel Syndrome
1999
Rapid chromosome territory relocation by nuclear motor activity in response to serum removal in primary human fibroblasts
2010
The human olfactory receptor gene family
2004 StandoutNobel
Embryo Implantation
2000 Standout
Chromosome Territories
2010
Thyroid cancer
2016 Standout
Hidden chromosome abnormalities in haematological malignancies detected by multicolour spectral karyotyping
1997
Clinical and molecular aspects of the Simpson-Golabi-Behmel syndrome
1998
The von Hippel–Lindau Tumor Suppressor Gene
2001 StandoutNobel
Chromosomal Dynamics at the Shh Locus: Limb Bud-Specific Differential Regulation of Competence and Active Transcription
2008
Visualizing Spatiotemporal Dynamics of Multicellular Cell-Cycle Progression
2008 Standout
Loss of Olfactory Receptor Genes Coincides with the Acquisition of Full Trichromatic Vision in Primates
2004 StandoutNobel
Mouse mutant embryos overexpressing IGF-II exhibit phenotypic features of the Beckwith–Wiedemann and Simpson–Golabi–Behmel syndromes
1997
Distribution of olfactory receptor genes in the human genome
1998
von Hippel-Lindau Disease
1997 StandoutNobel
Mammalian karyotype evolution
2007
A DNA damage checkpoint response in telomere-initiated senescence
2003 StandoutNature
Domain organization of human chromosomes revealed by mapping of nuclear lamina interactions
2008 StandoutNature
FGF signaling pathways in endochondral and intramembranous bone development and human genetic disease
2002 Standout
Short Telomeres Limit Tumor Progression In Vivo by Inducing Senescence
2007 StandoutNobel
Methylation of a CTCF-dependent boundary controls imprinted expression of the Igf2 gene
2000 StandoutNature
Management of Hepatocellular Carcinoma *
2005 Standout
Quantum dot bioconjugates for imaging, labelling and sensing
2005 Standout
Synthetic peptides define critical contacts between elongin C, elongin B, and the von Hippel-Lindau protein
1999 StandoutNobel
Extracellular matrix structure
2015 Standout
Telomere fusion to chromosome breaks reduces oncogenic translocations and tumour formation
2005 StandoutNobel
Mutations of theRET proto-oncogene in the multiple endocrine neoplasia type 2 syndromes, related sporadic tumours, and Hirschsprung disease
1997
Glypican-3, overexpressed specifically in human hepatocellular carcinoma, is a novel tumor marker
2003
The 5‐HT2B receptor plays a key regulatory role in both neuroendocrine tumor cell proliferation and the modulation of the fibroblast component of the neoplastic microenvironment
2010
Transcription factors: from enhancer binding to developmental control
2012 Standout
The role of glypicans in mammalian development
2002
The Shortest Telomere, Not Average Telomere Length, Is Critical for Cell Viability and Chromosome Stability
2001 StandoutNobel
Fluorescence in situ hybridization: A brief review
1996
Transcriptional regulation and nuclear reprogramming: roles of nuclear actin and actin-binding proteins
2012 StandoutNobel
Activation of the DNA damage checkpoint and genomic instability in human precancerous lesions
2005 StandoutNature
A p53-Dependent Checkpoint Pathway Prevents Rereplication
2003
Simpson Golabi Behmel Syndrome: Progress toward Understanding the Molecular Basis for Overgrowth, Malformation, and Cancer Predisposition
2001
Phosphorylation of H2AX at Short Telomeres in T Cells and Fibroblasts
2004 StandoutNobel
Multicolour spectral karyotyping of mouse chromosomes
1996
Autoregulatory effects of serotonin on proliferation and signaling pathways in lung and small intestine neuroendocrine tumor cell lines
2009
A census of human cancer genes
2004 Standout
Chromosome territories, nuclear architecture and gene regulation in mammalian cells
2001 Standout
Topological domains in mammalian genomes identified by analysis of chromatin interactions
2012 StandoutNature
DNA microarrays for comparative genomic hybridization based on DOP‐PCR amplification of BAC and PAC clones
2003
A 3D Map of the Human Genome at Kilobase Resolution Reveals Principles of Chromatin Looping
2014 Standout
Long Noncoding RNAs: Cellular Address Codes in Development and Disease
2013 Standout
The VHL tumour-suppressor gene paradigm
1998 StandoutNobel
Reverse chromosome painting: a method for the rapid analysis of aberrant chromosomes in clinical cytogenetics.
1992
Glycosaminoglycans and their proteoglycans: host‐associated molecular patterns for initiation and modulation of inflammation
2006 Standout
The Three-Dimensional Structure of Human Interphase Chromosomes Is Related to the Transcriptome Map
2007
AID-deficient Bcl-xL transgenic mice develop delayed atypical plasma cell tumors with unusual Ig/Myc chromosomal rearrangements
2007 StandoutNobel
Upconversion Nanoparticles: Design, Nanochemistry, and Applications in Theranostics
2014 Standout
A map of the human immunoglobulin VH locus completed by analysis of the telomeric region of chromosome 14q
1994 StandoutNobel
Fluorescence intermittency in single cadmium selenide nanocrystals
1996 StandoutNatureNobel
De novo assembly of the Aedes aegypti genome using Hi-C yields chromosome-length scaffolds
2017 StandoutScience
von Hippel-Lindau Disease
2006 StandoutNobel
Genomes in Focus: Development and Applications of CRISPR‐Cas9 Imaging Technologies
2017 StandoutNobel
Quantum Dot-Based Multiplexed Fluorescence Resonance Energy Transfer
2005 StandoutNobel
Self-Assembly of CdSe−ZnS Quantum Dot Bioconjugates Using an Engineered Recombinant Protein
2000 StandoutNobel
AnFgf8mouse mutant phenocopies human 22q11 deletion syndrome
2002 StandoutNobel
Combination therapy in combating cancer
2017 Standout
The mouse olfactory receptor gene family
2004 StandoutNobel
Spatial Relationship between Transcription Sites and Chromosome Territories
1999
Normal cardiovascular development in mice deficient for 16 genes in 550 kb of the velocardiofacial/ DiGeorge syndrome region
2000
Constitutive Expression of AID Leads to Tumorigenesis
2003 StandoutNobel
Semiconductor Nanocrystals as Fluorescent Biological Labels
1998 StandoutScience
Twenty years of lesson learning: how does the RET genetic screening test impact the clinical management of medullary thyroid cancer?
2014
Mutations in the RET proto-oncogene and the von Hippel-Lindau disease tumour suppressor gene in sporadic and syndromic phaeochromocytomas.
1995
The Importance of Diagnostic Cytogenetics on Outcome in AML: Analysis of 1,612 Patients Entered Into the MRC AML 10 Trial
1998 Standout
Guidelines for the management of thyroid cancer
2014 Standout
Functions of Cell Surface Heparan Sulfate Proteoglycans
1999 Standout
Bioconjugation of Highly Luminescent Colloidal CdSe-ZnS Quantum Dots with an Engineered Two-Domain Recombinant Protein
2001 StandoutNobel
Role ofVHLGene Mutation in Human Cancer
2004 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
Multicolor Spectral Karyotyping of Human Chromosomes
1996 Science

Works of A. Behmel being referenced

A new X-linked dysplasia gigantism syndrome: Identical with the Simpson dysplasia syndrome?
1984
Mutation of the RET protooncogene in sporadic medullary thyroid carcinoma
1995
Cytogenetic analysis by chromosome painting using dop‐pcr amplified flow‐sorted chromosomes
1992
A new X‐linked dysplasia gigantism syndrome: Follow up in the first family and report on a second Austrian family
1988
Establishment of a continuous cell line from a human carcinoid of the small intestine (KRJ-I)
1996
Gene for Simpson‐Golabi‐Behmel syndrome is linked to HPRT in Xq26 in two European families
1994
Rankless by CCL
2026