₈Hans Joenje

Summary for 2004 [at-glance overview of Hans Joenje work for the selected year as suggested by data mining algorithms]

This is an Authoratory overview of author Hans Joenje. According to available data, in 2004 Hans Joenje published at least 8 articles. This work was completed in collaboration with several authors including de Winter, Johan P and Arwert, Fré. Many other authors have collaborated with Hans Joenje as well. There is no information about the funding or the grants awarded to support this work.

Hans Joenje is a key opinion leader in the specific area of Fanconi Anemia. This author's rank is 1 when compared to all other authors using the same keyword. Analysis of the article abstracts and the titles suggests that Hans Joenje professional interests are focused around "fanconi anemia fa", "fanconi anemia complementation" and "defects atr-signalling pathway". These might also be referred to as "fanconi anemia", "seckel syndrome" or "cell lines". Statistical analysis shows that Hans Joenje's writing is likely to contains terms "fanconi", "anemia", "fa", "protein", "cell" and "syndrome".

Unfortunately, there is not enough information to establish Hans Joenje affiliation. Luckily, one email address is on file.

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Alternative names (1) [other authors with names similar to Hans Joenje]

₂₀Joenje, H

Year 2004 Charts [Hans Joenje frequent coauthors and the most common unique vocabulary terms for the selected year]

Historical Performance Charts [graphical overview of Hans Joenje publication and funding history for the range of years]

Emails (1) [email addresses extracted from Hans Joenje affiliations]

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Hans Joenje Coauthors (37) [all coauthors with the number of joint publications]

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₁₁Snijders, Peter J F

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₄Mathew, Christopher G

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₂van de Vrugt, Henri J

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₁Herterich, Sabine

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₁Kalb, Reinhard

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₁Meetei, Amom Ruhikanta

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Affiliations (6) [condensed summary of the Hans Joenje affiliations, the leading number and the color conveys importance]

₂Department of Clinical Genetics and Human Genetics, VU University Medical Center, Van der Boechorststraat 7, NL-1081BT NL-1081 BT, Amsterdam, The Netherlands.
₁Genome Damage and Stability Centre, University of Sussex, East Sussex, BN1 9RQ, UK.
₁Laboratory of Genetics, National Institute on Aging, National Institutes of Health, 333 Cassell Drive, TRIAD Center Room 3000, Baltimore, Maryland 21224, USA.
₁Group of Mutagenesis, Department of Genetics and Microbiology, Universitat Autonòma de Barcelona, 08193-Bellaterra, Barcelona, Spain.
₁Department of Clinical Genetics and Human Genetics, VU University Medical Center, Amsterdam, The Netherlands.
₁Department of Human Genetics, University of Wuerzburg, Biozentrum, Am Hubland, D-97074 Wuerzburg, Germany.

Key Opinion Leader In [Hans Joenje is considered a key opinion leader in any keyword where the rank of 5 is achieved, the leading number before the keyword shows the author's rank as compared to all other authors]

₁Fanconi Anemia

Keywords (32) [keywords assigned to Hans Joenje articles by PubMed, the leading number and the color conveys importance]

₈Humans | ₅Fanconi Anemia | ₃Animals | ₂Mutagenesis | ₂Cell Division | ₂Sequence Homology, Amino Acid | ₂Genetic Complementation Test | ₂Polymorphism, Genetic | ₂Signal Transduction | ₂Molecular Sequence Data | ₂Amino Acid Sequence | ₂Mutation | ₂Cell Line | ₂Cell Nucleus | ₁Oryzias | ₁Fanconi Anemia Complementation Group G Protein | ₁DNA-Binding Proteins | ₁Cell Cycle | ₁Protein Structure, Secondary | ₁Radiation Dosage | ₁Protein Structure, Tertiary | ₁Linkage (Genetics) | ₁Cell Fusion | ₁Xenopus | ₁Child | ₁Genes, Recessive | ₁Pedigree | ₁Tumor Suppressor Protein p53 | ₁Protein-Serine-Threonine Kinases | ₁Transfection | ₁Ultraviolet Rays | ₁DNA, Viral

Hans Joenje Unique Vocabulary (96) [single words, word pairs and phrases obtained by analysis of abstracts and titles, the leading number and the color conveys importance; Hans Joenje might be a good expert witness on these terms]

₂₁fanconi | ₂₀anemia | ₂₀fa | ₁₇protein | ₁₃cell | ₁₂syndrome | ₁₀fancf | ₁₀group | ₁₀pathway | ₉complementation | ₉seckel | ₉complex | ₈cells | ₈lines | ₇function | ₇fancg | ₇core | ₇radiation | ₆tpr | ₆genetic | ₆uv | ₆ionizing | ₆motifs | ₅complement | ₅defects | ₅primary | ₅fibroblasts | ₅patients | ₅response | ₅nuclear | ₅evidence | ₄atr
₂₀fanconi anemia | ₉seckel syndrome | ₈cell lines | ₇complementation group | ₇core complex | ₄anemia fa | ₄ionizing radiation | ₄atr-seckel cells | ₃sensitivity primary | ₃following exposure | ₃tpr motifs | ₃fancg protein | ₃anemia complementation | ₃flexible adaptor | ₃x-linked inheritance | ₃adaptor protein | ₃genetic subtypes | ₃atr-signalling pathway | ₃defects atr-signalling | ₃function fancf | ₃uv radiation | ₃fa pathway | ₂colony formation | ₂key role | ₂formation following | ₂hypoxic cell | ₂cellular features | ₂ataxia telangiectasia | ₂interstrain variation | ₂ionizing uv | ₂essential component | ₂component nuclear
₄fanconi anemia fa | ₃fanconi anemia complementation | ₃defects atr-signalling pathway | ₃flexible adaptor protein | ₂lack sensitivity primary | ₂sensitivity primary fanconi | ₂x-linked inheritance fanconi | ₂anemia fancg protein | ₂essential component nuclear | ₂anemia belonging complementation | ₂anemia evidence genetic | ₂fibroblasts uv ionizing | ₂fanconi anemia belonging | ₂multiple tpr motifs | ₂product fancf flexible | ₂cell culture conditions | ₂formation following exposure | ₂autosomal recessive syndrome | ₂fanconi anemia evidence | ₂motifs characterize fanconi | ₂hypoxic cell culture | ₂heterogeneity fanconi anemia | ₂fanconi anemia gene | ₂fancf flexible adaptor | ₂cellular features demonstrating | ₂mn formation following | ₂primary fanconi anemia | ₂ionizing uv radiation | ₂fanconi anemia fibroblasts | ₂anemia fibroblasts uv | ₂characterize fanconi anemia | ₂belonging complementation group

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