Serveur d'exploration Hippolyte Bernheim

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Atlas of Genetics and Cytogenetics in Oncology and Haematology in 2013

Identifieur interne : 000167 ( Main/Merge ); précédent : 000166; suivant : 000168

Atlas of Genetics and Cytogenetics in Oncology and Haematology in 2013

Auteurs : Jean-Loup Huret [France] ; Mohammad Ahmad ; Mélanie Arsaban ; Alain Bernheim [France] ; Jérémy Cigna ; François Desangles [France] ; Jean-Christophe Guignard ; Marie-Christine Jacquemot-Perbal [France] ; Maureen Labarussias ; Vanessa Leberre ; Anne Malo ; Catherine Morel-Pair [France] ; Hossein Mossafa [France] ; Jean-Claude Potier [France] ; Guillaume Texier [France] ; Franck Viguié [France] ; Sylvie Yau Chun Wan-Senon ; Alain Zasadzinski [France] ; Philippe Dessen [France]

Source :

RBID : PMC:3531131

English descriptors

Abstract

The Atlas of Genetics and Cytogenetics in Oncology and Haematology (http://AtlasGeneticsOncology.org) is a peer-reviewed internet journal/encyclopaedia/database focused on genes implicated in cancer, cytogenetics and clinical entities in cancer and cancer-prone hereditary diseases. The main goal of the Atlas is to provide review articles that describe complementary topics, namely, genes, genetic abnormalities, histopathology, clinical diagnoses and a large iconography. This description, which was historically based on karyotypic abnormalities and in situ hybridization (fluorescence in situ hybridization) techniques, now benefits from comparative genomic hybridization and massive sequencing, uncovering a tremendous amount of genetic rearrangements. As the Atlas combines different types of information (genes, genetic abnormalities, histopathology, clinical diagnoses and external links), its content is currently unique. The Atlas is a cognitive tool for fundamental and clinical research and has developed into an encyclopaedic work. In clinical practice, it contributes to the cytogenetic diagnosis and may guide treatment decision making, particularly regarding rare diseases (because they are numerous and are frequently encountered). Readers as well as the authors of the Atlas are researchers and/or clinicians.


Url:
DOI: 10.1093/nar/gks1082
PubMed: 23161685
PubMed Central: 3531131

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Links to Exploration step

PMC:3531131

Le document en format XML

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<p>The Atlas of Genetics and Cytogenetics in Oncology and Haematology (
<ext-link ext-link-type="uri" xlink:href="http://AtlasGeneticsOncology.org">http://AtlasGeneticsOncology.org</ext-link>
) is a peer-reviewed internet journal/encyclopaedia/database focused on genes implicated in cancer, cytogenetics and clinical entities in cancer and cancer-prone hereditary diseases. The main goal of the Atlas is to provide review articles that describe complementary topics, namely, genes, genetic abnormalities, histopathology, clinical diagnoses and a large iconography. This description, which was historically based on karyotypic abnormalities and
<italic>in situ</italic>
hybridization (fluorescence
<italic>in situ</italic>
hybridization) techniques, now benefits from comparative genomic hybridization and massive sequencing, uncovering a tremendous amount of genetic rearrangements. As the Atlas combines different types of information (genes, genetic abnormalities, histopathology, clinical diagnoses and external links), its content is currently unique. The Atlas is a cognitive tool for fundamental and clinical research and has developed into an encyclopaedic work. In clinical practice, it contributes to the cytogenetic diagnosis and may guide treatment decision making, particularly regarding rare diseases (because they are numerous and are frequently encountered). Readers as well as the authors of the Atlas are researchers and/or clinicians.</p>
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<div type="abstract" xml:lang="en">The Atlas of Genetics and Cytogenetics in Oncology and Haematology (http://AtlasGeneticsOncology.org) is a peer-reviewed internet journal/encyclopaedia/database focused on genes implicated in cancer, cytogenetics and clinical entities in cancer and cancer-prone hereditary diseases. The main goal of the Atlas is to provide review articles that describe complementary topics, namely, genes, genetic abnormalities, histopathology, clinical diagnoses and a large iconography. This description, which was historically based on karyotypic abnormalities and in situ hybridization (fluorescence in situ hybridization) techniques, now benefits from comparative genomic hybridization and massive sequencing, uncovering a tremendous amount of genetic rearrangements. As the Atlas combines different types of information (genes, genetic abnormalities, histopathology, clinical diagnoses and external links), its content is currently unique. The Atlas is a cognitive tool for fundamental and clinical research and has developed into an encyclopaedic work. In clinical practice, it contributes to the cytogenetic diagnosis and may guide treatment decision making, particularly regarding rare diseases (because they are numerous and are frequently encountered). Readers as well as the authors of the Atlas are researchers and/or clinicians.</div>
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<name sortKey="Zasadzinski, Alain" sort="Zasadzinski, Alain" uniqKey="Zasadzinski A" first="Alain" last="Zasadzinski">Alain Zasadzinski</name>
<affiliation wicri:level="3">
<nlm:aff id="gks1082-AFF1">INIST-CNRS, 95310 Nancy, France,</nlm:aff>
<country xml:lang="fr">France</country>
<wicri:regionArea>INIST-CNRS, 95310 Nancy</wicri:regionArea>
<placeName>
<region type="region" nuts="2">Île-de-France</region>
<settlement type="city">Nancy</settlement>
</placeName>
</affiliation>
</author>
<author>
<name sortKey="Dessen, Philippe" sort="Dessen, Philippe" uniqKey="Dessen P" first="Philippe" last="Dessen">Philippe Dessen</name>
<affiliation wicri:level="3">
<nlm:aff id="gks1082-AFF1">Génétique des Tumeurs, 985 INSERM, Institut Gustave Roussy, 94805 Villejuif, France,</nlm:aff>
<country xml:lang="fr">France</country>
<wicri:regionArea>Génétique des Tumeurs, 985 INSERM, Institut Gustave Roussy, 94805 Villejuif</wicri:regionArea>
<placeName>
<region type="region" nuts="2">Île-de-France</region>
<settlement type="city">Villejuif</settlement>
</placeName>
</affiliation>
</author>
</analytic>
<series>
<title level="j">Nucleic Acids Research</title>
<idno type="ISSN">0305-1048</idno>
<idno type="eISSN">1362-4962</idno>
<imprint>
<date when="2012">2012</date>
</imprint>
</series>
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<front>
<div type="abstract" xml:lang="en">
<p>The Atlas of Genetics and Cytogenetics in Oncology and Haematology (
<ext-link ext-link-type="uri" xlink:href="http://AtlasGeneticsOncology.org">http://AtlasGeneticsOncology.org</ext-link>
) is a peer-reviewed internet journal/encyclopaedia/database focused on genes implicated in cancer, cytogenetics and clinical entities in cancer and cancer-prone hereditary diseases. The main goal of the Atlas is to provide review articles that describe complementary topics, namely, genes, genetic abnormalities, histopathology, clinical diagnoses and a large iconography. This description, which was historically based on karyotypic abnormalities and
<italic>in situ</italic>
hybridization (fluorescence
<italic>in situ</italic>
hybridization) techniques, now benefits from comparative genomic hybridization and massive sequencing, uncovering a tremendous amount of genetic rearrangements. As the Atlas combines different types of information (genes, genetic abnormalities, histopathology, clinical diagnoses and external links), its content is currently unique. The Atlas is a cognitive tool for fundamental and clinical research and has developed into an encyclopaedic work. In clinical practice, it contributes to the cytogenetic diagnosis and may guide treatment decision making, particularly regarding rare diseases (because they are numerous and are frequently encountered). Readers as well as the authors of the Atlas are researchers and/or clinicians.</p>
</div>
</front>
<back>
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