BernheimV1, Hal, Corpus, bibRecord, 000016

Atlas of Genetics and Cytogenetics in Oncology and Haematology in 2013

Identifieur interne : 000016 ( Hal/Corpus ); précédent : 000015; suivant : 000017

Atlas of Genetics and Cytogenetics in Oncology and Haematology in 2013

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

Source :

Nucleic Acids Research [ 0305-1048 ] ; 2013.

RBID : Hal:hal-01587507

English descriptors

mix :
- database, haematology, internet journal, oncology.

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:

http://hal.upmc.fr/hal-01587507

DOI: 10.1093/nar/gks1082

Links to Exploration step

Hal:hal-01587507

Le document en format XML

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<idno type="DOI">10.1093/nar/gks1082</idno>
<series><title level="j">Nucleic Acids Research</title>
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<front><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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                <author role="aut">                  <persName>                    <forename type="first">Jean-Loup</forename>
                    <surname>Huret</surname>
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                <author role="aut">                  <persName>                    <forename type="first">Mélanie</forename>
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                <author role="aut">                  <persName>                    <forename type="first">Alain</forename>
                    <surname>Bernheim</surname>
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                <author role="aut">                  <persName>                    <forename type="first">Jérémy</forename>
                    <surname>Cigna</surname>
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                <author role="aut">                  <persName>                    <forename type="first">François</forename>
                    <surname>Desangles</surname>
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                <author role="aut">                  <persName>                    <forename type="first">Jean-christophe</forename>
                    <surname>Guignard</surname>
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                  <idno type="halauthorid">1615804</idno>
                  <affiliation ref="#struct-506615"></affiliation>
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                <author role="aut">                  <persName>                    <forename type="first">Marie-Christine</forename>
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                <author role="aut">                  <persName>                    <forename type="first">Vanessa</forename>
                    <surname>Leberre</surname>
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                <author role="aut">                  <persName>                    <forename type="first">Anne</forename>
                    <surname>Malo</surname>
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                <author role="aut">                  <persName>                    <forename type="first">Catherine</forename>
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                <author role="aut">                  <persName>                    <forename type="first">Hossein</forename>
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                <author role="aut">                  <persName>                    <forename type="first">Jean-claude</forename>
                    <surname>Potier</surname>
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                <author role="aut">                  <persName>                    <forename type="first">Guillaume</forename>
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                <author role="aut">                  <persName>                    <forename type="first">Franck</forename>
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                <author role="aut">                  <persName>                    <forename type="first">Sylvie</forename>
                    <surname>Yau Chun Wan-Senon</surname>
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                  <idno type="halauthorid">1615812</idno>
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                <author role="aut">                  <persName>                    <forename type="first">Alain</forename>
                    <surname>Zasadzinski</surname>
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                  <idno type="halauthorid">86996</idno>
                  <affiliation ref="#struct-1814"></affiliation>
                </author>
                <author role="aut">                  <persName>                    <forename type="first">Philippe</forename>
                    <surname>Dessen</surname>
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                <idno type="issn">0305-1048</idno>
                <idno type="eissn">1362-4962</idno>
                <title level="j">Nucleic Acids Research</title>
                <imprint>                  <publisher>Oxford University Press</publisher>
                  <biblScope unit="volume">41</biblScope>
                  <biblScope unit="issue">D1</biblScope>
                  <biblScope unit="pp">D920-D924</biblScope>
                  <date type="datePub">2013</date>
                  <date type="dateEpub">2013-09-01</date>
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              <idno type="doi">10.1093/nar/gks1082</idno>
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            <textClass>              <keywords scheme="author">                <term xml:lang="en">oncology</term>
                <term xml:lang="en">haematology</term>
                <term xml:lang="en">internet journal</term>
                <term xml:lang="en">database</term>
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            <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.</abstract>
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Serveur d'exploration Hippolyte Bernheim

Atlas of Genetics and Cytogenetics in Oncology and Haematology in 2013

Atlas of Genetics and Cytogenetics in Oncology and Haematology in 2013

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