Concepedia

Author

Sylviane Olschwang

InsermORCID

Also Known As

OLSCHWANG S, OLSCHWANG, Sylviane, Olschwang S, Olschwang, Sylviane, Olschwang, Sylviane M.D., Ph.D., S Olschwang, S. OLSCHWANG, S. Olschwang, Sylviane OLSCHWANG, Sylviane Olschwang

280

Publications

18.1K

Citations

58

H-Index

111

Concepts

All Affiliations

InsermInstitut Paoli-CalmettesInstitut CurieSorbonne UniversitéCentre de Recherche en Cancérologie de Marseille
SO

About

Sylviane Olschwang is an author at Inserm specializing in medicine, pathology, and cancer research.

Top Concepts

#ConceptH-IndexPublicationsCitations

1

Medicine

37

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9.9K

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Public Health

9

9

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Engineering

3

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Natural Sciences

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Health Sciences

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Sylviane Olschwang

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118

Publications

17.1K

Citations

56

H-Index

YearCitations

A serine/threonine kinase gene defective in Peutz–Jeghers syndrome

Akseli Hemminki, David Markie, Ian Tomlinson,

Nature

1998

1.6K

Gene Expression Classification of Colon Cancer into Molecular Subtypes: Characterization, Validation, and Prognostic Value

Laëtitia Marisa, Aurélien de Reyniès, Alex Duval,

PLoS Medicine

2013

1.5K

Long-term effect of aspirin on cancer risk in carriers of hereditary colorectal cancer: an analysis from the CAPP2 randomised controlled trial

John Burn, Anne‐Marie Gerdes, Finlay Macrae,

The Lancet

2011

940

Kisten ras mutations in patients with colorectal cancer: the “RASCAL II” study.

David Cunningham, J. Oates, Joanne Young,

IRIS UNIMORE (University of Modena and Reggio Emilia)

2001

886

Frequency and Spectrum of Cancers in the Peutz-Jeghers Syndrome

Nicholas Hearle, Valerié Schumacher, Fred H. Menko,

Clinical Cancer Research

2006

841

Genome-wide association scan identifies a colorectal cancer susceptibility locus on chromosome 8q24

Brent W. Zanke, Celia M.T. Greenwood, Jagadish Rangrej,

Nature Genetics

2007

727

Alleles of the APC gene: An attenuated form of familial polyposis

Lisa Spirio, Sylviane Olschwang, Joanna Groden,

Cell

1993

619

Mutations of polycomb‐associated gene <i>ASXL1</i> in myelodysplastic syndromes and chronic myelomonocytic leukaemia

Véronique Gelsi‐Boyer, Virginie Trouplin, José Adélaı̈de,

British Journal of Haematology

2009

555

Germline mutations in the Von Hippel-Lindau disease (VHL) gene in families from North America, Europe, and Japan

Berton Zbar, Takeshi Kishida, Fan Chen,

Human Mutation

1996

502

Chromosomes in Ewing's sarcoma. I. An evaluation of 85 cases and remarkable consistency of t(11;22)(q24;q12)

Claude Turc‐Carel, Alain Aurias, Francine Mugneret,

Cancer Genetics and Cytogenetics

1988

465

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