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S. Olschwang · SciRah

Researcher profile · Semantic Scholar

S. Olschwang

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S. Olschwang — researcher profile on SciRah

h-index: 56
Works: 227
Citations: 18K

Most-cited papers

Gene Expression Classification of Colon Cancer into Molecular Subtypes: Characterization, Validation, and Prognostic Value
L. Marisa, A. de Reyniès, A. Duval, J. Sèlves +20 more
2013PLoS Medicine1,376 citations Open access
Semantic Scholar
Cancer risks associated with germline mutations in MLH1, MSH2, and MSH6 genes in Lynch syndrome.
V. Bonadona, Bernard Bonaïti, S. Olschwang, S. Grandjouan +22 more
2011Journal of the American Medical Association (JAMA)1,066 citations Open access
Semantic Scholar
Mutations of polycomb‐associated gene ASXL1 in myelodysplastic syndromes and chronic myelomonocytic leukaemia
V. Gelsi-Boyer, V. Trouplin, J. Adélaı̈de, Julien Bonansea +12 more
2009British Journal of Haematology627 citations
Semantic Scholar
Long-term effect of aspirin on cancer risk in carriers of hereditary colorectal cancer: an analysis from the CAPP2 randomised controlled trial
J. Burn, A. Gerdes, F. Macrae, J. Mecklin +29 more
2011The Lancet372 citations Open access
Semantic Scholar
Point Mutations in Exon 1B of APC Reveal Gastric Adenocarcinoma and Proximal Polyposis of the Stomach as a Familial Adenomatous Polyposis Variant.
Jun Li, S. Woods, S. Healey, J. Beesley +71 more
2016American Journal of Human Genetics251 citations Open access
Semantic Scholar
Combined mutations of ASXL1, CBL, FLT3, IDH1, IDH2, JAK2, KRAS, NPM1, NRAS, RUNX1, TET2 and WT1 genes in myelodysplastic syndromes and acute myeloid leukemias
J. Rocquain, N. Carbuccia, V. Trouplin, S. Raynaud +8 more
2010BMC Cancer196 citations Open access
Semantic Scholar
A large fraction of unclassified variants of the mismatch repair genes MLH1 and MSH2 is associated with splicing defects
I. Tournier, M. Vezain, A. Martins, F. Charbonnier +8 more
2008Human Mutation173 citations Open access
Semantic Scholar
Effect of aspirin or resistant starch on colorectal neoplasia in the Lynch syndrome.
J. Burn, D. Bishop, J. Mecklin, F. Macrae +24 more
2008New England Journal of Medicine168 citations Open access
Semantic Scholar
Clinical practice guidelines for BRCA1 and BRCA2 genetic testing.
P. Pujol, M. Barberis, Philp Beer, E. Friedman +50 more
2021European Journal of Cancer142 citations Open access
Semantic Scholar
Identification in Daily Practice of Patients With Lynch Syndrome (Hereditary Nonpolyposis Colorectal Cancer): Revised Bethesda Guidelines-Based Approach Versus Molecular Screening
C. Julié, C. Trésallet, A. Brouquet, C. Vallot +16 more
2008American Journal of Gastroenterology140 citations
Semantic Scholar
Obesity, Aspirin, and Risk of Colorectal Cancer in Carriers of Hereditary Colorectal Cancer: A Prospective Investigation in the CAPP2 Study.
M. Movahedi, D. Bishop, F. Macrae, J. Mecklin +21 more
2015Journal of Clinical Oncology114 citations Open access
Semantic Scholar
The Balance Between Cytotoxic T-cell Lymphocytes and Immune Checkpoint Expression in the Prognosis of Colon Tumors
L. Marisa, M. Svrcek, A. Collura, E. Becht +22 more
2018Journal of the National Cancer Institute113 citations Open access
Semantic Scholar
Leiden open variation database of the MUTYH gene
Astrid A. Out, C. Tops, M. Nielsen, M. Weiss +27 more
2010Human Mutation93 citations Open access
Semantic Scholar
A polymorphism of EGFR extracellular domain is associated with progression free-survival in metastatic colorectal cancer patients receiving cetuximab-based treatment
A. Gonçalves, Séverine Esteyriès, Brynn Taylor-Smedra, A. Lagarde +12 more
2008BMC Cancer85 citations Open access
Semantic Scholar
Quantitative PCR high‐resolution melting (qPCR‐HRM) curve analysis, a new approach to simultaneously screen point mutations and large rearrangements: application to MLH1 germline mutations in Lynch syndrome
E. Rouleau, C. Lefol, V. Bourdon, F. Coulet +6 more
2009Human Mutation78 citations Open access
Semantic Scholar
A Seven-Gene Signature Aggregates a Subgroup of Stage II Colon Cancers with Stage III
S. Laibe, A. Lagarde, A. Ferrari, G. Monges +2 more
2012Omics77 citations
Semantic Scholar
SMARCB1/INI1 germline mutations contribute to 10% of sporadic schwannomatosis
G. Rousseau, T. Noguchi, V. Bourdon, H. Sobol +1 more
2011BMC Neurology75 citations Open access
Semantic Scholar
Variation in the Risk of Colorectal Cancer for Lynch Syndrome: A retrospective family cohort study
Aung Ko Win, J. Dowty, J. Reece, Grant Lee +208 more
2021The Lancet Oncology64 citations Open access
Semantic Scholar
Guidelines for reporting secondary findings of genome sequencing in cancer genes: the SFMPP recommendations
P. Pujol, Pierre Vande-Perre, L. Faivre, D. Sanlaville +42 more
2018European Journal of Human Genetics60 citations Open access
Semantic Scholar
Molecular combing reveals complex 4q35 rearrangements in Facioscapulohumeral dystrophy
K. Nguyen, F. Puppo, Stéphane Roche, Marie-Cécile Gaillard +11 more
2017Human Mutation54 citations Open access
Semantic Scholar
Germline APC mutation spectrum derived from 863 genomic variations identified through a 15-year medical genetics service to French patients with FAP
A. Lagarde, E. Rouleau, A. Ferrari, T. Noguchi +10 more
2010Journal of Medical Genetics48 citations
Semantic Scholar
8q24 Cancer Risk Allele Associated with Major Metastatic Risk in Inflammatory Breast Cancer
F. Bertucci, A. Lagarde, A. Ferrari, P. Finetti +7 more
2012PLoS ONE42 citations Open access
Semantic Scholar
Multicenter study of ZAP-70 expression in patients with B-cell chronic lymphocytic leukemia using an optimized flow cytometry method
N. Gachard, Aurélie Salviat, C. Boutet, C. Arnoulet +11 more
2008Haematologica42 citations Open access
Semantic Scholar
The LKB1 complex-AMPK pathway: the tree that hides the forest
M. Sebbagh, S. Olschwang, M. Santoni, J. Borg
2011Familial Cancer39 citations Open access
Semantic Scholar
PIK3CA mutations predict recurrence in localized microsatellite stable colon cancer
G. Manceau, L. Marisa, V. Boige, A. Duval +14 more
2015Cancer Medicine33 citations Open access
Semantic Scholar
A multicenter blinded study evaluating EGFR and KRAS mutation testing methods in the clinical non-small cell lung cancer setting--IFCT/ERMETIC2 Project Part 1: Comparison of testing methods in 20 French molecular genetic National Cancer Institute platforms.
M. Beau-Faller, H. Blons, C. Domerg, D. Gajda +23 more
2014Journal of Molecular Diagnostics32 citations Open access
Semantic Scholar
Array CGH and DNA sequencing to personalize targeted treatment of metastatic breast cancer (MBC) patients (pts): A prospective multicentric trial (SAFIR01).
F. André, T. Bachelot, M. Campone, M. Arnedos +16 more
201327 citations
Semantic Scholar
Vascular Endothelial Growth Factor A c.*237C>T polymorphism is associated with bevacizumab efficacy and related hypertension in metastatic colorectal cancer.
Camille Sibertin-Blanc, J. Mancini, A. Fabre, A. Lagarde +5 more
2015Digestive and Liver Disease26 citations
Semantic Scholar
High Frequency of Chromosome 14 Deletion in Early-Onset Colon Cancer
N. Mourra, G. Zeitoun, B. Buecher, P. Finetti +5 more
2007Diseases of the Colon & Rectum24 citations
Semantic Scholar
Colon‐specific phenotype in Lynch syndrome associated with EPCAM deletion
P. Grandval, S. Baert-Desurmont, F. Bonnet, M. Bronner +8 more
2012Clinical Genetics23 citations
Semantic Scholar
Expression Profiles in Stage II Colon Cancer According to APC Gene Status.
D. J. Birnbaum, S. Laibe, A. Ferrari, A. Lagarde +13 more
2012Translational Oncology22 citations Open access
Semantic Scholar
Contribution of Ultrasonography to Endometrial Cancer Screening in Patients With Hereditary Nonpolyposis Colorectal Cancer/Lynch Syndrome
F. Lécuru, C. Huchon, U. Metzger, A. Bats +3 more
2010International Journal of Gynecologic Cancer22 citations Open access
Semantic Scholar
[Cancer genetics: estimation of the needs of the population in France for the next ten years].
C. Bonaïti-pellié, N. Andrieu, P. Arveux, V. Bonadona +14 more
2009Bulletin du Cancer21 citations
Semantic Scholar
The UMD–APC Database, a Model of Nation‐Wide Knowledge Base: Update with Data from 3,581 Variations
P. Grandval, M. Blayau, M. Buisine, F. Coulet +7 more
2014Human Mutation20 citations Open access
Semantic Scholar
Mitochondrial D310 mutations in colorectal adenomas: An early but not causative genetic event during colorectal carcinogenesis
A. Legras, A. Lièvre, C. BonaÎti-Pellié, V. Cottet +9 more
2008International Journal of Cancer20 citations Open access
Semantic Scholar
UMD-MLH1/MSH2/MSH6 databases: description and analysis of genetic variations in French Lynch syndrome families
P. Grandval, A. Fabre, P. Gaildrat, S. Baert-Desurmont +5 more
2013Database J. Biol. Databases Curation17 citations Open access
Semantic Scholar
Clinical utility gene card for: Lynch syndrome (MLH1, MSH2, MSH6, PMS2, EPCAM) - update 2012
N. Rahner, V. Steinke, B. Schlegelberger, F. Eisinger +2 more
2012European Journal of Human Genetics17 citations Open access
Semantic Scholar
First large rearrangement in the MUTYH gene and attenuated familial adenomatous polyposis syndrome
E. Rouleau, H. Zattara, C. Lefol, T. Noguchi +6 more
2011Clinical Genetics16 citations Open access
Semantic Scholar
Improving Mutation Screening in Patients with Colorectal Cancer Predisposition Using Next-Generation Sequencing.
J. Rey, Vincent Ducros, P. Pujol, Qing Wang +4 more
2017Journal of Molecular Diagnostics15 citations Open access
Semantic Scholar
Clinical utility gene card for: Familial adenomatous polyposis (FAP) and attenuated FAP (AFAP)
S. Aretz, H. Vasen, S. Olschwang
2011European Journal of Human Genetics15 citations Open access
Semantic Scholar
Genomic profile concordance between pancreatic cyst fluid and neoplastic tissue
A. Laquière, A. Lagarde, B. Napoléon, R. Bourdariat +12 more
2019World Journal of Gastroenterology14 citations Open access
Semantic Scholar
Clinical utility gene card for: Lynch syndrome (MLH1, MSH2, MSH6, PMS2)
N. Rahner, V. Steinke, B. Schlegelberger, S. Olschwang +2 more
2010European Journal of Human Genetics14 citations Open access
Semantic Scholar
Characterisation of heterozygous PMS2 variants in French patients with Lynch syndrome
Qing Wang, J. Leclerc, G. Bougeard, S. Olschwang +8 more
2020Journal of Medical Genetics13 citations
Semantic Scholar
Is the controversy on breast cancer as part of the Lynch-related tumor spectrum still open?
P. Grandval, E. Barouk-Simonet, M. Bronner, M. Buisine +3 more
2012Familial Cancer12 citations
Semantic Scholar
Y253H mutation appearing in a μ-BCR-ABL (e19a2) CML
C. Popovici, A. Charbonnier, O. Gisserot, P. Aguilon +3 more
200812 citations
Semantic Scholar
Duodenal adenocarcinoma and Mut Y human homologue-associated polyposis
B. Buecher, S. Baert-Desurmont, J. Leborgne, Benoît Humeau +2 more
2008European Journal of Gastroenterology and Hepathology12 citations
Semantic Scholar
Pan Aurora Kinase Inhibitor: A Promising Targeted-Therapy in Dedifferentiated Liposarcomas With Differential Efficiency Depending on Sarcoma Molecular Profile
J. Mattei, C. Bouvier‐Labit, Doriane Barets, Nicolas Macagno +8 more
2020Cancers11 citations Open access
Semantic Scholar
SMAD4 protein expression and cell proliferation in colorectal adenocarcinomas
A. Handra-Luca, S. Olschwang, J. Fléjou
2011Virchows Archiv10 citations
Semantic Scholar
High-resolution Genotyping of Chromosome 8 in Colon Adenocarcinomas Reveals Recurrent Break Point But No Gene Mutation in the 8p21 Region
N. Mourra, G. Zeitoun, G. Portier, H. Blanché +6 more
2008Diagnostic molecular pathology (Print)10 citations
Semantic Scholar
Genomic profile of colon cancer metastases.
G. Zeitoun, N. Mourra, Hélène Blanché-Koch, G. Thomas +1 more
2008Anticancer Research10 citations
Semantic Scholar

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