Marine Guillaud-Bataille

Marine Guillaud-Bataille

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Marine Guillaud-Bataille

Marine Guillaud-Bataille

Publications by authors named "Marine Guillaud-Bataille"

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26Publications

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Large scale multifactorial likelihood quantitative analysis of BRCA1 and BRCA2 variants: An ENIGMA resource to support clinical variant classification.

Authors:
Michael T Parsons Emma Tudini Hongyan Li Eric Hahnen Barbara Wappenschmidt Lidia Feliubadaló Cora M Aalfs Simona Agata Kristiina Aittomäki Elisa Alducci María Concepción Alonso-Cerezo Norbert Arnold Bernd Auber Rachel Austin Jacopo Azzollini Judith Balmaña Elena Barbieri Claus R Bartram Ana Blanco Britta Blümcke Sandra Bonache Bernardo Bonanni Åke Borg Beatrice Bortesi Joan Brunet Carla Bruzzone Karolin Bucksch Giulia Cagnoli Trinidad Caldés Almuth Caliebe Maria A Caligo Mariarosaria Calvello Gabriele L Capone Sandrine M Caputo Ileana Carnevali Estela Carrasco Virginie Caux-Moncoutier Pietro Cavalli Giulia Cini Edward M Clarke Paola Concolino Elisa J Cops Laura Cortesi Fergus J Couch Esther Darder Miguel de la Hoya Michael Dean Irmgard Debatin Jesús Del Valle Capucine Delnatte Nicolas Derive Orland Diez Nina Ditsch Susan M Domchek Véronique Dutrannoy Diana M Eccles Hans Ehrencrona Ute Enders D Gareth Evans Ulrike Faust Ute Felbor Irene Feroce Miriam Fine Henrique C R Galvao Gaetana Gambino Andrea Gehrig Francesca Gensini Anne-Marie Gerdes Aldo Germani Jutta Giesecke Viviana Gismondi Carolina Gómez Encarna B Gómez Garcia Sara González Elia Grau Sabine Grill Eva Gross Aliana Guerrieri-Gonzaga Marine Guillaud-Bataille Sara Gutiérrez-Enríquez Thomas Haaf Karl Hackmann Thomas V O Hansen Marion Harris Jan Hauke Tilman Heinrich Heide Hellebrand Karen N Herold Ellen Honisch Judit Horvath Claude Houdayer Verena Hübbel Silvia Iglesias Angel Izquierdo Paul A James Linda A M Janssen Udo Jeschke Silke Kaulfuß Katharina Keupp Marion Kiechle Alexandra Kölbl Sophie Krieger Torben A Kruse Anders Kvist Fiona Lalloo Mirjam Larsen Vanessa L Lattimore Charlotte Lautrup Susanne Ledig Elena Leinert Alexandra L Lewis Joanna Lim Markus Loeffler Adrià López-Fernández Emanuela Lucci-Cordisco Nicolai Maass Siranoush Manoukian Monica Marabelli Laura Matricardi Alfons Meindl Rodrigo D Michelli Setareh Moghadasi Alejandro Moles-Fernández Marco Montagna Gemma Montalban Alvaro N Monteiro Eva Montes Luigi Mori Lidia Moserle Clemens R Müller Christoph Mundhenke Nadia Naldi Katherine L Nathanson Matilde Navarro Heli Nevanlinna Cassandra B Nichols Dieter Niederacher Henriette R Nielsen Kai-Ren Ong Nicholas Pachter Edenir I Palmero Laura Papi Inge Sokilde Pedersen Bernard Peissel Pedro Pérez-Segura Katharina Pfeifer Marta Pineda Esther Pohl-Rescigno Nicola K Poplawski Berardino Porfirio Anne S Quante Juliane Ramser Rui M Reis Françoise Revillion Kerstin Rhiem Barbara Riboli Julia Ritter Daniela Rivera Paula Rofes Andreas Rump Monica Salinas Ana María Sánchez de Abajo Gunnar Schmidt Ulrike Schoenwiese Jochen Seggewiß Ares Solanes Doris Steinemann Mathias Stiller Dominique Stoppa-Lyonnet Kelly J Sullivan Rachel Susman Christian Sutter Sean V Tavtigian Soo H Teo Alex Teulé Mads Thomassen Maria Grazia Tibiletti Silvia Tognazzo Amanda E Toland Eva Tornero Therese Törngren Sara Torres-Esquius Angela Toss Alison H Trainer Christi J van Asperen Marion T van Mackelenbergh Liliana Varesco Gardenia Vargas-Parra Raymonda Varon Ana Vega Ángela Velasco Anne-Sophie Vesper Alessandra Viel Maaike P G Vreeswijk Sebastian A Wagner Anke Waha Logan C Walker Rhiannon J Walters Shan Wang-Gohrke Bernhard H F Weber Wilko Weichert Kerstin Wieland Lisa Wiesmüller Isabell Witzel Achim Wöckel Emma R Woodward Silke Zachariae Valentina Zampiga Christine Zeder-Göß Conxi Lázaro Arcangela De Nicolo Paolo Radice Christoph Engel Rita K Schmutzler David E Goldgar Amanda B Spurdle

Hum Mutat 2019 May 27. Epub 2019 May 27.

Department of Genetics and Computational Biology, QIMR Berghofer Medical Research Institute, Brisbane, Queensland, Australia.

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http://dx.doi.org/10.1002/humu.23818DOI Listing
May 2019

Multiple skin hamartomata: a possible novel clinical presentation of SUFU neoplasia syndrome.

Fam Cancer 2015 Mar;14(1):151-5

Genetic Medicine and Familial Cancer Centre, Royal Melbourne Hospital, Grattan Street, Parkville, VIC, 3050, Australia,

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http://dx.doi.org/10.1007/s10689-014-9752-1DOI Listing
March 2015

p.Ala541Thr variant of MEN1 gene: a non deleterious polymorphism or a pathogenic mutation?

Ann Endocrinol (Paris) 2014 Jul 2;75(3):133-40. Epub 2014 Jul 2.

UMR 5201 génétique, signalisation et cancer, centre Léon-Bérard, 69008 Lyon, France; Laboratoire de génétique moléculaire, hôpital Édouard-Herriot, bâtiment B7, 69347 Lyon cedex 03, France. Electronic address:

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http://dx.doi.org/10.1016/j.ando.2014.05.003DOI Listing
July 2014

TMEM127 screening in a large cohort of patients with pheochromocytoma and/or paraganglioma.

J Clin Endocrinol Metab 2012 May 14;97(5):E805-9. Epub 2012 Mar 14.

Département de Génétique, Assistance Publique-Hôpitaux de Paris, Hôpital Européen Georges Pompidou, 75015 Paris, France.

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http://dx.doi.org/10.1210/jc.2011-3360DOI Listing
May 2012

The pathophysiology, diagnosis and prognosis of adrenocortical tumors revisited by transcriptome analyses.

Trends Endocrinol Metab 2010 May 25;21(5):325-34. Epub 2010 Jan 25.

Department of Endocrinology, Metabolism and Cancer, Institut Cochin, INSERM U567, University Paris Descartes, CNRS UMR8104, Paris, France.

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http://dx.doi.org/10.1016/j.tem.2009.12.009DOI Listing
May 2010

Mutations and polymorphisms in the gene encoding regulatory subunit type 1-alpha of protein kinase A (PRKAR1A): an update.

Hum Mutat 2010 Apr;31(4):369-79

Section on Endocrinology and Genetics, Program in Developmental Endocrinology & Genetics, Eunice Kennedy Shriver National Institute of Child Health & Human Development, National Institutes of Health, Bethesda, MD 20892, USA.

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http://doi.wiley.com/10.1002/humu.21178
Publisher Site
http://dx.doi.org/10.1002/humu.21178DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2936101PMC
April 2010

Mutations of the gene for the aryl hydrocarbon receptor-interacting protein in pituitary adenomas.

Horm Res 2009 3;71(3):132-41. Epub 2009 Feb 3.

INSERM, U567, Département d'Endocrinologie, Métabolisme et Cancer, CNRSURM8104, Institut Cochin, Université Paris V, Faculté de Médecine René Descartes, Paris, France.

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http://dx.doi.org/10.1159/000197869DOI Listing
May 2009

Expression of C-terminal deleted p53 isoforms in neuroblastoma.

Nucleic Acids Res 2006 5;34(19):5603-12. Epub 2006 Oct 5.

Centre National de Recherche Scientifique, UMR 8126, Institut Gustave Roussy, 94805 Villejuif, France.

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http://dx.doi.org/10.1093/nar/gkl619DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1636465PMC
December 2006

Alternative pathways of MYCN gene copy number increase in primary neuroblastoma tumors.

Cancer Genet Cytogenet 2004 Aug;153(1):10-5

Laboratoire de Génomique Cellulaire des Cancers, Institut Gustave Roussy, Unité Mixte de Recherche 8125, Centre National de la Recherche Scientifique, rue Camille Desmoulins 39, 94805 Villejuif Cedex, France.

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http://dx.doi.org/10.1016/j.cancergencyto.2003.12.007DOI Listing
August 2004

Detecting single DNA copy number variations in complex genomes using one nanogram of starting DNA and BAC-array CGH.

Nucleic Acids Res 2004 Jul 29;32(13):e112. Epub 2004 Jul 29.

Génomique Cellulaire des Cancers, CNRS UMR 8125, Institut Gustave Roussy, 39 rue Camille Desmoulins, 94805 Villejuif Cedex, France.

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http://dx.doi.org/10.1093/nar/gnh108DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC506828PMC
July 2004

[Cytogenetics, cytogenomics and cancer: 2004 update].

Bull Cancer 2004 Jan;91(1):29-43

UMR 8125 CNRS, Institut Gustave-Roussy, Villejuif, France.

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January 2004