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Gabriela Möslein

ResearcherPublications, citations & collaboration network

Gabriela Möslein is a researcher indexed in ScholarIQ from OpenAlex & ORCID.

How many works does Gabriela Möslein have?

ScholarIQindexed works

Gabriela Möslein has 276 works in the ScholarIQ index. The count is the OpenAlex total, not the number of papers listed on this page.

How many citations does Gabriela Möslein have?

ScholarIQcitation count

Gabriela Möslein has 16,289 citations in the OpenAlex counts ScholarIQ stores.

What is the h-index of Gabriela Möslein?

ScholarIQh-index

Gabriela Möslein has an h-index of 58 in OpenAlex.

What is the i10-index of Gabriela Möslein?

ScholarIQi10-index

Gabriela Möslein has an i10-index of 107 in OpenAlex.

What is the ORCID of Gabriela Möslein?

ScholarIQorcid

The ORCID for Gabriela Möslein is on the source record.

What is the OpenAlex record for Gabriela Möslein?

ScholarIQopenalex

The OpenAlex for Gabriela Möslein is on the source record.

What are the most-cited papers on Gabriela Möslein?

ScholarIQmost cited works
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, Jukka‐Pekka Mecklin, Gabriela Möslein, Sylviane Olschwang, Diana Eccles, D. Gareth Evans, Eamonn R. Maher, Lucio Bertario, Marie-Luise Bisgaard, Malcolm G. Dunlop, Judy Ho, Shirley V. Hodgson, Annika Lindblom, Jan Lubiński, Patrick J. Morrison, Victoria Murday, Raj Ramesar, Lucy Side, Rodney J. Scott, Huw Thomas, Hans F. A. Vasen, G Barker, Gillian Crawford, Faye Elliott, Mohammad Movahedi, Kirsi Pylvänäinen, Juul Wijnen, Riccardo Fodde, Henry T. Lynch, John C. Mathers, D. Timothy Bishop
The Lancet. 2011958 CitationsOPEN ACCESS
Peutz–Jeghers syndrome: a systematic review and recommendations for management
Andrew D. Beggs, Andrew Latchford, Hans F. A. Vasen, Gabriela Möslein, Ángel Alonso, Stefan Aretz, Lucio Bertario, Ignacio Blanco, S Bülow, John Burn, Gabriel Capellá, C. Colás, Waltraut Friedl, Pål Møller, Frederik J. Hes, Heikki Järvinen, J-P Mecklin, Fokko M. Nagengast, Yann Parc, R K S Phillips, Warren Hyer, Maurizio Ponz de Leòn, Laura Renkonen‐Sinisalo, Julian R. Sampson, Astrid Stormorken, Sabine Tejpar, H. J. W. Thomas, Juul Wijnen, S. K. Clark, S V Hodgson
Gut. 2010822 CitationsOPEN ACCESS
Revised guidelines for the clinical management of Lynch syndrome (HNPCC): recommendations by a group of European experts
Hans F. A. Vasen, Ignacio Blanco, Katja Aktan–Collan, Jessica P. Gopie, Ángel Alonso, Stefan Aretz, Inge Bernstein, Lucio Bertario, John Burn, Gabriel Capellá, Chrystelle Colas, Christoph Engel, Ian M. Frayling, Maurizio Genuardi, Karl Heinimann, Frederik J. Hes, Shirley V. Hodgson, John A. Karagiannis, Fiona Lalloo, Annika Lindblom, Jukka‐Pekka Mecklin, Pål Møller, T Myrhøj, Fokko M. Nagengast, Yann Parc, Maurizio Ponz de Leòn, Laura Renkonen‐Sinisalo, Julian R. Sampson, Astrid Stormorken, Rolf H. Sijmons, Sabine Tejpar, Huw Thomas, Nils Rahner, Juul Wijnen, Heikki Järvinen, Gabriela Möslein
Gut. 2013749 CitationsOPEN ACCESS
Guidelines for the clinical management of familial adenomatous polyposis (FAP)
Hans F. A. Vasen, Gabriela Möslein, Ángel Alonso, Stefan Aretz, Inge Bernstein, Lucio Bertario, Ignacio Blanco, S Bülow, John Burn, Gabriel Capellá, Chrystelle Colas, Christoph Engel, Ian M. Frayling, Waltraut Friedl, Frederik J. Hes, Shirley Hodgson, Heikki Järvinen, J-P Mecklin, Pål Møller, T. Myrhoi, Fokko M. Nagengast, Yann Parc, R Phillips, Susan K. Clark, Maurizio Ponz de Leòn, Laura Renkonen‐Sinisalo, Julian R. Sampson, Astrid Stormorken, Sabine Tejpar, Huw Thomas, Juul Wijnen
Gut. 2008703 CitationsOPEN ACCESS
Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome Database
Mev Dominguez–Valentin, Julian R. Sampson, Toni T. Seppälä, Sanne W. ten Broeke, John‐Paul Plazzer, Sigve Nakken, Christoph Engel, Stefan Aretz, Mark A. Jenkins, Lone Sunde, Inge Bernstein, Gabriel Capellá, Francesc Balaguer, Huw Thomas, D. Gareth Evans, John Burn, Marc S. Greenblatt, Eivind Hovig, Wouter H. de Vos tot Nederveen Cappel, Rolf H. Sijmons, Lucio Bertario, Maria Grazia Tibiletti, Giulia Martina Cavestro, Annika Lindblom, Adriana Della Valle, Francisco López‐Köstner, Nathan Gluck, Lior H. Katz, Karl Heinimann, Carlos Vaccaro, Reinhard Büttner, Heike Görgens, Elke Holinski‐Feder, Monika Morak, Stefanie Holzapfel, Robert Hüneburg, Magnus von Knebel Doeberitz, Markus Loeffler, Nils Rahner, Hans K. Schackert, Verena Steinke‐Lange, Wolff Schmiegel, Deepak Vangala, Kirsi Pylvänäinen, Laura Renkonen‐Sinisalo, John L. Hopper, Aung Ko Win, Robert W. Haile, Noralane M. Lindor, Steven Gallinger, Loı̈c Le Marchand, Polly A. Newcomb, Jane C. Figueiredo, Stephen N. Thibodeau, Karin Wadt, Christina Therkildsen, Henrik Okkels, Zohreh Ketabi, Leticia Moreira, Ariadna Sánchez, Miquel Serra‐Burriel, Marta Pineda, Matilde Navarro, Ignacio Blanco, Kate Green, Fiona Lalloo, Emma J. Crosbie, James Hill, Oliver G. Denton, Ian M. Frayling, Einar Andreas Rødland, Hans F. A. Vasen, Miriam Mints, Florencia Neffa, Patricia Esperón, Karin Álvarez, Revital Kariv, Guy Rosner, Tamara Alejandra Piñero, María Laura González, Pablo Kalfayan, Douglas Tjandra, Ingrid Winship, Finlay Macrae, Gabriela Möslein, Jukka‐Pekka Mecklin, Maartje Nielsen, Pål Møller
Genetics in Medicine. 2019664 CitationsOPEN ACCESS

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