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Jukka‐Pekka Mecklin

ResearcherPublications, citations & collaboration network

Jukka‐Pekka Mecklin is a researcher indexed in ScholarIQ from OpenAlex & ORCID.

How many works does Jukka‐Pekka Mecklin have?

ScholarIQindexed works

Jukka‐Pekka Mecklin has 504 works in the ScholarIQ index. The count is the OpenAlex total, not the number of papers listed on this page.

How many citations does Jukka‐Pekka Mecklin have?

ScholarIQcitation count

Jukka‐Pekka Mecklin has 44,179 citations in the OpenAlex counts ScholarIQ stores.

What is the h-index of Jukka‐Pekka Mecklin?

ScholarIQh-index

Jukka‐Pekka Mecklin has an h-index of 95 in OpenAlex.

What is the i10-index of Jukka‐Pekka Mecklin?

ScholarIQi10-index

Jukka‐Pekka Mecklin has an i10-index of 251 in OpenAlex.

What is the ORCID of Jukka‐Pekka Mecklin?

ScholarIQorcid

The ORCID for Jukka‐Pekka Mecklin is on the source record.

What is the OpenAlex record for Jukka‐Pekka Mecklin?

ScholarIQopenalex

The OpenAlex for Jukka‐Pekka Mecklin is on the source record.

What are the most-cited papers on Jukka‐Pekka Mecklin?

ScholarIQmost cited works
Mutations of a mutS homolog in hereditary nonpolyposis colorectal cancer
Fredrick S. Leach, Nicholas C. Nicolaides, Nickolas Papadopoulos, Bo Liu, Jin Jen, Ramon Parsons, Païvi Peltomäki, Pertti Sistonen, Lauri A. Aaltonen, Minna Nyström, Xin‐Yuan Guan, Ji Zhang, Paul S. Meltzer, Jingwei Yu, Fa‐Ten Kao, David J. Chen, Karen Cerosaletti, R. E. K. Fournier, S. Todd, Tracey Lewis, Robin J. Leach, Susan L. Naylor, Jean Weissenbach, Jukka‐Pekka Mecklin, Heikki Järvinen, Gloria M. Petersen, Stanley R. Hamilton, Jane Green, Jeremy R. Jass, Patrice Watson, Henry T. Lynch, Jeffrey M. Trent, Albert de la Chapelle, Kenneth W. Kinzler, Bert Vogelstein
Cell. 19932,286 Citations
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
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
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
Cancer risk and survival in <i>path_MMR</i> carriers by gene and gender up to 75 years of age: a report from the Prospective Lynch Syndrome Database
Pål Møller, Toni T. Seppälä, Inge Bernstein, Elke Holinski‐Feder, Paulo Sala, D. Gareth Evans, Annika Lindblom, Finlay Macrae, Ignacio Blanco, Rolf H. Sijmons, Jacqueline Jeffries, Hans F. A. Vasen, John Burn, Sigve Nakken, Eivind Hovig, Einar Andreas Rødland, Kukatharmini Tharmaratnam, Wouter H. de Vos tot Nederveen Cappel, James Hill, Juul Wijnen, Mark A. Jenkins, Kate Green, Fiona Lalloo, Lone Sunde, Miriam Mints, Lucio Bertario, Marta Pineda, Matilde Navarro, Monika Morak, Laura Renkonen‐Sinisalo, Mev Dominguez–Valentin, Ian M. Frayling, John‐Paul Plazzer, Kirsi Pylvänäinen, Maurizio Genuardi, Jukka‐Pekka Mecklin, Gabriela Moeslein, Julian R. Sampson, Gabriel Capellá
Gut. 2017582 CitationsOPEN ACCESS

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