Anders Kvist

Scopus Author ID ORCID

Publication Activity (10 Years)

Years Active: 2016-2023
Publications (10 Years): 13

Top Venues

Nature communications

Cancers

Nature genetics

Scientific reports

This page only lists publications with an associated author ORCID identifier.

Publications

Naomi Wilcox, Martine Dumont, Anna González-Neira, Sara Carvalho, Charles Joly Beauparlant, Marco Crotti, Craig Luccarini, Penny Soucy, Stéphane Dubois, Rocio Nuñez-Torres, Guillermo Pita, Eugene J Gardner, Joe Dennis, M Rosario Alonso, Nuria Álvarez, Caroline Baynes, Annie Claude Collin-Deschesnes, Sylvie Desjardins, Heiko Becher, Sabine Behrens, Manjeet K Bolla, Jose E Castelao, Jenny Chang-Claude, Sten Cornelissen, Thilo Dörk, Christoph Engel, Manuela Gago-Dominguez, Pascal Guénel, Andreas Hadjisavvas, Eric Hahnen, Mikael Hartman, Belén Herráez, null null, Audrey Jung, Renske Keeman, Marion Kiechle, Jingmei Li, Maria A Loizidou, Michael Lush, Kyriaki Michailidou, Mihalis I Panayiotidis, Xueling S Sim, Soo-Hwang Teo, Jonathan P Tyrer, Lizet E van der Kolk, Cecilia Wahlström, Qin Wang, John R B Perry, Javier Benitez, Marjanka K Schmidt, Rita K Schmutzler, Paul David Peter Pharoah, Arnaud Droit, Alison M Dunning, Anders Kvist, Peter Devilee, Douglas F Easton, Jacques Simard
Author Correction: Exome sequencing identifies breast cancer susceptibility genes and defines the contribution of coding variants to breast cancer risk. Nature genetics (2023)
Gisella Figlioli, Amandine Billaud, Qin Wang, Manjeet K Bolla, Joe G Dennis, Michael Lush, Anders Kvist, Muriel A Adank, Thomas U Ahearn, Natalia N Antonenkova, Päivi Auvinen, Sabine Behrens, Marina Bermisheva, Natalia V Bogdanova, Stig E Bojesen, Bernardo Bonanni, Thomas Brüning, Nicola J Camp, Archie I Campbell, Jose E Castelao, Melissa H Cessna, null Nbcs Collaborators, Kamila Czene, Peter Devilee, Thilo Dörk, Mikael Eriksson, Peter Andreas Fasching, Henrik Flyger, Marike Gabrielson, Manuela Gago-Dominguez, Montserrat García-Closas, Gord Glendon, Encarna B Gómez Garcia, Anna González-Neira, Felix Grassmann, Pascal Guénel, Eric Hahnen, Ute Hamann, Peter Hillemanns, Maartje J Hooning, Reiner Hoppe, Anthony Howell, Keith Humphreys, null kConFab Investigators, Anna Jakubowska, Elza K Khusnutdinova, Vessela N Kristensen, Annika Lindblom, Maria A Loizidou, Jan Lubiński, Arto Mannermaa, Tabea Maurer, Dimitrios Mavroudis, William G Newman, Nadia Obi, Mihalis I Panayiotidis, Paolo Radice, Muhammad Usman Rashid, Valerie Rhenius, Matthias Ruebner, Emmanouil Saloustros, Elinor J Sawyer, Marjanka K Schmidt, Rita K Schmutzler, Mitul Shah, Melissa C Southey, Ian Tomlinson, Thérèse Truong, Elke Maria van Veen, Camilla Wendt, Xiaohong R Yang, Kyriaki Michailidou, Alison M Dunning, Paul David Peter Pharoah, Douglas F Easton, Irene L Andrulis, Dafydd Gareth Evans, Antoinette Hollestelle, Jenny Chang-Claude, Roger L Milne, Paolo Peterlongo
Spectrum and Frequency of Germline FANCM Protein-Truncating Variants in 44,803 European Female Breast Cancer Cases. Cancers 15 (13) (2023)
Naomi Wilcox, Martine Dumont, Anna González-Neira, Sara Carvalho, Charles Joly Beauparlant, Marco Crotti, Craig Luccarini, Penny Soucy, Stéphane Dubois, Rocio Nuñez-Torres, Guillermo Pita, Eugene J Gardner, Joe Dennis, M Rosario Alonso, Nuria Álvarez, Caroline Baynes, Annie Claude Collin-Deschesnes, Sylvie Desjardins, Heiko Becher, Sabine Behrens, Manjeet K Bolla, Jose E Castelao, Jenny Chang-Claude, Sten Cornelissen, Thilo Dörk, Christoph Engel, Manuela Gago-Dominguez, Pascal Guénel, Andreas Hadjisavvas, Eric Hahnen, Mikael Hartman, Belén Herráez, null null, Audrey Jung, Renske Keeman, Marion Kiechle, Jingmei Li, Maria A Loizidou, Michael Lush, Kyriaki Michailidou, Mihalis I Panayiotidis, Xueling S Sim, Soo-Hwang Teo, Jonathan P Tyrer, Lizet E van der Kolk, Cecilia Wahlström, Qin Wang, John R B Perry, Javier Benitez, Marjanka K Schmidt, Rita K Schmutzler, Paul David Peter Pharoah, Arnaud Droit, Alison M Dunning, Anders Kvist, Peter Devilee, Douglas F Easton, Jacques Simard
Exome sequencing identifies breast cancer susceptibility genes and defines the contribution of coding variants to breast cancer risk. Nature genetics (2023)
Angelica A Palm, Joakim Esbjörnsson, Anders Kvist, Fredrik Månsson, Antonio Biague, Hans Norrgren, Marianne Jansson, Patrik Medstrand
Intra-Patient Evolution of HIV-2 Molecular Properties. Viruses 14 (11) (2022)
Sandra Wessman, Beatriz Bohorquez Fuentes, Therese Törngren, Anders Kvist, Georgia Kokaraki, Hanna Menkens, Elisabet Hjerpe, Ythalo Hugo, Tirzah Braz Petta, Åke Borg, Joseph W Carlson
Precision Oncology of High-Grade Ovarian Cancer Defined through Targeted Sequencing. Cancers 13 (20) (2021)
Dominik Glodzik, Ana Bosch, Johan Hartman, Mattias Aine, Johan Vallon-Christersson, Christel Reuterswärd, Anna Karlsson, Shamik Mitra, Emma Niméus, Karolina Holm, Jari Häkkinen, Cecilia Hegardt, Lao H Saal, Christer Larsson, Martin Malmberg, Lisa Rydén, Anna Ehinger, Niklas Loman, Anders Kvist, Hans Ehrencrona, Serena Nik-Zainal, Åke Borg, Johan Staaf
Comprehensive molecular comparison of BRCA1 hypermethylated and BRCA1 mutated triple negative breast cancers. Nature communications 11 (1) (2020)
Martin Lauss, Marco Donia, Katja Harbst, Rikke Andersen, Shamik Mitra, Frida Rosengren, Maryem Salim, Johan Vallon-Christersson, Therese Törngren, Anders Kvist, Markus Ringnér, Inge Marie Svane, Göran Jönsson
Author Correction: Mutational and putative neoantigen load predict clinical benefit of adoptive T cell therapy in melanoma. Nature communications 11 (1) (2020)
Mattias Brofelth, Anna Isinger Ekstrand, Shashank Gour, Ronnie Jansson, My Hedhammar, Björn Elleby, Anders Kvist, Christer Wingren, Ulrika Axelsson, Carl A K Borrebaeck
Multiplex profiling of serum proteins in solution using barcoded antibody fragments and next generation sequencing. Communications biology 3 (1) (2020)
Rita D Brandão, Klaas Mensaert, Irene López-Perolio, Demis Tserpelis, Markos Xenakis, Vanessa L Lattimore, Logan C Walker, Anders Kvist, Ana Vega, Sara Gutiérrez-Enríquez, Orland Diez, null null, Miguel de la Hoya, Amanda B Spurdle, Tim De Meyer, Marinus J Blok
Targeted RNA-seq successfully identifies normal and pathogenic splicing events in breast/ovarian cancer susceptibility and Lynch syndrome genes. International journal of cancer 145 (2) (2019)
Martin Lauss, Marco Donia, Katja Harbst, Rikke Andersen, Shamik Mitra, Frida Rosengren, Maryem Salim, Johan Vallon-Christersson, Therese Törngren, Anders Kvist, Markus Ringnér, Inge Marie Svane, Göran Jönsson
Mutational and putative neoantigen load predict clinical benefit of adoptive T cell therapy in melanoma. Nature communications 8 (1) (2017)
Helena Persson, Rolf Søkilde, Jari Häkkinen, Anna Chiara Pirona, Johan Vallon-Christersson, Anders Kvist, Fredrik Mertens, Åke Borg, Felix Mitelman, Mattias Höglund, Carlos Rovira
Frequent miRNA-convergent fusion gene events in breast cancer. Nature communications 8 (1) (2017)
Tuomo Mantere, Anna Tervasmäki, Anna Nurmi, Katrin Rapakko, Saila Kauppila, Jiangbo Tang, Johanna Schleutker, Anne Kallioniemi, Jaana M Hartikainen, Arto Mannermaa, Pentti Nieminen, Riitta Hanhisalo, Sini Lehto, Maija Suvanto, Mervi Grip, Arja Jukkola-Vuorinen, Maria Tengström, Päivi Auvinen, Anders Kvist, Åke Borg, Carl Blomqvist, Kristiina Aittomäki, Roger A Greenberg, Robert Winqvist, Heli Nevanlinna, Katri Pylkäs
Case-control analysis of truncating mutations in DNA damage response genes connects TEX15 and FANCD2 with hereditary breast cancer susceptibility. Scientific reports 7 (1) (2017)
Justyna Rak, Katie Foster, Katarzyna Potrzebowska, Mehrnaz Safaee Talkhoncheh, Natsumi Miharada, Karolina Komorowska, Therese Torngren, Anders Kvist, Åke Borg, Lena M Svensson, Dominique Bonnet, Jonas Larsson
Cytohesin 1 regulates homing and engraftment of human hematopoietic stem and progenitor cells. Blood 129 (8) (2016)

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Publication Activity (10 Years)

Top Topics

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Anders Kvist