Search

Author/Creator Wirta, Valtteri

1. Bioinformatory‐assisted analysis of next‐generation sequencing data for precision medicine in pancreatic cancer. Issue 10 (8th August 2017)

Authors:
Malgerud, Linnéa; Lindberg, Johan; Wirta, Valtteri; Gustafsson‐Liljefors, Maria; Karimi, Masoud; Moro, Carlos Fernández; Stecker, Katrin; Picker, Alexander; Huelsewig, Carolin; Stein, Martin; Bohnert, Regina; Del Chiaro, Marco; Haas, Stephan L.; Heuchel, Rainer L.; Permert, Johan; Maeurer, Markus...
Journal:
Molecular oncology
Issue:
Volume 11:Issue 10(2017)
Page Start:
1413
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

2. Bioinformatory‐assisted analysis of next‐generation sequencing data for precision medicine in pancreatic cancer. Issue 10 (8th August 2017)

Authors:
Malgerud, Linnéa; Lindberg, Johan; Wirta, Valtteri; Gustafsson‐Liljefors, Maria; Karimi, Masoud; Moro, Carlos Fernández; Stecker, Katrin; Picker, Alexander; Huelsewig, Carolin; Stein, Martin; Bohnert, Regina; Chiaro, Marco Del; Haas, Stephan L.; Heuchel, Rainer L.; Permert, Johan; Maeurer, Markus...
Journal:
Molecular oncology
Issue:
Volume 11:Issue 10(2017)
Page Start:
1413
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

3. Building a precision medicine infrastructure at a national level: The Swedish experience. (27th February 2023)

Authors:
Edsjö, Anders; Lindstrand, Anna; Gisselsson, David; Mölling, Paula; Friedman, Mikaela; Cavelier, Lucia; Johansson, Maria; Ehrencrona, Hans; Fagerqvist, Therese; Strid, Tobias; Lovmar, Lovisa; Jacobsson, Bo; Johansson, Åsa; Engstrand, Lars; Wheelock, Craig E.; Sikora, Per; Wirta, Valtteri; Fioreto...
Journal:
Cambridge prisms
Issue:
Volume 1(2023)
Page Start:
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

4. CTNND2—a candidate gene for reading problems and mild intellectual disability. Issue 2 (3rd December 2014)

Authors:
Hofmeister, Wolfgang; Nilsson, Daniel; Topa, Alexandra; Anderlid, Britt-Marie; Darki, Fahimeh; Matsson, Hans; Tapia Páez, Isabel; Klingberg, Torkel; Samuelsson, Lena; Wirta, Valtteri; Vezzi, Francesco; Kere, Juha; Nordenskjöld, Magnus; Syk Lundberg, Elisabeth; Lindstrand, Anna
Journal:
Journal of medical genetics
Issue:
Volume 52:Issue 2(2015)
Page Start:
111
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

5. PatientMatcher: A customizable Python‐based open‐source tool for matching undiagnosed rare disease patients via the Matchmaker Exchange network. Issue 6 (7th March 2022)

Authors:
Rasi, Chiara; Nilsson, Daniel; Magnusson, Måns; Lesko, Nicole; Lagerstedt‐Robinson, Kristina; Wedell, Anna; Lindstrand, Anna; Wirta, Valtteri; Stranneheim, Henrik
Other Names:
Boycott Kym guestEditor.; Hamosh Ada guestEditor.; Rehm Heidi guestEditor.
Journal:
Human mutation
Issue:
Volume 43:Issue 6(2022)
Page Start:
708
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

6. Trailblazing precision medicine in Europe: A joint view by Genomic Medicine Sweden and the Centers for Personalized Medicine, ZPM, in Germany. (September 2022)

Authors:
Stenzinger, Albrecht; Edsjö, Anders; Ploeger, Carolin; Friedman, Mikaela; Fröhling, Stefan; Wirta, Valtteri; Seufferlein, Thomas; Botling, Johan; Duyster, Justus; Akhras, Michael; Thimme, Robert; Fioretos, Thoas; Bitzer, Michael; Cavelier, Lucia; Schirmacher, Peter; Malek, Nisar; Rosenquist, Rich...
Journal:
Seminars in cancer biology
Issue:
Volume 84(2022)
Page Start:
242
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

7. Whole‐Genome Sequencing of Cytogenetically Balanced Chromosome Translocations Identifies Potentially Pathological Gene Disruptions and Highlights the Importance of Microhomology in the Mechanism of Formation. Issue 2 (5th December 2016)

Authors:
Nilsson, Daniel; Pettersson, Maria; Gustavsson, Peter; Förster, Alisa; Hofmeister, Wolfgang; Wincent, Josephine; Zachariadis, Vasilios; Anderlid, Britt‐Marie; Nordgren, Ann; Mäkitie, Outi; Wirta, Valtteri; Käller, Max; Vezzi, Francesco; Lupski, James R; Nordenskjöld, Magnus; Syk Lundberg, Elisabe...
Journal:
Human mutation
Issue:
Volume 38:Issue 2(2017)
Page Start:
180
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗