Björn Nilsson (Bjorn Nilsson)

Publication Activity (10 Years)

Years Active: 2017-2024
Publications (10 Years): 19

Top Topics

Multiple Myeloma

Dna Methylation

Gene Expression

Top Venues

Nature communications

Blood cancer journal

EMBO molecular medicine

medRxiv : the preprint server for health sciences

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

Publications

Molly Went, Laura Duran-Lozano, Gisli Hreinn Halldorsson, Andrea Gunnell, Nerea Ugidos-Damboriena, Philip J Law, Ludvig Ekdahl, Amit Sud, Gudmar Thorleifsson, Malte Thodberg, Thorunn Asta Olafsdottir, Antton Lamarca-Arrizabalaga, Caterina Cafaro, Abhishek Niroula, Ram Ajore, Aitzkoa Lopez de Lapuente Portilla, Zain Ali, Maroulio Pertesi, Hartmut Goldschmidt, Lilja Stefansdottir, Sigurdur Y Kristinsson, Simon N Stacey, Thorvardur J Love, Saemundur Rognvaldsson, Roman Hájek, Pavel Vodicka, Ulrika Pettersson-Kymmer, Florentin Späth, Carolina D Schinke, Frits Van Rhee, Patrick Sulem, Egil Ferkingstad, Grimur Hjorleifsson Eldjarn, Ulf-Henrik Mellqvist, Ingileif Jónsdóttir, Gareth J Morgan, Pieter Sonneveld, Anders Waage, Niels Weinhold, Hauke Thomsen, Asta Försti, Markus Hansson, Annette Juul Vangsted, Unnur Thorsteinsdottir, Kari Hemminki, Martin F Kaiser, Thorunn Rafnar, Kári Stefánsson, Richard S Houlston, Björn Nilsson
Deciphering the genetics and mechanisms of predisposition to multiple myeloma. Nature communications 15 (1) (2024)
Ram Ajore, Jenny Mattsson, Maroulio Pertesi, Ludvig Ekdahl, Zain Ali, Markus Hansson, Björn Nilsson
Genome-wide CRISPR/Cas9 screen identifies regulators of BCMA expression on multiple myeloma cells. Blood cancer journal 14 (1) (2024)
Ram Ajore, Jenny Mattsson, Maroulio Pertesi, Ludvig Ekdahl, Zain Ali, Markus Hansson, Björn Nilsson
Genome-wide CRISPR/Cas9 screen identifies regulators of BCMA expression on multiple myeloma cells. Blood cancer journal 14 (1) (2024)
Ram Ajore, Jenny Mattsson, Maroulio Pertesi, Ludvig Ekdahl, Zain Ali, Markus Hansson, Björn Nilsson
Genome-wide CRISPR/Cas9 screen identifies regulators of BCMA expression on multiple myeloma cells. Blood cancer journal 14 (1) (2024)
Thorunn Asta Olafsdottir, Gudmar Thorleifsson, Aitzkoa Lopez de Lapuente Portilla, Stefan Jonsson, Lilja Stefansdottir, Abhishek Niroula, Aslaug Jonasdottir, Hannes Petur Eggertsson, Gisli Hreinn Halldorsson, Gudny E Thorlacius, Asgeir O Arnthorsson, Unnur S Bjornsdottir, Folkert W. Asselbergs, Arthur E H Bentlage, Gudmundur I Eyjolfsson, Steinunn Gudmundsdottir, Kristbjorg Gunnarsdottir, Bjarni V Halldórsson, Hilma Hólm, Bjorn R Ludviksson, Pall Melsted, Gudmundur L Norddahl, Isleifur Olafsson, Saedis Saevarsdottir, Olof Sigurdardottir, Asgeir Sigurdsson, Robin Temming, Pall T Önundarson, Unnur Thorsteinsdottir, Gestur Vidarsson, Patrick Sulem, Daníel F Guðbjartsson, Ingileif Jónsdóttir, Björn Nilsson, Kári Stefánsson
Sequence variants influencing the regulation of serum IgG subclass levels. Nature communications 15 (1) (2024)
Ram Ajore, Jenny Mattsson, Maroulio Pertesi, Ludvig Ekdahl, Zain Ali, Markus Hansson, Björn Nilsson
Genome-wide CRISPR/Cas9 screen identifies regulators of BCMA expression on multiple myeloma cells. Blood cancer journal 14 (1) (2024)
Molly Went, Laura Duran-Lozano, Gisli Hreinn Halldorsson, Andrea Gunnell, Nerea Ugidos-Damboriena, Philip J Law, Ludvig Ekdahl, Amit Sud, Gudmar Thorleifsson, Malte Thodberg, Thorunn Asta Olafsdottir, Antton Lamarca-Arrizabalaga, Caterina Cafaro, Abhishek Niroula, Ram Ajore, Aitzkoa Lopez de Lapuente Portilla, Zain Ali, Maroulio Pertesi, Hartmut Goldschmidt, Lilja Stefansdottir, Sigurdur Y Kristinsson, Simon N Stacey, Thorvardur J Love, Saemundur Rognvaldsson, Roman Hájek, Pavel Vodicka, Ulrika Pettersson-Kymmer, Florentin Späth, Carolina D Schinke, Frits Van Rhee, Patrick Sulem, Egil Ferkingstad, Grimur Hjorleifsson Eldjarn, Ulf-Henrik Mellqvist, Ingileif Jónsdóttir, Gareth J Morgan, Pieter Sonneveld, Anders Waage, Niels Weinhold, Hauke Thomsen, Asta Försti, Markus Hansson, Annette Juul Vangsted, Unnur Thorsteinsdottir, Kari Hemminki, Martin F Kaiser, Thorunn Rafnar, Kári Stefánsson, Richard S Houlston, Björn Nilsson
Deciphering the genetics and mechanisms of predisposition to multiple myeloma. Nature communications 15 (1) (2024)
Molly Went, Laura Duran-Lozano, Gisli Hreinn Halldorsson, Andrea Gunnell, Nerea Ugidos-Damboriena, Philip J Law, Ludvig Ekdahl, Amit Sud, Gudmar Thorleifsson, Malte Thodberg, Thorunn Asta Olafsdottir, Antton Lamarca-Arrizabalaga, Caterina Cafaro, Abhishek Niroula, Ram Ajore, Aitzkoa Lopez de Lapuente Portilla, Zain Ali, Maroulio Pertesi, Hartmut Goldschmidt, Lilja Stefansdottir, Sigurdur Y Kristinsson, Simon N Stacey, Thorvardur J Love, Saemundur Rognvaldsson, Roman Hájek, Pavel Vodicka, Ulrika Pettersson-Kymmer, Florentin Späth, Carolina D Schinke, Frits Van Rhee, Patrick Sulem, Egil Ferkingstad, Grimur Hjorleifsson Eldjarn, Ulf-Henrik Mellqvist, Ingileif Jónsdóttir, Gareth J Morgan, Pieter Sonneveld, Anders Waage, Niels Weinhold, Hauke Thomsen, Asta Försti, Markus Hansson, Annette Juul Vangsted, Unnur Thorsteinsdottir, Kari Hemminki, Martin F Kaiser, Thorunn Rafnar, Kári Stefánsson, Richard S Houlston, Björn Nilsson
Deciphering the genetics and mechanisms of predisposition to multiple myeloma. Nature communications 15 (1) (2024)
Asmundur Oddsson, Patrick Sulem, Gardar Sveinbjörnsson, Gudny Anna Arnadottir, Valgerdur Steinthorsdottir, Gisli Hreinn Halldorsson, Bjarni A Atlason, Gudjon R Oskarsson, Hannes Helgason, Henriette Svarre Nielsen, David Westergaard, Juha M Karjalainen, Hildigunnur Katrinardottir, Run Fridriksdottir, Brynjar Orn Jensson, Vinicius Tragante, Egil Ferkingstad, Hákon Jónsson, Sigurjon A Gudjonsson, Doruk Beyter, Kristjan Helgi Swerford Moore, Helga B Thordardottir, Snaedis Kristmundsdottir, Olafur A Stefansson, Solbritt Rantapää Dahlqvist, Ida Elken Sonderby, Maria Didriksen, Pernilla Stridh, Jan Haavik, Laufey Tryggvadottir, Oleksandr Frei, G Bragi Walters, Ingrid Kockum, Henrik Hjalgrim, Thorunn Asta Olafsdottir, Geir Selbaek, Mette Nygaard, Christian Erikstrup, Thorsten Brodersen, Saedis Saevarsdottir, Tomas Olsson, Kaspar Rene Nielsen, Asgeir Haraldsson, Mie Topholm Bruun, Thomas Folkmann Hansen, null null, Thora Steingrimsdottir, Rikke Louise Jacobsen, Rolv Terje Lie, Srdjan Djurovic, Lars Alfredsson, Aitzkoa Lopez de Lapuente Portilla, Soren Brunak, Pall Melsted, Bjarni V Halldórsson, Jona Saemundsdottir, Olafur Th Magnusson, Leonid Padyukov, Karina Banasik, Thorunn Rafnar, Johan Askling, Lars Klareskog, Ole Birger Vesterager Pedersen, Gisli Masson, Karoline Alexandra Havdahl, Björn Nilsson, Ole Andreas Andreassen, Mark Daly, Sisse Rye Ostrowski, Ingileif Jónsdóttir, Hreinn Stefansson, Hilma Hólm, Agnar Helgason, Unnur Thorsteinsdottir, Kári Stefánsson, Daníel F Guðbjartsson
Deficit of homozygosity among 1.52 million individuals and genetic causes of recessive lethality. Nature communications 14 (1) (2023)
Liam David Cato, Rick Li, Henry Y Lu, Fulong Yu, Mariel Wissman, Baraka S Mkumbe, Supachai Ekwattanakit, Patrick Deelen, Liberata Alexander Mwita, Raphael Zozimus Sangeda, Thidarat Suksangpleng, Suchada Riolueang, Paola G Bronson, Dirk S Paul, Emily Kawabata, William John Astle, François Aguet, Kristin G Ardlie, Aitzkoa Lopez de Lapuente Portilla, Guolian Kang, Yingze Zhang, Seyed Mehdi Nouraie, Victor R Gordeuk, Mark T Gladwin, Melanie E Garrett, Allison Elizabeth Ashley-Koch, Marilyn J Telen, Brian S Custer, Shannon Kelly, Carla Dinardo, Ester Cerdeira Sabino, Paula Loureiro, Anna Barbara Carneiro-Proietti, Cláudia Máximo, null null, null null, Adriana Mendez, Angelika Hammerer-Lercher, Vivien A Sheehan, Mitchell J Weiss, Lude H Franke, Björn Nilsson, Adam S Butterworth, Vip Viprakasit, Siana Nkya, Vijay G Sankaran
Genetic regulation of fetal hemoglobin across global populations. medRxiv : the preprint server for health sciences (2023)
Asmundur Oddsson, Patrick Sulem, Gardar Sveinbjörnsson, Gudny Anna Arnadottir, Valgerdur Steinthorsdottir, Gisli Hreinn Halldorsson, Bjarni A Atlason, Gudjon R Oskarsson, Hannes Helgason, Henriette Svarre Nielsen, David Westergaard, Juha M Karjalainen, Hildigunnur Katrinardottir, Run Fridriksdottir, Brynjar Orn Jensson, Vinicius Tragante, Egil Ferkingstad, Hákon Jónsson, Sigurjon A Gudjonsson, Doruk Beyter, Kristjan Helgi Swerford Moore, Helga B Thordardottir, Snaedis Kristmundsdottir, Olafur A Stefansson, Solbritt Rantapää Dahlqvist, Ida Elken Sonderby, Maria Didriksen, Pernilla Stridh, Jan Haavik, Laufey Tryggvadottir, Oleksandr Frei, G Bragi Walters, Ingrid Kockum, Henrik Hjalgrim, Thorunn Asta Olafsdottir, Geir Selbaek, Mette Nygaard, Christian Erikstrup, Thorsten Brodersen, Saedis Saevarsdottir, Tomas Olsson, Kaspar Rene Nielsen, Asgeir Haraldsson, Mie Topholm Bruun, Thomas Folkmann Hansen, null null, Thora Steingrimsdottir, Rikke Louise Jacobsen, Rolv Terje Lie, Srdjan Djurovic, Lars Alfredsson, Aitzkoa Lopez de Lapuente Portilla, Soren Brunak, Pall Melsted, Bjarni V Halldórsson, Jona Saemundsdottir, Olafur Th Magnusson, Leonid Padyukov, Karina Banasik, Thorunn Rafnar, Johan Askling, Lars Klareskog, Ole Birger Vesterager Pedersen, Gisli Masson, Karoline Alexandra Havdahl, Björn Nilsson, Ole Andreas Andreassen, Mark Daly, Sisse Rye Ostrowski, Ingileif Jónsdóttir, Hreinn Stefansson, Hilma Hólm, Agnar Helgason, Unnur Thorsteinsdottir, Kári Stefánsson, Daníel F Guðbjartsson
Publisher Correction: Deficit of homozygosity among 1.52 million individuals and genetic causes of recessive lethality. Nature communications 14 (1) (2023)
Ram Ajore, Abhishek Niroula, Maroulio Pertesi, Caterina Cafaro, Malte Thodberg, Molly Went, Erik L Bao, Laura Duran-Lozano, Aitzkoa Lopez de Lapuente Portilla, Thorunn Asta Olafsdottir, Nerea Ugidos-Damboriena, Olafur Magnusson, Mehmet Kemal Samur, Caleb A Lareau, Gisli Hreinn Halldorsson, Gudmar Thorleifsson, Gudmundur L Norddahl, Kristbjorg Gunnarsdottir, Asta Försti, Hartmut Goldschmidt, Kari Hemminki, Frits van Rhee, Scott Kimber, Adam S Sperling, Martin F Kaiser, Kenneth C Anderson, Ingileif Jónsdóttir, Nikhil C Munshi, Thorunn Rafnar, Anders Waage, Niels Weinhold, Unnur Thorsteinsdottir, Vijay G Sankaran, Kári Stefánsson, Richard S Houlston, Björn Nilsson
Functional dissection of inherited non-coding variation influencing multiple myeloma risk. Nature communications 13 (1) (2022)
Ram Ajore, Abhishek Niroula, Maroulio Pertesi, Caterina Cafaro, Malte Thodberg, Molly Went, Erik L Bao, Laura Duran-Lozano, Aitzkoa Lopez de Lapuente Portilla, Thorunn Asta Olafsdottir, Nerea Ugidos-Damboriena, Olafur Magnusson, Mehmet Kemal Samur, Caleb A Lareau, Gisli Hreinn Halldorsson, Gudmar Thorleifsson, Gudmundur L Norddahl, Kristbjorg Gunnarsdottir, Asta Försti, Hartmut Goldschmidt, Kari Hemminki, Frits van Rhee, Scott Kimber, Adam S Sperling, Martin F Kaiser, Kenneth C Anderson, Ingileif Jónsdóttir, Nikhil C Munshi, Thorunn Rafnar, Anders Waage, Niels Weinhold, Unnur Thorsteinsdottir, Vijay G Sankaran, Kári Stefánsson, Richard S Houlston, Björn Nilsson
Author Correction: Functional dissection of inherited non-coding variation influencing multiple myeloma risk. Nature communications 13 (1) (2022)
Ram Ajore, Abhishek Niroula, Maroulio Pertesi, Caterina Cafaro, Malte Thodberg, Molly Went, Erik L Bao, Laura Duran-Lozano, Aitzkoa Lopez de Lapuente Portilla, Thorunn Asta Olafsdottir, Nerea Ugidos-Damboriena, Olafur Magnusson, Mehmet Kemal Samur, Caleb A Lareau, Gisli Hreinn Halldorsson, Gudmar Thorleifsson, Gudmundur L Norddahl, Kristbjorg Gunnarsdottir, Asta Försti, Hartmut Goldschmidt, Kari Hemminki, Frits van Rhee, Scott Kimber, Adam S Sperling, Martin F Kaiser, Kenneth C Anderson, Ingileif Jónsdóttir, Nikhil C Munshi, Thorunn Rafnar, Anders Waage, Niels Weinhold, Unnur Thorsteinsdottir, Vijay G Sankaran, Kári Stefánsson, Richard S Houlston, Björn Nilsson
Author Correction: Functional dissection of inherited non-coding variation influencing multiple myeloma risk. Nature communications 13 (1) (2022)
Laura Duran-Lozano, Gudmar Thorleifsson, Aitzkoa Lopez de Lapuente Portilla, Abhishek Niroula, Molly Went, Malte Thodberg, Maroulio Pertesi, Ram Ajore, Caterina Cafaro, Pall I Olason, Lilja Stefansdottir, G Bragi Walters, Gisli Hreinn Halldorsson, Ingemar Turesson, Martin F Kaiser, Niels Weinhold, Niels Abildgaard, Niels Frost Andersen, Ulf-Henrik Mellqvist, Anders Waage, Annette Juul Vangsted, Unnur Thorsteinsdottir, Markus Hansson, Richard S Houlston, Thorunn Rafnar, Kari Stefansson, Björn Nilsson
Author Correction: Germline variants at SOHLH2 influence multiple myeloma risk. Blood cancer journal 11 (11) (2021)
Laura Duran-Lozano, Gudmar Thorleifsson, Aitzkoa Lopez de Lapuente Portilla, Abhishek Niroula, Molly Went, Malte Thodberg, Maroulio Pertesi, Ram Ajore, Caterina Cafaro, Pall I Olason, Lilja Stefansdottir, G Bragi Walters, Gisli Hreinn Halldorsson, Ingemar Turesson, Martin F Kaiser, Niels Weinhold, Niels Abildgaard, Niels Frost Andersen, Ulf-Henrik Mellqvist, Anders Waage, Annette Juul Vangsted, Unnur Thorsteinsdottir, Markus Hansson, Richard S Houlston, Thorunn Rafnar, Kari Stefansson, Björn Nilsson
Germline variants at SOHLH2 influence multiple myeloma risk. Blood cancer journal 11 (4) (2021)
Calogerina Catalano, Nagarajan Paramasivam, Joanna Blocka, Sara Giangiobbe, Stefanie Huhn, Matthias Schlesner, Niels Weinhold, Rolf Sijmons, Mirjam de Jong, Christian Langer, Klaus-Dieter Preuss, Björn Nilsson, Brian Durie, Hartmut Goldschmidt, Obul Reddy Bandapalli, Kari Hemminki, Asta Försti
Characterization of rare germline variants in familial multiple myeloma. Blood cancer journal 11 (2) (2021)
Jenny Mattsson, Ludvig Ekdahl, Fredrik Junghus, Ram Ajore, Eva Erlandsson, Abhishek Niroula, Maroulio Pertesi, Björn Frendéus, Ingrid Teige, Björn Nilsson
Accelerating target deconvolution for therapeutic antibody candidates using highly parallelized genome editing. Nature communications 12 (1) (2021)
Ram Ajore, David Raiser, Marie McConkey, Magnus Jöud, Bernd Boidol, Brenton Mar, Gordon Saksena, David M Weinstock, Scott Armstrong, Steven R Ellis, Benjamin L Ebert, Björn Nilsson
Deletion of ribosomal protein genes is a common vulnerability in human cancer, especially in concert with TP53 mutations. EMBO molecular medicine 9 (4) (2017)