All papers authored by Patrick Sulem
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2021
Astros T.-H. Skuladottir 
,
Gyda Bjornsdottir,
Muhammad Sulaman Nawaz ,
Hannes Petersen,
Solvi Rognvaldsson ,
Kristjan Helgi Swerford Moore ,
Pall I. Olafsson,
Sigurður H. Magnusson ,
Anna Bjornsdottir,
Olafur A. Sveinsson,
Gudrun R. Sigurdardottir,
Saedis Saevarsdottir ,
Erna V. Ivarsdottir ,
Lilja Stefansdottir,
Bjarni Gunnarsson
and 16 other authors
,
Gyda Bjornsdottir,
Muhammad Sulaman Nawaz ,
Hannes Petersen,
Solvi Rognvaldsson ,
Kristjan Helgi Swerford Moore ,
Pall I. Olafsson,
Sigurður H. Magnusson ,
Anna Bjornsdottir,
Olafur A. Sveinsson,
Gudrun R. Sigurdardottir,
Saedis Saevarsdottir ,
Erna V. Ivarsdottir ,
Lilja Stefansdottir,
Bjarni Gunnarsson
and 16 other authors
A genome-wide meta-analysis uncovers six sequence variants conferring risk of vertigo
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2020
Ioanna Ntalla,
Lu-Chen Weng ,
James H. Cartwright,
Amelia Weber Hall ,
Gardar Sveinbjornsson,
Nathan R. Tucker ,
Seung Hoan Choi,
Mark D. Chaffin ,
Carolina Roselli ,
Michael R. Barnes ,
Borbala Mifsud ,
Helen R. Warren,
Caroline Hayward ,
Jonathan Marten,
James J. Cranley
and 172 other authors
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,
James H. Cartwright,
Amelia Weber Hall ,
Gardar Sveinbjornsson,
Nathan R. Tucker ,
Seung Hoan Choi,
Mark D. Chaffin ,
Carolina Roselli ,
Michael R. Barnes ,
Borbala Mifsud ,
Helen R. Warren,
Caroline Hayward ,
Jonathan Marten,
James J. Cranley
and 172 other authors
Download from doi.org
2019
David W. Clark ,
Yukinori Okada ,
Kristjan H. S. Moore ,
Dan Mason ,
Nicola Pirastu ,
Ilaria Gandin ,
Hannele Mattsson,
Catriona L. K. Barnes,
Kuang Lin,
Jing Hua Zhao,
Patrick Deelen ,
Rebecca Rohde,
Claudia Schurmann ,
Xiuqing Guo,
Franco Giulianini
and 421 other authors
,
Yukinori Okada ,
Kristjan H. S. Moore ,
Dan Mason ,
Nicola Pirastu ,
Ilaria Gandin ,
Hannele Mattsson,
Catriona L. K. Barnes,
Kuang Lin,
Jing Hua Zhao,
Patrick Deelen ,
Rebecca Rohde,
Claudia Schurmann ,
Xiuqing Guo,
Franco Giulianini
and 421 other authors
Associations of autozygosity with a broad range of human phenotypes
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2017
Gudny A. Arnadottir,
Brynjar O. Jensson,
Sigurdur E. Marelsson,
Gerald Sulem,
Asmundur Oddsson,
Ragnar P. Kristjansson,
Stefania Benonisdottir,
Sigurjon A. Gudjonsson,
Gisli Masson,
Gudmundur A. Thorisson,
Jona Saemundsdottir,
Olafur T.-H. Magnusson,
Adalbjorg Jonasdottir,
Aslaug Jonasdottir,
Asgeir Sigurdsson
and 5 other authors
Compound heterozygous mutations in UBA5 causing early-onset epileptic encephalopathy in two sisters
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Stefan Jonsson ,
Gardar Sveinbjornsson,
Aitzkoa Lopez de Lapuente Portilla,
Bhairavi Swaminathan,
Rosina Plomp,
Gillian Dekkers ,
Ram Ajore,
Mina Ali,
Arthur E. H. Bentlage,
Evelina Elmér,
Gudmundur I. Eyjolfsson,
Sigurjon A. Gudjonsson,
Urban Gullberg,
Arnaldur Gylfason,
Bjarni V. Halldorsson
and 23 other authors
,
Gardar Sveinbjornsson,
Aitzkoa Lopez de Lapuente Portilla,
Bhairavi Swaminathan,
Rosina Plomp,
Gillian Dekkers ,
Ram Ajore,
Mina Ali,
Arthur E. H. Bentlage,
Evelina Elmér,
Gudmundur I. Eyjolfsson,
Sigurjon A. Gudjonsson,
Urban Gullberg,
Arnaldur Gylfason,
Bjarni V. Halldorsson
and 23 other authors
Identification of sequence variants influencing immunoglobulin levels
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Unnur Styrkarsdottir ,
Hannes Helgason,
Asgeir Sigurdsson,
Gudmundur L. Norddahl,
Arna B. Agustsdottir,
Louise N. Reynard,
Amanda Villalvilla ,
Gisli H. Halldorsson,
Aslaug Jonasdottir,
Audur Magnusdottir,
Asmundur Oddson ,
Gerald Sulem,
Florian Zink,
Gardar Sveinbjornsson,
Agnar Helgason
and 33 other authors
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,
Hannes Helgason,
Asgeir Sigurdsson,
Gudmundur L. Norddahl,
Arna B. Agustsdottir,
Louise N. Reynard,
Amanda Villalvilla ,
Gisli H. Halldorsson,
Aslaug Jonasdottir,
Audur Magnusdottir,
Asmundur Oddson ,
Gerald Sulem,
Florian Zink,
Gardar Sveinbjornsson,
Agnar Helgason
and 33 other authors
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2015
K. de Lange,
K. de Lane,
Manuel A. Rivas,
Daniel Graham,
Patrick Sulem ,
Christine Stevens,
A. Nicole Desch,
A. Nicole Desch,
Philippe Goyette,
Daniel Gudbjartsson ,
Ingileif Jonsdottir,
Mauro D’amato,
Soren Mucha,
Unnur Thorsteinsdottir,
Frauke Degenhardt
and 83 other authors
,
Christine Stevens,
A. Nicole Desch,
A. Nicole Desch,
Philippe Goyette,
Daniel Gudbjartsson ,
Ingileif Jonsdottir,
Mauro D’amato,
Soren Mucha,
Unnur Thorsteinsdottir,
Frauke Degenhardt
and 83 other authors
A protein truncating R179X variant in RNF186 confers protection against ulcerative colitis
Download from dx.doi.org
Reedik Mägi,
Kathryn L. Lunetta,
Daphne L. van der A.,
Yvonne T. van der Schouw ,
Felix R. Day ,
Patrick Sulem ,
Katherine S. Ruth,
Joyce Y. Tung,
David A. Hinds,
Tõnu Esko,
Doris Stockl,
Cathy E. Elks,
Chunyan He,
Elisabeth Altmaier,
Jennifer E. Huffman
and 124 other authors
,
Felix R. Day ,
Patrick Sulem ,
Katherine S. Ruth,
Joyce Y. Tung,
David A. Hinds,
Tõnu Esko,
Doris Stockl,
Cathy E. Elks,
Chunyan He,
Elisabeth Altmaier,
Jennifer E. Huffman
and 124 other authors
Rare coding variants and X-linked loci associated with age at menarche
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Bhairavi Swaminathan,
Gudmar Thorleifsson,
Magnus Jöud,
Mina Ali,
Ellinor Johnsson,
Ram Ajore,
Patrick Sulem ,
Britt-Marie Halvarsson,
Guðmundur I. Eyjolfsson,
Vilhelmina Haraldsdottir,
Christina Hultman,
Erik Ingelsson,
Sigurdur Y. Kristinsson,
Anna K. Kahler,
Anna Katarina Kähler
and 22 other authors
,
Britt-Marie Halvarsson,
Guðmundur I. Eyjolfsson,
Vilhelmina Haraldsdottir,
Christina Hultman,
Erik Ingelsson,
Sigurdur Y. Kristinsson,
Anna K. Kahler,
Anna Katarina Kähler
and 22 other authors
Variants in ELL2 influencing immunoglobulin levels associate with multiple myeloma
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Aree Witoelar,
Stacy Steinberg,
Linda R. White,
Lars Tjelta Westlye ,
Thorlakur Jonsson,
Hreinn Stefansson,
Hrefna Johannsdottir,
T. Jonsson,
Andres Ingason,
Olafur Th Magnusson,
Sigurjon A. Gudjonsson,
Hannes Helgason,
Sigurjon A. Gudjunsson,
Patrick Sulem ,
James J. Lah
and 35 other authors
,
Thorlakur Jonsson,
Hreinn Stefansson,
Hrefna Johannsdottir,
T. Jonsson,
Andres Ingason,
Olafur Th Magnusson,
Sigurjon A. Gudjonsson,
Hannes Helgason,
Sigurjon A. Gudjunsson,
Patrick Sulem ,
James J. Lah
and 35 other authors
Loss-of-function variants in ABCA7 confer risk of Alzheimer's disease
Download from brage.bibsys.no
2014
Martin Hrabé de Angelis,
Martijn van de Bunt,
Steven Wiltshire,
Sungho Won,
Andrew Wood,
Wang Xu,
Joon Yoon,
Matthew Zawistowski,
Eleftheria Zeggini,
Weihua Zhang,
Sebastian Zöllner,
James G. Wilson,
Sara Willems,
Amy Williams,
Tiinamaija Toumi
and 219 other authors
Loss-of-function mutations in SLC30A8 protect against type 2 diabetes
Download from www.ncbi.nlm.nih.gov
Valgerdur Steinthorsdottir,
Gudmar Thorleifsson,
Patrick Sulem ,
Hannes Helgason,
Niels Grarup ,
Asgeir Sigurdsson,
Hafdis T. Helgadottir,
Hrefna Johannsdottir,
Olafur T. Magnusson,
Sigurjon A. Gudjonsson,
Johanne M. Justesen ,
Marie N. Harder,
Marit E. Jørgensen,
Cramer Christensen,
Ivan Brandslund
and 19 other authors
Download from www.researchgate.net
,
Hannes Helgason,
Niels Grarup ,
Asgeir Sigurdsson,
Hafdis T. Helgadottir,
Hrefna Johannsdottir,
Olafur T. Magnusson,
Sigurjon A. Gudjonsson,
Johanne M. Justesen ,
Marie N. Harder,
Marit E. Jørgensen,
Cramer Christensen,
Ivan Brandslund
and 19 other authors
Download from www.researchgate.net
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