Zobrazeno 1 - 10
of 199
pro vyhledávání: '"Ulf, Kristoffersson"'
Autor:
Kristoffer von Stedingk, Karl-Johan Stjernfelt, Anders Kvist, Cecilia Wahlström, Ulf Kristoffersson, Marie Stenmark-Askmalm, Thomas Wiebe, Lars Hjorth, Jan Koster, Håkan Olsson, Ingrid Øra
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-10 (2021)
Abstract Up to 10% of pediatric cancer patients harbor pathogenic germline variants in one or more cancer susceptibility genes. A recent study from the US reported pathogenic variants in 22 out of 60 analyzed autosomal dominant cancer susceptibility
Externí odkaz:
https://doaj.org/article/ed016924109146f38844d6ecd8f06a5b
Publikováno v:
Hereditas, Vol 157, Iss 1, Pp 1-19 (2020)
Abstract Background The Mendelian Society of Lund launched Hereditas in 1920. The purpose of this article is to give an overview of Hereditas’s hundred-year existence, focusing on the conditions for a learned society to publish a scientific journal
Externí odkaz:
https://doaj.org/article/49876da610c0499486820c41973a46e1
Autor:
Andreea Ilinca, Andreas Puschmann, Jukka Putaala, Frank Erik de Leeuw, John Cole, Stephen Kittner, Ulf Kristoffersson, Arne G. Lindgren
Publikováno v:
European Journal of Human Genetics, 31, 2, pp. 239-242
European Journal of Human Genetics, 31, 239-242
European Journal of Human Genetics, 31, 239-242
Contains fulltext : 291290.pdf (Publisher’s version ) (Open Access) This article updates our previous Stroke Gene Panels (SGP) from 2017. Online Mendelian Inheritance in Man and PubMed were searched. We divided detected genes into two SGP groups, S
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::275f94a2565d066fa992a2f05a34d502
https://hdl.handle.net/2066/291290
https://hdl.handle.net/2066/291290
Publikováno v:
Hereditas, Vol 158, Iss 1, Pp 1-1 (2021)
An amendment to this paper has been published and can be accessed via the original article.
Externí odkaz:
https://doaj.org/article/9a51d44b8c634c66adf9f087c7cdb194
Autor:
Håkan Olsson, Ulf Kristoffersson, Hans Ehrencrona, Carolina Ellberg, Annelie Augustinsson, Martin P. Nilsson
Publikováno v:
Breast Cancer Research and Treatment
Purpose In Sweden, a Traceback approach, i.e., a retrospective genetic outreach activity, among cancer patients is not normally used in clinical practice. In this pilot study, we wanted to evaluate a Traceback strategy for possible future clinical im
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4174bf58ec909ff14bd26d0e8aec1d1d
https://doi.org/10.1007/s10549-021-06351-z
https://doi.org/10.1007/s10549-021-06351-z
Publikováno v:
J Community Genet
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::df58efcc7c3518a847e40254b7d49c20
https://europepmc.org/articles/PMC8141078/
https://europepmc.org/articles/PMC8141078/
Autor:
Marie Stenmark-Askmalm, Cecilia Wahlström, Håkan Olsson, Anders Kvist, Ingrid Øra, Jan Koster, Lars Hjorth, Ulf Kristoffersson, Karl Johan Stjernfelt, Thomas Wiebe, Kristoffer von Stedingk
Publikováno v:
Scientific reports, 11(1):5307. Nature Publishing Group
Scientific Reports
Scientific Reports, Vol 11, Iss 1, Pp 1-10 (2021)
Scientific Reports
Scientific Reports, Vol 11, Iss 1, Pp 1-10 (2021)
Up to 10% of pediatric cancer patients harbor pathogenic germline variants in one or more cancer susceptibility genes. A recent study from the US reported pathogenic variants in 22 out of 60 analyzed autosomal dominant cancer susceptibility genes, im
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f3861b623c556b0088d3ec547e1e8f91
https://doi.org/10.1038/s41598-021-84502-4
https://doi.org/10.1038/s41598-021-84502-4
Publikováno v:
Hereditas
Hereditas, Vol 158, Iss 1, Pp 1-1 (2021)
Hereditas, Vol 158, Iss 1, Pp 1-1 (2021)
The Mendelian Society of Lund launched Hereditas in 1920. The purpose of this article is to give an overview of Hereditas's hundred-year existence, focusing on the conditions for a learned society to publish a scientific journal, and the journal's im
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3a40c0eda9d969a371d1bd4c7f87e105
http://europepmc.org/articles/PMC7856806
http://europepmc.org/articles/PMC7856806
Publikováno v:
Public Health Genomics
Swedish national breast cancer guidelines recommend that all women diagnosed with breast cancer (BC) at the age of 35 years or younger should be referred to their regional oncogenetic clinic for genetic counseling and testing, regardless of family hi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6d8b427fdf242507886388904fe600c9
https://europepmc.org/articles/PMC7592930/
https://europepmc.org/articles/PMC7592930/
Autor:
Sofie Samuelsson, Ulf Kristoffersson, Katarina Truvé, Nicolas Martinez-Majander, Andreas Puschmann, Steven J. Kittner, Paul Piccinelli, Turgut Tatlisumak, Arne Lindgren, John W. Cole, Maria Soller, Jukka Putaala, Andreea Ilinca
Publikováno v:
Stroke. 51(4)
Backgrounds and Purpose— Although new methods for genetic analyses are rapidly evolving, there are currently knowledge gaps in how to detect Mendelian forms of stroke. Methods— We performed whole-exome sequencing in 22 probands, under 56 years at
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::87f7c98fa5764020544a4e8a883c3590
https://pubmed.ncbi.nlm.nih.gov/32716824
https://pubmed.ncbi.nlm.nih.gov/32716824