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Petersen, Britt Sabina
103
results:
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english (100)
german (1)
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1
GS-10-A germline mutation in SEMA4D leads to a familial syn..:
Jiang, Xiaojun
;
Bergquist, Annika M
;
Petersen, Britt Sabina
...
Journal of Hepatology. 70 (2019) 1 - p. e46-e47 , 2019
Link:
https://doi.org/10.1016/..
?
2
Author Correction: CEACAM1 regulates TIM-3-mediated toleran..:
Huang, Yu-Hwa
;
Zhu, Chen
;
Kondo, Yasuyuki
...
Nature. 626 (2024) 8001 - p. E19-E19 , 2024
Link:
https://doi.org/10.1038/..
?
3
IL-17A is functionally relevant and a potential therapeutic..:
Chakievska, Lenche
;
Holtsche, Maike M.
;
Künstner, Axel
...
Journal of Autoimmunity. 96 (2019) - p. 104-112 , 2019
Link:
https://doi.org/10.1016/..
?
4
Correction: Insights into the genetic epidemiology of Crohn..:
Rivas, Manuel A.
;
Avila, Brandon E.
;
Koskela, Jukka
...
PLOS Genetics. 15 (2019) 5 - p. e1008190 , 2019
Link:
https://doi.org/10.1371/..
?
5
Identifying Crohn's disease signal from variome analysis:
Wang, Yanran
;
Miller, Maximilian
;
Astrakhan, Yuri
...
Genome Medicine. 11 (2019) 1 - p. , 2019
Link:
https://doi.org/10.1186/..
?
6
First known case of paediatric inflammatory bowel disease i..:
Petersen, Britt-Sabina
;
Bokemeyer, Bernd
;
Wenker, Christian
...
Gut. 69 (2019) 6 - p. 1153-1154 , 2019
Link:
https://doi.org/10.1136/..
?
7
Insights into the genetic epidemiology of Crohn's and rare ..:
Rivas, Manuel A.
;
Avila, Brandon E.
;
Koskela, Jukka
...
PLOS Genetics. 14 (2018) 5 - p. e1007329 , 2018
Link:
https://doi.org/10.1371/..
?
8
Whole-exome sequencing identifies rare genetic variations i..:
Kishore, Amit
;
Petersen, Britt-Sabina
;
Nutsua, Marcel
...
Human Genetics. 137 (2018) 9 - p. 705-716 , 2018
Link:
https://doi.org/10.1007/..
?
9
Exome Sequencing Identifies a Novel MAP3K14 Mutation in Rec..:
Schlechter, Nikola
;
Glanzmann, Brigitte
;
Hoal, Eileen Garner
...
Frontiers in Immunology. 8 (2017) - p. , 2017
Link:
https://doi.org/10.3389/..
?
10
Opportunities and challenges of whole-genome and -exome seq..:
Petersen, Britt-Sabina
;
Fredrich, Broder
;
Hoeppner, Marc P.
..
BMC Genetics. 18 (2017) 1 - p. , 2017
Link:
https://doi.org/10.1186/..
?
11
Exome Analysis of Rare and Common Variants within the NOD S..:
Andreoletti, Gaia
;
Shakhnovich, Valentina
;
Christenson, Kathy
...
Scientific Reports. 7 (2017) 1 - p. , 2017
Link:
https://doi.org/10.1038/..
?
12
Iterative Sequencing and Variant Screening (ISVS) as a nove..:
Lechowicz, Urszula
;
Gambin, Tomasz
;
Pollak, Agnieszka
...
Scientific Reports. 7 (2017) 1 - p. , 2017
Link:
https://doi.org/10.1038/..
?
13
Targeted Gene Panel Sequencing for Early-onset Inflammatory..:
Petersen, Britt-Sabina
;
August, Dietrich
;
Abt, Renate
...
Inflammatory Bowel Diseases. 23 (2017) 12 - p. 2109-2120 , 2017
Link:
https://doi.org/10.1097/..
?
14
Genetic Factors of the Disease Course After Sepsis: Rare De..:
Taudien, Stefan
;
Lausser, Ludwig
;
Giamarellos-Bourboulis, Evangelos J.
...
EBioMedicine. 12 (2016) - p. 227-238 , 2016
Link:
https://doi.org/10.1016/..
?
15
Homozygous SYNE1 mutation causes congenital onset of muscul..:
Baumann, Matthias
;
Steichen-Gersdorf, Elisabeth
;
Krabichler, Birgit
...
European Journal of Human Genetics. 25 (2016) 2 - p. 262-266 , 2016
Link:
https://doi.org/10.1038/..
1-15