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Petersen, Britt Sabina
129  results:
Online X
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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