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Petersen, Britt Sabina
26
results:
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1
First known case of paediatric inflammatory bowel disease i..:
Petersen, Britt-Sabina
;
Bokemeyer, Bernd
;
Wenker, Christian
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7282558/. , 2020
Link:
http://www.ncbi.nlm.nih...
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2
Identifying Crohn's disease signal from variome analysis:
Wang, Yanran
;
Miller, Maximilian
;
Astrakhan, Yuri
...
https://mediatum.ub.tum.de/1545258. , 2019
Link:
https://mediatum.ub.tum...
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3
Correction: Insights into the genetic epidemiology of Crohn..:
Manuel A Rivas
;
Brandon E Avila
;
Jukka Koskela
...
https://doi.org/10.1371/journal.pgen.1008190. , 2019
Link:
https://doi.org/10.1371/..
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4
Working toward precision medicine: Predicting phenotypes fr..:
Daneshjou, Roxana
;
Wang, Yanran
;
Bromberg, Yana
...
http://dx.doi.org/10.1002/HUMU.23280. , 2019
Link:
https://hdl.handle.net/1..
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5
Identifying Crohn's disease signal from variome analysis:
Yanran Wang
;
Maximilian Miller
;
Yuri Astrakhan
...
http://link.springer.com/article/10.1186/s13073-019-0670-6. , 2019
Link:
https://doi.org/10.1186/..
?
6
Insights into the genetic epidemiology of Crohn's and rare ..:
Manuel A Rivas
;
Brandon E Avila
;
Jukka Koskela
...
https://doi.org/10.1371/journal.pgen.1007329. , 2018
Link:
https://doi.org/10.1371/..
?
7
Iterative Sequencing and Variant Screening (ISVS) as a nove..:
Urszula Lechowicz
;
Tomasz Gambin
;
Agnieszka Pollak
...
https://doi.org/10.1038/s41598-017-02315-w. , 2017
Link:
https://doi.org/10.1038/..
?
8
Iterative Sequencing and Variant Screening (ISVS) as a nove..:
Lechowicz, Urszula
;
Gambin, Tomasz
;
Pollak, Agnieszka
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5451398/. , 2017
Link:
http://www.ncbi.nlm.nih...
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9
c.207C>G mutation in sepiapterin reductase causes autosomal..:
Shalash, Ali S
;
Rösler, Thomas W
;
Müller, Stefanie H
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5682855/. , 2017
Link:
http://www.ncbi.nlm.nih...
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10
Homozygous SYNE1 mutation causes congenital onset of muscul..:
Baumann, Matthias
;
Steichen-Gersdorf, Elisabeth
;
Krabichler, Birgit
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5255944/. , 2017
Link:
http://www.ncbi.nlm.nih...
?
11
Working toward precision medicine: Predicting phenotypes fr..:
Daneshjou, Roxana
;
Wang, Yanran
;
Bromberg, Yana
...
info:eu-repo/semantics/altIdentifier/pmid/28634997. , 2017
Link:
http://hdl.handle.net/11..
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12
Exome Sequencing Identifies a Novel MAP3K14 Mutation in Rec..:
Nikola Schlechter
;
Brigitte Glanzmann
;
Eileen Garner Hoal
...
http://journal.frontiersin.org/article/10.3389/fimmu.2017.01624/full. , 2017
Link:
https://doi.org/10.3389/..
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13
Exome Sequencing Identifies a Novel MAP3K14 Mutation in Rec..:
Schlechter, Nikola
;
Glanzmann, Brigitte
;
Hoal, Eileen Garner
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5712007/. , 2017
Link:
http://www.ncbi.nlm.nih...
?
14
Exome Sequencing Identifies a Novel MAP3K14 Mutation in Rec..:
Schlechter, Nikola
;
Glanzmann, Brigitte
;
Hoal, Eileen Garner
...
Frontiers in immunology -- 1664-3224. , 2017
Link:
https://doi.org/10.3389/..
?
15
Exome analysis of rare and common variants within the NOD s..:
Andreoletti, Gaia
;
Shakhnovich, Valentina
;
Christenson, Kathy
...
https://eprints.soton.ac.uk/406935/1/Merged_102237_1_art_file_3514266_zhfdw4.pdf. , 2017
Link:
https://eprints.soton.ac..
1-15