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Petersen, Britt Sabina
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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

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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3

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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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/..
 
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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/..
 
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7

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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8

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/..
 
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9

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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10

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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11

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...
 
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12

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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13

c.207C>G mutation in sepiapterin reductase causes autosomal..:

Shalash, Ali S ; Rösler, Thomas W ; Müller, Stefanie H...
https://mediatum.ub.tum.de/1440347.  , 2017
Link: https://mediatum.ub.tum...
 
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14

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..
 
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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/..
 
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