Britt‐Sabina Petersen

3.9k citations

24 papers · 885 indexed · h-index 15

Immunology top 10%
- Immunodeficiency and Autoimmune Disorders 7
Genetics top 10%
- Inflammatory Bowel Disease 7
- Genomic variations and chromosomal abnormalities 3
- Genomics and Rare Diseases 2
Hepatology top 10%
Genetics top 10%
- Inflammatory Bowel Disease 7
- Genomic variations and chromosomal abnormalities 3
- Genomics and Rare Diseases 2
Gastroenterology top 10%
Surgery
- Helicobacter pylori-related gastroenterology studies 5
Cancer Research
- Cancer Genomics and Diagnostics 2
Molecular Biology
- RNA Research and Splicing 2
Hematology
- Acute Myeloid Leukemia Research 1

Co-authors: André Franke David Ellinghaus Marc P. Hoeppner Jörn Bethune Stefan Schreiber Björn Stade Sebastian Zeißig Philip Rosenstiel
Cited by: Immunology Genetics Hepatology
Journals: Nucleic Acids Research (1 paper)Blood (1 paper)Gut (3 papers)
Partner nations: Germany United States Austria

In The Last Decade

Britt‐Sabina Petersen

24 papers receiving 876 citations

Peers

Countries citing papers authored by Britt‐Sabina Petersen

Since Specialization

Citations

This map shows the geographic impact of Britt‐Sabina Petersen's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Britt‐Sabina Petersen with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Britt‐Sabina Petersen more than expected).

Fields of papers citing papers by Britt‐Sabina Petersen

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Britt‐Sabina Petersen. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Britt‐Sabina Petersen. The network helps show where Britt‐Sabina Petersen may publish in the future.

Co-authorship network

The 25 scholars most cited alongside Britt‐Sabina Petersen, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Britt‐Sabina Petersen Line = papers co-authored together Britt‐Sabina Petersen links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Identifying Crohn’s disease signal from variome analysis Genome Medicine ·Yanran Wang,Maximilian Miller,Yuri Astrakhan,Britt‐Sabina Petersen,Stefan Schreiber,André Franke,Yana Bromberg	2019	18
2	Whole-exome sequencing identifies rare genetic variations in German families with pulmonary sarcoidosis Human Genetics ·Amit Kishore,Britt‐Sabina Petersen,Marcel Nutsua,Joachim Müller‐Quernheim,André Franke,Annegret Fischer,Stefan Schreiber,Martin Petřek	2018	12
3	IL-17A is functionally relevant and a potential therapeutic target in bullous pemphigoid Journal of Autoimmunity ·Lenche Chakievska,Maike M. Holtsche,Axel Künstner,Stephanie Goletz,Britt‐Sabina Petersen,Diamant Thaçi,Saleh Ibrahim,Ralf J. Ludwig,André Franke,Christian D. Sadik,Detlef Zillikens,Christoph Hölscher,Hauke Busch,Enno Schmidt	2018	78
4	Compound heterozygous mutations in IL10RA combined with a complement factor properdin mutation in infantile-onset inflammatory bowel disease European Journal of Gastroenterology & Hepatology ·Eun Suk Jung,Britt‐Sabina Petersen,Gabriele Mayr,Jae Hee Cheon,Yunkoo Kang,Seok Joo Lee,Xiumei Che,Won Ho Kim,Seung Kim,Stefan Schreiber,André Franke,Hong Koh	2018	5
5	Exome Sequencing Identifies a Novel MAP3K14 Mutation in Recessive Atypical Combined Immunodeficiency Frontiers in Immunology ·Nikola Schlechter,Brigitte Glanzmann,Eileen Garner Hoal,Mardelle Schoeman,Britt‐Sabina Petersen,André Franke,YL Lau,Michael Urban,Paul David van Helden,Monika Esser,Marlo Möller,Craig Kinnear	2017	14
6	Exome Analysis of Rare and Common Variants within the NOD Signaling Pathway Scientific Reports ·Gaia Andreoletti,Valentina Shakhnovich,Kathy Christenson,Tracy Coelho,Rachel Haggarty,Nadeem Afzal,Akshay Batra,Britt‐Sabina Petersen,Matthew Mort,R Mark Beattie,Sarah Ennis	2017	12
7	Opportunities and challenges of whole-genome and -exome sequencing BMC Genetics ·Britt‐Sabina Petersen,Broder Fredrich,Marc P. Hoeppner,David Ellinghaus,André Franke	2017	140
8	Iterative Sequencing and Variant Screening (ISVS) as a novel pathogenic mutations search strategy - application for TMPRSS3 mutations screen Scientific Reports ·Urszula Lechowicz,Tomasz Gambin,Agnieszka Pollak,Anna Podgórska,Piotr Stawiński,André Franke,Britt‐Sabina Petersen,Małgorzata Firczuk,Monika Ołdak,Henryk Skarżyńśki,Rafał Płoski	2017	7
9	c.207C>G mutation in sepiapterin reductase causes autosomal dominant dopa-responsive dystonia Neurology Genetics ·Ali Shalash,Thomas W. Rösler,Stefanie H. Müller,Mohamed Salama,Günther Deuschl,Ulrich Müller,Thomas Opladen,Britt‐Sabina Petersen,Andre Franke,Franziska Hopfner,Gregor Kuhlenbäumer,Günter U. Höglinger	2017	7
10	Homozygous SYNE1 mutation causes congenital onset of muscular weakness with distal arthrogryposis: a genotype–phenotype correlation European Journal of Human Genetics ·Matthias Baumann,Elisabeth Steichen‐Gersdorf,Birgit Krabichler,Britt‐Sabina Petersen,U. Weber,Wolfgang M. Schmidt,Johannes Zschocke,Thomas Müller,Reginald E. Bittner,Andreas Janecke	2016	30
11	Targeted Resequencing and Functional Testing Identifies Low-Frequency Missense Variants in the Gene Encoding GARP as Significant Contributors to Atopic Dermatitis Risk Journal of Investigative Dermatology ·Judith Manz,Elke Rodríguez,Abdou ElSharawy,Eva-Maria Oesau,Britt‐Sabina Petersen,Hansjörg Baurecht,Gabriele Mayr,Susanne Weber,Jürgen Harder,Eva Reischl,Agatha Schwarz,Natalija Novak,André Franke,Stephan Weidinger	2016	29
12	Impaired hepcidin expression in alpha-1-antitrypsin deficiency associated with iron overload and progressive liver disease Human Molecular Genetics ·Benedikt Schaefer,David Haschka,Armin Finkenstedt,Britt‐Sabina Petersen,Igor Theurl,Benjamin Henninger,Andreas Janecke,Chia‐Yu Wang,Herbert Y. Lin,Lothar Veits,Wolfgang Vogel,Günter Weiß,André Franke,Heinz Zoller	2015	22
13	XIAP variants in male Crohn's disease Gut ·Yvonne Zeißig,Britt‐Sabina Petersen,Snezana Milutinovic,Esther Bosse,Gabriele Mayr,Kenneth Peuker,Jelka Hartwig,Andreas Keller,Martina Kohl,Martin W. Laaß,Susanne Billmann-Born,Heide Brandau,Alfred C. Feller,Christoph Röcken,Martin Schrappe,Philip Rosenstiel,John C. Reed,Stefan Schreiber,André Franke,Sebastian Zeißig	2014	103
14	Reduced FOXP3+ regulatory T cells in patients with primary sclerosing cholangitis are associated with IL2RA gene polymorphisms Journal of Hepatology ·Marcial Sebode,Moritz Peiseler,Björn Franke,Dorothee Schwinge,Tanja Schoknecht,Frederike Wortmann,Alexander Quaas,Britt‐Sabina Petersen,Eva Ellinghaus,Udo Baron,Sven Olek,Christiane Wiegard,Christina Weiler‐Normann,Ansgar W. Lohse,Johannes Herkel,Christoph Schramm	2014	84
15	The genetics of Crohn’s disease and ulcerative colitis –status quoand beyond Scandinavian Journal of Gastroenterology ·David Ellinghaus,Jörn Bethune,Britt‐Sabina Petersen,André Franke	2014	67
16	Early-onset Crohn’s disease and autoimmunity associated with a variant in CTLA-4 Gut ·Sebastian Zeißig,Britt‐Sabina Petersen,Michal Tomczak,Espen Melum,Emilie Huc‐Claustre,Stephanie K. Dougan,Jon K. Laerdahl,Björn Stade,Michael Förster,Stefan Schreiber,Dascha C. Weir,Alan M. Leichtner,André Franke,Richard S. Blumberg	2014	96
17	Whole genome and exome sequencing of monozygotic twins discordant for Crohn’s disease BMC Genomics ·Britt‐Sabina Petersen,Martina E. Spehlmann,Andreas Raedler,Björn Stade,Ingo Thomsen,Raquel Rabionet,Philip Rosenstiel,Stefan Schreiber,André Franke	2014	34
18	Analyses of a Pair of Concordant Twins with Infant ALL and Discordant Clinical Outcome Reveals Immunoescape As a Mechanism of Disease Persistence in MLL-Rearranged Leukemia Blood ·Henning Fedders,Ameera Alsadeq,Britt‐Sabina Petersen,Christian Kellner,Matthias Peipp,Thomas Valerius,Robert Haesler,Julia Alten,Anja Möricke,S Strube,Thomas Wiesel,Gunnar Cario,Martin Schrappe,André Franke,Martin Stanulla,Denis M. Schewe	2014	1
19	From next-generation sequencing alignments to accurate comparison and validation of single-nucleotide variants: the pibase software Nucleic Acids Research ·Michael Förster,Peter Forster,Abdou ElSharawy,Georg Hemmrich,Benjamin Kreck,Michael Wittig,Ingo Thomsen,Björn Stade,Matthias Barann,David Ellinghaus,Britt‐Sabina Petersen,Sandra May,Espen Melum,Markus B. Schilhabel,Andreas Keller,Stefan Schreiber,Philip Rosenstiel,André Franke	2012	18
20	Improving mapping and SNP-calling performance in multiplexed targeted next-generation sequencing BMC Genomics ·Abdou ElSharawy,Michael Förster,Nadine Schracke,Andreas Keller,Ingo Thomsen,Britt‐Sabina Petersen,Björn Stade,Peer F. Stähler,Stefan Schreiber,Philip Rosenstiel,André Franke	2012	3

About Britt‐Sabina Petersen

Britt‐Sabina Petersen is a scholar working on Genetics, Immunology and Transplantation, having authored 24 papers that have together received 885 indexed citations. Recurring topics across this work include Immunodeficiency and Autoimmune Disorders (7 papers), Inflammatory Bowel Disease (7 papers), Helicobacter pylori-related gastroenterology studies (5 papers), Genomic variations and chromosomal abnormalities (3 papers), Genomics and Rare Diseases (2 papers), Cancer Genomics and Diagnostics (2 papers), RNA Research and Splicing (2 papers) and Acute Myeloid Leukemia Research (1 paper). The work is most often cited by research in Immunology (269 citations), Genetics (328 citations) and Hepatology (72 citations). Britt‐Sabina Petersen has collaborated with scholars based in Germany, United States and Austria. Frequent co-authors include André Franke, David Ellinghaus, Marc P. Hoeppner, Jörn Bethune, Stefan Schreiber, Björn Stade, Sebastian Zeißig, Philip Rosenstiel, Stefan Schreiber and Gabriele Mayr. Their work appears in journals such as Nucleic Acids Research, Blood and Gut.

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