A citation-based method for searching scientific literature

Helmut Fuchs, Valérie Gailus-Durner, Thure Adler, Juan Antonio Aguilar-Pimentel, Lore Becker, Julia Calzada-Wack, Patricia Da Silva-Buttkus, Frauke Neff, Alexander Götz, Wolfgang Hans, Sabine M Hölter, Marion Horsch, Gabi Kastenmüller, Elisabeth Kemter, Christoph Lengger, Holger Maier, Mikolaj Matloka, Gabriele Möller, Beatrix Naton, Cornelia Prehn, Oliver Puk, Ildikó Rácz, Birgit Rathkolb, Werner Römisch-Margl, Jan Rozman, Rui Wang-Sattler, Anja Schrewe, Claudia Stöger, Monica Tost, Jerzy Adamski, Bernhard Aigner, Johannes Beckers, Heidrun Behrendt, Dirk H Busch, Irene Esposito, Jochen Graw, Thomas Illig, Boris Ivandic, Martin Klingenspor, Thomas Klopstock, Elisabeth Kremmer, Martin Mempel, Susanne Neschen, Markus Ollert, Holger Schulz, Karsten Suhre, Eckhard Wolf, Wolfgang Wurst, Andreas Zimmer, Martin Hrabě de Angelis. Methods 2011
Times Cited: 97







List of co-cited articles
348 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


Introducing the German Mouse Clinic: open access platform for standardized phenotyping.
Valérie Gailus-Durner, Helmut Fuchs, Lore Becker, Ines Bolle, Markus Brielmeier, Julia Calzada-Wack, Ralf Elvert, Nicole Ehrhardt, Claudia Dalke, Tobias J Franz,[...]. Nat Methods 2005
138
49

Systemic first-line phenotyping.
Valérie Gailus-Durner, Helmut Fuchs, Thure Adler, Antonio Aguilar Pimentel, Lore Becker, Ines Bolle, Julia Calzada-Wack, Claudia Dalke, Nicole Ehrhardt, Barbara Ferwagner,[...]. Methods Mol Biol 2009
60
55

Innovations in phenotyping of mouse models in the German Mouse Clinic.
Helmut Fuchs, Valérie Gailus-Durner, Susanne Neschen, Thure Adler, Luciana Caminha Afonso, Juan Antonio Aguilar-Pimentel, Lore Becker, Alexander Bohla, Julia Calzada-Wack, Christian Cohrs,[...]. Mamm Genome 2012
34
58

The German Mouse Clinic: a platform for systemic phenotype analysis of mouse models.
H Fuchs, V Gailus-Durner, T Adler, J A Aguilar Pimentel, L Becker, I Bolle, M Brielmeier, J Calzada-Wack, C Dalke, N Ehrhardt,[...]. Curr Pharm Biotechnol 2009
40
45

Reliability, robustness, and reproducibility in mouse behavioral phenotyping: a cross-laboratory study.
Silvia Mandillo, Valter Tucci, Sabine M Hölter, Hamid Meziane, Mumna Al Banchaabouchi, Magdalena Kallnik, Heena V Lad, Patrick M Nolan, Abdel-Mouttalib Ouagazzal, Emma L Coghill,[...]. Physiol Genomics 2008
163
15

Genome-wide, large-scale production of mutant mice by ENU mutagenesis.
M H Hrabé de Angelis, H Flaswinkel, H Fuchs, B Rathkolb, D Soewarto, S Marschall, S Heffner, W Pargent, K Wuensch, M Jung,[...]. Nat Genet 2000
498
13

Systematic gene expression profiling of mouse model series reveals coexpressed genes.
Marion Horsch, Sandra Schädler, Valerie Gailus-Durner, Helmut Fuchs, Helmut Meyer, Martin Hrabé de Angelis, Johannes Beckers. Proteomics 2008
26
38

EMPReSS: standardized phenotype screens for functional annotation of the mouse genome.
S D M Brown, P Chambon, M Hrabé de Angelis. Nat Genet 2005
121
9

Behavioral and functional analysis of mouse phenotype: SHIRPA, a proposed protocol for comprehensive phenotype assessment.
D C Rogers, E M Fisher, S D Brown, J Peters, A J Hunter, J E Martin. Mamm Genome 1997
565
9

Towards better mouse models: enhanced genotypes, systemic phenotyping and envirotype modelling.
Johannes Beckers, Wolfgang Wurst, Martin Hrabé de Angelis. Nat Rev Genet 2009
65
13

Clinical Chemistry and Other Laboratory Tests on Mouse Plasma or Serum.
Birgit Rathkolb, Wolfgang Hans, Cornelia Prehn, Helmut Fuchs, Valérie Gailus-Durner, Bernhard Aigner, Jerzy Adamski, Eckhard Wolf, Martin Hrabě de Angelis. Curr Protoc Mouse Biol 2013
26
34

High-throughput mouse phenotyping.
Hilary Gates, Ann-Marie Mallon, Steve D M Brown. Methods 2011
23
30

Significance analysis of microarrays applied to the ionizing radiation response.
V G Tusher, R Tibshirani, G Chu. Proc Natl Acad Sci U S A 2001
7

Screening for dysmorphological abnormalities--a powerful tool to isolate new mouse mutants.
H Fuchs, K Schughart, E Wolf, R Balling, M Hrabé de Angelis. Mamm Genome 2000
32
18

EuroPhenome: a repository for high-throughput mouse phenotyping data.
Hugh Morgan, Tim Beck, Andrew Blake, Hilary Gates, Niels Adams, Guillaume Debouzy, Sophie Leblanc, Christoph Lengger, Holger Maier, David Melvin,[...]. Nucleic Acids Res 2010
56
10

Systematic, standardized and comprehensive neurological phenotyping of inbred mice strains in the German Mouse Clinic.
Ilka Schneider, Werner S Tirsch, Theresa Faus-Kessler, Lore Becker, Eva Kling, Rose-Leah Austin Busse, Andreas Bender, Berend Feddersen, Johannes Tritschler, Helmut Fuchs,[...]. J Neurosci Methods 2006
27
22

ENU mutagenesis, a way forward to understand gene function.
Abraham Acevedo-Arozena, Sara Wells, Paul Potter, Michelle Kelly, Roger D Cox, Steve D M Brown. Annu Rev Genomics Hum Genet 2008
113
6

Recommendations for the health monitoring of rodent and rabbit colonies in breeding and experimental units.
W Nicklas, P Baneux, R Boot, T Decelle, A A Deeny, M Fumanelli, B Illgen-Wilcke. Lab Anim 2002
387
6

Generation of N-ethyl-N-nitrosourea-induced mouse mutants with deviations in hematological parameters.
Bernhard Aigner, Birgit Rathkolb, Martina Klempt, Sibylle Wagner, Dian Michel, Matthias Klaften, Jürgen Laufs, Boris Schneider, Reinhard Sedlmeier, Martin Hrabé de Angelis,[...]. Mamm Genome 2011
18
33

Novel missense mutation of uromodulin in mice causes renal dysfunction with alterations in urea handling, energy, and bone metabolism.
Elisabeth Kemter, Birgit Rathkolb, Jan Rozman, Wolfgang Hans, Anja Schrewe, Christina Landbrecht, Matthias Klaften, Boris Ivandic, Helmut Fuchs, Valérie Gailus-Durner,[...]. Am J Physiol Renal Physiol 2009
32
18

The functional annotation of mammalian genomes: the challenge of phenotyping.
Steve D M Brown, Wolfgang Wurst, Ralf Kühn, John M Hancock. Annu Rev Genet 2009
44
11

A systematic, genome-wide, phenotype-driven mutagenesis programme for gene function studies in the mouse.
P M Nolan, J Peters, M Strivens, D Rogers, J Hagan, N Spurr, I C Gray, L Vizor, D Brooker, E Whitehill,[...]. Nat Genet 2000
500
5

Initial sequencing and comparative analysis of the mouse genome.
Robert H Waterston, Kerstin Lindblad-Toh, Ewan Birney, Jane Rogers, Josep F Abril, Pankaj Agarwal, Richa Agarwala, Rachel Ainscough, Marina Alexandersson, Peter An,[...]. Nature 2002
5

The Mouse Genome Database (MGD): premier model organism resource for mammalian genomics and genetics.
Judith A Blake, Carol J Bult, James A Kadin, Joel E Richardson, Janan T Eppig. Nucleic Acids Res 2011
190
5

A mouse for all reasons.
Francis S Collins, Janet Rossant, Wolfgang Wurst. Cell 2007
308
5

The mouse ascending: perspectives for human-disease models.
Nadia Rosenthal, Steve Brown. Nat Cell Biol 2007
223
5

A conditional knockout resource for the genome-wide study of mouse gene function.
William C Skarnes, Barry Rosen, Anthony P West, Manousos Koutsourakis, Wendy Bushell, Vivek Iyer, Alejandro O Mujica, Mark Thomas, Jennifer Harrow, Tony Cox,[...]. Nature 2011
5


Mutation of the Na(+)-K(+)-2Cl(-) cotransporter NKCC2 in mice is associated with severe polyuria and a urea-selective concentrating defect without hyperreninemia.
Elisabeth Kemter, Birgit Rathkolb, Lise Bankir, Anja Schrewe, Wolfgang Hans, Christina Landbrecht, Matthias Klaften, Boris Ivandic, Helmut Fuchs, Valérie Gailus-Durner,[...]. Am J Physiol Renal Physiol 2010
31
16



The use of behavioral test batteries: effects of training history.
K L McIlwain, M Y Merriweather, L A Yuva-Paylor, R Paylor. Physiol Behav 2001
383
4

The mammalian phenotype ontology: enabling robust annotation and comparative analysis.
Cynthia L Smith, Janan T Eppig. Wiley Interdiscip Rev Syst Biol Med 2009
142
4

EuroPhenome and EMPReSS: online mouse phenotyping resource.
Ann-Marie Mallon, Andrew Blake, John M Hancock. Nucleic Acids Res 2008
55
7

The European dimension for the mouse genome mutagenesis program.
Johan Auwerx, Phil Avner, Richard Baldock, Andrea Ballabio, Rudi Balling, Mariano Barbacid, Anton Berns, Allan Bradley, Steve Brown, Peter Carmeliet,[...]. Nat Genet 2004
154
4

A gene-driven ENU-based approach to generating an allelic series in any gene.
Mohamed Mohideen Quwailid, Alison Hugill, Neil Dear, Lucie Vizor, Sara Wells, Emma Horner, Shelly Fuller, Jessica Weedon, Hamish McMath, Paul Woodman,[...]. Mamm Genome 2004
126
4

Knockouts model the 100 best-selling drugs--will they model the next 100?
Brian P Zambrowicz, Arthur T Sands. Nat Rev Drug Discov 2003
280
4

Linking human diseases to animal models using ontology-based phenotype annotation.
Nicole L Washington, Melissa A Haendel, Christopher J Mungall, Michael Ashburner, Monte Westerfield, Suzanna E Lewis. PLoS Biol 2009
175
4


Different data from different labs: lessons from studies of gene-environment interaction.
Douglas Wahlsten, Pamela Metten, Tamara J Phillips, Stephen L Boehm, Sue Burkhart-Kasch, Janet Dorow, Sharon Doerksen, Chris Downing, Jennifer Fogarty, Kristina Rodd-Henricks,[...]. J Neurobiol 2003
323
4

The knockout mouse project.
Christopher P Austin, James F Battey, Allan Bradley, Maja Bucan, Mario Capecchi, Francis S Collins, William F Dove, Geoffrey Duyk, Susan Dymecki, Janan T Eppig,[...]. Nat Genet 2004
416
4

Mouse genomic variation and its effect on phenotypes and gene regulation.
Thomas M Keane, Leo Goodstadt, Petr Danecek, Michael A White, Kim Wong, Binnaz Yalcin, Andreas Heger, Avigail Agam, Guy Slater, Martin Goodson,[...]. Nature 2011
963
4

The clinical-chemical screen in the Munich ENU Mouse Mutagenesis Project: screening for clinically relevant phenotypes.
B Rathkolb, T Decker, E Fuchs, D Soewarto, C Fella, S Heffner, W Pargent, R Wanke, R Balling, M Hrabé de Angelis,[...]. Mamm Genome 2000
41
9


Implementing large-scale ENU mutagenesis screens in North America.
Amander T Clark, Daniel Goldowitz, Joseph S Takahashi, Martha Hotz Vitaterna, Sandra M Siepka, Luanne L Peters, Wayne N Frankel, George A Carlson, Janet Rossant, Joseph H Nadeau,[...]. Genetica 2004
69
5

Rapid quantification of adult and developing mouse spatial vision using a virtual optomotor system.
Glen T Prusky, Nazia M Alam, Steven Beekman, Robert M Douglas. Invest Ophthalmol Vis Sci 2004
510
4

Screening for increased plasma urea levels in a large-scale ENU mouse mutagenesis project reveals kidney disease models.
Bernhard Aigner, Birgit Rathkolb, Nadja Herbach, Elisabeth Kemter, Christina Schessl, Matthias Klaften, Martina Klempt, Martin Hrabé de Angelis, Rüdiger Wanke, Eckhard Wolf. Am J Physiol Renal Physiol 2007
20
20

Type of uromodulin mutation and allelic status influence onset and severity of uromodulin-associated kidney disease in mice.
Elisabeth Kemter, Petra Prueckl, Stefanie Sklenak, Birgit Rathkolb, Felix A Habermann, Wolfgang Hans, Valérie Gailus-Durner, Helmut Fuchs, Martin Hrabě de Angelis, Eckhard Wolf,[...]. Hum Mol Genet 2013
20
20

Rapamycin extends murine lifespan but has limited effects on aging.
Frauke Neff, Diana Flores-Dominguez, Devon P Ryan, Marion Horsch, Susanne Schröder, Thure Adler, Luciana Caminha Afonso, Juan Antonio Aguilar-Pimentel, Lore Becker, Lillian Garrett,[...]. J Clin Invest 2013
232
4

High mobility group N proteins modulate the fidelity of the cellular transcriptional profile in a tissue- and variant-specific manner.
Jamie E Kugler, Marion Horsch, Di Huang, Takashi Furusawa, Mark Rochman, Lillian Garrett, Lore Becker, Alexander Bohla, Sabine M Hölter, Cornelia Prehn,[...]. J Biol Chem 2013
26
15


Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.