A citation-based method for searching scientific literature

Viola Kretschmer, Sarita Rani Patnaik, Friedrich Kretschmer, Mira Manilal Chawda, Victor Hernandez-Hernandez, Helen Louise May-Simera. Invest Ophthalmol Vis Sci 2019
Times Cited: 6







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



Times Cited
  Times     Co-cited
Similarity


Disruption of Bardet-Biedl syndrome ciliary proteins perturbs planar cell polarity in vertebrates.
Alison J Ross, Helen May-Simera, Erica R Eichers, Masatake Kai, Josephine Hill, Daniel J Jagger, Carmen C Leitch, J Paul Chapple, Peter M Munro, Shannon Fisher,[...]. Nat Genet 2005
448
66

Bardet-Biedl syndrome-8 (BBS8) protein is crucial for the development of outer segments in photoreceptor neurons.
Tanya L Dilan, Ratnesh K Singh, Thamaraiselvi Saravanan, Abigail Moye, Andrew F X Goldberg, Peter Stoilov, Visvanathan Ramamurthy. Hum Mol Genet 2018
30
66

A core complex of BBS proteins cooperates with the GTPase Rab8 to promote ciliary membrane biogenesis.
Maxence V Nachury, Alexander V Loktev, Qihong Zhang, Christopher J Westlake, Johan Peränen, Andreas Merdes, Diane C Slusarski, Richard H Scheller, J Fernando Bazan, Val C Sheffield,[...]. Cell 2007
957
50

Bardet-Biedl syndrome.
Elizabeth Forsythe, Philip L Beales. Eur J Hum Genet 2013
280
50

A novel protein LZTFL1 regulates ciliary trafficking of the BBSome and Smoothened.
Seongjin Seo, Qihong Zhang, Kevin Bugge, David K Breslow, Charles C Searby, Maxence V Nachury, Val C Sheffield. PLoS Genet 2011
121
50


The BBSome controls IFT assembly and turnaround in cilia.
Qing Wei, Yuxia Zhang, Yujie Li, Qing Zhang, Kun Ling, Jinghua Hu. Nat Cell Biol 2012
142
50

The conserved Bardet-Biedl syndrome proteins assemble a coat that traffics membrane proteins to cilia.
Hua Jin, Susan Roehl White, Toshinobu Shida, Stefan Schulz, Mike Aguiar, Steven P Gygi, J Fernando Bazan, Maxence V Nachury. Cell 2010
397
50

Bbs2-null mice have neurosensory deficits, a defect in social dominance, and retinopathy associated with mislocalization of rhodopsin.
Darryl Y Nishimura, Melissa Fath, Robert F Mullins, Charles Searby, Michael Andrews, Roger Davis, Jeaneen L Andorf, Kirk Mykytyn, Ruth E Swiderski, Baoli Yang,[...]. Proc Natl Acad Sci U S A 2004
272
50

Loss of C. elegans BBS-7 and BBS-8 protein function results in cilia defects and compromised intraflagellar transport.
Oliver E Blacque, Michael J Reardon, Chunmei Li, Jonathan McCarthy, Moe R Mahjoub, Stephen J Ansley, Jose L Badano, Allan K Mah, Philip L Beales, William S Davidson,[...]. Genes Dev 2004
258
50

Accumulation of non-outer segment proteins in the outer segment underlies photoreceptor degeneration in Bardet-Biedl syndrome.
Poppy Datta, Chantal Allamargot, Joseph S Hudson, Emily K Andersen, Sajag Bhattarai, Arlene V Drack, Val C Sheffield, Seongjin Seo. Proc Natl Acad Sci U S A 2015
73
33

Genotype-phenotype correlations in Bardet-Biedl syndrome.
Anthony B Daniels, Michael A Sandberg, Jianjun Chen, Carol Weigel-DiFranco, J Fielding Hejtmancic, Eliot L Berson. Arch Ophthalmol 2012
38
33

BBSome function is required for both the morphogenesis and maintenance of the photoreceptor outer segment.
Ying Hsu, Janelle E Garrison, Gunhee Kim, Addison R Schmitz, Charles C Searby, Qihong Zhang, Poppy Datta, Darryl Y Nishimura, Seongjin Seo, Val C Sheffield. PLoS Genet 2017
30
33

Predominantly Cone-System Dysfunction as Rare Form of Retinal Degeneration in Patients With Molecularly Confirmed Bardet-Biedl Syndrome.
Sophie Scheidecker, Sarah Hull, Yaumara Perdomo, Fouzia Studer, Valérie Pelletier, Jean Muller, Corinne Stoetzel, Elise Schaefer, Sabine Defoort-Dhellemmes, Isabelle Drumare,[...]. Am J Ophthalmol 2015
10
33

Bardet-Biedl syndrome type 4 (BBS4)-null mice implicate Bbs4 in flagella formation but not global cilia assembly.
Kirk Mykytyn, Robert F Mullins, Michael Andrews, Annie P Chiang, Ruth E Swiderski, Baoli Yang, Terry Braun, Thomas Casavant, Edwin M Stone, Val C Sheffield. Proc Natl Acad Sci U S A 2004
241
33

Comparative genomics identifies a flagellar and basal body proteome that includes the BBS5 human disease gene.
Jin Billy Li, Jantje M Gerdes, Courtney J Haycraft, Yanli Fan, Tanya M Teslovich, Helen May-Simera, Haitao Li, Oliver E Blacque, Linya Li, Carmen C Leitch,[...]. Cell 2004
563
33

Bardet-Biedl syndrome 3 (Bbs3) knockout mouse model reveals common BBS-associated phenotypes and Bbs3 unique phenotypes.
Qihong Zhang, Darryl Nishimura, Seongjin Seo, Tim Vogel, Donald A Morgan, Charles Searby, Kevin Bugge, Edwin M Stone, Kamal Rahmouni, Val C Sheffield. Proc Natl Acad Sci U S A 2011
91
33

Bardet-Biedl syndrome proteins control the cilia length through regulation of actin polymerization.
Victor Hernandez-Hernandez, Priyanka Pravincumar, Anna Diaz-Font, Helen May-Simera, Dagan Jenkins, Martin Knight, Philip L Beales. Hum Mol Genet 2013
65
33

Cilia - The sensory antennae in the eye.
Helen May-Simera, Kerstin Nagel-Wolfrum, Uwe Wolfrum. Prog Retin Eye Res 2017
66
33

The primary cilium: a signalling centre during vertebrate development.
Sarah C Goetz, Kathryn V Anderson. Nat Rev Genet 2010
33

Disruption of intraflagellar transport in adult mice leads to obesity and slow-onset cystic kidney disease.
James R Davenport, Amanda J Watts, Venus C Roper, Mandy J Croyle, Thomas van Groen, J Michael Wyss, Tim R Nagy, Robert A Kesterson, Bradley K Yoder. Curr Biol 2007
314
33

Managing Bardet-Biedl Syndrome-Now and in the Future.
Elizabeth Forsythe, Joanna Kenny, Chiara Bacchelli, Philip L Beales. Front Pediatr 2018
56
33

Ciliopathies: an expanding disease spectrum.
Aoife M Waters, Philip L Beales. Pediatr Nephrol 2011
387
33

Requirement of Bardet-Biedl syndrome proteins for leptin receptor signaling.
Seongjin Seo, Deng-Fu Guo, Kevin Bugge, Donald A Morgan, Kamal Rahmouni, Val C Sheffield. Hum Mol Genet 2009
194
33

Understanding photoreceptor outer segment phagocytosis: use and utility of RPE cells in culture.
Francesca Mazzoni, Hussein Safa, Silvia C Finnemann. Exp Eye Res 2014
106
33

Ciliary proteins Bbs8 and Ift20 promote planar cell polarity in the cochlea.
Helen L May-Simera, Ronald S Petralia, Mireille Montcouquiol, Ya-Xian Wang, Katherine B Szarama, Yun Liu, Weichun Lin, Michael R Deans, Gregory J Pazour, Matthew W Kelley. Development 2015
44
33

Bardet-Biedl Syndrome proteins regulate cilia disassembly during tissue maturation.
Sarita Rani Patnaik, Viola Kretschmer, Lena Brücker, Sandra Schneider, Ann-Kathrin Volz, Liliana Del Rocio Oancea-Castillo, Helen Louise May-Simera. Cell Mol Life Sci 2019
15
33

Tissue-dependent differences in Bardet-Biedl syndrome gene expression.
Sarita Rani Patnaik, Aalaa Farag, Lena Brücker, Ann-Kathrin Volz, Sandra Schneider, Viola Kretschmer, Helen Louise May-Simera. Biol Cell 2020
4
50

Structural basis for membrane targeting of the BBSome by ARL6.
André Mourão, Andrew R Nager, Maxence V Nachury, Esben Lorentzen. Nat Struct Mol Biol 2014
50
33

BBS7 is required for BBSome formation and its absence in mice results in Bardet-Biedl syndrome phenotypes and selective abnormalities in membrane protein trafficking.
Qihong Zhang, Darryl Nishimura, Tim Vogel, Jianqiang Shao, Ruth Swiderski, Terry Yin, Charles Searby, Calvin S Carter, Gunhee Kim, Kevin Bugge,[...]. J Cell Sci 2013
74
33

Identification of a novel Bardet-Biedl syndrome protein, BBS7, that shares structural features with BBS1 and BBS2.
José L Badano, Stephen J Ansley, Carmen C Leitch, Richard Alan Lewis, James R Lupski, Nicholas Katsanis. Am J Hum Genet 2003
160
33

The BBSome Controls Energy Homeostasis by Mediating the Transport of the Leptin Receptor to the Plasma Membrane.
Deng-Fu Guo, Huxing Cui, Qihong Zhang, Donald A Morgan, Daniel R Thedens, Darryl Nishimura, Justin L Grobe, Val C Sheffield, Kamal Rahmouni. PLoS Genet 2016
55
33

BBS proteins interact genetically with the IFT pathway to influence SHH-related phenotypes.
Qihong Zhang, Seongjin Seo, Kevin Bugge, Edwin M Stone, Val C Sheffield. Hum Mol Genet 2012
90
33

Intraflagellar transport protein RABL5/IFT22 recruits the BBSome to the basal body through the GTPase ARL6/BBS3.
Bin Xue, Yan-Xia Liu, Bin Dong, Jenna L Wingfield, Mingfu Wu, Jun Sun, Karl F Lechtreck, Zhen-Chuan Fan. Proc Natl Acad Sci U S A 2020
10
33

BBS6, BBS10, and BBS12 form a complex with CCT/TRiC family chaperonins and mediate BBSome assembly.
Seongjin Seo, Lisa M Baye, Nathan P Schulz, John S Beck, Qihong Zhang, Diane C Slusarski, Val C Sheffield. Proc Natl Acad Sci U S A 2010
194
33

Loss of Bardet-Biedl syndrome protein-8 (BBS8) perturbs olfactory function, protein localization, and axon targeting.
Abigail L D Tadenev, Heather M Kulaga, Helen L May-Simera, Matthew W Kelley, Nicholas Katsanis, Randall R Reed. Proc Natl Acad Sci U S A 2011
67
33

Exploring Key Challenges of Understanding the Pathogenesis of Kidney Disease in Bardet-Biedl Syndrome.
Emanuela Marchese, Margherita Ruoppolo, Alessandra Perna, Giovambattista Capasso, Miriam Zacchia. Kidney Int Rep 2020
8
33

BBSome Component BBS5 Is Required for Cone Photoreceptor Protein Trafficking and Outer Segment Maintenance.
Katie L Bales, Melissa R Bentley, Mandy J Croyle, Robert A Kesterson, Bradley K Yoder, Alecia K Gross. Invest Ophthalmol Vis Sci 2020
6
33

A recombinant BBSome core complex and how it interacts with ciliary cargo.
Björn Udo Klink, Eldar Zent, Puneet Juneja, Anne Kuhlee, Stefan Raunser, Alfred Wittinghofer. Elife 2017
43
16


[Bardet-Biedl syndrome and Kidney failure: a case report].
Fabio Tattoli, Daniela Falconi, Chiara Bottaro, Maurizio Gherzi, Federico Marazzi, Marita Marengo, Ilaria Serra, Michela Tamagnone, Marco Formica. G Ital Nefrol 2018
1
100


New criteria for improved diagnosis of Bardet-Biedl syndrome: results of a population survey.
P L Beales, N Elcioglu, A S Woolf, D Parker, F A Flinter. J Med Genet 1999
495
16

Ciliopathies.
Friedhelm Hildebrandt, Thomas Benzing, Nicholas Katsanis. N Engl J Med 2011
830
16

Three-dimensional architecture of the rod sensory cilium and its disruption in retinal neurodegeneration.
Jared C Gilliam, Juan T Chang, Ivette M Sandoval, Youwen Zhang, Tiansen Li, Steven J Pittler, Wah Chiu, Theodore G Wensel. Cell 2012
104
16

The Bardet-Biedl protein BBS4 targets cargo to the pericentriolar region and is required for microtubule anchoring and cell cycle progression.
Jun Chul Kim, Jose L Badano, Sonja Sibold, Muneer A Esmail, Josephine Hill, Bethan E Hoskins, Carmen C Leitch, Kerrie Venner, Stephen J Ansley, Alison J Ross,[...]. Nat Genet 2004
318
16

Reconstructing the evolutionary history of the centriole from protein components.
Matthew E Hodges, Nicole Scheumann, Bill Wickstead, Jane A Langdale, Keith Gull. J Cell Sci 2010
161
16

Arrestin 1 and Cone Arrestin 4 Have Unique Roles in Visual Function in an All-Cone Mouse Retina.
Janise D Deming, Joseph S Pak, Jung-A Shin, Bruce M Brown, Moon K Kim, Moe H Aung, Eun-Jin Lee, Machelle T Pardue, Cheryl Mae Craft. Invest Ophthalmol Vis Sci 2015
5
20

Cone opsin determines the time course of cone photoreceptor degeneration in Leber congenital amaurosis.
Tao Zhang, Ning Zhang, Wolfgang Baehr, Yingbin Fu. Proc Natl Acad Sci U S A 2011
62
16

Phenotypic characterization of Bbs4 null mice reveals age-dependent penetrance and variable expressivity.
Erica R Eichers, Muhammad M Abd-El-Barr, Richard Paylor, Richard Alan Lewis, Weimin Bi, Xiaodi Lin, Thomas P Meehan, David W Stockton, Samuel M Wu, Elizabeth Lindsay,[...]. Hum Genet 2006
73
16


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.