A citation-based method for searching scientific literature

Qiuping Zhang, Cornelia Bethmann, Nathalie F Worth, John D Davies, Christina Wasner, Anja Feuer, Cassandra D Ragnauth, Qijian Yi, Jason A Mellad, Derek T Warren, Matthew A Wheeler, Juliet A Ellis, Jeremy N Skepper, Matthias Vorgerd, Beate Schlotter-Weigel, Peter L Weissberg, Roland G Roberts, Manfred Wehnert, Catherine M Shanahan. Hum Mol Genet 2007
Times Cited: 357







List of co-cited articles
1214 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


Coupling of the nucleus and cytoplasm: role of the LINC complex.
Melissa Crisp, Qian Liu, Kyle Roux, J B Rattner, Catherine Shanahan, Brian Burke, Phillip D Stahl, Didier Hodzic. J Cell Biol 2006
900
31

Novel nesprin-1 mutations associated with dilated cardiomyopathy cause nuclear envelope disruption and defects in myogenesis.
Can Zhou, Chen Li, Bin Zhou, Huaqin Sun, Victoria Koullourou, Ian Holt, Megan J Puckelwartz, Derek T Warren, Robert Hayward, Ziyuan Lin,[...]. Hum Mol Genet 2017
62
41

Muscular dystrophy-associated SUN1 and SUN2 variants disrupt nuclear-cytoskeletal connections and myonuclear organization.
Peter Meinke, Elisabetta Mattioli, Farhana Haque, Susumu Antoku, Marta Columbaro, Kees R Straatman, Howard J Worman, Gregg G Gundersen, Giovanna Lattanzi, Manfred Wehnert,[...]. PLoS Genet 2014
107
26

Mutations in SYNE1 lead to a newly discovered form of autosomal recessive cerebellar ataxia.
François Gros-Louis, Nicolas Dupré, Patrick Dion, Michael A Fox, Sandra Laurent, Steve Verreault, Joshua R Sanes, Jean-Pierre Bouchard, Guy A Rouleau. Nat Genet 2007
222
24

Identification of a novel X-linked gene responsible for Emery-Dreifuss muscular dystrophy.
S Bione, E Maestrini, S Rivella, M Mancini, S Regis, G Romeo, D Toniolo. Nat Genet 1994
680
23

Disruption of nesprin-1 produces an Emery Dreifuss muscular dystrophy-like phenotype in mice.
Megan J Puckelwartz, Eric Kessler, Yuan Zhang, Didier Hodzic, K Natalie Randles, Glenn Morris, Judy U Earley, Michele Hadhazy, James M Holaska, Stephanie K Mewborn,[...]. Hum Mol Genet 2009
139
23

Mutations in the gene encoding lamin A/C cause autosomal dominant Emery-Dreifuss muscular dystrophy.
G Bonne, M R Di Barletta, S Varnous, H M Bécane, E H Hammouda, L Merlini, F Muntoni, C R Greenberg, F Gary, J A Urtizberea,[...]. Nat Genet 1999
966
22

LINC complexes form by binding of three KASH peptides to domain interfaces of trimeric SUN proteins.
Brian A Sosa, Andrea Rothballer, Ulrike Kutay, Thomas U Schwartz. Cell 2012
258
21

Nesprin-1 mutations in human and murine cardiomyopathy.
Megan J Puckelwartz, Eric J Kessler, Gene Kim, Megan M Dewitt, Yuan Zhang, Judy U Earley, Frederic F S Depreux, James Holaska, Stephanie K Mewborn, Peter Pytel,[...]. J Mol Cell Cardiol 2010
101
20

Nesprin 1 is critical for nuclear positioning and anchorage.
Jianlin Zhang, Amanda Felder, Yujie Liu, Ling T Guo, Stephan Lange, Nancy D Dalton, Yusu Gu, Kirk L Peterson, Andrew P Mizisin, G Diane Shelton,[...]. Hum Mol Genet 2010
109
18

Nesprins: a novel family of spectrin-repeat-containing proteins that localize to the nuclear membrane in multiple tissues.
Q Zhang, J N Skepper, F Yang, J D Davies, L Hegyi, R G Roberts, P L Weissberg, J A Ellis, C M Shanahan. J Cell Sci 2001
300
18

Targeted ablation of nesprin 1 and nesprin 2 from murine myocardium results in cardiomyopathy, altered nuclear morphology and inhibition of the biomechanical gene response.
Indroneal Banerjee, Jianlin Zhang, Thomas Moore-Morris, Emily Pfeiffer, Kyle S Buchholz, Ao Liu, Kunfu Ouyang, Matthew J Stroud, Larry Gerace, Sylvia M Evans,[...]. PLoS Genet 2014
87
19

Nuclear lamin-A scales with tissue stiffness and enhances matrix-directed differentiation.
Joe Swift, Irena L Ivanovska, Amnon Buxboim, Takamasa Harada, P C Dave P Dingal, Joel Pinter, J David Pajerowski, Kyle R Spinler, Jae-Won Shin, Manorama Tewari,[...]. Science 2013
17

Nesprin 1α2 is essential for mouse postnatal viability and nuclear positioning in skeletal muscle.
Matthew J Stroud, Wei Feng, Jianlin Zhang, Jennifer Veevers, Xi Fang, Larry Gerace, Ju Chen. J Cell Biol 2017
40
40

SYNE1 ataxia is a common recessive ataxia with major non-cerebellar features: a large multi-centre study.
Matthis Synofzik, Katrien Smets, Martial Mallaret, Daniela Di Bella, Constanze Gallenmüller, Jonathan Baets, Martin Schulze, Stefania Magri, Elisa Sarto, Mona Mustafa,[...]. Brain 2016
67
23

Nesprins: from the nuclear envelope and beyond.
Dipen Rajgor, Catherine M Shanahan. Expert Rev Mol Med 2013
125
16

Mutation of SYNE-1, encoding an essential component of the nuclear lamina, is responsible for autosomal recessive arthrogryposis.
Ruben Attali, Nasim Warwar, Ariel Israel, Irina Gurt, Elizabeth McNally, Megan Puckelwartz, Benjamin Glick, Yoram Nevo, Ziva Ben-Neriah, Judith Melki. Hum Mol Genet 2009
100
16

Mammalian SUN protein interaction networks at the inner nuclear membrane and their role in laminopathy disease processes.
Farhana Haque, Daniela Mazzeo, Jennifer T Patel, Dawn T Smallwood, Juliet A Ellis, Catherine M Shanahan, Sue Shackleton. J Biol Chem 2010
189
16

Lamin A/C deficiency causes defective nuclear mechanics and mechanotransduction.
Jan Lammerding, P Christian Schulze, Tomosaburo Takahashi, Serguei Kozlov, Teresa Sullivan, Roger D Kamm, Colin L Stewart, Richard T Lee. J Clin Invest 2004
703
15

SUN1/2 and Syne/Nesprin-1/2 complexes connect centrosome to the nucleus during neurogenesis and neuronal migration in mice.
Xiaochang Zhang, Kai Lei, Xiaobing Yuan, Xiaohui Wu, Yuan Zhuang, Tian Xu, Rener Xu, Min Han. Neuron 2009
341
15

Isolated nuclei adapt to force and reveal a mechanotransduction pathway in the nucleus.
Christophe Guilluy, Lukas D Osborne, Laurianne Van Landeghem, Lisa Sharek, Richard Superfine, Rafael Garcia-Mata, Keith Burridge. Nat Cell Biol 2014
349
15

Loss of A-type lamin expression compromises nuclear envelope integrity leading to muscular dystrophy.
T Sullivan, D Escalante-Alcalde, H Bhatt, M Anver, N Bhat, K Nagashima, C L Stewart, B Burke. J Cell Biol 1999
925
15

Accumulation of the inner nuclear envelope protein Sun1 is pathogenic in progeric and dystrophic laminopathies.
Chia-Yen Chen, Ya-Hui Chi, Rafidah Abdul Mutalif, Matthew F Starost, Timothy G Myers, Stasia A Anderson, Colin L Stewart, Kuan-Teh Jeang. Cell 2012
154
15

TMEM43 mutations in Emery-Dreifuss muscular dystrophy-related myopathy.
Wen-Chen Liang, Hiroaki Mitsuhashi, Etsuko Keduka, Ikuya Nonaka, Satoru Noguchi, Ichizo Nishino, Yukiko K Hayashi. Ann Neurol 2011
79
17

Abnormal nuclear shape and impaired mechanotransduction in emerin-deficient cells.
Jan Lammerding, Janet Hsiao, P Christian Schulze, Serguei Kozlov, Colin L Stewart, Richard T Lee. J Cell Biol 2005
262
14

Nesprin 4 is an outer nuclear membrane protein that can induce kinesin-mediated cell polarization.
Kyle J Roux, Melissa L Crisp, Qian Liu, Daein Kim, Serguei Kozlov, Colin L Stewart, Brian Burke. Proc Natl Acad Sci U S A 2009
242
14


Recurrent de novo point mutations in lamin A cause Hutchinson-Gilford progeria syndrome.
Maria Eriksson, W Ted Brown, Leslie B Gordon, Michael W Glynn, Joel Singer, Laura Scott, Michael R Erdos, Christiane M Robbins, Tracy Y Moses, Peter Berglund,[...]. Nature 2003
14

The inner nuclear membrane protein Sun1 mediates the anchorage of Nesprin-2 to the nuclear envelope.
V C Padmakumar, Thorsten Libotte, Wenshu Lu, Hafida Zaim, Sabu Abraham, Angelika A Noegel, Josef Gotzmann, Roland Foisner, Iakowos Karakesisoglou. J Cell Sci 2005
313
13


Lamin A/C and emerin regulate MKL1-SRF activity by modulating actin dynamics.
Chin Yee Ho, Diana E Jaalouk, Maria K Vartiainen, Jan Lammerding. Nature 2013
304
13

Syne-1 and Syne-2 play crucial roles in myonuclear anchorage and motor neuron innervation.
Xiaochang Zhang, Rener Xu, Binggen Zhu, Xiujuan Yang, Xu Ding, Shumin Duan, Tian Xu, Yuan Zhuang, Min Han. Development 2007
201
13

Nesprin-3, a novel outer nuclear membrane protein, associates with the cytoskeletal linker protein plectin.
Kevin Wilhelmsen, Sandy H M Litjens, Ingrid Kuikman, Ntambua Tshimbalanga, Hans Janssen, Iman van den Bout, Karine Raymond, Arnoud Sonnenberg. J Cell Biol 2005
342
13

Multiple novel nesprin-1 and nesprin-2 variants act as versatile tissue-specific intracellular scaffolds.
Dipen Rajgor, Jason A Mellad, Flavia Autore, Qiuping Zhang, Catherine M Shanahan. PLoS One 2012
82
15

SUN1 interacts with nuclear lamin A and cytoplasmic nesprins to provide a physical connection between the nuclear lamina and the cytoskeleton.
Farhana Haque, David J Lloyd, Dawn T Smallwood, Carolyn L Dent, Catherine M Shanahan, Andrew M Fry, Richard C Trembath, Sue Shackleton. Mol Cell Biol 2006
363
12

Mechanotransduction at a distance: mechanically coupling the extracellular matrix with the nucleus.
Ning Wang, Jessica D Tytell, Donald E Ingber. Nat Rev Mol Cell Biol 2009
12

Missense mutations in the rod domain of the lamin A/C gene as causes of dilated cardiomyopathy and conduction-system disease.
D Fatkin, C MacRae, T Sasaki, M R Wolff, M Porcu, M Frenneaux, J Atherton, H J Vidaillet, S Spudich, U De Girolami,[...]. N Engl J Med 1999
940
12

Nuclear envelope rupture and repair during cancer cell migration.
Celine M Denais, Rachel M Gilbert, Philipp Isermann, Alexandra L McGregor, Mariska te Lindert, Bettina Weigelin, Patricia M Davidson, Peter Friedl, Katarina Wolf, Jan Lammerding. Science 2016
670
12

Accessorizing and anchoring the LINC complex for multifunctionality.
Wakam Chang, Howard J Worman, Gregg G Gundersen. J Cell Biol 2015
193
12

Nesprin-1α-Dependent Microtubule Nucleation from the Nuclear Envelope via Akap450 Is Necessary for Nuclear Positioning in Muscle Cells.
Petra Gimpel, Yin Loon Lee, Radoslaw M Sobota, Alessandra Calvi, Victoria Koullourou, Rutti Patel, Kamel Mamchaoui, François Nédélec, Sue Shackleton, Jan Schmoranzer,[...]. Curr Biol 2017
79
15

Nesprin-2 is a multi-isomeric protein that binds lamin and emerin at the nuclear envelope and forms a subcellular network in skeletal muscle.
Qiuping Zhang, Cassandra D Ragnauth, Jeremy N Skepper, Nathalie F Worth, Derek T Warren, Roland G Roberts, Peter L Weissberg, Juliet A Ellis, Catherine M Shanahan. J Cell Sci 2005
201
12

Lamin a truncation in Hutchinson-Gilford progeria.
Annachiara De Sandre-Giovannoli, Rafaëlle Bernard, Pierre Cau, Claire Navarro, Jeanne Amiel, Irène Boccaccio, Stanislas Lyonnet, Colin L Stewart, Arnold Munnich, Martine Le Merrer,[...]. Science 2003
988
12

Mutations of the FHL1 gene cause Emery-Dreifuss muscular dystrophy.
Lucie Gueneau, Anne T Bertrand, Jean-Philippe Jais, Mustafa A Salih, Tanya Stojkovic, Manfred Wehnert, Maria Hoeltzenbein, Simone Spuler, Shinji Saitoh, Annie Verschueren,[...]. Am J Hum Genet 2009
150
12

ESCRT III repairs nuclear envelope ruptures during cell migration to limit DNA damage and cell death.
M Raab, M Gentili, H de Belly, H R Thiam, P Vargas, A J Jimenez, F Lautenschlaeger, Raphaël Voituriez, A M Lennon-Duménil, N Manel,[...]. Science 2016
509
11

The interaction between nesprins and sun proteins at the nuclear envelope is critical for force transmission between the nucleus and cytoskeleton.
Maria L Lombardi, Diana E Jaalouk, Catherine M Shanahan, Brian Burke, Kyle J Roux, Jan Lammerding. J Biol Chem 2011
324
11

The nuclear lamins: flexibility in function.
Brian Burke, Colin L Stewart. Nat Rev Mol Cell Biol 2013
348
11

SYNE1 mutations in autosomal recessive cerebellar ataxia.
Anne Noreau, Cynthia V Bourassa, Anna Szuto, Annie Levert, Sylvia Dobrzeniecka, Julie Gauthier, Sylvie Forlani, Alexandra Durr, Mathieu Anheim, Giovanni Stevanin,[...]. JAMA Neurol 2013
40
27

De novo LMNA mutations cause a new form of congenital muscular dystrophy.
Susana Quijano-Roy, Blaise Mbieleu, Carsten G Bönnemann, Pierre-Yves Jeannet, Jaume Colomer, Nigel F Clarke, Jean-Marie Cuisset, Helen Roper, Linda De Meirleir, Adele D'Amico,[...]. Ann Neurol 2008
187
11

Accumulation of mutant lamin A causes progressive changes in nuclear architecture in Hutchinson-Gilford progeria syndrome.
Robert D Goldman, Dale K Shumaker, Michael R Erdos, Maria Eriksson, Anne E Goldman, Leslie B Gordon, Yosef Gruenbaum, Satya Khuon, Melissa Mendez, Renée Varga,[...]. Proc Natl Acad Sci U S A 2004
772
11



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.