A citation-based method for searching scientific literature

Grace Yoon, Zeenat Malam, Tara Paton, Christian R Marshall, Ella Hyatt, Zhenya Ivakine, Stephen W Scherer, Kyong-Soon Lee, Cynthia Hawkins, Ronald D Cohn. J Pediatr 2016
Times Cited: 44







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



Times Cited
  Times     Co-cited
Similarity


A lethal defect of mitochondrial and peroxisomal fission.
Hans R Waterham, Janet Koster, Carlo W T van Roermund, Petra A W Mooyer, Ronald J A Wanders, James V Leonard. N Engl J Med 2007
512
93

DNM1L-related mitochondrial fission defect presenting as refractory epilepsy.
Jason R Vanstone, Amanda M Smith, Skye McBride, Turaya Naas, Martin Holcik, Ghadi Antoun, Mary-Ellen Harper, Jean Michaud, Erick Sell, Pranesh Chakraborty,[...]. Eur J Hum Genet 2016
79
88

Postnatal microcephaly and pain insensitivity due to a de novo heterozygous DNM1L mutation causing impaired mitochondrial fission and function.
Ruth Sheffer, Liza Douiev, Simon Edvardson, Avraham Shaag, Khaled Tamimi, Devorah Soiferman, Vardiella Meiner, Ann Saada. Am J Med Genet A 2016
57
61

A novel de novo dominant negative mutation in DNM1L impairs mitochondrial fission and presents as childhood epileptic encephalopathy.
Jill A Fahrner, Raymond Liu, Michael Scott Perry, Jessica Klein, David C Chan. Am J Med Genet A 2016
74
59

Mitochondrial fission factor Drp1 is essential for embryonic development and synapse formation in mice.
Naotada Ishihara, Masatoshi Nomura, Akihiro Jofuku, Hiroki Kato, Satoshi O Suzuki, Keiji Masuda, Hidenori Otera, Yae Nakanishi, Ikuya Nonaka, Yu-Ichi Goto,[...]. Nat Cell Biol 2009
663
56

Biallelic Mutations in DNM1L are Associated with a Slowly Progressive Infantile Encephalopathy.
Alessia Nasca, Andrea Legati, Enrico Baruffini, Cecilia Nolli, Isabella Moroni, Anna Ardissone, Paola Goffrini, Daniele Ghezzi. Hum Mutat 2016
44
54

The dynamin-related GTPase Drp1 is required for embryonic and brain development in mice.
Junko Wakabayashi, Zhongyan Zhang, Nobunao Wakabayashi, Yasushi Tamura, Masahiro Fukaya, Thomas W Kensler, Miho Iijima, Hiromi Sesaki. J Cell Biol 2009
409
47

Disturbed mitochondrial and peroxisomal dynamics due to loss of MFF causes Leigh-like encephalopathy, optic atrophy and peripheral neuropathy.
Johannes Koch, René G Feichtinger, Peter Freisinger, Mechthild Pies, Falk Schrödl, Arcangela Iuso, Wolfgang Sperl, Johannes A Mayr, Holger Prokisch, Tobias B Haack. J Med Genet 2016
64
38

Missense variants in the middle domain of DNM1L in cases of infantile encephalopathy alter peroxisomes and mitochondria when assayed in Drosophila.
Yu-Hsin Chao, Laurie A Robak, Fan Xia, Mary K Koenig, Adekunle Adesina, Carlos A Bacino, Fernando Scaglia, Hugo J Bellen, Michael F Wangler. Hum Mol Genet 2016
39
43

Mutations in the mitochondrial GTPase mitofusin 2 cause Charcot-Marie-Tooth neuropathy type 2A.
Stephan Züchner, Irina V Mersiyanova, Maria Muglia, Nisrine Bissar-Tadmouri, Julie Rochelle, Elena L Dadali, Mario Zappia, Eva Nelis, Alessandra Patitucci, Jan Senderek,[...]. Nat Genet 2004
36

ER tubules mark sites of mitochondrial division.
Jonathan R Friedman, Laura L Lackner, Matthew West, Jared R DiBenedetto, Jodi Nunnari, Gia K Voeltz. Science 2011
36

Mutations in DNM1L, as in OPA1, result in dominant optic atrophy despite opposite effects on mitochondrial fusion and fission.
Sylvie Gerber, Majida Charif, Arnaud Chevrollier, Tanguy Chaumette, Claire Angebault, Mariame Selma Kane, Aurélien Paris, Jennifer Alban, Mélanie Quiles, Cécile Delettre,[...]. Brain 2017
60
36

Genomic analysis of mitochondrial diseases in a consanguineous population reveals novel candidate disease genes.
Hanan E Shamseldin, Muneera Alshammari, Tarfa Al-Sheddi, Mustafa A Salih, Hisham Alkhalidi, Amal Kentab, Gabriela M Repetto, Mais Hashem, Fowzan S Alkuraya. J Med Genet 2012
110
34

Dynamin-related protein Drp1 is required for mitochondrial division in mammalian cells.
E Smirnova, L Griparic, D L Shurland, A M van der Bliek. Mol Biol Cell 2001
34

Mitofusins Mfn1 and Mfn2 coordinately regulate mitochondrial fusion and are essential for embryonic development.
Hsiuchen Chen, Scott A Detmer, Andrew J Ewald, Erik E Griffin, Scott E Fraser, David C Chan. J Cell Biol 2003
34

Dynamin-like protein 1 is involved in peroxisomal fission.
Annett Koch, Meinolf Thiemann, Markus Grabenbauer, Yisang Yoon, Mark A McNiven, Michael Schrader. J Biol Chem 2003
247
29

Multiple dynamin family members collaborate to drive mitochondrial division.
Jason E Lee, Laura M Westrate, Haoxi Wu, Cynthia Page, Gia K Voeltz. Nature 2016
235
29

DNM1L-related encephalopathy in infancy with Leigh syndrome-like phenotype and suppression-burst.
K Zaha, H Matsumoto, M Itoh, H Saitsu, K Kato, M Kato, S Ogata, K Murayama, Y Kishita, Y Mizuno,[...]. Clin Genet 2016
20
65

A lethal de novo mutation in the middle domain of the dynamin-related GTPase Drp1 impairs higher order assembly and mitochondrial division.
Chuang-Rung Chang, Cara Marie Manlandro, Damien Arnoult, Julia Stadler, Ammon E Posey, R Blake Hill, Craig Blackstone. J Biol Chem 2010
117
27

Fis1, Mff, MiD49, and MiD51 mediate Drp1 recruitment in mitochondrial fission.
Oliver C Losón, Zhiyin Song, Hsiuchen Chen, David C Chan. Mol Biol Cell 2013
557
27

Conformational changes in Dnm1 support a contractile mechanism for mitochondrial fission.
Jason A Mears, Laura L Lackner, Shunming Fang, Elena Ingerman, Jodi Nunnari, Jenny E Hinshaw. Nat Struct Mol Biol 2011
267
27

Fission and selective fusion govern mitochondrial segregation and elimination by autophagy.
Gilad Twig, Alvaro Elorza, Anthony J A Molina, Hibo Mohamed, Jakob D Wikstrom, Gil Walzer, Linsey Stiles, Sarah E Haigh, Steve Katz, Guy Las,[...]. EMBO J 2008
27

Structural insights into oligomerization and mitochondrial remodelling of dynamin 1-like protein.
Chris Fröhlich, Stefan Grabiger, David Schwefel, Katja Faelber, Eva Rosenbaum, Jason Mears, Oliver Rocks, Oliver Daumke. EMBO J 2013
138
25

An actin-dependent step in mitochondrial fission mediated by the ER-associated formin INF2.
Farida Korobova, Vinay Ramabhadran, Henry N Higgs. Science 2013
426
25


Mff is an essential factor for mitochondrial recruitment of Drp1 during mitochondrial fission in mammalian cells.
Hidenori Otera, Chunxin Wang, Megan M Cleland, Kiyoko Setoguchi, Sadaki Yokota, Richard J Youle, Katsuyoshi Mihara. J Cell Biol 2010
612
22

Nuclear gene OPA1, encoding a mitochondrial dynamin-related protein, is mutated in dominant optic atrophy.
C Delettre, G Lenaers, J M Griffoin, N Gigarel, C Lorenzo, P Belenguer, L Pelloquin, J Grosgeorge, C Turc-Carel, E Perret,[...]. Nat Genet 2000
22

Opa1 deficiency in a mouse model of autosomal dominant optic atrophy impairs mitochondrial morphology, optic nerve structure and visual function.
Vanessa J Davies, Andrew J Hollins, Malgorzata J Piechota, Wanfen Yip, Jennifer R Davies, Kathryn E White, Phillip P Nicols, Michael E Boulton, Marcela Votruba. Hum Mol Genet 2007
281
20

OPA1 mutations induce mitochondrial DNA instability and optic atrophy 'plus' phenotypes.
Patrizia Amati-Bonneau, Maria Lucia Valentino, Pascal Reynier, Maria Esther Gallardo, Belén Bornstein, Anne Boissière, Yolanda Campos, Henry Rivera, Jesús González de la Aleja, Rosanna Carroccia,[...]. Brain 2008
342
20

During autophagy mitochondria elongate, are spared from degradation and sustain cell viability.
Ligia C Gomes, Giulietta Di Benedetto, Luca Scorrano. Nat Cell Biol 2011
20

The i-AAA protease YME1L and OMA1 cleave OPA1 to balance mitochondrial fusion and fission.
Ruchika Anand, Timothy Wai, Michael J Baker, Nikolay Kladt, Astrid C Schauss, Elena Rugarli, Thomas Langer. J Cell Biol 2014
370
20

Mitofusin 2 tethers endoplasmic reticulum to mitochondria.
Olga Martins de Brito, Luca Scorrano. Nature 2008
20

De novo DNM1L mutation associated with mitochondrial epilepsy syndrome with fever sensitivity.
Emma Ladds, Andrea Whitney, Eszter Dombi, Monika Hofer, Geetha Anand, Victoria Harrison, Carl Fratter, Janet Carver, Ines A Barbosa, Michael Simpson,[...]. Neurol Genet 2018
16
56

Mutations in the pleckstrin homology domain of dynamin 2 cause dominant intermediate Charcot-Marie-Tooth disease.
Stephan Züchner, Maher Noureddine, Marina Kennerson, Kristien Verhoeven, Kristl Claeys, Peter De Jonghe, John Merory, Sofia A Oliveira, Marcy C Speer, Judith E Stenger,[...]. Nat Genet 2005
248
18

Multi-system neurological disease is common in patients with OPA1 mutations.
P Yu-Wai-Man, P G Griffiths, G S Gorman, C M Lourenco, A F Wright, M Auer-Grumbach, A Toscano, O Musumeci, M L Valentino, L Caporali,[...]. Brain 2010
259
18

Titration of mitochondrial fusion rescues Mff-deficient cardiomyopathy.
Hsiuchen Chen, Shuxun Ren, Clary Clish, Mohit Jain, Vamsi Mootha, J Michael McCaffery, David C Chan. J Cell Biol 2015
80
18

ER-mitochondria contacts couple mtDNA synthesis with mitochondrial division in human cells.
Samantha C Lewis, Lauren F Uchiyama, Jodi Nunnari. Science 2016
262
18

MiD49 and MiD51, new components of the mitochondrial fission machinery.
Catherine S Palmer, Laura D Osellame, David Laine, Olga S Koutsopoulos, Ann E Frazier, Michael T Ryan. EMBO Rep 2011
368
18

OPA1, encoding a dynamin-related GTPase, is mutated in autosomal dominant optic atrophy linked to chromosome 3q28.
C Alexander, M Votruba, U E Pesch, D L Thiselton, S Mayer, A Moore, M Rodriguez, U Kellner, B Leo-Kottler, G Auburger,[...]. Nat Genet 2000
919
18

A novel mechanism causing imbalance of mitochondrial fusion and fission in human myopathies.
Marina Bartsakoulia, Angela Pyle, Diego Troncoso-Chandía, Josefa Vial-Brizzi, Marysol V Paz-Fiblas, Jennifer Duff, Helen Griffin, Veronika Boczonadi, Hanns Lochmüller, Stephanie Kleinle,[...]. Hum Mol Genet 2018
33
24

De Novo DNM1L Variant in a Teenager With Progressive Paroxysmal Dystonia and Lethal Super-refractory Myoclonic Status Epilepticus.
Conor S Ryan, Anthony L Fine, Alexander L Cohen, Brenda M Schiltz, Deborah L Renaud, Elaine C Wirrell, Marc C Patterson, Nicole J Boczek, Raymond Liu, Dusica Babovic-Vuksanovic,[...]. J Child Neurol 2018
11
72

De novo missense variant in the GTPase effector domain (GED) of DNM1L leads to static encephalopathy and seizures.
Nurit Assia Batzir, Pranjali K Bhagwat, Tanya N Eble, Pengfei Liu, Christine M Eng, Sarah H Elsea, Laurie A Robak, Fernando Scaglia, Alica M Goldman, Shweta U Dhar,[...]. Cold Spring Harb Mol Case Stud 2019
13
61


Dynamin-related protein 1 is required for normal mitochondrial bioenergetic and synaptic function in CA1 hippocampal neurons.
L Y Shields, H Kim, L Zhu, D Haddad, A Berthet, D Pathak, M Lam, R Ponnusamy, L G Diaz-Ramirez, T M Gill,[...]. Cell Death Dis 2015
52
15

Mitochondrial fission and fusion factors reciprocally orchestrate mitophagic culling in mouse hearts and cultured fibroblasts.
Moshi Song, Katsuyoshi Mihara, Yun Chen, Luca Scorrano, Gerald W Dorn. Cell Metab 2015
260
15

Mitotic phosphorylation of dynamin-related GTPase Drp1 participates in mitochondrial fission.
Naoko Taguchi, Naotada Ishihara, Akihiro Jofuku, Toshihiko Oka, Katsuyoshi Mihara. J Biol Chem 2007
756
15

A role for myosin II in mammalian mitochondrial fission.
Farida Korobova, Timothy J Gauvin, Henry N Higgs. Curr Biol 2014
131
15

Metabolism. AMP-activated protein kinase mediates mitochondrial fission in response to energy stress.
Erin Quan Toyama, Sébastien Herzig, Julien Courchet, Tommy L Lewis, Oliver C Losón, Kristina Hellberg, Nathan P Young, Hsiuchen Chen, Franck Polleux, David C Chan,[...]. Science 2016
485
15

Tubular network formation protects mitochondria from autophagosomal degradation during nutrient starvation.
Angelika S Rambold, Brenda Kostelecky, Natalie Elia, Jennifer Lippincott-Schwartz. Proc Natl Acad Sci U S A 2011
659
15

MFN1 structures reveal nucleotide-triggered dimerization critical for mitochondrial fusion.
Yu-Lu Cao, Shuxia Meng, Yang Chen, Jian-Xiong Feng, Dong-Dong Gu, Bing Yu, Yu-Jie Li, Jin-Yu Yang, Shuang Liao, David C Chan,[...]. Nature 2017
122
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.