A citation-based method for searching scientific literature

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
Times Cited: 528







List of co-cited articles
1860 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


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
701
40

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
39

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
36

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
85
41

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
81
38

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
428
31

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
70
41

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
942
29

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
29

Mitofusin 2 tethers endoplasmic reticulum to mitochondria.
Olga Martins de Brito, Luca Scorrano. Nature 2008
28

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
612
27

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
27

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
27

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
68
38

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
649
25

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
25

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
116
24

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
388
23

An actin-dependent step in mitochondrial fission mediated by the ER-associated formin INF2.
Farida Korobova, Vinay Ramabhadran, Henry N Higgs. Science 2013
460
23

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
62
35

Lethal Disorder of Mitochondrial Fission Caused by Mutations in DNM1L.
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
47
44


Structural basis of mitochondrial receptor binding and constriction by DRP1.
Raghav Kalia, Ray Yu-Ruei Wang, Ali Yusuf, Paul V Thomas, David A Agard, Janet M Shaw, Adam Frost. Nature 2018
108
19

Multiple dynamin family members collaborate to drive mitochondrial division.
Jason E Lee, Laura M Westrate, Haoxi Wu, Cynthia Page, Gia K Voeltz. Nature 2016
263
19

During autophagy mitochondria elongate, are spared from degradation and sustain cell viability.
Ligia C Gomes, Giulietta Di Benedetto, Luca Scorrano. Nat Cell Biol 2011
19

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
787
18

ER-mitochondria contacts couple mtDNA synthesis with mitochondrial division in human cells.
Samantha C Lewis, Lauren F Uchiyama, Jodi Nunnari. Science 2016
294
18

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
407
18

Parkin-independent mitophagy requires Drp1 and maintains the integrity of mammalian heart and brain.
Yusuke Kageyama, Masahiko Hoshijima, Kinya Seo, Djahida Bedja, Polina Sysa-Shah, Shaida A Andrabi, Weiran Chen, Ahmet Höke, Valina L Dawson, Ted M Dawson,[...]. EMBO J 2014
264
17

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
46
36

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
360
16

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
86
18

Clinical-genetic features and peculiar muscle histopathology in infantile DNM1L-related mitochondrial epileptic encephalopathy.
Daniela Verrigni, Michela Di Nottia, Anna Ardissone, Enrico Baruffini, Alessia Nasca, Andrea Legati, Emanuele Bellacchio, Gigliola Fagiolari, Diego Martinelli, Lucia Fusco,[...]. Hum Mutat 2019
21
76

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
154
16

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
290
16

Dynamin-related protein 1 has membrane constricting and severing abilities sufficient for mitochondrial and peroxisomal fission.
Sukrut C Kamerkar, Felix Kraus, Alice J Sharpe, Thomas J Pucadyil, Michael T Ryan. Nat Commun 2018
80
18

S-nitrosylation of Drp1 mediates beta-amyloid-related mitochondrial fission and neuronal injury.
Dong-Hyung Cho, Tomohiro Nakamura, Jianguo Fang, Piotr Cieplak, Adam Godzik, Zezong Gu, Stuart A Lipton. Science 2009
752
14

The cell biology of mitochondrial membrane dynamics.
Marta Giacomello, Aswin Pyakurel, Christina Glytsou, Luca Scorrano. Nat Rev Mol Cell Biol 2020
227
14

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
254
13

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
555
13

Mitochondrial fusion protects against neurodegeneration in the cerebellum.
Hsiuchen Chen, J Michael McCaffery, David C Chan. Cell 2007
616
13

Critical reappraisal confirms that Mitofusin 2 is an endoplasmic reticulum-mitochondria tether.
Deborah Naon, Marta Zaninello, Marta Giacomello, Tatiana Varanita, Francesca Grespi, Sowmya Lakshminaranayan, Annalisa Serafini, Martina Semenzato, Stephanie Herkenne, Maria Isabel Hernández-Alvarez,[...]. Proc Natl Acad Sci U S A 2016
274
13

Mitochondrial fusion is required for mtDNA stability in skeletal muscle and tolerance of mtDNA mutations.
Hsiuchen Chen, Marc Vermulst, Yun E Wang, Anne Chomyn, Tomas A Prolla, J Michael McCaffery, David C Chan. Cell 2010
729
13

Clinical and Biochemical Features in a Patient With Mitochondrial Fission Factor Gene Alteration.
Alessia Nasca, Francesca Nardecchia, Anna Commone, Michela Semeraro, Andrea Legati, Barbara Garavaglia, Daniele Ghezzi, Vincenzo Leuzzi. Front Genet 2018
24
54


Loss of OPA1 perturbates the mitochondrial inner membrane structure and integrity, leading to cytochrome c release and apoptosis.
Aurélien Olichon, Laurent Baricault, Nicole Gas, Emmanuelle Guillou, Annie Valette, Pascale Belenguer, Guy Lenaers. J Biol Chem 2003
812
13

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
43
30

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
272
13

Mitochondrial Dynamics and Metabolic Regulation.
Timothy Wai, Thomas Langer. Trends Endocrinol Metab 2016
571
13

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
687
13


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.