A citation-based method for searching scientific literature

Sarah L Stenton, Laura S Kremer, Robert Kopajtich, Christina Ludwig, Holger Prokisch. J Inherit Metab Dis 2020
Times Cited: 17







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



Times Cited
  Times     Co-cited
Similarity


MitoCarta2.0: an updated inventory of mammalian mitochondrial proteins.
Sarah E Calvo, Karl R Clauser, Vamsi K Mootha. Nucleic Acids Res 2016
752
35

Genetic diagnosis of Mendelian disorders via RNA sequencing.
Laura S Kremer, Daniel M Bader, Christian Mertes, Robert Kopajtich, Garwin Pichler, Arcangela Iuso, Tobias B Haack, Elisabeth Graf, Thomas Schwarzmayr, Caterina Terrile,[...]. Nat Commun 2017
204
35

Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy.
D C Wallace, G Singh, M T Lott, J A Hodge, T G Schurr, A M Lezza, L J Elsas, E K Nikoskelainen. Science 1988
29


A mitochondrial protein compendium elucidates complex I disease biology.
David J Pagliarini, Sarah E Calvo, Betty Chang, Sunil A Sheth, Scott B Vafai, Shao-En Ong, Geoffrey A Walford, Canny Sugiana, Avihu Boneh, William K Chen,[...]. Cell 2008
29

Expanding the Boundaries of RNA Sequencing as a Diagnostic Tool for Rare Mendelian Disease.
Hernan D Gonorazky, Sergey Naumenko, Arun K Ramani, Viswateja Nelakuditi, Pouria Mashouri, Peiqui Wang, Dennis Kao, Krish Ohri, Senthuri Viththiyapaskaran, Mark A Tarnopolsky,[...]. Am J Hum Genet 2019
71
29

Complexome profiling identifies TMEM126B as a component of the mitochondrial complex I assembly complex.
Heinrich Heide, Lea Bleier, Mirco Steger, Jörg Ackermann, Stefan Dröse, Bettina Schwamb, Martin Zörnig, Andreas S Reichert, Ina Koch, Ilka Wittig,[...]. Cell Metab 2012
183
23

High-throughput, pooled sequencing identifies mutations in NUBPL and FOXRED1 in human complex I deficiency.
Sarah E Calvo, Elena J Tucker, Alison G Compton, Denise M Kirby, Gabriel Crawford, Noel P Burtt, Manuel Rivas, Candace Guiducci, Damien L Bruno, Olga A Goldberger,[...]. Nat Genet 2010
265
23

The Assembly Pathway of Mitochondrial Respiratory Chain Complex I.
Sergio Guerrero-Castillo, Fabian Baertling, Daniel Kownatzki, Hans J Wessels, Susanne Arnold, Ulrich Brandt, Leo Nijtmans. Cell Metab 2017
182
23

Improving genetic diagnosis in Mendelian disease with transcriptome sequencing.
Beryl B Cummings, Jamie L Marshall, Taru Tukiainen, Monkol Lek, Sandra Donkervoort, A Reghan Foley, Veronique Bolduc, Leigh B Waddell, Sarah A Sandaradura, Gina L O'Grady,[...]. Sci Transl Med 2017
275
23

Advancing genomic approaches to the molecular diagnosis of mitochondrial disease.
Sarah Louise Stenton, Holger Prokisch. Essays Biochem 2018
33
23

Use of whole-exome sequencing to determine the genetic basis of multiple mitochondrial respiratory chain complex deficiencies.
Robert W Taylor, Angela Pyle, Helen Griffin, Emma L Blakely, Jennifer Duff, Langping He, Tania Smertenko, Charlotte L Alston, Vivienne C Neeve, Andrew Best,[...]. JAMA 2014
213
17

New perspective in diagnostics of mitochondrial disorders: two years' experience with whole-exome sequencing at a national paediatric centre.
Ewa Pronicka, Dorota Piekutowska-Abramczuk, Elżbieta Ciara, Joanna Trubicka, Dariusz Rokicki, Agnieszka Karkucińska-Więckowska, Magdalena Pajdowska, Elżbieta Jurkiewicz, Paulina Halat, Joanna Kosińska,[...]. J Transl Med 2016
114
17

The T9176G mtDNA mutation severely affects ATP production and results in Leigh syndrome.
R Carrozzo, A Tessa, M E Vázquez-Memije, F Piemonte, C Patrono, A Malandrini, C Dionisi-Vici, L Vilarinho, M Villanova, H Schägger,[...]. Neurology 2001
73
17

The genetics and pathology of mitochondrial disease.
Charlotte L Alston, Mariana C Rocha, Nichola Z Lax, Doug M Turnbull, Robert W Taylor. J Pathol 2017
177
17

NDUFA4 mutations underlie dysfunction of a cytochrome c oxidase subunit linked to human neurological disease.
Robert D S Pitceathly, Shamima Rahman, Yehani Wedatilake, James M Polke, Sebahattin Cirak, A Reghan Foley, Anna Sailer, Matthew E Hurles, Jim Stalker, Iain Hargreaves,[...]. Cell Rep 2013
72
17

NDUFAF4 variants are associated with Leigh syndrome and cause a specific mitochondrial complex I assembly defect.
Fabian Baertling, Laura Sánchez-Caballero, Mariël A M van den Brand, Liesbeth T Wintjes, Maaike Brink, Frans A van den Brandt, Callum Wilson, Richard J T Rodenburg, Leo G J Nijtmans. Eur J Hum Genet 2017
16
18

Clinical spectrum of BCS1L Mitopathies and their underlying structural relationships.
Rachael A Baker, Jessica R C Priestley, Amy M Wilstermann, Kalina J Reese, Paul R Mark. Am J Med Genet A 2019
14
21

Nuclear gene mutations as the cause of mitochondrial complex III deficiency.
Erika Fernández-Vizarra, Massimo Zeviani. Front Genet 2015
74
17


Novel TTC19 mutation in a family with severe psychiatric manifestations and complex III deficiency.
Célia Nogueira, José Barros, Maria José Sá, Luísa Azevedo, Ricardo Taipa, Alessandra Torraco, Maria Chiara Meschini, Daniela Verrigni, Claudia Nesti, Teresa Rizza,[...]. Neurogenetics 2013
29
17

Architecture of mammalian respiratory complex I.
Kutti R Vinothkumar, Jiapeng Zhu, Judy Hirst. Nature 2014
276
17

Sequence and organization of the human mitochondrial genome.
S Anderson, A T Bankier, B G Barrell, M H de Bruijn, A R Coulson, J Drouin, I C Eperon, D P Nierlich, B A Roe, F Sanger,[...]. Nature 1981
17

Structure of mammalian respiratory complex I.
Jiapeng Zhu, Kutti R Vinothkumar, Judy Hirst. Nature 2016
287
17

TIMMDC1/C3orf1 functions as a membrane-embedded mitochondrial complex I assembly factor through association with the MCIA complex.
Virginia Guarani, Joao Paulo, Bo Zhai, Edward L Huttlin, Steven P Gygi, J Wade Harper. Mol Cell Biol 2014
57
17

NDUFAF7 methylates arginine 85 in the NDUFS2 subunit of human complex I.
Virginie F Rhein, Joe Carroll, Shujing Ding, Ian M Fearnley, John E Walker. J Biol Chem 2013
69
17

Whole exome sequencing of suspected mitochondrial patients in clinical practice.
Saskia B Wortmann, David A Koolen, Jan A Smeitink, Lambert van den Heuvel, Richard J Rodenburg. J Inherit Metab Dis 2015
121
17

Mitochondrial Protein Interaction Mapping Identifies Regulators of Respiratory Chain Function.
Brendan J Floyd, Emily M Wilkerson, Mike T Veling, Catie E Minogue, Chuanwu Xia, Emily T Beebe, Russell L Wrobel, Holly Cho, Laura S Kremer, Charlotte L Alston,[...]. Mol Cell 2016
145
17

Building a complex complex: Assembly of mitochondrial respiratory chain complex I.
Luke E Formosa, Marris G Dibley, David A Stroud, Michael T Ryan. Semin Cell Dev Biol 2018
68
17

Mitochondrial medicine in the omics era.
Joyeeta Rahman, Shamima Rahman. Lancet 2018
98
17

Mutations in the gene encoding C8orf38 block complex I assembly by inhibiting production of the mitochondria-encoded subunit ND1.
Matthew McKenzie, Elena J Tucker, Alison G Compton, Michael Lazarou, Christa George, David R Thorburn, Michael T Ryan. J Mol Biol 2011
48
17


Mutation of C20orf7 disrupts complex I assembly and causes lethal neonatal mitochondrial disease.
Canny Sugiana, David J Pagliarini, Matthew McKenzie, Denise M Kirby, Renato Salemi, Khaled K Abu-Amero, Hans-Henrik M Dahl, Wendy M Hutchison, Katherine A Vascotto, Stacey M Smith,[...]. Am J Hum Genet 2008
135
17

Mitochondria: in sickness and in health.
Jodi Nunnari, Anu Suomalainen. Cell 2012
17

Accessory subunits are integral for assembly and function of human mitochondrial complex I.
David A Stroud, Elliot E Surgenor, Luke E Formosa, Boris Reljic, Ann E Frazier, Marris G Dibley, Laura D Osellame, Tegan Stait, Traude H Beilharz, David R Thorburn,[...]. Nature 2016
197
17

Exome sequencing identifies ACAD9 mutations as a cause of complex I deficiency.
Tobias B Haack, Katharina Danhauser, Birgit Haberberger, Jonathan Hoser, Valentina Strecker, Detlef Boehm, Graziella Uziel, Eleonora Lamantea, Federica Invernizzi, Joanna Poulton,[...]. Nat Genet 2010
169
17

OUTRIDER: A Statistical Method for Detecting Aberrantly Expressed Genes in RNA Sequencing Data.
Felix Brechtmann, Christian Mertes, Agnė Matusevičiūtė, Vicente A Yépez, Žiga Avsec, Maximilian Herzog, Daniel M Bader, Holger Prokisch, Julien Gagneur. Am J Hum Genet 2018
25
17

Targeted exome sequencing of suspected mitochondrial disorders.
Daniel S Lieber, Sarah E Calvo, Kristy Shanahan, Nancy G Slate, Shangtao Liu, Steven G Hershman, Nina B Gold, Brad A Chapman, David R Thorburn, Gerard T Berry,[...]. Neurology 2013
107
17

SSBP1 mutations cause mtDNA depletion underlying a complex optic atrophy disorder.
Valentina Del Dotto, Farid Ullah, Ivano Di Meo, Pamela Magini, Mirjana Gusic, Alessandra Maresca, Leonardo Caporali, Flavia Palombo, Francesca Tagliavini, Evan Harris Baugh,[...]. J Clin Invest 2020
32
17

A Comprehensive Genomic Analysis Reveals the Genetic Landscape of Mitochondrial Respiratory Chain Complex Deficiencies.
Masakazu Kohda, Yoshimi Tokuzawa, Yoshihito Kishita, Hiromi Nyuzuki, Yohsuke Moriyama, Yosuke Mizuno, Tomoko Hirata, Yukiko Yatsuka, Yzumi Yamashita-Sugahara, Yutaka Nakachi,[...]. PLoS Genet 2016
148
17

Molecular diagnosis of infantile mitochondrial disease with targeted next-generation sequencing.
Sarah E Calvo, Alison G Compton, Steven G Hershman, Sze Chern Lim, Daniel S Lieber, Elena J Tucker, Adrienne Laskowski, Caterina Garone, Shangtao Liu, David B Jaffe,[...]. Sci Transl Med 2012
307
17

New genes and pathomechanisms in mitochondrial disorders unraveled by NGS technologies.
Andrea Legati, Aurelio Reyes, Alessia Nasca, Federica Invernizzi, Eleonora Lamantea, Valeria Tiranti, Barbara Garavaglia, Costanza Lamperti, Anna Ardissone, Isabella Moroni,[...]. Biochim Biophys Acta 2016
65
17


Heteroplasmic mtDNA mutation (T----G) at 8993 can cause Leigh disease when the percentage of abnormal mtDNA is high.
Y Tatuch, J Christodoulou, A Feigenbaum, J T Clarke, J Wherret, C Smith, N Rudd, R Petrova-Benedict, B H Robinson. Am J Hum Genet 1992
395
17

Mutations in COX7B cause microphthalmia with linear skin lesions, an unconventional mitochondrial disease.
Alessia Indrieri, Vanessa Alexandra van Rahden, Valeria Tiranti, Manuela Morleo, Daniela Iaconis, Roberta Tammaro, Ilaria D'Amato, Ivan Conte, Isabelle Maystadt, Stephanie Demuth,[...]. Am J Hum Genet 2012
73
17

Diverse phenotype in patients with complex I deficiency due to mutations in NDUFB11.
Karit Reinson, Reka Kovacs-Nagy, Eve Õiglane-Shlik, Sander Pajusalu, Margit Nõukas, Liesbeth T Wintjes, Frans C A van den Brandt, Maaike Brink, Till Acker, Uwe Ahting,[...]. Eur J Med Genet 2019
7
42


Mutation of a nuclear succinate dehydrogenase gene results in mitochondrial respiratory chain deficiency.
T Bourgeron, P Rustin, D Chretien, M Birch-Machin, M Bourgeois, E Viegas-Péquignot, A Munnich, A Rötig. Nat Genet 1995
529
17

Mutations in NDUFB11, encoding a complex I component of the mitochondrial respiratory chain, cause microphthalmia with linear skin defects syndrome.
Vanessa A van Rahden, Erika Fernandez-Vizarra, Malik Alawi, Kristina Brand, Florence Fellmann, Denise Horn, Massimo Zeviani, Kerstin Kutsche. Am J Hum Genet 2015
38
17

A new mitochondrial disease associated with mitochondrial DNA heteroplasmy.
I J Holt, A E Harding, R K Petty, J A Morgan-Hughes. Am J Hum Genet 1990
796
17


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.