A citation-based method for searching scientific literature

Elizabeth M McCormick, Marie T Lott, Matthew C Dulik, Lishuang Shen, Marcella Attimonelli, Ornella Vitale, Amel Karaa, Renkui Bai, Daniel E Pineda-Alvarez, Larry N Singh, Christine M Stanley, Stacey Wong, Anshu Bhardwaj, Daria Merkurjev, Rong Mao, Neal Sondheimer, Shiping Zhang, Vincent Procaccio, Douglas C Wallace, Xiaowu Gai, Marni J Falk. Hum Mutat 2020
Times Cited: 14







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



Times Cited
  Times     Co-cited
Similarity


Mitochondrial diseases.
Gráinne S Gorman, Patrick F Chinnery, Salvatore DiMauro, Michio Hirano, Yasutoshi Koga, Robert McFarland, Anu Suomalainen, David R Thorburn, Massimo Zeviani, Douglass M Turnbull. Nat Rev Dis Primers 2016
456
28

Molecular poltergeists: mitochondrial DNA copies (numts) in sequenced nuclear genomes.
Einat Hazkani-Covo, Raymond M Zeller, William Martin. PLoS Genet 2010
329
28

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
21

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
21

ClinVar: improving access to variant interpretations and supporting evidence.
Melissa J Landrum, Jennifer M Lee, Mark Benson, Garth R Brown, Chen Chao, Shanmuga Chitipiralla, Baoshan Gu, Jennifer Hart, Douglas Hoffman, Wonhee Jang,[...]. Nucleic Acids Res 2018
955
21

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
21

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
21


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
21

Fidelity of capture-enrichment for mtDNA genome sequencing: influence of NUMTs.
Mingkun Li, Roland Schroeder, Albert Ko, Mark Stoneking. Nucleic Acids Res 2012
68
21

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.
Sue Richards, Nazneen Aziz, Sherri Bale, David Bick, Soma Das, Julie Gastier-Foster, Wayne W Grody, Madhuri Hegde, Elaine Lyon, Elaine Spector,[...]. Genet Med 2015
21

Comprehensive next-generation sequence analyses of the entire mitochondrial genome reveal new insights into the molecular diagnosis of mitochondrial DNA disorders.
Hong Cui, Fangyuan Li, David Chen, Guoli Wang, Cavatina K Truong, Gregory M Enns, Brett Graham, Margherita Milone, Megan L Landsverk, Jing Wang,[...]. Genet Med 2013
64
21

Comprehensive molecular characterization of mitochondrial genomes in human cancers.
Yuan Yuan, Young Seok Ju, Youngwook Kim, Jun Li, Yumeng Wang, Christopher J Yoon, Yang Yang, Inigo Martincorena, Chad J Creighton, John N Weinstein,[...]. Nat Genet 2020
71
21

Clinical and laboratory interpretation of mitochondrial mRNA variants.
Lee-Jun C Wong, Ting Chen, Eric S Schmitt, Jing Wang, Sha Tang, Megan Landsverk, Fangyuan Li, Shulin Zhang, Yue Wang, Victor W Zhang,[...]. Hum Mutat 2020
4
75

UCSF Chimera--a visualization system for exploratory research and analysis.
Eric F Pettersen, Thomas D Goddard, Conrad C Huang, Gregory S Couch, Daniel M Greenblatt, Elaine C Meng, Thomas E Ferrin. J Comput Chem 2004
14



Mitochondria and cancer.
Douglas C Wallace. Nat Rev Cancer 2012
14

A bacterial cytidine deaminase toxin enables CRISPR-free mitochondrial base editing.
Beverly Y Mok, Marcos H de Moraes, Jun Zeng, Dustin E Bosch, Anna V Kotrys, Aditya Raguram, FoSheng Hsu, Matthew C Radey, S Brook Peterson, Vamsi K Mootha,[...]. Nature 2020
130
14

mtDNA Variation and Analysis Using Mitomap and Mitomaster.
Marie T Lott, Jeremy N Leipzig, Olga Derbeneva, H Michael Xie, Dimitra Chalkia, Mahdi Sarmady, Vincent Procaccio, Douglas C Wallace. Curr Protoc Bioinformatics 2013
238
14

Advancing genomic approaches to the molecular diagnosis of mitochondrial disease.
Sarah Louise Stenton, Holger Prokisch. Essays Biochem 2018
33
14


Mutation Load of Single, Large-Scale Deletions of mtDNA in Mitotic and Postmitotic Tissues.
Tina D Jeppesen, Morten Duno, John Vissing. Front Genet 2020
3
66

Diagnosis and management of mitochondrial disease: a consensus statement from the Mitochondrial Medicine Society.
Sumit Parikh, Amy Goldstein, Mary Kay Koenig, Fernando Scaglia, Gregory M Enns, Russell Saneto, Irina Anselm, Bruce H Cohen, Marni J Falk, Carol Greene,[...]. Genet Med 2015
203
14

Using urine to diagnose large-scale mtDNA deletions in adult patients.
Kristin N Varhaug, Gonzalo S Nido, Irenaeus de Coo, Pirjo Isohanni, Anu Suomalainen, Charalampos Tzoulis, Per Knappskog, Laurence A Bindoff. Ann Clin Transl Neurol 2020
6
33

Pathogenic mitochondrial DNA mutations are common in the general population.
Hannah R Elliott, David C Samuels, James A Eden, Caroline L Relton, Patrick F Chinnery. Am J Hum Genet 2008
357
14

Recent Advances in Mitochondrial Disease.
Lyndsey Craven, Charlotte L Alston, Robert W Taylor, Doug M Turnbull. Annu Rev Genomics Hum Genet 2017
114
14

Mitochondrial energy generation disorders: genes, mechanisms, and clues to pathology.
Ann E Frazier, David R Thorburn, Alison G Compton. J Biol Chem 2019
94
14


PCR-Free Enrichment of Mitochondrial DNA from Human Blood and Cell Lines for High Quality Next-Generation DNA Sequencing.
Meetha P Gould, Colleen M Bosworth, Sarah McMahon, Sneha Grandhi, Brian T Grimberg, Thomas LaFramboise. PLoS One 2015
16
14

Nuclear-mitochondrial DNA segments resemble paternally inherited mitochondrial DNA in humans.
Wei Wei, Alistair T Pagnamenta, Nicholas Gleadall, Alba Sanchis-Juan, Jonathan Stephens, John Broxholme, Salih Tuna, Christopher A Odhams, Carl Fratter, Ernest Turro,[...]. Nat Commun 2020
27
14

Myoclonic epilepsy and ragged-red fiber disease (MERRF) is associated with a mitochondrial DNA tRNA(Lys) mutation.
J M Shoffner, M T Lott, A M Lezza, P Seibel, S W Ballinger, D C Wallace. Cell 1990
14

Interpretation of mitochondrial tRNA variants.
Lee-Jun C Wong, Ting Chen, Jing Wang, Sha Tang, Eric S Schmitt, Megan Landsverk, Fangyuan Li, Yue Wang, Shulin Zhang, Victor Wei Zhang,[...]. Genet Med 2020
8
25

Sensitive detection of mitochondrial DNA variants for analysis of mitochondrial DNA-enriched extracts from frozen tumor tissue.
M J A Weerts, E C Timmermans, R H A M Vossen, D van Strijp, M C G N Van den Hout-van Vroonhoven, W F J van IJcken, P J van der Zaag, S Y Anvar, S Sleijfer, J W M Martens. Sci Rep 2018
8
25

MitoCarta3.0: an updated mitochondrial proteome now with sub-organelle localization and pathway annotations.
Sneha Rath, Rohit Sharma, Rahul Gupta, Tslil Ast, Connie Chan, Timothy J Durham, Russell P Goodman, Zenon Grabarek, Mary E Haas, Wendy H W Hung,[...]. Nucleic Acids Res 2021
78
14

Decrease of 3243 A-->G mtDNA mutation from blood in MELAS syndrome: a longitudinal study.
S Rahman, J Poulton, D Marchington, A Suomalainen. Am J Hum Genet 2001
162
14

Prevalence of nuclear and mitochondrial DNA mutations related to adult mitochondrial disease.
Gráinne S Gorman, Andrew M Schaefer, Yi Ng, Nicholas Gomez, Emma L Blakely, Charlotte L Alston, Catherine Feeney, Rita Horvath, Patrick Yu-Wai-Man, Patrick F Chinnery,[...]. Ann Neurol 2015
404
14

Mitochondrial Diseases: Hope for the Future.
Oliver M Russell, Gráinne S Gorman, Robert N Lightowlers, Doug M Turnbull. Cell 2020
68
14

Patient care standards for primary mitochondrial disease: a consensus statement from the Mitochondrial Medicine Society.
Sumit Parikh, Amy Goldstein, Amel Karaa, Mary Kay Koenig, Irina Anselm, Catherine Brunel-Guitton, John Christodoulou, Bruce H Cohen, David Dimmock, Gregory M Enns,[...]. Genet Med 2017
92
14

Mitochondria and cancer: past, present, and future.
M L Verschoor, R Ungard, A Harbottle, J P Jakupciak, R L Parr, G Singh. Biomed Res Int 2013
48
14

Mitochondrial determinants of cancer health disparities.
Aaheli Roy Choudhury, Keshav K Singh. Semin Cancer Biol 2017
41
14

Reanalysis and revision of the Cambridge reference sequence for human mitochondrial DNA.
R M Andrews, I Kubacka, P F Chinnery, R N Lightowlers, D M Turnbull, N Howell. Nat Genet 1999
14

Deletions of mitochondrial DNA in Kearns-Sayre syndrome.
M Zeviani, C T Moraes, S DiMauro, H Nakase, E Bonilla, E A Schon, L P Rowland. Neurology 1988
635
14

Mitochondrial genetic medicine.
Douglas C Wallace. Nat Genet 2018
101
14

MToolBox: a highly automated pipeline for heteroplasmy annotation and prioritization analysis of human mitochondrial variants in high-throughput sequencing.
Claudia Calabrese, Domenico Simone, Maria Angela Diroma, Mariangela Santorsola, Cristiano Guttà, Giuseppe Gasparre, Ernesto Picardi, Graziano Pesole, Marcella Attimonelli. Bioinformatics 2014
108
14

Origins and functional consequences of somatic mitochondrial DNA mutations in human cancer.
Young Seok Ju, Ludmil B Alexandrov, Moritz Gerstung, Inigo Martincorena, Serena Nik-Zainal, Manasa Ramakrishna, Helen R Davies, Elli Papaemmanuil, Gunes Gundem, Adam Shlien,[...]. Elife 2014
211
14

HmtDB, a human mitochondrial genomic resource based on variability studies supporting population genetics and biomedical research.
Marcella Attimonelli, Matteo Accetturo, Monica Santamaria, Daniela Lascaro, Gaetano Scioscia, Graziano Pappadà, Luigi Russo, Luigi Zanchetta, Mila Tommaseo-Ponzetta. BMC Bioinformatics 2005
44
14

The genomic landscape of polymorphic human nuclear mitochondrial insertions.
Gargi Dayama, Sarah B Emery, Jeffrey M Kidd, Ryan E Mills. Nucleic Acids Res 2014
86
14


The Genomic Landscape of Renal Oncocytoma Identifies a Metabolic Barrier to Tumorigenesis.
Shilpy Joshi, Denis Tolkunov, Hana Aviv, Abraham A Hakimi, Ming Yao, James J Hsieh, Shridar Ganesan, Chang S Chan, Eileen White. Cell Rep 2015
86
14


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.