A citation-based method for searching scientific literature

Weiwei Zou, Jesse Slone, Yunxia Cao, Taosheng Huang. DNA Cell Biol 2020
Times Cited: 4







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



Times Cited
  Times     Co-cited
Similarity


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
50

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
25

Maternally inherited essential hypertension is associated with the novel 4263A>G mutation in the mitochondrial tRNAIle gene in a large Han Chinese family.
Shiwen Wang, Ronghua Li, Andrea Fettermann, Zongbin Li, Yaping Qian, Yuqi Liu, Xinjian Wang, Anna Zhou, Jun Qin Mo, Li Yang,[...]. Circ Res 2011
92
25

DNA from buccal swab is suitable for rapid genotyping of angiotensin-converting enzyme insertion/deletion (I/D) polymorphism.
Angelo Minucci, Giulia Canu, Paola Concolino, Donatella Guarino, Stefania Boccia, Silvana Ficarra, Cecilia Zuppi, Bruno Giardina, Ettore Capoluongo. Clin Chim Acta 2014
7
25

Mitochondrial genetic medicine.
Douglas C Wallace. Nat Genet 2018
101
25

Collection of buccal cell DNA using treated cards.
L C Harty, M Garcia-Closas, N Rothman, Y A Reid, M A Tucker, P Hartge. Cancer Epidemiol Biomarkers Prev 2000
63
25

The tRNAMet 4435A>G mutation in the mitochondrial haplogroup G2a1 is responsible for maternally inherited hypertension in a Chinese pedigree.
Zhongqiu Lu, Hong Chen, Yanzi Meng, Yan Wang, Ling Xue, Shaoce Zhi, Qiaomeng Qiu, Li Yang, Jun Qin Mo, Min-Xin Guan. Eur J Hum Genet 2011
32
25

Rapid screening of genetic polymorphisms using buccal cell DNA with detection by matrix-assisted laser desorption/ionization mass spectrometry.
Y H Liu, J Bai, Y Zhu, X Liang, D Siemieniak, P J Venta, D M Lubman. Rapid Commun Mass Spectrom 1995
69
25

Maternal transmission of mitochondrial diseases.
Marcos R Chiaratti, Carolina H Macabelli, José Djaci Augusto Neto, Mateus Priolo Grejo, Anand Kumar Pandey, Felipe Perecin, Maite Del Collado. Genet Mol Biol 2020
5
25

Noninvasive and Accurate Detection of Hereditary Hearing Loss Mutations with Buccal Swab Based on Droplet Digital PCR.
Fang Wang, Lingxiang Zhu, Baoxia Liu, Xiurui Zhu, Nan Wang, Tao Deng, Dongyang Kang, Junmin Pan, Wenjun Yang, Huafang Gao,[...]. Anal Chem 2018
5
25


Mitochondrial transfer RNAMet 4435A>G mutation is associated with maternally inherited hypertension in a Chinese pedigree.
Yuqi Liu, Ronghua Li, Zongbin Li, Xin-Jian Wang, Li Yang, Shiwen Wang, Min-Xin Guan. Hypertension 2009
72
25

Leber's hereditary optic neuropathy caused by a mutation in mitochondrial tRNAThr in eight Chinese pedigrees.
Juanjuan Zhang, Yanchun Ji, Xiaoling Liu, Jie Chen, Bibin Wang, Minglian Zhang, Min-Xin Guan. Mitochondrion 2018
8
25

Coronary heart disease is associated with a mutation in mitochondrial tRNA.
Zidong Jia, Xinjian Wang, Yanwen Qin, Ling Xue, Pingping Jiang, Yanzi Meng, Suxue Shi, Yan Wang, Jun Qin Mo, Min-Xin Guan. Hum Mol Genet 2013
45
25

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
25

Mitochondria and mitochondrial DNA as relevant targets for environmental contaminants.
Deborah A Roubicek, Nadja C de Souza-Pinto. Toxicology 2017
46
25

Universal rules and idiosyncratic features in tRNA identity.
R Giegé, M Sissler, C Florentz. Nucleic Acids Res 1998
568
25


Mitochondrial haplotypes may modulate the phenotypic manifestation of the deafness-associated 12S rRNA 1555A>G mutation.
Jianxin Lu, Yaping Qian, Zhiyuan Li, Aifen Yang, Yi Zhu, Ronghua Li, Li Yang, Xiaowen Tang, Bobei Chen, Yu Ding,[...]. Mitochondrion 2010
71
25

Detection of cytochrome P450 2C19 gene polymorphism from noninvasive samples by cycling probe technology.
Saori Nakagawa, Naoko Kuwabara, Yu Takamatsu, Sadahiko Shimoeda, Shin Ohta, Susumu Yamato. Ann Clin Biochem 2014
3
33

Biochemical characterization of the mitochondrial tRNASer(UCN) T7511C mutation associated with nonsyndromic deafness.
Xiaoming Li, Nathan Fischel-Ghodsian, Faina Schwartz, Qingfeng Yan, Rick A Friedman, Min-Xin Guan. Nucleic Acids Res 2004
106
25

A coronary artery disease-associated tRNAThr mutation altered mitochondrial function, apoptosis and angiogenesis.
Zidong Jia, Ye Zhang, Qiang Li, Zhenzhen Ye, Yuqi Liu, Changzhu Fu, Xiaohui Cang, Meng Wang, Min-Xin Guan. Nucleic Acids Res 2019
33
25

Stool-based DNA testing, a new noninvasive method for colorectal cancer screening, the first report from Iran.
Mohammad Reza Abbaszadegan, Alireza Tavasoli, Arash Velayati, Hamid Reza Sima, Hassan Vosooghinia, Mehdi Farzadnia, Hamid Asadzedeh, Mehran Gholamin, Ezzat Dadkhah, Azadeh Aarabi. World J Gastroenterol 2007
33
25

Human leukocyte antigen typing using buccal swabs as accurate and non-invasive substitute for venipuncture in children at risk for celiac disease.
Marlou P M Adriaanse, Anita C E Vreugdenhil, Véronique Vastmans, Lisette Groeneveld, Stefan Molenbroeck, Dina A Schott, Christina E M Voorter, Marcel G J Tilanus. J Gastroenterol Hepatol 2016
5
25

A comparative analysis approach to determining the pathogenicity of mitochondrial tRNA mutations.
John W Yarham, Mazhor Al-Dosary, Emma L Blakely, Charlotte L Alston, Robert W Taylor, Joanna L Elson, Robert McFarland. Hum Mutat 2011
133
25

A Newly Developed Nested PCR Assay for the Detection of Helicobacter pylori in the Oral Cavity.
Hawazen Ismail, Claire Morgan, Paul Griffiths, John Williams, Gareth Jenkins. J Clin Gastroenterol 2016
13
25

Automated genomic DNA extraction from saliva using the QIAxtractor.
Henry Keijzer, Silvia C Endenburg, Marcel G Smits, Miriam Koopmann. Clin Chem Lab Med 2010
5
25

Human mitochondrial tRNAs in health and disease.
C Florentz, B Sohm, P Tryoen-Tóth, J Pütz, M Sissler. Cell Mol Life Sci 2003
187
25

Expanding insights of mitochondrial dysfunction in Parkinson's disease.
Patrick M Abou-Sleiman, Miratul M K Muqit, Nicholas W Wood. Nat Rev Neurosci 2006
620
25

A deafness-associated tRNAHis mutation alters the mitochondrial function, ROS production and membrane potential.
Shasha Gong, Yanyan Peng, Pingping Jiang, Meng Wang, Mingjie Fan, Xinjian Wang, Hong Zhou, Huawei Li, Qingfeng Yan, Taosheng Huang,[...]. Nucleic Acids Res 2014
74
25

STR typing of ancient DNA extracted from hair shafts of Siberian mummies.
S Amory, C Keyser, E Crubézy, B Ludes. Forensic Sci Int 2007
25
25

A simple, low cost and non-invasive method for screening Y-chromosome microdeletions in infertile men.
I E Aknin-Seifer, R L Touraine, H Lejeune, J L Laurent, B Lauras, R Levy. Hum Reprod 2003
25
25

Comparison of different collection procedures and two methods for DNA isolation from saliva.
Jaroslava Durdiaková, Natália Kamodyová, Daniela Ostatníková, Barbora Vlková, Peter Celec. Clin Chem Lab Med 2012
11
25


New Frontiers in IVF: mtDNA and autologous germline mitochondrial energy transfer.
Mauro Cozzolino, Diego Marin, Giovanni Sisti. Reprod Biol Endocrinol 2019
16
25

Ovarian ageing: the role of mitochondria in oocytes and follicles.
Pascale May-Panloup, Lisa Boucret, Juan-Manuel Chao de la Barca, Valérie Desquiret-Dumas, Véronique Ferré-L'Hotellier, Catherine Morinière, Philippe Descamps, Vincent Procaccio, Pascal Reynier. Hum Reprod Update 2016
164
25


During autophagy mitochondria elongate, are spared from degradation and sustain cell viability.
Ligia C Gomes, Giulietta Di Benedetto, Luca Scorrano. Nat Cell Biol 2011
25

Cryopreservation and xenotransplantation of human ovarian tissue: an ultrastructural study.
Stefania A Nottola, Alessandra Camboni, Anne Van Langendonckt, Dominique Demylle, Guido Macchiarelli, Marie-Madeleine Dolmans, Belen Martinez-Madrid, Silvia Correr, Jacques Donnez. Fertil Steril 2008
75
25


Mitochondrial content reflects oocyte variability and fertilization outcome.
Teresa Almeida Santos, Shahy El Shourbagy, Justin C St John. Fertil Steril 2006
242
25

Vitrification and xenografting of human ovarian tissue.
Christiani Andrade Amorim, Marie-Madeleine Dolmans, Anu David, Jonathan Jaeger, Julie Vanacker, Alessandra Camboni, Jacques Donnez, Anne Van Langendonckt. Fertil Steril 2012
77
25

Controls for immunohistochemistry: the Histochemical Society's standards of practice for validation of immunohistochemical assays.
Stephen M Hewitt, Denis G Baskin, Charles W Frevert, William L Stahl, Eduardo Rosa-Molinar. J Histochem Cytochem 2014
127
25

The primordial pool of follicles and nest breakdown in mammalian ovaries.
Candace Tingen, Alison Kim, Teresa K Woodruff. Mol Hum Reprod 2009
132
25

Dynamic changes in mitochondrial DNA, distribution and activity within cat oocytes during folliculogenesis.
N Songsasen, L H Henson, W Tipkantha, C Thongkittidilok, J H Henson, K Chatdarong, P Comizzoli. Reprod Domest Anim 2017
5
25




Mitochondrial aggregation patterns and activity in human oocytes and preimplantation embryos.
M Wilding, B Dale, M Marino, L di Matteo, C Alviggi, M L Pisaturo, L Lombardi, G De Placido. Hum Reprod 2001
332
25

A modified and tailored human follicle isolation procedure improves follicle recovery and survival.
Maria Costanza Chiti, Marie-Madeleine Dolmans, Maria Hobeika, Alice Cernogoraz, Jacques Donnez, Christiani Andrade Amorim. J Ovarian Res 2017
12
25


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.