A citation-based method for searching scientific literature

Tiago M Bernardino Gomes, Yi Shiau Ng, Sarah J Pickett, Doug M Turnbull, Amy E Vincent. Hum Mol Genet 2021
Times Cited: 1







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



Times Cited
  Times     Co-cited
Similarity


Mitochondrial Syndromes Revisited.
Daniele Orsucci, Elena Caldarazzo Ienco, Andrea Rossi, Gabriele Siciliano, Michelangelo Mancuso. J Clin Med 2021
5
100

Cardiac involvement in mitochondrial DNA disease: clinical spectrum, diagnosis, and management.
Matthew G D Bates, John P Bourke, Carla Giordano, Giulia d'Amati, Douglass M Turnbull, Robert W Taylor. Eur Heart J 2012
120
100


Renal involvement in MELAS syndrome - a series of 5 cases and review of the literature.
Alexandre Seidowsky, Maxime Hoffmann, François Glowacki, Claire-Marie Dhaenens, Jean-Philippe Devaux, Celia Lessore de Sainte Foy, François Provot, Jean-Dominique Gheerbrant, Aurelie Hummel, Marc Hazzan,[...]. Clin Nephrol 2013
31
100

Risk factors for poor bone health in primary mitochondrial disease.
Shifa S Gandhi, Colleen Muraresku, Elizabeth M McCormick, Marni J Falk, Shana E McCormack. J Inherit Metab Dis 2017
12
100

Solid organ transplantation in primary mitochondrial disease: Proceed with caution.
Sumit Parikh, Amel Karaa, Amy Goldstein, Yi S Ng, Grainne Gorman, Annette Feigenbaum, John Christodoulou, Richard Haas, Mark Tarnopolsky, Bruce K Cohen,[...]. Mol Genet Metab 2016
27
100

LRPPRC mutations cause a phenotypically distinct form of Leigh syndrome with cytochrome c oxidase deficiency.
François-Guillaume Debray, Charles Morin, Annie Janvier, Josée Villeneuve, Bruno Maranda, Rachel Laframboise, Jacques Lacroix, Jean-Claude Decarie, Yves Robitaille, Marie Lambert,[...]. J Med Genet 2011
51
100

Expanding the genotypic spectrum of Perrault syndrome.
L A M Demain, J E Urquhart, J O'Sullivan, S G Williams, S S Bhaskar, E M Jenkinson, C M Lourenco, A Heiberg, S H Pearce, S A Shalev,[...]. Clin Genet 2017
46
100

Maternally inherited diabetes and deafness is a distinct subtype of diabetes and associates with a single point mutation in the mitochondrial tRNA(Leu(UUR)) gene.
J M van den Ouweland, H H Lemkes, R C Trembath, R Ross, G Velho, D Cohen, P Froguel, J A Maassen. Diabetes 1994
173
100

Retrospective natural history of thymidine kinase 2 deficiency.
Caterina Garone, Robert W Taylor, Andrés Nascimento, Joanna Poulton, Carl Fratter, Cristina Domínguez-González, Julie C Evans, Mariana Loos, Pirjo Isohanni, Anu Suomalainen,[...]. J Med Genet 2018
40
100

Age-related mitochondrial DNA depletion and the impact on pancreatic Beta cell function.
Donna L Nile, Audrey E Brown, Meutia A Kumaheri, Helen R Blair, Alison Heggie, Satomi Miwa, Lynsey M Cree, Brendan Payne, Patrick F Chinnery, Louise Brown,[...]. PLoS One 2014
29
100

Mitochondrial Donation - Which Women Could Benefit?
Sarah J Pickett, Alasdair Blain, Yi Shiau Ng, Ian J Wilson, Robert W Taylor, Robert McFarland, Doug M Turnbull, Gráinne S Gorman. N Engl J Med 2019
10
100

Recessive twinkle mutations cause severe epileptic encephalopathy.
Tuula Lönnqvist, Anders Paetau, Leena Valanne, Helena Pihko. Brain 2009
69
100

Strategies for fighting mitochondrial diseases.
C Viscomi, M Zeviani. J Intern Med 2020
19
100

Impaired insulin secretion and beta-cell loss in tissue-specific knockout mice with mitochondrial diabetes.
J P Silva, M Köhler, C Graff, A Oldfors, M A Magnuson, P O Berggren, N G Larsson. Nat Genet 2000
321
100

Mitochondrial DNA mutation analysis from exome sequencing-A more holistic approach in diagnostics of suspected mitochondrial disease.
Matias Wagner, Riccardo Berutti, Bettina Lorenz-Depiereux, Elisabeth Graf, Gertrud Eckstein, Johannes A Mayr, Thomas Meitinger, Uwe Ahting, Holger Prokisch, Tim M Strom,[...]. J Inherit Metab Dis 2019
30
100

Mutations in the DBP-deficiency protein HSD17B4 cause ovarian dysgenesis, hearing loss, and ataxia of Perrault Syndrome.
Sarah B Pierce, Tom Walsh, Karen M Chisholm, Ming K Lee, Anne M Thornton, Agata Fiumara, John M Opitz, Ephrat Levy-Lahad, Rachel E Klevit, Mary-Claire King. Am J Hum Genet 2010
171
100


Pronuclear transfer in human embryos to prevent transmission of mitochondrial DNA disease.
Lyndsey Craven, Helen A Tuppen, Gareth D Greggains, Stephen J Harbottle, Julie L Murphy, Lynsey M Cree, Alison P Murdoch, Patrick F Chinnery, Robert W Taylor, Robert N Lightowlers,[...]. Nature 2010
286
100

Defining the importance of mitochondrial gene defects in maternally inherited diabetes by sequencing the entire mitochondrial genome.
Alan T W Choo-Kang, Stephen Lynn, Geoffrey A Taylor, Mark E Daly, Sarbpreet S Sihota, Teressa M Wardell, Patrick F Chinnery, Douglass M Turnbull, Mark Walker. Diabetes 2002
28
100

Latent Autoimmune Diabetes in Adults: Current Status and New Horizons.
Paolo Pozzilli, Silvia Pieralice. Endocrinol Metab (Seoul) 2018
23
100

Mitochondrial DNA sequence characteristics modulate the size of the genetic bottleneck.
Ian J Wilson, Phillipa J Carling, Charlotte L Alston, Vasileios I Floros, Angela Pyle, Gavin Hudson, Suzanne C E H Sallevelt, Costanza Lamperti, Valerio Carelli, Laurence A Bindoff,[...]. Hum Mol Genet 2016
38
100

Phenotypic heterogeneity in m.3243A>G mitochondrial disease: The role of nuclear factors.
Sarah J Pickett, John P Grady, Yi Shiau Ng, Gráinne S Gorman, Andrew M Schaefer, Ian J Wilson, Heather J Cordell, Doug M Turnbull, Robert W Taylor, Robert McFarland. Ann Clin Transl Neurol 2018
44
100

Mitochondrial respiratory dysfunction caused by a heteroplasmic mitochondrial DNA mutation blocks cellular reprogramming.
Mutsumi Yokota, Hideyuki Hatakeyama, Saki Okabe, Yasuha Ono, Yu-ichi Goto. Hum Mol Genet 2015
30
100

Towards germline gene therapy of inherited mitochondrial diseases.
Masahito Tachibana, Paula Amato, Michelle Sparman, Joy Woodward, Dario Melguizo Sanchis, Hong Ma, Nuria Marti Gutierrez, Rebecca Tippner-Hedges, Eunju Kang, Hyo-Sang Lee,[...]. Nature 2013
230
100

The impact of gender, puberty, and pregnancy in patients with POLG disease.
Omar Hikmat, Karin Naess, Martin Engvall, Claus Klingenberg, Magnhild Rasmussen, Chantal M E Tallaksen, Christian Samsonsen, Eylert Brodtkorb, Elsebet Ostergaard, Rene de Coo,[...]. Ann Clin Transl Neurol 2020
2
100

Incidence and predictors of total mortality in 267 adults presenting with mitochondrial diseases.
Constantinos Papadopoulos, Karim Wahbi, Anthony Behin, Wulfran Bougouin, Tanya Stojkovic, Sarah Leonard-Louis, Nawal Berber, Anne Lombès, Denis Duboc, Claude Jardel,[...]. J Inherit Metab Dis 2020
3
100

Metabolic rescue in pluripotent cells from patients with mtDNA disease.
Hong Ma, Clifford D L Folmes, Jun Wu, Robert Morey, Sergio Mora-Castilla, Alejandro Ocampo, Li Ma, Joanna Poulton, Xinjian Wang, Riffat Ahmed,[...]. Nature 2015
113
100

Sudden adult death syndrome in m.3243A>G-related mitochondrial disease: an unrecognized clinical entity in young, asymptomatic adults.
Yi Shiau Ng, John P Grady, Nichola Z Lax, John P Bourke, Charlotte L Alston, Steven A Hardy, Gavin Falkous, Andrew G Schaefer, Aleksandar Radunovic, Saidi A Mohiddin,[...]. Eur Heart J 2016
31
100

Maternally transmitted diabetes and deafness associated with a 10.4 kb mitochondrial DNA deletion.
S W Ballinger, J M Shoffner, E V Hedaya, I Trounce, M A Polak, D A Koontz, D C Wallace. Nat Genet 1992
531
100

Mitochondrial diabetes is associated with insulin resistance in subcutaneous adipose tissue but not with increased liver fat content.
Markus M Lindroos, Ronald Borra, Nina Mononen, Terho Lehtimäki, Kirsi A Virtanen, Virva Lepomäki, Letizia Guiducci, Patricia Iozzo, Kari Majamaa, Pirjo Nuutila. J Inherit Metab Dis 2011
6
100

Monogenic Diabetes: From Genetic Insights to Population-Based Precision in Care. Reflections From a Diabetes Care Editors' Expert Forum.
Matthew C Riddle, Louis H Philipson, Stephen S Rich, Annelie Carlsson, Paul W Franks, Siri Atma W Greeley, John J Nolan, Ewan R Pearson, Philip S Zeitler, Andrew T Hattersley. Diabetes Care 2020
9
100

Hearing impairment in patients with 3243A-->G mtDNA mutation: phenotype and rate of progression.
S Uimonen, J S Moilanen, M Sorri, I E Hassinen, K Majamaa. Hum Genet 2001
36
100

High risk of severe cardiac adverse events in patients with mitochondrial m.3243A>G mutation.
Edoardo Malfatti, Pascal Laforêt, Claude Jardel, Tanya Stojkovic, Anthony Behin, Bruno Eymard, Anne Lombès, Amria Benmalek, Henri-Marc Bécane, Nawal Berber,[...]. Neurology 2013
39
100

Inappropriate liver transplantation in a child with Alpers-Huttenlocher syndrome misdiagnosed as valproate-induced acute liver failure.
A Delarue, O Paut, J M Guys, M F Montfort, V Lethel, B Roquelaure, J F Pellissier, J Sarles, J Camboulives. Pediatr Transplant 2000
43
100

Mitochondrial medicine therapies: rationale, evidence, and dosing guidelines.
Isabella Barcelos, Edward Shadiack, Rebecca D Ganetzky, Marni J Falk. Curr Opin Pediatr 2020
9
100

Prevalence of A-to-G mutation at nucleotide 3243 of the mitochondrial tRNA(Leu(UUR)) gene in Japanese patients with diabetes mellitus and end stage renal disease.
N Iwasaki, T Babazono, K Tsuchiya, O Tomonaga, A Suzuki, M Togashi, N Ujihara, Y Sakka, H Yokokawa, M Ogata,[...]. J Hum Genet 2001
24
100

Molecular and histological evaluation of pancreata from patients with a mitochondrial gene mutation associated with impaired insulin secretion.
S Otabe, K Yasuda, Y Mori, K Shimokawa, H Kadowaki, A Jimi, K Nonaka, Y Akanuma, Y Yazaki, T Kadowaki. Biochem Biophys Res Commun 1999
24
100


Association between HLA and islet cell antibodies in diabetic patients with a mitochondrial DNA mutation at base pair 3243.
T Kobayashi, Y Oka, H Katagiri, A Falorni, A Kasuga, I Takei, K Nakanishi, T Murase, K Kosaka, A Lernmark. Diabetologia 1996
29
100

Systematic review and meta-analysis of cardiac involvement in mitochondrial myopathy.
Asfia Quadir, Carly Sabine Pontifex, Helen Lee Robertson, Christopher Labos, Gerald Pfeffer. Neurol Genet 2019
10
100

Growth hormone deficiency in a patient with mitochondrial disease.
Vera Rocha, Dalila Rocha, Helena Santos, Jorge Sales Marques. J Pediatr Endocrinol Metab 2015
12
100

Lack of paternal inheritance of muscle mitochondrial DNA in sporadic mitochondrial myopathies.
Massimiliano Filosto, Michelangelo Mancuso, Cristofol Vives-Bauza, Maya R Vilà, Sara Shanske, Michio Hirano, Antoni L Andreu, Salvatore DiMauro. Ann Neurol 2003
42
100

Urine heteroplasmy is the best predictor of clinical outcome in the m.3243A>G mtDNA mutation.
R G Whittaker, J K Blackwood, C L Alston, E L Blakely, J L Elson, R McFarland, P F Chinnery, D M Turnbull, R W Taylor. Neurology 2009
66
100

Clinical and genetic heterogeneity in progressive external ophthalmoplegia due to mutations in polymerase gamma.
Massimiliano Filosto, Michelangelo Mancuso, Yutaka Nishigaki, Jacklyn Pancrudo, Yadollah Harati, Clifton Gooch, Ami Mankodi, Lydia Bayne, Eduardo Bonilla, Sara Shanske,[...]. Arch Neurol 2003
91
100

Mutations in LARS2, encoding mitochondrial leucyl-tRNA synthetase, lead to premature ovarian failure and hearing loss in Perrault syndrome.
Sarah B Pierce, Ksenija Gersak, Rachel Michaelson-Cohen, Tom Walsh, Ming K Lee, Daniel Malach, Rachel E Klevit, Mary-Claire King, Ephrat Levy-Lahad. Am J Hum Genet 2013
129
100

Clinical features of diabetes mellitus with the mitochondrial DNA 3243 (A-G) mutation in Japanese: maternal inheritance and mitochondria-related complications.
Susumu Suzuki, Yoshitomo Oka, Takashi Kadowaki, Azuma Kanatsuka, Takeshi Kuzuya, Masashi Kobayashi, Tokio Sanke, Yutaka Seino, Kishio Nanjo. Diabetes Res Clin Pract 2003
49
100

Mitochondrial disease in pregnancy: a systematic review.
R E Say, R G Whittaker, H E Turnbull, R McFarland, R W Taylor, D M Turnbull. Obstet Med 2011
14
100

The clinical, biochemical and genetic features associated with RMND1-related mitochondrial disease.
Yi Shiau Ng, Charlotte L Alston, Daria Diodato, Andrew A Morris, Nicole Ulrick, Stanislav Kmoch, Josef Houštěk, Diego Martinelli, Alireza Haghighi, Mehnaz Atiq,[...]. J Med Genet 2016
20
100



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.