Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 66 Records) |
Query Trace: ND5[original query] |
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Mitochondrial DNA sequencing reveals association of variants and haplogroup M33a2'3 with High altitude pulmonary edema susceptibility in Indian male lowlanders. Scientific reports 2019 Jul 9 (1): 10975. Sharma Swati, Singh Sayar, Gupta Rajinder K, Ganju Lilly, Singh Shashi Bala, Kumar Bhuvnesh, Singh Yami |
Maternally Inherited Differences within Mitochondrial Complex I Control Murine Healthspan. Genes 2019 7 10 (7): . Hirose Misa, Schilf Paul, Zarse Kim, Busch Hauke, Fuellen Georg, Jöhren Olaf, Köhling Rüdiger, König Inke R, Richer Barbara, Rupp Jan, Schwaninger Markus, Seeger Karsten, Sina Christian, Ristow Michael, Ibrahim Saleh |
Landscape of Germline and Somatic Mitochondrial DNA Mutations in Pediatric Malignancies. Cancer research 2019 2 79 (7): 1318-1330. Triska Petr, Kaneva Kristiyana, Merkurjev Daria, Sohail Noor, Falk Marni J, Triche Timothy J, Biegel Jaclyn A, Gai Xiao |
Four novel mutations in the mitochondrial ND4 gene of complex I in patients with multiple sclerosis. Biomedical reports 2019 12 11 (6): 257-268. Alharbi Maram Atallah, Al-Kafaji Ghada, Khalaf Noureddine Ben, Messaoudi Safia Abdulsalam, Taha Safa, Daif Abdulqader, Bakhiet Mo |
The conflict within: origin, proliferation and persistence of a spontaneously arising selfish mitochondrial genome. Philosophical transactions of the Royal Society of London. Series B, Biological sciences 2019 12 375 (1790): 20190174. Dubie Joseph James, Caraway Avery Robert, Stout McKenna Margaret, Katju Vaishali, Bergthorsson Ulf |
Genomic profiling of mitochondrial DNA reveals novel complex gene mutations in familial type 2 diabetes mellitus individuals from Mizo ethnic population, Northeast India. Mitochondrion 2019 Dec 51 7-14. Lalrohlui Freda, Zohmingthanga John, Hruaii Vanlal, Kumar Nachimuthu Senth |
A novel mutation in the mitochondrial MT-ND5 gene in a family with MELAS. The relevance of genetic analysis on targeted tissues. Mitochondrion 2019 10 50 14-18. Panadés-de Oliveira Luísa, Montoya Julio, Emperador Sonia, Ruiz-Pesini Eduardo, Jericó Ivonne, Arenas Joaquín, Hernández-Lain Aurelio, Blázquez Alberto, Martín Miguel Á, Domínguez-González Cristi |
Cardiomyopathy in children with mitochondrial disease: Prognosis and genetic background. International journal of cardiology 2019 1 279 115-121. Imai-Okazaki Atsuko, Kishita Yoshihito, Kohda Masakazu, Mizuno Yosuke, Fushimi Takuya, Matsunaga Ayako, Yatsuka Yukiko, Hirata Tomoko, Harashima Hiroko, Takeda Atsuhito, Nakaya Akihiro, Sakata Yasushi, Kogaki Shigetoyo, Ohtake Akira, Murayama Kei, Okazaki Yasus |
Associations of Mitochondrial and Nuclear Mitochondrial Variants and Genes with Seven Metabolic Traits. American journal of human genetics 2019 Jan 104 (1): 112-138. Kraja Aldi T, Liu Chunyu, Fetterman Jessica L, Graff Mariaelisa, Have Christian Theil, Gu Charles, Yanek Lisa R, Feitosa Mary F, Arking Dan E, Chasman Daniel I, Young Kristin, Ligthart Symen, Hill W David, Weiss Stefan, Luan Jian'an, Giulianini Franco, Li-Gao Ruifang, Hartwig Fernando P, Lin Shiow J, Wang Lihua, Richardson Tom G, Yao Jie, Fernandez Eliana P, Ghanbari Mohsen, Wojczynski Mary K, Lee Wen-Jane, Argos Maria, Armasu Sebastian M, Barve Ruteja A, Ryan Kathleen A, An Ping, Baranski Thomas J, Bielinski Suzette J, Bowden Donald W, Broeckel Ulrich, Christensen Kaare, Chu Audrey Y, Corley Janie, Cox Simon R, Uitterlinden Andre G, Rivadeneira Fernando, Cropp Cheryl D, Daw E Warwick, van Heemst Diana, de Las Fuentes Lisa, Gao He, Tzoulaki Ioanna, Ahluwalia Tarunveer S, de Mutsert Renée, Emery Leslie S, Erzurumluoglu A Mesut, Perry James A, Fu Mao, Forouhi Nita G, Gu Zhenglong, Hai Yang, Harris Sarah E, Hemani Gibran, Hunt Steven C, Irvin Marguerite R, Jonsson Anna E, Justice Anne E, Kerrison Nicola D, Larson Nicholas B, Lin Keng-Hung, Love-Gregory Latisha D, Mathias Rasika A, Lee Joseph H, Nauck Matthias, Noordam Raymond, Ong Ken K, Pankow James, Patki Amit, Pattie Alison, Petersmann Astrid, Qi Qibin, Ribel-Madsen Rasmus, Rohde Rebecca, Sandow Kevin, Schnurr Theresia M, Sofer Tamar, Starr John M, Taylor Adele M, Teumer Alexander, Timpson Nicholas J, de Haan Hugoline G, Wang Yujie, Weeke Peter E, Williams Christine, Wu Hongsheng, Yang Wei, Zeng Donglin, Witte Daniel R, Weir Bruce S, Wareham Nicholas J, Vestergaard Henrik, Turner Stephen T, Torp-Pedersen Christian, Stergiakouli Evie, Sheu Wayne Huey-Herng, Rosendaal Frits R, Ikram M Arfan, Franco Oscar H, Ridker Paul M, Perls Thomas T, Pedersen Oluf, Nohr Ellen A, Newman Anne B, Linneberg Allan, Langenberg Claudia, Kilpeläinen Tuomas O, Kardia Sharon L R, Jørgensen Marit E, Jørgensen Torben, Sørensen Thorkild I A, Homuth Georg, Hansen Torben, Goodarzi Mark O, Deary Ian J, Christensen Cramer, Chen Yii-Der Ida, Chakravarti Aravinda, Brandslund Ivan, Bonnelykke Klaus, Taylor Kent D, Wilson James G, Rodriguez Santiago, Davies Gail, Horta Bernardo L, Thyagarajan Bharat, Rao D C, Grarup Niels, Davila-Roman Victor G, Hudson Gavin, Guo Xiuqing, Arnett Donna K, Hayward Caroline, Vaidya Dhananjay, Mook-Kanamori Dennis O, Tiwari Hemant K, Levy Daniel, Loos Ruth J F, Dehghan Abbas, Elliott Paul, Malik Afshan N, Scott Robert A, Becker Diane M, de Andrade Mariza, Province Michael A, Meigs James B, Rotter Jerome I, North Kari |
Germline and somatic mtDNA mutation spectrum of rheumatoid arthritis patients in the Taizhou area, China. Rheumatology (Oxford, England) 2020 3 59 (10): 2982-2991. Du Juping, Yu Sufei, Wang Donglian, Chen Shuaishuai, Chen Suyun, Zheng Yufen, Wang Na, Chen Shiyong, Li Jun, Shen |
Multisystem mitochondrial diseases due to mutations in mtDNA-encoded subunits of complex I. BMC pediatrics 2020 1 20 (1): 41. Danhelovska Tereza, Kolarova Hana, Zeman Jiri, Hansikova Hana, Vaneckova Manuela, Lambert Lukas, Kucerova-Vidrova Vendula, Berankova Kamila, Honzik Tomas, Tesarova Marke |
The relationship between mitochondrial ND5 gene polymorphisms and in vitro embryo production in Sanjabi sheep. Zygote (Cambridge, England) 2021 Sep 1-3. Teymouri Fereshteh, Foroutanifar Saheb, Abdolmohammadi Alireza, Hajarian Ha |
Variations of Mitochondrial ND4 and ND5 Genes and their Association with Temporal Lobe Epilepsy in a Northern Han Chinese Population. Annals of Indian Academy of Neurology 0 24 (2): 266-267. Zhang Wuqiong, Wang Qilong, Cheng Yingying, Meng Hongm |
Mitochondrial genome variations are associated with amyotrophic lateral sclerosis in patients from mainland China. Journal of neurology 2021 Jun . Ni Jie, Liu Zhen, Yuan Yanchun, Li Wanzhen, Hu Yiting, Liu Pan, Hou Xiaorong, Zhu Xiangyu, Tang Xuxiong, Liang Mingyu, Zheng Siqi, Hou Xuan, Du Juan, Tang Jianguang, Jiang Hong, Shen Lu, Tang Beisha, Wang Junli |
NGS-based mtDNA Profiling Could Reveal Genetic Alterations in Schizophrenia. Current topics in medicinal chemistry 2021 6 21 (11): 938-948. Ivanova Elena Mihailova, Kandilarova Snezhina Mihailova, Lukanov Tzvetelin Ivanov, Naumova Elissaveta Jordanova, Akabalieva Katerina Valentinova, Milanova Vihra Krumo |
MELAS/LS Overlap Syndrome Associated With Mitochondrial DNA Mutations: Clinical, Genetic, and Radiological Studies. Frontiers in neurology 2021 5 12 648740. Wei Yanping, Huang Yan, Yang Yingmai, Qian M |
Genetic associations with polycystic ovary syndrome: the role of the mitochondrial genome; a systematic review and meta-analysis. Journal of clinical pathology 2022 9 75 (12): 815-824. Moosa Almira, Ghani Meeladah, O'Neill Helen Clai |
A Pilot Mitochondrial Genome-Wide Association on Migraine Among Saudi Arabians. International journal of general medicine 2022 7 15 6249-6258. Al Asoom Lubna, Khan Johra, Al Sunni Ahmad, Rafique Nazish, Latif Rabia, Alabdali Majed, AbdulAzeez Sayed, Borgio J Franc |
Examining the Association between Mitochondrial Genome Variation and Coronary Artery Disease. Genes 2022 3 13 (3): . Vilne Baiba, Sawant Aniket, Rudaka Iri |
Mutation profile of neurodegenerative mitochondriopathy - LHON in Southern India. Gene 2022 Apr 819 146202. Gowri Poigaialwar, Sathish Ponraj, Mahesh Kumar Shanmugam, Sundaresan Periasa |
Association analyses of the autosomal genome and mitochondrial DNA with accelerometry-derived sleep parameters in depressed UK biobank subjects.
Journal of psychiatric research 2022 12 157 152-161. Melhuish Beaupre Lindsay M, Wainberg Michael, Zai Clement C, Milic Milos, Felsky Daniel, Brown Gregory, Goldstein Benjamin I, Tripathy Shreejoy J, Kennedy James L, Gonçalves Vanessa |
Mitochondrial DNA haplogroup analysis in Saudi Arab patients with multiple sclerosis. PloS one 2022 12 17 (12): e0279237. Al-Kafaji Ghada, Alwehaidah Materah Salem, Alsabbagh Manahel Mahmood, Alharbi Maram A, Bakhiet Mo |
Heteroplasmic Mutant Load Differences in Mitochondrial DNA-Associated Leigh Syndrome. Pediatric neurology 2022 11 138 27-32. Na Ji-Hoon, Lee Young-Mo |
[Leber's hereditary optic neuropathy clinical features in patients with mitochondrial DNA m.13513G>A candidate mutation]. Vestnik oftalmologii 2022 10 138 (5. Vyp. 2): 208-214. Andreeva N A, Murakhovskaya Yu K, Tsygankova P G, Krilova T D, Sheremet N |
The mutational analysis of mitochondrial DNA in maternal inheritance of polycystic ovarian syndrome. Frontiers in endocrinology 2023 9 14 1093353. Shaheen Bibi, Ghulam Abbas, Muhammad Zahoor Khan, Tanzeela Nawaz, Qudrat Ullah, Aziz Uddin, Muhammad Fiaz Khan, Sajid Ul Ghafoor, Muhammad Shahid Nadeem, Sadia Tabassum, Muhammad Zaho |
Use of dual genomic sequencing to screen mitochondrial diseases in pediatrics: a retrospective analysis. Scientific reports 2023 3 13 (1): 4193. Wu Teng-Hui, Peng Jing, Yang Li, Chen Yan-Hui, Lu Xiu-Lan, Huang Jiao-Tian, You Jie-Yu, Ou-Yang Wen-Xian, Sun Yue-Yu, Xue Yi-Nan, Mao Xiao, Yan Hui-Ming, Ren Rong-Na, Xie Jing, Chen Zhi-Heng, Zhang Victor-Wei, Lyu Gui-Zhen, He Fa |
Prognostic landscape of mitochondrial genome in myelodysplastic syndrome after stem-cell transplantation. Journal of hematology & oncology 2023 3 16 (1): 21. Dong Jing, Buradagunta Christopher Staffi, Zhang Tao, Spellman Stephen, Bolon Yung-Tsi, DeZern Amy E, Gadalla Shahinaz M, Deeg H Joachim, Nazha Aziz, Cutler Corey, Cheng Chao, Urrutia Raul, Auer Paul, Saber Wa |
"Mitochondrial pathogenic mutations and metabolic alterations associated with COVID-19 disease severity". Journal of medical virology 2023 2 95 (2): e28553. Kumari Diksha, Singh Yamini, Singh Sayar, Dogra Vikas, Srivastava Ashish Kumar, Srivastava Swati, Garg Iti, Bargotya Mona, Hussain Javid, Ganju Lilly, Varshney Raje |
Association of Mitochondrial Variants with the Joint Occurrence of Polycystic Ovary Syndrome and Hashimoto's Thyroiditis. Antioxidants (Basel, Switzerland) 2023 11 12 (11): . Natalia Zeber-Lubecka, Maria Kulecka, Katarzyna Suchta, Michalina D?browska, Micha? Ciebiera, Ewa E Henn |
Leigh Syndrome: Spectrum of Molecular Defects and Clinical Features in Russia. International journal of molecular sciences 2023 1 24 (2): . Kistol Denis, Tsygankova Polina, Krylova Tatiana, Bychkov Igor, Itkis Yulia, Nikolaeva Ekaterina, Mikhailova Svetlana, Sumina Maria, Pechatnikova Natalia, Kurbatov Sergey, Bostanova Fatima, Migiaev Ochir, Zakharova Ekateri |
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- Page last updated:Apr 29, 2024
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