Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 206 Records) |
Query Trace: NKX2-8[original query] |
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Migraine, Stroke, and Cervical Arterial Dissection: Shared Genetics for a Triad of Brain Disorders With Vascular Involvement.
Neurology. Genetics 2022 2 8 (1): e653. Daghals Iyas, Sargurupremraj Muralidharan, Danning Rebecca, Gormley Padhraig, Malik Rainer, Amouyel Philippe, Metso Tiina, Pezzini Alessandro, Kurth Tobias, Debette Stéphanie, Chasman Dani |
Association of NFKB1, NKX2-5, GATA4 and RANKL Gene Polymorphisms with Sporadic Congenital Heart Disease in Greek Patients. Balkan journal of medical genetics : BJMG 2021 8 24 (1): 15-20. Aidinidou L, Chatzikyriakidou A, Giannopoulos A, Karpa V, Tzimou I, Aidinidou E, Fidani |
Genetic and clinical heterogeneity of permanent neonatal diabetes mellitus: a single tertiary centre experience. Acta diabetologica 2021 8 58 (12): 1689-1700. Laimon Wafaa, El-Ziny Magdy, El-Hawary Amany, Elsharkawy Ashraf, Salem Nanees Abdel-Badie, Aboelenin Hadil Mohamed, Awad Mohammad Hosny, Flanagan Sarah E, De Franco Eli |
The role of NKX2-5 gene polymorphisms in congenital heart disease (CHD): a systematic review and meta-analysis. The Egyptian heart journal : (EHJ) : official bulletin of the Egyptian Society of Cardiology 2021 Aug 73 (1): 72. Ashiq Sana, Ashiq Kanwal, Sabar Muhammad Faro |
Genomic characteristics of invasive mucinous adenocarcinoma of the lung with multiple pulmonary sites of involvement. Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc 2021 Jul . Kim Moonsik, Hwang Jinha, Kim Kyung A, Hwang Sohyun, Lee Hye-Jeong, Jung Ji Ye, Lee Jin Gu, Cha Yoon Jin, Shim Hyo S |
Genetic Variants Associated with Thyroid Cancer Risk: Comprehensive Research Synopsis, Meta-Analysis, and Cumulative Epidemiological Evidence. Journal of oncology 2021 12 2021 9967599. Ran Ran, Tu Gang, Li Hui, Wang Hao, Mou Exian, Liu Caiya |
Genetic variants involved in innate immunity modulate the risk of inflammatory bowel diseases in an understudied Malaysian population. Journal of gastroenterology and hepatology 2021 12 37 (2): 342-351. Luu Laurence Don Wai, Popple Georgia, Tsang Samuel Pok Wei, Vinasco Karla, Hilmi Ida, Ng Ruey Terng, Chew Kee Seang, Wong Shin Yee, Riordan Stephen, Lee Way Seah, Mitchell Hazel M, Kaakoush Nadeem O, Castaño-Rodríguez Natal |
NKX2.1 (TTF1) germline mutation associated with pulmonary fibrosis and lung cancer. ERJ open research 2021 11 7 (4): . Borie Raphael, Funalot Benoit, Epaud Ralph, Delestrain Céline, Cazes Aurélie, Gounant Valerie, Frija Justine, Debray Marie-Pierre, Zalcman Gérard, Crestani Bru |
Implication of rare genetic variants of NODAL and ACVR1B in congenital heart disease patients from Indian population. Experimental cell research 2021 10 409 (1): 112869. Yadav Manohar Lal, Ranjan Prashant, Das Parimal, Jain Dharmendra, Kumar Ashok, Mohapatra Bhagyalax |
Stochastic epigenetic mutations as possible explanation for phenotypical discordance among twins with congenital hypothyroidism. Journal of endocrinological investigation 2022 9 46 (2): 393-404. Gentilini D, Muzza M, de Filippis T, Vigone M C, Weber G, Calzari L, Cassio A, Di Frenna M, Bartolucci M, Grassi E S, Carbone E, Olivieri A, Persani |
Rare surfactant-related variants in familial and sporadic pulmonary fibrosis. Human mutation 2022 Sep . Sutton Rachel M, Bittar Humberto Trejo, Sullivan Daniel I, Silva Agustin Gil, Bahudhanapati Harinath, Parikh Anishka H, Zhang Yingze, Gibson Kevin, McDyer John F, Kass Daniel J, Alder Jonathan |
Mutational Assessment in NKX2-5 and ACTC1 Genes in Patients with Congenital Cardiac Septal Defect (CCSD) from Ethnic Kashmiri Population. International journal of environmental research and public health 2022 8 19 (16): . Nazeer Nadeem Ul, Bhat Mohammad Akbar, Rah Bilal, Bhat Gh Rasool, Wani Shadil Ibrahim, Yousuf Adfar, Dar Abdul Majeed, Afroze D |
Germline Variants Associated with Nasopharyngeal Carcinoma Predisposition Identified through Whole-Exome Sequencing. Cancers 2022 Jul 14 (15): . Lee Ning-Yuan, Hum Melissa, Ong Pei-Yi, Myint Matthew Khine, Ong Enya H W, Low Kar-Perng, Li Zheng, Goh Boon-Cher, Tay Joshua K, Loh Kwok-Seng, Chua Melvin L K, Lee Soo-Chin, Khor Chiea-Chuen, Lee Ann S |
Mutational and bioinformatics analysis of the NKX2.1 gene in a cohort of Iranian pediatric patients with congenital hypothyroidism (CH). Physiology international 2022 Jun 109 (2): 261-277. Heidari Mohammad Mehdi, Madani Manshadi Seyed Ali, Eshghi Ahmad Reza, Talebi Fatemeh, Khatami Mehri, Bragança José, Ordooei Mahtab, Chamani Reyhane, Ghasemi Farzan |
Association between single-nucleotide polymorphisms of NKX2.5 and congenital heart disease in Chinese population: A meta-analysis. Open life sciences 2022 6 17 (1): 473-482. Chen Huan, Li Tianjiao, Wu Yuqing, Wang Xi, Wang Mingyuan, Wang Xin, Fang Xiaoli |
Mutational screening of the TPO and DUOX2 genes in Argentinian children with congenital hypothyroidism due to thyroid dyshormonogenesis. Endocrine 2022 5 77 (1): 86-101. Molina Maricel F, Papendieck Patricia, Sobrero Gabriela, Balbi Viviana A, Belforte Fiorella S, Martínez Elena Bueno, Adrover Ezequiela, Olcese María C, Chiesa Ana, Miras Mirta B, González Verónica G, Pio Mauricio Gomes, González-Sarmiento Rogelio, Targovnik Héctor M, Rivolta Carina |
Clinicopathologic and Genomic Landscape of Non-Small Cell Lung Cancer Brain Metastases. The oncologist 2022 May . Huang Richard S P, Harries Lukas, Decker Brennan, Hiemenz Matthew C, Murugesan Karthikeyan, Creeden James, Tolba Khaled, Stabile Laura P, Ramkissoon Shakti H, Burns Timothy F, Ross Jeffrey |
NKX2-5 variants screening in patients with atrial septal defect in Indonesia. BMC medical genomics 2022 4 15 (1): 91. Rozqie Royhan, Satwiko Muhammad Gahan, Anggrahini Dyah Wulan, Sadewa Ahmad Hamim, Gunadi , Hartopo Anggoro Budi, Mumpuni Hasanah, Dinarti Lucia Kr |
Deleterious Pulmonary Surfactant System Gene Mutations in Lung Adenocarcinomas Associated With Usual Interstitial Pneumonia. JCO precision oncology 2022 2 2 1-24. Honda Takayuki, Sakashita Hiroyuki, Masai Kyohei, Totsuka Hirohiko, Motoi Noriko, Kobayashi Masashi, Akashi Takumi, Mimaki Sachiyo, Tsuchihara Katsuya, Chiku Suenori, Shiraishi Kouya, Shimada Yoko, Otsuka Ayaka, Kanai Yae, Okubo Kenichi, Watanabe Shun-Ichi, Tsuta Koji, Inase Naohiko, Kohno Takas |
Associations between NKX2-5 gene polymorphisms and congenital heart disease in the Chinese Tibetan population. American journal of translational research 2022 12 14 (11): 8407-8415. Ma Qiang, Yang Yingzhong, Liu Yongni |
Identification of TCR rearrangements specific for genetic alterations in EGFR-mutated non-small cell lung cancer: results from the ADJUVANT-CTONG1104 trial. Cancer immunology, immunotherapy : CII 2022 11 . Chen Cunte, Liu Siyang Maggie, Chen Yedan, Ou Qiuxiang, Bao Hua, Xu Ling, Zhang Yikai, Zhang Jia-Tao, Zhong Wenzhao, Zhou Qing, Yang Xue-Ning, Shao Yang, Wu Yi-Long, Liu Si-Yang, Li Yangq |
Genetic Variants Close to TTN, NKX2-5, and MYH6 Associate With AVNRT. Circulation research 2022 10 131 (10): 862-865. Andreasen Laura, Ahlberg Gustav, Ægisdottir Hildur M, Sveinbjörnsson Gardar, Lundegaard Pia R, Hartmann Jacob P, Paludan-Müller Christian, Hadji-Turdeghal Katra, Ghouse Jonas, Pehrson Steen, Jensen Henrik K, Riahi Sam, Hansen Jim, Sandgaard Niels, Sørensen Erik, Banasik Karina, Sækmose Susanne G, Bruun Mie T, Hjalgrim Henrik, Erikstrup Christian, Pedersen Ole B, Wittig Michael, Haunsø Stig, Ostrowski Sisse R, , Franke Andre, Brunak Søren, Kanters Jørgen K, Ellervik Christina, Bundgaard Henning, Ullum Henrik, Gudbjartsson Daniel F, Thorsteinsdottir Unnur, Holm Hilma, Arnar David O, Stefansson Kari, Svendsen Jesper H, Olesen Morten |
Prioritizing Cardiovascular Disease-Associated Variants Altering NKX2-5 Binding through an Integrative Computational Approach. medRxiv : the preprint server for health sciences 2023 9 . Edwin G Peña-Martínez, Diego A Pomales-Matos, Alejandro Rivera-Madera, Jean L Messon-Bird, Joshua G Medina-Feliciano, Leandro Sanabria-Alberto, Adriana C Barreiro-Rosario, Jessica M Rodriguez-Rios, José A Rodríguez-Martín |
A Case-Control Study of the Relationship Between Genetic Polymorphism and Cretinism in Xinjiang. Pharmacogenomics and personalized medicine 2023 8 16 785-794. Jia Huang, Haiyan Wu, Guiqiang Zhao, Yan Ma, Yunping An, Li Sun, Fuye Li, Shengling Wa |
Novel Gene Polymorphisms for Stable Warfarin Dose in a Korean Population: Genome-Wide Association Study. Biomedicines 2023 8 11 (8): . Jung Sun Kim, Sak Lee, Jeong Yee, Kyemyung Park, Eun Jeong Jang, Byung Chul Chang, Hye Sun Gw |
Maternal Age at Menarche Gene Polymorphisms Are Associated with Offspring Birth Weight. Life (Basel, Switzerland) 2023 7 13 (7): . Yuliya Reshetnikova, Maria Churnosova, Vadim Stepanov, Anna Bocharova, Victoria Serebrova, Ekaterina Trifonova, Irina Ponomarenko, Inna Sorokina, Olga Efremova, Valentina Orlova, Irina Batlutskaya, Marina Ponomarenko, Vladimir Churnosov, Natalya Eliseeva, Inna Aristova, Alexey Polonikov, Evgeny Reshetnikov, Mikhail Churnos |
Association of maternal hypertension and diabetes with variants of the NKX2-5, LEFTY1 and LEFTY2 genes in children with congenital heart defects: a case-control study from Pakistani Population. Molecular biology reports 2023 4 . Sana Ashiq, Muhammad Farooq Sab |
eQTL colocalization analysis highlights novel susceptibility genes in Autism Spectrum Disorders (ASD). Translational psychiatry 2023 11 13 (1): 336. S Dominguez-Alonso, A Carracedo, C Rodriguez-Fonten |
Identification of BMP10 as a Novel Gene Contributing to Dilated Cardiomyopathy. Diagnostics (Basel, Switzerland) 2023 1 13 (2): . Gu Jia-Ning, Yang Chen-Xi, Ding Yuan-Yuan, Qiao Qi, Di Ruo-Min, Sun Yu-Min, Wang Jun, Yang Ling, Xu Ying-Jia, Yang Yi-Qi |
High risk of lung cancer in surfactant-related gene variant carriers. The European respiratory journal 2024 4 . Alexandre Brudon, Marie Legendre, Arthur Mageau, Julien Bermudez, Philippe Bonniaud, Diane Bouvry, Jacques Cadranel, Aurélie Cazes, Bruno Crestani, Tristan Dégot, Céline Delestrain, Rémi Diesler, Ralph Epaud, Quentin Philippot, Nathalie Theou-Anton, Caroline Kannengiesser, Ibrahima Ba, Marie-Pierre Debray, Pascale Fanen, Efrosine Manali, Spyros Papiris, Nadia Nathan, Serge Amselem, Antoine Gondouin, Anne Guillaumot, Claire Andréjak, Stephane Jouneau, Guillaume Beltramo, Yurdagul Uzunhan, François Galodé, Virginie Westeel, Anas Mehdaoui, Sandrine Hirschi, Sylvie Leroy, Sylvain Marchand-Adam, Hilario Nunes, Clément Picard, Grégoire Prevot, Martine Reynaud-Gaubert, Paul De Vuyst, Lidwine Wemeau, Gautier Defossez, Gérard Zalcman, Vincent Cottin, Raphael Borie, |
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- Page last updated:Apr 29, 2024
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