Human Genome Epidemiology Literature Finder
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Records 1 - 14 (of 14 Records) |
| Query Trace: Disease and PRKG1[original query] |
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| Fine mapping of the chromosome 10q11-q21 linkage region in Alzheimer's disease cases and controls. Neurogenetics 2010 Jul 11 (3): 335-48. Fallin Margaret Daniele, Szymanski Megan, Wang Ruihua, Gherman Adrian, Bassett Susan S, Avramopoulos Dimitri |
| Association study of 167 candidate genes for schizophrenia selected by a multi-domain evidence-based prioritization algorithm and neurodevelopmental hypothesis. PloS one 2013 8 (7): e67776. Zhao Zhongming, Webb Bradley T, Jia Peilin, Bigdeli T Bernard, Maher Brion S, van den Oord Edwin, Bergen Sarah E, Amdur Richard L, O'Neill Francis A, Walsh Dermot, Thiselton Dawn L, Chen Xiangning, Pato Carlos N, , Riley Brien P, Kendler Kenneth S, Fanous Ayman |
Genetic analysis of the pathogenic molecular sub-phenotype interferon-alpha identifies multiple novel loci involved in systemic lupus erythematosus.
Genes and immunity 0 16 (1): 15-23. Kariuki S N, Ghodke-Puranik Y, Dorschner J M, Chrabot B S, Kelly J A, Tsao B P, Kimberly R P, Alarcón-Riquelme M E, Jacob C O, Criswell L A, Sivils K L, Langefeld C D, Harley J B, Skol A D, Niewold T |
| Genome wide association and linkage analyses identified three loci-4q25, 17q23.2, and 10q11.21-associated with variation in leukocyte telomere length: the Long Life Family Study.
Frontiers in genetics 2013 4 310. Lee Joseph H, Cheng Rong, Honig Lawrence S, Feitosa Mary, Kammerer Candace M, Kang Min S, Schupf Nicole, Lin Shiow J, Sanders Jason L, Bae Harold, Druley Todd, Perls Thomas, Christensen Kaare, Province Michael, Mayeux Richa |
| Genetic susceptibility to salt-sensitive hypertension in a Han Chinese population: a validation study of candidate genes. Hypertension research : official journal of the Japanese Society of Hypertension 2017 Apr . Liu Zheng, Qi Han, Liu Bin, Liu Kuo, Wu Jingjing, Cao Han, Zhang Jie, Yan Yuxiang, He Yan, Zhang Li |
| Association of modifiers and other genetic factors explain Marfan syndrome clinical variability.
European journal of human genetics : EJHG 2018 12 26 (12): 1759-1772. Aubart Melodie, Gazal Steven, Arnaud Pauline, Benarroch Louise, Gross Marie-Sylvie, Buratti Julien, Boland Anne, Meyer Vincent, Zouali Habib, Hanna Nadine, Milleron Olivier, Stheneur Chantal, Bourgeron Thomas, Desguerre Isabelle, Jacob Marie-Paule, Gouya Laurent, Génin Emmanuelle, Deleuze Jean-François, Jondeau Guillaume, Boileau Catheri |
| Whole exome sequencing identifies MRVI1 as a susceptibility gene for moyamoya syndrome in neurofibromatosis type 1. PloS one 2018 13 (7): e0200446. Santoro Claudia, Giugliano Teresa, Kraemer Markus, Torella Annalaura, Schwitalla Jan Claudius, Cirillo Mario, Melis Daniela, Berlit Peter, Nigro Vincenzo, Perrotta Silverio, Piluso Giul |
| Identification of 26 novel loci that confer susceptibility to early-onset coronary artery disease in a Japanese population.
Biomedical reports 2018 Nov 9 (5): 383-404. Yamada Yoshiji, Yasukochi Yoshiki, Kato Kimihiko, Oguri Mitsutoshi, Horibe Hideki, Fujimaki Tetsuo, Takeuchi Ichiro, Sakuma J |
| Clinical Implications of Identifying Pathogenic Variants in Individuals With Thoracic Aortic Dissection. Circulation. Genomic and precision medicine 2019 6 12 (6): e002476. Wolford Brooke N, Hornsby Whitney E, Guo Dongchuan, Zhou Wei, Lin Maoxuan, Farhat Linda, McNamara Jennifer, Driscoll Anisa, Wu Xiaoting, Schmidt Ellen M, Norton Elizabeth L, Mathis Michael R, Ganesh Santhi K, Douville Nicholas J, Brummett Chad M, Kitzman Jacob, Chen Y Eugene, Kim Karen, Deeb G Michael, Patel Himanshu, Eagle Kim A, Milewicz Dianna M, J Willer Cristen, Yang |
| Association analysis of juvenile idiopathic arthritis genetic susceptibility factors in Estonian patients.
Clinical rheumatology 2021 Jun . Nikopensius Tiit, Niibo Priit, Haller Toomas, Jagomägi Triin, Voog-Oras Ülle, Tõnisson Neeme, Metspalu Andres, Saag Mare, Pruunsild Chr |
| Next Generation Exome Sequencing of Pediatric Asthma Identifies Rare and Novel Variants in Candidate Genes. Disease markers 2021 2 2021 8884229. Bogari Neda M, Amin Amr A, Rayes Husni H, Abdelmotelb Ahmed, Taher Mohiuddin M, Al-Allaf Faisal A, Bouazzaoui Abdellatif, O'Gorman Luke, Holloway John |
| Interferon pathway lupus risk alleles modulate risk of death from acute COVID-19. medRxiv : the preprint server for health sciences 2021 Nov . Nln Ilona, Fernandez-Ruiz Ruth, Wampler Muskardin Theresa L, Paredes Jacqueline L, Blazer Ashira D, Tuminello Stephanie, Attur Mukundan, Iturrate Eduardo, Petrilli Christopher M, Abramson Steven B, Chakravarti Aravinda, Niewold Timothy |
| Comparative Risks of Initial Aortic Events Associated With Genetic Thoracic Aortic Disease. Journal of the American College of Cardiology 2022 Aug 80 (9): 857-869. Regalado Ellen S, Morris Shaine A, Braverman Alan C, Hostetler Ellen M, De Backer Julie, Li Ruosha, Pyeritz Reed E, Yetman Anji T, Cervi Elena, Shalhub Sherene, Jeremy Richmond, LeMaire Scott, Ouzounian Maral, Evangelista Arturo, Boileau Catherine, Jondeau Guillaume, Milewicz Dianna |
| Spontaneous coronary artery dissection is infrequent in individuals with heritable thoracic aortic disease despite partially shared genetic susceptibility. American journal of medical genetics. Part A 2022 Jan . Murad Andrea M, Hill Hannah L, Wang Yu, Ghannam Michael, Yang Min-Lee, Pugh Norma L, Asch Federico M, Hornsby Whitney, Driscoll Anisa, McNamara Jennifer, Willer Cristen J, Regalado Ellen S, , , Milewicz Dianna M, Eagle Kim A, Ganesh Santhi |
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