Human Genome Epidemiology Literature Finder
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Records 1 - 30 (of 70 Records) |
| Query Trace: Disease and CAMP[original query] |
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Genome-Wide Association Study Reveals Genetic Link between Diarrhea-Associated Entamoeba histolytica Infection and Inflammatory Bowel Disease.
mBio 2018 09 9 (5): . Wojcik Genevieve L, Marie Chelsea, Abhyankar Mayuresh M, Yoshida Nobuya, Watanabe Koji, Mentzer Alexander J, Carstensen Tommy, Mychaleckyj Josyf, Kirkpatrick Beth D, Rich Stephen S, Concannon Patrick, Haque Rashidul, Tsokos George C, Petri William A, Duggal Pri |
| Clinical and genetic associations with prostacyclin response in pulmonary arterial hypertension. Pulmonary circulation 2018 8 8 (4): 2045894018800544. Halliday Stephen J, Xu Meng, Thayer Timothy E, Mosley Jonathan D, Sheng Quanhu, Ye Fei, Farber-Eger Eric H, Pugh Meredith E, Robbins Ivan R, Assad Tufik R, West James D, Brittain Evan L, Hemnes Anna |
| Weibel-Palade Body Localized Syntaxin-3 Modulates Von Willebrand Factor Secretion From Endothelial Cells. Arteriosclerosis, thrombosis, and vascular biology 2018 Jun . Schillemans Maaike, Karampini Ellie, van den Eshof Bart, Gangaev Anastasia, Hofman Menno, van Breevoort Dorothee, Meems Henriët, Janssen Hans, Mulder Aat A, Jost Carolina R, Escher Johanna C, Adam Rüdiger, Carter Tom, Koster Abraham J, van den Biggelaar Maartje, Voorberg Jan, Bierings Rub |
| PDE8B mutation is not associated with Parkinson's disease in a Taiwanese population. Neurobiology of aging 2018 May . Fan Tian-Sin, Wu Ruey-Meei, Lin Han-I, Cheng Chieh, Lin Chin-Hsi |
| Identification of Key Genes and Pathways Associated with RUNX1 Mutations in Acute Myeloid Leukemia Using Bioinformatics Analysis. Medical science monitor : international medical journal of experimental and clinical research 2018 Oct 24 7100-7108. Zhu Fangxiao, Huang Rui, Li Jing, Liao Xiwen, Huang Yumei, Lai Yongro |
| How Rap and its GEFs control liver physiology and cancer development. C3G alterations in human hepatocarcinoma. Hepatic oncology 2018 10 5 (1): HEP05. Sequera Celia, Manzano Sara, Guerrero Carmen, Porras Almude |
| Whole-Exome Sequencing of Nasopharyngeal Carcinoma Families Reveals Novel Variants Potentially Involved in Nasopharyngeal Carcinoma. Scientific reports 2019 7 9 (1): 9916. Yu Guoqin, Hsu Wan-Lun, Coghill Anna E, Yu Kelly J, Wang Cheng-Ping, Lou Pei-Jen, Liu Zhiwei, Jones Kristie, Vogt Aurelie, Wang Mingyi, Mbulaiteye Sam M, Chen Hao-Hui, Boland Joseph, Yeager Meredith, Diehl Scott R, Chen Chien-Jen, Hildesheim Allan, Goldstein Alisa |
| Systems Approach to Identify Common Genes and Pathways Associated with Response to Selective Serotonin Reuptake Inhibitors and Major Depression Risk. International journal of molecular sciences 2019 4 20 (8): . Srivastava Ankit, Singh Priyanka, Gupta Hitesh, Kaur Harpreet, Kanojia Neha, Guin Debleena, Sood Mamta, Chadda Rakesh Kumar, Yadav Jyoti, Vohora Divya, Saso Luciano, Kukreti Ritushr |
| Mutant RAMP2 causes primary open-angle glaucoma via the CRLR-cAMP axis. Genetics in medicine : official journal of the American College of Medical Genetics 2019 Apr . Gong Bo, Zhang Houbin, Huang Lulin, Chen Yuhong, Shi Yi, Tam Pancy Oi-Sin, Zhu Xianjun, Huang Yi, Lei Bo, Sundaresan Periasamy, Li Xi, Jiang Linxin, Yang Jialiang, Lin Ying, Lu Fang, Chen Lijia, Li Yuanfeng, Leung Christopher Kai-Shun, Guo Xiaoxin, Zhang Shanshan, Huang Guo, Wu Yaqi, Zhou Tongdan, Shuai Ping, Tham Clement Chee-Yung, Weisschuh Nicole, Krishnadas Subbaiah Ramasamy, Mardin Christian, Reis André, Yang Jiyun, Zhang Lin, Zhou Yu, Wang Ziyan, Qu Chao, Shaw Peter X, Pang Chi-Pui, Sun Xinghuai, Zhu Weiquan, Li Dean Yaw, Pasutto Francesca, Yang Zhengl |
| Impact of USP8 Gene Mutations on Protein Deregulation in Cushing Disease. The Journal of clinical endocrinology and metabolism 2019 Mar . Weigand Isabel, Knobloch Lisanne, Flitsch Jörg, Saeger Wolfgang, Monoranu Camelia M, Höfner Kerstin, Herterich Sabine, Rotermund Roman, Ronchi Cristina L, Buchfelder Michael, Glatzel Markus, Hagel Christian, Fassnacht Martin, Deutschbein Timo, Sbiera Silv |
| Characterization of Rare Variants in MC4R in African American and Latino Children With Severe Early-Onset Obesity. The Journal of clinical endocrinology and metabolism 2019 2 104 (7): 2961-2970. De Rosa Maria Caterina, Chesi Alessandra, McCormack Shana, Zhou Justin, Weaver Benjamin, McDonald Molly, Christensen Sinead, Liimatta Kalle, Rosenbaum Michael, Hakonarson Hakon, Doege Claudia A, Grant Struan F A, Hirschhorn Joel N, Thaker Vidhu |
| PDE4B gene polymorphism in Russian patients with panic disorder. AIMS genetics 2019 6 (3): 55-63. Malakhova Alena V, Rudko Olga I, Sobolev Vladimir V, Tretiakov Artemii V, Naumova Elena A, Kokaeva Zarema G, Azimova Julia E, Klimov Eugene |
| The impact of the rs8005161 polymorphism on G protein-coupled receptor GPR65 (TDAG8) pH-associated activation in intestinal inflammation. BMC gastroenterology 2019 1 19 (1): 2. Tcymbarevich Irina V, Eloranta Jyrki J, Rossel Jean-Benoît, Obialo Nicole, Spalinger Marianne, Cosin-Roger Jesus, Lang Silvia, Kullak-Ublick Gerd A, Wagner Carsten A, Scharl Michael, Seuwen Klaus, Ruiz Pedro A, Rogler Gerhard, de Vallière Cheryl, Misselwitz Benjamin, |
| Genome-wide association analyses of chronotype in 697,828 individuals provides insights into circadian rhythms.
Nature communications 2019 01 10 (1): 343. Jones Samuel E, Lane Jacqueline M, Wood Andrew R, van Hees Vincent T, Tyrrell Jessica, Beaumont Robin N, Jeffries Aaron R, Dashti Hassan S, Hillsdon Melvyn, Ruth Katherine S, Tuke Marcus A, Yaghootkar Hanieh, Sharp Seth A, Jie Yingjie, Thompson William D, Harrison Jamie W, Dawes Amy, Byrne Enda M, Tiemeier Henning, Allebrandt Karla V, Bowden Jack, Ray David W, Freathy Rachel M, Murray Anna, Mazzotti Diego R, Gehrman Philip R, Lawlor Debbie A, Frayling Timothy M, Rutter Martin K, Hinds David A, Saxena Richa, Weedon Michael |
| Influence of rs1042713 and rs1042714 polymorphisms of ?2-adrenergic receptor gene with erythrocyte cAMP in sickle cell disease patients from Odisha State, India. Annals of hematology 2020 Sep . Sinha Shalini, Jit Bimal Prasad, Patro A Raj Kumar, Ray Aisurya, Dehury Snehadhini, Sahoo Sarmila, Behera Rajendra Kumar, Mohanty Pradeep Kumar, Panigrahi Pinaki, Das Padmala |
| Exome Sequencing Reveals Signal Transduction Genes Involved in Impulse Control Disorders in Parkinson's Disease. Frontiers in neurology 2020 8 11 641. Prud'hon Sabine, Bekadar Samir, Rastetter Agnès, Guégan Justine, Cormier-Dequaire Florence, Lacomblez Lucette, Mangone Graziella, You Hana, Daniau Mailys, Marie Yannick, Bertrand Hélène, Lesage Suzanne, Tezenas Du Montcel Sophie, Anheim Mathieu, Brice Alexis, Danjou Fabrice, Corvol Jean-Christop |
| Regulatory SNP rs5743417 impairs constitutive expression of human ?-defensin 1 and has high frequency in Africans and Afro-Americans. International journal of immunogenetics 2020 1 47 (4): 332-341. Cruz Díaz Luis Antonio, Gutiérrez Ortega Abel, Chávez Álvarez Rocío Del Carmen, Velarde Félix Jesús Salvador, Prado Montes de Oca Ernes |
| The PRKAR1B p.R115K Variant is Associated with Lipoprotein Profile in African American Youth with Metabolic Challenges. Journal of the Endocrine Society 2021 7 5 (8): bvab071. Bloyd Michelle, Settas Nikolaos, Faucz Fabio Rueda, Sinaii Ninet, Bathon Kerstin, Iben James, Coon Steven, Caprio Sonia, Stratakis Constantine A, London Ed |
| Exome sequencing revealed PDE11A as a novel candidate gene for early-onset Alzheimer's disease. Human molecular genetics 2021 4 30 (9): 811-822. Qin Wei, Zhou Aihong, Zuo Xiumei, Jia Longfei, Li Fangyu, Wang Qi, Li Ying, Wei Yiping, Jin Hongmei, Cruchaga Carlos, Benitez Bruno A, Jia Jianpi |
| Predicted regulatory SNPs reveal potential drug targets and novel companion diagnostics in psoriasis. Journal of translational autoimmunity 2021 4 100096. Ruiz Ramírez Andrea Virginia, Flores-Saiffe Farías Adolfo, Chávez Álvarez Rocío Del Carmen, Prado Montes de Oca Ernes |
| DDX58 Is Associated With Susceptibility to Severe Influenza Virus Infection in Children and Adolescents. The Journal of infectious diseases 2022 Aug . Lee Sanghun, Zhang Yu, Newhams Margaret, Novak Tanya, Thomas Paul G, Mourani Peter M, Hall Mark W, Loftis Laura L, Cvijanovich Natalie Z, Tarquinio Keiko M, Schwarz Adam J, Weiss Scott L, Thomas Neal J, Markovitz Barry, Cullimore Melissa L, Sanders Ronald C, Zinter Matt S, Sullivan Janice E, Halasa Natasha B, Bembea Melania M, Giuliano John S, Typpo Katri V, Nofziger Ryan A, Shein Steven L, Kong Michele, Coates Bria M, Weiss Scott T, Lange Christoph, Su Helen C, Randolph Adrienne G, |
| The relationship between phosphodiesterase 4D gene polymorphism and coronary heart disease. Cellular and molecular biology (Noisy-le-Grand, France) 2022 Feb 67 (6): 26-32. Yan Laixing, Li Ketao, Zhang Weiwei, Shen Chengji, Ma Liping, Sun |
| Whole-genome sequencing identifies rare missense variants of WNT16 and ERVW-1 causing the systemic lupus erythematosus. Genomics 2022 3 114 (3): 110332. Chen Jianhai, Zhang Ping, Chen Haidi, Wang Xin, He Xuefei, Zhong Jie, Zheng HuaPing, Li Xiaoyu, Jakovli? Ivan, Zhang Yong, Chen Younan, Shen Bairong, Deng Cheng, Wu Yongka |
| Carriers of rare damaging CCR2 genetic variants are at lower risk of atherosclerotic disease. medRxiv : the preprint server for health sciences 2023 8 . Marios K Georgakis, Rainer Malik, Natalie R Hasbani, Gabrielle Shakt, Alanna C Morrison, Noah L Tsao, Renae Judy, Braxton D Mitchell, Huichun Xu, May E Montasser, Ron Do, Eimear E Kenny, Ruth J F Loos, James G Terry, John Jeffrey Carr, Joshua C Bis, Bruce M Psaty, W T Longstreth, Kendra A Young, Sharon M Lutz, Michael H Cho, Jai Broome, Alyna T Khan, Fei Fei Wang, Nancy Heard-Costa, Sudha Seshadri, Ramachandran S Vasan, Nicholette D Palmer, Barry I Freedman, Donald W Bowden, Lisa R Yanek, Brian G Kral, Lewis C Becker, Patricia A Peyser, Lawrence F Bielak, Farah Ammous, April P Carson, Michael E Hall, Laura M Raffield, Stephen S Rich, Wendy S Post, Russel P Tracy, Kent D Taylor, Xiuqing Guo, Michael C Mahaney, Joanne E Curran, John Blangero, Shoa L Clarke, Jeffrey W Haessler, Yao Hu, Themistocles L Assimes, Charles Kooperberg, Scott M Damrauer, Jerome I Rotter, Paul S de Vries, Martin Dichga |
| KLKB1 and CLSTN2 are associated with HDL-mediated cholesterol efflux capacity in a genome-wide association study. Atherosclerosis 2023 2 368 1-11. Schachtl-Riess Johanna F, Schönherr Sebastian, Lamina Claudia, Forer Lukas, Coassin Stefan, Streiter Gertraud, Kheirkhah Azin, Li Yong, Meiselbach Heike, Di Maio Silvia, Eckardt Kai-Uwe, Köttgen Anna, Kronenberg Florian, |
| NOTCH1 and CREBBP co-mutations negatively affect the benefit of adjuvant therapy in completely resected EGFR-mutated NSCLC: translational research of phase III IMPACT study. Molecular oncology 2023 10 . Satoshi Ikeda, Masahiro Tsuboi, Kazuko Sakai, Toshihiro Misumi, Hiroaki Akamatsu, Hiroyasu Shoda, Noriaki Sakakura, Atsushi Nakamura, Yasuhisa Ohde, Hidetoshi Hayashi, Kyoichi Okishio, Morihito Okada, Ichiro Yoshino, Jiro Okami, Kazuhisa Takahashi, Norihiko Ikeda, Masayuki Tanahashi, Yuichi Tambo, Haruhiro Saito, Shinichi Toyooka, Hidetoshi Inokawa, Toyofumi Chen-Yoshikawa, Toshihide Yokoyama, Tatsuro Okamoto, Noriko Yanagitani, Masahide Oki, Makoto Takahama, Kenji Sawa, Hirohito Tada, Kazuhiko Nakagawa, Tetsuya Mitsudomi, Kazuto Nish |
| Defective monocyte plasticity and altered cAMP pathway characterize USB1-mutated poikiloderma with neutropenia Clericuzio type. British journal of haematology 2023 10 . Prahlad Parajuli, Douglas B Craig, Manisha Gadgeel, Shruti Bagla, Robert E Wright, Roland Chu, Christina M Shanti, Rajeev Thirunagari, Sudershan K Grover, Yaddanapudi Ravindrana |
| Correlation between variants of the CREB1 and GRM7 genes and risk of depression. BMC psychiatry 2023 1 23 (1): 3. Wang Li, Tang Xingming, Liang Peng, Zhou Chuan, Sun Yingjie, Liang Yund |
| Determinants of plasma levels of proglucagon and the metabolic impact of glucagon receptor signalling: a UK Biobank study. Diabetologia 2024 5 . Marie Winther-Sørensen, Sara L Garcia, Andreas Bartholdy, Maud E Ottenheijm, Karina Banasik, Søren Brunak, Charlotte M Sørensen, Lise Lotte Gluud, Filip K Knop, Jens J Holst, Mette M Rosenkilde, Majken K Jensen, Nicolai J Wewer Albrechts |
| Transcriptomic analysis reveals a critical role for activating G? mutations in spontaneous feline hyperthyroidism. Scientific reports 2024 11 14 (1): 28749. Thomas K Hiron, Joana Aguiar, Jonathan M Williams, Sara Falcone, Paul A Norman, Jonathan Elliott, Robert C Fowkes, Harriet M Syme, Lucy J Davis |
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