Human Genome Epidemiology Literature Finder
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Records 1 - 30 (of 336 Records) |
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| BIRC5 Gene Polymorphisms Are Associated with a Higher Stage of Local and Regional Disease in Oral and Oropharyngeal Squamous Cell Carcinomas. International journal of molecular sciences 2023 12 24 (24): . Ivan Mumlek, Petar Ozreti?, Maja Sabol, Matko Leovi?, Ljubica Glavaš-Obrovac, Dinko Leovi?, Vesna Musa |
| Whole-genome analysis of plasma fibrinogen reveals population-differentiated genetic regulators with putative liver roles. Blood 2024 9 . Jennifer E Huffman, Jayna Nicholas, Julie Hahn, Adam S Heath, Laura M Raffield, Lisa R Yanek, Jennifer A Brody, Florian Thibord, Laura Almasy, Traci M Bartz, Lawrence F Bielak, Russell P Bowler, German D Carrasquilla, Daniel I Chasman, Ming-Huei Chen, David B Emmert, Mohsen Ghanbari, Jeffrey Haessler, Jouke J Hottenga, Marcus E Kleber, Ngoc-Quynh Le, Jiwon Lee, Joshua P Lewis, Ruifang Li-Gao, Jian'an Luan, Anni Liisi Malmberg, Massimo Mangino, Riccardo Marioni, Angel Martinez-Perez, Nathan Pankratz, Ozren Polasek, Anne Richmond, Benjamin A T Rodriguez, Jerome I Rotter, Maristella Steri, Pierre Suchon, Stella Trompet, Stefan Weiss, Marjan Zare, Paul L Auer, Michael Cho, Paraskevi Christofidou, Gail Davies, Eco Jc de Geus, Jean-François Deleuze, Graciela E Delgado, Lynette Ekunwe, Nauder Faraday, Martin Gogele, Andreas Greinacher, He Gao, Tom E Howard, Peter K Joshi, Tuomas O Kilpeläinen, Jari Lahti, Allan Linneberg, Silvia Naitza, Raymond Noordam, Ferran Paüls Vergés, Stephen S Rich, Frits R Rosendaal, Igor Rudan, Kathleen A Ryan, Juan Carlos Carlos Souto, Frank J A van Rooij, Heming Wang, Wei Zhao, Lewis Becker, Andrew Beswick, Michael R Brown, Brian Cade, Harry Campbell, Kelly Cho, James Crapo, Joanne Curran, Moniek P M de Maat, Margaret F Doyle, Paul Elliott, James S Floyd, Christian Fuchsberger, Niels Grarup, Xiuqing Guo, Sarah Harris, Lifang Hou, Ivana Kolcic, Charles Kooperberg, Cristina Menni, Matthias Nauck, Jeffrey R O'Connell, Valeria Orru, Bruce M Psaty, Katri Räikkönen, Jennifer A Smith, Jose Manuel Soria, David Stott, Astrid van Hylckama Vlieg, Hugh Watkins, Gonneke Willemsen, Peter Wf Wilson, Yoav Ben-Shlomo, John Blangero, Dorret Boomsma, Simon R Cox, Abbas Dehghan, Johan G Eriksson, Edoardo Fiorillo, Myriam Fornage, Torben Hansen, Caroline Hayward, Mohammad Arfan Ikram, J Wouter Jukema, Sharon Kardia, Leslie Lange, Winfried Maerz, Rasika Mathias, Braxton D Mitchell, Dennis O Mook-Kanamori, Pierre-Emmanuel Morange, Oluf Pedersen, Peter P Pramstaller, Susan Redline, Alex P Reiner, Paul M Ridker, Edwin K Silverman, Tim D Spector, Uwe Volker, Nick Wareham, James Wilson, Jie Yao, David-Alexandre Tregouet, Andrew D Johnson, Alisa S Wolberg, Paul S de Vries, Maria Sabater-Lleal, Alanna Morrison, Nicholas L Smi |
| Fat Mass and Obesity-Related (FTO) Gene Variant Is a Predictor of CVD in T2DM Patients. Journal of diabetes research 2024 9 2024 5914316. Mazhar Hussain, Akbar Waheed, Asim Elahi, Ghulam Musta |
| Whole-exome and whole-genome sequencing of 1064 individuals with type 1 diabetes reveals novel genes for diabetic kidney disease. Diabetologia 2024 8 . Jani K Haukka, Anni A Antikainen, Erkka Valo, Anna Syreeni, Emma H Dahlström, Bridget M Lin, Nora Franceschini, Andrzej S Krolewski, Valma Harjutsalo, Per-Henrik Groop, Niina Sandholm, |
| Start codon variant in LAG3 is associated with decreased LAG-3 expression and increased risk of autoimmune thyroid disease. Nature communications 2024 7 15 (1): 5748. Saedis Saevarsdottir, Kristbjörg Bjarnadottir, Thorsteinn Markusson, Jonas Berglund, Thorunn A Olafsdottir, Gisli H Halldorsson, Gudrun Rutsdottir, Kristbjorg Gunnarsdottir, Asgeir Orn Arnthorsson, Sigrun H Lund, Lilja Stefansdottir, Julius Gudmundsson, Ari J Johannesson, Arni Sturluson, Asmundur Oddsson, Bjarni Halldorsson, Björn R Ludviksson, Egil Ferkingstad, Erna V Ivarsdottir, Gardar Sveinbjornsson, Gerdur Grondal, Gisli Masson, Grimur Hjorleifsson Eldjarn, Gudmundur A Thorisson, Katla Kristjansdottir, Kirk U Knowlton, Kristjan H S Moore, Sigurjon A Gudjonsson, Solvi Rognvaldsson, Stacey Knight, Lincoln D Nadauld, Hilma Holm, Olafur T Magnusson, Patrick Sulem, Daniel F Gudbjartsson, Thorunn Rafnar, Gudmar Thorleifsson, Pall Melsted, Gudmundur L Norddahl, Ingileif Jonsdottir, Kari Stefanss |
| Extended genome-wide association study employing the African genome resources panel identifies novel susceptibility loci for Alzheimer's disease in individuals of African ancestry. Alzheimer's & dementia : the journal of the Alzheimer's Association 2024 7 . Nicholas R Ray, Brian W Kunkle, Kara Hamilton-Nelson, Jiji T Kurup, Farid Rajabli, Min Qiao, Badri N Vardarajan, Mehmet I Cosacak, Caghan Kizil, Melissa Jean-Francois, Michael Cuccaro, Dolly Reyes-Dumeyer, Laura Cantwell, Amanda Kuzma, Jeffery M Vance, Sujuan Gao, Hugh C Hendrie, Olusegun Baiyewu, Adesola Ogunniyi, Rufus O Akinyemi, , Wan-Ping Lee, Eden R Martin, Li-San Wang, Gary W Beecham, William S Bush, Wanying Xu, Fulai Jin, Liyong Wang, Lindsay A Farrer, Jonathan L Haines, Goldie S Byrd, Gerard D Schellenberg, Richard Mayeux, Margaret A Pericak-Vance, Christiane Rei |
| Exome-wide evidence of compound heterozygous effects across common phenotypes in the UK Biobank. Cell genomics 2024 6 100602. Frederik H Lassen, Samvida S Venkatesh, Nikolas Baya, Barney Hill, Wei Zhou, Alex Bloemendal, Benjamin M Neale, Benedikt M Kessler, Nicola Whiffin, Cecilia M Lindgren, Duncan S Palm |
| Whole Exome Sequencing Revealed Paternal Inheritance of Obesity-related Genetic Variants in a Family with an Exclusively Breastfed Infant. Journal of clinical research in pediatric endocrinology 2024 6 . Hazal Banu Olgun Celebioglu, Ayse Pinar Ozturk, Sukran Poyrazoglu, Feyza Nur Tunc |
| Somatic KMT2D loss-of-function mutations in lung squamous cell carcinoma: a single-center cohort study. Journal of thoracic disease 2024 6 16 (5): 3338-3349. Zekui Fang, Xiping Wu, Li Xiao, Chunli Wang, Yanyan Zhao, Qingchao Zhang, Paola Anna Jablonska, Alonso La Rosa, Wolfram C M Dempke, Muhammad Furqan, Huizhen F |
| Clinical exome sequencing unravels the diverse spectrum of genetic heterogeneity and genotype-phenotype correlations in hypertrophic cardiomyopathy. International journal of cardiology 2024 6 132273. Sivadasanpillai Harikrishnan, Linda Koshy, Sanjay Ganapathi, Panniyammakal Jeemon, N K Ramya Das, Madhusoodanan Urulangodi, M Madhuma, Y Vysakh, Anjana Subran, L R Lakshmikan |
| A novel locus in CSMD1 gene is associated with increased susceptibility to severe malaria in Malian children. Frontiers in genetics 2024 6 15 1390786. Delesa Damena, Amadou Barry, Robert Morrison, Santara Gaoussou, Almahamoudou Mahamar, Oumar Attaher, Djibrilla Issiaka, Yahia Dicko, Alassane Dicko, Patrick Duffy, Michal Fri |
| Association of Renin-Angiotensin Pathway Gene Polymorphisms with COVID-19 Susceptibility and Severity in Moroccans: A Case-Control Study. Biochemical genetics 2024 5 . Fatima-Zahra El Yousfi, Samia El Hilali, Jihane Belayachi, Khalid Ennibi, Rachid Razine, Redouane Abouqal, Ahmed Bouhouc |
| Characterization of the Common Genetic Variation in the Spanish Population of Navarre. Genes 2024 5 15 (5): . Alberto Maillo, Estefania Huergo, María Apellániz-Ruiz, Edurne Urrutia-Lafuente, María Miranda, Josefa Salgado, Sara Pasalodos-Sanchez, Luna Delgado-Mora, Óscar Teijido, Ibai Goicoechea, Rosario Carmona, Javier Perez-Florido, Virginia Aquino, Daniel Lopez-Lopez, María Peña-Chilet, Sergi Beltran, Joaquín Dopazo, Iñigo Lasa, Juan José Beloqui, Nagen-Scheme, Ángel Alonso, David Gomez-Cabre |
| Mutations in the tail and rod domains of the neurofilament heavy-chain gene increase the risk of ALS. Annals of clinical and translational neurology 2024 5 . Heather Marriott, Thomas P Spargo, Ahmad Al Khleifat, Peter M Andersen, Nazli A Ba?ak, Johnathan Cooper-Knock, Philippe Corcia, Philippe Couratier, Mamede de Carvalho, Vivian Drory, Marc Gotkine, John E Landers, Russell McLaughlin, Jesús S Mora Pardina, Karen E Morrison, Susana Pinto, Christopher E Shaw, Pamela J Shaw, Vincenzo Silani, Nicola Ticozzi, Philip van Damme, Leonard H van den Berg, Patrick Vourc'h, Markus Weber, Jan H Veldink, , Richard J Dobson, Patrick Schwab, Ammar Al-Chalabi, Alfredo Iacoange |
| Increased prevalence of CFTR variants and susceptibility to CRS: A real-world study based on Chinese children. Heliyon 2024 4 10 (7): e27681. Yang Han, Jinhao Zhao, Wenjing Liu, Xiaojian Yang, Wei Zhang, Xiao Xiao, Xiaoge Liu, Xiaoxu Chen, Lixing Tang, Pengpeng Wang, Wentong |
| Prognostic Model for High-Grade Neuroendocrine Carcinoma of the Lung Incorporating Genomic Profiling and Poly (ADP-ribose) Polymerase-1 Expression. JCO precision oncology 2024 4 8 e2300495. Hye Sook Kim, Jong Kwang Kim, Jeong Hyeon Lee, Young Joo Lee, Geon-Kuk Lee, Ji-Youn H |
| The ABCG8 polymorphism increases the risk of gallbladder cancer in the general population and gallstones in obese patients from Poland. European journal of clinical investigation 2024 4 e14213. Lukasz Krupa, Piotr Kalinowski, Joanna Ligocka, Marc Dauer, Krzysztof Jankowski, Jolanta Gozdowska, Beata Kruk, Piotr Milkiewicz, Krzysztof Zieniewicz, Marek Krawczyk, Susanne N Weber, Frank Lammert, Marcin Krawcz |
| Assessment of Stx-1A gene polymorphism (rs1569061) in relation to the development of multiple sclerosis in Egyptian patients. The Egyptian journal of immunology 2024 4 31 (2): 18-27. Christine A Habib, Aziza A El-Sebai, Mohamed M Fouad, Marwa A El-Mohamdy, Amani M Abdel Ghani, Somia A Bawa |
| Common Mutations in the Surfactant Protein-C Gene in Iranian Patients with Diffuse Parenchymal Lung Disease. Tanaffos 2024 12 23 (1): 65-72. Mihan Pourabdollah Toutkaboni, Elham Askari, Jalal Heshmatnia, Mitra Rezaei, Maryam Hasanzad, Atosa Dorudinia, Mehrdad Bakhshayesh Karam, Leila Mohammadi Ziazi, Maryam-Fatemeh Sheikholesla |
| Hemodynamic and Genetic Associations with the Risk of Idiopathic Pulmonary Arterial Hypertension Development in an Ethnic Cohort of Kazakhs. Diagnostics (Basel, Switzerland) 2024 12 14 (23): . Dana Taizhanova, Togzhan Nurpissova, Gulshara Abildinova, Tamilla Martynyuk, Nazgul Kulmyrzayeva, Elena Zholdybaye |
| Clinical features and search for genetic determinants of postprandial hypoglycemia. Endocrine connections 2024 11 . Qian Ren, Xueyao Han, Siqian Gong, Simin Zhang, Tianhao Ba, Yilin Zhao, Yating Li, Yanai Wang, Xianghai Zhou, Yufeng Li, Linong |
| Low-frequency variants in genes involved in glutamic acid metabolism and ?-glutamyl cycle and risk of coronary artery disease in type 2 diabetes. Cardiovascular diabetology 2024 11 23 (1): 406. Fernando M A Giuffrida, Sharan K Rai, Yaling Tang, Christine Mendonça, Scott G Frodsham, Hetal S Shah, Marcus G Pezzolesi, Qi Sun, Alessandro Dor |
| Loss of Function in Protein Z (PROZ) is Associated with Increased Risk of Ischemic Stroke in the UK Biobank. Journal of thrombosis and haemostasis : JTH 2024 10 . Amelia K Haj, Justine Ryu, Sean J Jurgens, Sharjeel Chaudhry, Satoshi Koyama, Xin Wang, Seung Hoan Choi, Cody Hou, Simone Sanna-Cherchi, Christopher D Anderson, Patrick T Ellinor, Pavan K Bendapu |
| A Novel AKT1, ERBB2, ESR1, KRAS, PIK3CA, and TP53 NGS Assay: A Non-Invasive Tool to Monitor Resistance Mechanisms to Hormonal Therapy and CDK4/6 Inhibitors. Biomedicines 2024 10 12 (10): . Alessandra Virga, Caterina Gianni, Michela Palleschi, Davide Angeli, Filippo Merloni, Roberta Maltoni, Paola Ulivi, Giovanni Martinelli, Ugo De Giorgi, Sara Bravacci |
| ENaC gene variants and their involvement in Covid?19 severity. Biomedical reports 2024 10 21 (6): 176. Eleni Koniari, Kyriaki Hatziagapiou, Alexandra Olti Nikola, Konstantina Georgoulia, Nikolaos Marinakis, Petros Bakakos, Athanasia Athanasopoulou, Athanasios Koromilias, Nikoletta Rovina, Vasiliki Efthymiou, Eleni Papakonstantinou, Dimitrios Vlachakis, Sophia Mavrikou, Antonia Koutsoukou, Joanne Traeger-Synodinos, George P Chrous |
| Genetic determinants of IgG antibody response to COVID-19 vaccination. American journal of human genetics 2024 1 111 (1): 181-199. Shengzhe Bian, Xinxin Guo, Xilai Yang, Yuandan Wei, Zijing Yang, Shiyao Cheng, Jiaqi Yan, Yongkun Chen, Guo-Bo Chen, Xiangjun Du, Stephen S Francis, Yuelong Shu, Siyang L |
| A scalable and robust variance components method reveals insights into the architecture of gene-environment interactions underlying complex traits. bioRxiv : the preprint server for biology 2024 1 . Ali Pazokitoroudi, Andrew Dahl, Noah Zaitlen, Saharon Rosset, Sriram Sankararam |
| Short-term serial circulating tumor DNA assessment predicts therapeutic efficacy for patients with advanced pancreatic cancer. Journal of cancer research and clinical oncology 2024 1 150 (2): 35. Hideki Motobayashi, Yuji Kitahata, Ken-Ichi Okada, Motoki Miyazawa, Masaki Ueno, Shinya Hayami, Atsushi Miyamoto, Atsushi Shimizu, Masatoshi Sato, Tomohiro Yoshimura, Yuki Nakamura, Norio Takemoto, Tomoki Nakai, Takahiko Hyo, Kyohei Matsumoto, Hiroki Yamaue, Manabu Kaw |
| Whole exome sequencing identifies ABHD14A and MRNIP as novel candidate genes for developmental language disorder. Scientific reports 2025 1 15 (1): 367. Amal Bouzid, Malek Belcadhi, Amal Souissi, Meryam Chelly, Fakher Frikha, Hela Gargouri, Crystel Bonnet, Fida Jebali, Salma Loukil, Christine Petit, Saber Masmoudi, Rifat Hamoudi, Mariem Ben Sa |
| CYP2C19 and CES1 gene variants affecting clopidogrel metabolism in a South Asian population from Sri Lanka. Pharmacogenomics 2025 1 1-4. Priyanga Ranasinghe, Pulasthi B Gunarathna, Hajanthy Jeyapragasam, Nirmala Sirisena, D P Bhagya Hendalage, Vajira H W Dissanaya |
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