Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 43 Records) |
Query Trace: HRC[original query] |
---|
Adiponectin and resistin in PCOS: a clinical, biochemical and molecular genetic study. Human reproduction (Oxford, England) 2006 Sep 21 (9): 2257-65. Escobar-Morreale H F, Villuendas G, Botella-Carretero J I, Alvarez-Blasco F, Sanchón R, Luque-Ramírez M, San Millán J |
Haplotype analysis of common vitamin D receptor variants and colon and rectal cancers. Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 2006 Apr 15 (4): 744-9. Sweeney Carol, Curtin Karen, Murtaugh Maureen A, Caan Bette J, Potter John D, Slattery Martha |
ESR1, AR, body size, and breast cancer risk in Hispanic and non-Hispanic white women living in the Southwestern United States. Breast Cancer Res Treat 2006 Dec (): . Slattery ML, Sweeney C, Herrick J, Wolff R, Baumgartner K, Giuliano A, Byers T |
Genetic variation in IGF1, IGFBP3, IRS1, IRS2 and risk of breast cancer in women living in Southwestern United States. Breast cancer research and treatment 2007 Aug 104 (2): 197-209. Slattery M L, Sweeney C, Wolff R, Herrick J, Baumgartner K, Giuliano A, Byers |
IL6 genotypes and colon and rectal cancer. Cancer causes & control : CCC 2007 Dec 18 (10): 1095-105. Slattery Martha L, Wolff Roger K, Herrick Jennifer S, Caan Bette J, Potter John |
IL6, aspirin, nonsteroidal anti-inflammatory drugs, and breast cancer risk in women living in the southwestern United States. Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 2007 Apr 16 (4): 747-55. Slattery Martha L, Curtin Karen, Baumgartner Richard, Sweeney Carol, Byers Tim, Giuliano Anna R, Baumgartner Kathy B, Wolff Roger |
The Ser96Ala variant in histidine-rich calcium-binding protein is associated with life-threatening ventricular arrhythmias in idiopathic dilated cardiomyopathy. European heart journal 2008 Oct 29 (20): 2514-25. Arvanitis Demetrios A, Sanoudou Despina, Kolokathis Fotis, Vafiadaki Elizabeth, Papalouka Vasiliki, Kontrogianni-Konstantopoulos Aikaterini, Theodorakis George N, Paraskevaidis Ioannis A, Adamopoulos Stamatios, Dorn Gerald W, Kremastinos Dimitrios Th, Kranias Evangelia |
Transcription factor 7-like 2 polymorphism and colon cancer. Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 2008 Apr 17 (4): 978-82. Slattery Martha L, Folsom Aaron R, Wolff Roger, Herrick Jenifer, Caan Bette J, Potter John |
LINGO1 and risk for essential tremor: results of a meta-analysis of rs9652490 and rs11856808. Journal of the neurological sciences 2012 Jun 317 (1-2): 52-7. Jiménez-Jiménez Félix Javier, García-Martín Elena, Lorenzo-Betancor Oswaldo, Pastor Pau, Alonso-Navarro Hortensia, Agúndez José A |
Vitamin D3 receptor ( VDR ) gene rs2228570 (Fok1) and rs731236 (Taq1) variants are not associated with the risk for multiple sclerosis: results of a new study and a meta-analysis. PloS one 2013 8 (6): e65487. García-Martín Elena, Agúndez José A G, Martínez Carmen, Benito-León Julián, Millán-Pascual Jorge, Calleja Patricia, Díaz-Sánchez María, Pisa Diana, Turpín-Fenoll Laura, Alonso-Navarro Hortensia, Ayuso-Peralta Lucía, Torrecillas Dolores, Plaza-Nieto José Francisco, Jiménez-Jiménez Félix Javi |
Exploration of haplotype research consortium imputation for genome-wide association studies in 20,032 Generation Scotland participants.
Genome medicine 2017 Mar 9 (1): 23. Nagy Reka, Boutin Thibaud S, Marten Jonathan, Huffman Jennifer E, Kerr Shona M, Campbell Archie, Evenden Louise, Gibson Jude, Amador Carmen, Howard David M, Navarro Pau, Morris Andrew, Deary Ian J, Hocking Lynne J, Padmanabhan Sandosh, Smith Blair H, Joshi Peter, Wilson James F, Hastie Nicholas D, Wright Alan F, McIntosh Andrew M, Porteous David J, Haley Chris S, Vitart Veronique, Hayward Caroli |
Accuracy of Inferred APOE Genotypes for a Range of Genotyping Arrays and Imputation Reference Panels. Journal of Alzheimer's disease : JAD 2018 6 64 (1): 49-54. Lupton Michelle K, Medland Sarah E, Gordon Scott D, Goncalves Tabatha, MacGregor Stuart, Mackey David A, Young Terri L, Duffy David L, Visscher Peter M, Wray Naomi R, Nyholt Dale R, Bain Lisa, Ferreira Manuel A, Henders Anjali K, Wallace Leanne, Montgomery Grant W, Wright Margaret J, Martin Nicholas |
Genotype imputation for Han Chinese population using Haplotype Reference Consortium as reference. Human genetics 2018 May . Lin Yuan, Liu Lu, Yang Sen, Li Yun, Lin Dongxin, Zhang Xuejun, Yin Xianyo |
Genotype imputation performance of three reference panels using African ancestry individuals. Human genetics 2018 Apr 137 (4): 281-292. Vergara Candelaria, Parker Margaret M, Franco Liliana, Cho Michael H, Valencia-Duarte Ana V, Beaty Terri H, Duggal Pri |
Shared genetic risk contributes to type 1 and type 2 diabetes etiology. Human molecular genetics 2018 11 . Aylward Anthony, Chiou Joshua, Okino Mei-Lin, Kadakia Nikita, Gaulton Kyle |
Gene-based analysis in HRC imputed genome wide association data identifies three novel genes for Alzheimer's disease. PloS one 2019 7 14 (7): e0218111. Baker Emily, Sims Rebecca, Leonenko Ganna, Frizzati Aura, Harwood Janet C, Grozeva Detelina, , , , , , Morgan Kevin, Passmore Peter, Holmes Clive, Powell John, Brayne Carol, Gill Michael, Mead Simon, Bossù Paola, Spalletta Gianfranco, Goate Alison M, Cruchaga Carlos, Maier Wolfgang, Heun Reinhard, Jessen Frank, Peters Oliver, Dichgans Martin, FröLich Lutz, Ramirez Alfredo, Jones Lesley, Hardy John, Ivanov Dobril, Hill Matthew, Holmans Peter, Allen Nicholas D, Morgan B Paul, Seshadri Sudha, Schellenberg Gerard D, Amouyel Philippe, Williams Julie, Escott-Price Valenti |
Rare Variants Imputation in Admixed Populations: Comparison Across Reference Panels and Bioinformatics Tools. Frontiers in genetics 2019 4 10 239. Sariya Sanjeev, Lee Joseph H, Mayeux Richard, Vardarajan Badri N, Reyes-Dumeyer Dolly, Manly Jennifer J, Brickman Adam M, Lantigua Rafael, Medrano Martin, Jimenez-Velazquez Ivonne Z, Tosto Giusep |
Ser96Ala genetic variant of the human histidine-rich calcium-binding protein is a genetic predictor of recurrence after catheter ablation in patients with paroxysmal atrial fibrillation. PloS one 2019 14 (3): e0213208. Amioka Michitaka, Nakano Yukiko, Ochi Hidenori, Onohara Yuko, Sairaku Akinori, Tokuyama Takehito, Motoda Chikaaki, Matsumura Hiroya, Tomomori Shunsuke, Hironobe Naoya, Okubo Yousaku, Okamura Sho, Chayama Kazuaki, Kihara Yasu |
Are serum brain-derived neurotrophic factor concentrations related to brain structure and psychopathology in late childhood and early adolescence? CNS spectrums 2019 Dec 1-7. de Araujo Celia Maria, Swardfager Walter, Zugman Andre, Cogo-Moreira Hugo, Belangero Sintia I, Ota Vanessa K, Spindola Leticia M, Hakonarson Hakon, Pellegrino Renata, Gadelha Ary, Salum Giovanni A, Pan Pedro M, Mansur Rodrigo B, Hoexter Marcelo, Picon Felipe, Sato João R, Brietzke Elisa, Grassi-Oliveira Rodrigo, Rohde Luis A P, Miguel Euripedes C, Bressan Rodrigo A, Jackowski Andrea |
Transcriptomic Heterogeneity of Alzheimer's Disease Associated with Lipid Genetic Risk. Neuromolecular medicine 2020 Aug . Miao Xiao, Liu Weifeng, Fan Bin, Lin Honghua |
Genome-wide meta-analysis identified novel variant associated with hallux valgus in Caucasians.
Journal of foot and ankle research 2020 Mar 13 (1): 11. Arbeeva Liubov, Yau Michelle, Mitchell Braxton D, Jackson Rebecca D, Ryan Kathleen, Golightly Yvonne M, Hannan Marian T, Nelson Amanda, Jordan Joanne M, Hochberg Marc |
Effect of longevity genetic variants on the molecular aging rate.
GeroScience 2021 5 43 (3): 1237-1251. Gurinovich Anastasia, Song Zeyuan, Zhang William, Federico Anthony, Monti Stefano, Andersen Stacy L, Jennings Lori L, Glass David J, Barzilai Nir, Millman Sofiya, Perls Thomas T, Sebastiani Pao |
Common and Rare Variants Genetic Association Analysis of Circulating Neutrophil Extracellular Traps.
Frontiers in immunology 2021 12 615527. Donkel Samantha J, Portilla Fernández Eliana, Ahmad Shahzad, Rivadeneira Fernando, van Rooij Frank J A, Ikram M Arfan, Leebeek Frank W G, de Maat Moniek P M, Ghanbari Mohs |
The impact of non-additive genetic associations on age-related complex diseases.
Nature communications 2021 4 12 (1): 2436. Guindo-Martínez Marta, Amela Ramon, Bonàs-Guarch Silvia, Puiggròs Montserrat, Salvoro Cecilia, Miguel-Escalada Irene, Carey Caitlin E, Cole Joanne B, Rüeger Sina, Atkinson Elizabeth, Leong Aaron, Sanchez Friman, Ramon-Cortes Cristian, Ejarque Jorge, Palmer Duncan S, Kurki Mitja, , Aragam Krishna, Florez Jose C, Badia Rosa M, Mercader Josep M, Torrents Dav |
Genotype imputation and polygenic score estimation in northwestern Russian population. PloS one 2022 6 17 (6): e0269434. Kolosov Nikita, Rezapova Valeriia, Rotar Oxana, Loboda Alexander, Freylikhman Olga, Melnik Olesya, Sergushichev Alexey, Stevens Christine, Voortman Trudy, Kostareva Anna, Konradi Alexandra, Daly Mark J, Artomov Myky |
Spatial Distribution of Missense Variants within Complement Proteins Associates with Age Related Macular Degeneration. medRxiv : the preprint server for health sciences 2023 9 . Michelle Grunin, Sarah de Jong, Ellen L Palmer, Bowen Jin, David Rinker, Christopher Moth, Anthony Capra, Jonathan L Haines, William S Bush, Anneke I den Hollander, |
Rare genetic variants correlate with better processing speed. Neurobiology of aging 2023 2 . Song Zeyuan, Gurinovich Anastasia, Nygaard Marianne, Mengel-From Jonas, Andersen Stacy, Cosentino Stephanie, Schupf Nicole, Lee Joseph, Zmuda Joseph, Ukraintseva Svetlana, Arbeev Konstantin, Christensen Kaare, Perls Thomas, Sebastiani Pao |
Non?synonymous polymorphisms in the HRC and ADRB1 genes may be associated with all?cause death in patients with non?ischemic heart failure. Experimental and therapeutic medicine 2023 12 27 (1): 48. Tanise Machado Telles, Bruna Miers May, Mauricio Pimentel, Bruna Letícia Da Silva Pereira, Michael Andrades, Luis Eduardo Rohde, Kátia Gonçalves Dos Sant |
Lack of Evidence for the Role of the p.(Ser96Ala) Polymorphism in Histidine-Rich Calcium Binding Protein as a Secondary Hit in Cardiomyopathies. International journal of molecular sciences 2023 11 24 (21): . Stephanie M van der Voorn, Esmée van Drie, Virginnio Proost, Kristina Dimitrova, Netherlands Acm/Pln Registry, Robert F Ernst, Cynthia A James, Crystal Tichnell, Brittney Murray, Hugh Calkins, Ardan M Saguner, Firat Duru, Patrick T Ellinor, Connie R Bezzina, Sean J Jurgens, J Peter van Tintelen, Toon A B van Ve |
Protective effect of uridine on atrial fibrillation: a Mendelian randomisation study. Scientific reports 2023 11 13 (1): 19639. Xintian Xu, Xiaoyu Zhang, Shiyao Cheng, Qinglang Li, Cai Chen, Mao Ouya |
- Page last reviewed:Feb 1, 2024
- Page last updated:Apr 16, 2024
- Content source: