Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 82 Records) |
Query Trace: RXRA[original query] |
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Single-Nucleotide Polymorphisms in Vitamin D-Related Genes May Modify Vitamin D-Breast Cancer Associations. Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 2017 Aug . O'Brien Katie M, Sandler Dale P, Kinyamu H Karimi, Taylor Jack A, Weinberg Clarice |
Titers of antibodies to the surface antigen of hepatitis B virus after vaccination in relation to immunity-related gene variants. A prospective study among hemodialysis patients. Polish archives of internal medicine 2017 8 127 (7-8): 481-489. Jod?owska-Siewert El?bieta, Jagodzi?ski Pawe? P, Grzegorzewska Alicja |
Genetic associations for keratoconus: a systematic review and meta-analysis. Scientific reports 2017 Jul 7 (1): 4620. Rong Shi Song, Ma Sarah Tsz Ue, Yu Xin Ting, Ma Li, Chu Wai Kit, Chan Tommy Chung Yan, Wang Yu Meng, Young Alvin L, Pang Chi Pui, Jhanji Vishal, Chen Li J |
Pseudoexfoliation syndrome-associated genetic variants affect transcription factor binding and alternative splicing of LOXL1. Nature communications 2017 May 8 15466. Pasutto Francesca, Zenkel Matthias, Hoja Ursula, Berner Daniel, Uebe Steffen, Ferrazzi Fulvia, Schödel Johannes, Liravi Panah, Ozaki Mineo, Paoli Daniela, Frezzotti Paolo, Mizoguchi Takanori, Nakano Satoko, Kubota Toshiaki, Manabe Shinichi, Salvi Erika, Manunta Paolo, Cusi Daniele, Gieger Christian, Wichmann Heinz-Erich, Aung Tin, Khor Chiea Chuen, Kruse Friedrich E, Reis André, Schlötzer-Schrehardt Ursu |
Genome-wide association study identifies WNT7B as a novel locus for central corneal thickness in Latinos.
Human molecular genetics 2016 11 25 (22): 5035-5045. Gao Xiaoyi, Nannini Drew R, Corrao Kristen, Torres Mina, Chen Yii-Der I, Fan Bao J, Wiggs Janey L, , Taylor Kent D, Gauderman W James, Rotter Jerome I, Varma Roh |
Prevalence, determinants and clinical correlates of vitamin D deficiency in patients with Chronic Obstructive Pulmonary Disease in London, UK. The Journal of steroid biochemistry and molecular biology 2018 01 175 138-145. Jolliffe David A, James Wai Yee, Hooper Richard L, Barnes Neil C, Greiller Claire L, Islam Kamrul, Bhowmik Angshu, Timms Peter M, Rajakulasingam Raj K, Choudhury Aklak B, Simcock David E, Hyppönen Elina, Walton Robert T, Corrigan Christopher J, Griffiths Christopher J, Martineau Adrian |
Association of a 3' untranslated region polymorphism in proprotein convertase subtilisin/kexin type 9 with HIV viral load and CD4+ levels in HIV/hepatitis C virus coinfected women. AIDS (London, England) 2017 Nov 31 (18): 2483-2492. Kuniholm Mark H, Liang Hua, Anastos Kathryn, Gustafson Deborah, Kassaye Seble, Nowicki Marek, Sha Beverly E, Pawlowski Emilia J, Gange Stephen J, Aouizerat Bradley E, Pushkarsky Tatiana, Bukrinsky Michael I, Prasad Vinayaka |
Plasma 25-Hydroxyvitamin D Concentration and Risk of Islet Autoimmunity. Diabetes 2017 Oct . Norris Jill M, Lee Hye-Seung, Frederiksen Brittni, Erlund Iris, Uusitalo Ulla, Yang Jimin, Lernmark Åke, Simell Olli, Toppari Jorma, Rewers Marian, Ziegler Anette-G, She Jin-Xiong, Onengut-Gumuscu Suna, Chen Wei-Min, Rich Stephen S, Sundvall Jouko, Akolkar Beena, Krischer Jeffrey, Virtanen Suvi M, Hagopian William, |
Vitamin D receptor genotype influences risk of upper respiratory infection. The British journal of nutrition 2018 Aug 1-10. Jolliffe David A, Greiller Claire L, Mein Charles A, Hoti Mimoza, Bakhsoliani Eteri, Telcian Aurica G, Simpson Angela, Barnes Neil C, Curtin John A, Custovic Adnan, Johnston Sebastian L, Griffiths Christopher J, Walton Robert T, Martineau Adrian |
An African-specific profile of pharmacogene variants for rosuvastatin plasma variability: limited role for SLCO1B1 c.521T>C and ABCG2 c.421A>C. The pharmacogenomics journal 2018 Aug . Soko Nyarai Desiree, Chimusa Emile, Masimirembwa Collen, Dandara Coll |
Implication of OPRM1 A118G Polymorphism in Opioids Addicts in Pakistan: In vitro and In silico Analysis. Journal of molecular neuroscience : MN 2018 Jul . Ahmed Madiha, Ul Haq Ihsan, Faisal Muhammad, Waseem Durdana, Taqi Malik Mumt |
Rare, potentially pathogenic variants in 21 keratoconus candidate genes are not enriched in cases in a large Australian cohort of European descent. PloS one 2018 13 (6): e0199178. Lucas Sionne E M, Zhou Tiger, Blackburn Nicholas B, Mills Richard A, Ellis Jonathan, Leo Paul, Souzeau Emmanuelle, Ridge Bronwyn, Charlesworth Jac C, Lindsay Richard, Craig Jamie E, Burdon Kathryn |
ENHO, RXRA, and LXRA polymorphisms and dyslipidaemia, related comorbidities and survival in haemodialysis patients. BMC medical genetics 2018 Nov 19 (1): 194. Grzegorzewska Alicja E, Niepolski Leszek, ?widerska Monika K, Mostowska Adrianna, Stolarek Ireneusz, Warcho? Wojciech, Figlerowicz Marek, Jagodzi?ski Pawe? |
Nuclear receptor gene polymorphisms and warfarin dose requirements in the Quebec Warfarin Cohort. The pharmacogenomics journal 2018 Jan . Shahabi Payman, Lamothe Félix, Dumas Stéphanie, Rouleau-Mailloux Étienne, Feroz Zada Yassamin, Provost Sylvie, Asselin Geraldine, Mongrain Ian, Valois Diane, Gaulin Marion Marie-Josée, Lemieux Perreault Louis-Philippe, Perreault Sylvie, Dubé Marie-Pier |
Smoking and Parkinson disease: Evidence for gene-by-smoking interactions. Neurology 2018 Jan . Lee Pei-Chen, Ahmed Ismaïl, Loriot Marie-Anne, Mulot Claire, Paul Kimberly C, Bronstein Jeff M, Ritz Beate, Elbaz Alex |
In silico genome-wide identification of m6A-associated SNPs as potential functional variants for periodontitis. Journal of cellular physiology 2019 Jun . Lin Weimin, Xu Hao, Wu Yunshu, Wang Jun, Yuan Qu |
Epigenome-wide association analysis of daytime sleepiness in the Multi-Ethnic Study of Atherosclerosis reveals African-American-specific associations. Sleep 2019 May . Barfield Richard, Wang Heming, Liu Yongmei, Brody Jennifer A, Swenson Brenton, Li Ruitong, Bartz Traci M, Sotoodehnia Nona, Chen Yii-der I, Cade Brian E, Chen Han, Patel Sanjay R, Zhu Xiaofeng, Gharib Sina A, Johnson W Craig, Rotter Jerome I, Saxena Richa, Purcell Shaun, Lin Xihong, Redline Susan, Sofer Tam |
Genetic associations of the vitamin D and antiviral pathways with natural resistance to HIV-1 infection are influenced by interpopulation variability. Infection, genetics and evolution : journal of molecular epidemiology and evolutionary genetics in infectious diseases 2019 May 73 276-286. Aguilar-Jimenez Wbeimar, Zapata Wildeman, Rivero-Juárez Antonio, Pineda Juan A, Laplana Marina, Taborda Natalia A, Biasin Mara, Clerici Mario, Caruz Antonio, Fibla Joan, Rugeles María |
Targeted deep sequencing of urothelial bladder cancers and associated urinary DNA: a 23-gene panel with utility for non-invasive diagnosis and risk stratification. BJU international 2019 May . Ward Douglas G, Gordon Naheema S, Boucher Rebecca H, Pirrie Sarah J, Baxter Laura, Ott Sascha, Silcock Lee, Whalley Celina M, Stockton Joanne D, Beggs Andrew D, Griffiths Mike, Abbotts Ben, Ijakipour Hanieh, Latheef Fathimath N, Robinson Robert A, White Andrew J, James Nicholas D, Zeegers Maurice P, Cheng K K, Bryan Richard |
Epigenomic signatures in liver and blood of Wilson disease patients include hypermethylation of liver-specific enhancers. Epigenetics & chromatin 2019 02 12 (1): 10. Mordaunt Charles E, Kieffer Dorothy A, Shibata Noreene M, Cz?onkowska Anna, Litwin Tomasz, Weiss Karl-Heinz, Zhu Yihui, Bowlus Christopher L, Sarkar Souvik, Cooper Stewart, Wan Yu-Jui Yvonne, Ali Mohamed R, LaSalle Janine M, Medici Valenti |
Calcium-sensing receptor gene (CASR) polymorphisms and CASR transcript level concerning dyslipidemia in hemodialysis patients: a cross-sectional study. BMC nephrology 2019 Nov 20 (1): 436. Grzegorzewska Alicja E, Frycz Bartosz A, ?widerska Monika, Niepolski Leszek, Mostowska Adrianna, Jagodzi?ski Pawe? |
Genome-wide association study in two populations to determine genetic variants associated with Toxoplasma gondii infection and relationship to schizophrenia risk.
Progress in neuro-psychopharmacology & biological psychiatry 2019 06 92 133-147. Wang Alex W, Avramopoulos Dimitrios, Lori Adriana, Mulle Jennifer, Conneely Karen, Powers Abigail, Duncan Erica, Almli Lynn, Massa Nicholas, McGrath John, Schwartz Ann C, Goes Fernando S, Weng Lei, Wang Ruihua, Yolken Robert, Ruczinski Ingo, Gillespie Charles F, Jovanovic Tanja, Ressler Kerry, Pulver Ann E, Pearce Brad |
Association of VDBP rs4701 Variant, but not VDR/RXR-? Over-Expression with Bone Mineral Density in Pediatric Well-Chelated ?-Thalassemia Patients. Mediterranean journal of hematology and infectious diseases 2020 7 12 (1): e2020037. Sahmoud Shaimaa, Ibrahim Mostafa S, Toraih Eman A, Kamel Noha, Fawzy Manal S, Elfiky Sam |
Assessment of prognostic implication of a panel of oncogenes in bladder cancer and identification of a 3-gene signature associated with recurrence and progression risk in non-muscle-invasive bladder cancer. Scientific reports 2020 10 10 (1): 16641. Le Goux Constance, Vacher Sophie, Schnitzler Anne, Barry Delongchamps Nicolas, Zerbib Marc, Peyromaure Michael, Sibony Mathilde, Allory Yves, Bieche Ivan, Damotte Diane, Pignot Geraldi |
Multifaceted regulation of hepatic lipid metabolism by YY1. Life science alliance 2021 6 4 (7): . Pan Gang, Diamanti Klev, Cavalli Marco, Lara Gutiérrez Ariadna, Komorowski Jan, Wadelius Cla |
Multi-omics integration identifies key upstream regulators of pathomechanisms in hypertrophic cardiomyopathy due to truncating MYBPC3 mutations. Clinical epigenetics 2021 3 13 (1): 61. Pei J, Schuldt M, Nagyova E, Gu Z, El Bouhaddani S, Yiangou L, Jansen M, Calis J J A, Dorsch L M, Blok C Snijders, van den Dungen N A M, Lansu N, Boukens B J, Efimov I R, Michels M, Verhaar M C, de Weger R, Vink A, van Steenbeek F G, Baas A F, Davis R P, Uh H W, Kuster D W D, Cheng C, Mokry M, van der Velden J, Asselbergs F W, Harakalova |
A Non-coding HES1 Variant Predisposes Children to Congenital Heart Disease in Chinese Population. Frontiers in cell and developmental biology 2021 2 9 631942. Song Yangliu, Chen Weicheng, Huang Zitong, Tian Guixiang, Li Mengru, Zhao Zhengshan, Feng Zhiyu, Wu Feizhen, Qian Maoxiang, Ma Xiaojing, Sheng Wei, Huang Guoyi |
Association Between Retinoid X Receptor Gene Variants and Dyslipidemia Risk in an Iranian Population. Cureus 2021 10 13 (9): e17730. Vafaeie Farzane, Kazemi Toba, Khosravi Saeede, Miri Moghaddam Ebrah |
Polymorphisms analysis for association between ADIPO signaling pathway and genetic susceptibility to T2DM in Chinese han population. Adipocyte 2021 Dec 10 (1): 463-474. Yu Haibing, Hu Wei, Lin Chunwen, Xu Lin, Liu Hao, Luo Ling, Chen Rong, Huang Jialu, Chen Weiying, Yang Chen, Kong Danli, Ding Yuanl |
SNP rs11185644 in RXRA gene and SNP rs2235544 in DIO1 gene predict dosage requirements in a cross-sectional sample of hypothyroid patients. BMC endocrine disorders 2023 8 23 (1): 167. Rowan AlEjielat, Anas Khaleel, Yazan S Batarseh, Luay Abu-Qatouseh, Suzan Al-Wawi, Toleen AlSun |
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