Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 54 Records) |
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Association between the ABO locus and hematological traits in Korean. BMC genetics 2012 13 (1): 78. Hong Kyung-Won, Moon Sanghoon, Kim Young Jin, Kim Yun Kyoung, Kim Dong-Joon, Kim Cheong-sik, Kim Sung Soo, Kim Bong- |
Fibrinolysis alterations in infertile women during controlled ovarian stimulation: influence of BMI and genetic components. Thrombosis research 2012 Jul . Sticchi E, Romagnuolo I, Cellai AP, Lami D, Fedi S, Prisco D, Noci I, Abbate R, Fatini C |
Folic acid supplementation, MTHFR and MTRR polymorphisms, and the risk of childhood leukemia: the ESCALE study (SFCE). Cancer causes & control : CCC 2012 Aug 23 (8): 1265-77. Amigou Alicia, Rudant Jérémie, Orsi Laurent, Goujon-Bellec Stéphanie, Leverger Guy, Baruchel André, Bertrand Yves, Nelken Brigitte, Plat Geneviève, Michel Gérard, Haouy Stéphanie, Chastagner Pascal, Ducassou Stéphane, Rialland Xavier, Hémon Denis, Clavel Jacqueli |
Prognostic significance and gene expression profiles of p53 mutations in microsatellite-stable stage III colorectal adenocarcinomas. PloS one 2012 7 (1): e30020. Katkoori Venkat R, Shanmugam Chandrakumar, Jia Xu, Vitta Swaroop P, Sthanam Meenakshi, Callens Tom, Messiaen Ludwine, Chen Dongquan, Zhang Bin, Bumpers Harvey L, Samuel Temesgen, Manne Upend |
Association of genetic variants of fibrinolytic system with stroke and stroke subtypes. Gene 2012 Mar 495 (1): 76-80. Babu M Sai, Prabha T Surya, Kaul Subhash, Al-Hazzani Amal, Shafi Gowhar, Roy Sitara, Balakrishna N, Jyothy A, Munshi Anja |
Prevalence of genetic risk factors related with thrombophilia and hypofibrinolysis in patients with osteonecrosis of the femoral head in Poland. BMC musculoskeletal disorders 2013 14 (1): 264. Gagala Jacek, Buraczynska Monika, Mazurkiewicz Tomasz, Ksiazek Andrz |
Clinical effectiveness and cost-effectiveness of first-line chemotherapy for adult patients with locally advanced or metastatic non-small cell lung cancer: a systematic review and economic evaluation. Health technology assessment (Winchester, England) 2013 Jul 17 (31): 1-278. Brown T, Pilkington G, Bagust A, Boland A, Oyee J, Tudur-Smith C, Blundell M, Lai M, Martin Saborido C, Greenhalgh J, Dundar Y, Dickson |
Genetic variation in FADS genes and plasma cholesterol levels in 2-year-old infants: KOALA Birth Cohort Study. PloS one 2013 8 (5): e61671. Moltó-Puigmartí Carolina, Jansen Eugène, Heinrich Joachim, Standl Marie, Mensink Ronald P, Plat Jogchum, Penders John, Mommers Monique, Koppelman Gerard H, Postma Dirkje S, Thijs Car |
tPA Alu (I/D) polymorphism associates with bacterial osteomyelitis. The Journal of infectious diseases 2013 Jul 208 (2): 218-23. Valle-Garay Eulalia, Montes Angel H, Corte Jose R, Meana Alvaro, Fierer Joshua, Asensi Vict |
Maternal but not fetal FADS gene variants modify the association between maternal long-chain PUFA intake in pregnancy and birth weight. The Journal of nutrition 2014 Sep 144 (9): 1430-7. Moltó-Puigmartí Carolina, van Dongen Martien C J M, Dagnelie Pieter C, Plat Jogchum, Mensink Ronald P, Tan Frans E S, Heinrich Joachim, Thijs Car |
HBsAg loss in patients treated with peginterferon alfa-2a and adefovir is associated with SLC16A9 gene variation and lower plasma carnitine levels. Journal of hepatology 2014 Oct 61 (4): 730-7. Jansen Louis, de Niet Annikki, Stelma Femke, van Iperen Erik P A, van Dort Karel A, Plat-Sinnige Marjan J Tempelmans, Takkenberg R Bart, Chin Daniel J, Zwinderman A H Koos, Lopatin Uri, Kootstra Neeltje A, Reesink Hendrik |
Genome-wide association study for circulating tissue plasminogen activator levels and functional follow-up implicates endothelial STXBP5 and STX2.
Arteriosclerosis, thrombosis, and vascular biology 2014 May 34 (5): 1093-101. Huang Jie, Huffman Jennifer E, Yamakuchi Munekazu, Yamkauchi Munekazu, Trompet Stella, Asselbergs Folkert W, Sabater-Lleal Maria, Trégouët David-Alexandre, Chen Wei-Min, Smith Nicholas L, Kleber Marcus E, Shin So-Youn, Becker Diane M, Tang Weihong, Dehghan Abbas, Johnson Andrew D, Truong Vinh, Folkersen Lasse, Yang Qiong, Oudot-Mellkah Tiphaine, Buckley Brendan M, Moore Jason H, Williams Frances M K, Campbell Harry, Silbernagel Günther, Vitart Veronique, Rudan Igor, Tofler Geoffrey H, Navis Gerjan J, Destefano Anita, Wright Alan F, Chen Ming-Huei, de Craen Anton J M, Worrall Bradford B, Rudnicka Alicja R, Rumley Ann, Bookman Ebony B, Psaty Bruce M, Chen Fang, Keene Keith L, Franco Oscar H, Böhm Bernhard O, Uitterlinden Andre G, Carter Angela M, Jukema J Wouter, Sattar Naveed, Bis Joshua C, Ikram Mohammad A, , Sale Michèle M, McKnight Barbara, Fornage Myriam, Ford Ian, Taylor Kent, Slagboom P Eline, McArdle Wendy L, Hsu Fang-Chi, Franco-Cereceda Anders, Goodall Alison H, Yanek Lisa R, Furie Karen L, Cushman Mary, Hofman Albert, Witteman Jacqueline C M, Folsom Aaron R, Basu Saonli, Matijevic Nena, van Gilst Wiek H, Wilson James F, Westendorp Rudi G J, Kathiresan Sekar, Reilly Muredach P, , Tracy Russell P, Polasek Ozren, Winkelmann Bernhard R, Grant Peter J, Hillege Hans L, Cambien Francois, Stott David J, Lowe Gordon D, Spector Timothy D, Meigs James B, Marz Winfried, Eriksson Per, Becker Lewis C, Morange Pierre-Emmanuel, Soranzo Nicole, Williams Scott M, Hayward Caroline, van der Harst Pim, Hamsten Anders, Lowenstein Charles J, Strachan David P, O'Donnell Christopher J, |
[Analysis of Eight Polymorphic Alu Elements in the Teleuts Population]. Genetika 2015 Aug 51 (8): 963-6. Swarovskaya M G, Marusin A V, Tacheeva T I, Khitrinskaya I Yu, Gafarov N I, Stepanov V |
Clinical characteristics of a Japanese family with hearing loss accompanied by compound heterozygous mutations in LOXHD1. Auris, nasus, larynx 2016 Mar . Minami Shujiro B, Mutai Hideki, Namba Kazunori, Sakamoto Hirozazu, Matsunaga Tats |
Microsatellite instability derived JAK1 frameshift mutations are associated with tumor immune evasion in endometrioid endometrial cancer. Oncotarget 2016 Jun 7 (26): 39885-39893. Stelloo Ellen, Versluis Marco A, Nijman Hans W, de Bruyn Marco, Plat Annechien, Osse Elisabeth M, van Dijk Reinhardt H, Nout Remi A, Creutzberg Carien L, de Bock Geertruida H, Smit Vincent T, Bosse Tjalling, Hollema Har |
Interaction of Alu Polymorphisms and Novel Measures of Discrimination in Association with Blood Pressure in African Americans Living in Tallahassee, Florida. Human biology 2015 Oct 87 (4): 295-305. Boulter Alexis C, Quinlan Jacklyn, Miró-Herrans Aida T, Pearson Laurel N, Todd Nubiana L, , Gravlee Clarence C, Mulligan Connie |
A Prothrombotic Score Based on Genetic Polymorphisms of the Hemostatic System Differs in Patients with Ischemic Stroke, Myocardial Infarction, or Peripheral Arterial Occlusive Disease. Frontiers in cardiovascular medicine 2017 4 39. Herm Juliane, Hoppe Berthold, Siegerink Bob, Nolte Christian H, Koscielny Jürgen, Haeusler Karl Geo |
Role of the tissue-type plasminogen activator -7351C > T and plasminogen activator inhibitor 1 4G/5G gene polymorphisms in central serous chorioretinopathy. Ophthalmic genetics 2018 Nov 1-3. Malle Eva Maria, Posch-Pertl Laura, Renner Wilfried, Pinter-Hausberger Silke, Singer Christoph, Haas Anton, Wedrich Andreas, Weger Mart |
Mutation burden profile in familial Alzheimer's disease cases from India. Neurobiology of aging 2017 Dec . Syama Adhikarla, Sen Somdatta, Kota Lakshmi Narayanan, Viswanath Biju, Purushottam Meera, Varghese Mathew, Jain Sanjeev, Panicker Mitradas M, Mukherjee Odi |
Association of homozygous variants of STING1 with outcome in human cervical cancer. Cancer science 2020 Oct . Lubbers Joyce M, Koopman Bart, de Klerk-Sluis Jessica M, van Rooij Nienke, Plat Annechien, Pijper Harry, Koopman Timco, van Hemel Bettien M, Hollema Harry, Wisman Bea, Nijman Hans W, de Bruyn Mar |
Genetic Determinants for Bacterial Osteomyelitis: A Focused Systematic Review of Published Literature. Frontiers in genetics 2021 7 12 654792. Xie Xiaoping, Li Jiangbi, Gu Feng, Zhang Ke, Su Zilong, Wen Qiangqiang, Sui Zhenjiang, Zhou Pengcheng, Yu Tieche |
Recessive LOXHD1 variants cause a prelingual down-sloping hearing loss: genotype-phenotype correlation and three additional children with novel variants. International journal of pediatric otorhinolaryngology 2021 4 145 110715. Yu Sha, Chen Wen-Xia, Zhang Yun-Fei, Chen Chao, Ni Yihua, Duan Bo, Wang Huijun, Xu Zheng-M |
Associations between SNPs in Intestinal Cholesterol Absorption and Endogenous Cholesterol Synthesis Genes with Cholesterol Metabolism. Biomedicines 2021 Oct 9 (10): . Schroor Maite M, Mokhtar Fatma B A, Plat Jogchum, Mensink Ronald |
Allergies, genetic polymorphisms of Th2 interleukins, and childhood acute lymphoblastic leukemia: The ESTELLE study. Pediatric blood & cancer 2021 10 69 (3): e29402. Ajrouche Roula, Chandab Ghinaj, Petit Arnaud, Strullu Marion, Nelken Brigitte, Plat Geneviève, Michel Gérard, Domenech Carine, Clavel Jacqueline, Bonaventure Audr |
Heritability Estimation of Multiple Sclerosis Related Plasma Protein Levels in Sardinian Families with Immunochip Genotyping Data. Life (Basel, Switzerland) 2022 7 12 (7): . Nova Andrea, Baldrighi Giulia Nicole, Fazia Teresa, Graziano Francesca, Saddi Valeria, Piras Marialuisa, Beecham Ashley, McCauley Jacob L, Bernardinelli Lui |
Occurrence and severity of cocaine-induced hallucinations: Two distinct phenotypes with shared clinical factors but specific genetic risk factors. Drug and alcohol dependence 2022 Mar 232 109270. Zerdazi El-Hadi, Curis Emmanuel, Karsinti Emily, Icick Romain, Fortias Maeva, Batel Philippe, Cottencin Olivier, Orizet Cyrille, Gay Aurélia, Coeuru Philippe, Deschenau Alice, Lack Philippe, Moisan Delphine, Pelissier-Alicot Anne-Laure, Plat Arnaud, Trabut Jean-Baptiste, Kousignian Isabelle, Boumendil Luana, Vicaut Eric, Prince Nathalie, Laplanche Jean-Louis, Bellivier Frank, Lépine Jean-Pierre, Marie-Claire Cynthia, Brousse Georges, Vorspan Florence, Bloch Vanes |
Alu Deletions in LAMA2 and CDH4 Genes Are Key Components of Polygenic Predictors of Longevity. International journal of molecular sciences 2022 11 23 (21): . Erdman Vera V, Karimov Denis D, Tuktarova Ilsia A, Timasheva Yanina R, Nasibullin Timur R, Korytina Gulnaz |
Identification of Prominent Genes between 3D Glioblastoma Models and Clinical Samples via GEO/TCGA/CGGA Data Analysis. Biology 2023 5 12 (5): . Brandon Wee Siang Phon, Saatheeyavaane Bhuvanendran, Qasim Ayub, Ammu Kutty Radhakrishnan, Muhamad Noor Alfarizal Kamarud |
Relation between single nucleotide polymorphisms in circadian clock relevant genes and cholesterol metabolism. Molecular genetics and metabolism 2023 4 138 (4): 107561. Schroor Maite M, Plat Jogchum, Mensink Ronald |
The breast cancer coagulome in the tumor microenvironment and its role in prognosis and treatment response to chemotherapy. Journal of thrombosis and haemostasis : JTH 2024 1 . Mari Tinholt, Xavier Tekpli, Lilly Anne Torland, Andliena Tahiri, Jürgen Geisler, Vessela Kristensen, Per Morten Sandset, Nina Ivers |
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