Human Genome Epidemiology Literature Finder
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Heme oxygenase-1 genotype of the donor is associated with graft survival after liver transplantation. American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons 2008 Feb 8 (2): 377-85. Buis C I, van der Steege G, Visser D S, Nolte I M, Hepkema B G, Nijsten M, Slooff M J H, Porte R |
Screening for six Mediterranean mutations in 90 Egyptian patients with phenylketonuria. Bratislavské lekárske listy 2008 109 (1): 17-9. Effat L K, Essawi M L, Abd El Hamid M S, Hawari N, Gad Y |
Gene polymorphisms of renin angiotensin system and serotonin transporter gene in patients with vasovagal syncope. Bratislavské lekárske listy 2009 110 (2): 73-6. Mudrakova K, Mitro P, Salagovic J, Habalova V, Kirsch P, Tkac |
Laboratory testing of hereditary thrombophilia: previous data in the face of verification. Bratislavské lekárske listy 2009 110 (1): 18-20. Melus V, Kiricova G, Simek |
Distribution of the 22 cytokine gene polymorphisms in healthy Macedonian population. Bratislavské lekárske listy 2009 110 (1): 7-17. Trajkov D, Arsov T, Petlichkovski A, Strezova A, Efinska-Mladenovska O, Gogusev J, Spiroski |
Plasma homocysteine level and 677C-->T mutation on the MTHFR gene in patients with venous thromboembolism. Bratislavské lekárske listy 2010 111 (2): 70-3. Hanta I, Soydas Y, Karatasli M, Koseoglu Z, Satar S, Hasturk |
Implication of glutathione S-transferase M1 and T1 polymorphisms in the development of senile cataract among Egyptians. Bratislavské lekárske listy 2009 110 (11): 678-83. Abdel Azeem Amira A, Mahmoud Amany A, Salaheldine Mostafa M, Amr Khal |
SnapShot: Renal Cell Carcinoma. Cancer cell 2016 Apr 29 (4): 610-610.e1. Ricketts Christopher J, Crooks Daniel R, Sourbier Carole, Schmidt Laura S, Srinivasan Ramaprasad, Linehan W Marst |
Genetic polymorphisms for 19 X-STR loci of Sichuan Han ethnicity and its comparison with Chinese populations. Legal medicine (Tokyo, Japan) 2017 9 29 6-12. He Guanglin, Li Ye, Zou Xing, Wang Mengge, Chen Pengyu, Liao Miao, Wu J |
First Approved Kinase Inhibitor for AML. Cell 2017 11 171 (5): 981. Rasko John E J, Hughes Timothy |
Publisher Correction: Genetic variants in systemic lupus erythematosus susceptibility loci, XKR6 and GLT1D1 are associated with childhood-onset SLE in a Korean cohort. Scientific reports 2018 Jul 8 (1): 11713. Joo Young Bin, Lim Jiwoo, Tsao Betty P, Nath Swapan K, Kim Kwangwoo, Bae Sang-Che |
Correction: Patient experience and utility of genetic information: a cross-sectional study among patients tested for cancer susceptibility and thrombophilia. European journal of human genetics : EJHG 2018 7 26 (9): 1398. D'Andrea Elvira, Lagerberg Tyra, De Vito Corrado, Pitini Erica, Marzuillo Carolina, Massimi Azzurra, Vacchio Maria Rosaria, Grammatico Paola, Villari Pao |
Correction: Association between interleukin family gene polymorphisms and recurrent aphthous stomatitis risk. Genes and immunity 2018 Jul . Zhou Ying, Wu Jun, Wang Wei, Sun Mingfa |
Author Correction: Population genetics analysis of the Nujiang catfish Creteuchiloglanis macropterus through a genome-wide single nucleotide polymorphisms resource generated by RAD-seq. Scientific reports 2018 6 8 (1): 9703. Kang Jingliang, Ma Xiuhui, He Shunpi |
Author Correction: The prognostic effects of somatic mutations in ER-positive breast cancer. Nature communications 2018 11 9 (1): 4850. Griffith Obi L, Spies Nicholas C, Anurag Meenakshi, Griffith Malachi, Luo Jingqin, Tu Dongsheng, Yeo Belinda, Kunisaki Jason, Miller Christopher A, Krysiak Kilannin, Hundal Jasreet, Ainscough Benjamin J, Skidmore Zachary L, Campbell Katie, Kumar Runjun, Fronick Catrina, Cook Lisa, Snider Jacqueline E, Davies Sherri, Kavuri Shyam M, Chang Eric C, Magrini Vincent, Larson David E, Fulton Robert S, Liu Shuzhen, Leung Samuel, Voduc David, Bose Ron, Dowsett Mitch, Wilson Richard K, Nielsen Torsten O, Mardis Elaine R, Ellis Matthew |
Correction: Variants in MED12L, encoding a subunit of the Mediator kinase module, are responsible for intellectual disability associated with transcriptional defect. Genetics in medicine : official journal of the American College of Medical Genetics 2019 7 21 (11): 2663. Nizon Mathilde, Laugel Vincent, Flanigan Kevin M, Pastore Matthew, Waldrop Megan A, Rosenfeld Jill A, Marom Ronit, Xiao Rui, Gerard Amanda, Pichon Olivier, Le Caignec Cédric, Gérard Marion, Dieterich Klaus, Truitt Cho Megan, McWalter Kirsty, Hiatt Susan, Thompson Michelle L, Bézieau Stéphane, Wadley Alexandrea, Wierenga Klaas J, Egly Jean-Marc, Isidor Bertra |
Author Correction: Combination of KIR2DS4 and Fc?RIIa polymorphisms predicts the response to cetuximab in KRAS mutant metastatic colorectal cancer. Scientific reports 2019 5 9 (1): 7706. Borrero-Palacios A, Cebrián A, Gómez Del Pulgar M T, García-Carbonero R, Garcia-Alfonso P, Aranda E, Elez E, López-López R, Cervantes A, Valladares M, Nadal C, Viéitez J M, Guillén-Ponce C, Rodríguez J, Hernández I, García J L, Vega-Bravo R, Puime-Otin A, Martínez-Useros J, Del Puerto-Nevado L, Rincón R, Rodríguez-Remírez M, Rojo F, García-Foncillas |
Correction: Polymorphisms at phase I-metabolizing enzyme and hormone receptor loci influence the response to anti-TNF therapy in rheumatoid arthritis patients. The pharmacogenomics journal 2019 2 19 (6): 582. Canet Luz M, Sánchez-Maldonado Jose M, Cáliz Rafael, Rodríguez-Ramos Ana, Lupiañez Carmen B, Canhão Helena, Martínez-Bueno Manuel, Escudero Alejandro, Segura-Catena Juana, Sorensen Signe B, Hetland Merete L, Soto-Pino María José, Ferrer Miguel A, García Antonio, Glintborg Bente, Filipescu Ileana, Pérez-Pampin Eva, González-Utrilla Alfonso, Nevot Miguel Ángel López, Conesa-Zamora Pablo, den Broeder Alfons, De Vita Salvatore, Jacobsen Sven Erik Hobe, Collantes-Estevez Eduardo, Quartuccio Luca, Canzian Federico, Fonseca João E, Coenen Marieke J H, Andersen Vibeke, Sainz Ju |
Correction: Epistasis of HTR1A and BDNF risk genes alters cortical 5-HT1A receptor binding: PET results link genotype to molecular phenotype in depression. Translational psychiatry 2019 10 9 (1): 246. Kautzky Alexander, James Gregory M, Philippe Cecile, Baldinger-Melich Pia, Kraus Christoph, Kranz Georg S, Vanicek Thomas, Gryglewski Gregor, Hartmann Annette M, Hahn Andreas, Wadsak Wolfgang, Mitterhauser Markus, Rujescu Dan, Kasper Siegfried, Lanzenberger Rupe |
Author Correction: Genome-wide association study of classical Hodgkin lymphoma identifies key regulators of disease susceptibility. Nature communications 2019 1 10 (1): 157. Sud Amit, Thomsen Hauke, Law Philip J, Försti Asta, da Silva Filho Miguel Inacio, Holroyd Amy, Broderick Peter, Orlando Giulia, Lenive Oleg, Wright Lauren, Cooke Rosie, Easton Douglas, Pharoah Paul, Dunning Alison, Peto Julian, Canzian Federico, Eeles Rosalind, Kote-Jarai Zsofia, Muir Kenneth, Pashayan Nora, , Hoffmann Per, Nöthen Markus M, Jöckel Karl-Heinz, von Strandmann Elke Pogge, Lightfoot Tracy, Kane Eleanor, Roman Eve, Lake Annette, Montgomery Dorothy, Jarrett Ruth F, Swerdlow Anthony J, Engert Andreas, Orr Nick, Hemminki Kari, Houlston Richard |
Publisher Correction: A downy mildew effector evades recognition by polymorphism of expression and subcellular localization. Nature communications 2019 1 10 (1): 174. Asai Shuta, Furzer Oliver J, Cevik Volkan, Kim Dae Sung, Ishaque Naveed, Goritschnig Sandra, Staskawicz Brian J, Shirasu Ken, Jones Jonathan D |
Genetic polymorphism investigation of 16 X-STR loci in the Bai ethnic minority in Yunnan Province, Southwest China. International journal of legal medicine 2020 11 136 (2): 543-545. Qing Lili, Li Yi, Liu Linlin, Chen Dengyong, Han Jianli, Shi Yuchao, Huang Renwu, Zhang Xiufeng, Nie Shengjie, Hu Lipi |
Linkage of blood pressure, obesity and diabetes mellitus with angiotensinogen gene (AGT 704T>C/rs699) polymorphism in hypertensive patients. Bratislavske lekarske listy 2021 122 (10): 715-720. Repchuk Y, Sydorchuk L P, Sydorchuk A R, Fedonyuk L Y, Kamyshnyi O, Korovenkova O, Plehutsa I M, Dzhuryak V S, Myshkovskii Y M, Iftoda O M, Sydorchuk R |
Genome-wide association study meta-analysis identifies three novel loci for circulating anti-Müllerian hormone levels in women.
Human reproduction (Oxford, England) 2022 3 37 (5): 1069-1082. Verdiesen Renée M G, van der Schouw Yvonne T, van Gils Carla H, Verschuren W M Monique, Broekmans Frank J M, Borges Maria C, Gonçalves Soares Ana L, Lawlor Deborah A, Eliassen A Heather, Kraft Peter, Sandler Dale P, Harlow Siobán D, Smith Jennifer A, Santoro Nanette, Schoemaker Minouk J, Swerdlow Anthony J, Murray Anna, Ruth Katherine S, Onland-Moret N Charlot |
Role of genetics in the development of cardiac allograft vasculopathy. Bratislavske lekarske listy 2023 1 124 (3): 193-200. Mayerova Lucie, Chaloupka Anna, Wohlfahrt Peter, Hubacek Jaroslav Alois, Bedanova Helena, Chen Zhi, Kautzner Josef, Melenovsky Vojtech, Malek Ivan, Tomasek Ales, Ozabalova Eva, Krejci Jan, Kovarnik Tomas, Sonka Milan, Pazdernik Mich |
The effects of angiotensinogen M235T/T174M and angiotensin type 1 receptor a1166c gene polymorphisms on the development of diabetic nephropathy in type 2 diabetes mellitus patients. Bratislavske lekarske listy 2023 1 124 (3): 175-181. Yukcu Fulya, Sipahi Tammam, Guldiken S?bel, Ustundag Sedat, Sut Necd |
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- Page last updated:Apr 22, 2024
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