HuGE Literature Finder
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Records 1-100
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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, Czlonkowska 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 |
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A Systematic Review of Genetic Influence on Psychological Resilience.
Biological research for nursing 2018 Sep 1099800418800396. Niitsu Kosuke, Rice Michael J, Houfek Julia F, Stoltenberg Scott F, Kupzyk Kevin A, Barron Cecilia |
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Genetic variation affecting DNA methylation and the human imprinting disorder, Beckwith-Wiedemann syndrome.
Clinical epigenetics 2018 Aug 10 (1): 114. Dagar Vinod, Hutchison Wendy, Muscat Andrea, Krishnan Anita, Hoke David, Buckle Ashley, Siswara Priscillia, Amor David J, Mann Jeffrey, Pinner Jason, Colley Alison, Wilson Meredith, Sachdev Rani, McGillivray George, Edwards Matthew, Kirk Edwin, Collins Felicity, Jones Kristi, Taylor Juliet, Hayes Ian, Thompson Elizabeth, Barnett Christopher, Haan Eric, Freckmann Mary-Louise, Turner Anne, White Susan, Kamien Ben, Ma Alan, Mackenzie Fiona, Baynam Gareth, Kiraly-Borri Cathy, Field Michael, Dudding-Byth Tracey, Algar Elizabeth |
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Specific alterations in the circulating levels of the SIRT1, TLR4, and IL7 proteins in patients with dementia.
Experimental gerontology 2018 Jul 111 203-209. Kilic Ulkan, Elibol Birsen, Uysal Omer, Kilic Ertugrul, Yulug Burak, Sayin Sakul Arzu, Babacan Yildiz Guls |
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No evidence for association of MTHFR 677C>T and 1298A>C variants with placental DNA methylation.
Clinical epigenetics 2018 10 34. Del Gobbo Giulia F, Price E Magda, Hanna Courtney W, Robinson Wendy |
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[Genetic factors in alcohol dependence].
Presse medicale (Paris, France : 1983) 2017 Dec . Ramoz Nicolas, Gorwood Phil |
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Potential for diagnosis versus therapy monitoring of attention deficit hyperactivity disorder: a new epigenetic biomarker interacting with both genotype and auto-immunity.
European child & adolescent psychiatry 2017 Aug . Adriani Walter, Romano Emilia, Pucci Mariangela, Pascale Esterina, Cerniglia Luca, Cimino Silvia, Tambelli Renata, Curatolo Paolo, Granstrem Oleg, Maccarrone Mauro, Laviola Giovanni, D'Addario Claud |
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Targeted Exome Sequencing Identifies PBX1 as Involved in Monogenic Congenital Anomalies of the Kidney and Urinary Tract.
Journal of the American Society of Nephrology : JASN 2017 May . Heidet Laurence, Morinière Vincent, Henry Charline, De Tomasi Lara, Reilly Madeline Louise, Humbert Camille, Alibeu Olivier, Fourrage Cécile, Bole-Feysot Christine, Nitschké Patrick, Tores Frédéric, Bras Marc, Jeanpierre Marc, Pietrement Christine, Gaillard Dominique, Gonzales Marie, Novo Robert, Schaefer Elise, Roume Joëlle, Martinovic Jelena, Malan Valérie, Salomon Rémi, Saunier Sophie, Antignac Corinne, Jeanpierre Céci |
Identification of unique venous thromboembolism-susceptibility variants in African-Americans.
Thrombosis and haemostasis 2017 Feb . Heit John A, Armasu Sebastian M, McCauley Bryan M, Kullo Iftikhar J, Sicotte Hugues, Pathak Jyotishman, Chute Christopher G, Gottesman Omri, Bottinger Erwin P, Denny Joshua C, Roden Dan M, Li Rongling, Ritchie Marylyn D, de Andrade Mari |
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MTHFR Gene Polymorphism-Mutations and Air Pollution as Risk Factors for Breast Cancer: A Metaprediction Study.
Nursing research 2017 Jan . Gonzales Mildred C, Yu Pojui, Shiao S Pamela |
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[A search of target regions for association studies between DNA methylation and cognitive impairment in schizophrenia].
Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova 2017 117 (8): 72-75. Kondratiev N V, Alfimova M V, Golimbet V |
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Differential methylation at MHC in CD4(+) T cells is associated with multiple sclerosis independently of HLA-DRB1.
Clinical epigenetics 2017 9 71. Maltby Vicki E, Lea Rodney A, Sanders Katherine A, White Nicole, Benton Miles C, Scott Rodney J, Lechner-Scott Jeannet |
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Epigenetic regulation of AXL and risk of childhood asthma symptoms.
Clinical epigenetics 2017 9 121. Gao Lu, Millstein Joshua, Siegmund Kimberly D, Dubeau Louis, Maguire Rachel, Gilliland Frank D, Murphy Susan K, Hoyo Cathrine, Breton Carrie |
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The dynamic DNA methylation landscape of the mutL homolog 1 shore is altered by MLH1-93G>A polymorphism in normal tissues and colorectal cancer.
Clinical epigenetics 2017 9 26. Savio Andrea J, Mrkonjic Miralem, Lemire Mathieu, Gallinger Steven, Knight Julia A, Bapat Bhar |
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MeQTL analysis of childhood obesity links epigenetics with a risk SNP rs17782313 near MC4R from meta-analysis.
Oncotarget 2016 Dec . Tang Yuping, Jin Bo, Zhou Lingling, Lu Weife |
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LBH Gene Transcription Regulation by the Interplay of an Enhancer Risk Allele and DNA Methylation in Rheumatoid Arthritis.
Arthritis & rheumatology (Hoboken, N.J.) 2016 Nov 68 (11): 2637-2645. Hammaker Deepa, Whitaker John W, Maeshima Keisuke, Boyle David L, Ekwall Anna-Karin H, Wang Wei, Firestein Gary |
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The framework for population epigenetic study.
Briefings in bioinformatics 2016 Oct . Zhao Linna, Liu Di, Xu Jing, Wang Zhaoyang, Chen Yang, Lei Changgui, Li Ying, Liu Guiyou, Jiang Yongshu |
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DNA methylation profiling in human lung tissue identifies genes associated with COPD.
Epigenetics 2016 Aug 0. Morrow Jarrett D, Cho Michael H, Hersh Craig P, Pinto-Plata Victor, Celli Bartolome, Marchetti Nathaniel, Criner Gerard, Bueno Raphael, Washko George, Glass Kimberly, Choi Augustine M K, Quackenbush John, Silverman Edwin K, DeMeo Dawn |
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Genetic contribution to variation in DNA methylation at maternal smoking sensitive loci in exposed neonates.
Epigenetics 2016 Jul 0. Gonseth Semira, de Smith Adam J, Roy Ritu, Zhou Mi, Lee Seung-Tae, Shao Xiaorong, Ohja Juhi, Wrensch Margaret R, Walsh Kyle M, Metayer Catherine, Wiemels Joseph |
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Genomics, Telomere Length, Epigenetics, and Metabolomics in the Nurses' Health Studies.
American journal of public health 2016 Jul e1-e6. Townsend Mary K, Aschard Hugues, De Vivo Immaculata, Michels Karin B, Kraft Pet |
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Homocysteine metabolism and the associations of global DNA methylation with selected gene polymorphisms and nutritional factors in patients with dementia.
Experimental gerontology 2016 May . Bednarska-Makaruk Ma?gorzata, Graban A??a, Sobczy?ska-Malefora Agata, Harrington Dominic J, Mitchell Michael, Voong Kieran, Dai Letian, ?ojkowska Wanda, Bochy?ska Anna, Ryglewicz Danuta, Wi?niewska Anna, Wehr Han |
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Role of DNA methylation at the placental RTL1 gene locus in type 1 diabetes.
Pediatric diabetes 2016 May . Belot Marie-Pierre, Nadéri Kambiz, Mille Clémence, Boëlle Pierre-Yves, Benachi Alexandra, Bougnères Pierre, Fradin Delphi |
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BDNF rs6265 methylation and genotype interact on risk for schizophrenia.
Epigenetics 2016 Feb 1-13. Ursini Gianluca, Cavalleri Tommaso, Fazio Leonardo, Angrisano Tiziana, Iacovelli Luisa, Porcelli Annamaria, Maddalena Giancarlo, Punzi Giovanna, Mancini Marina, Gelao Barbara, Romano Raffaella, Masellis Rita, Calabrese Francesca, Rampino Antonio, Taurisano Paolo, Giorgio Annabella Di, Keller Simona, Tarantini Letizia, Sinibaldi Lorenzo, Quarto Tiziana, Popolizio Teresa, Caforio Grazia, Blasi Giuseppe, Riva Marco A, Blasi Antonio De, Chiariotti Lorenzo, Bollati Valentina, Bertolino Alessand |
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DNA methylation profiling to assess pathogenicity of BRCA1 unclassified variants in breast cancer.
Epigenetics 2016 Jan 0. Flower Kirsty J, Shenker Natalie S, El-Bahrawy Mona, Goldgar David E, Parsons Michael T, Investigators KConFab, Study Group Affect, Spurdle Amanda B, Morris Joanna R, Brown Robert, Flanagan James |
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A Genome-Wide mQTL Analysis in Human Adipose Tissue Identifies Genetic Variants Associated with DNA Methylation, Gene Expression and Metabolic Traits.
PloS one 2016 11 (6): e0157776. Volkov Petr, Olsson Anders H, Gillberg Linn, Jørgensen Sine W, Brøns Charlotte, Eriksson Karl-Fredrik, Groop Leif, Jansson Per-Anders, Nilsson Emma, Rönn Tina, Vaag Allan, Ling Charlot |
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A STAT6 Intronic Single-Nucleotide Polymorphism is Associated with Clinical Malaria in Ghanaian Children.
Genetics & epigenetics 2016 8 7-14. Amoako-Sakyi Daniel, Adukpo Selorme, Kusi Kwadwo A, Dodoo Daniel, Ofori Michael F, Adjei George O, Edoh Dominic E, Asmah Richard H, Brown Charles, Adu Bright, Obiri-Yeboah Dorcas, Futagbi Godfred, Abubakari Sharif Buari, Troye-Blomberg Marita, Akanmori Bartholomew D, Goka Bamenla Q, Arko-Mensah John, Gyan Ben |
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Assessing the Causality Factors in the Association between (Abdominal) Obesity and Physical Activity among the Newfoundland Population-A Mendelian Randomization Analysis.
Genetics & epigenetics 2016 8 15-24. Barning Frank, Abarin Taran |
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DNA methylation in a Scottish family multiply affected by bipolar disorder and major depressive disorder.
Clinical epigenetics 2016 8 5. Walker Rosie May, Christoforou Andrea Nikie, McCartney Daniel L, Morris Stewart W, Kennedy Nicholas A, Morten Peter, Anderson Susan Maguire, Torrance Helen Scott, Macdonald Alix, Sussmann Jessika Elizabeth, Whalley Heather Clare, Blackwood Douglas H R, McIntosh Andrew Mark, Porteous David John, Evans Kathryn Loui |
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Genetic and epigenetic studies of atopic dermatitis.
Allergy, asthma, and clinical immunology : official journal of the Canadian Society of Allergy and Clinical Immunology 2016 12 52. Bin Lianghua, Leung Donald Y |
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Genome- and epigenome-wide association study of hypertriglyceridemic waist in Mexican American families.
Clinical epigenetics 2016 8 6. Mamtani Manju, Kulkarni Hemant, Dyer Thomas D, Göring Harald H H, Neary Jennifer L, Cole Shelley A, Kent Jack W, Kumar Satish, Glahn David C, Mahaney Michael C, Comuzzie Anthony G, Almasy Laura, Curran Joanne E, Duggirala Ravindranath, Blangero John, Carless Melanie |
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The cardiovascular and hypothalamus-pituitary-adrenal axis response to stress is controlled by glucocorticoid receptor sequence variants and promoter methylation.
Clinical epigenetics 2016 8 12. Li-Tempel Ting, Larra Mauro F, Sandt Estelle, Mériaux Sophie B, Schote Andrea B, Schächinger Hartmut, Muller Claude P, Turner Jonathan |
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HPA AXIS RELATED GENES AND RESPONSE TO PSYCHOLOGICAL THERAPIES: GENETICS AND EPIGENETICS.
Depression and anxiety 2015 Dec 32 (12): 861-70. Roberts Susanna, Keers Robert, Lester Kathryn J, Coleman Jonathan R I, Breen Gerome, Arendt Kristian, Blatter-Meunier Judith, Cooper Peter, Creswell Cathy, Fjermestad Krister, Havik Odd E, Herren Chantal, Hogendoorn Sanne M, Hudson Jennifer L, Krause Karen, Lyneham Heidi J, Morris Talia, Nauta Maaike, Rapee Ronald M, Rey Yasmin, Schneider Silvia, Schneider Sophie C, Silverman Wendy K, Thastum Mikael, Thirlwall Kerstin, Waite Polly, Eley Thalia C, Wong Chloe C |
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The Genetic Epidemiological Landscape of Hip and Knee Osteoarthritis: Where Are We Now and Where Are We Going?
The Journal of rheumatology 2015 Dec . Zengini Eleni, Finan Chris, Wilkinson J Ma |
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Genetic, Epigenetic and Pharmacogenetic Aspects of Psoriasis and Psoriatic Arthritis.
Rheumatic diseases clinics of North America 2015 Nov 41 (4): 623-42. O'Rielly Darren D, Rahman Prot |
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The impact of genetic variation and cigarette smoke on DNA methylation in current and former smokers from the COPDGene study.
Epigenetics 2015 Nov 10 (11): 1064-73. Qiu Weiliang, Wan Emily, Morrow Jarrett, Cho Michael H, Crapo James D, Silverman Edwin K, DeMeo Dawn |
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DNA methylation provides insight into intergenerational risk for preterm birth in African Americans.
Epigenetics 2015 Sep 10 (9): 784-92. Parets Sasha E, Conneely Karen N, Kilaru Varun, Menon Ramkumar, Smith Alicia |
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Mitochondrial Citrate Transporter-dependent Metabolic Signature in the 22q11.2 Deletion Syndrome.
The Journal of biological chemistry 2015 Sep 290 (38): 23240-53. Napoli Eleonora, Tassone Flora, Wong Sarah, Angkustsiri Kathleen, Simon Tony J, Song Gyu, Giulivi Cecil |
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Associations between genetic variation in one-carbon metabolism and LINE-1 DNA methylation in histologically normal breast tissues.
Epigenetics 2015 Aug 10 (8): 727-35. Llanos Adana A M, Marian Catalin, Brasky Theodore M, Dumitrescu Ramona G, Liu Zhenhua, Mason Joel B, Makambi Kepher H, Spear Scott L, Kallakury Bhaskar V S, Freudenheim Jo L, Shields Peter |
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Differential DNA methylation identified in the blood and retina of AMD patients.
Epigenetics 2015 Aug 10 (8): 698-707. Oliver Verity F, Jaffe Andrew E, Song Jin, Wang Guohua, Zhang Pingwu, Branham Kari E, Swaroop Anand, Eberhart Charles G, Zack Donald J, Qian Jiang, Merbs Shannath |
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PON1 as a model for integration of genetic, epigenetic, and expression data on candidate susceptibility genes.
Environmental epigenetics 2015 Jan 1 (1): . Huen Karen, Yousefi Paul, Street Kelly, Eskenazi Brenda, Holland Ni |
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Combined epigenetic and intraspecific variation of the DRD4 and SERT genes influence novelty seeking behavior in great tit Parus major.
Epigenetics 2015 10 (6): 516-25. Riyahi Sepand, Sánchez-Delgado Marta, Calafell Francesc, Monk David, Senar Juan Carl |
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DNA methylation analysis of Homeobox genes implicates HOXB7 hypomethylation as risk factor for neural tube defects.
Epigenetics 2015 10 (1): 92-101. Rochtus Anne, Izzi Benedetta, Vangeel Elise, Louwette Sophie, Wittevrongel Christine, Lambrechts Diether, Moreau Yves, Winand Raf, Verpoorten Carla, Jansen Katrien, Van Geet Chris, Freson Kathle |
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Genome-scale hypomethylation in the cord blood DNAs associated with early onset preeclampsia.
Clinical epigenetics 2015 7 (1): 21. Ching Travers, Ha James, Song Min-Ae, Tiirikainen Maarit, Molnar Janos, Berry Marla J, Towner Dena, Garmire Lana |
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Increased DNA methylation of the SLC30A8 gene promoter is associated with type 2 diabetes in a Malay population.
Clinical epigenetics 2015 7 (1): 30. Seman Norhashimah Abu, Mohamud Wan Nazaimoon Wan, Östenson Claes-Göran, Brismar Kerstin, Gu Harvest |
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Isocitrate dehydrogenase 1 R132C mutation occurs exclusively in microsatellite stable colorectal cancers with the CpG island methylator phenotype.
Epigenetics 2014 Nov 9 (11): 1454-60. Whitehall V L J, Dumenil T D, McKeone D M, Bond C E, Bettington M L, Buttenshaw R L, Bowdler L, Montgomery G W, Wockner L F, Leggett B |
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DNA methyltransferase haplotype is associated with Alzheimer's disease.
Neuroscience letters 2014 Sep 579 70-4. Pezzi Julio Carlos, Ens Cintia Monique Boschmann, Borba Ericksen Mielle, Schumacher-Schuh Artur F, de Andrade Fabiana Michelsen, Chaves Marcia Lorena Fagundes, Fiegenbaum Marilu, Camozzato Ana Lui |
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The effect of genotype and in utero environment on interindividual variation in neonate DNA methylomes.
Genome research 2014 Jul 24 (7): 1064-74. Teh Ai Ling, Pan Hong, Chen Li, Ong Mei-Lyn, Dogra Shaillay, Wong Johnny, MacIsaac Julia L, Mah Sarah M, McEwen Lisa M, Saw Seang-Mei, Godfrey Keith M, Chong Yap-Seng, Kwek Kenneth, Kwoh Chee-Keong, Soh Shu-E, Chong Mary F F, Barton Sheila, Karnani Neerja, Cheong Clara Y, Buschdorf Jan Paul, Stünkel Walter, Kobor Michael S, Meaney Michael J, Gluckman Peter D, Holbrook Joanna |
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CpG island methylator phenotype and its association with malignancy in sporadic duodenal adenomas.
Epigenetics 2014 May 9 (5): 738-46. Sun Lifeng, Guzzetta Angela A, Fu Tao, Chen Jinming, Jeschke Jana, Kwak Ruby, Vatapalli Rajita, Baylin Stephen B, Iacobuzio-Donahue Christine A, Wolfgang Christopher L, Ahuja Ni |
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Gene promoter methylation in colorectal cancer and healthy adjacent mucosa specimens: correlation with physiological and pathological characteristics, and with biomarkers of one-carbon metabolism.
Epigenetics 2014 Apr 9 (4): 621-33. Coppedè Fabio, Migheli Francesca, Lopomo Angela, Failli Alessandra, Legitimo Annalisa, Consolini Rita, Fontanini Gabriella, Sensi Elisa, Servadio Adele, Seccia Massimo, Zocco Giuseppe, Chiarugi Massimo, Spisni Roberto, Migliore Luc |
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Oral contraceptives modify the effect of GATA3 polymorphisms on the risk of asthma at the age of 18 years via DNA methylation.
Clinical epigenetics 2014 6 (1): 17. Guthikonda Kranthi, Zhang Hongmei, Nolan Vikki G, Soto-Ramírez Nelís, Ziyab Ali H, Ewart Susan, Arshad Hasan S, Patil Veeresh, Holloway John W, Lockett Gabrielle A, Karmaus Wilfri |
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The interplay of DNA methylation over time with Th2 pathway genetic variants on asthma risk and temporal asthma transition.
Clinical epigenetics 2014 6 (1): 8. Zhang Hongmei, Tong Xin, Holloway John W, Rezwan Faisal I, Lockett Gabrielle A, Patil Veeresh, Ray Meredith, Everson Todd M, Soto-Ramírez Nelís, Arshad S Hasan, Ewart Susan, Karmaus Wilfri |
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Vitamin D Receptor Genotype Modulates the Correlation between Vitamin D and Circulating Levels of let-7a/b and Vitamin D Intake in an Elderly Cohort.
Journal of nutrigenetics and nutrigenomics 2014 7 (4-6): 264-73. Beckett Emma Louise, Martin Charlotte, Duesing Konsta, Jones Patrice, Furst John, Yates Zoe, Veysey Martin, Lucock Ma |
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Interaction of prenatal maternal smoking, interleukin 13 genetic variants and DNA methylation influencing airflow and airway reactivity.
Clinical epigenetics 2013 Dec 5 (1): 1. Patil VK, Holloway JW, Zhang H, Soto-Ramirez N, Ewart S, Arshad SH, Karmaus W |
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PIK3CA hypomethylation plays a key role in activation of the PI3K/AKT pathway in esophageal cancer in Chinese patients.
Acta pharmacologica Sinica 2013 Dec 34 (12): 1560-7. Wang Wei-feng, Xie Yan, Zhou Zhi-hua, Qin Zheng-hong, Wu Jun-chao, He Jing-ka |
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Prospective analysis of the association between estrogen receptor gene variants and the risk of cognitive decline in elderly women.
European neuropsychopharmacology : the journal of the European College of Neuropsychopharmacology 2013 Dec 23 (12): 1763-8. Ryan Joanne, Carrière Isabelle, Amieva Helene, Rouaud Olivier, Berr Claudine, Ritchie Karen, Scarabin Pierre-Yves, Ancelin Marie-Lau |
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Integrated analysis of genome-wide genetic and epigenetic association data for identification of disease mechanisms.
Epigenetics 2013 Nov 8 (11): 1236-44. Ke Xiayi, Cortina-Borja Mario, Silva Bruno Cesar, Lowe Robert, Rakyan Vardhman, Balding Dav |
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Ten years of progress in the Hokkaido birth cohort study on environment and children's health: cohort profile--updated 2013.
Environmental health and preventive medicine 2013 Nov 18 (6): 429-50. Kishi Reiko, Kobayashi Sachiko, Ikeno Tamiko, Araki Atsuko, Miyashita Chihiro, Itoh Sachiko, Sasaki Seiko, Okada Emiko, Kobayashi Sumitaka, Kashino Ikuko, Itoh Kumiko, Nakajima Sonomi, |
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Brain volumes in late life: gender, hormone treatment, and estrogen receptor variants.
Neurobiology of aging 2013 Oct . Ryan J, Artero S, Carrière I, Scali J, Maller JJ, Meslin C, Ritchie K, Scarabin PY, Ancelin ML |
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A prospective study of duration of smoking cessation and colorectal cancer risk by epigenetics-related tumor classification.
American journal of epidemiology 2013 Jul 178 (1): 84-100. Nishihara Reiko, Morikawa Teppei, Kuchiba Aya, Lochhead Paul, Yamauchi Mai, Liao Xiaoyun, Imamura Yu, Nosho Katsuhiko, Shima Kaori, Kawachi Ichiro, Qian Zhi Rong, Fuchs Charles S, Chan Andrew T, Giovannucci Edward, Ogino Shu |
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Endocrine profile and phenotype-(epi)genotype correlation in Spanish patients with pseudohypoparathyroidism.
The Journal of clinical endocrinology and metabolism 2013 May 98 (5): E996-1006. Fernández-Rebollo Eduardo, Lecumberri Beatriz, Gaztambide Sonia, Martinez-Indart Lorea, Perez de Nanclares Guiomar, Castaño Luis, |
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Mutations of the epigenetics-modifying gene (DNMT3a, TET2, IDH1/2) at diagnosis may induce FLT3-ITD at relapse in de novo acute myeloid leukemia.
Leukemia 2013 Apr 27 (5): 1044-52. Wakita S, Yamaguchi H, Omori I, Terada K, Ueda T, Manabe E, Kurosawa S, Iida S, Ibaraki T, Sato Y, Todoroki T, Hirakawa T, Ryotokuji T, Arai K, Kitano T, Mitamura Y, Kosaka F, Dan K, Inokuchi |
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Genetic and epigenetic factors in regulation of microRNA in colorectal cancers.
Methods (San Diego, Calif.) 2013 Jan 59 (1): 138-46. Vinci Serena, Gelmini Stefania, Mancini Irene, Malentacchi Francesca, Pazzagli Mario, Beltrami Cristina, Pinzani Pamela, Orlando Claud |
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The interaction of genetic variants and DNA methylation of the interleukin-4 receptor gene increase the risk of asthma at age 18 years.
Clinical epigenetics 2013 Jan 5 (1): 1. Soto-Ramírez N, Arshad SH, Holloway J, Zhang H, Schauberger E, Ewart S, Patil V, Karmaus W |
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Association of the DNMT3B -579G>T polymorphism with risk of thymomas in patients with myasthenia gravis.
PloS one 2013 8 (11): e80846. Coppedè Fabio, Ricciardi Roberta, Denaro Maria, De Rosa Anna, Provenzano Carlo, Bartoccioni Emanuela, Baggiani Angelo, Lucchi Marco, Mussi Alfredo, Migliore Luc |
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Association of the HLA-DQA1 and HLA-DQB1 Alleles in Type 2 Diabetes Mellitus and Diabetic Nephropathy in the Han Ethnicity of China.
Journal of diabetes research 2013 2013 452537. Ma Ze-Jun, Sun Pei, Guo Gang, Zhang Rui, Chen Li-Mi |
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DNA methyltransferase candidate polymorphisms, imprinting methylation, and birth outcome.
PloS one 2013 8 (7): e68896. Haggarty Paul, Hoad Gwen, Horgan Graham W, Campbell Doris |
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DNMT1 genetic polymorphisms affect breast cancer risk in the central European Caucasian population.
Clinical epigenetics 2013 5 (1): 7. Kullmann Kathrin, Deryal Mustafa, Ong Mei Fang, Schmidt Werner, Mahlknecht Ulri |
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Aberrant keap1 methylation in breast cancer and association with clinicopathological features.
Epigenetics : official journal of the DNA Methylation Society 2012 Dec 8 (1): 1. Barbano R, Muscarella LA, Pasculli B, Valori VM, Fontana A, Coco M, la Torre A, Balsamo T, Poeta ML, Marangi GF, Maiello E, Castelvetere M, Pellegrini F, Murgo R, Fazio VM, Parrella P |
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Evidence that the methylation state of the monoamine oxidase A (MAOA) gene predicts brain activity of MAO A enzyme in healthy men.
Epigenetics 2012 Oct 7 (10): 1151-60. Shumay Elena, Logan Jean, Volkow Nora D, Fowler Joanna |
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IGF2 DNA methylation is a modulator of newborn's fetal growth and development.
Epigenetics 2012 Oct 7 (10): 1125-32. St-Pierre Julie, Hivert Marie-France, Perron Patrice, Poirier Paul, Guay Simon-Pierre, Brisson Diane, Bouchard Lui |
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Sirtuin1 single nucleotide polymorphism (A2191G) is a diagnostic marker for vibration-induced white finger disease.
Clinical epigenetics 2012 Oct 4 (1): 1. Voelter-Mahlknecht S, Rossbach B, Schleithoff C, Dransfeld CL, Letzel S, Mahlknecht U |
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Epigenetic dysregulation of secreted frizzled-related proteins in myeloproliferative neoplasms complements the JAK2V617F-mutation.
Clinical epigenetics 2012 Aug 4 (1): 1. Bennemann K, Galm O, Wilop S, Schubert C, Bruemmendorf TH, Jost E |
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No associations found between the genes situated at 6p22.1, HIST1H2BJ, PRSS16, and PGBD1 in Japanese patients diagnosed with schizophrenia.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2012 Jun 159B (4): 456-64. Kitazawa Maiko, Ohnuma Tohru, Takebayashi Yuto, Shibata Nobuto, Baba Hajime, Ohi Kazutaka, Yasuda Yuka, Nakamura Yukako, Aleksic Branko, Yoshimi Akira, Okochi Tomo, Ikeda Masashi, Naitoh Hiroshi, Hashimoto Ryota, Iwata Nakao, Ozaki Norio, Takeda Masatoshi, Arai He |
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[Correlation between RARbeta gene promoter methylation and P53 gene mutations in non-small cell lung cancer].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2012 Apr 29 (2): 131-6. Tan Cong, Jin Yong-tang, Xu He-yun, Zhang Chen-ye, Zhang Hu, Zhang Wei-min, Chen Chun-mei, Sun Xiao- |
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[Effects of CYP1A1 and GSTM1 gene polymorphisms and BPDE-DNA adducts on lung cancer].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2012 Feb 29 (1): 23-7. Chen Chun-mei, Jin Yong-tang, Xu He-yun, Zhang Chen-ye, Zhang Hu, Zhang Wei-min, Tan Cong, Sun Xiao- |
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Effects of TET2 mutations on DNA methylation in chronic myelomonocytic leukemia.
Epigenetics 2012 Feb 7 (2): 201-7. Yamazaki Jumpei, Taby Rodolphe, Vasanthakumar Aparna, Macrae Trisha, Ostler Kelly R, Shen Lanlan, Kantarjian Hagop M, Estecio Marcos R, Jelinek Jaroslav, Godley Lucy A, Issa Jean-Pierre |
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[Chromosomal instability, microsatellite instability and CpG island methylator phenotype: roles in small intestinal carcinogenesis].
Der Pathologe 2011 Nov 32 Suppl 2 181-4. Bläker H, Warth A, Kloor M, Schirmacher |
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Effect of CYP1A1 MSPI polymorphism on the relationship between TP53 mutation and CDKN2A hypermethylation in non-small cell lung cancer.
Archives of medical research 2011 Nov 42 (8): 669-76. Tan Cong, Xu He-Yun, Zhang Chen-Ye, Zhang Hu, Chen Chun-Mei, Zhang Wei-Min, Sun Xiao-Yu, Jin Yong-Ta |
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Genotype of an individual single nucleotide polymorphism regulates DNA methylation at the TRPC3 alternative promoter.
Epigenetics 2011 Oct 6 (10): 1236-41. Martin-Trujillo Alex, Iglesias-Platas Isabel, Coto Eliecer, Corral-Juan Marc, San Nicolás Hector, Corral Jordi, Volpini Victor, Matilla-Dueñas Antoni, Monk Dav |
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Common genetic variants related to genomic integrity and risk of papillary thyroid cancer.
Carcinogenesis 2011 Aug 32 (8): 1231-7. Neta Gila, Brenner Alina V, Sturgis Erich M, Pfeiffer Ruth M, Hutchinson Amy A, Aschebrook-Kilfoy Briseis, Yeager Meredith, Xu Li, Wheeler William, Abend Michael, Ron Elaine, Tucker Margaret A, Chanock Stephen J, Sigurdson Alice |
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Role of complement factor H I62V and age-related maculopathy susceptibility 2 A69S variants in the clinical expression of polypoidal choroidal vasculopathy.
Ophthalmology 2011 Jul 118 (7): 1402-7. Sakurada Yoichi, Kubota Takeo, Imasawa Mitsuhiro, Mabuchi Fumihiko, Tateno Yasushi, Tanabe Naohiko, Iijima Hiroyu |
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Methylenetetrahydrofolate reductase 677 C->T polymorphism: a link between birth weight and insulin resistance in obese adolescents.
International journal of pediatric obesity : IJPO : an official journal of the International Association for the Study of Obesity 2011 Jun 6 (2-2): e312-7. Frelut Marie-Laure, Nicolas Jean-Pierre, Guilland Jean-Claude, de Courcy Genevieve Poti |
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Identification of polymorphisms in ultraconserved elements (UCEs) associated with clinical outcomes in patients (pts) with stage II/III colorectal cancer (CRC).
Journal of clinical oncology : official journal of the American Society of Clinical Oncology 2011 May 29 (15_suppl): 3529. Lin M, Hawk E, Huang M, Lin J, Gu J, Ellis L M, Wu X, Eng |
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Genetics and epigenetics of small bowel adenocarcinoma: the interactions of CIN, MSI, and CIMP.
Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc 2011 Apr 24 (4): 564-70. Warth Arne, Kloor Matthias, Schirmacher Peter, Bläker Hendr |
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Evaluation of 64 candidate single nucleotide polymorphisms as risk factors for neural tube defects in a large Irish study population.
American journal of medical genetics. Part A 2011 Jan 155A (1): 14-21. Carter Tonia C, Pangilinan Faith, Troendle James F, Molloy Anne M, VanderMeer Julia, Mitchell Adam, Kirke Peadar N, Conley Mary R, Shane Barry, Scott John M, Brody Lawrence C, Mills James |
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Genetic variation in PCAF, a key mediator in epigenetics, is associated with reduced vascular morbidity and mortality: evidence for a new concept from three independent prospective studies.
Heart (British Cardiac Society) 2011 Jan 97 (2): 143-50. Pons Douwe, Trompet Stella, de Craen Anton J M, Thijssen Peter E, Quax Paul H A, de Vries Margreet R, Wierda Rutger J, van den Elsen Peter J, Monraats Pascalle S, Ewing Mark M, Heijmans Bastiaan T, Slagboom P Eline, Zwinderman Aeilko H, Doevendans Pieter A F M, Tio René A, de Winter Robbert J, de Maat Moniek P M, Iakoubova Olga A, Sattar Naveed, Shepherd Jim, Westendorp Rudi G J, Jukema J Wouter, , , |
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Evaluation of 64 candidate single nucleotide polymorphisms as risk factors for neural tube defects in a large Irish study population.
American journal of medical genetics. Part A 2010 Dec . Carter TC, Pangilinan F, Troendle JF, Molloy AM, Vandermeer J, Mitchell A, Kirke PN, Conley MR, Shane B, Scott JM, Brody LC, Mills JL |
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A functional polymorphism in the reduced folate carrier gene and DNA hypomethylation in mothers of children with autism.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2010 Sep 153B (6): 1209-20. James S Jill, Melnyk Stepan, Jernigan Stefanie, Pavliv Oleksandra, Trusty Timothy, Lehman Sara, Seidel Lisa, Gaylor David W, Cleves Mario |
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Association of histone deacetylase genes with schizophrenia in Korean population.
Psychiatry research 2010 Jul 178 (2): 266-9. Kim Tae, Park Jin Kyung, Kim Hak-Jae, Chung Joo-Ho, Kim Jong W |
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Influence of IL1B polymorphism on CpG island hypermethylation in Helicobacter pylori-infected gastric cancer.
Virchows Archiv : an international journal of pathology 2010 Jun 456 (6): 647-52. Yoo Eun Joo, Park Seog-Yun, Cho Nam-Yun, Kim Nayoung, Lee Hye Seung, Kim Donguk, Kang Gyeong Ho |
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Human intelligence and polymorphisms in the DNA methyltransferase genes involved in epigenetic marking.
PloS one 2010 5 (6): e11329. Haggarty Paul, Hoad Gwen, Harris Sarah E, Starr John M, Fox Helen C, Deary Ian J, Whalley Lawrence |
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Single nucleotide polymorphism in the methyl-CpG binding domain 4 gene and the risk for immune thrombocytopenic purpura in Chinese population.
Platelets 2010 21 (2): 132-6. Zhao Haifeng, Du Weiting, Wang Donghai, Gu Dongsheng, Xue Feng, Ge Jing, Sui Tao, Yang Renc |
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Genetic diagnosis strategy of hereditary non-polyposis colorectal cancer.
World journal of gastroenterology : WJG 2009 Feb 15 (8): 983-9. Sheng Jian-Qiu, Zhang Hong, Ji Min, Fu Lei, Mu Hong, Zhang Ming-Zhi, Huang Ji-Sheng, Han Min, Li Ai-Qin, Wei Zhi, Sun Zi-Qin, Wu Zi-Tao, Xia Chang-Hong, Li Shi-Ro |
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Epigenetics in multiple sclerosis susceptibility: difference in transgenerational risk localizes to the major histocompatibility complex.
Human molecular genetics 2009 Jan 18 (2): 261-6. Chao Michael J, Ramagopalan Sreeram V, Herrera Blanca M, Lincoln Matthew R, Dyment David A, Sadovnick A Dessa, Ebers George |
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DNMT3B 579G>T promoter polymorphism and the risk for idiopathic thrombocytopenic purpura in a Chinese population.
Acta haematologica 2009 122 (1): 31-5. Zhao Haifeng, Du Weiting, Gu Dongsheng, Wang Donghai, Xue Feng, Ge Jing, Sui Tao, Yang Renc |
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Folic acid use in pregnancy and embryo selection.
BJOG : an international journal of obstetrics and gynaecology 2008 Jun 115 (7): 851-6. Haggarty P, Campbell D M, Duthie S, Andrews K, Hoad G, Piyathilake C, Fraser I, McNeill |
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Effect of B vitamins and genetics on success of in-vitro fertilisation: prospective cohort study.
Lancet (London, England) 2006 May 367 (9521): 1513-9. Haggarty P, McCallum H, McBain H, Andrews K, Duthie S, McNeill G, Templeton A, Haites N, Campbell D, Bhattacharya |
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Mutations and sequence variants in GDF9 and BMP15 in patients with premature ovarian failure.
European journal of endocrinology / European Federation of Endocrine Societies 2006 May 154 (5): 739-44. Laissue Paul, Christin-Maitre Sophie, Touraine Philippe, Kuttenn Frederique, Ritvos Olli, Aittomaki Kristiina, Bourcigaux Nathalie, Jacquesson Laetitia, Bouchard Philippe, Frydman Rene, Dewailly Didier, Reyss Anne-Céline, Jeffery Luke, Bachelot Anne, Massin Nathalie, Fellous Marc, Veitia Reiner |
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Germ-line variants in methyl-group metabolism genes and susceptibility to DNA methylation in normal tissues and human primary tumors.
Cancer research 2002 Aug 62 (15): 4519-24. Paz Maria F, Avila Sonia, Fraga Mario F, Pollan Marina, Capella Gabriel, Peinado Miquel Angel, Sanchez-Cespedes Montserrat, Herman James G, Esteller Man |
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The study of the rs9939609 FTO gene polymorphism in association with obesity and the management of obesity in a Romanian cohort.
Journal of medicine and life 0 8 (2): 232-8. Ursu R I, Badiu C, Cucu N, Ursu G F, Craciunescu I, Severin |
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