Human Genome Epidemiology Literature Finder
Records 1 - 14 (of 14 Records) |
Query Trace: EHMT1[original query] |
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Genetic variants in epigenetic genes and breast cancer risk. Carcinogenesis 2006 Aug 27 (8): 1661-9. Cebrian Arancha, Pharoah Paul D, Ahmed Shahana, Ropero Santiago, Fraga Mario F, Smith Paula L, Conroy Don, Luben Robert, Perkins Barbara, Easton Douglas F, Dunning Alison M, Esteller Manel, Ponder Bruce A |
Genetic variants of methyl metabolizing enzymes and epigenetic regulators: associations with promoter CpG island hypermethylation in colorectal cancer. Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 2009 Nov 18 (11): 3086-96. de Vogel Stefan, Wouters Kim A D, Gottschalk Ralph W H, van Schooten Frederik J, de Goeij Anton F P M, de Bruïne Adriaan P, Goldbohm Royle A, van den Brandt Piet A, Weijenberg Matty P, van Engeland Man |
De novo CNV analysis implicates specific abnormalities of postsynaptic signalling complexes in the pathogenesis of schizophrenia. Molecular psychiatry 2012 Feb 17 (2): 142-53. Kirov G, Pocklington A J, Holmans P, Ivanov D, Ikeda M, Ruderfer D, Moran J, Chambert K, Toncheva D, Georgieva L, Grozeva D, Fjodorova M, Wollerton R, Rees E, Nikolov I, van de Lagemaat L N, Bayés A, Fernandez E, Olason P I, Böttcher Y, Komiyama N H, Collins M O, Choudhary J, Stefansson K, Stefansson H, Grant S G N, Purcell S, Sklar P, O'Donovan M C, Owen M |
Exon resequencing of H3K9 methyltransferase complex genes, EHMT1, EHTM2 and WIZ, in Japanese autism subjects. Molecular autism 2014 5 (1): 49. Balan Shabeesh, Iwayama Yoshimi, Maekawa Motoko, Toyota Tomoko, Ohnishi Tetsuo, Toyoshima Manabu, Shimamoto Chie, Esaki Kayoko, Yamada Kazuo, Iwata Yasuhide, Suzuki Katsuaki, Ide Masayuki, Ota Motonori, Fukuchi Satoshi, Tsujii Masatsugu, Mori Norio, Shinkai Yoichi, Yoshikawa Tak |
De Novo and Rare Variants at Multiple Loci Support the Oligogenic Origins of Atrioventricular Septal Heart Defects. PLoS genetics 2016 Apr 12 (4): e1005963. Priest James R, Osoegawa Kazutoyo, Mohammed Nebil, Nanda Vivek, Kundu Ramendra, Schultz Kathleen, Lammer Edward J, Girirajan Santhosh, Scheetz Todd, Waggott Daryl, Haddad Francois, Reddy Sushma, Bernstein Daniel, Burns Trudy, Steimle Jeffrey D, Yang Xinan H, Moskowitz Ivan P, Hurles Matthew, Lifton Richard P, Nickerson Debbie, Bamshad Michael, Eichler Evan E, Mital Seema, Sheffield Val, Quertermous Thomas, Gelb Bruce D, Portman Michael, Ashley Euan |
CTCF-Mediated Chromatin Loops between Promoter and Gene Body Regulate Alternative Splicing across Individuals. Cell systems 2017 12 5 (6): 628-637.e6. Ruiz-Velasco Mariana, Kumar Manjeet, Lai Mang Ching, Bhat Pooja, Solis-Pinson Ana Belen, Reyes Alejandro, Kleinsorg Stefan, Noh Kyung-Min, Gibson Toby J, Zaugg Judith |
[Kleefstra syndrome 1 and ring chromosome 9 in a case]. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2019 8 36 (8): 837-840. Lyu Nan, Li Dongxiao, Li Jingjie, Shang Qing, Ma Caiy |
Comprehensive genetic analysis of 57 families with clinically suspected Cornelia de Lange syndrome. Journal of human genetics 2019 Jul . Aoi Hiromi, Mizuguchi Takeshi, Ceroni José Ricard, Kim Veronica Eun Hue, Furquim Isabel, Honjo Rachel S, Iwaki Takuma, Suzuki Toshifumi, Sekiguchi Futoshi, Uchiyama Yuri, Azuma Yoshiteru, Hamanaka Kohei, Koshimizu Eriko, Miyatake Satoko, Mitsuhashi Satomi, Takata Atsushi, Miyake Noriko, Takeda Satoru, Itakura Atsuo, Bertola Débora R, Kim Chong Ae, Matsumoto Naomic |
Excess of de novo variants in genes involved in chromatin remodelling in patients with marfanoid habitus and intellectual disability. Journal of medical genetics 2020 4 57 (7): 466-474. Chevarin Martin, Duffourd Yannis, A Barnard Rebecca, Moutton Sébastien, Lecoquierre François, Daoud Fatma, Kuentz Paul, Cabret Caroline, Thevenon Julien, Gautier Elodie, Callier Patrick, St-Onge Judith, Jouan Thibaud, Lacombe Didier, Delrue Marie Ange, Goizet Cyril, Morice-Picard Fanny, Van-Gils Julien, Munnich Arnold, Lyonnet Stanislas, Cormier-Daire Valérie, Baujat Geneviève, Holder Muriel, Petit Florence, Leheup Bruno, Odent Sylvie, Jouk Pierre-Simon, Lopez Gipsy, Geneviève David, Collignon Patrick, Martin-Coignard Dominique, Jacquette Aurélia, Perrin Laurence, Putoux Audrey, Sarrazin Elisabeth, Amarof Khadija, Missotte Isabelle, Coubes Christine, Jagadeesh Sujatha, Lapi Elisabetta, Demurger Florence, Goldenberg Alice, Doco-Fenzy Martine, Mignot Cyril, Héron Delphine, Jean-Marçais Nolwenn, Masurel Alice, El Chehadeh Salima, Marle Nathalie, Huet Frédéric, Binquet Christine, Collod-Beroud Gwenaëlle, Arnaud Pauline, Hanna Nadine, Boileau Catherine, Jondeau Guillaume, Olaso Robert, Lechner Doris, Poe Charlotte, Assoum Mirna, Carmignac Virginie, Duplomb Laurence, Tran Mau-Them Frédéric, Philippe Christophe, Vitobello Antonio, Bruel Ange-Line, Boland Anne, Deleuze Jean-François, Thauvin-Robinet Christel, Rivière Jean-Baptiste, O'Roak Brian J, Faivre Lauren |
Eight novel susceptibility loci and putative causal variants in atopic dermatitis.
The Journal of allergy and clinical immunology 2021 Jun . Tanaka Nao, Koido Masaru, Suzuki Akari, Otomo Nao, Suetsugu Hiroyuki, Kochi Yuta, Tomizuka Kouhei, Momozawa Yukihide, Kamatani Yoichiro, , Ikegawa Shiro, Yamamoto Kazuhiko, Terao Chikas |
[Genetic analysis of three patients with Kleefstra syndrome]. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2021 4 38 (4): 347-350. Gong Yuhong, Zhu Xiaoming, Li Wen, Dong Guizhen, Xu Biao, Zhao Hongli |
Genetic investigation of syndromic forms of obesity. International journal of obesity (2005) 2022 May . Carvalho Laura Machado Lara, D'Angelo Carla Sustek, Villela Darine, da Costa Silvia Souza, de Lima Jorge Alexander Augusto, da Silva Israel Tojal, de Oliveira Scliar Marília, Chaves Luiza Dias, Krepischi Ana Cristina Victorino, Koiffmann Celia Priszkulnik, Rosenberg Car |
Overlapping pathogenic de novo CNVs in neurodevelopmental disorders and congenital anomalies impacting constraint genes regulating early development. Human genetics 2022 11 . Safizadeh Shabestari Seyed Ali, Nassir Nasna, Sopariwala Samana, Karimov Islam, Tambi Richa, Zehra Binte, Kosaji Noor, Akter Hosneara, Berdiev Bakhrom K, Uddin Mohamm |
The role of the gut microbiota in patients with Kleefstra syndrome. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2023 1 . Bloemendaal Mirjam, Vlaming Priscilla, de Boer Anneke, Vermeulen-Kalk Karlijn, Bouman Arianne, Kleefstra Tjitske, Arias Vasquez Alejand |
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