HuGE Literature Finder
Records 1-6
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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 |
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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 |
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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 |
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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 |
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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 |
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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 |
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- Page last updated:Apr 15, 2021
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