Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 62 Records) |
Query Trace: Genomic medicine[original query] |
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A genome-wide association study identifies locus at 10q22 associated with clinical outcomes of adjuvant tamoxifen therapy for breast cancer patients in Japanese.
Human molecular genetics 2012 Apr 21 (7): 1665-72. Kiyotani Kazuma, Mushiroda Taisei, Tsunoda Tatsuhiko, Morizono Takashi, Hosono Naoya, Kubo Michiaki, Tanigawara Yusuke, Imamura Chiyo K, Flockhart David A, Aki Fuminori, Hirata Koichi, Takatsuka Yuichi, Okazaki Minoru, Ohsumi Shozo, Yamakawa Takashi, Sasa Mitsunori, Nakamura Yusuke, Zembutsu Hitos |
A genome-wide association study identifies common variants near LBX1 associated with adolescent idiopathic scoliosis.
Nature genetics 2011 Dec 43 (12): 1237-40. Takahashi Yohei, Kou Ikuyo, Takahashi Atsushi, Johnson Todd A, Kono Katsuki, Kawakami Noriaki, Uno Koki, Ito Manabu, Minami Shohei, Yanagida Haruhisa, Taneichi Hiroshi, Tsuji Taichi, Suzuki Teppei, Sudo Hideki, Kotani Toshiaki, Watanabe Kota, Chiba Kazuhiro, Hosono Naoya, Kamatani Naoyuki, Tsunoda Tatsuhiko, Toyama Yoshiaki, Kubo Michiaki, Matsumoto Morio, Ikegawa Shi |
Meta-analysis identifies multiple loci associated with kidney function-related traits in east Asian populations.
Nature genetics 2012 Aug 44 (8): 904-9. Okada Yukinori, Sim Xueling, Go Min Jin, Wu Jer-Yuarn, Gu Dongfeng, Takeuchi Fumihiko, Takahashi Atsushi, Maeda Shiro, Tsunoda Tatsuhiko, Chen Peng, Lim Su-Chi, Wong Tien-Yin, Liu Jianjun, Young Terri L, Aung Tin, Seielstad Mark, Teo Yik-Ying, Kim Young Jin, Lee Jong-Young, Han Bok-Ghee, Kang Daehee, Chen Chien-Hsiun, Tsai Fuu-Jen, Chang Li-Ching, Fann S-J Cathy, Mei Hao, Rao Dabeeru C, Hixson James E, Chen Shufeng, Katsuya Tomohiro, Isono Masato, Ogihara Toshio, Chambers John C, Zhang Weihua, Kooner Jaspal S, , , Albrecht Eva, , Yamamoto Kazuhiko, Kubo Michiaki, Nakamura Yusuke, Kamatani Naoyuki, Kato Norihiro, He Jiang, Chen Yuan-Tsong, Cho Yoon Shin, Tai E-Shyong, Tanaka Toshihi |
Genetic polymorphisms of the human PNPLA3 gene are strongly associated with severity of non-alcoholic fatty liver disease in Japanese.
PloS one 2012 7 (6): e38322. Kawaguchi Takahisa, Sumida Yoshio, Umemura Atsushi, Matsuo Keitaro, Takahashi Meiko, Takamura Toshinari, Yasui Kohichiroh, Saibara Toshiji, Hashimoto Etsuko, Kawanaka Miwa, Watanabe Sumio, Kawata Sumio, Imai Yasuharu, Kokubo Miki, Shima Toshihide, Park Hyohun, Tanaka Hideo, Tajima Kazuo, Yamada Ryo, Matsuda Fumihiko, , Japan Study Group of Nonalcoholic Fatty Liver Diseas |
A single-nucleotide polymorphism in ANK1 is associated with susceptibility to type 2 diabetes in Japanese populations.
Human molecular genetics 2012 Mar . Imamura M, Maeda S, Yamauchi T, Hara K, Yasuda K, Morizono T, Takahashi A, Horikoshi M, Nakamura M, Fujita H, Tsunoda T, Kubo M, Watada H, Maegawa H, Okada-Iwabu M, Iwabu M, Shojima N, Ohshige T, Omori S, Iwata M, Hirose H, Kaku K, Ito C, Tanaka Y, Tobe K, Kashiwagi A, Kawamori R, Kasuga M, Kamatani N, Nakamura Y, Kadowaki T |
Meta-analysis identifies nine new loci associated with rheumatoid arthritis in the Japanese population.
Nature genetics 2012 May 44 (5): 511-6. Okada Yukinori, Terao Chikashi, Ikari Katsunori, Kochi Yuta, Ohmura Koichiro, Suzuki Akari, Kawaguchi Takahisa, Stahl Eli A, Kurreeman Fina A S, Nishida Nao, Ohmiya Hiroko, Myouzen Keiko, Takahashi Meiko, Sawada Tetsuji, Nishioka Yuichi, Yukioka Masao, Matsubara Tsukasa, Wakitani Shigeyuki, Teshima Ryota, Tohma Shigeto, Takasugi Kiyoshi, Shimada Kota, Murasawa Akira, Honjo Shigeru, Matsuo Keitaro, Tanaka Hideo, Tajima Kazuo, Suzuki Taku, Iwamoto Takuji, Kawamura Yoshiya, Tanii Hisashi, Okazaki Yuji, Sasaki Tsukasa, Gregersen Peter K, Padyukov Leonid, Worthington Jane, Siminovitch Katherine A, Lathrop Mark, Taniguchi Atsuo, Takahashi Atsushi, Tokunaga Katsushi, Kubo Michiaki, Nakamura Yusuke, Kamatani Naoyuki, Mimori Tsuneyo, Plenge Robert M, Yamanaka Hisashi, Momohara Shigeki, Yamada Ryo, Matsuda Fumihiko, Yamamoto Kazuhi |
A genome-wide association study identifies three new risk loci for Kawasaki disease.
Nature genetics 2012 May 44 (5): 517-21. Onouchi Yoshihiro, Ozaki Kouichi, Burns Jane C, Shimizu Chisato, Terai Masaru, Hamada Hiromichi, Honda Takafumi, Suzuki Hiroyuki, Suenaga Tomohiro, Takeuchi Takashi, Yoshikawa Norishige, Suzuki Yoichi, Yasukawa Kumi, Ebata Ryota, Higashi Kouji, Saji Tsutomu, Kemmotsu Yasushi, Takatsuki Shinichi, Ouchi Kazunobu, Kishi Fumio, Yoshikawa Tetsushi, Nagai Toshiro, Hamamoto Kunihiro, Sato Yoshitake, Honda Akihito, Kobayashi Hironobu, Sato Junichi, Shibuta Shoichi, Miyawaki Masakazu, Oishi Ko, Yamaga Hironobu, Aoyagi Noriyuki, Iwahashi Seiji, Miyashita Ritsuko, Murata Yuji, Sasago Kumiko, Takahashi Atsushi, Kamatani Naoyuki, Kubo Michiaki, Tsunoda Tatsuhiko, Hata Akira, Nakamura Yusuke, Tanaka Toshihiro, , |
Common variants at CDKAL1 and KLF9 are associated with body mass index in east Asian populations.
Nature genetics 2012 Mar 44 (3): 302-6. Okada Yukinori, Kubo Michiaki, Ohmiya Hiroko, Takahashi Atsushi, Kumasaka Natsuhiko, Hosono Naoya, Maeda Shiro, Wen Wanqing, Dorajoo Rajkumar, Go Min Jin, Zheng Wei, Kato Norihiro, Wu Jer-Yuarn, Lu Qi, , Tsunoda Tatsuhiko, Yamamoto Kazuhiko, Nakamura Yusuke, Kamatani Naoyuki, Tanaka Toshihi |
A genome-wide association study identifies four genetic markers for hematological toxicities in cancer patients receiving gemcitabine therapy.
Pharmacogenetics and genomics 2012 Apr 22 (4): 229-35. Kiyotani Kazuma, Uno Satoko, Mushiroda Taisei, Takahashi Atsushi, Kubo Michiaki, Mitsuhata Naoki, Ina Shinomi, Kihara Chikashi, Kimura Yasutoshi, Yamaue Hiroki, Hirata Koichi, Nakamura Yusuke, Zembutsu Hitos |
A genome-wide association study identified AFF1 as a susceptibility locus for systemic lupus eyrthematosus in Japanese.
PLoS genetics 2012 Jan 8 (1): e1002455. Okada Yukinori, Shimane Kenichi, Kochi Yuta, Tahira Tomoko, Suzuki Akari, Higasa Koichiro, Takahashi Atsushi, Horita Tetsuya, Atsumi Tatsuya, Ishii Tomonori, Okamoto Akiko, Fujio Keishi, Hirakata Michito, Amano Hirofumi, Kondo Yuya, Ito Satoshi, Takada Kazuki, Mimori Akio, Saito Kazuyoshi, Kamachi Makoto, Kawaguchi Yasushi, Ikari Katsunori, Mohammed Osman Wael, Matsuda Koichi, Terao Chikashi, Ohmura Koichiro, Myouzen Keiko, Hosono Naoya, Tsunoda Tatsuhiko, Nishimoto Norihiro, Mimori Tsuneyo, Matsuda Fumihiko, Tanaka Yoshiya, Sumida Takayuki, Yamanaka Hisashi, Takasaki Yoshinari, Koike Takao, Horiuchi Takahiko, Hayashi Kenshi, Kubo Michiaki, Kamatani Naoyuki, Yamada Ryo, Nakamura Yusuke, Yamamoto Kazuhi |
A genome-wide association study identifies 2 susceptibility Loci for Crohn's disease in a Japanese population.
Gastroenterology 2012 Dec . Yamazaki K, Umeno J, Takahashi A, Hirano A, Johnson TA, Kumasaka N, Morizono T, Hosono N, Kawaguchi T, Takazoe M, Yamada T, Suzuki Y, Tanaka H, Motoya S, Hosokawa M, Arimura Y, Shinomura Y, Matsui T, Matsumoto T, Iida M, Tsunoda T, Nakamura Y, Kamatani N, Kubo M |
HLA-DQ strikes again: genome-wide association study further confirms HLA-DQ in the diagnosis of asthma among adults.
Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology 2012 Dec 42 (12): 12. Lasky-Su J, Himes BE, Raby BA, Klanderman BJ, Sylvia JS, Lange C, Melen E, Martinez FD, Israel E, Gauderman J, Gilliland F, Sleiman P, Hakonarson H, Celedón JC, Soto-Quiros M, Avila L, Lima JJ, Irvin CG, Peters SP, Boushey H, Chinchilli VM, Mauger D, Tantisira K, Weiss ST |
Whole-genome-wide association study in the Bulgarian population reveals HHAT as schizophrenia susceptibility gene.
Psychiatric genetics 2013 Feb 23 (1): 11-9. Betcheva Elitza T, Yosifova Adelina G, Mushiroda Taisei, Kubo Michiaki, Takahashi Atsushi, Karachanak Sena K, Zaharieva Irina T, Hadjidekova Savina P, Dimova Ivanka I, Vazharova Radoslava V, Stoyanov Drozdstoy S, Milanova Vihra K, Tolev Todor, Kirov George, Kamatani Naoyuki, Toncheva Draga I, Nakamura Yusu |
Genome-wide association study identifies eight new susceptibility loci for atopic dermatitis in the Japanese population.
Nature genetics 2012 Nov 44 (11): 1222-6. Hirota Tomomitsu, Takahashi Atsushi, Kubo Michiaki, Tsunoda Tatsuhiko, Tomita Kaori, Sakashita Masafumi, Yamada Takechiyo, Fujieda Shigeharu, Tanaka Shota, Doi Satoru, Miyatake Akihiko, Enomoto Tadao, Nishiyama Chiharu, Nakano Nobuhiro, Maeda Keiko, Okumura Ko, Ogawa Hideoki, Ikeda Shigaku, Noguchi Emiko, Sakamoto Tohru, Hizawa Nobuyuki, Ebe Koji, Saeki Hidehisa, Sasaki Takashi, Ebihara Tamotsu, Amagai Masayuki, Takeuchi Satoshi, Furue Masutaka, Nakamura Yusuke, Tamari Mayu |
Functional variants in NFKBIE and RTKN2 involved in activation of the NF-?B pathway are associated with rheumatoid arthritis in Japanese.
PLoS genetics 2012 Sep 8 (9): 9. Myouzen K, Kochi Y, Okada Y, Terao C, Suzuki A, Ikari K, Tsunoda T, Takahashi A, Kubo M, Taniguchi A, Matsuda F, Ohmura K, Momohara S, Mimori T, Yamanaka H, Kamatani N, Yamada R, Nakamura Y, Yamamoto K |
Haplotypes with copy number and single nucleotide polymorphisms in CYP2A6 locus are associated with smoking quantity in a Japanese population.
PloS one 2012 7 (9): e44507. Kumasaka Natsuhiko, Aoki Masayuki, Okada Yukinori, Takahashi Atsushi, Ozaki Kouichi, Mushiroda Taisei, Hirota Tomomitsu, Tamari Mayumi, Tanaka Toshihiro, Nakamura Yusuke, Kamatani Naoyuki, Kubo Michia |
Genome-wide association of implantable cardioverter-defibrillator activation with life-threatening arrhythmias.
PloS one 2012 7 (1): e25387. Murray Sarah S, Smith Erin N, Villarasa Nikki, Nahey Tara, Lande Jeff, Goldberg Harold, Shaw Marian, Rosenthal Lawrence, Ramza Brian, Alaeddini Jamshid, Han Xinqiang, Damani Samir, Soykan Orhan, Kowal Robert C, Topol Eric J, |
Genome-wide association study of chemotherapeutic agent-induced severe neutropenia/leucopenia for patients in Biobank Japan.
Cancer science 2013 Aug 104 (8): 1074-82. Low Siew-Kee, Chung Suyoun, Takahashi Atsushi, Zembutsu Hitoshi, Mushiroda Taisei, Kubo Michiaki, Nakamura Yusu |
A GWAS in uveal melanoma identifies risk polymorphisms in the CLPTM1L locus.
NPJ genomic medicine 2017 2 . Mobuchon Lenha, Battistella Aude, Bardel Claire, Scelo Ghislaine, Renoud Alexia, Houy Alexandre, Cassoux Nathalie, Milder Maud, Cancel-Tassin Géraldine, Cussenot Olivier, Delattre Olivier, Besse Céline, Boland Anne, Deleuze Jean-François, Cox David G, Stern Marc-Hen |
The eMERGE genotype set of 83,717 subjects imputed to ~40?million variants genome wide and association with the herpes zoster medical record phenotype.
Genetic epidemiology 2019 02 43 (1): 63-81. Stanaway Ian B, Hall Taryn O, Rosenthal Elisabeth A, Palmer Melody, Naranbhai Vivek, Knevel Rachel, Namjou-Khales Bahram, Carroll Robert J, Kiryluk Krzysztof, Gordon Adam S, Linder Jodell, Howell Kayla Marie, Mapes Brandy M, Lin Frederick T J, Joo Yoonjung Yoonie, Hayes M Geoffrey, Gharavi Ali G, Pendergrass Sarah A, Ritchie Marylyn D, de Andrade Mariza, Croteau-Chonka Damien C, Raychaudhuri Soumya, Weiss Scott T, Lebo Matt, Amr Sami S, Carrell David, Larson Eric B, Chute Christopher G, Rasmussen-Torvik Laura Jarmila, Roy-Puckelwartz Megan J, Sleiman Patrick, Hakonarson Hakon, Li Rongling, Karlson Elizabeth W, Peterson Josh F, Kullo Iftikhar J, Chisholm Rex, Denny Joshua Charles, Jarvik Gail P, , Crosslin David |
Genome-wide association study for proliferative diabetic retinopathy in Africans.
NPJ genomic medicine 2019 4 20. Liu Chang, Chen Guanjie, Bentley Amy R, Doumatey Ayo, Zhou Jie, Adeyemo Adebowale, Yang Jinkui, Rotimi Charl |
A genome-wide association and replication study of blood pressure in Ugandan early adolescents.
Molecular genetics & genomic medicine 2019 Aug e950. Lule Swaib A, Mentzer Alexander J, Namara Benigna, Muwenzi Allan G, Nassanga Beatrice, Kizito Dennison, Akurut Helen, Lubyayi Lawrence, Tumusiime Josephine, Zziwa Christopher, Akello Florence, Gurdasani Deept, Sandhu Manjinder, Smeeth Liam, Elliott Alison M, Webb Emily |
Genome-wide meta-analysis of SNP and antihypertensive medication interactions on left ventricular traits in African Americans.
Molecular genetics & genomic medicine 2019 Aug e788. Do Anh N, Zhao Wei, Baldridge Abigail S, Raffield Laura M, Wiggins Kerri L, Shah Sanjiv J, Aslibekyan Stella, Tiwari Hemant K, Limdi Nita, Zhi Degui, Sitlani Colleen M, Taylor Kent D, Psaty Bruce M, Sotoodehnia Nona, Brody Jennifer A, Rasmussen-Torvik Laura J, Lloyd-Jones Donald, Lange Leslie A, Wilson James G, Smith Jennifer A, Kardia Sharon L R, Mosley Thomas H, Vasan Ramachandran S, Arnett Donna K, Irvin Marguerite |
Both rare and common genetic variants contribute to autism in the Faroe Islands.
NPJ genomic medicine 2019 4 1. Leblond Claire S, Cliquet Freddy, Carton Coralie, Huguet Guillaume, Mathieu Alexandre, Kergrohen Thomas, Buratti Julien, Lemière Nathalie, Cuisset Laurence, Bienvenu Thierry, Boland Anne, Deleuze Jean-François, Stora Tormodur, Biskupstoe Rannva, Halling Jónrit, Andorsdóttir Guðrið, Billstedt Eva, Gillberg Christopher, Bourgeron Thom |
Genome-wide association study of café-au-lait macule number in neurofibromatosis type 1.
Molecular genetics & genomic medicine 2020 (10): e1400. Sung Heejong, Hyland Paula L, Pemov Alexander, Sabourin Jeremy A, Baldwin Andrea M, Bass Sara, Teshome Kedest, Luo Wen, , Widemann Brigitte C, Stewart Douglas R, Wilson Alexander |
The impact of adjusting for baseline in pharmacogenomic genome-wide association studies of quantitative change.
NPJ genomic medicine 2020 5 1. Oni-Orisan Akinyemi, Haldar Tanushree, Ranatunga Dilrini K, Medina Marisa W, Schaefer Catherine, Krauss Ronald M, Iribarren Carlos, Risch Neil, Hoffmann Thomas |
A UGT1A1 variant is associated with serum total bilirubin levels, which are causal for hypertension in African-ancestry individuals.
NPJ genomic medicine 2021 6 6 (1): 44. Chen Guanjie, Adeyemo Adebowale, Zhou Jie, Doumatey Ayo P, Bentley Amy R, Ekoru Kenneth, Shriner Daniel, Rotimi Charles |
Mapping of susceptible variants for cold medicine-related Stevens-Johnson syndrome by whole-genome resequencing.
NPJ genomic medicine 2021 2 6 (1): 9. Kawai Yosuke, Hitomi Yuki, Ueta Mayumi, Khor Seik-Soon, Nakatani Ken, Sotozono Chie, Kinoshita Shigeru, Nagasaki Masao, Tokunaga Katsus |
Heritability and genome-wide association study of blood pressure in Chinese adult twins.
Molecular genetics & genomic medicine 2021 9 9 (11): e1828. Chen Jiahao, Wang Weijing, Li Zhaoying, Xu Chunsheng, Tian Xiaocao, Zhang Dongfe |
A common variant in 11q23.3 associated with hyperlipidemia is mediated by the binding and regulation of GATA4.
NPJ genomic medicine 2022 Jan 7 (1): 4. Chou Wen-Cheng, Chen Wei-Ting, Shen Chen-Ya |
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