Human Genome Epidemiology Literature Finder
Records 1 - 13 (of 13 Records) |
Query Trace: PDE3B[original query] |
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Analysis of the insulin-sensitive phosphodiesterase 3B gene in type 2 diabetes. Diabetes research and clinical practice 2001 Nov 54 (2): 79-88. Sano R, Miki T, Suzuki Y, Shimada F, Taira M, Kanatsuka A, Makino H, Hashimoto N, Saito |
The absence of evidence for major effects of the frequent SNP +299G>A in the resistin gene on susceptibility to insulin resistance syndrome associated with Japanese type 2 diabetes. Diabetes research and clinical practice 2003 Sep 61 (3): 191-8. Ochi Masaaki, Osawa Haruhiko, Onuma Hiroshi, Murakami Akiko, Nishimiya Tatsuya, Shimada Fumio, Kato Kenichi, Shimizu Ikki, Shishino Koji, Murase Mitsuharu, Fujii Yasuhisa, Ohashi Jun, Makino Hideic |
Systematic search for single nucleotide polymorphisms in the 5' flanking region of the human phosphodiesterase 3B gene: absence of evidence for major effects of identified polymorphisms on susceptibility to Japanese type 2 diabetes. Molecular genetics and metabolism 2003 May 79 (1): 43-51. Osawa Haruhiko, Niiya Toshiyuki, Onuma Hiroshi, Murakami Akiko, Ochi Masaaki, Nishimiya Tatsuya, Ogura Takahiro, Kato Kenichi, Shimizu Ikki, Fujii Yasuhisa, Ohashi Jun, Yamada Kazuya, Liang Shu-Jian, Manganiello Vincent C, Fujita-Yamaguchi Yoko, Makino Hideic |
Genome-wide association study of vitamin D levels in children: replication in the Western Australian Pregnancy Cohort (Raine) study.
Genes and immunity 2014 Dec 15 (8): 578-83. Anderson D, Holt B J, Pennell C E, Holt P G, Hart P H, Blackwell J |
Discovery and fine-mapping of adiposity loci using high density imputation of genome-wide association studies in individuals of African ancestry: African Ancestry Anthropometry Genetics Consortium.
PLoS genetics 2017 Apr 13 (4): e1006719. Ng Maggie C Y, Graff Mariaelisa, Lu Yingchang, Justice Anne E, Mudgal Poorva, Liu Ching-Ti, Young Kristin, Yanek Lisa R, Feitosa Mary F, Wojczynski Mary K, Rand Kristin, Brody Jennifer A, Cade Brian E, Dimitrov Latchezar, Duan Qing, Guo Xiuqing, Lange Leslie A, Nalls Michael A, Okut Hayrettin, Tajuddin Salman M, Tayo Bamidele O, Vedantam Sailaja, Bradfield Jonathan P, Chen Guanjie, Chen Wei-Min, Chesi Alessandra, Irvin Marguerite R, Padhukasahasram Badri, Smith Jennifer A, Zheng Wei, Allison Matthew A, Ambrosone Christine B, Bandera Elisa V, Bartz Traci M, Berndt Sonja I, Bernstein Leslie, Blot William J, Bottinger Erwin P, Carpten John, Chanock Stephen J, Chen Yii-Der Ida, Conti David V, Cooper Richard S, Fornage Myriam, Freedman Barry I, Garcia Melissa, Goodman Phyllis J, Hsu Yu-Han H, Hu Jennifer, Huff Chad D, Ingles Sue A, John Esther M, Kittles Rick, Klein Eric, Li Jin, McKnight Barbara, Nayak Uma, Nemesure Barbara, Ogunniyi Adesola, Olshan Andrew, Press Michael F, Rohde Rebecca, Rybicki Benjamin A, Salako Babatunde, Sanderson Maureen, Shao Yaming, Siscovick David S, Stanford Janet L, Stevens Victoria L, Stram Alex, Strom Sara S, Vaidya Dhananjay, Witte John S, Yao Jie, Zhu Xiaofeng, Ziegler Regina G, Zonderman Alan B, Adeyemo Adebowale, Ambs Stefan, Cushman Mary, Faul Jessica D, Hakonarson Hakon, Levin Albert M, Nathanson Katherine L, Ware Erin B, Weir David R, Zhao Wei, Zhi Degui, , Arnett Donna K, Grant Struan F A, Kardia Sharon L R, Oloapde Olufunmilayo I, Rao D C, Rotimi Charles N, Sale Michele M, Williams L Keoki, Zemel Babette S, Becker Diane M, Borecki Ingrid B, Evans Michele K, Harris Tamara B, Hirschhorn Joel N, Li Yun, Patel Sanjay R, Psaty Bruce M, Rotter Jerome I, Wilson James G, Bowden Donald W, Cupples L Adrienne, Haiman Christopher A, Loos Ruth J F, North Kari |
Analysis of predicted loss-of-function variants in UK Biobank identifies variants protective for disease. Nature communications 2018 4 9 (1): 1613. Emdin Connor A, Khera Amit V, Chaffin Mark, Klarin Derek, Natarajan Pradeep, Aragam Krishna, Haas Mary, Bick Alexander, Zekavat Seyedeh M, Nomura Akihiro, Ardissino Diego, Wilson James G, Schunkert Heribert, McPherson Ruth, Watkins Hugh, Elosua Roberto, Bown Matthew J, Samani Nilesh J, Baber Usman, Erdmann Jeanette, Gupta Namrata, Danesh John, Chasman Daniel, Ridker Paul, Denny Joshua, Bastarache Lisa, Lichtman Judith H, D'Onofrio Gail, Mattera Jennifer, Spertus John A, Sheu Wayne H-H, Taylor Kent D, Psaty Bruce M, Rich Stephen S, Post Wendy, Rotter Jerome I, Chen Yii-Der Ida, Krumholz Harlan, Saleheen Danish, Gabriel Stacey, Kathiresan Sek |
Investigation of genetic variation and lifestyle determinants in vitamin D levels in Arab individuals. Journal of translational medicine 2018 Jan 16 (1): 20. Mezzavilla Massimo, Tomei Sara, Alkayal Fadi, Melhem Motasem, Ali Maisa M, Al-Arouj Monira, Bennakhi Abdullah, Alsmadi Osama, Elkum Nas |
Genetics of blood lipids among ~300,000 multi-ethnic participants of the Million Veteran Program.
Nature genetics 2018 Oct . Klarin Derek, Damrauer Scott M, Cho Kelly, Sun Yan V, Teslovich Tanya M, Honerlaw Jacqueline, Gagnon David R, DuVall Scott L, Li Jin, Peloso Gina M, Chaffin Mark, Small Aeron M, Huang Jie, Tang Hua, Lynch Julie A, Ho Yuk-Lam, Liu Dajiang J, Emdin Connor A, Li Alexander H, Huffman Jennifer E, Lee Jennifer S, Natarajan Pradeep, Chowdhury Rajiv, Saleheen Danish, Vujkovic Marijana, Baras Aris, Pyarajan Saiju, Di Angelantonio Emanuele, Neale Benjamin M, Naheed Aliya, Khera Amit V, Danesh John, Chang Kyong-Mi, Abecasis Gonçalo, Willer Cristen, Dewey Frederick E, Carey David J, , , , , Concato John, Gaziano J Michael, O'Donnell Christopher J, Tsao Philip S, Kathiresan Sekar, Rader Daniel J, Wilson Peter W F, Assimes Themistocles |
Components of genetic associations across 2,138 phenotypes in the UK Biobank highlight adipocyte biology. Nature communications 2019 9 10 (1): 4064. Tanigawa Yosuke, Li Jiehan, Justesen Johanne M, Horn Heiko, Aguirre Matthew, DeBoever Christopher, Chang Chris, Narasimhan Balasubramanian, Lage Kasper, Hastie Trevor, Park Chong Y, Bejerano Gill, Ingelsson Erik, Rivas Manuel |
Rare and low-frequency exonic variants and gene-by-smoking interactions in pulmonary function. Scientific reports 2021 Sep 11 (1): 19365. Yang Tianzhong, Jackson Victoria E, Smith Albert V, Chen Han, Bartz Traci M, Sitlani Colleen M, Psaty Bruce M, Gharib Sina A, O'Connor George T, Dupuis Josée, Xu Jiayi, Lohman Kurt, Liu Yongmei, Kritchevsky Stephen B, Cassano Patricia A, Flexeder Claudia, Gieger Christian, Karrasch Stefan, Peters Annette, Schulz Holger, Harris Sarah E, Starr John M, Deary Ian J, Manichaikul Ani, Oelsner Elizabeth C, Barr R G, Taylor Kent D, Rich Stephen S, Bonten Tobias N, Mook-Kanamori Dennis O, Noordam Raymond, Li-Gao Ruifang, Jarvelin Marjo-Riitta, Wielscher Matthias, Terzikhan Natalie, Lahousse Lies, Brusselle Guy, Weiss Stefan, Ewert Ralf, Gläser Sven, Homuth Georg, Shrine Nick, Hall Ian P, Tobin Martin, London Stephanie J, Wei Peng, Morrison Alanna |
Unveiling Genetic Variants Underlying Vitamin D Deficiency in Multiple Korean Cohorts by a Genome-Wide Association Study.
Endocrinology and metabolism (Seoul, Korea) 2021 Dec . Kim Ye An, Yoon Ji Won, Lee Young, Choi Hyuk Jin, Yun Jae Won, Bae Eunsin, Kwon Seung-Hyun, Ahn So Eun, Do Ah-Ra, Jin Heejin, Won Sungho, Park Do Joon, Shin Chan Soo, Seo Je Hy |
Inherited basis of visceral, abdominal subcutaneous and gluteofemoral fat depots.
Nature communications 2022 7 13 (1): 3771. Agrawal Saaket, Wang Minxian, Klarqvist Marcus D R, Smith Kirk, Shin Joseph, Dashti Hesam, Diamant Nathaniel, Choi Seung Hoan, Jurgens Sean J, Ellinor Patrick T, Philippakis Anthony, Claussnitzer Melina, Ng Kenney, Udler Miriam S, Batra Puneet, Khera Amit |
Exome-wide sequencing study identified genetic variants associated with sarcopenic obesity. The journals of gerontology. Series A, Biological sciences and medical sciences 2024 1 . Qian Xu, Qi-Gang Zhao, Xin-Ling Ma, Shan-Shan Yan, Bai-Xue Han, Zi-Tong Song, Fan Bu, Kuan Li, Lei Zhang, Yu-Fang P |
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