Human Genome Epidemiology Literature Finder
Records 1 - 7 (of 7 Records) |
Query Trace: DNAH10[original query] |
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Forty-three loci associated with plasma lipoprotein size, concentration, and cholesterol content in genome-wide analysis.
PLoS genetics 2009 Nov 5 (11): e1000730. Chasman Daniel I, Paré Guillaume, Mora Samia, Hopewell Jemma C, Peloso Gina, Clarke Robert, Cupples L Adrienne, Hamsten Anders, Kathiresan Sekar, Mälarstig Anders, Ordovas José M, Ripatti Samuli, Parker Alex N, Miletich Joseph P, Ridker Paul |
Identification of four novel genes contributing to familial elevated plasma HDL cholesterol in humans. Journal of lipid research 2014 Jun 55 (8): 1693-1701. Singaraja Roshni R, Tietjen Ian, Hovingh G Kees, Franchini Patrick L, Radomski Chris, Wong Kenny, vanHeek Margaret, Stylianou Ioannis M, Lin Linus, Wang Liangsu, Mitnaul Lyndon, Hubbard Brian, Winther Michael, Mattice Maryanne, Legendre Annick, Sherrington Robin, Kastelein John J, Akinsanya Karen, Plump Andrew, Hayden Michael |
Protein-coding variants implicate novel genes related to lipid homeostasis contributing to body-fat distribution.
Nature genetics 2019 03 51 (3): 452-469. Justice Anne E, Karaderi Tugce, Highland Heather M, Young Kristin L, Graff Mariaelisa, Lu Yingchang, Turcot Valérie, Auer Paul L, Fine Rebecca S, Guo Xiuqing, Schurmann Claudia, Lempradl Adelheid, Marouli Eirini, Mahajan Anubha, Winkler Thomas W, Locke Adam E, Medina-Gomez Carolina, Esko Tõnu, Vedantam Sailaja, Giri Ayush, Lo Ken Sin, Alfred Tamuno, Mudgal Poorva, Ng Maggie C Y, Heard-Costa Nancy L, Feitosa Mary F, Manning Alisa K, Willems Sara M, Sivapalaratnam Suthesh, Abecasis Goncalo, Alam Dewan S, Allison Matthew, Amouyel Philippe, Arzumanyan Zorayr, Balkau Beverley, Bastarache Lisa, Bergmann Sven, Bielak Lawrence F, Blüher Matthias, Boehnke Michael, Boeing Heiner, Boerwinkle Eric, Böger Carsten A, Bork-Jensen Jette, Bottinger Erwin P, Bowden Donald W, Brandslund Ivan, Broer Linda, Burt Amber A, Butterworth Adam S, Caulfield Mark J, Cesana Giancarlo, Chambers John C, Chasman Daniel I, Chen Yii-Der Ida, Chowdhury Rajiv, Christensen Cramer, Chu Audrey Y, Collins Francis S, Cook James P, Cox Amanda J, Crosslin David S, Danesh John, de Bakker Paul I W, Denus Simon de, Mutsert Renée de, Dedoussis George, Demerath Ellen W, Dennis Joe G, Denny Josh C, Di Angelantonio Emanuele, Dörr Marcus, Drenos Fotios, Dubé Marie-Pierre, Dunning Alison M, Easton Douglas F, Elliott Paul, Evangelou Evangelos, Farmaki Aliki-Eleni, Feng Shuang, Ferrannini Ele, Ferrieres Jean, Florez Jose C, Fornage Myriam, Fox Caroline S, Franks Paul W, Friedrich Nele, Gan Wei, Gandin Ilaria, Gasparini Paolo, Giedraitis Vilmantas, Girotto Giorgia, Gorski Mathias, Grallert Harald, Grarup Niels, Grove Megan L, Gustafsson Stefan, Haessler Jeff, Hansen Torben, Hattersley Andrew T, Hayward Caroline, Heid Iris M, Holmen Oddgeir L, Hovingh G Kees, Howson Joanna M M, Hu Yao, Hung Yi-Jen, Hveem Kristian, Ikram M Arfan, Ingelsson Erik, Jackson Anne U, Jarvik Gail P, Jia Yucheng, Jørgensen Torben, Jousilahti Pekka, Justesen Johanne M, Kahali Bratati, Karaleftheri Maria, Kardia Sharon L R, Karpe Fredrik, Kee Frank, Kitajima Hidetoshi, Komulainen Pirjo, Kooner Jaspal S, Kovacs Peter, Krämer Bernhard K, Kuulasmaa Kari, Kuusisto Johanna, Laakso Markku, Lakka Timo A, Lamparter David, Lange Leslie A, Langenberg Claudia, Larson Eric B, Lee Nanette R, Lee Wen-Jane, Lehtimäki Terho, Lewis Cora E, Li Huaixing, Li Jin, Li-Gao Ruifang, Lin Li-An, Lin Xu, Lind Lars, Lindström Jaana, Linneberg Allan, Liu Ching-Ti, Liu Dajiang J, Luan Jian'an, Lyytikäinen Leo-Pekka, MacGregor Stuart, Mägi Reedik, Männistö Satu, Marenne Gaëlle, Marten Jonathan, Masca Nicholas G D, McCarthy Mark I, Meidtner Karina, Mihailov Evelin, Moilanen Leena, Moitry Marie, Mook-Kanamori Dennis O, Morgan Anna, Morris Andrew P, Müller-Nurasyid Martina, Munroe Patricia B, Narisu Narisu, Nelson Christopher P, Neville Matt, Ntalla Ioanna, O'Connell Jeffrey R, Owen Katharine R, Pedersen Oluf, Peloso Gina M, Pennell Craig E, Perola Markus, Perry James A, Perry John R B, Pers Tune H, Ewing Ailith, Polasek Ozren, Raitakari Olli T, Rasheed Asif, Raulerson Chelsea K, Rauramaa Rainer, Reilly Dermot F, Reiner Alex P, Ridker Paul M, Rivas Manuel A, Robertson Neil R, Robino Antonietta, Rudan Igor, Ruth Katherine S, Saleheen Danish, Salomaa Veikko, Samani Nilesh J, Schreiner Pamela J, Schulze Matthias B, Scott Robert A, Segura-Lepe Marcelo, Sim Xueling, Slater Andrew J, Small Kerrin S, Smith Blair H, Smith Jennifer A, Southam Lorraine, Spector Timothy D, Speliotes Elizabeth K, Stefansson Kari, Steinthorsdottir Valgerdur, Stirrups Kathleen E, Strauch Konstantin, Stringham Heather M, Stumvoll Michael, Sun Liang, Surendran Praveen, Swart Karin M A, Tardif Jean-Claude, Taylor Kent D, Teumer Alexander, Thompson Deborah J, Thorleifsson Gudmar, Thorsteinsdottir Unnur, Thuesen Betina H, Tönjes Anke, Torres Mina, Tsafantakis Emmanouil, Tuomilehto Jaakko, Uitterlinden André G, Uusitupa Matti, van Duijn Cornelia M, Vanhala Mauno, Varma Rohit, Vermeulen Sita H, Vestergaard Henrik, Vitart Veronique, Vogt Thomas F, Vuckovic Dragana, Wagenknecht Lynne E, Walker Mark, Wallentin Lars, Wang Feijie, Wang Carol A, Wang Shuai, Wareham Nicholas J, Warren Helen R, Waterworth Dawn M, Wessel Jennifer, White Harvey D, Willer Cristen J, Wilson James G, Wood Andrew R, Wu Ying, Yaghootkar Hanieh, Yao Jie, Yerges-Armstrong Laura M, Young Robin, Zeggini Eleftheria, Zhan Xiaowei, Zhang Weihua, Zhao Jing Hua, Zhao Wei, Zheng He, Zhou Wei, Zillikens M Carola, Rivadeneira Fernando, Borecki Ingrid B, Pospisilik J Andrew, Deloukas Panos, Frayling Timothy M, Lettre Guillaume, Mohlke Karen L, Rotter Jerome I, Kutalik Zoltán, Hirschhorn Joel N, Cupples L Adrienne, Loos Ruth J F, North Kari E, Lindgren Cecilia M, , , , , , , , , , |
Bi-allelic mutations of DNAH10 cause primary male infertility with asthenoteratozoospermia in humans and mice. American journal of human genetics 2021 Jun . Tu Chaofeng, Cong Jiangshan, Zhang Qianjun, He Xiaojin, Zheng Rui, Yang Xiaoxuan, Gao Yang, Wu Huan, Lv Mingrong, Gu Yayun, Lu Shuai, Liu Chunyu, Tian Shixiong, Meng Lanlan, Wang Weili, Tan Chen, Nie Hongchuan, Li Dongyan, Zhang Huan, Gong Fei, Hu Liang, Lu Guangxiu, Xu Wenming, Lin Ge, Zhang Feng, Cao Yunxia, Tan Yue-Q |
Genome-wide discovery of genetic loci that uncouple excess adiposity from its comorbidities.
Nature metabolism 2021 02 3 (2): 228-243. Huang Lam O, Rauch Alexander, Mazzaferro Eugenia, Preuss Michael, Carobbio Stefania, Bayrak Cigdem S, Chami Nathalie, Wang Zhe, Schick Ursula M, Yang Nancy, Itan Yuval, Vidal-Puig Antonio, den Hoed Marcel, Mandrup Susanne, Kilpeläinen Tuomas O, Loos Ruth J |
FUS-P525L Juvenile Amyotrophic Lateral Sclerosis and Intellectual Disability: Evidence for Association and Oligogenic Inheritance. Neurology. Genetics 2022 7 8 (4): e200009. Goldstein Orly, Inbar Talya, Kedmi Merav, Gana-Weisz Mali, Abramovich Beatrice, Orr-Urtreger Avi, Drory Vivian |
A general framework for identifying oligogenic combinations of rare variants in complex disorders. Genome research 2022 3 32 (5): 904-915. Pounraja Vijay Kumar, Girirajan Santho |
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