Human Genome Epidemiology Literature Finder
Records 1 - 16 (of 16 Records) |
Query Trace: SLC30A10[original query] |
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Association studies of novel obesity-related gene variants with quantitative metabolic phenotypes in a population-based sample of 6,039 Danish individuals. Diabetologia 2012 Jan 55 (1): 105-13. Burgdorf K S, Gjesing A P, Grarup N, Justesen J M, Sandholt C H, Witte D R, Jørgensen T, Madsbad S, Hansen T, Pedersen |
Genetic variants on chromosome 1q41 influence ocular axial length and high myopia.
![]() PLoS genetics 2012 8 (6): e1002753. Fan Qiao, Barathi Veluchamy A, Cheng Ching-Yu, Zhou Xin, Meguro Akira, Nakata Isao, Khor Chiea-Chuen, Goh Liang-Kee, Li Yi-Ju, Lim Wan'e, Ho Candice E H, Hawthorne Felicia, Zheng Yingfeng, Chua Daniel, Inoko Hidetoshi, Yamashiro Kenji, Ohno-Matsui Kyoko, Matsuo Keitaro, Matsuda Fumihiko, Vithana Eranga, Seielstad Mark, Mizuki Nobuhisa, Beuerman Roger W, Tai E-Shyong, Yoshimura Nagahisa, Aung Tin, Young Terri L, Wong Tien-Yin, Teo Yik-Ying, Saw Seang-M |
Sex-stratified genome-wide association studies including 270,000 individuals show sexual dimorphism in genetic loci for anthropometric traits.
![]() PLoS genetics 2013 Jun 9 (6): e1003500. Randall Joshua C, Winkler Thomas W, Kutalik Zoltán, Berndt Sonja I, Jackson Anne U, Monda Keri L, Kilpeläinen Tuomas O, Esko Tõnu, Mägi Reedik, Li Shengxu, Workalemahu Tsegaselassie, Feitosa Mary F, Croteau-Chonka Damien C, Day Felix R, Fall Tove, Ferreira Teresa, Gustafsson Stefan, Locke Adam E, Mathieson Iain, Scherag Andre, Vedantam Sailaja, Wood Andrew R, Liang Liming, Steinthorsdottir Valgerdur, Thorleifsson Gudmar, Dermitzakis Emmanouil T, Dimas Antigone S, Karpe Fredrik, Min Josine L, Nicholson George, Clegg Deborah J, Person Thomas, Krohn Jon P, Bauer Sabrina, Buechler Christa, Eisinger Kristina, , Bonnefond Amélie, Froguel Philippe, , Hottenga Jouke-Jan, Prokopenko Inga, Waite Lindsay L, Harris Tamara B, Smith Albert Vernon, Shuldiner Alan R, McArdle Wendy L, Caulfield Mark J, Munroe Patricia B, Grönberg Henrik, Chen Yii-Der Ida, Li Guo, Beckmann Jacques S, Johnson Toby, Thorsteinsdottir Unnur, Teder-Laving Maris, Khaw Kay-Tee, Wareham Nicholas J, Zhao Jing Hua, Amin Najaf, Oostra Ben A, Kraja Aldi T, Province Michael A, Cupples L Adrienne, Heard-Costa Nancy L, Kaprio Jaakko, Ripatti Samuli, Surakka Ida, Collins Francis S, Saramies Jouko, Tuomilehto Jaakko, Jula Antti, Salomaa Veikko, Erdmann Jeanette, Hengstenberg Christian, Loley Christina, Schunkert Heribert, Lamina Claudia, Wichmann H Erich, Albrecht Eva, Gieger Christian, Hicks Andrew A, Johansson Asa, Pramstaller Peter P, Kathiresan Sekar, Speliotes Elizabeth K, Penninx Brenda, Hartikainen Anna-Liisa, Jarvelin Marjo-Riitta, Gyllensten Ulf, Boomsma Dorret I, Campbell Harry, Wilson James F, Chanock Stephen J, Farrall Martin, Goel Anuj, Medina-Gomez Carolina, Rivadeneira Fernando, Estrada Karol, Uitterlinden André G, Hofman Albert, Zillikens M Carola, den Heijer Martin, Kiemeney Lambertus A, Maschio Andrea, Hall Per, Tyrer Jonathan, Teumer Alexander, Völzke Henry, Kovacs Peter, Tönjes Anke, Mangino Massimo, Spector Tim D, Hayward Caroline, Rudan Igor, Hall Alistair S, Samani Nilesh J, Attwood Antony Paul, Sambrook Jennifer G, Hung Joseph, Palmer Lyle J, Lokki Marja-Liisa, Sinisalo Juha, Boucher Gabrielle, Huikuri Heikki, Lorentzon Mattias, Ohlsson Claes, Eklund Niina, Eriksson Johan G, Barlassina Cristina, Rivolta Carlo, Nolte Ilja M, Snieder Harold, Van der Klauw Melanie M, Van Vliet-Ostaptchouk Jana V, Gejman Pablo V, Shi Jianxin, Jacobs Kevin B, Wang Zhaoming, Bakker Stephan J L, Mateo Leach Irene, Navis Gerjan, van der Harst Pim, Martin Nicholas G, Medland Sarah E, Montgomery Grant W, Yang Jian, Chasman Daniel I, Ridker Paul M, Rose Lynda M, Lehtimäki Terho, Raitakari Olli, Absher Devin, Iribarren Carlos, Basart Hanneke, Hovingh Kees G, Hyppönen Elina, Power Chris, Anderson Denise, Beilby John P, Hui Jennie, Jolley Jennifer, Sager Hendrik, Bornstein Stefan R, Schwarz Peter E H, Kristiansson Kati, Perola Markus, Lindström Jaana, Swift Amy J, Uusitupa Matti, Atalay Mustafa, Lakka Timo A, Rauramaa Rainer, Bolton Jennifer L, Fowkes Gerry, Fraser Ross M, Price Jackie F, Fischer Krista, Krjutå Kov Kaarel, Metspalu Andres, Mihailov Evelin, Langenberg Claudia, Luan Jian'an, Ong Ken K, Chines Peter S, Keinanen-Kiukaanniemi Sirkka M, Saaristo Timo E, Edkins Sarah, Franks Paul W, Hallmans Göran, Shungin Dmitry, Morris Andrew David, Palmer Colin N A, Erbel Raimund, Moebus Susanne, Nöthen Markus M, Pechlivanis Sonali, Hveem Kristian, Narisu Narisu, Hamsten Anders, Humphries Steve E, Strawbridge Rona J, Tremoli Elena, Grallert Harald, Thorand Barbara, Illig Thomas, Koenig Wolfgang, Müller-Nurasyid Martina, Peters Annette, Boehm Bernhard O, Kleber Marcus E, März Winfried, Winkelmann Bernhard R, Kuusisto Johanna, Laakso Markku, Arveiler Dominique, Cesana Giancarlo, Kuulasmaa Kari, Virtamo Jarmo, Yarnell John W G, Kuh Diana, Wong Andrew, Lind Lars, de Faire Ulf, Gigante Bruna, Magnusson Patrik K E, Pedersen Nancy L, Dedoussis George, Dimitriou Maria, Kolovou Genovefa, Kanoni Stavroula, Stirrups Kathleen, Bonnycastle Lori L, Njølstad Inger, Wilsgaard Tom, Ganna Andrea, Rehnberg Emil, Hingorani Aroon, Kivimaki Mika, Kumari Meena, Assimes Themistocles L, Barroso Inês, Boehnke Michael, Borecki Ingrid B, Deloukas Panos, Fox Caroline S, Frayling Timothy, Groop Leif C, Haritunians Talin, Hunter David, Ingelsson Erik, Kaplan Robert, Mohlke Karen L, O'Connell Jeffrey R, Schlessinger David, Strachan David P, Stefansson Kari, van Duijn Cornelia M, Abecasis Gonçalo R, McCarthy Mark I, Hirschhorn Joel N, Qi Lu, Loos Ruth J F, Lindgren Cecilia M, North Kari E, Heid Iris |
Genome-wide association study of toxic metals and trace elements reveals novel associations.
![]() Human molecular genetics 2015 Aug 24 (16): 4739-45. Ng Esther, Lind P Monica, Lindgren Cecilia, Ingelsson Erik, Mahajan Anubha, Morris Andrew, Lind La |
Common Polymorphisms in the Solute Carrier SLC30A10 are Associated With Blood Manganese and Neurological Function. Toxicological sciences : an official journal of the Society of Toxicology 2015 Dec . Wahlberg Karin, Kippler Maria, Alhamdow Ayman, Rahman Syed Moshfiqur, Smith Donald R, Vahter Marie, Lucchini Roberto, Broberg Kar |
Polymorphisms in manganese transporters show developmental stage and sex specific associations with manganese concentrations in primary teeth. Neurotoxicology 2017 Sep . Wahlberg Karin, Arora Manish, Curtin Austen, Curtin Paul, Wright Robert O, Smith Donald R, Lucchini Roberto G, Broberg Karin, Austin Christi |
Sexual Dimorphism of a Genetic Risk Score for Obesity and Related Traits among Chinese Patients with Type 2 Diabetes. Obesity facts 2019 Jun 12 (3): 328-343. Kong Xiaomu, Xing Xiaoyan, Zhang Xuelian, Hong Jing, Yang Wenyi |
Manganese transporter genetics and sex modify the association between environmental manganese exposure and neurobehavioral outcomes in children. Environment international 2019 6 130 104908. Broberg Karin, Taj Tahir, Guazzetti Stefano, Peli Marco, Cagna Giuseppa, Pineda Daniela, Placidi Donatella, Wright Robert O, Smith Donald R, Lucchini Roberto G, Wahlberg Kar |
Polymorphisms in Manganese Transporters SLC30A10 and SLC39A8 Are Associated With Children's Neurodevelopment by Influencing Manganese Homeostasis. Frontiers in genetics 2019 1 9 664. Wahlberg Karin E, Guazzetti Stefano, Pineda Daniela, Larsson Susanna C, Fedrighi Chiara, Cagna Giuseppa, Zoni Silvia, Placidi Donatella, Wright Robert O, Smith Donald R, Lucchini Roberto G, Broberg Kar |
Genome-wide and Mendelian randomisation studies of liver MRI yield insights into the pathogenesis of steatohepatitis.
![]() Journal of hepatology 2020 Aug 73 (2): 241-251. Parisinos Constantinos A, Wilman Henry R, Thomas E Louise, Kelly Matt, Nicholls Rowan C, McGonigle John, Neubauer Stefan, Hingorani Aroon D, Patel Riyaz S, Hemingway Harry, Bell Jimmy D, Banerjee Rajarshi, Yaghootkar Hani |
GWAS of serum ALT and AST reveals an association of SLC30A10 Thr95Ile with hypermanganesemia symptoms.
![]() Nature communications 2021 7 12 (1): 4571. Ward Lucas D, Tu Ho-Chou, Quenneville Chelsea B, Tsour Shira, Flynn-Carroll Alexander O, Parker Margaret M, Deaton Aimee M, Haslett Patrick A J, Lotta Luca A, Verweij Niek, Ferreira Manuel A R, , , Baras Aris, Hinkle Gregory, Nioi Pa |
GWAS of allometric body-shape indices in UK Biobank identifies loci suggesting associations with morphogenesis, organogenesis, adrenal cell renewal and cancer.
![]() Scientific reports 2021 5 11 (1): 10688. Christakoudi Sofia, Evangelou Evangelos, Riboli Elio, Tsilidis Konstantinos |
Germline Mutations in CIDEB and Protection against Liver Disease. The New England journal of medicine 2022 8 387 (4): 332-344. Verweij Niek, Haas Mary E, Nielsen Jonas B, Sosina Olukayode A, Kim Minhee, Akbari Parsa, De Tanima, Hindy George, Bovijn Jonas, Persaud Trikaldarshi, Miloscio Lawrence, Germino Mary, Panagis Lampros, Watanabe Kyoko, Mbatchou Joelle, Jones Marcus, LeBlanc Michelle, Balasubramanian Suganthi, Lammert Craig, Enhörning Sofia, Melander Olle, Carey David J, Still Christopher D, Mirshahi Tooraj, Rader Daniel J, Parasoglou Prodromos, Walls Johnathon R, Overton John D, Reid Jeffrey G, Economides Aris, Cantor Michael N, Zambrowicz Brian, Murphy Andrew J, Abecasis Goncalo R, Ferreira Manuel A R, Smagris Eriks, Gusarova Viktoria, Sleeman Mark, Yancopoulos George D, Marchini Jonathan, Kang Hyun M, Karalis Katia, Shuldiner Alan R, Della Gatta Giusy, Locke Adam E, Baras Aris, Lotta Luca |
Association of SNPs in zinc transporter genes on seminal plasma zinc levels in humans. Biometals : an international journal on the role of metal ions in biology, biochemistry, and medicine 2022 7 35 (5): 955-965. Deng Peipei, Han Xiaoke, Ma Jing, Huang Xin, Sun Bo, Geng Yasong, Zheng Bo, Wang Shuso |
A rare genetic variant in the manganese transporter SLC30A10 and elevated liver enzymes in the general population. Hepatology international 2022 4 16 (3): 702-711. Seidelin Anne-Sofie, Nordestgaard Børge Grønne, Tybjærg-Hansen Anne, Yaghootkar Hanieh, Stender Stef |
Ancestry- and sex-specific effects underlying inguinal hernia susceptibility identified in a multiethnic genome-wide association study meta-analysis.
![]() Human molecular genetics 2022 1 31 (13): 2279-2293. Choquet Hélène, Li Weiyu, Yin Jie, Bradley Rachael, Hoffmann Thomas J, Nandakumar Priyanka, , Mostaedi Rouzbeh, Tian Chao, Ahituv Nadav, Jorgenson Er |
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