Human Genome Epidemiology Literature Finder
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Records 1 - 30 (of 33 Records) |
| Query Trace: Disease and MTNR1B[original query] |
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| Common genetic variation in the melatonin receptor 1B gene (MTNR1B) is associated with decreased early-phase insulin response. Diabetologia 2009 Aug 52 (8): 1537-42. Langenberg C, Pascoe L, Mari A, Tura A, Laakso M, Frayling T M, Barroso I, Loos R J F, Wareham N J, Walker M, |
| Genetic predisposition to long-term nondiabetic deteriorations in glucose homeostasis: Ten-year follow-up of the GLACIER study. Diabetes 2011 Jan 60 (1): 345-54. Renström Frida, Shungin Dmitry, Johansson Ingegerd, , Florez Jose C, Hallmans Göran, Hu Frank B, Franks Paul |
| Common genetic variation in MTNR1B is associated with serum testosterone, glucose tolerance, and insulin secretion in polycystic ovary syndrome patients. Fertility and sterility 2010 Nov 94 (6): 2486-9, 2489.e1-2. Wang Lei, Wang Ying, Zhang Xiaoping, Shi Juanzi, Wang Min, Wei Zhiyun, Zhao Aman, Li Baojie, Zhao Xinzhi, Xing Qinghe, He L |
| Association of disease-predisposition polymorphisms of the melatonin receptors and sunshine duration in the global human populations. Journal of pineal research 2010 Mar 48 (2): 133-41. Ji Lin-dan, Xu Jin, Wu Dong-dong, Xie Si-da, Tang Nelson L S, Zhang Ya-pi |
| Melatonin receptor 1 B polymorphisms associated with the risk of gestational diabetes mellitus. BMC medical genetics 2011 12 (1): 82. Kim Jason Y, Cheong Hyun Sub, Park Byung-Lae, Baik Sei Hyun, Park Sunmin, Lee Si Won, Kim Min-Hyoung, Chung Jin Hoon, Choi June Seek, Kim Moon-Young, Yang Jae-Hyug, Cho Dong-Hee, Shin Hyoung Doo, Kim Sung-Ho |
A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium.
Diabetes 2011 Apr 60 (4): 1329-39. Kraja Aldi T, Vaidya Dhananjay, Pankow James S, Goodarzi Mark O, Assimes Themistocles L, Kullo Iftikhar J, Sovio Ulla, Mathias Rasika A, Sun Yan V, Franceschini Nora, Absher Devin, Li Guo, Zhang Qunyuan, Feitosa Mary F, Glazer Nicole L, Haritunians Talin, Hartikainen Anna-Liisa, Knowles Joshua W, North Kari E, Iribarren Carlos, Kral Brian, Yanek Lisa, O'Reilly Paul F, McCarthy Mark I, Jaquish Cashell, Couper David J, Chakravarti Aravinda, Psaty Bruce M, Becker Lewis C, Province Michael A, Boerwinkle Eric, Quertermous Thomas, Palotie Leena, Jarvelin Marjo-Riitta, Becker Diane M, Kardia Sharon L R, Rotter Jerome I, Chen Yii-Der Ida, Borecki Ingrid |
| Association of six single nucleotide polymorphisms with gestational diabetes mellitus in a Chinese population. PloS one 2011 6 (11): e26953. Wang Ying, Nie Min, Li Wei, Ping Fan, Hu Yingying, Ma Liangkun, Gao Jinsong, Liu Junt |
| Variations with modest effects have an important role in the genetic background of type 2 diabetes and diabetes-related traits. Journal of human genetics 2012 Dec 57 (12): 776-9. Fujita Hayato, Hara Kazuo, Shojima Nobuhiro, Horikoshi Momoko, Iwata Minoru, Hirota Yushi, Tobe Kazuyuki, Seino Susumu, Kadowaki Takas |
| Melatonin pathway genes are associated with progressive subtypes and disability status in multiple sclerosis among Finnish patients. Journal of neuroimmunology 2012 Sep 250 (1-2): 106-10. Natarajan Renuka, Einarsdottir Elisabet, Riutta Asko, Hagman Sanna, Raunio Minna, Mononen Nina, Lehtimäki Terho, Elovaara Iri |
| Association of type 2 diabetes susceptibility loci with one-year weight loss in the look AHEAD clinical trial. Obesity (Silver Spring, Md.) 2012 Feb . Peter I, McCaffery JM, Kelley-Hedgepeth A, Hakonarson H, Reis S, Wagenknecht LE, Kopin AS, Huggins GS |
| Polymorphisms in genes involved in the free-radical process in patients with sudden sensorineural hearing loss and Ménière's disease. Free radical research 2013 Jul 47 (6-7): 498-506. Teranishi M, Uchida Y, Nishio N, Kato K, Otake H, Yoshida T, Suzuki H, Sone M, Sugiura S, Ando F, Shimokata H, Nakashima |
| Genetics of melatonin receptor type 2 is associated with left ventricular function in hypertensive patients treated according to guidelines. European journal of internal medicine 2013 Oct 24 (7): 650-5. Huber Matthias, Treszl Andras, Reibis Rona, Teichmann Christopher, Zergibel Irina, Bolbrinker Juliane, Scholze Jürgen, Wegscheider Karl, Völler Heinz, Kreutz Reinho |
| Impact of type 2 diabetes susceptibility variants on quantitative glycemic traits reveals mechanistic heterogeneity. Diabetes 2013 Dec . Dimas AS, Lagou V, Barker A, Knowles JW, Mägi R, Hivert MF, Benazzo A, Rybin D, Jackson AU, Stringham HM, Song C, Fischer-Rosinsky A, Boesgaard TW, Grarup N, Abbasi FA, Assimes TL, Hao K, Yang X, Lecoeur C, Barroso I, Bonnycastle LL, Böttcher Y, Bumpstead S, Chines PS, Erdos MR, Graessler J, Kovacs P, Morken MA, Narisu N, Payne F, Stancakova A, Swift AJ, Tönjes A, Bornstein SR, Cauchi S, Froguel P, Meyre D, Schwarz PE, Häring HU, Smith U, Boehnke M, Bergman RN, Collins FS, Mohlke KL, Tuomilehto J, Quertemous T, Lind L, Hansen T, Pedersen O, Walker M, Pfeiffer AF, Spranger J, Stumvoll M, Meigs JB, Wareham NJ, Kuusisto J, Laakso M, Langenberg C, Dupuis J, Watanabe RM, Florez JC, Ingelsson E, McCarthy MI, Prokopenko I |
| Association of common genetic variants with diabetes and metabolic syndrome related traits in the Arizona Insulin Resistance registry: a focus on Mexican American families in the Southwest. Human heredity 2014 78 (1): 47-58. DeMenna Jacob, Puppala Sobha, Chittoor Geetha, Schneider Jennifer, Kim Joon Young, Shaibi Gabriel Q, Mandarino Lawrence J, Duggirala Ravindranath, Coletta Dawn |
| Type 2 diabetes susceptibility gene variants predispose to adult-onset autoimmune diabetes. Diabetologia 2014 Sep 57 (9): 1859-68. Andersen Mette K, Sterner Maria, Forsén Tom, Käräjämäki Annemari, Rolandsson Olov, Forsblom Carol, Groop Per-Henrik, Lahti Kaj, Nilsson Peter M, Groop Leif, Tuomi Tiinamai |
| MTNR1B gene polymorphisms and susceptibility to Type 2 Diabetes: A pilot study in South Indians. Gene 2015 Jul 566 (2): 189-93. Salman Mohammed, Dasgupta Shruti, Cholendra A, Venugopal P N, Lakshmi G L, Xaviour D, Rao Jayashankar, D'Souza Cletus J |
| Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci. Nature genetics 2015 Nov . Gaulton Kyle J, Ferreira Teresa, Lee Yeji, Raimondo Anne, Mägi Reedik, Reschen Michael E, Mahajan Anubha, Locke Adam, William Rayner N, Robertson Neil, Scott Robert A, Prokopenko Inga, Scott Laura J, Green Todd, Sparso Thomas, Thuillier Dorothee, Yengo Loic, Grallert Harald, Wahl Simone, Frånberg Mattias, Strawbridge Rona J, Kestler Hans, Chheda Himanshu, Eisele Lewin, Gustafsson Stefan, Steinthorsdottir Valgerdur, Thorleifsson Gudmar, Qi Lu, Karssen Lennart C, van Leeuwen Elisabeth M, Willems Sara M, Li Man, Chen Han, Fuchsberger Christian, Kwan Phoenix, Ma Clement, Linderman Michael, Lu Yingchang, Thomsen Soren K, Rundle Jana K, Beer Nicola L, van de Bunt Martijn, Chalisey Anil, Kang Hyun Min, Voight Benjamin F, Abecasis Gonçalo R, Almgren Peter, Baldassarre Damiano, Balkau Beverley, Benediktsson Rafn, Blüher Matthias, Boeing Heiner, Bonnycastle Lori L, Bottinger Erwin P, Burtt Noël P, Carey Jason, Charpentier Guillaume, Chines Peter S, Cornelis Marilyn C, Couper David J, Crenshaw Andrew T, van Dam Rob M, Doney Alex S F, Dorkhan Mozhgan, Edkins Sarah, Eriksson Johan G, Esko Tonu, Eury Elodie, Fadista João, Flannick Jason, Fontanillas Pierre, Fox Caroline, Franks Paul W, Gertow Karl, Gieger Christian, Gigante Bruna, Gottesman Omri, Grant George B, Grarup Niels, Groves Christopher J, Hassinen Maija, Have Christian T, Herder Christian, Holmen Oddgeir L, Hreidarsson Astradur B, Humphries Steve E, Hunter David J, Jackson Anne U, Jonsson Anna, Jørgensen Marit E, Jørgensen Torben, Kao Wen-Hong L, Kerrison Nicola D, Kinnunen Leena, Klopp Norman, Kong Augustine, Kovacs Peter, Kraft Peter, Kravic Jasmina, Langford Cordelia, Leander Karin, Liang Liming, Lichtner Peter, Lindgren Cecilia M, Lindholm Eero, Linneberg Allan, Liu Ching-Ti, Lobbens Stéphane, Luan Jian'an, Lyssenko Valeriya, Männistö Satu, McLeod Olga, Meyer Julia, Mihailov Evelin, Mirza Ghazala, Mühleisen Thomas W, Müller-Nurasyid Martina, Navarro Carmen, Nöthen Markus M, Oskolkov Nikolay N, Owen Katharine R, Palli Domenico, Pechlivanis Sonali, Peltonen Leena, Perry John R B, Platou Carl G P, Roden Michael, Ruderfer Douglas, Rybin Denis, van der Schouw Yvonne T, Sennblad Bengt, Sigurðsson Gunnar, Stan?áková Alena, Steinbach Gerald, Storm Petter, Strauch Konstantin, Stringham Heather M, Sun Qi, Thorand Barbara, Tikkanen Emmi, Tonjes Anke, Trakalo Joseph, Tremoli Elena, Tuomi Tiinamaija, Wennauer Roman, Wiltshire Steven, Wood Andrew R, Zeggini Eleftheria, Dunham Ian, Birney Ewan, Pasquali Lorenzo, Ferrer Jorge, Loos Ruth J F, Dupuis Josée, Florez Jose C, Boerwinkle Eric, Pankow James S, van Duijn Cornelia, Sijbrands Eric, Meigs James B, Hu Frank B, Thorsteinsdottir Unnur, Stefansson Kari, Lakka Timo A, Rauramaa Rainer, Stumvoll Michael, Pedersen Nancy L, Lind Lars, Keinanen-Kiukaanniemi Sirkka M, Korpi-Hyövälti Eeva, Saaristo Timo E, Saltevo Juha, Kuusisto Johanna, Laakso Markku, Metspalu Andres, Erbel Raimund, Jöcke Karl-Heinz, Moebus Susanne, Ripatti Samuli, Salomaa Veikko, Ingelsson Erik, Boehm Bernhard O, Bergman Richard N, Collins Francis S, Mohlke Karen L, Koistinen Heikki, Tuomilehto Jaakko, Hveem Kristian, Njølstad Inger, Deloukas Panagiotis, Donnelly Peter J, Frayling Timothy M, Hattersley Andrew T, de Faire Ulf, Hamsten Anders, Illig Thomas, Peters Annette, Cauchi Stephane, Sladek Rob, Froguel Philippe, Hansen Torben, Pedersen Oluf, Morris Andrew D, Palmer Collin N A, Kathiresan Sekar, Melander Olle, Nilsson Peter M, Groop Leif C, Barroso Inês, Langenberg Claudia, Wareham Nicholas J, O'Callaghan Christopher A, Gloyn Anna L, Altshuler David, Boehnke Michael, Teslovich Tanya M, McCarthy Mark I, Morris Andrew P, |
| Associations of melatonin receptor gene polymorphisms with Graves' disease. PloS one 2017 12 (9): e0185529. Lin Jiunn-Diann, Yang Shun-Fa, Wang Yuan-Hung, Fang Wen-Fang, Lin Ying-Chin, Liou Bing-Chun, Lin Yuh-Feng, Tang Kam-Tsun, Cheng Chao-W |
| Analysis of MTNR1B gene polymorphisms in relationship with IRS2 gene variants, epicardial fat thickness, glucose homeostasis and cognitive performance in the elderly. Chronobiology international 2017 Jul 1-11. Mazzoccoli Gianluigi, Dagostino Mariangela Pia, Paroni Giulia, Seripa Davide, Ciccone Filomena, Addante Filomena, Favuzzi Giovanni, Grandone Elvira, Avola Roberto, Mazza Tommaso, Fusilli Caterina, Greco Antonio, De Cosmo Salvato |
| Association of melatonin membrane receptor 1A/1B gene polymorphisms with the occurrence and metastasis of hepatocellular carcinoma. Oncotarget 2017 Oct 8 (49): 85655-85669. Su Shih-Chi, Ho Yung-Chuan, Liu Yu-Fan, Reiter Russel J, Chou Chia-Hsuan, Yeh Chia-Ming, Lee Hsiang-Lin, Chung Wen-Hung, Hsieh Ming-Ju, Yang Shun- |
| The genetic overlap between mood disorders and cardiometabolic diseases: a systematic review of genome wide and candidate gene studies. Translational psychiatry 2017 Jan 7 (1): e1007. Amare A T, Schubert K O, Klingler-Hoffmann M, Cohen-Woods S, Baune B |
| Effects of variants of 50 genes on diabetes risk among the Chinese population born in the early 1960s. Journal of diabetes 2019 Mar . Song Chao, Wang Meng, Fang Hongyun, Gong Weiyan, Mao Deqian, Ding Caicui, Fu Qiqi, Feng Ganyu, Chen Zheng, Ma Yanning, Yao Yecheng, Liu Aili |
| Genome-wide by environment interaction studies of depressive symptoms and psychosocial stress in UK Biobank and Generation Scotland.
Translational psychiatry 2019 02 9 (1): 14. Arnau-Soler Aleix, Macdonald-Dunlop Erin, Adams Mark J, Clarke Toni-Kim, MacIntyre Donald J, Milburn Keith, Navrady Lauren, , , Hayward Caroline, McIntosh Andrew M, Thomson Pippa |
| MTNR1B genetic polymorphisms as risk factors for gestational diabetes mellitus: a case-control study in a single tertiary care center. Annals of Saudi medicine 0 39 (5): 309-318. Alharbi Khalid Khalaf, Al-Sulaiman Abdulrahman Mohammed, Shedaid Khalid Muath Bin, Al-Shangiti Ali M, Marie Mohammed, Al-Sheikh Yazeed A, Ali Khan Imr |
| Genetic determinants of gestational diabetes mellitus: a case-control study in two independent populations. Acta diabetologica 2020 Feb . Shen Yi, Jia Yulong, Li Yuandong, Gu Xuefeng, Wan Guoqing, Zhang Peng, Zhang Yafeng, Jiang Liyi |
| Genome-wide association study of metabolic syndrome in Korean populations.
PloS one 2020 15 (1): e0227357. Oh Seung-Won, Lee Jong-Eun, Shin Eunsoon, Kwon Hyuktae, Choe Eun Kyung, Choi Su-Yeon, Rhee Hwanseok, Choi Seung |
| Analysis of Evolution and Ethnic Diversity at Glucose-Associated SNPs of Circadian Clock-Related Loci with Cryptochrome 1, Cryptochrome 2, and Melatonin receptor 1B. Biochemical genetics 2021 3 59 (5): 1173-1184. Yoshiuchi Iss |
| No association between a common type 2 diabetes risk gene variant in the melatonin receptor gene (MTNR1B) and mortality among type 2 diabetes patients. Journal of pineal research 2021 12 72 (2): e12785. Xue Pei, Tan Xiao, Wu Jiafei, Tang Xiangdong, Benedict Christi |
| Aggregation of Genome-Wide Association Data from FinnGen and UK Biobank Replicates Multiple Risk Loci for Pregnancy Complications.
Genes 2022 12 13 (12): . Changalidis Anton I, Maksiutenko Evgeniia M, Barbitoff Yury A, Tkachenko Alexander A, Vashukova Elena S, Pachuliia Olga V, Nasykhova Yulia A, Glotov Andrey |
| Decoding type 2 diabetes mellitus genetic risk variants in Pakistani Pashtun ethnic population using the nascent whole exome sequencing and MassARRAY genotyping: A case-control association study. PloS one 2023 2 18 (1): e0281070. Jan Asif, Zakiullah , Ali Sajid, Muhammad Basir, Arshad Amina, Shah Yasar, Bahadur Haji, Khan Hamayun, Khuda Fazli, Akbar Rani, Ijaz Kir |
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