Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 38 Records) |
Query Trace: MADD[original query] |
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Variants from GIPR, TCF7L2, DGKB, MADD, CRY2, GLIS3, PROX1, SLC30A8 and IGF1 are associated with glucose metabolism in the Chinese. PloS one 2010 5 (11): e15542. Hu Cheng, Zhang Rong, Wang Congrong, Wang Jie, Ma Xiaojing, Hou Xuhong, Lu Jingyi, Yu Weihui, Jiang Feng, Bao Yuqian, Xiang Kunsan, Jia Weipi |
Glucose-raising genetic variants in MADD and ADCY5 impair conversion of proinsulin to insulin. PloS one 2011 6 (8): e23639. Wagner Robert, Dudziak Katarzyna, Herzberg-Schäfer Silke A, Machicao Fausto, Stefan Norbert, Staiger Harald, Häring Hans-Ulrich, Fritsche Andre |
Genome-wide association identifies nine common variants associated with fasting proinsulin levels and provides new insights into the pathophysiology of type 2 diabetes.
Diabetes 2011 Oct 60 (10): 2624-34. Strawbridge Rona J, Dupuis Josée, Prokopenko Inga, Barker Adam, Ahlqvist Emma, Rybin Denis, Petrie John R, Travers Mary E, Bouatia-Naji Nabila, Dimas Antigone S, Nica Alexandra, Wheeler Eleanor, Chen Han, Voight Benjamin F, Taneera Jalal, Kanoni Stavroula, Peden John F, Turrini Fabiola, Gustafsson Stefan, Zabena Carina, Almgren Peter, Barker David J P, Barnes Daniel, Dennison Elaine M, Eriksson Johan G, Eriksson Per, Eury Elodie, Folkersen Lasse, Fox Caroline S, Frayling Timothy M, Goel Anuj, Gu Harvest F, Horikoshi Momoko, Isomaa Bo, Jackson Anne U, Jameson Karen A, Kajantie Eero, Kerr-Conte Julie, Kuulasmaa Teemu, Kuusisto Johanna, Loos Ruth J F, Luan Jian'an, Makrilakis Konstantinos, Manning Alisa K, Martínez-Larrad María Teresa, Narisu Narisu, Nastase Mannila Maria, Ohrvik John, Osmond Clive, Pascoe Laura, Payne Felicity, Sayer Avan A, Sennblad Bengt, Silveira Angela, Stancáková Alena, Stirrups Kathy, Swift Amy J, Syvänen Ann-Christine, Tuomi Tiinamaija, van 't Hooft Ferdinand M, Walker Mark, Weedon Michael N, Xie Weijia, Zethelius Björn, , , , , , Ongen Halit, Mälarstig Anders, Hopewell Jemma C, Saleheen Danish, Chambers John, Parish Sarah, Danesh John, Kooner Jaspal, Ostenson Claes-Göran, Lind Lars, Cooper Cyrus C, Serrano-Ríos Manuel, Ferrannini Ele, Forsen Tom J, Clarke Robert, Franzosi Maria Grazia, Seedorf Udo, Watkins Hugh, Froguel Philippe, Johnson Paul, Deloukas Panos, Collins Francis S, Laakso Markku, Dermitzakis Emmanouil T, Boehnke Michael, McCarthy Mark I, Wareham Nicholas J, Groop Leif, Pattou François, Gloyn Anna L, Dedoussis George V, Lyssenko Valeriya, Meigs James B, Barroso Inês, Watanabe Richard M, Ingelsson Erik, Langenberg Claudia, Hamsten Anders, Florez Jose |
Variants in GLIS3 and CRY2 are associated with type 2 diabetes and impaired fasting glucose in Chinese Hans. PloS one 2011 6 (6): e21464. Liu Chen, Li Huaixing, Qi Lu, Loos Ruth J F, Qi Qibin, Lu Ling, Gan Wei, Lin |
Association study of type 2 diabetes genetic susceptibility variants and risk of pancreatic cancer: an analysis of PanScan-I data. Cancer causes & control : CCC 2011 Jun 22 (6): 877-83. Pierce Brandon L, Austin Melissa A, Ahsan Habib |
Replication of association of DENND1A and THADA variants with polycystic ovary syndrome in European cohorts. Journal of medical genetics 2012 Feb 49 (2): 90-5. Goodarzi Mark O, Jones Michelle R, Li Xiaohui, Chua Angela K, Garcia Obed A, Chen Yii-Der I, Krauss Ronald M, Rotter Jerome I, Ankener Wendy, Legro Richard S, Azziz Ricardo, Strauss Jerome F, Dunaif Andrea, Urbanek Margr |
Effects of genetic variants previously associated with fasting glucose and insulin in the Diabetes Prevention Program. PloS one 2012 7 (9): e44424. Florez Jose C, Jablonski Kathleen A, McAteer Jarred B, Franks Paul W, Mason Clinton C, Mather Kieren, Horton Edward, Goldberg Ronald, Dabelea Dana, Kahn Steven E, Arakaki Richard F, Shuldiner Alan R, Knowler William C, |
Exome array analysis identifies new loci and low-frequency variants influencing insulin processing and secretion.
Nature genetics 2012 Dec . Huyghe JR, Jackson AU, Fogarty MP, Buchkovich ML, Stan?áková A, Stringham HM, Sim X, Yang L, Fuchsberger C, Cederberg H, Chines PS, Teslovich TM, Romm JM, Ling H, McMullen I, Ingersoll R, Pugh EW, Doheny KF, Neale BM, Daly MJ, Kuusisto J, Scott LJ, Kang HM, Collins FS, Abecasis GR, Watanabe RM, Boehnke M, Laakso M, Mohlke KL |
Association of the rs7395662 SNP in the MADD-FOLH1 and several environmental factors with serum lipid levels in the Mulao and Han populations. International journal of medical sciences 2013 10 (11): 1537-46. Huang Ke-Ke, Yin Rui-Xing, Zeng Xiao-Na, Huang Ping, Lin Quan-Zhen, Wu Jian, Guo Tao, Wang Wei, Yang De-Zhai, Lin Wei-Xio |
Association of levels of fasting glucose and insulin with rare variants at the chromosome 11p11.2-MADD locus: Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium Targeted Sequencing Study. Circulation. Cardiovascular genetics 2014 Jun 7 (3): 374-82. Cornes Belinda K, Brody Jennifer A, Nikpoor Naghmeh, Morrison Alanna C, Dang Huan Chu Pham, Ahn Byung Soo, Wang Shuai, Dauriz Marco, Barzilay Joshua I, Dupuis Josée, Florez Jose C, Coresh Josef, Gibbs Richard A, Kao W H Linda, Liu Ching-Ti, McKnight Barbara, Muzny Donna, Pankow James S, Reid Jeffrey G, White Charles C, Johnson Andrew D, Wong Tien Y, Psaty Bruce M, Boerwinkle Eric, Rotter Jerome I, Siscovick David S, Sladek Robert, Meigs James |
Family-based genome scan for age at onset of late-onset Alzheimer's disease in whole exome sequencing data. Genes, brain, and behavior 2015 Sep . Saad M, Brkanac Z, Wijsman E |
Associations of lipid levels susceptibility loci with coronary artery disease in Chinese population. Lipids in health and disease 2015 14 (1): 80. Wang Xue-Bin, Han Ya-di, Cui Ning-Hua, Gao Jia-Jia, Yang Jie, Huang Zhu-Liang, Zhu Qiang, Zheng Fa |
Polycystic ovary syndrome susceptibility single nucleotide polymorphisms in women with a single PCOS clinical feature. Human reproduction (Oxford, England) 2015 Mar 30 (3): 732-6. Cui Linlin, Li Guangyu, Zhong Wanxia, Bian Yuehong, Su Shizhen, Sheng Yan, Shi Yuhua, Wei Daimin, Zhang Wei, Zhao Han, Chen Zi-Jia |
MADD-FOLH1 Polymorphisms and Their Haplotypes with Serum Lipid Levels and the Risk of Coronary Heart Disease and Ischemic Stroke in a Chinese Han Population. Nutrients 2016 8 (4): . Wu Dong-Feng, Yin Rui-Xing, Cao Xiao-Li, Huang Feng, Wu Jin-Zhen, Chen Wu-Xi |
Bivariate Genome-Wide Association Study of Depressive Symptoms With Type 2 Diabetes and Quantitative Glycemic Traits. Psychosomatic medicine 2017 Dec . Haljas Kadri, Amare Azmeraw T, Alizadeh Behrooz Z, Hsu Yi-Hsiang, Mosley Thomas, Newman Anne, Murabito Joanne, Tiemeier Henning, Tanaka Toshiko, van Duijn Cornelia, Ding Jingzhong, Llewellyn David J, Bennett David A, Terracciano Antonio, Launer Lenore, Ladwig Karl-Heinz, Cornelis Marylin C, Teumer Alexander, Grabe Hans, Kardia Sharon L R, Ware Erin B, Smith Jennifer A, Snieder Harold, Eriksson Johan G, Groop Leif, Räikkönen Katri, Lahti Ja |
A novel mutation in ETFDH manifesting as severe neonatal-onset multiple acyl-CoA dehydrogenase deficiency. Journal of the neurological sciences 2017 12 384 121-125. van der Westhuizen Francois H, Smuts Izelle, Honey Engela, Louw Roan, Schoonen Maryke, Jonck Lindi-Maryn, Dercksen Mar |
Association between genetic loci linked to HDL-C levels and Indian patients with CAD: a pilot study. Heart Asia 2017 9 (1): 9-13. Stanley Ashley, Ponde C K, Rajani R M, Ashavaid T |
Genome-wide association analyses identify new loci influencing intraocular pressure.
Human molecular genetics 2018 Mar . Gao X Raymond, Huang Hua, Nannini Drew R, Fan Fangda, Kim Heej |
Measuring gene-gene interaction using Kullback-Leibler divergence. Annals of human genetics 2019 6 83 (6): 405-417. Chen Guanjie, Yuan Ao, Cai Tao, Li Chuan-Ming, Bentley Amy R, Zhou Jie, N Shriner Daniel, A Adeyemo Adebowale, N Rotimi Charl |
Expression and significance of ETFDH in hepatocellular carcinoma. Pathology, research and practice 2019 Oct 152702. Wu Yaxun, Zhang Xingsong, Shen Rong, Huang Jieyu, Lu Xiaoyun, Zheng Guihua, Chen Xudo |
Genome-wide Association Study Identifies 2 New Loci Associated With Anti-NMDAR Encephalitis.
Neurology(R) neuroimmunology & neuroinflammation 2021 Nov 8 (6): . Tietz Anja K, Angstwurm Klemens, Baumgartner Tobias, Doppler Kathrin, Eisenhut Katharina, Elisak Martin, Franke Andre, Golombeck Kristin S, Handreka Robert, Kaufmann Max, Kraemer Markus, Kraft Andrea, Lewerenz Jan, Lieb Wolfgang, Madlener Marie, Melzer Nico, Mojzisova Hana, Möller Peter, Pfefferkorn Thomas, Prüss Harald, Rostásy Kevin, Schnegelsberg Margret, Schröder Ina, Siebenbrodt Kai, Sühs Kurt-Wolfram, Wickel Jonathan, Wandinger Klaus-Peter, Leypoldt Frank, Kuhlenbäumer Gregor, |
GWAS-Top Polymorphisms Associated With Late-Onset Alzheimer Disease in Brazil: Pointing Out Possible New Culprits Among Non-Coding RNAs. Frontiers in molecular biosciences 2021 8 632314. Kretzschmar Gabriela Canalli, Alencar Nina Moura, da Silva Saritha Suellen Lopes, Sulzbach Carla Daniela, Meissner Caroline Grisbach, Petzl-Erler Maria Luiza, Souza Ricardo Lehtonen R, Boldt Angelica Beate Wint |
Newborn screening and molecular features of patients with multiple acyl-CoA dehydrogenase deficiency in Quanzhou, China. Journal of pediatric endocrinology & metabolism : JPEM 2021 4 34 (5): 649-652. Lin Yiming, Zhang Weifeng, Chen Zhixu, Lin Chunmei, Lin Weihua, Fu Qingliu, Peng Weilin, Chen Dongm |
A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers.
Nature communications 2021 02 12 (1): 1078. Coignard Juliette, Lush Michael, Beesley Jonathan, O'Mara Tracy A, Dennis Joe, Tyrer Jonathan P, Barnes Daniel R, McGuffog Lesley, Leslie Goska, Bolla Manjeet K, Adank Muriel A, Agata Simona, Ahearn Thomas, Aittomäki Kristiina, Andrulis Irene L, Anton-Culver Hoda, Arndt Volker, Arnold Norbert, Aronson Kristan J, Arun Banu K, Augustinsson Annelie, Azzollini Jacopo, Barrowdale Daniel, Baynes Caroline, Becher Heiko, Bermisheva Marina, Bernstein Leslie, Bia?kowska Katarzyna, Blomqvist Carl, Bojesen Stig E, Bonanni Bernardo, Borg Ake, Brauch Hiltrud, Brenner Hermann, Burwinkel Barbara, Buys Saundra S, Caldés Trinidad, Caligo Maria A, Campa Daniele, Carter Brian D, Castelao Jose E, Chang-Claude Jenny, Chanock Stephen J, Chung Wendy K, Claes Kathleen B M, Clarke Christine L, , , Collée J Margriet, Conroy Don M, Czene Kamila, Daly Mary B, Devilee Peter, Diez Orland, Ding Yuan Chun, Domchek Susan M, Dörk Thilo, Dos-Santos-Silva Isabel, Dunning Alison M, Dwek Miriam, Eccles Diana M, Eliassen A Heather, Engel Christoph, Eriksson Mikael, Evans D Gareth, Fasching Peter A, Flyger Henrik, Fostira Florentia, Friedman Eitan, Fritschi Lin, Frost Debra, Gago-Dominguez Manuela, Gapstur Susan M, Garber Judy, Garcia-Barberan Vanesa, García-Closas Montserrat, García-Sáenz José A, Gaudet Mia M, Gayther Simon A, Gehrig Andrea, Georgoulias Vassilios, Giles Graham G, Godwin Andrew K, Goldberg Mark S, Goldgar David E, González-Neira Anna, Greene Mark H, Guénel Pascal, Haeberle Lothar, Hahnen Eric, Haiman Christopher A, Håkansson Niclas, Hall Per, Hamann Ute, Harrington Patricia A, Hart Steven N, He Wei, Hogervorst Frans B L, Hollestelle Antoinette, Hopper John L, Horcasitas Darling J, Hulick Peter J, Hunter David J, Imyanitov Evgeny N, , , , Jager Agnes, Jakubowska Anna, James Paul A, Jensen Uffe Birk, John Esther M, Jones Michael E, Kaaks Rudolf, Kapoor Pooja Middha, Karlan Beth Y, Keeman Renske, Khusnutdinova Elza, Kiiski Johanna I, Ko Yon-Dschun, Kosma Veli-Matti, Kraft Peter, Kurian Allison W, Laitman Yael, Lambrechts Diether, Le Marchand Loic, Lester Jenny, Lesueur Fabienne, Lindstrom Tricia, Lopez-Fernández Adria, Loud Jennifer T, Luccarini Craig, Mannermaa Arto, Manoukian Siranoush, Margolin Sara, Martens John W M, Mebirouk Noura, Meindl Alfons, Miller Austin, Milne Roger L, Montagna Marco, Nathanson Katherine L, Neuhausen Susan L, Nevanlinna Heli, Nielsen Finn C, O'Brien Katie M, Olopade Olufunmilayo I, Olson Janet E, Olsson Håkan, Osorio Ana, Ottini Laura, Park-Simon Tjoung-Won, Parsons Michael T, Pedersen Inge Sokilde, Peshkin Beth, Peterlongo Paolo, Peto Julian, Pharoah Paul D P, Phillips Kelly-Anne, Polley Eric C, Poppe Bruce, Presneau Nadege, Pujana Miquel Angel, Punie Kevin, Radice Paolo, Rantala Johanna, Rashid Muhammad U, Rennert Gad, Rennert Hedy S, Robson Mark, Romero Atocha, Rossing Maria, Saloustros Emmanouil, Sandler Dale P, Santella Regina, Scheuner Maren T, Schmidt Marjanka K, Schmidt Gunnar, Scott Christopher, Sharma Priyanka, Soucy Penny, Southey Melissa C, Spinelli John J, Steinsnyder Zoe, Stone Jennifer, Stoppa-Lyonnet Dominique, Swerdlow Anthony, Tamimi Rulla M, Tapper William J, Taylor Jack A, Terry Mary Beth, Teulé Alex, Thull Darcy L, Tischkowitz Marc, Toland Amanda E, Torres Diana, Trainer Alison H, Truong Thérèse, Tung Nadine, Vachon Celine M, Vega Ana, Vijai Joseph, Wang Qin, Wappenschmidt Barbara, Weinberg Clarice R, Weitzel Jeffrey N, Wendt Camilla, Wolk Alicja, Yadav Siddhartha, Yang Xiaohong R, Yannoukakos Drakoulis, Zheng Wei, Ziogas Argyrios, Zorn Kristin K, Park Sue K, Thomassen Mads, Offit Kenneth, Schmutzler Rita K, Couch Fergus J, Simard Jacques, Chenevix-Trench Georgia, Easton Douglas F, Andrieu Nadine, Antoniou Antonis |
Phenotype and genotype spectrum of variants in guanine nucleotide exchange factor genes in a broad cohort of Iranian patients. Molecular genetics & genomic medicine 2022 2 10 (4): e1894. Mosallaei Meysam, Ehtesham Naeim, Beheshtian Maryam, Khoshbakht Shahrouz, Davarnia Behzad, Kahrizi Kimia, Najmabadi Hosse |
Large-scale exome sequence analysis identifies sex- and age-specific determinants of obesity. Cell genomics 2023 8 3 (8): 100362. Lena R Kaisinger, Katherine A Kentistou, Stasa Stankovic, Eugene J Gardner, Felix R Day, Yajie Zhao, Alexander Mörseburg, Christopher J Carnie, Guido Zagnoli-Vieira, Fabio Puddu, Stephen P Jackson, Stephen O'Rahilly, I Sadaf Farooqi, Laura Dearden, Lucas C Pantaleão, Susan E Ozanne, Ken K Ong, John R B Per |
Co-existence of multiple functional variants and genes underlie genetic risk locus 11p11.2 of Alzheimer's disease. Biological psychiatry 2023 6 . Min Xu, Qianjin Liu, Rui Bi, Yu Li, Hongli Li, Wei-Bo Kang, Zhongjiang Yan, Quanzhen Zheng, Chunli Sun, Maosen Ye, Bo-Lin Xiang, Xiong-Jian Luo, Ming Li, Deng-Feng Zhang, Yong-Gang Y |
Genetic Background of Metabolically Healthy and Unhealthy Obesity Phenotypes in Hungarian Adult Sample Population. International journal of molecular sciences 2023 3 24 (6): . Piko Peter, Llanaj Erand, Nagy Karoly, Adany Ro |
Newborn screening for fatty acid oxidation disorders in a southern Chinese population. Heliyon 2024 1 10 (1): e23671. Yiming Lin, Chunmei Lin, Bangbang Lin, Zhenzhu Zheng, Weihua Lin, Yanru Chen, Dongmei Chen, Weilin Pe |
Clinical, biochemical, and genetic spectrum of MADD in a South African cohort: an ICGNMD study. Orphanet journal of rare diseases 2024 1 19 (1): 15. Michelle Bisschoff, Izelle Smuts, Marli Dercksen, Maryke Schoonen, Barend C Vorster, George van der Watt, Careni Spencer, Kireshnee Naidu, Franclo Henning, Surita Meldau, Robert McFarland, Robert W Taylor, Krutik Patel, Mahmoud R Fassad, Jana Vandrovcova, , Ronald J A Wanders, Francois H van der Westhuiz |
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