Human Genome Epidemiology Literature Finder
Records 1 - 11 (of 11 Records) |
Query Trace: LEKR1[original query] |
---|
Variants in ADCY5 and near CCNL1 are associated with fetal growth and birth weight.
Nature genetics 2010 May 42 (5): 430-5. Freathy Rachel M, Mook-Kanamori Dennis O, Sovio Ulla, Prokopenko Inga, Timpson Nicholas J, Berry Diane J, Warrington Nicole M, Widen Elisabeth, Hottenga Jouke Jan, Kaakinen Marika, Lange Leslie A, Bradfield Jonathan P, Kerkhof Marjan, Marsh Julie A, Mägi Reedik, Chen Chih-Mei, Lyon Helen N, Kirin Mirna, Adair Linda S, Aulchenko Yurii S, Bennett Amanda J, Borja Judith B, Bouatia-Naji Nabila, Charoen Pimphen, Coin Lachlan J M, Cousminer Diana L, de Geus Eco J C, Deloukas Panos, Elliott Paul, Evans David M, Froguel Philippe, , Glaser Beate, Groves Christopher J, Hartikainen Anna-Liisa, Hassanali Neelam, Hirschhorn Joel N, Hofman Albert, Holly Jeff M P, Hyppönen Elina, Kanoni Stavroula, Knight Bridget A, Laitinen Jaana, Lindgren Cecilia M, , McArdle Wendy L, O'Reilly Paul F, Pennell Craig E, Postma Dirkje S, Pouta Anneli, Ramasamy Adaikalavan, Rayner Nigel W, Ring Susan M, Rivadeneira Fernando, Shields Beverley M, Strachan David P, Surakka Ida, Taanila Anja, Tiesler Carla, Uitterlinden Andre G, van Duijn Cornelia M, , Wijga Alet H, Willemsen Gonneke, Zhang Haitao, Zhao Jianhua, Wilson James F, Steegers Eric A P, Hattersley Andrew T, Eriksson Johan G, Peltonen Leena, Mohlke Karen L, Grant Struan F A, Hakonarson Hakon, Koppelman Gerard H, Dedoussis George V, Heinrich Joachim, Gillman Matthew W, Palmer Lyle J, Frayling Timothy M, Boomsma Dorret I, Davey Smith George, Power Chris, Jaddoe Vincent W V, Jarvelin Marjo-Riitta, , McCarthy Mark |
Replication of a genome-wide association study of birth weight in preterm neonates. The Journal of pediatrics 2012 Jan 160 (1): 19-24.e4. Ryckman Kelli K, Feenstra Bjarke, Shaffer John R, Bream Elise N A, Geller Frank, Feingold Eleanor, Weeks Daniel E, Gadow Enrique, Cosentino Viviana, Saleme Cesar, Simhan Hyagriv N, Merrill David, Fong Chin-To, Busch Tamara, Berends Susan K, Comas Belen, Camelo Jorge L, Boyd Heather, Laurie Cathy C, Crosslin David, Zhang Qi, Doheny Kimberly F, Pugh Elizabeth, Melbye Mads, Marazita Mary L, Dagle John M, Murray Jeffrey |
Variants near CCNL1/LEKR1 and in ADCY5 and fetal growth characteristics in different trimesters. The Journal of clinical endocrinology and metabolism 2011 May 96 (5): E810-5. Mook-Kanamori Dennis O, Marsh Julie A, Warrington Nicole M, Taal H Rob, Newnham John P, Beilin Lawrie J, Lye Stephen J, Palmer Lyle J, Hofman Albert, Steegers Eric A P, Pennell Craig E, , Jaddoe Vincent W |
The birth weight lowering C-allele of rs900400 near LEKR1 and CCNL1 associates with elevated insulin release following an oral glucose challenge. PloS one 2011 6 (11): e27096. Andersson Ehm A, Harder Marie N, Pilgaard Kasper, Pisinger Charlotta, Stan?áková Alena, Kuusisto Johanna, Grarup Niels, Færch Kristine, Poulsen Pernille, Witte Daniel R, Jørgensen Torben, Vaag Allan, Laakso Markku, Pedersen Oluf, Hansen Torb |
The chromosome 3q25 genomic region is associated with measures of adiposity in newborns in a multi-ethnic genome-wide association study.
Human molecular genetics 2013 Sep 22 (17): 3583-96. Urbanek Margrit, Hayes M Geoffrey, Armstrong Loren L, Morrison Jean, Lowe Lynn P, Badon Sylvia E, Scheftner Doug, Pluzhnikov Anna, Levine David, Laurie Cathy C, McHugh Caitlin, Ackerman Christine M, Mirel Daniel B, Doheny Kimberly F, Guo Cong, Scholtens Denise M, Dyer Alan R, Metzger Boyd E, Reddy Timothy E, Cox Nancy J, Lowe William L, |
Genetic variants in LEKR1 and GALNT10 modulate sex-difference in carotid intima-media thickness: a genome-wide interaction study.
Atherosclerosis 2015 Jun 240 (2): 462-7. Dong Chuanhui, Della-Morte David, Beecham Ashley, Wang Liyong, Cabral Digna, Blanton Susan H, Sacco Ralph L, Rundek Tatja |
Exome genotyping arrays to identify rare and low frequency variants associated with epithelial ovarian cancer risk. Human molecular genetics 2016 Jul . Permuth Jennifer B, Pirie Ailith, Chen Y Ann, Lin Hui-Yi, Reid Brett M, Chen Zhihua, Monteiro Alvaro, Dennis Joe, Mendoza-Fandino Gustavo, , , Anton-Culver Hoda, Bandera Elisa V, Bisogna Maria, Brinton Louise, Brooks-Wilson Angela, Carney Michael E, Chenevix-Trench Georgia, Cook Linda S, Cramer Daniel W, Cunningham Julie M, Cybulski Cezary, D'Aloisio Aimee A, Doherty Jennifer Anne, Earp Madalene, Edwards Robert P, Fridley Brooke L, Gayther Simon A, Gentry-Maharaj Aleksandra, Goodman Marc T, Gronwald Jacek, Hogdall Estrid, Iversen Edwin S, Jakubowska Anna, Jensen Allan, Karlan Beth Y, Kelemen Linda E, Kjaer Suzanne K, Kraft Peter, Le Nhu D, Levine Douglas A, Lissowska Jolanta, Lubinski Jan, Matsuo Keitaro, Menon Usha, Modugno Rosemary, Moysich Kirsten B, Nakanishi Toru, Ness Roberta B, Olson Sara, Orlow Irene, Pearce Celeste L, Pejovic Tanja, Poole Elizabeth M, Ramus Susan J, Rossing Mary Anne, Sandler Dale P, Shu Xiao-Ou, Song Honglin, Taylor Jack A, Teo Soo-Hwang, Terry Kathryn L, Thompson Pamela J, Tworoger Shelley S, Webb Penelope M, Wentzensen Nicolas, Wilkens Lynne R, Winham Stacey, Woo Yin-Ling, Wu Anna H, Yang Hannah, Zheng Wei, Ziogas Argyrios, Phelan Catherine M, Schildkraut Joellen M, Berchuck Andrew, Goode Ellen L, Pharoah Paul Dp, Sellers Thomas A, |
Association between LEKR1-CCNL1 and IGSF21-KLHDC7A gene polymorphisms and diabetic retinopathy of type 2 diabetes mellitus in the Chinese Han population. The journal of gene medicine 2016 Sep . Lin Xiaohui, Wang Jihong, Yun Lixia, Jiang Shuhong, Li Langen, Chen Xiaohai, Li Zhen, Lu Qiang, Zhang Yihui, Ma Xiaoche |
Genetic determinants of adiponectin regulation revealed by pregnancy.
Obesity (Silver Spring, Md.) 2017 Mar . Hivert Marie-France, Scholtens Denise M, Allard Catherine, Nodzenski Michael, Bouchard Luigi, Brisson Diane, Lowe Lynn P, McDowell Ian, Reddy Tim, Dastani Zari, Richards J Brent, Hayes M Geoffrey, Lowe William |
Founder Mutations for Early Onset Melanoma as Revealed by Whole Exome Sequencing Suggests That This is Not Associated with the Increasing Incidence of Melanoma in Poland. Cancer research and treatment 2018 May . D?bniak Tadeusz, Scott Rodney J, Lea Rodney A, Górski Bohdan, Masoj? Bart?omiej, Cybulski Cezary, Kram Andrzej, Maleszka Romuald, Gromowski Tomasz, Paszkowska-Szczur Katarzyna, Kashyap Aniruddh, Lener Marcin R, Mali?ska Karolina, Rogo?a Emilia, Murawa Dawid, Rudnicka Helena, Deptu?a Jakub, Lubi?ski J |
Genetic Study on Small Insertions and Deletions in Psoriasis Reveals a Role in Complex Human Diseases. The Journal of investigative dermatology 2019 5 139 (11): 2302-2312.e14. Zhen Qi, Yang Zhenjun, Wang Wenjun, Li Bao, Bai Mingzhou, Wu Jing, Ge Huiyao, Dong Zirui, Shen Juan, Tang Huayang, Sun Silong, Qiu Ying, Xu Jinjin, Qu Xiaoxiao, Wang Ying, Yi Meihui, Hu Huaqing, Xu Yuanhong, Cheng Hui, Liang Bo, Gao Jinping, Shao Haojing, Jiang Zhengwen, Gao Qiang, Sun Liangd |
- Page last reviewed:Feb 1, 2024
- Page last updated:Apr 16, 2024
- Content source: