Human Genome Epidemiology Literature Finder
Records 1 - 7 (of 7 Records) |
Query Trace: SYTL3[original query] |
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Genetic determinants of the ankle-brachial index: a meta-analysis of a cardiovascular candidate gene 50K SNP panel in the candidate gene association resource (CARe) consortium. Atherosclerosis 2012 May 222 (1): 138-47. Wassel Christina L, Lamina Claudia, Nambi Vijay, Coassin Stefan, Mukamal Kenneth J, Ganesh Santhi K, Jacobs David R, Franceschini Nora, Papanicolaou George J, Gibson Quince, Yanek Lisa R, van der Harst Pim, Ferguson Jane F, Crawford Dana C, Waite Lindsay L, Allison Matthew A, Criqui Michael H, McDermott Mary M, Mehra Reena, Cupples L Adrienne, Hwang Shih-Jen, Redline Susan, Kaplan Robert C, Heiss Gerardo, Rotter Jerome I, Boerwinkle Eric, Taylor Herman A, Eraso Luis H, Haun Margot, Li Mingyao, Meisinger Christa, O'Connell Jeffrey R, Shuldiner Alan R, Tybjærg-Hansen Anne, Frikke-Schmidt Ruth, Kollerits Barbara, Rantner Barbara, Dieplinger Benjamin, Stadler Marietta, Mueller Thomas, Haltmayer Meinhard, Klein-Weigel Peter, Summerer Monika, Wichmann H-Erich, Asselbergs Folkert W, Navis Gerjan, Mateo Leach Irene, Brown-Gentry Kristin, Goodloe Robert, Assimes Themistocles L, Becker Diane M, Cooke John P, Absher Devin M, Olin Jeffrey W, Mitchell Braxton D, Reilly Muredach P, Mohler Emile R, North Kari E, Reiner Alexander P, Kronenberg Florian, Murabito Joanne |
Whole-Exome Sequencing Study of Thyrotropin-Secreting Pituitary Adenomas. The Journal of clinical endocrinology and metabolism 2016 Nov jc20162261. Sapkota Santosh, Horiguchi Kazuhiko, Tosaka Masahiko, Yamada Syozo, Yamada Masano |
Whole-genome sequencing reveals new Alzheimer's disease-associated rare variants in loci related to synaptic function and neuronal development. medRxiv : the preprint server for health sciences 2020 Nov . Prokopenko Dmitry, Morgan Sarah L, Mullin Kristina, Hofmann Oliver, Chapman Brad, Kirchner Rory, Amberkar Sandeep, Wohlers Inken, Lange Christoph, Hide Winston, Bertram Lars, Tanzi Rudolph |
SYTL3-SLC22A3 Single-Nucleotide Polymorphisms and Gene-Gene/Environment Interactions on the Risk of Hyperlipidemia. Frontiers in genetics 2021 8 12 679027. Zheng Peng-Fei, Yin Rui-Xing, Cao Xiao-Li, Guan Yao-Zong, Deng Guo-Xiong, Wei Bi-Liu, Liu Chun-Xi |
Effect of SYTL3-SLC22A3 Variants, Their Haplotypes, and G × E Interactions on Serum Lipid Levels and the Risk of Coronary Artery Disease and Ischaemic Stroke. Frontiers in cardiovascular medicine 2021 8 8 713068. Zheng Peng-Fei, Yin Rui-Xing, Cao Xiao-Li, Chen Wu-Xian, Wu Jin-Zhen, Huang Fe |
Whole-genome sequencing reveals new Alzheimer's disease-associated rare variants in loci related to synaptic function and neuronal development. Alzheimer's & dementia : the journal of the Alzheimer's Association 2021 Apr . Prokopenko Dmitry, Morgan Sarah L, Mullin Kristina, Hofmann Oliver, Chapman Brad, Kirchner Rory, , Amberkar Sandeep, Wohlers Inken, Lange Christoph, Hide Winston, Bertram Lars, Tanzi Rudolph |
Identification of Neurotransmission and Synaptic Biological Processes Disrupted in Autism Spectrum Disorder Using Interaction Networks and Community Detection Analysis. Biomedicines 2023 11 11 (11): . Joana Vilela, Hugo Martiniano, Ana Rita Marques, João Xavier Santos, Muhammad Asif, Célia Rasga, Guiomar Oliveira, Astrid Moura Vicen |
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- Page last updated:Mar 25, 2024
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