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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 25, 2025. (Total: 235671Documents)
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Records 1 - 5 (of 5 Records)

Query Trace: Disease and PLD2[original query]
Genome-wide association study identifies novel loci associated with circulating phospho- and sphingolipid concentrations. GWAS Catalog
PLoS genetics 2012 8 (2): e1002490.
Demirkan Ay?e, van Duijn Cornelia M, Ugocsai Peter, Isaacs Aaron, Pramstaller Peter P, Liebisch Gerhard, Wilson James F, Johansson Åsa, Rudan Igor, Aulchenko Yurii S, Kirichenko Anatoly V, Janssens A Cecile J W, Jansen Ritsert C, Gnewuch Carsten, Domingues Francisco S, Pattaro Cristian, Wild Sarah H, Jonasson Inger, Polasek Ozren, Zorkoltseva Irina V, Hofman Albert, Karssen Lennart C, Struchalin Maksim, Floyd James, Igl Wilmar, Biloglav Zrinka, Broer Linda, Pfeufer Arne, Pichler Irene, Campbell Susan, Zaboli Ghazal, Kolcic Ivana, Rivadeneira Fernando, Huffman Jennifer, Hastie Nicholas D, Uitterlinden Andre, Franke Lude, Franklin Christopher S, Vitart Veronique, , Nelson Christopher P, Preuss Michael, , Bis Joshua C, O'Donnell Christopher J, Franceschini Nora, , Witteman Jacqueline C M, Axenovich Tatiana, Oostra Ben A, Meitinger Thomas, Hicks Andrew A, Hayward Caroline, Wright Alan F, Gyllensten Ulf, Campbell Harry, Schmitz Gerd,
Joint linkage and association analysis with exome sequence data implicates SLC25A40 in hypertriglyceridemia.
American journal of human genetics 2013 Nov .
Rosenthal EA, Ranchalis J, Crosslin DR, Burt A, Brunzell JD, Motulsky AG, Nickerson DA, Wijsman EM, Jarvik GP
PLD3 in Alzheimer's Disease: a Modest Effect as Revealed by Updated Association and Expression Analyses.
Molecular neurobiology 2015 Jul .
Zhang Deng-Feng, Fan Yu, Wang Dong, Bi Rui, Zhang Chen, Fang Yiru, Yao Yong-Ga
Recapitulation of Candidate Systemic Lupus Erythematosus-Associated Variants in Koreans.
Genomics & informatics 2016 Sep 14 (3): 85-89.
Kwon Ki-Sung, Cho Hye-Young, Chung Yeun-J
Clinical exome sequencing identified POLB c.C1002A as a possible genetic cause in a family with hereditary cancer-predisposing syndrome.
Cancer genetics 2020 7 245 49-52.
Zhu Zhenxin, Wang Jieshi, Jiang Lisha, Lin Ling, Meng Peng, Zhao Jiangman, Cai Qingpi
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