Human Genome Epidemiology Literature Finder
Records 1 - 6 (of 6 Records) |
Query Trace: SYT9[original query] |
---|
Genome-wide association study identifies novel loci associated with circulating phospho- and sphingolipid concentrations.
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, |
Polymorphisms in genes related to one-carbon metabolism are not related to pancreatic cancer in PanScan and PanC4. Cancer causes & control : CCC 2013 Mar 24 (3): 595-602. Leenders Max, Bhattacharjee Samsiddhi, Vineis Paolo, Stevens Victoria, Bueno-de-Mesquita H Bas, Shu Xiao-Ou, Amundadottir Laufey, Gross Myron, Tobias Geoffrey S, Wactawski-Wende Jean, Arslan Alan A, Duell Eric J, Fuchs Charles S, Gallinger Steven, Hartge Patricia, Hoover Robert N, Holly Elizabeth A, Jacobs Eric J, Klein Alison P, Kooperberg Charles, LaCroix Andrea, Li Donghui, Mandelson Margaret T, Olson Sara H, Petersen Gloria, Risch Harvey A, Yu Kai, Wolpin Brian M, Zheng Wei, Agalliu Ilir, Albanes Demetrius, Boutron-Ruault Marie-Christine, Bracci Paige M, Buring Julie E, Canzian Federico, Chang Kenneth, Chanock Stephen J, Cotterchio Michelle, Gaziano J Michael, Giovanucci Edward L, Goggins Michael, Hallmans Göran, Hankinson Susan E, Hoffman-Bolton Judith A, Hunter David J, Hutchinson Amy, Jacobs Kevin B, Jenab Mazda, Khaw Kay-Tee, Kraft Peter, Krogh Vittorio, Kurtz Robert C, McWilliams Robert R, Mendelsohn Julie B, Patel Alpa V, Rabe Kari G, Riboli Elio, Tjønneland Anne, Trichopoulos Dimitrios, Virtamo Jarmo, Visvanathan Kala, Elena Joanne W, Yu Herbert, Zeleniuch-Jacquotte Anne, Stolzenberg-Solomon Rachael |
Whole genome analyses reveal no pathogenetic single nucleotide or structural differences between monozygotic twins discordant for amyotrophic lateral sclerosis. Amyotrophic lateral sclerosis & frontotemporal degeneration 2015 May 1-8. Meltz Steinberg Karyn, Nicholas Thomas J, Koboldt Daniel C, Yu Bing, Mardis Elaine, Pamphlett Rog |
Identification of Candidate Gene Variants in Korean MODY Families by Whole-Exome Sequencing. Hormone research in pædiatrics 2015 83 (4): 242-51. Shim Ye Jee, Kim Jung Eun, Hwang Su-Kyeong, Choi Bong Seok, Choi Byung Ho, Cho Eun-Mi, Jang Kyoung Mi, Ko Cheol W |
A genetic variant in a homocysteine metabolic gene that increases the risk of congenital cardiac septal defects in Han Chinese populations. IUBMB life 2017 Sep 69 (9): 700-705. Xie Han-Hui, Li Jiong, Li Pei-Qiang, Zhang An-An, Li Yi, Wang Yan-Zhen, Xie Ding-Xiong, Xie Xiao-Do |
A Genetic Variant in FIGN Gene Reduces the Risk of Congenital Heart Disease in Han Chinese Populations. Pediatric cardiology 2017 May . Wang Dan, Chu Maoping, Wang Feng, Zhou Aihua, Ruan Miaohua, Chen Yimi |
- Page last reviewed:Feb 1, 2024
- Page last updated:Mar 25, 2024
- Content source: