Human Genome Epidemiology Literature Finder
Records 1 - 25 (of 25 Records) |
Query Trace: HK1[original query] |
---|
Coagulation factor V G allele and HR2 haplotype: factor V activity, activated protein C resistance and risk of venous thrombosis. Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis 2003 Jan 14 (1): 49-56. Kostka Heike, Schwarz Thomas, Schellong Sebastian, Mix Cornelia, Kuhlisch Eberhard, Temelkova-Kurktschiev Theodora, Henkel Elena, Köhler Carsta, Gehrisch Siegmund, Siegert Gabrie |
Novel association of HK1 with glycated hemoglobin in a non-diabetic population: a genome-wide evaluation of 14,618 participants in the Women's Genome Health Study.
PLoS genetics 2008 Dec 4 (12): e1000312. Paré Guillaume, Chasman Daniel I, Parker Alexander N, Nathan David M, Miletich Joseph P, Zee Robert Y, Ridker Paul |
Genes in glucose metabolism and association with spina bifida. Reproductive sciences (Thousand Oaks, Calif.) 2008 Jan 15 (1): 51-8. Davidson Christina M, Northrup Hope, King Terri M, Fletcher Jack M, Townsend Irene, Tyerman Gayle H, Au Kit Si |
Genetic variant in HK1 is associated with a proanemic state and A1C but not other glycemic control-related traits. Diabetes 2009 Nov 58 (11): 2687-97. Bonnefond Amélie, Vaxillaire Martine, Labrune Yann, Lecoeur Cécile, Chèvre Jean-Claude, Bouatia-Naji Nabila, Cauchi Stéphane, Balkau Beverley, Marre Michel, Tichet Jean, Riveline Jean-Pierre, Hadjadj Samy, Gallois Yves, Czernichow Sébastien, Hercberg Serge, Kaakinen Marika, Wiesner Susanne, Charpentier Guillaume, Lévy-Marchal Claire, Elliott Paul, Jarvelin Marjo-Riitta, Horber Fritz, Dina Christian, Pedersen Oluf, Sladek Robert, Meyre David, Froguel Philip |
Common variants at 10 genomic loci influence hemoglobin A1(C) levels via glycemic and nonglycemic pathways.
Diabetes 2010 Dec 59 (12): 3229-39. Soranzo Nicole, Sanna Serena, Wheeler Eleanor, Gieger Christian, Radke Dörte, Dupuis Josée, Bouatia-Naji Nabila, Langenberg Claudia, Prokopenko Inga, Stolerman Elliot, Sandhu Manjinder S, Heeney Matthew M, Devaney Joseph M, Reilly Muredach P, Ricketts Sally L, Stewart Alexandre F R, Voight Benjamin F, Willenborg Christina, Wright Benjamin, Altshuler David, Arking Dan, Balkau Beverley, Barnes Daniel, Boerwinkle Eric, Böhm Bernhard, Bonnefond Amélie, Bonnycastle Lori L, Boomsma Dorret I, Bornstein Stefan R, Böttcher Yvonne, Bumpstead Suzannah, Burnett-Miller Mary Susan, Campbell Harry, Cao Antonio, Chambers John, Clark Robert, Collins Francis S, Coresh Josef, de Geus Eco J C, Dei Mariano, Deloukas Panos, Döring Angela, Egan Josephine M, Elosua Roberto, Ferrucci Luigi, Forouhi Nita, Fox Caroline S, Franklin Christopher, Franzosi Maria Grazia, Gallina Sophie, Goel Anuj, Graessler Jürgen, Grallert Harald, Greinacher Andreas, Hadley David, Hall Alistair, Hamsten Anders, Hayward Caroline, Heath Simon, Herder Christian, Homuth Georg, Hottenga Jouke-Jan, Hunter-Merrill Rachel, Illig Thomas, Jackson Anne U, Jula Antti, Kleber Marcus, Knouff Christopher W, Kong Augustine, Kooner Jaspal, Köttgen Anna, Kovacs Peter, Krohn Knut, Kühnel Brigitte, Kuusisto Johanna, Laakso Markku, Lathrop Mark, Lecoeur Cécile, Li Man, Li Mingyao, Loos Ruth J F, Luan Jian'an, Lyssenko Valeriya, Mägi Reedik, Magnusson Patrik K E, Mälarstig Anders, Mangino Massimo, Martínez-Larrad María Teresa, März Winfried, McArdle Wendy L, McPherson Ruth, Meisinger Christa, Meitinger Thomas, Melander Olle, Mohlke Karen L, Mooser Vincent E, Morken Mario A, Narisu Narisu, Nathan David M, Nauck Matthias, O'Donnell Chris, Oexle Konrad, Olla Nazario, Pankow James S, Payne Felicity, Peden John F, Pedersen Nancy L, Peltonen Leena, Perola Markus, Polasek Ozren, Porcu Eleonora, Rader Daniel J, Rathmann Wolfgang, Ripatti Samuli, Rocheleau Ghislain, Roden Michael, Rudan Igor, Salomaa Veikko, Saxena Richa, Schlessinger David, Schunkert Heribert, Schwarz Peter, Seedorf Udo, Selvin Elizabeth, Serrano-Ríos Manuel, Shrader Peter, Silveira Angela, Siscovick David, Song Kjioung, Spector Timothy D, Stefansson Kari, Steinthorsdottir Valgerdur, Strachan David P, Strawbridge Rona, Stumvoll Michael, Surakka Ida, Swift Amy J, Tanaka Toshiko, Teumer Alexander, Thorleifsson Gudmar, Thorsteinsdottir Unnur, Tönjes Anke, Usala Gianluca, Vitart Veronique, Völzke Henry, Wallaschofski Henri, Waterworth Dawn M, Watkins Hugh, Wichmann H-Erich, Wild Sarah H, Willemsen Gonneke, Williams Gordon H, Wilson James F, Winkelmann Juliane, Wright Alan F, , Zabena Carina, Zhao Jing Hua, Epstein Stephen E, Erdmann Jeanette, Hakonarson Hakon H, Kathiresan Sekar, Khaw Kay-Tee, Roberts Robert, Samani Nilesh J, Fleming Mark D, Sladek Robert, Abecasis Gonçalo, Boehnke Michael, Froguel Philippe, Groop Leif, McCarthy Mark I, Kao W H Linda, Florez Jose C, Uda Manuela, Wareham Nicholas J, Barroso Inês, Meigs James |
Case-control genome-wide association study of attention-deficit/hyperactivity disorder. Journal of the American Academy of Child and Adolescent Psychiatry 2010 Sep 49 (9): 906-20. Neale Benjamin M, Medland Sarah, Ripke Stephan, Anney Richard J L, Asherson Philip, Buitelaar Jan, Franke Barbara, Gill Michael, Kent Lindsey, Holmans Peter, Middleton Frank, Thapar Anita, Lesch Klaus-Peter, Faraone Stephen V, Daly Mark, Nguyen Thuy Trang, Schäfer Helmut, Steinhausen Hans-Christoph, Reif Andreas, Renner Tobias J, Romanos Marcel, Romanos Jasmin, Warnke Andreas, Walitza Susanne, Freitag Christine, Meyer Jobst, Palmason Haukur, Rothenberger Aribert, Hawi Ziarih, Sergeant Joseph, Roeyers Herbert, Mick Eric, Biederman Joseph, |
Studies of a genetic variant in HK1 in relation to quantitative metabolic traits and to the prevalence of type 2 diabetes. BMC medical genetics 2011 12 (1): 99. Gjesing Anette P, Nielsen Aneta A, Brandslund Ivan, Christensen Cramer, Sandbæk Anneli, Jørgensen Torben, Witte Daniel, Bonnefond Amélie, Froguel Phillippe, Hansen Torben, Pedersen Ol |
Race-ethnic differences in the association of genetic loci with HbA1c levels and mortality in U.S. adults: the third National Health and Nutrition Examination Survey (NHANES III). BMC medical genetics 2012 13 (1): 30. Grimsby Jonna L, Porneala Bianca C, Vassy Jason L, Yang Quanhe, Florez José C, Dupuis Josée, Liu Tiebin, Yesupriya Ajay, Chang Man-Huei, Ned Renee M, Dowling Nicole F, Khoury Muin J, Meigs James B, |
Family-based association study between SLC2A1, HK1, and LEPR polymorphisms with myelomeningocele in Chile. Reproductive sciences (Thousand Oaks, Calif.) 2013 Oct 20 (10): 1207-14. Suazo José, Pardo Rosa, Castillo Silvia, Martin Luz Maria, Rojas Francisca, Santos José Luis, Rotter Karin, Solar Margarita, Tapia E |
Association between maternal single nucleotide polymorphisms in genes regulating glucose metabolism and risk for neural tube defects in offspring. Birth defects research. Part A, Clinical and molecular teratology 2015 Jun 103 (6): 471-8. Fu Yunting, Wang Lin-lin, Yi Deqing, Jin Lei, Liu Jufen, Zhang Yali, Ren Aig |
Genome-wide association study identifies common loci influencing circulating glycated hemoglobin (HbA1c) levels in non-diabetic subjects: the Long Life Family Study (LLFS).
Metabolism: clinical and experimental 2014 Apr 63 (4): 461-8. An Ping, Miljkovic Iva, Thyagarajan Bharat, Kraja Aldi T, Daw E Warwick, Pankow James S, Selvin Elizabeth, Kao W H Linda, Maruthur Nisa M, Nalls Micahel A, Liu Yongmei, Harris Tamara B, Lee Joseph H, Borecki Ingrid B, Christensen Kaare, Eckfeldt John H, Mayeux Richard, Perls Thomas T, Newman Anne B, Province Michael |
c-Src phosphorylation and activation of hexokinase promotes tumorigenesis and metastasis. Nature communications 2017 1 8 13732. Zhang Jia, Wang Suili, Jiang Bin, Huang Lihong, Ji Zhiliang, Li Xiaotong, Zhou Huamin, Han Aidong, Chen Ai, Wu Yanan, Ma Huanhuan, Zhao Wentao, Zhao Qingwen, Xie Changchuan, Sun Xiaoyan, Zhou Yanming, Huang Huiying, Suleman Muhammad, Lin Furong, Zhou Lin, Tian Fang, Jin Meijun, Cai Yana, Zhang Nan, Li Qin |
mRNA Expression of SLC5A5 and SLC2A Family Genes in Papillary Thyroid Cancer: An Analysis of The Cancer Genome Atlas. Yonsei medical journal 2018 Aug 59 (6): 746-753. Suh Sunghwan, Kim Yun Hak, Goh Tae Sik, Jeong Dae Cheon, Lee Chi Seung, Jang Jeon Yeob, Cha Wonjae, Han Myoung Eun, Kim Seong Jang, Kim In Joo, Pak Kyoungju |
Associations of variants In the hexokinase 1 and interleukin 18 receptor regions with oxyhemoglobin saturation during sleep. PLoS genetics 2019 Apr 15 (4): e1007739. Cade Brian E, Chen Han, Stilp Adrienne M, Louie Tin, Ancoli-Israel Sonia, Arens Raanan, Barfield Richard, Below Jennifer E, Cai Jianwen, Conomos Matthew P, Evans Daniel S, Frazier-Wood Alexis C, Gharib Sina A, Gleason Kevin J, Gottlieb Daniel J, Hillman David R, Johnson W Craig, Lederer David J, Lee Jiwon, Loredo Jose S, Mei Hao, Mukherjee Sutapa, Patel Sanjay R, Post Wendy S, Purcell Shaun M, Ramos Alberto R, Reid Kathryn J, Rice Ken, Shah Neomi A, Sofer Tamar, Taylor Kent D, Thornton Timothy A, Wang Heming, Yaffe Kristine, Zee Phyllis C, Hanis Craig L, Palmer Lyle J, Rotter Jerome I, Stone Katie L, Tranah Gregory J, Wilson James G, Sunyaev Shamil R, Laurie Cathy C, Zhu Xiaofeng, Saxena Richa, Lin Xihong, Redline Sus |
An EGLN1 mutation may regulate hypoxic response in cyanotic congenital heart disease through the PHD2/HIF-1A pathway. Genes & diseases 2019 3 6 (1): 35-42. Zhou Yuanlin, Ouyang Na, Liu Lingjuan, Tian Jie, Huang Xupei, Lu Tiew |
Characterization of glycolysis-related gene expression in malignant melanoma. Pathology, research and practice 2019 12 216 (1): 152752. Koch Andreas, Ebert Eva Vanessa, Seitz Tatjana, Dietrich Peter, Berneburg Mark, Bosserhoff Anja, Hellerbrand Cla |
Condemned or Not to Die? Gene Polymorphisms Associated With Cell Death in Pemphigus Foliaceus. Frontiers in immunology 2019 10 2416. Bumiller-Bini Valéria, Cipolla Gabriel Adelman, Spadoni Mariana Basso, Augusto Danillo Gardenal, Petzl-Erler Maria Luiza, Beltrame Marcia Holsbach, Boldt Angelica Beate Wint |
Impact of Rare and Common Genetic Variants on Diabetes Diagnosis by Hemoglobin A1c in Multi-Ancestry Cohorts: The Trans-Omics for Precision Medicine Program. American journal of human genetics 2019 Oct 105 (4): 706-718. Sarnowski Chloé, Leong Aaron, Raffield Laura M, Wu Peitao, de Vries Paul S, DiCorpo Daniel, Guo Xiuqing, Xu Huichun, Liu Yongmei, Zheng Xiuwen, Hu Yao, Brody Jennifer A, Goodarzi Mark O, Hidalgo Bertha A, Highland Heather M, Jain Deepti, Liu Ching-Ti, Naik Rakhi P, O'Connell Jeffrey R, Perry James A, Porneala Bianca C, Selvin Elizabeth, Wessel Jennifer, Psaty Bruce M, Curran Joanne E, Peralta Juan M, Blangero John, Kooperberg Charles, Mathias Rasika, Johnson Andrew D, Reiner Alexander P, Mitchell Braxton D, Cupples L Adrienne, Vasan Ramachandran S, Correa Adolfo, Morrison Alanna C, Boerwinkle Eric, Rotter Jerome I, Rich Stephen S, Manning Alisa K, Dupuis Josée, Meigs James B, , , , |
Novel homozygous mutations in Pakistani families with Charcot-Marie-Tooth disease. BMC medical genomics 2021 7 14 (1): 174. Kanwal Sumaira, Choi Yu JIn, Lim Si On, Choi Hee Ji, Park Jin Hee, Nuzhat Rana, Khan Aneela, Perveen Shazia, Choi Byung-Ok, Chung Ki W |
Multiple-ancestry genome-wide association study identifies 27 loci associated with measures of hemolysis following blood storage.
The Journal of clinical investigation 2021 May . Page Grier P, Kanias Tamir, Guo Yuelong J, Lanteri Marion C, Zhang Xu, Mast Alan E, Cable Ritchard G, Spencer Bryan R, Kiss Joseph E, Fang Fang, Endres-Dighe Stacy M, Brambilla Donald, Nouraie Mehdi, Gordeuk Victor R, Kleinman Steve, Busch Michael P, Gladwin Mark T, |
Latent trait modeling of tau neuropathology in progressive supranuclear palsy.
Acta neuropathologica 2021 2 141 (5): 667-680. Kouri Naomi, Murray Melissa E, Reddy Joseph S, Serie Daniel J, Soto-Beasley Alexandra, Allen Mariet, Carrasquillo Minerva M, Wang Xue, Castanedes Monica Casey, Baker Matthew C, Rademakers Rosa, Uitti Ryan J, Graff-Radford Neill R, Wszolek Zbigniew K, Schellenberg Gerard D, Crook Julia E, Ertekin-Taner Nilüfer, Ross Owen A, Dickson Dennis |
Variants influencing age at diagnosis of HNF1A-MODY. Molecular medicine (Cambridge, Mass.) 2022 9 28 (1): 113. Ludwig-S?omczy?ska Agnieszka H, Seweryn Micha? T, Radkowski Piotr, Kapusta Przemys?aw, Machlowska Julita, Pruhova Stepanka, Gasperikova Daniela, Bellanne-Chantelot Christine, Hattersley Andrew, Kandasamy Balamurugan, Letourneau-Freiberg Lisa, Philipson Louis, Doria Alessandro, Wo?kow Pawe? P, Ma?ecki Maciej T, Klupa Toma |
Driving with retinitis pigmentosa. Ophthalmic genetics 2023 4 1-9. Heath Jeffery Rachael C, Lo Johnny, Thompson Jennifer A, Lamey Tina M, McLaren Terri L, DeRoach John N, Kabilio Miguel S, Chen Fred |
Genetic predisposition, lifestyle inflammation score, food-based dietary inflammatory index, and the risk for incident diabetes: Findings from the KoGES data. Nutrition, metabolism, and cardiovascular diseases : NMCD 2023 12 . Hye Ah Lee, Hyesook Park, Bomi Pa |
Metabolic heterogeneity in early-stage lung adenocarcinoma revealed by RNA-seq and scRNA-seq. Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico 2023 1 . Zhang Yang, Shi Jiang, Luo Junfang, Liu Cong, Zhu Li |
- Page last reviewed:Feb 1, 2024
- Page last updated:Apr 22, 2024
- Content source: