Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 61 Records) |
Query Trace: CUBN[original query] |
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Cubilin Single Nucleotide Polymorphism Variants are Associated with Macroangiopathy While a Matrix Metalloproteinase-9 Single Nucleotide Polymorphism Flip-Flop may Indicate Susceptibility of Diabetic Nephropathy in Type-2 Diabetic Patients. Nephron 2019 141 (3): 156-165. Albert Christian, Kube Johanna, Albert Annemarie, Schanze Denny, Zenker Martin, Mertens Peter |
A novel rare CUBN variant and three additional genes identified in Europeans with and without diabetes: results from an exome-wide association study of albuminuria.
Diabetologia 2019 02 62 (2): 292-305. Ahluwalia Tarunveer S, Schulz Christina-Alexandra, Waage Johannes, Skaaby Tea, Sandholm Niina, van Zuydam Natalie, Charmet Romain, Bork-Jensen Jette, Almgren Peter, Thuesen Betina H, Bedin Mathilda, Brandslund Ivan, Christensen Cramer K, Linneberg Allan, Ahlqvist Emma, Groop Per-Henrik, Hadjadj Samy, Tregouet David-Alexandre, Jørgensen Marit E, Grarup Niels, Pedersen Oluf, Simons Matias, Groop Leif, Orho-Melander Marju, McCarthy Mark I, Melander Olle, Rossing Peter, Kilpeläinen Tuomas O, Hansen Torb |
Vitamin D-Related Genes, Blood Vitamin D Levels and Colorectal Cancer Risk in Western European Populations. Nutrients 2019 Aug 11 (8): . Fedirko Veronika, Mandle Hannah B, Zhu Wanzhe, Hughes David J, Siddiq Afshan, Ferrari Pietro, Romieu Isabelle, Riboli Elio, Bueno-de-Mesquita Bas, van Duijnhoven Fränzel J B, Siersema Peter D, Tjønneland Anne, Olsen Anja, Perduca Vittorio, Carbonnel Franck, Boutron-Ruault Marie-Christine, Kühn Tilman, Johnson Theron, Krasimira Aleksandrova, Trichopoulou Antonia, Makrythanasis Periklis, Thanos Dimitris, Panico Salvatore, Krogh Vittorio, Sacerdote Carlotta, Skeie Guri, Weiderpass Elisabete, Colorado-Yohar Sandra, Sala Núria, Barricarte Aurelio, Sanchez Maria-Jose, Quirós Ramón, Amiano Pilar, Gylling Björn, Harlid Sophia, Perez-Cornago Aurora, Heath Alicia K, Tsilidis Konstantinos K, Aune Dagfinn, Freisling Heinz, Murphy Neil, Gunter Marc J, Jenab Maz |
Identification of 22 novel loci associated with urinary biomarkers of albumin, sodium, and potassium excretion.
Kidney international 2019 May 95 (5): 1197-1208. Zanetti Daniela, Rao Abhiram, Gustafsson Stefan, Assimes Themistocles L, Montgomery Stephen B, Ingelsson Er |
Exonic variants of genes related to the vitamin D signaling pathway in the families of familial multiple sclerosis using whole-exome next generation sequencing. Brain and behavior 2019 3 9 (4): e01272. Pytel Vanesa, Matías-Guiu Jordi A, Torre-Fuentes Laura, Montero-Escribano Paloma, Maietta Paolo, Botet Javier, Álvarez Sara, Gómez-Pinedo Ulises, Matías-Guiu Jor |
Not all proteinuria is created equal. The Journal of clinical investigation 2019 12 130 (1): 74-76. Beenken Andrew, Barasch Jonathan M, Gharavi Ali |
Association between CUBN gene variants, type 2 diabetes and vitamin D concentrations in an elderly Greek population. The Journal of steroid biochemistry and molecular biology 2019 11 198 105549. Tsekmekidou Xanthippi, Tsetsos Fotis, Koufakis Theocharis, Karras Spyridon N, Georgitsi Marianthi, Papanas Nikolaos, Papazoglou Dimitrios, Roumeliotis Athanasios, Panagoutsos Stylianos, Thodis Elias, Theodoridis Marios, Pasadakis Ploumis, Maltezos Eustratios, Paschou Peristera, Kotsa Kallio |
NF1 patient missense variants predict a role for ATM in modifying neurofibroma initiation. Acta neuropathologica 2019 10 139 (1): 157-174. Yu Yanan, Choi Kwangmin, Wu Jianqiang, Andreassen Paul R, Dexheimer Phillip J, Keddache Mehdi, Brems Hilde, Spinner Robert J, Cancelas Jose A, Martin Lisa J, Wallace Margaret R, Legius Eric, Vogel Kristine S, Ratner Nan |
A genome-wide association study implicates multiple mechanisms influencing raised urinary albumin-creatinine ratio.
Human molecular genetics 2019 Oct . Casanova Francesco, Tyrrell Jessica, Beaumont Robin N, Ji Yingjie, Jones Samuel E, Hattersley Andrew T, Weedon Michael N, Murray Anna, Shore Angela C, Frayling Timothy M, Wood Andrew |
Human C-terminal CUBN variants associate with chronic proteinuria and normal renal function. The Journal of clinical investigation 2019 10 130 (1): 335-344. Bedin Mathilda, Boyer Olivia, Servais Aude, Li Yong, Villoing-Gaudé Laure, Tête Marie-Josephe, Cambier Alexandra, Hogan Julien, Baudouin Veronique, Krid Saoussen, Bensman Albert, Lammens Florie, Louillet Ferielle, Ranchin Bruno, Vigneau Cecile, Bouteau Iseline, Isnard-Bagnis Corinne, Mache Christoph J, Schäfer Tobias, Pape Lars, Gödel Markus, Huber Tobias B, Benz Marcus, Klaus Günter, Hansen Matthias, Latta Kay, Gribouval Olivier, Morinière Vincent, Tournant Carole, Grohmann Maik, Kuhn Elisa, Wagner Timo, Bole-Feysot Christine, Jabot-Hanin Fabienne, Nitschké Patrick, Ahluwalia Tarunveer S, Köttgen Anna, Andersen Christian Brix Folsted, Bergmann Carsten, Antignac Corinne, Simons Mati |
Tuberculosis risk is associated with genetic polymorphisms in the LRP2, CUBN, and VDR genes. Genes & genomics 2020 8 42 (10): 1189-1196. Kim Sung-Soo, Lee Sang In, Jin Hyun-Seok, Park Sangju |
Variants in SNAI1, AMDHD1 and CUBN in vitamin D pathway genes are associated with breast cancer risk: a large-scale analysis of 14 GWASs in the DRIVE study. American journal of cancer research 2020 10 (7): 2160-2173. Wang Haijiao, Zhao Lingling, Liu Hongliang, Luo Sheng, Akinyemiju Tomi, Hwang Shelley, Wei Qing |
Smoking-by-genotype interaction in type 2 diabetes risk and fasting glucose. PloS one 2020 15 (5): e0230815. Wu Peitao, Rybin Denis, Bielak Lawrence F, Feitosa Mary F, Franceschini Nora, Li Yize, Lu Yingchang, Marten Jonathan, Musani Solomon K, Noordam Raymond, Raghavan Sridharan, Rose Lynda M, Schwander Karen, Smith Albert V, Tajuddin Salman M, Vojinovic Dina, Amin Najaf, Arnett Donna K, Bottinger Erwin P, Demirkan Ayse, Florez Jose C, Ghanbari Mohsen, Harris Tamara B, Launer Lenore J, Liu Jingmin, Liu Jun, Mook-Kanamori Dennis O, Murray Alison D, Nalls Mike A, Peyser Patricia A, Uitterlinden André G, Voortman Trudy, Bouchard Claude, Chasman Daniel, Correa Adolfo, de Mutsert Renée, Evans Michele K, Gudnason Vilmundur, Hayward Caroline, Kao Linda, Kardia Sharon L R, Kooperberg Charles, Loos Ruth J F, Province Michael M, Rankinen Tuomo, Redline Susan, Ridker Paul M, Rotter Jerome I, Siscovick David, Smith Blair H, van Duijn Cornelia, Zonderman Alan B, Rao D C, Wilson James G, Dupuis Josée, Meigs James B, Liu Ching-Ti, Vassy Jason |
Genetic Variability in the Iron Homeostasis Pathway and Patient Outcomes After Aneurysmal Subarachnoid Hemorrhage. Neurocritical care 2020 Apr . Heinsberg Lacey W, Alexander Sheila A, Crago Elizabeth A, Minster Ryan L, Poloyac Samuel M, Weeks Daniel E, Conley Yvette |
Novel CUBN Mutation in a Young Child With Megaloblastic Anemia. Journal of pediatric hematology/oncology 2020 10 43 (4): e546-e549. Falcon Corey, Hamm Austin J, Li Geling, Lebensburger Jeffrey, Howard Thomas H, Xavier Ana |
A study of associations between CUBN, HNF1A, and LIPC gene polymorphisms and coronary artery disease. Scientific reports 2020 10 10 (1): 16294. Park Han Sung, Kim In Jai, Kim Eun Gyo, Ryu Chang Soo, Lee Jeong Yong, Ko Eun Ju, Park Hyeon Woo, Sung Jung Hoon, Kim Nam Ke |
Genetic Analyses in Dent Disease and Characterization of CLCN5 Mutations in Kidney Biopsies. International journal of molecular sciences 2020 1 21 (2): . Gianesello Lisa, Ceol Monica, Bertoldi Loris, Terrin Liliana, Priante Giovanna, Murer Luisa, Peruzzi Licia, Giordano Mario, Paglialonga Fabio, Cantaluppi Vincenzo, Musetti Claudio, Valle Giorgio, Del Prete Dorella, Anglani Franca, Network Dent Disease Itali |
Whole-Exome Sequencing for Identification of Genetic Variants Involved in Vitamin D Metabolic Pathways in Families With Vitamin D Deficiency in Saudi Arabia. Frontiers in genetics 2021 6 12 677780. Alharazy Shatha, Naseer Muhammad Imran, Alissa Eman, Robertson Margaret Denise, Lanham-New Susan, Chaudhary Adeel |
Identification of recurrent variants implicated in disease in bicuspid aortic valve patients through whole-exome sequencing. Human genomics 2022 09 16 (1): 36. Chen Shasha, Jin Qinchun, Hou Shiqiang, Li Mingfei, Zhang Yuan, Guan Lihua, Pan Wenzhi, Ge Junbo, Zhou Dax |
Genetic Variants in Folate and Cobalamin Metabolism-Related Genes in Pregnant Women of a Homogeneous Spanish Population: The Need for Revisiting the Current Vitamin Supplementation Strategies. Nutrients 2022 Jun 14 (13): . Rodriguez-Carnero Gemma, Lorenzo Paula M, Canton-Blanco Ana, Mendizabal Leire, Arregi Maddi, Zulueta Mirella, Simon Laureano, Macia-Cortiñas Manuel, Casanueva Felipe F, Crujeiras Ana |
Molecular Genetic Testing for Kidney Disorders During the COVID-19 Pandemic. Delaware journal of public health 2022 5 7 (5): 24-27. Kirwin Susan M, Robbins Katherine M, Vinette Kathleen M B, Hirata Lee, Gripp Karen W, Funanage Vicky |
Vitamin B12 Transport Genes and Nonsyndromic Cleft Lip With or Without Cleft Palate in Chile. Reproductive sciences (Thousand Oaks, Calif.) 2022 4 29 (10): 2921-2926. Suazo José, Salamanca Carlos, Cáceres-Rojas Gabriela, González-Hormazábal Patricio, Pantoja Roberto, Leiva Noemi, Pardo Ro |
Vitamin B-related Gene Polymorphisms and Cardiovascular Disease. Endocrine, metabolic & immune disorders drug targets 2022 3 22 (10): 979-984. Katsa Maria Efthymia, Gil Andrea Paola Roj |
Vitamin D pathway gene variation rs3740165 is associated with serological uric acid levels in healthy Chinese women. Frontiers in endocrinology 2022 12 13 1059964. Gu Jiemei, Yue Hua, Wang Chun, Zhang Hao, Hu Weiwei, Zhang Zhenl |
Vitamin D-Related Genes and Thyroid Cancer-A Systematic Review. International journal of molecular sciences 2022 11 23 (21): . Maciejewski Adam, Lacka Katarzy |
Clinical relevance of vitamin B12 level and vitamin B12 metabolic gene variation in pulmonary tuberculosis. Frontiers in immunology 2022 13 947897. Zhang Tian-Ping, Li Rui, Wang Li-Jun, Tang Fei, Li Hong-Mi |
Genomic analyses reveal SCN7A is associated with the prognosis of esophageal squamous cell carcinoma. Esophagus : official journal of the Japan Esophageal Society 2022 1 19 (2): 303-315. Yuan Ping, Rao Wenqing, Lin Zheng, Liu Shuang, Lin Xiuquan, Wu Chaofeng, Lin Xu, Hu Zhijian, Ye Weim |
Albuminuria-Related Genetic Biomarkers: Replication and Predictive Evaluation in Individuals with and without Diabetes from the UK Biobank. International journal of molecular sciences 2023 7 24 (13): . Marisa Cañadas-Garre, Andrew T Kunzmann, Kerry Anderson, Eoin P Brennan, Ross Doyle, Christopher C Patterson, Catherine Godson, Alexander P Maxwell, Amy Jayne McKnig |
Four missense genetic variants in CUBN are associated with higher levels of eGFR in non-diabetes but not in diabetes mellitus or its subtypes: A genetic association study in Europeans. Frontiers in endocrinology 2023 3 14 1081741. Uglebjerg Nicoline, Ahmadizar Fariba, Aly Dina M, Cañadas-Garre Marisa, Hill Claire, Naber Annemieke, Oddsson Asmundur, Singh Sunny S, Smyth Laura, Trégouët David-Alexandre, Chaker Layal, Ghanbari Mohsen, Steinthorsdottir Valgerdur, Ahlqvist Emma, Hadjadj Samy, Van Hoek Mandy, Kavousi Maryam, McKnight Amy Jayne, Sijbrands Eric J, Stefansson Kari, Simons Matias, Rossing Peter, Ahluwalia Tarunveer |
Polymorphisms in LRP2 and CUBN genes and their association with serum vitamin D levels and sleep apnea. Sleep & breathing = Schlaf & Atmung 2023 11 . Dimitra Anatolou, Paschalis Steiropoulos, Athanasios Zissimopoulos, Konstantina Chadia, Kostas Archontogeorgis, George Kolios, Vangelis G Manolopoulos, Georgia Rag |
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- Page last updated:Apr 16, 2024
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