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Jun 15, 2014 (publication date) through Apr 20, 2024
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World Journal of Diabetes
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1948-9358
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Baishideng Publishing Group Inc, 7041 Koll Center Parkway, Suite 160, Pleasanton, CA 94566, USA
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Auburger G, Gispert S, Lahut S, Ömür &, Damrath E, Heck M, Başak N. 12q24 locus association with type 1 diabetes: |
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| URL: | https://www.wjgnet.com/1948-9358/full/v5/i3/316.htm |
| Number | Citing Articles |
| 1 |
Evridiki-Pandora G. Tsare, Maria I. Klapa, Nicholas K. Moschonas. Protein–protein interaction network-based integration of GWAS and functional data for blood pressure regulation analysis. Human Genomics 2024; 18(1) doi: 10.1186/s40246-023-00565-6
|
| 2 |
Varun Alur, Varshita Raju, Basavaraj Vastrad, Anandkumar Tengli, Chanabasayya Vastrad, Shivakumar Kotturshetti. Integrated bioinformatics analysis reveals novel key biomarkers and potential candidate small molecule drugs in gestational diabetes mellitus. Bioscience Reports 2021; 41(5) doi: 10.1042/BSR20210617
|
| 3 |
Feifei Yu, Yibin Guo, Hao Wang, Jian Feng, Zhichao Jin, Qi Chen, Yu Liu, Jia He. Type 2 diabetes mellitus and risk of colorectal adenoma: a meta-analysis of observational studies. BMC Cancer 2016; 16(1) doi: 10.1186/s12885-016-2685-3
|
| 4 |
Melanie Vanessa Halbach, Tanja Stehning, Ewa Damrath, Marina Jendrach, Nesli Ece Şen, A. Nazlı Başak, Georg Auburger, David R Borchelt. Both Ubiquitin Ligases FBXW8 and PARK2 Are Sequestrated into Insolubility by ATXN2 PolyQ Expansions, but Only FBXW8 Expression Is Dysregulated. PLOS ONE 2015; 10(3): e0121089 doi: 10.1371/journal.pone.0121089
|
| 5 |
Meihua Hao, Feng Yuan, Chenchen Jin, Zehong Zhou, Qi Cao, Ling Xu, Guanlei Wang, Hui Huang, Dongzi Yang, Meiqing Xie, Xiaomiao Zhao. Overexpression of Lnk in the Ovaries Is Involved in Insulin Resistance in Women With Polycystic Ovary Syndrome. Endocrinology 2016; 157(10): 3709 doi: 10.1210/en.2016-1234
|
| 6 |
Marten Hansen, Sabrina Zeddies, Marjolein Meinders, Franca di Summa, Ewa Rollmann, Floris P.J. van Alphen, Arjan J. Hoogendijk, Kat S. Moore, Melanie Halbach, Laura Gutiérrez, Maartje van den Biggelaar, Daphne C. Thijssen-Timmer, Georg W.J. Auburger, Emile van den Akker, Marieke von Lindern. The RNA-Binding Protein ATXN2 is Expressed during Megakaryopoiesis and May Control Timing of Gene Expression. International Journal of Molecular Sciences 2020; 21(3): 967 doi: 10.3390/ijms21030967
|
| 7 |
Daniel Z. Bar, Chayki Charar, Yosef Gruenbaum. Small GTPases in C. elegans metabolism. Small GTPases 2018; 9(5): 415 doi: 10.1080/21541248.2016.1247940
|
| 8 |
Baby Kumari, Pankaj Singh Dholaniya. Parkinson's disease gene prioritising using an efficient and biologically appropriate network-based consensus strategy. Journal of Computational Science 2022; 65: 101879 doi: 10.1016/j.jocs.2022.101879
|
| 9 |
Helen Ye Rim Huang, Andrew Awuah Wireko, Goshen David Miteu, Adan Khan, Sakshi Roy, Tomas Ferreira, Tulika Garg, Narjiss Aji, Faaraea Haroon, Farida Zakariya, Yasir Alshareefy, Anushka Gurunath Pujari, Djabir Madani, Marios Papadakis. Advancements and progress in juvenile idiopathic arthritis: A Review of pathophysiology and treatment. Medicine 2024; 103(13): e37567 doi: 10.1097/MD.0000000000037567
|
| 10 |
Boram Park, Eun Choe, Hae Kang, Eunsoon Shin, Sangwoo Lee, Sungho Won. Genetic Polymorphisms Associated with the Neutrophil–Lymphocyte Ratio and Their Clinical Implications for Metabolic Risk Factors. Journal of Clinical Medicine 2018; 7(8): 204 doi: 10.3390/jcm7080204
|
| 11 |
William B Horton, Jeremy S Taylor, Timothy J Ragland, Angela R Subauste. Diabetic muscle infarction: a systematic review. BMJ Open Diabetes Research & Care 2015; 3(1): e000082 doi: 10.1136/bmjdrc-2015-000082
|
| 12 |
Nesli E. Sen, Suzana Gispert, Georg Auburger. PINK1 and Ataxin-2 as modifiers of growth. Oncotarget 2017; 8(20): 32382 doi: 10.18632/oncotarget.16636
|
| 13 |
Hakeem Gh. Hassan, Arwa M. Al-Shuwaikh, Raid K.D. Al-Auqili. Evaluation of possible association of interferon-induced helicase (IFIH1) gene polymorphism with type one diabetes mellitus in a sample of Iraqi children. Human Gene 2022; 33: 201064 doi: 10.1016/j.humgen.2022.201064
|
| 14 |
Henning Jansen, Christina Willenborg, Sabrina Schlesinger, Paola G. Ferrario, Inke R. König, Jeanette Erdmann, Nilesh J. Samani, Wolfgang Lieb, Heribert Schunkert. Genetic variants associated with celiac disease and the risk for coronary artery disease. Molecular Genetics and Genomics 2015; 290(5): 1911 doi: 10.1007/s00438-015-1045-3
|
| 15 |
Daniel Z. Bar, Chayki Charar, Jehudith Dorfman, Tam Yadid, Lionel Tafforeau, Denis L. J. Lafontaine, Yosef Gruenbaum.
Cell size and fat content of dietary-restricted
Caenorhabditis elegans
are regulated by ATX-2, an mTOR repressor
. Proceedings of the National Academy of Sciences 2016; 113(32) doi: 10.1073/pnas.1512156113
|
| 16 |
Hongxiao Jiao, Miaomiao Zhang, Yuan Zhang, Yaogang Wang, Wei-Dong Li. Pathway Association Studies Reveal Gene Loci and Pathway Networks that Associated With Plasma Cystatin C Levels. Frontiers in Genetics 2021; 12 doi: 10.3389/fgene.2021.711155
|
| 17 |
N Maslah, B Cassinat, E Verger, J-J Kiladjian, L Velazquez. The role of LNK/SH2B3 genetic alterations in myeloproliferative neoplasms and other hematological disorders. Leukemia 2017; 31(8): 1661 doi: 10.1038/leu.2017.139
|
| 18 |
Júlia Canet-Pons, Nesli-Ece Sen, Aleksandar Arsović, Luis-Enrique Almaguer-Mederos, Melanie V. Halbach, Jana Key, Claudia Döring, Anja Kerksiek, Gina Picchiarelli, Raphaelle Cassel, Frédérique René, Stéphane Dieterlé, Nina V. Fuchs, Renate König, Luc Dupuis, Dieter Lütjohann, Suzana Gispert, Georg Auburger. Atxn2-CAG100-KnockIn mouse spinal cord shows progressive TDP43 pathology associated with cholesterol biosynthesis suppression. Neurobiology of Disease 2021; 152: 105289 doi: 10.1016/j.nbd.2021.105289
|
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David Meierhofer, Melanie Halbach, Nesli Ece Şen, Suzana Gispert, Georg Auburger. Ataxin-2 (Atxn2)-Knock-Out Mice Show Branched Chain Amino Acids and Fatty Acids Pathway Alterations. Molecular & Cellular Proteomics 2016; 15(5): 1728 doi: 10.1074/mcp.M115.056770
|
| 20 |
Jose S. Subauste, Angela Subauste. Diabetes Mellitus. 2020; : 275 doi: 10.1016/B978-0-12-820605-8.00013-9
|
| 21 |
Krishna Gundabolu, Bhavana J. Dave, Carmelita J. Alvares, Jeffrey J. Cannatella, Vijaya R. Bhatt, Lori J. Maness, Zaid S. Al-Kadhimi, Rana K. Zabad, Allison M. Cushman-Vokoun, Balraj Mittal. The Missing LNK: Evolution from Cytosis to Chronic Myelomonocytic Leukemia in a Patient with Multiple Sclerosis and Germline SH2B3 Mutation. Case Reports in Genetics 2022; 2022: 1 doi: 10.1155/2022/6977041
|
| 22 |
Omar I. Saadah, Noor Ahmad Shaik, Babajan Banaganapalli, Mohammed A. Salama, Sameer E. Al-Harthi, Jun Wang, Harbi A. Shawoosh, Sharifa A. Alghamdi, Yagoub Y. Bin-Taleb, Bakr H. Alhussaini, Ramu Elango, Jumana Y. Al-Aama. Replication of GWAS Coding SNPs Implicates MMEL1 as a Potential Susceptibility Locus among Saudi Arabian Celiac Disease Patients. Disease Markers 2015; 2015: 1 doi: 10.1155/2015/351673
|
| 23 |
Fateme Rajabi, Fahimeh Abdollahimajd, Navid Jabalameli, Mansour Nassiri Kashani, Alireza Firooz. The Immunogenetics of Dermatologic Diseases. Advances in Experimental Medicine and Biology 2022; 1367: 19 doi: 10.1007/978-3-030-92616-8_2
|
| 24 |
Kostas Kakleas, Alexandra Soldatou, Feneli Karachaliou, Kyriaki Karavanaki. Associated autoimmune diseases in children and adolescents with type 1 diabetes mellitus (T1DM). Autoimmunity Reviews 2015; 14(9): 781 doi: 10.1016/j.autrev.2015.05.002
|
| 25 |
Gunnar Seidel, David Meierhofer, Nesli-Ece Şen, Anika Guenther, Sylvia Krobitsch, Georg Auburger. Quantitative Global Proteomics of Yeast PBP1 Deletion Mutants and Their Stress Responses Identifies Glucose Metabolism, Mitochondrial, and Stress Granule Changes. Journal of Proteome Research 2017; 16(2): 504 doi: 10.1021/acs.jproteome.6b00647
|
| 26 |
Rosario Vasta, Fabrizio D’Ovidio, Giancarlo Logroscino, Adriano Chiò. The links between diabetes mellitus and amyotrophic lateral sclerosis. Neurological Sciences 2021; 42(4): 1377 doi: 10.1007/s10072-021-05099-0
|
| 27 |
Sara Carmo-Silva, Clevio Nobrega, Luís Pereira de Almeida, Claudia Cavadas. Unraveling the Role of Ataxin-2 in Metabolism. Trends in Endocrinology & Metabolism 2017; 28(4): 309 doi: 10.1016/j.tem.2016.12.006
|
| 28 |
Sara Carmo-Silva, Marisa Ferreira-Marques, Clévio Nóbrega, Mariana Botelho, Daniela Costa, Célia A Aveleira, Stefan M Pulst, Luís Pereira de Almeida, Claudia Cavadas. Ataxin-2 in the hypothalamus at the crossroads between metabolism and clock genes. Journal of Molecular Endocrinology 2023; 70(1) doi: 10.1530/JME-21-0272
|
| 29 |
Clara Albiñana, Zhihong Zhu, Nis Borbye-Lorenzen, Sanne Grundvad Boelt, Arieh S. Cohen, Kristin Skogstrand, Naomi R. Wray, Joana A. Revez, Florian Privé, Liselotte V. Petersen, Cynthia M. Bulik, Oleguer Plana-Ripoll, Katherine L. Musliner, Esben Agerbo, Anders D. Børglum, David M. Hougaard, Merete Nordentoft, Thomas Werge, Preben Bo Mortensen, Bjarni J. Vilhjálmsson, John J. McGrath. Genetic correlates of vitamin D-binding protein and 25-hydroxyvitamin D in neonatal dried blood spots. Nature Communications 2023; 14(1) doi: 10.1038/s41467-023-36392-5
|
| 30 |
Luka Brčić, Ana Barić, Sanda Gračan, Dubravka Brdar, Vesela Torlak Lovrić, Nikolina Vidan, Tatijana Zemunik, Ozren Polašek, Maja Barbalić, Ante Punda, Vesna Boraska Perica. Association of established thyroid peroxidase autoantibody (TPOAb) genetic variants with Hashimoto’s thyroiditis. Autoimmunity 2016; 49(7): 480 doi: 10.1080/08916934.2016.1191475
|
| 31 |
Mette K. Andersen. New Insights into the Genetics of Latent Autoimmune Diabetes in Adults. Current Diabetes Reports 2020; 20(9) doi: 10.1007/s11892-020-01330-y
|
| 32 |
Roberto Rodríguez‐Labrada, Luis Velázquez‐Pérez, Georg Auburger, Ulf Ziemann, Nalia Canales‐Ochoa, Jacqueline Medrano‐Montero, Yaimeé Vázquez‐Mojena, Yanetza González‐Zaldivar. Spinocerebellar ataxia type 2: Measures of saccade changes improve power for clinical trials. Movement Disorders 2016; 31(4): 570 doi: 10.1002/mds.26532
|
| 33 |
Melanie Vanessa Halbach, Suzana Gispert, Tanja Stehning, Ewa Damrath, Michael Walter, Georg Auburger. Atxn2 Knockout and CAG42-Knock-in Cerebellum Shows Similarly Dysregulated Expression in Calcium Homeostasis Pathway. The Cerebellum 2017; 16(1): 68 doi: 10.1007/s12311-016-0762-4
|
| 34 |
Nesli-Ece Sen, Júlia Canet-Pons, Melanie V. Halbach, Aleksandar Arsovic, Ulrich Pilatus, Woon-Hyung Chae, Zeynep-Ece Kaya, Kay Seidel, Ewa Rollmann, Michel Mittelbronn, David Meierhofer, Chris I. De Zeeuw, Laurens W.J. Bosman, Suzana Gispert, Georg Auburger. Generation of an Atxn2-CAG100 knock-in mouse reveals N-acetylaspartate production deficit due to early Nat8l dysregulation. Neurobiology of Disease 2019; 132: 104559 doi: 10.1016/j.nbd.2019.104559
|
| 35 |
Isabel Lastres-Becker, David Nonis, Florian Eich, Michael Klinkenberg, Myriam Gorospe, Peter Kötter, Fabrice A.C. Klein, Nancy Kedersha, Georg Auburger. Mammalian ataxin-2 modulates translation control at the pre-initiation complex via PI3K/mTOR and is induced by starvation. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease 2016; 1862(9): 1558 doi: 10.1016/j.bbadis.2016.05.017
|
| 36 |
Pablo Librado, Ludovic Orlando, Ryan Hernandez. Detecting Signatures of Positive Selection along Defined Branches of a Population Tree Using LSD. Molecular Biology and Evolution 2018; 35(6): 1520 doi: 10.1093/molbev/msy053
|
| 37 |
Nesli Ece Sen, Jessica Drost, Suzana Gispert, Sylvia Torres-Odio, Ewa Damrath, Michael Klinkenberg, Hamid Hamzeiy, Gülden Akdal, Halil Güllüoğlu, A. Nazlı Başak, Georg Auburger. Search for SCA2 blood RNA biomarkers highlights Ataxin-2 as strong modifier of the mitochondrial factor PINK1 levels. Neurobiology of Disease 2016; 96: 115 doi: 10.1016/j.nbd.2016.09.002
|
| 38 |
Elina Misicka, Mary F Davis, Woori Kim, Steven W Brugger, Jeremy Beales, Stephanie Loomis, Paola G Bronson, Farren BS Briggs. A higher burden of multiple sclerosis genetic risk confers an earlier onset. Multiple Sclerosis Journal 2022; 28(8): 1189 doi: 10.1177/13524585211053155
|
| 39 |
G Davies, R E Marioni, D C Liewald, W D Hill, S P Hagenaars, S E Harris, S J Ritchie, M Luciano, C Fawns-Ritchie, D Lyall, B Cullen, S R Cox, C Hayward, D J Porteous, J Evans, A M McIntosh, J Gallacher, N Craddock, J P Pell, D J Smith, C R Gale, I J Deary. Genome-wide association study of cognitive functions and educational attainment in UK Biobank (N=112 151). Molecular Psychiatry 2016; 21(6): 758 doi: 10.1038/mp.2016.45
|
| 40 |
In Human and Mouse Spino-Cerebellar Tissue, Ataxin-2 Expansion Affects Ceramide-Sphingomyelin Metabolism. International Journal of Molecular Sciences 2019; 20(23): 5854 doi: 10.3390/ijms20235854
|
| 41 |
Daniel Eriksson, Ellen Christine Røyrvik, Maribel Aranda-Guillén, Amund Holte Berger, Nils Landegren, Haydee Artaza, Åsa Hallgren, Marianne Aardal Grytaas, Sara Ström, Eirik Bratland, Ileana Ruxandra Botusan, Bergithe Eikeland Oftedal, Lars Breivik, Marc Vaudel, Øyvind Helgeland, Alberto Falorni, Anders Palmstrøm Jørgensen, Anna-Lena Hulting, Johan Svartberg, Olov Ekwall, Kristian Johan Fougner, Jeanette Wahlberg, Bjørn Gunnar Nedrebø, Per Dahlqvist, Helge Ræder, Nevena Jovanovic, Sigfrid Christine Reisegg, Geir Hølleland, Siri Carlsen, Tore Julsrud Berg, Jan Bertil Eggesbø, Thomas Svendsen, Kari Lima, Ingrid Nermoen, Rolf Whitfield, Stina Sollid, Dagfinn Aarskog, Elin Korsgaard, Solveig Sæta, Trine Finnes, Susanna Fonneland Valland, Christian Fossum, Eli Brevik, Ragnar Bekkhus Moe, Margrethe Svendsen, Aleksandra Debowska, Petya Milova, Synnøve Holte, Aneta Eva Tomkowicz, Dag Eirik Sørmo, Anders Svare, Marthe Landsverk Rensvik, Randi Revheim, Thor Haug, Ivar Blix, Lars Petter Jensen, Anna-Karin Åkerman, Anna-Lena Hulting, Bengt Lindberg, Berit Kriström, Erik Waldenström, Gudmundur Johannsson, Jakob Skov, Jeanette Wahlberg, Karel Duchen, Magnus Isaksson, Maria Elfving, Maria Halldin Stenlid, Ola Nilsson, Olle Kämpe, Olov Ekwall, Per Dahlqvist, Ragnhildur Bergthorsdottir, Ricard Nergårdh, Sigridur Björnsdottir, Sophie Bensing, Tommy Olsson, Per Morten Knappskog, Anette Susanne Bøe Wolff, Sophie Bensing, Stefan Johansson, Olle Kämpe, Eystein Sverre Husebye. GWAS for autoimmune Addison’s disease identifies multiple risk loci and highlights AIRE in disease susceptibility. Nature Communications 2021; 12(1) doi: 10.1038/s41467-021-21015-8
|
| 42 |
Helmut Schaschl, Tobias Göllner, David L. Morris. Positive selection acts on regulatory genetic variants in populations of European ancestry that affect ALDH2 gene expression. Scientific Reports 2022; 12(1) doi: 10.1038/s41598-022-08588-0
|
| 43 |
Aleksandra Krzewska, Iwona Ben-Skowronek. Effect of Associated Autoimmune Diseases on Type 1 Diabetes Mellitus Incidence and Metabolic Control in Children and Adolescents. BioMed Research International 2016; 2016: 1 doi: 10.1155/2016/6219730
|
| 44 |
L. J. Smyth, J. Kilner, V. Nair, H. Liu, E. Brennan, K. Kerr, N. Sandholm, J. Cole, E. Dahlström, A. Syreeni, R. M. Salem, R. G. Nelson, H. C. Looker, C. Wooster, K. Anderson, G. J. McKay, F. Kee, I. Young, D. Andrews, C. Forsblom, J. N. Hirschhorn, C. Godson, P. H. Groop, A. P. Maxwell, K. Susztak, M. Kretzler, J. C. Florez, A. J. McKnight. Assessment of differentially methylated loci in individuals with end-stage kidney disease attributed to diabetic kidney disease: an exploratory study. Clinical Epigenetics 2021; 13(1) doi: 10.1186/s13148-021-01081-x
|
| 45 |
A. Barić, L. Brčić, S. Gračan, V. Torlak Lovrić, I. Gunjača, M. Šimunac, M. Brekalo, M. Boban, O. Polašek, M. Barbalić, T. Zemunik, A. Punda, V. Boraska Perica. Association of established hypothyroidism-associated genetic variants with Hashimoto’s thyroiditis. Journal of Endocrinological Investigation 2017; 40(10): 1061 doi: 10.1007/s40618-017-0660-8
|
| 46 |
Georg Auburger, Nesli-Ece Sen, David Meierhofer, Ayşe-Nazlı Başak, Aaron D. Gitler. Efficient Prevention of Neurodegenerative Diseases by Depletion of Starvation Response Factor Ataxin-2. Trends in Neurosciences 2017; 40(8): 507 doi: 10.1016/j.tins.2017.06.004
|
| 47 |
Jennie Vagher, Luke Maese, Amanda Gammon, Wendy Kohlmann, Joshua D. Schiffman. The Hereditary Basis of Childhood Cancer. 2021; : 315 doi: 10.1007/978-3-030-74448-9_11
|
| 48 |
João M. Da Conceição Alves-Cruzeiro, Liliana Mendonça, Luís Pereira de Almeida, Clévio Nóbrega. Motor Dysfunctions and Neuropathology in Mouse Models of Spinocerebellar Ataxia Type 2: A Comprehensive Review. Frontiers in Neuroscience 2016; 10 doi: 10.3389/fnins.2016.00572
|