Human Genome Epidemiology Literature Finder
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Records 1 - 27 (of 27 Records) |
| Query Trace: Disease and PTPRD[original query] |
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| Identification of ZNF366 and PTPRD as novel determinants of plasma homocysteine in a family-based genome-wide association study. Blood 2009 Aug 114 (7): 1417-22. Mälarstig Anders, Buil Alfonso, Souto Juan Carolos, Clarke Robert, Blanco-Vaca Francisco, Fontcuberta Jordi, Peden John, Andersen Malin, Silveira Angela, Barlera Simona, Seedorf Udo, Watkins Hugh, Almasy Laura, Hamsten Anders, Soria José Manuel, |
Genome-wide association and meta-analysis in populations from Starr County, Texas, and Mexico City identify type 2 diabetes susceptibility loci and enrichment for expression quantitative trait loci in top signals.
Diabetologia 2011 Aug 54 (8): 2047-55. Below J E, Gamazon E R, Morrison J V, Konkashbaev A, Pluzhnikov A, McKeigue P M, Parra E J, Elbein S C, Hallman D M, Nicolae D L, Bell G I, Cruz M, Cox N J, Hanis C |
| MEIS1 and BTBD9: genetic association with restless leg syndrome in end stage renal disease. Journal of medical genetics 2011 Jul 48 (7): 462-6. Schormair Barbara, Plag Jens, Kaffe Maria, Gross Nadine, Czamara Darina, Samtleben Walter, Lichtner Peter, Ströhle Andreas, Stefanidis Ioannis, Vainas Andreas, Dardiotis Efthimios, Sakkas George K, Gieger Christian, Müller-Myhsok Bertram, Meitinger Thomas, Heemann Uwe, Hadjigeorgiou Georgios M, Oexle Konrad, Winkelmann Julia |
| Large scale association analysis identifies three susceptibility loci for coronary artery disease. PloS one 2011 6 (12): e29427. Saade Stephanie, Cazier Jean-Baptiste, Ghassibe-Sabbagh Michella, Youhanna Sonia, Badro Danielle A, Kamatani Yoichiro, Hager Jörg, Yeretzian Joumana S, El-Khazen Georges, Haber Marc, Salloum Angelique K, Douaihy Bouchra, Othman Raed, Shasha Nabil, Kabbani Samer, Bayeh Hamid El, Chammas Elie, Farrall Martin, Gauguier Dominique, Platt Daniel E, Zalloua Pierre A, |
| Association of restless legs syndrome variants in Korean patients with restless legs syndrome. Sleep 2013 Dec 36 (12): 1787-91. Kim Myeong-Kyu, Cho Yong Won, Shin Won Chul, Cho Jae Wook, Shon Young Min, Kim Jee Hyun, Yang Kwang Ik, Earley Christopher J, Allen Richard |
| Association of candidate genetic variants with restless legs syndrome in end stage renal disease: a multicenter case-control study in Taiwan. European journal of neurology : the official journal of the European Federation of Neurological Societies 2014 Mar 21 (3): 492-8. Lin C H, Chen M L, Wu V C, Li W Y, Sy H N, Wu S L, Chang C C, Chiu P F, Liou H H, Lin C Y, Chang H W, Lin S Y, Wu K D, Chen Y M, Wu R |
| Analysis of functional GLO1 variants in the BTBD9 locus and restless legs syndrome. Sleep medicine 2015 Sep 16 (9): 1151-5. Gan-Or Ziv, Zhou Sirui, Ambalavanan Amirthagowri, Leblond Claire S, Xie Pingxing, Johnson Amelie, Spiegelman Dan, Allen Richard P, Earley Christopher J, Desautels Alex, Montplaisir Jacques Y, Dion Patrick A, Xiong Lan, Rouleau Guy |
| CNV Analysis Associates AKNAD1 with Type-2 Diabetes in Jordan Subpopulations. Scientific reports 2015 5 13391. Dajani Rana, Li Jin, Wei Zhi, Glessner Joseph T, Chang Xiao, Cardinale Christopher J, Pellegrino Renata, Wang Tiancheng, Hakooz Nancy, Khader Yousef, Sheshani Amina, Zandaki Duaa, Hakonarson Hak |
| Genetic markers of Restless Legs Syndrome in Parkinson disease. Parkinsonism & related disorders 2015 Jun 21 (6): 582-5. Gan-Or Ziv, Alcalay Roy N, Bar-Shira Anat, Leblond Claire S, Postuma Ronald B, Ben-Shachar Shay, Waters Cheryl, Johnson Amelie, Levy Oren, Mirelman Anat, Gana-Weisz Mali, Dupré Nicolas, Montplaisir Jacques, Giladi Nir, Fahn Stanley, Xiong Lan, Dion Patrick A, Orr-Urtreger Avi, Rouleau Guy |
| 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 |
| Air pollution and diabetes association: Modification by type 2 diabetes genetic risk score. Environment international 2016 Jun 94 263-271. Eze Ikenna C, Imboden Medea, Kumar Ashish, von Eckardstein Arnold, Stolz Daiana, Gerbase Margaret W, Künzli Nino, Pons Marco, Kronenberg Florian, Schindler Christian, Probst-Hensch Nico |
| Prognostic Value of TERT Alterations, Mutational and Copy Number Alterations Burden in Urothelial Carcinoma. European urology focus 2017 Aug . Isharwal Sumit, Audenet François, Drill Esther, Pietzak Eugene J, Iyer Gopa, Ostrovnaya Irina, Cha Eugene, Donahue Timothy, Arcila Maria, Jayakumaran Gowtham, Berger Michael F, Rosenberg Jonathan E, Bajorin Dean F, Coleman Jonathan, Dalbagni Guido, Reuter Victor E, Bochner Bernard H, Solit David B, Al-Ahmadie Hikmat |
| Polymorphism of receptor-type tyrosine-protein phosphatase delta gene in the development of non-alcoholic fatty liver disease. Journal of gastroenterology and hepatology 2017 May . Nakajima Shunsuke, Tanaka Hiroki, Sawada Koji, Hayashi Hidemi, Hasebe Takumu, Abe Masami, Hasebe Chitomi, Fujiya Mikihiro, Okumura Toshikat |
| Susceptibility to neurofibrillary tangles: role of the PTPRD locus and limited pleiotropy with other neuropathologies.
Molecular psychiatry 2017 Mar . Chibnik L B, White C C, Mukherjee S, Raj T, Yu L, Larson E B, Montine T J, Keene C D, Sonnen J, Schneider J A, Crane P K, Shulman J M, Bennett D A, De Jager P |
| Genetics of restless legs syndrome: An update. Sleep medicine reviews 2018 06 39 108-121. Jiménez-Jiménez Félix J, Alonso-Navarro Hortensia, García-Martín Elena, Agúndez José A |
| Genome-wide association analysis of common genetic variants of resistant hypertension.
The pharmacogenomics journal 2018 Sep . El Rouby Nihal, McDonough Caitrin W, Gong Yan, McClure Leslie A, Mitchell Braxton D, Horenstein Richard B, Talbert Robert L, Crawford Dana C, , Gitzendanner Matthew A, Takahashi Atsushi, Tanaka Toshihiro, Kubo Michiaki, Pepine Carl J, Cooper-DeHoff Rhonda M, Benavente Oscar R, Shuldiner Alan R, Johnson Julie |
| Association analysis of copy number variations in type 2 diabetes-related susceptible genes in a Chinese population. Acta diabetologica 2018 Jun . Yan Yu-Xiang, Li Jia-Jiang-Hui, Xiao Huan-Bo, Wang Shuo, He Yan, Wu Li-Ju |
| Genetic overlap between endometriosis and endometrial cancer: evidence from cross-disease genetic correlation and GWAS meta-analyses.
Cancer medicine 2018 May 7 (5): 1978-1987. Painter Jodie N, O'Mara Tracy A, Morris Andrew P, Cheng Timothy H T, Gorman Maggie, Martin Lynn, Hodson Shirley, Jones Angela, Martin Nicholas G, Gordon Scott, Henders Anjali K, Attia John, McEvoy Mark, Holliday Elizabeth G, Scott Rodney J, Webb Penelope M, Fasching Peter A, Beckmann Matthias W, Ekici Arif B, Hein Alexander, Rübner Matthias, Hall Per, Czene Kamila, Dörk Thilo, Dürst Matthias, Hillemanns Peter, Runnebaum Ingo, Lambrechts Diether, Amant Frederic, Annibali Daniela, Depreeuw Jeroen, Vanderstichele Adriaan, Goode Ellen L, Cunningham Julie M, Dowdy Sean C, Winham Stacey J, Trovik Jone, Hoivik Erling, Werner Henrica M J, Krakstad Camilla, Ashton Katie, Otton Geoffrey, Proietto Tony, Tham Emma, Mints Miriam, Ahmed Shahana, Healey Catherine S, Shah Mitul, Pharoah Paul D P, Dunning Alison M, Dennis Joe, Bolla Manjeet K, Michailidou Kyriaki, Wang Qin, Tyrer Jonathan P, Hopper John L, Peto Julian, Swerdlow Anthony J, Burwinkel Barbara, Brenner Hermann, Meindl Alfons, Brauch Hiltrud, Lindblom Annika, Chang-Claude Jenny, Couch Fergus J, Giles Graham G, Kristensen Vessela N, Cox Angela, Zondervan Krina T, Nyholt Dale R, MacGregor Stuart, Montgomery Grant W, Tomlinson Ian, Easton Douglas F, Thompson Deborah J, Spurdle Amanda |
| Targeted next generation sequencing in 112 Chinese patients with intellectual disability/developmental delay: novel mutations and candidate gene. BMC medical genetics 2019 5 20 (1): 80. Yan Huifang, Shi Zhen, Wu Ye, Xiao Jiangxi, Gu Qiang, Yang Yanling, Li Ming, Gao Kai, Chen Yinyin, Yang Xiaoping, Ji Haoran, Cao Binbin, Duan Ruoyu, Jiang Yuwu, Wang Jingm |
| Genetic Determinants of Circulating Glycine Levels and Risk of Coronary Artery Disease.
Journal of the American Heart Association 2019 May 8 (10): e011922. Jia Qiong, Han Yi, Huang Pin, Woodward Nicholas C, Gukasyan Janet, Kettunen Johannes, Ala-Korpela Mika, Anufrieva Olga, Wang Qin, Perola Markus, Raitakari Olli, Lehtimäki Terho, Viikari Jorma, Järvelin Marjo-Riitta, Boehnke Michael, Laakso Markku, Mohlke Karen L, Fiehn Oliver, Wang Zeneng, Tang W H Wilson, Hazen Stanley L, Hartiala Jaana A, Allayee Hoom |
| TOX3 gene variant could be associated with painful restless legs. Sleep medicine 2019 Jul 65 4-7. Karroum Elias G, Saini Prabhjyot S, Trotti Lynn M, Rye David |
| Effect of dietary calcium on the gender-specific association between polymorphisms in the PTPRD locus and osteoporosis.
Clinical nutrition (Edinburgh, Scotland) 2022 2 41 (3): 680-686. Bae Ji-Hyun, Park Dongj |
| Identification of single nucleotide polymorphisms (SNPs) associated with chronic graft-versus-host disease in patients undergoing allogeneic hematopoietic cell transplantation. Supportive care in cancer : official journal of the Multinational Association of Supportive Care in Cancer 2023 9 31 (10): 587. Jean-Luc C Mougeot, Micaela F Beckman, Allan J Hovan, Bengt Hasséus, Karin Garming Legert, Jan-Erik Johansson, Inger von Bültzingslöwen, Michael T Brennan, Farah Bahrani Mouge |
| Genome-wide association meta-analysis identifies 17 loci associated with nonalcoholic fatty liver disease. Nature genetics 2023 9 . Yanhua Chen, Xiaomeng Du, Annapurna Kuppa, Mary F Feitosa, Lawrence F Bielak, Jeffrey R O'Connell, Solomon K Musani, Xiuqing Guo, Bratati Kahali, Vincent L Chen, Albert V Smith, Kathleen A Ryan, Gudny Eirksdottir, Matthew A Allison, Donald W Bowden, Matthew J Budoff, John Jeffrey Carr, Yii-Der I Chen, Kent D Taylor, Antonino Oliveri, Adolfo Correa, Breland F Crudup, Sharon L R Kardia, Thomas H Mosley, Jill M Norris, James G Terry, Jerome I Rotter, Lynne E Wagenknecht, Brian D Halligan, Kendra A Young, John E Hokanson, George R Washko, Vilmundur Gudnason, Michael A Province, Patricia A Peyser, Nicholette D Palmer, Elizabeth K Speliot |
| Next-generation sequencing of uveal melanoma with clinical and histological correlations: Prognostic value of new mutations in the PI3K/AKT/mTOR pathway. Clinical & experimental ophthalmology 2023 10 . Manuel Pérez-Pérez, Alessandro Agostino, Carmen García de Sola-Llamas, Michael Ruvolo, Angel Vilches-Arenas, M Isabel Relimpio-López, Francisco Espejo-Arjona, Laura Macías-García, Manuel De Miguel-Rodríguez, Antonio García-Escudero, Miguel A Idoate, Juan J Ríos-Mart |
| PTPRD gene variant rs10739150: A potential game-changer in hypertension diagnosis. PloS one 2024 6 19 (6): e0304950. Laith Al-Eit |
| Genetic and prognostic analysis of blastoid and pleomorphic mantle cell lymphoma: a multicenter analysis in China. Annals of hematology 2024 1 . Ping Yang, Shuo-Zi Liu, Chun-Yuan Li, Wei-Long Zhang, Jing Wang, Ying-Tong Chen, Sen Li, Cui-Ling Liu, Hui Liu, Qing-Qing Cai, Wei Zhang, Hong-Mei Ji |
- Page last reviewed:Feb 1, 2024
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