Human Genome Epidemiology Literature Finder
Records 1 - 28 (of 28 Records) |
Query Trace: SORCS1[original query] |
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Assessment of Alzheimer's disease case-control associations using family-based methods. Neurogenetics 2009 Feb 10 (1): 19-25. Schjeide Brit-Maren M, McQueen Matthew B, Mullin Kristina, DiVito Jason, Hogan Meghan F, Parkinson Michele, Hooli Basavaraj, Lange Christoph, Blacker Deborah, Tanzi Rudolph E, Bertram La |
A genome-wide association study identifies a novel major locus for glycemic control in type 1 diabetes, as measured by both A1C and glucose. Diabetes 2010 Feb 59 (2): 539-49. Paterson Andrew D, Waggott Daryl, Boright Andrew P, Hosseini S Mohsen, Shen Enqing, Sylvestre Marie-Pierre, Wong Isidro, Bharaj Bhupinder, Cleary Patricia A, Lachin John M, , Below Jennifer E, Nicolae Dan, Cox Nancy J, Canty Angelo J, Sun Lei, Bull Shelley B, |
Systematic analysis of candidate genes for Alzheimer's disease in a French, genome-wide association study. Journal of Alzheimer's disease : JAD 2010 20 (4): 1181-8. Laumet Geoffroy, Chouraki Vincent, Grenier-Boley Benjamin, Legry Vanessa, Heath Simon, Zelenika Diana, Fievet Nathalie, Hannequin Didier, Delepine Marc, Pasquier Florence, Hanon Olivier, Brice Alexis, Epelbaum Jacques, Berr Claudine, Dartigues Jean-Francois, Tzourio Christophe, Campion Dominique, Lathrop Mark, Bertram Lars, Amouyel Philippe, Lambert Jean-Charl |
Rare copy number variation discovery and cross-disorder comparisons identify risk genes for ADHD. Science translational medicine 2011 Aug 3 (95): 95ra75. Lionel Anath C, Crosbie Jennifer, Barbosa Nicole, Goodale Tara, Thiruvahindrapuram Bhooma, Rickaby Jessica, Gazzellone Matthew, Carson Andrew R, Howe Jennifer L, Wang Zhuozhi, Wei John, Stewart Alexandre F R, Roberts Robert, McPherson Ruth, Fiebig Andreas, Franke Andre, Schreiber Stefan, Zwaigenbaum Lonnie, Fernandez Bridget A, Roberts Wendy, Arnold Paul D, Szatmari Peter, Marshall Christian R, Schachar Russell, Scherer Stephen |
Evaluation of four novel genetic variants affecting hemoglobin A1c levels in a population-based type 2 diabetes cohort (the HUNT2 study). BMC medical genetics 2011 12 (1): 20. Hertel Jens K, Johansson Stefan, Ræder Helge, Platou Carl G P, Midthjell Kristian, Hveem Kristian, Molven Anders, Njølstad Pål |
SORCS1 alters amyloid precursor protein processing and variants may increase Alzheimer's disease risk. Annals of neurology 2011 Jan 69 (1): 47-64. Reitz Christiane, Tokuhiro Shinya, Clark Lorraine N, Conrad Christopher, Vonsattel Jean-Paul, Hazrati Lili-Naz, Palotás András, Lantigua Raphael, Medrano Martin, Z Jiménez-Velázquez Ivonne, Vardarajan Badri, Simkin Irene, Haines Jonathan L, Pericak-Vance Margaret A, Farrer Lindsay A, Lee Joseph H, Rogaeva Ekaterina, George-Hyslop Peter St, Mayeux Richa |
Genetics of late-onset Alzheimer's disease: update from the alzgene database and analysis of shared pathways. International journal of Alzheimer's disease 2011 2011 . Olgiati P, Politis AM, Papadimitriou GN, De Ronchi D, Serretti A |
A Multinomial Ordinal Probit Model with Singular Value Decomposition Method for a Multinomial Trait. Journal of probability and statistics 2012 2012 . Kwon Soonil, Goodarzi Mark O, Taylor Kent D, Cui Jinrui, Chen Y-D Ida, Rotter Jerome I, Hsueh Willa, Guo Xiuqi |
SORCS1 and APOE polymorphisms interact to confer risk for late-onset Alzheimer's disease in a Northern Han Chinese population. Brain research 2012 Apr 1448 111-6. Wang Hui-Fu, Yu Jin-Tai, Zhang Wei, Wang Wei, Liu Qiu-Yan, Ma Xiao-Ying, Ding Hua-Min, Tan L |
SORCS1 contributes to the development of renal disease in rats and humans. Physiological genomics 2013 Aug 45 (16): 720-8. Lazar Jozef, O'Meara Caitlin C, Sarkis Allison B, Prisco Sasha Z, Xu Haiyan, Fox Caroline S, Chen Ming-Huei, Broeckel Ulrich, Arnett Donna K, Moreno Carol, Provoost Abraham P, Jacob Howard |
The genetic variation of SORCS1 is associated with late-onset Alzheimer's disease in Chinese Han population. PloS one 2013 8 (5): e63621. Xu Wei, Xu Jun, Wang Ying, Tang Huidong, Deng Yulei, Ren Rujing, Wang Gang, Niu Wenquan, Ma Jianfang, Wu Yiwen, Zheng Jialin, Chen Shengdi, Ding Jianqi |
Independent and epistatic effects of variants in VPS10-d receptors on Alzheimer disease risk and processing of the amyloid precursor protein (APP). Translational psychiatry 2013 3 e256. Reitz C, Tosto G, Vardarajan B, Rogaeva E, Ghani M, Rogers R S, Conrad C, Haines J L, Pericak-Vance M A, Fallin M D, Foroud T, Farrer L A, Schellenberg G D, George-Hyslop P S, Mayeux R, |
Sortilin-related VPS10 domain containing receptor 1 and Alzheimer's disease-associated allelic variations preferentially exist in female or type 2 diabetes mellitus patients in southern Han Chinese. Psychogeriatrics : the official journal of the Japanese Psychogeriatric Society 2012 Dec 12 (4): 4. He Y, Fang Z, Yu G |
Genome-wide association study identifies new disease loci for isolated clubfoot.
Journal of medical genetics 2014 May 51 (5): 334-9. Zhang Tian-Xiao, Haller Gabe, Lin Peng, Alvarado David M, Hecht Jacqueline T, Blanton Susan H, Stephens Richards B, Rice John P, Dobbs Matthew B, Gurnett Christina |
The A-B-C for SORting APP. Journal of neurochemistry 2015 Oct 135 (1): 1-3. Coulson Elizabeth J, Andersen Olav |
Effects of genetic variation on the dynamics of neurodegeneration in Alzheimer's disease. Annual International Conference of the IEEE Engineering in Medicine and Biology Society. IEEE Engineering in Medicine and Biology Society. Annual International Conference 2014 2014 2464-7. Printy Blake P, Verma Nishant, Cowperthwaite Matthew C, Markey Mia K, |
SORCS1 polymorphism and insulin secretion in obese women with polycystic ovary syndrome. Gynecological endocrinology : the official journal of the International Society of Gynecological Endocrinology 2016 32 (5): 395-8. Hrovat Ana, Kravos Nika Aleksandra, Gori?ar Katja, Jensterle Sever Mojca, Janež Andrej, Dolžan Vi |
The common variants implicated in microstructural abnormality of first episode and drug-naïve patients with schizophrenia.
Scientific reports 2017 Sep 7 (1): 11750. Ren H Y, Wang Q, Lei W, Zhang C C, Li Y F, Li X J, Li M L, Deng W, Huang C H, Du F, Zhao L S, Wang Y C, Ma X H, Hu X, Li |
Genetic determinants of impaired awareness of hypoglycemia in type 1 diabetes. Pharmacogenetics and genomics 2017 Jul . Schouwenberg Bas J, Coenen Marieke J, Paterson Andrew D, Tack Cees J, Smits Paul, Kramers Cornelis, de Galan Bastiaan |
Heritability and genome-wide association study of benign prostatic hyperplasia (BPH) in the eMERGE network.
Scientific reports 2019 Apr 9 (1): 6077. Hellwege Jacklyn N, Stallings Sarah, Torstenson Eric S, Carroll Robert, Borthwick Kenneth M, Brilliant Murray H, Crosslin David, Gordon Adam, Hripcsak George, Jarvik Gail P, Linneman James G, Devi Parimala, Peissig Peggy L, Sleiman Patrick A M, Hakonarson Hakon, Ritchie Marylyn D, Verma Shefali Setia, Shang Ning, Denny Josh C, Roden Dan M, Velez Edwards Digna R, Edwards Todd |
Type 2 diabetes-associated single nucleotide polymorphism in Sorcs1 gene results in alternative processing of the Sorcs1 protein in INS1 ß-cells. Scientific reports 2019 Dec 9 (1): 19466. Yau Belinda, Blood Zachary, An Yousun, Su Zhiduan, Kebede Melkam |
Novel Alzheimer's disease risk variants identified based on whole-genome sequencing of APOE ?4 carriers.
Translational psychiatry 2021 May 11 (1): 296. Park Jong-Ho, Park Inho, Youm Emilia Moonkyung, Lee Sejoon, Park June-Hee, Lee Jongan, Lee Dong Young, Byun Min Soo, Lee Jun Ho, Yi Dahyun, Chung Sun Ju, Park Kye Won, Choi Nari, Kim Seong Yoon, Yoon Woon, An Hoyoung, Kim Ki Woong, Choi Seong Hye, Jeong Jee Hyang, Kim Eun-Joo, Kang Hyojin, Lee Junehawk, Kim Younghoon, Lee Eunjung Alice, Seo Sang Won, Na Duk L, Kim Jong-W |
Identification of Genetic Variants in 65 Obesity Related Genes in a Cohort of Portuguese Obese Individuals. Genes 2021 4 12 (4): . Ginete Catarina, Serrasqueiro Bernardo, Silva-Nunes José, Veiga Luísa, Brito Migu |
Genome-wide association study of fasting proinsulin, fasting insulin, 2-hour postprandial proinsulin, and 2-hour postprandial insulin in Chinese Han people.
Endokrynologia Polska 2022 8 . Lin Leweihua, Quan Huibiao, Fang Tuanyu, Lin Lu, Ou Qianying, Zhang Huachuan, Chen Kaining, Zhou Zhigua |
Targeted Exome Sequencing of Genes Involved in Rare CNVs in Early-Onset Severe Obesity. Frontiers in genetics 2022 3 13 839349. Loid Petra, Pekkinen Minna, Mustila Taina, Tossavainen Päivi, Viljakainen Heli, Lindstrand Anna, Mäkitie Ou |
Genome-wide association study of brain arteriolosclerosis. Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism 2022 Feb 271678X211066299. Shade Lincoln Mp, Katsumata Yuriko, Hohman Timothy J, Nho Kwangsik, Saykin Andrew J, Mukherjee Shubhabrata, Boehme Kevin L, Kauwe John Sk, Farrer Lindsay A, Schellenberg Gerard D, Haines Jonathan L, Mayeux Richard P, Schneider Julie A, Nelson Peter T, Fardo David |
Whole Exome Sequencing in Multi-Incident Families Identifies Novel Candidate Genes for Multiple Sclerosis. International journal of molecular sciences 2022 10 23 (19): . Horjus Julia, van Mourik-Banda Tineke, Heerings Marco A P, Hakobjan Marina, De Witte Ward, Heersema Dorothea J, Jansen Anne J, Strijbis Eva M M, de Jong Brigit A, Slettenaar Astrid E J, Zeinstra Esther M P E, Hoogervorst Erwin L J, Franke Barbara, Kruijer Wiebe, Jongen Peter J, Visser Leo J, Poelmans Gee |
The Association of Selected GWAS Reported AD Risk Loci with CSF Biomarker Levels and Cognitive Decline in Slovenian Patients. International journal of molecular sciences 2023 8 24 (16): . David Vogrinc, Milica Gregori? Kramberger, Andreja Emerši?, Saša ?u?nik, Katja Gori?ar, Vita Dolž |
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